Schizophrenia: Clinical Guidelines

Applies tochildren2024 editionF20.0, F20.1, F20.2, F20.3…

Clinical Guidelines of the Russian Ministry of Health, Pediatrics. 2024 edition, ICD-10 codes: F20.0, F20.1, F20.2, F20.3….

Receive research articles on «Schizophrenia»Every morning — fresh PubMed studies on this topic and specialty: in Russian, with numbers, sample size, and conclusions. Plus updates to Russian clinical guidelines.

Subscribe for 990 ₽

Brief for Practice

WhiteCoat Pro editorial summary based on the 2024 guideline text. Each item links to the original section — verify against it before prescribing.

Schizophrenia is a mental disorder characterized by a combination of positive, negative, cognitive, and behavioral symptoms; it may onset in childhood and follow an episodic or continuous course. These guidelines focus on the diagnosis and comprehensive treatment of children and adolescents: antipsychotics are the mainstay of therapy, while maintenance treatment, rehabilitation, and social functioning monitoring are essential after exacerbation is controlled.

Key points

Diagnostics

  1. Collect subjective and objective anamnesis from the child and parents: family psychiatric history, course of pregnancy and childbirth, early development, education, social adaptation, symptom dynamics, previous treatment, and its tolerability (Level of Reliability of Evidence: B, Level of Evidence: 2). → in text
  2. Perform an initial examination by a child psychiatrist to compare the anamnesis and current psychopathological picture with ICD-10 criteria (Level of Reliability of Evidence: B, Level of Evidence: 2). → in text
  3. Perform a clinical and psychological psychodiagnostic assessment to evaluate higher mental functions and subsequently plan psychocorrection and rehabilitation (Level of Reliability of Evidence: C, Level of Evidence: 5). → in text
  4. Verify diagnostic criteria: psychotic, catatonic, negative, speech, or behavioral symptoms must meet the required combination and persist for at least 1 month. → in text
  5. If substance use is suspected, involve a pediatric addiction psychiatrist to rule out a substance-induced psychotic episode (Level of Reliability of Evidence: C, Level of Evidence: 5). → in text
  6. Perform pediatric and neurological examinations to identify somatic and neurological pathology, as well as contraindications and therapy risks (Level of Reliability of Evidence: C, Level of Evidence: 5). → in text
  7. Include a complete blood count, urinalysis, and blood biochemistry in the initial examination, hospitalization workup, and follow-up (Level of Reliability of Evidence: C, Level of Evidence: 5). → in text
  8. Before initiating therapy, perform an EEG and neuroimaging according to indications; in diagnosed schizophrenia, perform an ECG with exercise to assess the safety of psychopharmacotherapy, especially given the risk of QT prolongation (Level of Reliability of Evidence: C, Level of Evidence: 4). → in text

Treatment

When to refer and how to monitor

Frequently asked questions

What symptoms allow for the diagnosis of schizophrenia according to ICD-10?

At least one distinct symptom from the groups of mental automatism, delusions of control, characteristic hallucinations, or persistent inappropriate delusions is required, or two less distinct symptoms from these groups; an option with two symptoms from other diagnostic groups is also possible. Symptoms must persist for at least 1 month. → in text

Are MRI and EEG necessary to confirm schizophrenia?

No, there is no specific instrumental diagnostic method for schizophrenia. MRI, CT, and EEG are prescribed according to clinical or anamnestic indications for differential diagnosis and risk assessment. → in text

How long should antipsychotic therapy be continued after psychosis resolution?

Maintenance therapy per the guidelines should continue for at least 1 year. If there is no effect within 4–6 weeks, the drug is replaced, provided it is well tolerated and prescribed at the optimal therapeutic dose. → in text

When is clozapine used in childhood schizophrenia?

Clozapine is indicated for suicide risk and resistance to other antipsychotics; the specified dose is 25–400 mg/day. The goals are the prevention of suicidal behavior and enhancement of treatment efficacy (Level of Reliability of Evidence: A, Level of Evidence: 1). → in text

When should a child with schizophrenia be hospitalized?

The main indications are the risk of suicide or harm to oneself and others, severe agitation and aggression, severe psychotic disorganization, a newly established diagnosis requiring a comprehensive examination, severe somatic pathology, ineffectiveness or poor tolerability of outpatient therapy, unavailability of adequate outpatient care, and the inability to meet basic living needs due to severe social maladjustment. → in the text

Status
Applied · approved by the Scientific and Practical Council of the Russian Ministry of Health
Database ID
674, edition 3 (ID 674_3)
Publication date
September 18, 2024
Age category
children
ICD-10 codes
F20.0F20.1F20.2F20.3F20.5F20.6F20.8F20.9
Specialties
PsychiatryPediatrics
Developers
Public Organization "Russian Society of Psychiatrists"
Official text
Russian Ministry of Health Guidelines — 674_3

List of Abbreviations

DSM-5 - Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition

PANSS - Positive and Negative Syndrome Scale

PSP - Personal and Social Performance Scale

SCI - Structured Clinical Interview

AT - autogenic training

ATC - Anatomical Therapeutic Chemical (Classification)

WHO — World Health Organization

GABA - gamma-aminobutyric acid

CBT - cognitive behavioral therapy

CG – clinical guidelines

CT — computed tomography

ICD-10 - International Classification of Diseases, 10th Revision

PET - Positron emission tomography

RCT - randomized controlled trial

RPS - Russian Society of Psychiatrists

SSRI - selective serotonin reuptake inhibitor

LoE – level of evidence

LER — level of evidence and recommendation

FSI - Federal State Budgetary Institution

fMRI - functional magnetic resonance imaging

SZ - schizophrenia

ECG - electrocardiography

EEG - electroencephalography

Terms and Definitions

Verschrobene-type defect - (from German *verschrobene* – "eccentric") – negative personality changes progressing over the course of schizophrenia, including oddness, eccentricity, emotional coldness, and a tendency to form overvalued ideas.

Progredience - the rate of accumulation of negative symptoms in the clinical picture of schizophrenia, determining the nature of personality and cognitive changes within the structure of the defect.

Mental dysontogenesis - a disorder of mental development as a whole or of its individual components, a disruption in the pace and timing of the development of specific mental spheres and their components.

Kandinsky-Clerambault syndrome - hallucinatory-paranoid syndrome or syndrome of psychic automatism, including delusions of persecution and influence, phenomena of psychic automatism, and pseudohallucinations.

Screening - the collection of information (typically via questionnaires) to identify a specific risk group from the general population, assess their need for further in-depth clinical diagnosis and necessary therapeutic/rehabilitative care (without precise qualification) based on key indicators of mental disorders. Screening is performed by primary care specialists (pediatricians, neurologists, medical psychologists).

1. Brief information on the disease or condition

1.1 Definition of the disease or condition

Schizophrenia (hereinafter referred to as SZ) is a mental disorder characterized by a combination of productive (hallucinatory-delusional, catatonic-hebephrenic, affective, etc.) and negative (apathy, abulia, alogia, emotional and social withdrawal, etc.) symptoms, behavioral and cognitive impairments (memory, attention, thinking, etc.), leading to adverse social and economic consequences. SZ can develop at various ages, including in childhood.

Schizophrenic disorders in childhood are typically accompanied by significant and characteristic distortions of thinking and perception, as well as inappropriate affect. Clear consciousness and intellectual abilities are usually preserved, although a certain decline in cognitive functions may occur over time. Crucial psychopathological symptoms include the experience of thought echo, thought insertion or withdrawal, and thought broadcasting; delusional perception and delusions of external control; inertia; auditory hallucinations commenting on or discussing the patient in the third person; loosening of associations and negativism symptoms. The course of schizophrenic disorders can be continuous or episodic, with progression or stabilization of deficits; it may consist of one or several episodes of the illness with complete or incomplete remission [1].

Comment: the definitions of SZ have changed depending on the prevailing concept of SZ and the paradigm of its perception by physicians and researchers. In the definition given above (based on ICD-10), the primary features of schizophrenia are impairments of the thought process and perceptual disturbances. In the 20th century, the definition by A.V. Snezhnevsky was considered classic: "SZ is a progressive mental illness characterized by the dissociation of mental functions, i.e., the loss of unity of mental processes with rapidly or slowly developing personality changes of a specific type (decreased energy potential, progressive introversion, emotional impoverishment) and diverse productive psychopathological disorders" [2]. Thus, the core elements in understanding schizophrenia were its process-like course and personality deformation, with a predominance of negative symptoms. In ICD-11, schizophrenia is defined differently: "Schizophrenia is characterized by disturbances in multiple mental modalities, including thinking (e.g., delusions, derailment of thought processes), perception (e.g., hallucinations), self-experience (e.g., the experience that one's feelings, impulses, thoughts, or behavior are under the control of an external force), cognition (e.g., deficits in attention, verbal memory, and social cognition), volition (e.g., loss of motivation), affect (e.g., blunted emotional responsiveness), and behavior (e.g., behavior that appears odd or purposeless or is disrupted in connection with unpredictable or inappropriate emotional responses). Psychomotor disturbances, including catatonia, may be present. Persistent delusions, persistent hallucinations, thinking disturbances, and experiences of passivity, influence, or control are considered core symptoms" [3]. Thus, the spectrum of manifestations of SZ in this definition is significantly expanded, with a particular emphasis on phenomena of psychic automatism, thought disorders, and perceptual disturbances. These clinical guidelines have been prepared in accordance with ICD-10 in effect in the Russian Federation at the time of their writing.

1.2 Etiology and pathogenesis of the disease or condition (group of diseases or conditions)

Schizophrenia is presumed to be a polyetiological disease, the etiology and pathogenesis of which remain unknown to date. There are a large number of theories and hypotheses regarding its origin, which to varying degrees emphasize various hereditary factors and environmental influences.

Numerous studies postulate a high role of hereditary pathology in the origin of schizophrenia [4]. Inheritance is complex and polygenic in nature, and the manifestation of the disease likely depends on the accumulation of pathological factors across generations, which at a certain point collectively reach a critical threshold. Convincing evidence of the role of heredity in the origin of schizophrenia is provided by genealogical and twin studies [5, 6]. At the same time, it is generally accepted that in half of schizophrenia cases, de novo mutations play a leading role, which are absent in the genome of the patient's parents.

The so-called dopamine hypothesis of schizophrenia, which arose as a consequence of studying the antipsychotic action of neuroleptics, is dedicated to explaining the mechanism of realization of genetic pathology in schizophrenia [7]. Studies have shown that patients with schizophrenia have an increased concentration of dopamine in a number of brain regions [8]. Similar hypotheses have also been advanced regarding the role of glutamate and dysfunctions in GABAergic and cholinergic neurotransmitter systems [9].

Modern neuroimaging methods, primarily PET-CT and fMRI, have revealed numerous changes in the structure and functional characteristics of the brain in patients with schizophrenia. Findings include gray matter degradation, ventricular enlargement, and altered functional activity of the frontal and temporal lobes, as well as the hippocampus [10, 11, 12]. However, it has not been proven that these changes are not associated, for example, with the use of psychotropic medications, alcohol, or the consequences of a sedentary and cognitively impoverished lifestyle.

Numerous social factors, such as poverty, migration, urbanization, physical (including sexual) and emotional abuse in childhood, insufficient emotional support from parents, loneliness, as well as socially conditioned factors such as alcoholism and marijuana use, have been studied over the past half-century, but none of them has shown a convincing causal relationship with the onset of schizophrenia [13].

In recent years, the autoimmune theory has become an established theory of the origin of schizophrenia, combining hypotheses of a selective inflammatory process as the cause of damage to a number of brain cells (or, in a broader context, structures) and neurodysontogenesis [14, 15].

Most researchers attribute the difficulties in identifying the causes and pathogenetic mechanisms of schizophrenia to the well-known blurriness of the boundaries of the schizophrenia spectrum disorder continuum and the non-specificity of most recorded symptoms and syndromes. In particular, in cases of childhood-onset schizophrenia and schizoaffective disorder, diagnostic discrepancies between the first and second examinations could reach up to 50% of cases [16], which precludes the uniformity so essential for research. It is also impossible to rule out the hypothesis that schizophrenia represents several closely related states that are difficult to distinguish clinically, yet have different etiologies (e.g., mutations in various genes or groups of genes) and pathogenesis.

1.3 Epidemiology of the Disease or Condition

According to the World Health Organization (WHO), 0.3% to 0.7% of people worldwide suffer from schizophrenia. At the same time, data indicate that morbidity rates can vary significantly depending on the calculation methods used. Prevalence and incidence may fluctuate considerably depending on age, sex, ethnicity, and place of residence, including in the Russian Federation [17, 27]. It is known that men are affected on average 1.4 times more often than women, with this difference being driven primarily by the age group under 30 [18]. Schizophrenia is rare in childhood [19], with the proportion of individuals developing childhood-onset schizophrenia being less than 1% [20] (according to other authors, up to 4%) [21]. Among children recognized as disabled due to mental disorders in Russia, children with schizophrenia account for 4.4% [22]. According to epidemiological data for 2018 in Russia, the overall incidence rate of schizophrenia in children increased by 6.5%, from 13.53 per 100,000 population in 2000 to 14.41 per 100,000 population in 2018, while in the adolescent group, the incidence rate of schizophrenia increased by 44.7%, from 54.61 per 100,000 population in 2000 to 79.03 per 100,000 population in 2018 [23]. However, the reasons for such a significant increase in statistical indicators may not be directly related to an increase in the number of cases.

According to 2019 data, Russia has seen a steady increase in the incidence of psychoses and dementia states in children under 14 (by 50% since 1995), and a 70% increase in morbidity. Schizophrenia morbidity among the pediatric population also tended to increase from 1995 to 2010 (by 70%), with a slight decrease (by 20%) observed in recent years. However, the number of children registered with this diagnosis remains one-third higher than it was 20 years ago. The incidence of childhood schizophrenia grew until 2008 and subsequently declined. In 2017, the diagnosis of schizophrenia was established for the first time in life in 300,000 children. There is also a steady upward trend in the population of patients with schizophrenia aged 15–17 years. While in 1995 there were 53.3 per 100,000 adolescents, by 2016 their number had increased by 50% to 75.1 cases per 100,000 adolescents. Compared to 2000, overall morbidity rates for psychoses and dementia among adolescents have also increased (from 152 to 162 cases per 100,000 adolescents). It is possible that some of these cases are attributable to schizophrenia [24].

1.4 Features of Coding the Disease or Condition

Neither ICD-10 nor DSM-5 contains a specific category for schizophrenia developing in children or adolescents. The view is expressed that since the clinical presentation of adult and childhood-onset schizophrenia is identical, childhood schizophrenia should not be a separate disorder [25]. In the version of ICD-10 adapted for use in the Russian Federation, the childhood type of schizophrenia is included under code F20.8 (other schizophrenia), with the specific code F20.8xx3. This subcategory includes cases of schizophrenia that begin in childhood and are characterized by a specific and polymorphic clinical presentation. It also includes early-childhood cases of schizophrenia with a pronounced oligophrenia-like defect (due to severe mental retardation similar to oligophrenia) [26]. According to studies, up to 50% of early-onset schizophrenia cases (onset before age 13) are comorbid with autism spectrum disorder [202, 203].

Thus, Chapter V of ICD-10, adapted for use in the Russian Federation, includes the following categories:

F20.0 - Paranoid schizophrenia

F20.1 - Hebephrenic schizophrenia

F20.2 - Catatonic schizophrenia

F20.3 - Undifferentiated schizophrenia

F20.5 - Residual schizophrenia

F20.6 - Simple schizophrenia

F20.8 - Other schizophrenia, including F20.8xx3 - childhood schizophrenia

F20.9 - Schizophrenia, unspecified

Comment: ICD-11 does not provide for the subdivision of schizophrenia into subtypes.

It provides for the identification of a first episode of schizophrenia (current state, partial remission, full remission), multiple episodes of schizophrenia (current state, partial remission, full remission), and continuous course. Thus, the symptomatology of psychosis characterized as an episode of schizophrenia will not be relevant within the framework of ICD-11 [3].

1.5 Classification of the disease or condition

For the classification and diagnosis of schizophrenia in both adults and children, two main classifications with international status are currently used worldwide: ICD-10, issued under the auspices of the WHO, and the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5), developed by the American Psychiatric Association. Russia uses Chapter V of ICD-10 adapted for use in the Russian Federation [1]. The diagnostic and classification categories used in ICD-10 are provided in Section 1.4 of these clinical guidelines.

Comments: traditional classifications of schizophrenia dating back to the times of E. Kraepelin and E. Bleuler, which in Russian psychiatry were most fully developed by A.V. Snezhnevsky and his pupils and colleagues [29], have not lost their relevance to this day. Thanks to the classical clinical approach, ICD-10 retains clinical forms of schizophrenia and takes into account the type of course, while research and clinical practice pay significant attention to such factors as the features of the course and therapy of the first episode, positive and negative symptoms, as well as affective and cognitive disorders within the clinical presentation of schizophrenia. In fact, it is precisely these features that determine such high variability of individual cases within the general continuum of schizophrenia spectrum disorders. The modern centrifugal trend present in the structure of ICD-10 and DSM-5, which led to the formation of independent diagnostic categories such as schizotypal disorder (latent schizophrenia, neurosis-like schizophrenia) or schizoaffective disorder, also has a flip side, manifested in the creation within DSM-5 of the category "schizophrenia spectrum and other psychotic disorders," indicating the etiopathogenetic and clinical affinity of these forms of mental pathology [30], even though certain forms of schizophrenia were removed from the classification

1.6 Clinical presentation of the disease or condition

The clinical presentation of schizophrenia is extremely polymorphic and may include various symptoms and syndromes of greater or lesser specificity. There are no absolute pathognomonic symptoms that allow for a definitive diagnosis of schizophrenia. In all cases, symptoms and syndromes are evaluated comprehensively. ICD-10 uses the following general criteria for diagnosing schizophrenia [1]:

1. Thought echo, thought insertion or withdrawal, and thought broadcasting;

2. Delusions of control, influence, or passivity, referred to body movements or specific limbs, thoughts, actions, or sensations; delusional perception;

3. Hallucinatory voices commenting on the patient's behavior or discussing them among themselves, or other types of hallucinatory voices coming from some part of the body;

4. Persistent delusions of other kinds that are culturally inappropriate and completely implausible in content;

5. Persistent hallucinations in any modality, when accompanied by fleeting or half-formed delusions without clear affective content, or persistent overvalued ideas that may occur daily for weeks or months;

6. Breaks or interpolations in the train of thought, resulting in incoherence or irrelevant speech, or neologisms;

7. Catatonic symptoms, such as undifferentiated, sometimes stereotyped excitement, impulsive actions, posturing or waxy flexibility, negativism, mutism, and stupor; exaggerated mannerisms and grimacing are also possible;

8. "Negative" symptoms, such as marked apathy, speech poverty, blunted or inappropriate emotional responses, typically leading to social withdrawal and reduced social productivity; these signs are not due to depression or drug-induced neuroleptic side effects;

9. A significant and consistent qualitative change in behavior, manifested by loss of interests, aimlessness, inactivity, self-absorption, and social withdrawal.

To diagnose schizophrenia, at least one clear symptom (or two less distinct symptoms) belonging to items 1-4 listed above, or two symptoms belonging to items 5-9, must be present for a duration of at least one month.

ICD-10 proposes both general diagnostic criteria (see above) and specific criteria required for diagnosing individual forms of schizophrenia (see sections 1.4 and 1.5 of these clinical guidelines).

Comment: childhood-onset schizophrenia has a number of features that distinguish its clinical presentation from the typical adult pattern. Clinical manifestations of schizophrenia in children are divided into 2 groups: (1) symptoms and syndromes characteristic of schizophrenia (catatonic, hebephrenic, hallucinatory, delusional, psychopathy-like, affective, etc.), which in children are characterized by fragmentation, rudimentariness, incompleteness of individual components and the entire syndrome as a whole, transitoriness, and variability; (2) syndromes characteristic of childhood (fears, fantasies, speech disorders) and adolescence (dysmorphophobia, anorexia acquiring the features of delusional conviction), differing in comparison with similar symptoms observed in children with other mental illnesses by a specific shade caused by schizophrenia. They may be atypical, grotesque, bizarre, absurd. Symptoms of schizophrenic defect in patients develop in parallel with the psychophysical development continuing against the background of the disease. Thus, in childhood schizophrenia with a continuous course type, manifestations of mental underdevelopment resembling intellectual deficit in mental retardation—the so-called "oligophrenia-like" defect—may appear in the defect symptoms alongside traits of a specific emotional and volitional impairment.

The diagnosis of paranoid schizophrenia (F20.0) is made when the clinical picture is dominated by delusions (persecution, reference, significance, jealousy, special mission, etc.) and perceptual disturbances, typically true auditory and pseudohallucinations (threatening, commenting, or insulting hallucinatory "voices" or non-verbalized sounds such as noise, whistling, knocking; visual, gustatory, and tactile hallucinations are less common; cenesthopathies are possible). In paranoid schizophrenia, speech disorders, emotional disturbances, and catatonia may occur, but do not typically occupy a dominant position in the clinical picture.

Comment: paranoid schizophrenia, generally similar to that in adults, is extremely rare in preschool age; as a rule, it develops no earlier than 7-9 years of age. In children, paranoid schizophrenia is characterized by high polymorphism and rudimentariness of psychopathological syndromes, poverty and monotony of affective manifestations, and rapid shifts of states. Paranoid schizophrenia can progress continuously (continuous form) or episodically (episodic-progressive form). In the first variant, the clinical picture in children (9-10 years) is dominated by syndromes of delusion-like fantasizing, often transforming into delusions of imagination, sometimes with pseudohallucinations. Delusions of imagination, in the structure of which confabulations occupy a significant place—"retrograde mythomania"—are less common. Hallucinations are typically rudimentary and unstable, characterized by fragmentation and a peculiar separation of hallucinatory images. They are combined with a sense of hostility and alienation, approaching pseudohallucinations, which gives grounds to consider them a component of the mental automatism syndrome. At the age of 15-18, the clinical picture of manifest forms of paranoid schizophrenia becomes more similar to that described in adults.

The diagnosis of hebephrenic schizophrenia (F20.1) is made when the clinical picture is dominated by gross affective disturbances (inappropriate, absurd, mannered reactions), thought and speech disorganization, and volitional disturbances manifested in bizarre, aimless, senseless behavior. Hallucinations and delusions do not dominate the clinical picture; they are fragmented and rudimentary. Hebephrenic schizophrenia is characteristic of adolescence.

Comment: in the early-onset hebephrenic form, the primary manifestations are silliness with grimacing, absurd actions, increased readiness for communication against the background of mutism, pronounced exposure of drives, impulsive destructive actions, and hypomanic states with phenomena of attention hypermetamorphosis.

In catatonia-type schizophrenia (F20.2), the dominant manifestations in the clinical picture are catatonic psychomotor disorders, manifested in their extreme forms by stupor or raptus, negativism, or automatic obedience. For the diagnosis, along with the general criteria for schizophrenia, the following are required: (1) stupor or mutism, (2) motor excitement not controlled by the patient and unresponsive to external stimuli, (3) freezing in inadequate, bizarre postures, (4) negativism or rigidity, (5) waxy flexibility or other symptoms. It should be noted that catatonic manifestations per se are not specific to schizophrenia, and without other criteria for schizophrenia, the diagnosis of the catatonic form is not made.

Comment: the catatonic form of schizophrenia is frequently encountered in preschool age. Children are characterized by specific catatonic symptoms such as vocalisms (outcries), stereotyped movements, walking on tiptoe, running in circles, and spinning in place. Catatonic schizophrenia in children is accompanied by severe behavioral disturbances (eating disorders, sleep-wake cycle disruptions) and regression of higher mental functions, with the loss of acquired knowledge and skills.

The diagnostic category "Undifferentiated schizophrenia (F20.3)" is used when the observed clinical picture meets the general criteria for schizophrenia but does not fully correspond to any of the above categories, nor to residual schizophrenia. Residual schizophrenia (F20.5) is a chronic stage (the so-called "end-state") of schizophrenia, when several acute episodes or a continuous course dominated by positive psychotic symptoms are replaced by a period of persistent negative symptoms ("defect"). Simple schizophrenia (F20.6) is diagnosed when pronounced negative symptoms develop insidiously without preceding distinct psychotic episodes.

The diagnostic category "Residual schizophrenia (F20.5)" is used when the observed clinical picture is represented mainly by negative symptoms (speech poverty, emotional flattening, impoverished facial expressions, decreased activity, motor slowing, marked reduction in social productivity, and diminished self-care skills) occurring after previous psychotic episodes that met the criteria for schizophrenia.

Comment: the diagnosis of residual schizophrenia corresponds to the traditional concept of a "persistent schizophrenic defect"

The diagnostic category "Simple schizophrenia (F20.6)" is used in the presence of a progressive character of the mental disorder, eventually leading to the formation of a "persistent schizophrenic defect" without preceding distinct hallucinatory, delusional, or catatonic symptoms. The patient's behavior is characterized by pronounced social withdrawal, aimlessness, inactivity, and loss of interests.

Comment: when adapting ICD-10 (1999) in the Russian Federation, the category "Other type of schizophrenia (F20.8)" includes "Childhood-type schizophrenia (F20.8xx3)", which manifests in childhood and is characterized by specific age-related peculiarities, polymorphism of the clinical picture, malignant course, and an oligophrenia-like defect. The clinical picture of childhood schizophrenia is significantly influenced by the course type (coded by the fifth character in ICD-10). In malignant continuous schizophrenia (F20.x0) the initial period is marked by alienation from close relatives, decreased interest in the environment, and lethargy combined with irritability and stubbornness. The clinical picture of manifest states is dominated by catatonic excitation or stupor, and subcortical motor stereotypies. Manege-like running, jumping in place, jactitation, grimacing, wing-like arm flapping, clapping, and "vermiform movements" of the fingers displace purposeful movements. Catatonic manifestations are accompanied by symptoms of gross regression of higher mental functions. An oligophrenia-like defect in patients begins to form as early as the manifest period of the disease and persists throughout life [32]. With partial reduction of catatonia, psychopathy-like manifestations emerge in the form of impulsive aggression toward others, auto-aggression, and eating disorders.

Fecal retention in patients is accompanied by bizarre methods of defecation and manipulation of feces. Subsequently, negative symptoms increase—decreased energy potential, passivity, fatiguability, autization, emotional impoverishment, and thought disorders. In episodic type with a progressive defect (F20.x1) Traditionally, several clinical courses are distinguished. In the (1) catatonic variant, the premanifest stage is characterized by autistic dysontogenesis, decreased cognitive activity, irritability, and phobias. The manifest stage of the disease typically appears at the age of 5 years or older. The clinical picture of the psychosis is polymorphic and changeable. Along with catatonic disorders (typically agitation with motor stereotypies) and regressive disorders, more distinct affective disturbances appear, as well as rudimentary hallucinations (auditory, visual, olfactory). The course of the disease is episodic-progredient. Remissions are incomplete and therapeutic, accompanied by residual catatonic stereotypies, echolalia, atypical affective disorders with a monotonous, prolonged course, and cognitive deficit. 2–4 years after the manifestation of schizophrenia in children of this group, an oligophrenia-like defect develops with autism, emotional flattening, and passivity. In the majority of patients with episodic-progredient schizophrenia in children, as the disease progresses, positive symptoms are complemented or replaced by negative ones, and a cognitive defect is formed. Children with malignant continuous and episodic-progredient schizophrenia who have undergone catatonic-regressive episodes, following the relief of acute states, are characterized by pronounced impairments in all areas of social functioning. Particularly prominent are a gross cognitive deficit, the inability to learn, and difficulties in social adaptation. Patients exhibit indifference toward loved ones, lack of interest in peers, and frequent manifestations of unmotivated aggression. Such patients require constant care and supervision; the majority of children in this group live in specialized orphanages (children's residential care facilities), and later in psycho-neurological boarding houses. Throughout their lives, they retain residual productive disorders: aimless wandering behavior (fleet behaviour), motor stereotypies, aggression, and auto-aggression. In the (2) hebephrenic variant, the premanifest stage is characterized by autistic dysontogenesis and atypical affective disorders. Manifest polymorphic episodes develop in the 3rd–4th year of life. Patients experience sleep disturbances and a distorted circadian rhythm. Catatonic manifestations in the form of unusual, loud, piercing, or monotonous screaming, and impulsive destructive actions are combined with silliness, grimacing, and absurd acts, while mutism and hypermetamorphosis of attention persist. The course of the disease is episodic-progredient. Remissions are therapeutic, with residual positive and negative disorders. 4–5 years after the manifestation of the disease, a deep cognitive deficit develops, characterized by a lack of cognitive activity, asthenia, severe autism, and thought disorders. Recurrent episodes are observed predominantly during critical periods of ontogenesis. In the (3) paranoid variant, the premanifest stage is marked by an accentuation of schizoid personality traits and cognitive dysontogenesis. Hallucinatory-delusional episodes occur predominantly at puberty and adolescence (13–17 years) and tend to be protracted (ranging from 3 months to 2 years). This form of the disease is distinguished by great polymorphism and the rudimentary nature of psychopathological syndromes, their rapid shift, and the absence of spontaneous remissions. Remissions are therapeutic, with residual productive symptoms. Over the years, the distortion of mental development increases, leading to the formation of a specific personality structure—profound schizoidism, infantilism, and peculiarities and oddities in thinking, motor skills, and behavior. A personality defect of the Verschroben type is formed. In episodic type with a stable defect (F20.x2) The premanifest stage manifests as personality accentuation, cognitive dysontogenesis, neurotic, and affective disorders. As the manifest episode approaches, the level of premorbid functioning declines. Manifest episodes are dominated by affective, affective-neurotic-like, affective-depersonalizational disorders, or polymorphic states with anxiety affect, perceptual distortions, elements of a dream-like state, and catatonic inclusions. Subsequently, the course may change either toward worsening or toward compensation of the state with the achievement of stable remission, the basis of whose clinical picture consists of psychopathy-like personality changes.

2. Diagnostics, medical indications and contraindications for diagnostic methods

Criteria for establishing the diagnosis/condition: general criteria for diagnosing schizophrenia are outlined in Section 1.6 of these clinical guidelines. Their identification and verification require and are sufficient with

1) objective and subjective medical history data

2) clinical psychopathological examination data

3) clinical pathopsychological assessment data

2.1 Complaints and Anamnesis

Recommended: Collection of complaints and history (objective and subjective) in psychiatry (service code - A01.29.001) for all children with suspected schizophrenia to identify diagnostically relevant circumstances. [33-41]

GCR BGrade of Recommendation — B

Level of Evidence — 2

Comment: The collection of complaints and medical history is performed by a psychiatrist. Information necessary for a comprehensive objective history may be contained in medical records or provided by the parents (or other legal representatives) of the minor. Objective history data are gathered from the parents of a child with suspected schizophrenia through a structured interview, generally conducted in chronological order. The interview may establish circumstances relevant to the diagnosis of schizophrenia, including: (1) a history of mental disorders in the family or close relatives; (2) characteristics of pregnancy and childbirth, including pathology or exposure to adverse factors; (3) early development characteristics, including physical and mental development, specifically speech, communication skills, self-care skills, knowledge of the surrounding world, and play behavior; (4) course of age-related crisis periods; (5) adaptation to kindergarten and school, interaction with peers and teachers, and academic performance; (6) mental status during various age periods, behavioral characteristics, presence of psychopathological symptoms and their dynamics; (7) previously diagnosed mental disorders, treatment characteristics and efficacy, and individual drug tolerability; (8) course of the current illness period immediately preceding the seek for psychiatric care. Complaints and subjective history data in children with suspected schizophrenia cannot always be successfully gathered. Children may report information inconsistently, conceal certain facts, or conversely, provide unreliable information or interpret details through the lens of illness. However, with clinical analysis, this information can be exceptionally important for diagnosis [42-43]. At the same time, children often report important anamnestic details unknown to their parents [44].

Recommended: Initial psychiatric examination (consultation/evaluation) in children (service code - B01.035.003) for all children with suspected schizophrenia to establish a diagnosis [45-48]

GCR BGrade of Recommendation — B

Level of Evidence — 2

Comment: the diagnosis of schizophrenia is established based on obtained objective and subjective history data and symptoms identified during the current psychiatric examination that form a clinical picture meeting ICD-10 diagnostic criteria (see Section 1.6. Clinical picture of the disease or condition (group of diseases or conditions) of these clinical guidelines).

Recommended: Initial addiction psychiatrist examination (consultation/evaluation) (service code - B01.036.001) for children with suspected use of narcotic or other psychoactive substances (PAS) to rule out a psychotic episode induced by PAS use [49-52]

GCR CGrade of Recommendation — C

Level of Evidence — 5

2.2 Physical Examination

Recommended: Initial pediatrician examination (consultation/evaluation) (service code - B01.031.001) for all children with suspected schizophrenia to identify concomitant somatic and functional disorders and evaluate contraindications and potential adverse effects of therapy [53-54]

GCR CGrade of Recommendation — C

Level of Evidence — 5

Recommended: Initial neurologist examination (consultation/evaluation) (service code - B01.023.001) for all children with suspected schizophrenia to identify concomitant neurological disorders and evaluate contraindications and potential adverse effects of therapy [55-57]

GCR CGrade of Recommendation — C

Level of Evidence — 5

Comment. Physical examination methods are not of decisive importance directly for diagnosing schizophrenia in children. Despite reports in scientific literature regarding somatic disorders and physical development features associated with childhood schizophrenia [58-61], there is no conclusive evidence of such a link. At the same time, physical examination data are important for detecting disorders comorbid with schizophrenia (e.g., organic brain damage, general somatic or endocrine pathology), the identification of which can significantly affect therapeutic tactics, including the list of medications and other therapeutic interventions used. The ordering of laboratory diagnostic tests (see Section 2.3 of these clinical guidelines) and instrumental diagnostic tests (see Section 2.4 of these clinical guidelines), as well as specialist consultations, is primarily within the purview of the pediatrician and neurologist. These examinations should not be overutilized, as they most frequently prove to have low diagnostic informativeness.

2.3 Laboratory Diagnostics

Recommended: General (clinical) urinalysis (service code - B03.016.006) for all children with suspected and diagnosed schizophrenia as part of the initial evaluation, upon hospital admission, and during follow-up monitoring to assess organ and system function prior to prescribing psychopharmacological treatment [48].

GCR CGrade of Recommendation — C

Level of Evidence — 5

Recommended: Complete blood count (CBC) with differential (service code - B03.016.003) for all children with suspected and diagnosed schizophrenia as part of the initial evaluation, upon hospital admission, and during follow-up monitoring to assess organ and system function prior to prescribing psychopharmacological treatment [48].

GCR CGrade of Recommendation — C

Level of Evidence — 5

Recommended: General general-medical blood chemistry panel (service code - B03.016.004) for all children with suspected and diagnosed schizophrenia as part of the initial evaluation, upon hospital admission, and during follow-up monitoring to assess organ and system function, specifically to evaluate renal and hepatic function and rule out inflammation prior to prescribing psychopharmacological treatment [48].

GCR CGrade of Recommendation — C

Level of Evidence — 5

Recommended: General general-medical blood chemistry panel (service code - B03.016.004) and biochemical blood lipid metabolism panel (service code - B03.016.005) for all children with diagnosed schizophrenia receiving antipsychotic treatment, to assess glucose levels and lipid profile [62]

GCR CGrade of Recommendation — C

Level of Evidence — 5

Recommended: Blood prolactin level testing (service code - A09.05.087) for all children with diagnosed schizophrenia receiving antipsychotic treatment known to affect blood prolactin levels (therapy-related adverse effect). [63-64]

GCR AGrade of Recommendation — A

Level of Evidence — 1

Comment. Laboratory diagnostic tests are not of decisive importance directly for diagnosing schizophrenia in children. At the same time, laboratory diagnostic tests are important for identifying conditions comorbid with schizophrenia (e.g., general somatic or endocrine pathology), the detection of which can significantly affect treatment tactics, including the list of medications used and other therapeutic interventions. The ordering of laboratory diagnostic tests, instrumental diagnostic tests (see section 2.4 of these clinical guidelines), and medical specialist consultations is primarily the competence of a pediatrician and neurologist.

2.4 Instrumental Diagnostics

There are no instrumental diagnostic methods for schizophrenia, including in childhood.

  • Before prescribing therapy, to perform differential diagnosis with other diseases, primarily of organic etiology, and to assess various somatic health risks, some patients are recommended to undergo additional examination methods [32, 37, et al.], which include:

- electroencephalography (EEG), electroencephalography with provocative tests, video-electroencephalography monitoring (service codes - A05.23.001, A05.23.001.001, A05.23.001.002) [65–66, 210],

GOR CGrade of Recommendation – C

Level of Evidence — 5

- magnetic resonance imaging (MRI) of the brain and other types of brain neuroimaging (computed tomography of the brain (service code - A05.23.009) [67–68].

Level of Evidence - 3

Grade of Recommendation BStrength of Recommendation - B.

Comments: MRI and EEG are recommended for initial patients who have never undergone these studies before, or if there are clinical or anamnestic indications. In case of suspected epilepsy, a space-occupying brain lesion, or other pathology, electroencephalography, computed tomography, or brain MRI may be ordered by a neurologist. Modern studies have yielded much data indicating a statistically traceable relationship between the anatomy of the brain and its individual structures and the presence, onset character, and course of schizophrenia in children and adolescents [73–75]; however, EEG and MRI data are not of decisive importance directly for diagnosing schizophrenia in children.

  • Electrocardiography (ECG) with exercise (service code - A12.10.001) is recommended for all children with diagnosed schizophrenia to assess the safety of psychopharmacological therapy, especially antipsychotics that prolong the QT interval [69–72].

GCR CGrade of Recommendation — C

Level of Evidence - 4

2.5 Other Procedures

Recommended: Clinical and psychological psychodiagnostic examination (service code - A13.29.003.001) for all children with suspected and diagnosed schizophrenia to assess higher mental functions and create an individual plan for psychocorrection and medical rehabilitation [76–77].

GCR CGrade of Recommendation — C

Level of Evidence — 5

Comment: Abroad, psychometric scales designed to assess the overall severity of the mental state, symptom severity, preservation of social skills, and adaptation to the educational process have recently become widespread. Before being approved for use, these techniques undergo a complex procedure of standardization and validation. Unfortunately, in Russia today there are no domestic methods with sufficiently high validity parameters that are easy to use and tested on representative samples. Many foreign methods, having been translated into Russian, require re-validation, which has not been performed to date. Therefore, it is not feasible to use the PANSS scale (child version), service type: Clinical and psychological counseling (service code - A13.29.006) for all children with suspected and diagnosed schizophrenia to assess symptom severity over time and evaluate treatment efficacy [80–84], although in some cases, when the general clinical impression is insufficient to assess the child's state, it is desirable to do so (see Appendix G1 to these clinical guidelines).

GCR BGrade of Recommendation — B

Level of Evidence — 2

Comment: despite the fact that foreign methods are not validated for use in Russia, the method can be used as a convenient guideline during a clinical interview with the patient, using data obtained from observation, which will objectify the dynamics of the state by comparing data from the same patient. An important additional option for using the scale is the Structured Clinical Interview for Positive and Negative Syndrome Scale (SCI-PANSS) [85]

The Personal and Social Performance Scale can also be used as a guideline, service type: Clinical and psychological counseling (service code - A13.29.006) for children with suspected and diagnosed schizophrenia to assess the ability to learn and acquire speech skills, relationships with relatives and others, self-care skills, and arousal and aggressive behavior, including during ongoing treatment, as well as to evaluate treatment efficacy and during the creation and implementation of an individual plan for psychocorrection and medical rehabilitation [86–90] (see Appendix G2 to these clinical guidelines).

GCR CGrade of Recommendation — C

Level of Evidence — 5

Comment: the same scale is used in children and adults; separate studies in children with schizophrenia have not been conducted. The method can be used as a convenient guideline during a clinical interview with the patient, using data obtained from observation, which will objectify the dynamics of the state by comparing data from the same patient.

3. Treatment, including drug and non-drug therapies, diet therapy, and pain management

Pharmacotherapy is an essential condition for the treatment of schizophrenia [91]. The main pharmacological class of drugs prescribed both to relieve psychotic symptoms and to prevent relapses is antipsychotics (neuroleptics) [92, 93]. Along with antipsychotics, drugs of other classes are used [94]. Psychotherapy is used as an adjunct to pharmacological therapy [95].

Not recommended: Electroconvulsive therapy (service code - A17.29.001) and other types of shock therapy in children with diagnosed schizophrenia [96–99]

GCR BGrade of Recommendation — B

Level of Evidence — 2

Comment: Although most guidelines do not recommend the use of ECT in childhood, there are no absolute contraindications to this method [204]. There are isolated indications of the efficacy of ECT in adolescents over 12 years of age with diagnosed schizophrenia in the presence of catatonic symptoms [204, 205]. Foreign literature contains data on the efficacy of ECT in adolescent and youth schizophrenia in 42% of cases, but these conclusions are based on a very limited number of observations [211]

3.1. Treatment with antipsychotics

Antipsychotics are used in the treatment of schizophrenia in children to relieve positive symptoms (perceptual distortions, delusions or their equivalents, aggression, catatonic symptoms). There is evidence of the efficacy of a number of antipsychotics against negative symptoms [78]. Due to limited safety data on the use of many antipsychotics in childhood, the range of drugs recommended for children is significantly narrower compared to adults [79]. The prescription of antipsychotics to children is based on several principles: (1) due to the risk of side effects (extrapyramidal symptoms), second-generation antipsychotics should be preferred; (2) monotherapy with a single drug at the minimum effective dose is preferred; in case of combination therapy, the increased risk of side effects and drug interactions of antipsychotics must be taken into account [28, 144]; (3) if therapy fails within 4–6 weeks (provided good tolerability and administration at the optimal therapeutic dose), the drug should be replaced; (4) using doses higher than recommended generally does not improve the therapeutic effect, but sharply increases the risk of side effects [100]; (5) prior to prescribing certain drugs, comorbid somatic (neuroendocrine, neurological, cardiological, etc.) pathology should be excluded; (6) the duration of antipsychotic therapy after relief of the acute state in maintenance doses must be at least 1 year.

Recommended: Prescribing medications for mental disorders (service code - A25.29.001) – first- and second-generation antipsychotics in all children with diagnosed schizophrenia to relieve psychotic symptoms [101-104].

LoE ALevel of Evidence – A

Level of Evidence — 1

Recommended: Prescribing medications for mental disorders (service code - A25.29.001) – antiparkinsonian drugs in all children with diagnosed schizophrenia receiving antipsychotic therapy, to relieve extrapyramidal disorders [105].

GCR CGrade of Recommendation – C

Level of Evidence — 5

Comment: the choice of a specific drug depends on a number of additional factors, in particular, the features of the clinical picture, the child's age, the presence of comorbid pathology, and the physician's experience.

Recommended: Prescribing medications for mental disorders (service code - A25.29.001) – haloperidol**. Drug class, ATC code: N05AD01, butyrophenone derivatives, antipsychotic agent. In children with diagnosed schizophrenia starting from 3 years of age for the reduction of hallucinations, delusions (or their equivalents characteristic of childhood), thought and consciousness disorders, and catatonic symptoms [103,104,107].

LoE BLevel of Evidence – B

Level of Evidence — 2

Recommended: Prescribing medications for mental disorders (service code - A25.29.001) – chlorpromazine**. Drug class, ATC code: N05AA01, phenothiazine derivatives, antipsychotic agent. In children with diagnosed schizophrenia starting from 12 years of age for the reduction of psychomotor agitation, agitation, hallucinations, delusions (or their equivalents characteristic of childhood), and catatonic symptoms [108,109]

LoE ALevel of Evidence – A

Level of Evidence — 1

Recommended: Prescribing medications for mental disorders (service code - A25.29.001) – risperidone**. Drug class, ATC code: N05AX08, antipsychotic agent. In children with diagnosed schizophrenia starting from 13 years of age for the correction of acute positive and negative symptoms and aggression [107,110,112].

LoE ALevel of Evidence – A

Level of Evidence — 1

Recommended: Prescribing medications for mental disorders (service code - A25.29.001) – thioridazine**. Drug class, ATC code: N05AC02, phenothiazine derivatives, antipsychotic agent. In children with diagnosed schizophrenia starting from 4 years of age for the correction of psychomotor agitation, restlessness, and severe behavioral disorders [113-115].

GCR CGrade of Recommendation — C

Level of Evidence - 4

Recommended: Prescribing medications for mental disorders (service code - A25.29.001) – levomepromazine**. Drug class, ATC code: N05AC02, piperidine derivatives of phenothiazine, antipsychotic agent. In children with diagnosed schizophrenia starting from 12 years of age for the correction of psychomotor agitation, restlessness, and severe behavioral disorders [116-118].

GCR CGrade of Recommendation — C

Level of Evidence - 4

Recommended: Prescribing medications for mental disorders (service code - A25.29.001) – tiapride. Drug class, ATC code: N05AL03, antipsychotic agent. In children with diagnosed schizophrenia starting from 6 years of age for the correction of psychomotor agitation, restlessness, severe behavioral disorders, and aggression [119].

LoE BLevel of Evidence – B

Level of Evidence - 3

Recommended: Prescribing medications for mental disorders (service code - A25.29.001) – sulpiride**. Drug class, ATC code: N05AL01, benzamide derivatives, antipsychotic agent. In children with diagnosed schizophrenia starting from 14 years of age for the correction of negative symptoms when affective and cognitive impairments predominate in the clinical picture [120-123].

GCR BGrade of Recommendation — B

Level of Evidence - 3

Recommended: Prescribing medications for mental disorders (service code - A25.29.001) – periciazine**. Drug class, ATC code: N05AC01, piperidine derivatives of phenothiazine, antipsychotic agent. In children with diagnosed schizophrenia starting from 3 years of age in oral solution for the correction of psychomotor agitation, restlessness, and severe behavioral disorders [124-125].

LoE BLevel of Evidence – B

Level of Evidence — 1

Recommended: Prescribing medications for mental disorders (service code - A25.29.001) – #olanzapine**. Drug class, ATC code: N05AH03, antipsychotic agent. In children aged 8 years and older with diagnosed schizophrenia for the reduction of psychotic symptoms, including catatonic disorders, overcoming resistance to other antipsychotics, and correction of psychomotor agitation, restlessness, and severe behavioral disorders at doses of 2.5–15 mg per day [126-128, 137].

LoE ALevel of Evidence – A

Level of Evidence — 1

Recommended: Prescribing medications for mental disorders (service code - A25.29.001) – #clozapine. Drug class, ATC code: N05AH02, antipsychotic agent. In children with diagnosed schizophrenia in the presence of suicidal risk and resistance to therapy with other antipsychotics for the prevention of suicidal behavior and increasing treatment efficacy at doses of 25–400 mg per day [107,127,130, 206-208].

LoE ALevel of Evidence – A

Level of Evidence — 1

Recommended: Prescribing medications for mental disorders (service code - A25.29.001) – paliperidone**. Drug class, ATC code: N05AX13, benzisoxazole derivatives, antipsychotic agent. In children with diagnosed schizophrenia starting from 12 years of age in tablet form in case of resistance to therapy with other antipsychotics for the correction of negative symptoms [103,127].

LoE ALevel of Evidence – A

Level of Evidence — 1

Recommended: Prescribing medications for mental disorders (service code - A25.29.001) – #paliperidone**, prolonged-release suspension for intramuscular injection. Drug class, ATC code: N05AX13, benzisoxazole derivatives, antipsychotic agent. In adolescents with diagnosed schizophrenia starting from 15 years of age as deep long-acting intramuscular injections for the prevention of relapses within 12 months after the first psychotic episode at a dose of 50–150 mg once a month [134-136].

GCR CGrade of Recommendation — C

Level of Evidence - 4

Recommended: Prescribing medications for mental disorders (service code - A25.29.001) – lurasidone**. Drug class, ATC code: N05AE05, indole derivatives, antipsychotic agent. In children with diagnosed schizophrenia starting from 13 years of age in tablet form for the correction of positive, negative, and depressive symptoms, as well as cognitive impairments [31,110,129,137,138,209].

LoE ALevel of Evidence – A

Level of Evidence — 1

Recommended: Prescribing medications for mental disorders (service code - A25.29.001) – #aripiprazole. Drug class, ATC code: N05AX12, antipsychotic agent. In adolescents over 15 years of age with diagnosed schizophrenia in case of resistance to therapy with other antipsychotics for the correction of negative symptoms [137,139-140] at a dose of 10–30 mg per day.

GCR CGrade of Recommendation — C

Level of Evidence — 2

Recommended: Prescribing medications for mental disorders (service code - A25.29.001) – #quetiapine**. Drug class, ATC code: N05AH04, antipsychotic agent. In adolescents starting from 15 years of age with diagnosed schizophrenia for the correction of negative symptoms or when neurosis-like and affective symptoms predominate in the clinical picture [102,141] at a dose of 50–600 mg/day.

LoE ALevel of Evidence – A

Level of Evidence — 1

Recommended: Prescribing medications for mental disorders (service code - A25.29.001) – biperiden**. Drug class, ATC code: N04AA02, tertiary amines. In children with diagnosed schizophrenia receiving antipsychotics, parenterally – without age restriction, tablets starting from 3 years of age, for the correction of extrapyramidal symptoms [105,142,143].

GCR CGrade of Recommendation – C

Level of Evidence - 4

3.2. Treatment with antidepressants

In schizophrenia, depression can occur both within the structure of psychosis and in the prodromal period, during remissions, and as residual symptoms of schizophrenia. According to established opinion, depressive symptoms during acute psychoses often resolve in parallel with hallucinatory-delusional symptoms and do not require a separate prescription of antidepressants. The prescription of antidepressants is mainly restricted to so-called post-psychotic depressions when other therapeutic measures are ineffective [132,145-146,196]. If antidepressants are necessary, SSRIs are preferred [147,196], although the increased probability and risk factors for suicide should be taken into account [106,111,196].

Recommended: Prescribing medications for mental disorders (service code - A25.29.001) – antidepressants in children with diagnosed schizophrenia to relieve depressive symptoms and/or obsessive-compulsive symptoms [148-149].

GCR CGrade of Recommendation — C

Recommended: Prescription of medications for mental disorders (service code - A25.29.001) - sertraline**. Drug class, ATC code: N06AB06, selective serotonin reuptake inhibitor (SSRI), antidepressant. For children diagnosed with schizophrenia from the age of 6, #sertraline** in the presence of depressive symptoms for their relief, starting at 25 mg per day, followed by a dose increase; sertraline** for obsessive-compulsive symptoms for their relief at a dose of 50 mg [150-152].

GCR CGrade of Recommendation — C

Level of Evidence - 4

Recommended: Prescription of medications for mental disorders (service code - A25.29.001) - #fluvoxamine. Drug class, ATC code: N06AB06, selective serotonin reuptake inhibitor (SSRI), antidepressant. For adolescents diagnosed with schizophrenia from the age of 16, fluvoxamine for the correction of obsessive-compulsive symptoms at a dose of 100-300 mg/day in combination with risperidone at doses of 2-3 mg/day [131,133,199].

GCR CGrade of Recommendation — C

Level of evidence validity - 4

3.3. Treatment with other drug classes

Recommended: Prescription of medications for mental disorders (service code - A25.29.001) - antiepileptic drugs for children diagnosed with schizophrenia in the presence of affective disorders (manic, depressive, and mixed) in the clinical presentation, with the aim of relieving symptoms of affective disorders [149,153-156].

GCR CGrade of Recommendation – C

Level of Evidence - 4

Recommended: Prescription of medications for mental disorders (service code - A25.29.001) - benzodiazepine anxiolytics for children diagnosed with schizophrenia in the presence of psychomotor agitation, stupor, and other catatonic symptoms in the clinical presentation for their correction [157-160].

GCR CGrade of Recommendation — C

Level of Evidence - 4

3.4. Other Treatment

Psychotherapy

Psychotherapy in Russia lacks a clear definition and strict legislative regulation. Numerous works aimed at finding psychotherapy approaches and methods that meet efficacy criteria have revealed proven efficacy for a very small spectrum of psychotherapeutic interventions in schizophrenia, especially in childhood [161-166]. No convincing data have been obtained regarding the efficacy of treating schizophrenia with diet therapy, physiotherapeutic methods, and other treatment modalities practiced in medicine.

Recommended: Individual cognitive behavioral therapy (CBT) (service code - A13.29.008.001) and group cognitive behavioral therapy (service code - A13.29.008.002) for children diagnosed with schizophrenia, provided they have preserved intellect and are outside of exacerbation periods, with the aim of improving quality of life, increasing compliance, and developing and restoring cognitive and emotional social interaction skills [167-169].

GCR AGrade of Recommendation — A

Level of Evidence – 1

Comment: within the framework of cognitive behavioral therapy, new techniques and methods frequently emerge, which typically receive new proprietary names. In particular, cognitive and behavioral approaches form the basis of ACT (acceptance and commitment therapy), DBT (dialectical behavior therapy), and schema therapy. Thus, these types of psychotherapy can also be used to provide care for children with schizophrenia.

Recommended: Clinical and psychological training (cognitive skills training, social skills training) (service code - A13.29.020) for children diagnosed with schizophrenia, provided they have preserved intellect and are outside of exacerbation periods, with the aim of improving quality of life, increasing compliance, and developing and restoring cognitive and emotional social interaction skills [170-171].

GCR BGrade of Recommendation — B

Level of Evidence — 2

Recommended: Art therapy (music, painting, dance therapy) (service code - A13.29.019) for children diagnosed with schizophrenia, provided they have preserved intellect and are outside of exacerbation periods, with the aim of improving quality of life, increasing compliance, and developing and restoring cognitive and emotional social interaction skills [172-174].

GCR BGrade of Recommendation — B

Level of Evidence — 1

Not recommended: Hypnotherapy (service code - A13.29.018) for children diagnosed with schizophrenia and suspected of having schizophrenia, due to existing data on the risk of exacerbating the schizophrenic process as a result of hypnotherapy [175-176].

GCR CGrade of Recommendation — C

Level of Evidence — 5

4. Medical Rehabilitation and Sanatorium-Resort Treatment

Medical rehabilitation for schizophrenia should be carried out at all stages of psychiatric care. It is aimed at forming or restoring cognitive, motivational, and emotional resources of the personality, skills, knowledge, and abilities that are deficient or lost as a result of the illness, enabling the individual to interact with others, solve everyday tasks, and cope with more complex problems [177], as well as building adherence to ongoing therapy [137].

Recommended: Group psychoeducational work with patients with mental disorders and behavioral disorders (service code B04.035.006) and Group psychoeducational work with relatives of a patient with mental disorders and behavioral disorders (service code B04.035.007) for children diagnosed with schizophrenia, provided they have preserved intellect and are outside of exacerbation periods, with the aim of improving quality of life, increasing compliance, and developing and restoring cognitive and emotional social interaction skills [178-180].

GCR AGrade of Recommendation — A

Level of Evidence — 1

Recommended: Psychosocial adaptation school for patients with mental disorders and behavioral disorders and their relatives (service code - B04.035.008) for children diagnosed with schizophrenia, provided they have preserved intellect and are outside of exacerbation periods, with the aim of improving quality of life, increasing compliance, and developing and restoring cognitive and emotional social interaction skills [181].

GCR BGrade of Recommendation — B

Level of Evidence - 3

Recommended: Clinical and psychological training (service code - A13.29.020) for children diagnosed with schizophrenia, provided there are no severe intellectual impairments and they are outside of exacerbation periods, with the aim of improving quality of life, increasing compliance, and developing and restoring cognitive and emotional social interaction skills [182-189].

GCR BGrade of Recommendation — B

Level of Evidence — 2

Comment: methods of cognitive remediation and social skills training are used, carried out, as a rule, by specialists in the field of psychology. There is no convincing data supporting the efficacy of rehabilitation methods based on natural therapeutic factors (balneotherapy, spa therapy, terrain cure, and other health resort treatment methods). No convincing data have been obtained regarding the benefits of animal-assisted therapy (AAT) using dogs, horses, dolphins, or petting zoos. Data obtained by some researchers on the efficacy of rehabilitating schizophrenia patients using video games [190] have an extremely low level of evidence due to exceptionally small patient samples.

5. Prevention and Dispensary Observation

Schizophrenia is a mental disorder for which there are no primary prevention measures. At the same time, early detection and timely initiated treatment can significantly influence the prognosis in schizophrenia [154]. By Order of the Russian Ministry of Health No. 396n dated June 13, 2019, "On Amending the Procedure for Preventive Medical Examinations of Minors, Approved by Order of the Ministry of Health of the Russian Federation No. 514n dated August 10, 2017," additions were made concerning screening within the framework of preventive medical examinations of two-year-old children to identify a risk group for the emergence or presence of mental development disorders through parental questionnaires. The psychiatrist examines only those children who are included in the specified risk group.

Recommended: Follow-up appointment (examination, consultation) by a child psychiatrist (service code - B01.035.004) for children diagnosed with schizophrenia outside of exacerbation periods, with the aim of assessing the condition dynamically, identifying exacerbations, and adjusting treatment at least once a year [191].

GCR CGrade of Recommendation — C

Level of Evidence — 5

Comment: Dispanserizatsiya (clinical dispansery observation) may be established regardless of the consent of the person suffering from a mental disorder or their legal representative in cases provided for by Part 1 of Art. 27 of the Law of the Russian Federation No. 3185-1 dated July 2, 1992, "On Psychiatric Care and Guarantees of Citizens' Rights in Its Provision" (hereinafter referred to as Law No. 3185-1).

"Decisions on the necessity of establishing clinical dispansery observation and its termination are made by a commission of psychiatrists appointed by the head of the medical organization providing outpatient psychiatric care, or by a commission of psychiatrists appointed by the executive authority of a constituent entity of the Russian Federation in the field of healthcare" (Part 2, Art. 27 of Law No. 3185-1). Such an examination is possible both upon a person's voluntary application for psychiatric care and involuntarily, if there are indications for involuntary examination.

The basis for establishing clinical dispansery observation is the presence of a chronic and protracted mental disorder with severe, persistent, or frequently exacerbating pathological manifestations (Part 1, Art. 27 of Law No. 3185-1).

The procedure for dispensary observation of a person suffering from a chronic and prolonged mental disorder with severe, persistent, or frequently exacerbating morbid manifestations is defined by Order of the Russian Ministry of Health No. 453n dated June 30, 2022, “On approval of the Procedure for dispensary observation of a person suffering from a chronic and prolonged mental disorder with severe, persistent, or frequently exacerbating morbid manifestations,” which entered into force on March 1, 2023. In accordance with the appendix to the Procedure, 5 dispensary observation groups are defined: D-1, D-2, D-3, D-4, D-5 (active dispensary observation), within which subgroups may be distinguished if necessary.

Upon recovery or significant and persistent improvement in a person's mental state, dispensary observation is terminated (Part 4, Article 27 of Law No. 3185-1).

Comment: secondary prevention of schizophrenia aims to prevent recurrent exacerbations, while tertiary prevention aims to restore patients' social functioning to the maximum possible extent (see the section “Medical rehabilitation and sanatorium-resort treatment, medical indications and contraindications for the use of medical rehabilitation methods, including those based on natural healing factors” of these guidelines).

6. Organization of Medical Care

Diagnosis, treatment, monitoring, and rehabilitation of children with schizophrenia can, in the vast majority of cases, be carried out on an outpatient basis or in a day hospital setting. In accordance with Federal Law No. 323-FZ dated November 21, 2011, “On the Fundamentals of Protecting the Health of Citizens in the Russian Federation,” parents or legal representatives of a child with schizophrenia have the right to seek medical care at their place of permanent registration. If this is not possible, they have the right to receive care in other medical institutions located outside their place of permanent residence.

Indications for hospitalization in a hospital for children with schizophrenia are: (1) pronounced manifestations of agitation and aggression, including the risk of harming others and oneself, (2) high suicide risk, (3) newly diagnosed schizophrenia, the need for additional comprehensive examination and selection of therapy, (4) prominent psychotic symptoms and grossly disorganized behavior, (5) severe concomitant somatic pathology complicating the selection of treatment, (6) manifestations of resistance and poor tolerability of therapy, (7) unavailability of adequate outpatient care at the place of residence, (8) pronounced social maladaptation of the child and family members with the inability to meet basic living needs (social indications).

Indications for discharge from the hospital for children with schizophrenia are: elimination of suicide risks, relief of pronounced manifestations of agitation and aggression, stabilization of the mental and somatic state with the reduction of pathological symptoms.

Comment: preschool-aged children with schizophrenia rarely have a high suicide risk and such grossly disorganized behavior that it cannot be controlled within the family; at the same time, placing them in a hospital, especially without parents, is often accompanied by the formation of psychogenically conditioned comorbid disorders and the risk of hospitalism [192-194]. Traditional concepts of the three stages of schizophrenia therapy (acute treatment stage — treatment of acute psychosis/exacerbation of psychotic symptoms, continuation stage — stabilization of the condition, and maintenance stage — relapse prevention) are fully applicable to adolescent patients with schizophrenia [195-198]. A differentiated, comprehensive approach to the management of children with schizophrenia has proven itself well in practice in Russia [197].

7. Additional Information

Given the specifics of the disease, in particular its chronic course and progressive nature of impairments, the "outcome" of the disease in the case of schizophrenia should be understood not as a final outcome, but as intermediate results achieved during treatment. Factors that worsen the course of schizophrenia and its prognosis are traditionally considered to be refusal of timely and effective treatment, abuse of alcohol and other psychoactive substances, lack of social rehabilitation and family support, and stress [200-201].

Criteria for Evaluating the Quality of Medical Care

№

Quality assessment criterion

Fulfilled / not fulfilled

1.

An initial examination (consultation) by a child psychiatrist was performed, including the collection of complaints and anamnesis

Yes / No

2.

Biochemical blood test performed

general therapeutic

Yes / No

3.

Blood prolactin level testing performed in all children with diagnosed schizophrenia receiving treatment with antipsychotics that affect the level

prolactin levels (regularly)

Yes / No

4.

Clinical and psychological counseling performed

Yes / No

5.

Prescription of medicinal products for mental disorders — first- or second-generation antipsychotics — carried out

Yes / No

6.

Individual and/or group cognitive behavioral therapy (CBT) performed

Yes / No

7.

Clinical and psychological training conducted (training

of cognitive abilities, social skills training)

Yes / No

8.

Group psychoeducational work conducted with

patients with mental and behavioral disorders and their relatives

Yes / No

9.

A psychosomatic adaptation school was conducted for patients with mental and behavioral disorders and their relatives

Yes / No

10.

Treatment efficacy evaluation was performed

Yes / No

References

Show references
  1. Mental and behavioral disorders (F00-F99). Chapter V of ICD-10, adapted for use in the Russian Federation. Edited by B.A. Kazakovtsev, V.B. Holland. Moscow: Russian Ministry of Health, 1998. 512 p.

  2. Guidelines on Psychiatry / Ed. by A.V. Snezhnevsky / Vol. 1. Moscow: Meditsina, 1983, 480 p.

  3. ICD-11. Chapter 06. Mental, behavioural and neurodevelopmental disorders. Statistical classification. Moscow: "KDU", "Universitetskaya kniga" - 2021. - 432 p.

  4. O"Donovan MC; Williams N.M., Owen M.J. Recent advances in the genetics of schizophrenia. // Human Molecular Genetics. 2003, 12 (2): 125 133. doi:10.1093/hmg/ddg302

  5. Nagel M, Jansen PR, Stringer S, Watanabe K, de Leeuw CA, et al. Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways. Nat Genet. 2018 50 (7): 920-927. doi:10.1038/s41588-018-0151-7

  6. Rasic D, Hajek T, Alda M, Uher R. Risk of mental illness in offspring of parents with schizophrenia, bipolar disorder, and major depressive disorder: a meta-analysis of family high-risk studies. Schizophr Bull. 2014 Jan; 40(1): 28-38. doi:10.1093/schbul/sbt114.

  7. Carlsson A., Lecrubier Y. Dopamine theory of schizophrenia pathogenesis. A guide for physicians / ed. by S.N. Mosolov. London, 2004.

  8. Stahl S.M. Stahl's Essential Psychopharmacology: Neuroscientific Basis and Practical Applications. Moscow: GEOTAR-Media, 2020. - 656 p.

  9. Mosolov S.N. Some current theoretical problems of diagnosis, classification, neurobiology and therapy of schizophrenia: comparison of foreign and domestic approaches. S.S. Korsakov Journal of Neurology and Psychiatry. 2010. Vol. 110. No. 6. P. 4-11

  10. Green M.F. Cognitive impairment and functional outcome in schizophrenia and bipolar disorder. Journal of Clinical Psychiatry 2006. 67 (9): 3—8.

  11. Molina V., Sanz J., Reig S., Martinez R., Sarramea F., Luque R. et al. Hypofrontality in men with first-episode psychosis . British Journal of Psychiatry 2005. 186: 203— 208. — doi:10.1192/bjp.186.3.203

  12. Models of Madness: Psychological, Social and Biological Approaches to Understanding Schizophrenia. Edited by J. Read, L.R. Mosher, R.P. Bentall. — Stavropol: Vozrozhdenie, 2008. — 412 p.

  13. Mueser K.T., McGurk S.R. Schizophrenia. The Lancet. 2004, 363 (9426): 2063— 2072. doi:10.1016/S0140-6736(04)16458-1

  14. Fraguas D, D^az-Caneja CM, Ayora M, Hernandez-Alvarez F, Rodriguez-Quiroga A, Recio S, Leza JC, Arango C. Oxidative Stress and Inflammation in First-Episode Psychosis: A Systematic Review and Meta-analysis. Schizophr Bull. 2019 45(4): 742-751. doi: 10.1093/schbul/sby125.

  15. Kostyukova A.B., Mosolov S.N. Neuroinflammatory hypothesis of schizophrenia and some new therapeutic approaches. // Modern Therapy of Mental Disorders. 2013. No. 4. P. 2-8

  16. Salamon S, Santelmann H, Franklin J, Baethge C. Test-retest reliability of the diagnosis of schizoaffective disorder in childhood and adolescence - A systematic review and meta-analysis. J Affect Disord. 2018. 230: 28-33. doi: 10.1016/j.jad.2017.12.070.

  17. Os J., Kapur S. Schizophrenia. Lancet. 2009, 374 (9690): 635-645. DOI: https://doi.org/10.1016/S0140-6736(09)60995-8

  18. Picchioni M.M., Murray R.M. Schizophrenia. BMJ. 2007, 335 (7610): 91 95. DOI:10.1136/bmj.39227.616447.BE

  19. Clemmensen L., Vernal D. L., Steinhausen H. C. A systematic review of the long¬term outcome of early onset schizophrenia. BMC Psychiatry. 2012, 12: 150 156. doi:10.1186/1471-244X-12-150

  20. Ishal Madaan, Yael Dvir, Daniel R Wilson. Child and adolescent schizophrenia: pharmacological approaches. Informa Healthcare. 2008, 9, (12): 2053-2068. doi:10.1517/14656566.9.12.2053

  21. Remschmidt H. Child and Adolescent Psychiatry: An Introduction. Moscow: EKSMO-Press, 2001. 624 p.

  22. Demcheva N.K., Pronina L.A., Polozhaya Z.B. Indices of childhood disability due to mental illness in the Russian Federation in 2002-2012. Bulletin of Neurology, Psychiatry and Neurosurgery. 2014, 1: 3-11

  23. Makushkin E.V., Demcheva N.K. Dynamics and comparative analysis of child and adolescent morbidity with mental disorders in the Russian Federation in 2000-2018. Russian Journal of Psychiatry. 2019, 4: 4-15.

  24. Shmatova Yu.E. Dynamics of statistical and sociological indicators of the mental health status of the Russian population // Problems of Territory's Development. 2019. No. 3 (101). P. 76-96. DOI: 10.15838/ptd.2019.3.101.5

  25. Robert L. Spitzer, Dennis P. Cantwell. The DSM-III Classification of the Psychiatric Disorders of Infancy, Childhood, and Adolescence. Journal of the American Academy of Child and Adolescent Psychiatry (Eng.) Elsevier BV, 1980, 19 (3): 356-370. doi:10.1016/s0002-7138(09)61059-1

  26. Schizophrenia (childhood and adolescence): a guide for physicians / E.E. Balakireva, A.V. Kulikov, A.A. Koval-Zaytsev [et al.] - Moscow: GEOTAR-Media, 2023. - 96 p.

  27. Neznanov N.G., Martynykhin I.A., Mosolov S.N. Diagnosis of schizophrenia in Russia: results of an online survey of psychiatrists. Part 1. Use of ICD-10. // Modern Therapy of Mental Disorders. - 2019, No. 1, p. 2-13

  28. Mosolov S.N., Malin D.I., Ryvkin P.V., Sychev D.A. Drug-drug interactions of medications used in psychiatric practice // Modern Therapy of Mental Disorders. 2019, S1, P. 2-35. DOI: 10.21265/PSYPH.2019.50.40828

  29. Schizophrenia: A Multidisciplinary Study / Ed. by A.V. Snezhnevsky; Acad. Med. Sci. - Moscow: Meditsina, 1972. - 400 p.

  30. American Psychiatric Association. Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5).- Arlington, VA: American Psychiatric Publishing, 2013. - 992 p

  31. Oleneva E.V. Effect of lurasidone on cognitive functioning in patients with schizophrenia: a systematic review of evidence-based studies of the drug // Modern Therapy of Mental Disorders. - 2021. - No. 1. - P. 23-33. - DOI: 10.21265/PSYPH.2021.74.13.004

  32. Bashina V.M., Simashkova N.V. Systematics of childhood schizophrenia. S.S. Korsakov Journal of Neurology and Psychiatry. 1989. 89 (8): 69-75

  33. Ambrosini PJ. Historical developments and present status of the schedule for affective disorders and schizophrenia for school age children (K-SADS). J Am Acad Child Adolesc Psychiatry 39:49-58, 2000

  34. Kelleher I, Connor D, Clarke MC, Devlin N, Harley M, Cannon M: Prevalence of psychotic symptoms in childhood and adolescence: a systematic review and meta-analysis of population-based studies. Psychol Med 42(9):1857-1863, 2012

  35. Kaplan and Sadock’s handbook of clinical psychiatry. Philadelphia, Williams&Wilkins, 2001. 480 p.

  36. Hollis C: Child and adolescent (juvenile onset) schizophrenia. A case control study of premorbid developmental impairments. Br J Psychiatry 166(4):489-495, 1995

  37. Laurens KR, Luo L, Matheson SL, et al.: Common or distinct pathways to psychosis? A systematic review of evidence from prospective studies for developmental risk factors and antecedents of the schizophrenia spectrum disorders and affective psychoses. BMC Psychiatry 15:205, 2015

  38. Schaeffer JL, Ross RG: Childhood-onset schizophrenia: premorbid and prodromal diagnostic and treatment histories. J Am Acad Child Adolesc Psychiatry 41(5):538- 545, 2002

  39. Lewis SW, Murray RM: Obstetric complications, neurodevelopmental deviance, and risk of schizophrenia. JPsychiatr Res 21(4):413-421, 1987

  40. Remschmidt H. Child and Adolescent Psychiatry: An Introduction. Moscow: EKSMO-Press, 2001. 624 p.

  41. Childhood Psychiatry. A Guide for Physicians / Ed. by I.V. Makarov. - St. Petersburg: Nauka i Tekhnika, 2019. - 992 p.

  42. Weissman MM, Wickramaratne P, Warner V, et al.: Assessing psychiatric disorders in children: discrepancies between mothers’ and children’s reports. Arch Gen Psychiatry 44:747-753, 1987

  43. Poulton R, Caspi A, Moffitt TE, Cannon M, Murray R, Harrington H: Children’s self-reported psychotic symptoms and adult schizophreniform disorder: a 15-year longitudinal study. Arch Gen Psychiatry 57(11):1053-1058, 2000

  44. Dhossche D, Ferdinand R, Van der Ende J, Hofstra MB, Verhulst F: Diagnostic outcome of self-reported hallucinations in a community sample of adolescents. Psychol Med 32(4):619-627, 2002

  45. Kelleher I, Connor D, Clarke MC, Devlin N, Harley M, Cannon M: Prevalence of psychotic symptoms in childhood and adolescence: a systematic review and meta-analysis of population-based studies. Psychol Med 42(9):1857-1863, 2012

  46. van Os J, Linscott RJ, Myin-Germeys I, Delespaul P, Krabbendam L: A systematic review and meta-analysis of the psychosis continuum: evidence for a psychosis proneness-persistence-impairment model of psychotic disorder. Psychol Med 39(2):179-195, 2009

  47. Driver DI, Gogtay N, Rapoport JL: Childhood onset schizophrenia and early onset schizophrenia spectrum disorders. ChildAdolesc Psychiatr Clin NAm 22(4):539-555, 2013

  48. Psychiatry: National Guidelines. Moscow: GEOTAR-Media, 2018. 1008 p.

  49. Glasner-Edwards S, Mooney L. J. Methamphetamine psychosis: epidemiology and management. CNS Drugs. 2014. 28(12): 1115-26. doi: 10.1007/s40263-014-0209-8.

  50. Rosenthal R.N, Miner C. R. Differential diagnosis of substance-induced psychosis and schizophrenia in patients with substance use disorders. Schizophr Bull. 1997; 23(2):187-93. doi: 10.1093/schbul/23.2.187

  51. Fastovtsov G. A., Osolkova S. N. The problem of diagnosing schizophrenia in patients substance use disorders. Rossiyskiy Psikhiatricheskiy Zhurnal. 2018. 5: 51-63

  52. Mendelevich V. D. Psychotic disorders due to drug use. Narkologiya. 2014. 7: 93-100

  53. Rimvall M.K, Jespersen C.P, Clemmensen L, Munkholm A, Skovgaard A.M, Verhulst F, van Os J, Rask C.U, Jeppesen P. Psychotic experiences are associated with health anxiety and functional somatic symptoms in preadolescence. J Child Psychol Psychiatry. 2019. 60(5): 524-532. doi: 10.1111/jcpp.12986.

  54. Frajerman A, Morin V, Chaumette B, Kebir O, Krebs M.O Management of cardiovascular co-morbidities in young patients with early onset psychosis: State of the art and therapeutic perspectives. Encephale. 2020. 46(5): 390-398. doi: 10.1016/j.encep.2020.03.007

  55. Godbout R. Treatment of sleep disorders in children with a psychiatric diagnosis. Sante Ment Que. 2015. 40(2): 257-74

  56. Bray T, Agius M. Soft neurological signs and schizophrenia - a looking glass into core pathology? Psychiatr Danub. 2009. 21(3): 327-8.

  57. Vonberg F.W, Bigdeli T.B. Genetic Correlation Between Schizophrenia and Epilepsy. JAMA Neurol. 2016. 73(1): 125-6. doi: 10.1001/jamaneurol.2015.3480.

  58. Brown AS, Gyllenberg D, Hinkka-Yli-Salomaki S, Sourander A, McKeague IW. Altered growth trajectory of head circumference during infancy and schizophrenia in a National Birth Cohort. Schizophr Res. 2017. 182: 115-119. doi: 10.1016/j.schres.2016.10.032.

  59. McCauley E, Carlson G.A, Calderon R. The role of somatic complaints in the diagnosis of depression in children and adolescents. J Am Acad Child Adolesc Psychiatry. 1991. 30(4): 631-5. doi: 10.1097/00004583-199107000-00016.

  60. Lukkari S, Hakko H, Taanila A, Rasanen P, Riala K, Herva A. Body size at birth and psychiatric disorders among adolescents: a clinical study of 310 under-age inpatient adolescents in Northern Finland. Compr Psychiatry. 2014. 55(3): 414-21. doi: 10.1016/j.comppsych.2013.10.005.

  61. Sormunen E, Saarinen MM, Salokangas RKR, Telama R, Hutri-Kahonen N, Tammelin T, Viikari J, Raitakari O, Hietala J. Effects of childhood and adolescence physical activity patterns on psychosis risk-a general population cohort study. NPJ Schizophr. 2017. 13: 3-5. doi: 10.1038/s41537-016-0007-z.

  62. Mitchell AJ, Delaffon V, Vancampfort D, et al: Guideline concordant monitoring of metabolic risk in people treated with antipsychotic medication: systematic review and meta-analysis of screening practices. Psychol Med 42(1):125-147, 2012 21846426

  63. Druyts E, Eapen S, Wu P, Thorlund K. The risk of elevated prolactin levels in pediatric patients exposed to antipsychotics for the treatment of schizophrenia and schizophrenia spectrum disorders: protocol for a systematic review and meta-analysis. Syst Rev. 2014. 13;3:116. doi: 10.1186/2046-4053-3-116

  64. Pringsheim T, Lam D, Ching H, Patten S. Metabolic and neurological complications of second-generation antipsychotic use in children: a systematic review and meta¬analysis of randomized controlled trials. Drug Saf. 2011 1;34(8):651-68. doi: 10.2165/11592020-000000000-00000

  65. Vonberg FW, Bigdeli TB. Genetic Correlation Between Schizophrenia and Epilepsy. JAMA Neurol. 2016. 73(1): 125-6. doi: 10.1001/jamaneurol.2015.3480.

  66. Ritvo E.R, Ornitz E.M, Walter R.D, Hanley J. Correlation of psychiatric diagnoses and EEG findings: a double-blind study of 184 hospitalized children. Am J Psychiatry. 1970 126(7): 988-96. doi: 10.1176/ajp.126.7.988.

  67. Levman J, Takahashi E. Multivariate analyses applied to fetal, neonatal and pediatric MRI of neurodevelopmental disorders. Neuroimage Clin. 2015 3;9: 532-44. doi: 10.1016/j.nicl.2015.09.017.

  68. Park MTM, Raznahan A, Shaw P, Gogtay N, Lerch JP, Chakravarty MM. Neuroanatomical phenotypes in mental illness: identifying convergent and divergent cortical phenotypes across autism, ADHD and schizophrenia. J Psychiatry Neurosci. 2018. 43(3):201-212. doi: 10.1503/jpn.170094.

  69. Correll CU, Harris J, Figen V, Kane JM, Manu P. Antipsychotic drug administration does not correlate with prolonged rate-corrected QT interval in children and adolescents: results from a nested case-control study. J Child Adolesc Psychopharmacol. 2011. 21(4):365-8. doi: 10.1089/cap.2011.0024.

  70. Jensen KG, Gartner S, Correll CU, Ruda D, Klauber DG, Stentebjerg-Olesen M, Fagerlund B, Jepsen JR, Fink-Jensen A, Juul K, Pagsberg AK. Change and dispersion of QT interval during treatment with quetiapine extended release versus aripiprazole in children and adolescents with first-episode psychosis: results from the TEA trial. Psychopharmacology 2018. 235(3): 681-693. doi: 10.1007/s00213-017-4784-5.

  71. Ho J.G, Caldwell R.L, McDougle C.J, Orsagh-Yentis D.K, Erickson C.A, Posey D.J, Stigler K.A The effects of aripiprazole on electrocardiography in children with pervasive developmental disorders. J Child Adolesc Psychopharmacol. 2012 22(4): 277-83. doi: 10.1089/cap.2011.0129.

  72. DelBello M.P, Versavel M, Ice K, Keller D, Miceli J. Tolerability of oral ziprasidone in children and adolescents with bipolar mania, schizophrenia, or schizoaffective disorder. J Child Adolesc Psychopharmacol. 2008. 18(5):491-9. doi: 10.1089/cap.2008.008

  73. van Erp T.G.M, Walton E, Hibar D.P, Schmaal L, Jiang W et all. White matter microstructural alterations across four major psychiatric disorders: mega-analysis study in 2937 individuals. Mol Psychiatry. 2020 25(4): 883-895. doi: 10.1038/s41380-019-0553-7.

  74. Walton E, Hibar D.P, van Erp T.G.M, Potkin S.G, Roiz-Santianez R et all. Prefrontal cortical thinning links to negative symptoms in schizophrenia via the ENIGMA consortium. Psychol Med. 2018. 48(1):82-94. doi: 10.1017/S0033291717001283.

  75. Dezhina Z, Ranlund S, Kyriakopoulos M, Williams SCR, Dima D. A systematic review of associations between functional MRI activity and polygenic risk for schizophrenia and bipolar disorder. Brain Imaging Behav. 2019.13(3):862-877. doi: 10.1007/s11682-018-9879-z.

  76. Zvereva N. V., Khromov A. I., Sergienko A. A., Koval-Zaytsev A. A. Clinical and psychological methods for assessing cognitive development in children and adolescents with endogenous mental pathology (memory and thinking). Moscow: «Sam Poligrafist», 2017. - 48 p.

  77. Zvereva N. V., Koval-Zaytsev A. A., Khromov A. I. Pathopsychological methods for assessing cognitive development in children and adolescents with endogenous mental pathology (visual perception and thinking). Moscow: «MBA Publishing House», 2014. - 40 p.

  78. Mosolov S.N., Yaltonskaya P.A. Treatment algorithm for primary negative symptoms in schizophrenia. // Sovremennaya Terapiya Psikhicheskikh Rasstroystv. 2020; №2, p. 33-44

  79. Malin D.I., Ryvkin P.V. Intolerance to antipsychotic therapy in the treatment of patients with schizophrenia: risk factors, clinical manifestations, and therapeutic approaches // Sovremennaya Terapiya Psikhicheskikh Rasstroystv. - 2022. - No 3. - P. 2-8. - DOI: 10.21265/PSYPH.2022.50.29.001

  80. 0stergaard S.D, Foldager L, Mors O, Bech P, Correll C.U. The validity and sensitivity of PANSS-6 in treatment-resistant schizophrenia. Acta Psychiatr Scand. 2018. 138(5): 420-431. doi: 10.1111/acps.12952

  81. Leucht S, Kane JM, Kissling W, Hamann J, Etschel E, Engel R.R. What does the PANSS mean? Schizophr Res. 2005.15; 79(2-3): 231-8. doi:

    10.1016/j.schres.2005.04.008.

  82. 0stergaard SD, Foldager L, Mors O, Bech P, Correll C.U. The Validity and Sensitivity of PANSS-6 in the Clinical Antipsychotic Trials of Intervention Effectiveness (CATIE) Study. Schizophr Bull. 2018 15;44(2): 453-462. doi: 10.1093/schbul/sbx076

  83. Mosolov S.N. Psychometric rating scales for schizophrenia symptoms and the concept of positive and negative disorders. Moscow, 2001. 238 p.

  84. Opler L.A., Kay S.R., Lindenmayer J.P., Fiszbein A. Structured Clinical Interview Positive and Negative Syndrome Scale (SCI-PANSS). // Multi-Health Systems Inc., Toronto, 1999, № 4, 15 p.

  85. Fields J. H. et al. A POSITIVE AND NEGATIVE SYMPTOM SCALE FOR CHILDREN AND ADOLESCENTS: THE KIDDIE-PANSS //Clinical

    Neuropharmacology. - 1992. - Vol. 15. - P. 52B.

  86. Schaub D, Juckel G. PSP Scale: German version of the Personal and Social Performance Scale: valid instrument for the assessment of psychosocial functioning in the treatment of schizophrenia Nervenarzt. 2011. 82(9):1178-84. doi: 10.1007/s00115-010-3204-4

  87. Juckel G., Morosini P.L. The new approach: Psychosocial functioning as a necessary outcome criterion for therapeutic success in schizophrenia. Current Opinion in Psychiatry, 2008. 21, 630-639

  88. Juckel G., de Bartolomeis A., Gorwood Ph., Mosolov S., Pani L., Rossi A., Sanjuan J. Towards a framework for treatment effectiveness in schizophrenia. // Neuropsychiatric Disease and Treatment, 2014, №10, P.1867-1878

  89. Morosini P.L, Magliano L, Brambilla L, Ugolini S, Pioli R. Development, reliability and acceptability of a new version of the DSM-IV Social and Occupational Functioning Assessment Scale (SOFAS) to assess routine social functioning. Acta Psychiatrica Scandinavica 2000. 101: 323-329.

  90. Tianmei S, Liang S, Yun"ai S, Chenghua T, Jun Y, Jia C, Xueni L, Qi L, Yantao M, Weihua Z, Hongyan Z. The Chinese version of the Personal and Social Performance Scale (PSP): validity and reliability. Psychiatry Res. 2011. 30;185(1-2): 275-9. doi: 10.1016/j.psychres.2010.05.001

  91. Biological Methods of Therapy for Mental Disorders (Evidence-Based Medicine in Clinical Practice). /Ed. by S.N. Mosolov/ - Moscow, «Sotsialno-Politicheskaya Mysl», 2012, 1073 p.

  92. Mosolov S.N., Tsukarzi E.E. Pharmacotherapy of schizophrenia // Psychiatry: National Guidelines / ed. by N.G. Neznanov, Yu.A. Alexandrovsky. Moscow: Geotar-Media, 2018. P. 299-328

  93. Mosolov S.N., Tsukarzi E.E., Kapiletti S.G. Antipsychotic pharmacotherapy of schizophrenia: from scientific data to clinical guidelines. In: Biological Methods of Therapy for Mental Disorders. Ed. by Mosolov S.N. Evidence-Based Medicine in Clinical Practice. Moscow, 2012. P. 11-61

  94. Mosolov S.N. Fundamentals of psychopharmacotherapy. Moscow: Vostok; 1996. 288 p. (In Russ.)

  95. Zimmermann G., Favrod J., Trieu V.H., Pomini V. The effect of cognitive behavioral treatment on the positive symptoms of schizophrenia spectrum disorders: a meta-analysis. Schizophrenia Research. 2005. 77(1): 1-9.

  96. Nelson A. I. Electroconvulsive Therapy in Psychiatry, Addiction Medicine, and Neurology. Moscow: BINOM. Laboratoriya Znaniy. 2005. - 368 p.

  97. Geretsegger C. Electroconvulsive therapy (ECT). Fortschr Neurol Psychiatr. 1986. 54(5): 139-53. doi: 10.1055/s-2007-1001859.

  98. Tharyan, P. Adams, C.E. Electroconvulsive therapy for schizophrenia. Cochrane Database of Systematic Reviews 2005. No. 2. P. CD000076. — doi:10.1002/14651858.CD000076.pub2

  99. Greenhalgh J. et al. Clinical and cost-effectiveness of electroconvulsive therapy for depressive illness, schizophrenia, catatonia and mania: systematic reviews and economic modelling studies // Health Technology Assessment (Winchester, England). - 2005. - Vol. 9. - No. 9. - P. 1-156

  100. Leucht S, Crippa A, Siafis S, Patel MX, Orsini N, Davis JM. Dose-Response Meta-Analysis of Antipsychotic Drugs for Acute Schizophrenia. Am J Psychiatry. 2020. 177(4):342-353. doi: 10.1176/appi.ajp.2019.19010034

  101. Kennedy E, Kumar A, Datta SS. Antipsychotic medication for childhood¬onset schizophrenia. Cochrane Database Syst Rev. 2007.18(3):CD004027. doi: 10.1002/14651858.CD004027.pub2

  102. Krause M, Zhu Y, Huhn M, Schneider-Thoma J, Bighelli I, Chaimani A, Leucht S. Efficacy, acceptability, and tolerability of antipsychotics in children and adolescents with schizophrenia: A network meta-analysis. Eur

    Neuropsychopharmacol. 2018. 28(6): 659-674. doi: 10.1016/j.euroneuro.2018.03.008

  103. Harvey RC, James AC, Shields GE. A Systematic Review and Network Meta-Analysis to Assess the Relative Efficacy of Antipsychotics for the Treatment of Positive and Negative Symptoms in Early-Onset Schizophrenia. CNS Drugs. 2016. 30(1): 27-39. doi: 10.1007/s40263-015-0308-1.

  104. Abidi S, Mian I, Garcia-Ortega I, Lecomte T, Raedler T, Jackson K, Jackson K, Pringsheim T, Addington D. Canadian Guidelines for the Pharmacological Treatment of Schizophrenia Spectrum and Other Psychotic Disorders in Children and Youth. Can J Psychiatry. 2017. 62(9): 635-647. doi: 10.1177/0706743717720197.

  105. Pringsheim T. et al. Treatment recommendations for extrapyramidal side effects associated with second-generation antipsychotic use in children and youth // Paediatrics & child health. - 2011. - Vol. 16. - No. 9. - P. 590-598.

  106. Fornaro M, Anastasia A, Valchera A, et al. (2018) The FDA “black box” warning on antidepressant suicide risk in young adults: more harm than benefits?. Front. Psychiatry 10:294. doi:10.3389/fpsyt.2019.00294

  107. Sarkar S, Grover S. Antipsychotics in children and adolescents with schizophrenia: a systematic review and meta-analysis. Indian J Pharmacol. 2013. 45(5): 439-46. doi: 10.4103/0253-7613.117720

  108. Pine DS, Cohen E. Therapeutics of aggression in children. Paediatr Drugs. 1999. 1(3): 183-96. doi: 10.2165/00128072-199901030-00003

  109. Saha KB, Bo L, Zhao S, Xia J, Sampson S, Zaman RU. Chlorpromazine versus atypical antipsychotic drugs for schizophrenia. Cochrane Database Syst Rev. 2016. 4(4):CD010631. doi: 10.1002/14651858.CD010631.pub2

  110. Kumar A, Datta SS, Wright SD, Furtado VA, Russell PS. Atypical antipsychotics for psychosis in adolescents. Cochrane Database Syst Rev. 2013. (10):CD009582. doi: 10.1002/14651858.CD009582.pub2

  111. Petrova N.N. Risk factors and prevention of suicide in schizophrenia: focus on the role of modern long-acting injectable antipsychotics // Sovremennaya Terapiya Psikhicheskikh Rasstroystv. - 2021. - No 3. - P. 31-37. - DOI: 10.21265/PSYPH.2021.15.71.003

  112. Xia L, Li WZ, Liu HZ, Hao R, Zhang XY. Olanzapine Versus Risperidone in Children and Adolescents with Psychosis: A Meta-Analysis of Randomized Controlled Trials. J Child Adolesc Psychopharmacol. 2018. 28(4): 244-251. doi: 10.1089/cap.2017.0120

  113. Avrutsky G. Ya., Neduva A. A. Treatment of Psychiatric Patients. — 2nd ed. — Moscow: Meditsina, 1988. — 528 p.

  114. Green W. H. et al. Schizophrenia with childhood onset: a phenomenological study of 38 cases // Journal of the American Academy of Child & Adolescent Psychiatry. - 1992. - Vol. 31. - No. 5. - P. 968-976.

  115. Alderton H. R., Hoddinott B. A. A controlled study of the use of thioridazine in the treatment of hyperactive and aggressive children in a children's psychiatric hospital // Canadian Psychiatric Association Journal. - 1964. - Vol. 9. - No. 3. - P. 239-247.

  116. Neznanov N.G., Mosolov S.N., Ivanov M.V. Psychopharmacotherapy. // In the book: Psychiatry: National Guidelines / ed. by Neznanov N.G.,

    Alexandrovsky Yu.A./ Moscow, 2018. P. 820-893.

  117. Bachmann C. J. et al. Antipsychotic prescription in children and adolescents: an analysis of data from a German statutory health insurance company from 2005 to 2012 // Deutsches Arzteblatt International. - 2014. - Vol. 111. - No. 3. - P. 25.

  118. Remschmidt H. E. et al. Childhood-onset schizophrenia: history of the concept and recent studies // Schizophrenia bulletin. - 1994. - Vol. 20. - No. 4. - P. 727-745.

  119. Toren P, Laor N, Weizman A. Use of atypical neuroleptics in child and adolescent psychiatry. J Clin Psychiatry. 1998. 59(12):644-56. doi: 10.4088/jcp.v59n1202

  120. Leucht S, Winter-van Rossum I, Heres S, et al. The optimization of treatment and management of schizophrenia in Europe (OPTiMiSE) trial: rationale for its methodology and a review of the effectiveness of switching antipsychotics. Schizophr Bull. 2015. 41(3):549-58. doi: 10.1093/schbul/sbv019.

  121. Wang J, Sampson S. Sulpiride versus placebo for schizophrenia. Cochrane database Syst Rev. 2014;(4):CD007811. doi: 10.1002/14651858.CD007811.pub2

  122. Omori IM, Wang J. Sulpiride versus placebo for schizophrenia. Cochrane Database Syst Rev. 2009. 15;(2):CD007811. doi: 10.1002/14651858.CD007811

  123. Bachmann C. J. et al. Antipsychotic prescription in children and adolescents: an analysis of data from a German statutory health insurance company from 2005 to 2012 // Deutsches Arzteblatt International. - 2014. - Vol. 111. - No. 3. - P. 25

  124. Hosam E Matar, Muhammad Qutayba Almerie, Samer Makhoul, Jun Xia, Pamela Humphreys Pericyazine for schizophrenia Cochrane Database Syst Rev. (5):CD007479. doi: 10.1002/14651858.CD007479.pub2.

  125. Lichko A. E. Schizophrenia in Adolescents. Leningrad: Meditsina : Leningr. otd-nie, 1989. - 214 p.

  126. Flank J, Sung L, Dvorak CC, Spettigue W, Dupuis LL. The safety of olanzapine in young children: a systematic review and meta-analysis. Drug Saf. 2014. 37(10): 791-804. doi: 10.1007/s40264-014-0219-y

  127. Pagsberg AK, Tarp S, Glintborg D, Stenstr0m AD, Fink-Jensen A, Correll CU, Christensen R. Acute Antipsychotic Treatment of Children and Adolescents With Schizophrenia-Spectrum Disorders: A Systematic Review and Network Meta¬Analysis. J Am Acad Child Adolesc Psychiatry. 2017. 56(3):191-202. doi:

    10.1016/j.jaac.2016.12.013

  128. Ardizzone I, Nardecchia F, Marconi A, Carratelli TI, Ferrara M. Antipsychotic medication in adolescents suffering from schizophrenia: a meta-analysis of randomized controlled trials. Psychopharmacol Bull. 2010; 43(2):45-66.

  129. Oleychik I. V., Baranov P.A., Shishkovskaya T. I., Sizov S. V. Efficacy and safety of the third-generation atypical antipsychotic lurasidone in the treatment of depressive states developing within the framework of schizophrenia // Sovremennaya Terapiya Psikhicheskikh Rasstroystv. - 2021. - No 2. - P. 28-35. - DOI: 10.21265/PSYPH.2021.57.2.004

  130. Armenteros JL, Davies M. Antipsychotics in early onset Schizophrenia: Systematic review and meta-analysis. Eur Child Adolesc Psychiatry. 2006. (3):141-8. doi: 10.1007/s00787-005-0515-2.

  131. Apter A, Ratzoni G, King RA, et al. Fluvoxamine open-label treatment of adolescent inpatients with obsessive-compulsive disorder or depression. // J Am Acad Child Adolesc Psychiatry. 1994;33(3):342-348. doi:10.1097/00004583-199403000- 00007

  132. Dorofeykova M.V., Petrova N.N. Personalized approach to the therapy of depression in schizophrenia // Sovremennaya Terapiya Psikhicheskikh Rasstroystv. - 2021. - No 3. - P. 39-46. - DOI: 10.21265/PSYPH.2021.99.14.004

  133. Faragian, S., Kurs, R. & Poyurovsky, M. Insight into Obsessive-Compulsive Symptoms and Awareness of Illness in Adolescent Schizophrenia Patients with and without OCD. // Child Psychiatry Hum Dev 39, 39-48 (2008).

    https://doi.org/10.1007/s10578-007-0069-2

  134. Fortea A, Ilzarbe D, Espinosa L, et al. Long-Acting Injectable Atypical Antipsychotic Use in Adolescents: An Observational Study // Journal of Child and Adolescent Psychopharmacology 2018, Vol. 28, N 4, Pp. 252-257 DOI: 10.1089/cap.2017.0096

  135. Petric D, Racki V, Gaco N, et al. Retrospective Analysis of the Effectiveness and Tolerability of Long-Acting Paliperidone Palmitate Antipsychotic in Adolescent First-Episode Schizophrenia Patients // Journal of Child and Adolescent Psychopharmacology 2019, Vol. 29, N 3, Pp. 1-8 DOI: 10.1089/cap.2018.0044

  136. Pereira Sanchez V, Arrieta M, Ferrer-Chinchilla M. et al. Retrospective follow-up data on the use of intramuscular paliperidone palmitate in adolescents and young adults // European Psychiatry 2018; 48S: S359-S566

  137. Chumakov E.M. Modern non-pharmacological and pharmacological treatment strategies for schizophrenia aimed at improving therapy adherence // Modern Therapy of Mental Disorders. - 2022. - No. 3. - P. 58-66. - DOI: 10.21265/PSYPH.2022.97.90.007

  138. Correll CU, Findling RL, Tocco M, Pikalov A, Deng L, Goldman R. Safety and effectiveness of lurasidone in adolescents with schizophrenia: results of a 2-year, open-label extension study [published correction appears in CNS Spectr. 2022 Feb;27(1):129]. CNS Spectr. 2022;27(1):118-128.

  139. Gentile S. Clinical usefulness of second-generation antipsychotics in treating children and adolescents diagnosed with bipolar or schizophrenic disorders. Paediatr Drugs. 2011. 13(5):291-302. doi: 10.2165/11591250-000000000-00000

  140. Putignano D. et al. The evidence-based choice for antipsychotics in children and adolescents should be guaranteed // European journal of clinical pharmacology. - 2019. - P. 1-8.

  141. Pagsberg A. K. et al. Quetiapine extended release versus aripiprazole in children and adolescents with first-episode psychosis: the multicentre, double-blind, randomised tolerability and efficacy of antipsychotics (TEA) trial // The Lancet Psychiatry. - 2017. - Vol. 4. - No. 8. - P. 605-618.

  142. Lerner V. Biperiden (Akineton): a literature review. Psychiatry and Psychopharmacotherapy, 2014. 10:36-43

  143. Lamberti M. et al. Aripiprazole-induced tardive dyskinesia in 13 years old girl successfully treated with biperiden: A case report // Clinical Psychopharmacology and Neuroscience. - 2017. - Vol. 15. - No. 3. - P. 285.

  144. Malin D.I., Ryvkin P.V. Clinically significant drug interactions in the treatment with second-generation antipsychotics // Sovremennaya Terapiya Psikhicheskikh Rasstroystv. - 2021. - No 2. - P. 36-45. - DOI: 10.21265/PSYPH.2021.57.2.005

  145. Maslenikov N.V., Tsukarzi E.E., Mosolov S.N. Algorithm for biological therapy of depression in schizophrenia. // Sovremennaya Terapiya Psikhicheskikh Rasstroystv. 2019. 1: 31-39

  146. Mosolov S.N. Clinical Application of Modern Antidepressants. St. Petersburg, «Meditsinskoe Informatsionnoe Agentstvo», 1995. - 568 p.

  147. Hasan A., Falkai P., Wobrock T., Lieberman J., Glenth0j B., Gattaz W.F., Thibaut F., Moller H.J., Mosolov S.N. World Federation of Societies of Biological Psychiatry (WFSBP) Guidelines for biological treatment of schizophrenia - A short version for primary care. // International Journal of Psychiatry in Clinical Practice. 2017, Vol. 21, № 2, P. 82-90.

  148. Jerrell J. M., McIntyre R. S., Deroche C. B. Pharmacotherapy effectiveness for clinical subgroups among children and adolescents with early onset schizophrenia // Human Psychopharmacology: Clinical and Experimental. - 2017. - Vol. 32. - No. 2. - P. e2585.

  149. Kang-Yi C. D. et al. Psychiatric Diagnoses and Treatment Preceding Schizophrenia in Adolescents Aged 9-17 Years // Frontiers in Psychiatry. - 2020. - Vol. 11. - P. 487.

  150. Coskun M., Zoroglu S. Clozapine induced obsessions treated with sertraline in an adolescent with schizophrenia // Klinik Psikofarmakoloji Bulteni. - 2009. - Vol. 19. - No. 2. - P. 155

  151. Jerath A. U., Mavrides N. A., Coffey B. J. Complexity in Evaluation and Pharmacological Treatment of Early Onset Psychosis with Mood Symptoms: Childhood Onset Schizophrenia or Affective Disorder? // Journal of child and adolescent psychopharmacology. - 2019. - Vol. 29. - No. 3. - P. 241-244

  152. Falkai P., Wobrock T., Lieberman J., Glenthoj B., Gattaz Wf., Moller H-J., et al. World Federation of Societies of Biological Psychiatry (WFSBP) Guidelines for Biological Treatment of Schizophrenia, Part 1: Acute Treatment of Schizophrenia. // The World Journal of Biological Psychiatry: the official journal of the World Federation of Societies of Biological Psychiatry. 2005, Vol. 6, № 3, P. 132-191.

  153. Jerrell J. M., McIntyre R. S., Deroche C. B. Pharmacotherapy effectiveness for clinical subgroups among children and adolescents with early onset schizophrenia // Human Psychopharmacology: Clinical and Experimental. - 2017. - Vol. 32. - No. 2. - P. e2585.

  154. Usov G.M., Kolomytsev D.Yu. The concept of early intervention in the therapy of schizophrenia // Sovremennaya Terapiya Psikhicheskikh Rasstroystv. - 2023. - No 1. - P. 3-13. - DOI: 10.21265/PSYPH.2023.69.86.001

  155. Abidi, S., Mian, I., Garcia-Ortega, I., Lecomte, T., Raedler, T., Jackson, K., Jackson, K., Pringsheim, T., & Addington, D. Canadian Guidelines for the

    Pharmacological Treatment of Schizophrenia Spectrum and Other Psychotic Disorders in Children and Youth. Canadian journal of psychiatry. 2017. 62(9): 635¬647. https://doi.org/10.1177/0706743717720197

  156. Huband N, Ferriter M, Nathan R, Jones H. Antiepileptics for aggression and associated impulsivity. Cochrane Database Syst Rev. 2010. 2010(2):CD003499. doi: 10.1002/14651858.CD003499.pub3

  157. Dold M, Li C, Tardy M, Khorsand V, Gillies D, Leucht S. Benzodiazepines for schizophrenia. Cochrane Database Syst Rev. 2012. 14;11(11):CD006391. doi:

    10.1002/14651858.CD006391.pub2

  158. Dedkova A.E. Experience of effective use of benzodiazepines in catatonia complicated by neuroleptic malignant syndrome. // Sovremennaya Terapiya Psikhicheskikh Rasstroystv 2016. 2: 29-34.

  159. Benarous X, Raffin M, Ferrafiat V, Consoli A, Cohen D. Catatonia in children and adolescents: New perspectives. Schizophr Res. 2018. 200:56-67. doi: 10.1016

  160. Sidorchuk A. et al. Benzodiazepine prescribing for children, adolescents, and young adults from 2006 through 2013: a total population register-linkage study // PLoS medicine. - 2018. - Vol. 15. - No. 8. - P. e1002635

  161. Sevi Tok ES, Arkar H, Bildik T.The Effectiveness of Cognitive Behavioral Therapy, Medication, or Combined Treatment For Child Hood Anxiety Disorders. Turk Psikiyatri Derg. 2016 27(2):10.

  162. Pharoah F, Mari J, Rathbone J, Wong W. Family intervention for schizophrenia. Cochrane Database Syst Rev. 2010. 8;(12) :CD000088. doi:

    10.1002/14651858.CD000088.pub2.

  163. Maurus I, Roh A, Falkai P, Malchow B, Schmitt A, Hasan A. Nonpharmacological treatment of dyscognition in schizophrenia: effects of aerobic exercise. Dialogues Clin Neurosci. 2019. 21(3):261-269. doi:

    10.31887/DCNS.2019.21.3/aschmitt.

  164. Broderick J, Crumlish N, Waugh A, Vancampfort D. Yoga versus non-standard care for schizophrenia. Cochrane Database Syst Rev. 2017 28;9(9):CD012052. doi: 10.1002/14651858.CD012052.pub2.

  165. Ruddy RA, Dent-Brown K. Drama therapy for schizophrenia or schizophrenia¬like illnesses. Cochrane Database Syst Rev. 2007 24;(1): CD005378. doi:

    10.1002/14651858.CD005378.pub2.

  166. Valiente C, Espinosa R, Trucharte A, Nieto J, Martinez-Prado L. The challenge of well-being and quality of life: A meta-analysis of psychological interventions in schizophrenia. Schizophr Res. 2019. 208:16-24. doi: 10.1016/j.schres.2019.01.040.

  167. Laws KR, Darlington N, Kondel TK, McKenna PJ, Jauhar S. Cognitive Behavioural Therapy for schizophrenia - outcomes for functioning, distress and quality of life: a meta-analysis. BMC Psychol. 2018. 17;6(1):32. doi: 10.1186/s40359- 018-0243-2.

  168. Jones C, Hacker D, Xia J, Meaden A, Irving CB, Zhao S, Chen J, Shi C. Cognitive behavioural therapy plus standard care versus standard care for people with schizophrenia. Cochrane Database Syst Rev. 2018. 20;12(12):CD007964. doi: 10.1002/14651858.CD007964.pub2.

  169. Ueland T., Rund B. R. A controlled randomized treatment study: the effects of a cognitive remediation program on adolescents with early onset psychosis // Acta Psychiatrica Scandinavica. - 2004. - Vol. 109. - No. 1. - P. 70-74.

  170. Ueland T, Rund BR. Cognitive remediation for adolescents with early onset psychosis: a 1-year follow-up study. // Acta Psychiatr Scand 2005;111:193-201

  171. van Oosterhout B, Smit F, Krabbendam L, Castelein S, Staring AB, van der Gaag M. Metacognitive training for schizophrenia spectrum patients: a meta-analysis on outcome studies. Psychol Med. 2016. 46(1):47-57. doi: 10.1017/S0033291715001105.

  172. Geretsegger M, Mossier KA, Bieleninik L, Chen XJ, Heldal TO, Gold C. Music therapy for people with schizophrenia and schizophrenia-like disorders. Cochrane Database Syst Rev. 2017. 29;5(5):CD004025. doi: 10.1002/14651858.CD004025.pub4

  173. Gold C, Heldal TO, Dahle T, Wigram T. Music therapy for schizophrenia or schizophrenia-like illnesses. Cochrane Database Syst Rev. 2005. 18;(2):CD004025. doi: 10.1002/14651858.CD004025.pub2.

  174. Potocky M. An art therapy group for clients with chronic schizophrenia // Social Work with Groups. - 1993. - Vol. 16. - No. 3. - P. 73-82.

  175. Izquierdo de Santiago A, Khan M. Hypnosis for schizophrenia. Cochrane Database Syst Rev. 2007. 17;2007(4):CD004160. doi:

    10.1002/14651858.CD004160.pub3

  176. Gruzelier J. Unwanted effects of hypnosis: a review of the evidence and its implications // Contemporary Hypnosis. - 2000. - Vol. 17. - No. 4. - P. 163-193

  177. Psychiatry: National Guidelines / Ed. by Alexandrovsky Yu.A., Neznanov N.G. et al. / Moscow. 2011, 1008 p.

  178. Law E, Fisher E, Eccleston C, Palermo TM. Psychological interventions for parents of children and adolescents with chronic illness. Cochrane Database Syst Rev. 2019 18;3(3):CD009660. doi: 10.1002/14651858.CD009660.pub4

  179. Buckley LA, Maayan N, Soares-Weiser K, Adams CE. Supportive therapy for schizophrenia. Cochrane Database Syst Rev. 2015. 14;2015(4):CD004716. doi:

    10.1002/14651858.CD004716.pub4.

  180. Gearing RE. Evidence-based family psychoeducational interventions for children and adolescents with psychotic disorders. Journal of the Canadian Academy of Child and Adolescent Psychiatry. 2008. 17(1): 2-11.

  181. Kupriyanova T.A., Koren E.V. Psychosocial therapy program (module) for children and adolescents with schizophrenia spectrum disorders.// Sovremennaya Terapiya Psikhicheskikh Rasstroystv. 2015. 3: 26-32.

  182. Ueland T., Rund B. R. A controlled randomized treatment study: the effects of a cognitive remediation program on adolescents with early onset psychosis // Acta Psychiatrica Scandinavica. - 2004. - Vol. 109. - No. 1. - P. 70-74.

  183. Ueland T, Rund BR. Cognitive remediation for adolescents with early onset

    psychosis: a 1-year follow-up study. // Acta Psychiatr Scand 2005;111:193-201

  184. Cella M, Preti A, Edwards C, Dow T, Wykes T. Cognitive remediation for negative symptoms of schizophrenia: A network meta-analysis. // Clin Psychol Rev. 2017. 52:43-51. doi: 10.1016/j.cpr.2016.11.009.

  185. Lewandowski KE. Cognitive Remediation for the Treatment

    of Cognitive Dysfunction in the Early Course of Psychosis. Harv Rev Psychiatry. 2016. 24(2):164-72. doi: 10.1097/HRP.0000000000000108.

  186. Bryce S, Sloan E, Lee S, Ponsford J, Rossell S. Cognitive remediation in schizophrenia: A methodological appraisal of systematic reviews and meta-analyses. J Psychiatr Res. 2016. 75:91-106. doi: 10.1016/j.jpsychires.2016.01.004.

  187. Wood L, Byrne R, Varese F, Morrison AP. Psychosocial interventions for internalised stigma in people with a schizophrenia-spectrum diagnosis: A systematic narrative synthesis and meta-analysis. Schizophr Res. 2016. 176(2-3):291-303. doi: 10.1016/j.schres.2016.05.001.

  188. Turner DT, McGlanaghy E, Cuijpers P, van der Gaag M, Karyotaki E, MacBeth A. A Meta-Analysis of Social Skills Training and Related Interventions for Psychosis. Schizophr Bull. 2018. 6;44(3):475-491. doi: 10.1093/schbul/sbx146

  189. Kurtz MM, Richardson CL. Social cognitive training for schizophrenia: a meta- analytic investigation of controlled research. Schizophr Bull. 2012. 38(5):1092-104. doi: 10.1093/schbul/sbr036.

  190. Shimizu N, Umemura T, Matsunaga M, Hirai T. An interactive sports video game as an intervention for rehabilitation of community-living patients with schizophrenia: A controlled, single-blind, crossover study. PLoS One. 2017 Nov 13;12(11):e0187480. doi: 10.1371/journal.pone.0187480

  191. Psychiatry: National Guidelines / Ed. by Alexandrovsky Yu.A., Neznanov N.G./ - Concise edition, revised and expanded. Moscow. 2021

  192. Lloyd A, Horan W, Borgaro SR, Stokes JM, Pogge DL, Harvey PD. Predictors of medication compliance after hospital discharge in adolescent psychiatric patients. J Child Adolesc Psychopharmacol. 1998; 8(2):133-41. doi: 10.1089/cap.1998.8.133.

  193. Krasnov V.N., Gurovich I.Ya., Mosolov S.N., Shmukler A.B. et al. Psychiatric Care for Patients with Schizophrenia. Clinical Guide - Moscow, 2007

  194. Hasan A., Falkai P., Wobrock T., Lieberman J., Glenthoj B., Gattaz W.F., Thibaut F., Moller H.J. World Federation of Societies of Biological Psychiatry (WFSBP) Guidelines for Biological Treatment of Schizophrenia, part 1: update 2012 on the acute treatment of schizophrenia and the management of treatment resistance. World J Biol Psychiatry 2012;13(5):318-78. doi: 10.3109/15622975.2012.696143.

  195. Hasan A, Falkai P, Wobrock T, Lieberman J, Glenthoj B, Gattaz WF, Thibaut F, Moller HJ. World Federation of Societies of Biological Psychiatry (WFSBP) guidelines for biological treatment of schizophrenia, part 2: update 2012 on the long¬term treatment of schizophrenia and management of antipsychotic-induced side effects. WFSBP Task force on Treatment Guidelines for Schizophrenia.World J Biol Psychiatry. 2013.14(1):2-44. doi: 10.3109/15622975.2012.739708.

  196. Hasan A, Falkai P, Wobrock T, Lieberman J, Glenth0j B, Gattaz WF, Thibaut F, Moller HJ. World Federation of Societies of Biological Psychiatry (WFSBP) Guidelines for Biological Treatment of Schizophrenia. Part 3: Update 2015 Management of special circumstances: Depression, Suicidality, substance use disorders and pregnancy and lactation. WFSBP Task Force on Treatment Guidelines for Schizophrenia. World J Biol Psychiatry. 2015.16(3): 142-70. doi: 10.3109/15622975.2015.1009163

  197. Makushkin E.V., Simashkova N.V., Goryunov A.V., Perezhogin L.O. Schizophrenia in childhood and adolescence. Rossiyskiy psikhiatricheskiy zhurnal. 2016;6:62-81. (In Russ.)

  198. Firth J, Cotter J, Elliott R, French P, Yung AR A systematic review and meta-analysis of exercise interventions in schizophrenia patients. Psychol Med.

    2015;45(7):1343-61. doi: 10.1017/S0033291714003110.

  199. Dwivedi S, Pavuluri M, Heidenreich J, Wright T. Response to fluvoxamine augmentation for obsessive and compulsive symptoms in schizophrenia. // J Child Adolesc Psychopharmacol. 2002;12(1):69-70. doi:10.1089/10445460252943597

  200. Fusar-Poli P, Cappucciati M, Bonoldi I, Hui LM, Rutigliano G, Stahl DR, Borgwardt S, Politi P, Mishara AL, Lawrie SM, Carpenter WT Jr, McGuire PK. Prognosis of Brief Psychotic Episodes: A Meta-analysis. JAMA Psychiatry. 2016;73(3):211-20. doi: 10.1001/jamapsychiatry.2015.2313.

  201. Jaaskelainen E, Juola P, Hirvonen N, McGrath JJ, Saha S, Isohanni M, Veijola J, Miettunen J. A systematic review and meta-analysis of recovery in schizophrenia. Schizophr Bull. 2013; 39(6):1296-306. doi: 10.1093/schbul/sbs130.

  202. Rapoport J, Chavez A, Greenstein D, Addington A, Gogtay N. Autism spectrum disorders and childhood-onset schizophrenia: clinical and biological contributions to a relation revisited. J Am Acad Child Adolesc Psychiatry. 2009 Jan;48(1):10-8. doi: 10.1097/CHI.0b013e31818b1c63

  203. Driver DI, Thomas S, Gogtay N, Rapoport JL. Childhood-Onset Schizophrenia and Early-onset Schizophrenia Spectrum Disorders: An Update. Child Adolesc Psychiatr Clin N Am. 2020 Jan;29(1):71-90. doi: 10.1016/j.chc.2019.08.017

  204. D0ssing E, Pagsberg AK. Electroconvulsive Therapy in Children and Adolescents: A Systematic Review of Current Literature and Guidelines. J ECT. 2021 Sep 1;37(3):158-170. doi: 10.1097/YCT.0000000000000761

  205. Patel RS, Hobart K, Wadhawan A, Chalia A, Youssef NA. Electroconvulsive Treatment Utilization for Inpatient Management of Catatonia in Adolescents With Schizophrenia Spectrum Disorders. J ECT. 2022 Dec 1;38(4):244-248. doi: 10.1097/YCT.0000000000000858

  206. Schneider C, Corrigall R, Hayes D, Kyriakopoulos M, Frangou S. Systematic review of the efficacy and tolerability of clozapine in the treatment of youth with early onset schizophrenia. Eur Psychiatry. 2014 Jan;29(1):1-10. doi:

    10.1016/j.eurpsy.2013.08.001

  207. Adnan M, Motiwala F, Trivedi C, Sultana T, Mansuri Z, Jain S. Clozapine for Management of Childhood and Adolescent-Onset Schizophrenia: A Systematic Review and Meta-Analysis. J Child Adolesc Psychopharmacol. 2022 Feb;32(1):2-11. doi: 10.1089/cap.2021.0092

  208. Shaw P, Sporn A, Gogtay N, Overman GP, Greenstein D, Gochman P, Tossell JW, Lenane M, Rapoport JL. Childhood-onset schizophrenia: A double-blind, randomized clozapine-olanzapine comparison. Arch Gen Psychiatry. 2006 Jul;63(7):721-30. doi: 10.1001/archpsyc.63.7.721

  209. Arango C, Ng-Mak D, Finn E, Byrne A, Loebel A. Lurasidone compared to other atypical antipsychotic monotherapies for adolescent schizophrenia: a systematic literature review and network meta-analysis. Eur Child Adolesc Psychiatry. 2020 Sep;29(9):1195-1205. doi: 10.1007/s00787-019-01425-2

  210. Nussbaum L.A., Hogea L.M., Chiriac D.V., Grigoraş M.L., Folescu R, Bredicean A.C., Roşca E.C.I., Muncan B., Nussbaum L.M., Simu M.A., Levai C.M. The effect of neurobiological changes in the brain of children with schizophrenia, ultra high-risk for psychosis and epilepsy: clinical correlations with EEG and neuroimagistic abnormalities. Rom J Morphol Embryol. 2017;58(4):1435-1446.

  211. Nelson A.I. Elektrosudorozhnaya terapiya v psikhiatrii, narkologii i nevrologii / A.I. Nelson. — M: BINOM. Laboratoriya znaniy, 2005. — 368 p.: ill. (In Russ.)

Appendix A1. Working Group Composition

  1. Balakireva Elena Evgenyevna, Candidate of Medical Sciences, Leading Researcher, Department of Child Psychiatry, Mental Health Research Center. Member of the Russian Society of Psychiatrists (RSP).

  2. Ivanov Mikhail Vladimirovich, Candidate of Psychological Sciences, Leading Researcher, Department of Child Psychiatry, Mental Health Research Center. Member of the Russian Society of Psychiatrists (RSP).

  3. Ivashchenko Dmitry Vladimirovich, Doctor of Medical Sciences, Associate Professor, Head of the Department of Child Psychiatry and Psychotherapy, Russian Medical Academy of Continuous Professional Education of the Russian Ministry of Health. Member of the Russian Society of Psychiatrists (RSP).

  4. Koval-Zaitsev Alexey Anatolyevich, Candidate of Psychological Sciences, Leading Researcher, Department of Child Psychiatry, Mental Health Research Center. Member of the Russian Society of Psychiatrists (RSP).

  5. Kulikov Anton Vladislavovich, Candidate of Medical Sciences, Senior Researcher, Department of Child Psychiatry, Mental Health Research Center. Member of the Russian Society of Psychiatrists (RSP).

  6. Makushkin Evgeny Vadimovich, Doctor of Medical Sciences, Professor, Head of the Scientific and Medical Center for Child Psychiatry, National Medical Research Center for Children's Health of the Russian Ministry of Health. Member of the Russian Society of Psychiatrists (RSP).

  7. Nikitina Svetlana Gennadyevna, Candidate of Medical Sciences, Senior Researcher, Department of Child Psychiatry, Mental Health Research Center. Member of the Russian Society of Psychiatrists (RSP).

  8. Perezhogin Lev Olegovich, Doctor of Medical Sciences, Head of the Department of Social Psychiatry of Children and Adolescents, V.P. Serbsky National Medical Research Center for Psychiatry and Narcology of the Russian Ministry of Health. Member of the Russian Society of Psychiatrists (RSP).

    The members of the working group for the development and revision of clinical guidelines declare no conflict of interest.

Appendix A2. Methodology for Developing Clinical Guidelines

Target audience of these clinical guidelines:

1. Psychiatrist

2. Psychotherapist

3. Medical psychologist

Table 1. Scale for assessing levels of evidence (LE) for diagnostic methods (diagnostic interventions)

LoE

Definition

1

Systematic reviews of studies with reference standard control or systematic reviews of randomized controlled trials with meta-analysis

2

Individual studies with reference standard control or individual randomized controlled trials and systematic reviews of studies of any design, except randomized controlled trials, with meta-analysis

3

Studies without consecutive reference standard control or studies with a reference standard not independent of the test method, or non-randomized comparative studies, including cohort studies

4

Non-comparative studies, case report

5

Only justification of mechanism of action or expert opinion is available

Table 2. Scale for assessing levels of evidence (LE) for prevention, treatment and rehabilitation methods (preventive, therapeutic, rehabilitation interventions)

LoE

Definition

1

Systematic review of RCTs with meta-analysis

2

Individual RCTs and systematic reviews of studies of any design except RCTs, with meta-analysis

3

Non-randomized comparative studies, including cohort studies

4

Non-comparative studies, case reports or case series, case-control studies

5

Only justification of the mechanism of action of the intervention (preclinical studies) or expert opinion is available

Table 3. Scale for assessing grades of recommendation (GR) for prevention, diagnosis, treatment and rehabilitation methods (preventive, diagnostic, therapeutic, rehabilitation interventions)

GoR

Definition

A

Strong recommendation (all evaluated efficacy criteria (outcomes) are important, all studies are of high or satisfactory methodological quality, and their conclusions regarding

the outcomes of interest are consistent)

B

Conditional recommendation (not all considered efficacy criteria (outcomes) are important, not all studies are of high or acceptable methodological quality, and/or their conclusions on the outcomes of interest are inconsistent)

C

Weak recommendation (lack of adequate quality evidence (all considered efficacy criteria (outcomes) are unimportant, all studies are of low methodological quality, and their conclusions on the outcomes of interest are inconsistent)

Procedure for updating clinical guidelines.

The mechanism for updating clinical guidelines provides for their systematic revision at least once every three years, as well as upon the emergence of new evidence-based medicine data regarding the diagnosis, treatment, prevention, and rehabilitation of specific diseases, or in the presence of justified additions/comments to previously approved clinical guidelines, but no more frequently than once every 6 months.

Appendix A3. Reference Materials

Legislative and regulatory acts governing the provision of care for schizophrenia

  1. Federal Law No. 323-FZ of November 21, 2011, "On the Fundamentals of Protecting the Health of Citizens in the Russian Federation";

  2. Law of the Russian Federation No. 3185-1 of July 2, 1992, "On Psychiatric Care and Guarantees of Citizens' Rights in Its Provision";

  3. Procedure for Providing Medical Care for Mental Disorders and Behavioral Disorders (Approved by Order of the Ministry of Health of the Russian Federation No. 566n of May 17, 2012);

  4. Order of the Ministry of Health of the Russian Federation No. 1233n of December 20, 2012, "On the Approval of the Standard of Specialized Medical Care for Schizophrenia, Acute (Subacute) Phase, with Treatment Resistance and Therapy Intolerance";

  5. Order of the Ministry of Health of the Russian Federation No. 1400n of December 24, 2012, "On the Approval of the Standard of Specialized Medical Care for Schizophrenia, Acute (Subacute) Phase with Protracted Course and Preponderance of Social Rehabilitation Problems";

  6. Order of the Ministry of Health of the Russian Federation No. 1421n of December 24, 2012, "On the Approval of the Standard of Specialized Medical Care for Schizophrenia, Subacute Phase in a Day Hospital Setting";

  7. Order of the Ministry of Health of the Russian Federation No. 420 of December 31, 2002, "On the Approval of Primary Medical Documentation Forms for Psychiatric and Narcological Facilities".

Information on indications for use, contraindications, methods of administration, and dosages of medicinal products is publicly available on the website of the State Register of Medicines grls.rosminzdrav.ru

Appendix B. Physician Action Algorithms

Appendix B. Physician Action Algorithms — Schizophrenia

Appendix C. Patient Information

Information for Parents

Schizophrenia is a chronic mental disorder occurring in both adults and children. Schizophrenia has been known since antiquity; patient descriptions corresponding to the modern concept of schizophrenia, which took shape in the early 20th century, are present even in ancient and medieval literature. Cases of schizophrenia have been described in people of all ages, from infants to the elderly, in men and women, and among all races. According to the World Health Organization, 0.3% to 0.7% of people worldwide suffer from schizophrenia, which amounts to approximately 20-30 million individuals. Schizophrenia is rare in childhood; the proportion of individuals who develop schizophrenia in childhood is less than 1% (according to other authors, up to 4%) of all affected individuals. Among children recognized as disabled due to mental disorders in Russia, children with schizophrenia account for 4.4%. According to recent epidemiological data in Russia, the overall incidence rates of schizophrenia in children have increased by 6.5% since 2000.

Schizophrenia is presumed to be a polyetiological disease, the etiology and pathogenesis of which remain unknown to date. There are numerous theories and hypotheses regarding its origin, which emphasize various hereditary factors and environmental influences to varying degrees, but none can claim absolute validity. In recent years, it is generally accepted that most cases of schizophrenia develop due to a random combination of several (possibly several dozen) common genes among people and spontaneous mutations leading to impaired metabolism of the brain's crucial neurotransmitters — dopamine, serotonin, and others. People with such abnormalities do not fall ill immediately, but constitute a risk group for the development of schizophrenia. Additional negative environmental factors are required for the disease to develop. Currently, the leading damaging factor hypothesized by scientists is an autoimmune process leading to alterations in brain structure at the cellular and functional levels. Numerous social factors, such as poverty, migration, urbanization, physical (including sexual) and emotional abuse in childhood, insufficient emotional support from parents, loneliness, as well as socially conditioned factors such as alcoholism and marijuana use, have been studied over the past half-century, but none have shown a convincing causal relationship with the onset of schizophrenia.

The clinical picture of schizophrenia is very diverse; individual forms of schizophrenia combined with different types of its course create a bizarre continuum of individual clinical cases. All symptoms of schizophrenia are nonspecific to varying degrees. Attempts to isolate symptoms that are pathognomonic and unique to schizophrenia, such as the famous "first-rank symptoms" proposed by K. Schneider, have been unsuccessful. Modern diagnostic approaches outlined in international classifications (diagnostic systems), such as the International Classification of Diseases, 10th Revision (ICD-10, used in Russia since 1999), rely on a categorical approach requiring the identification of a specific number of symptoms present in the clinical picture for a certain duration during diagnosis.

All symptoms of schizophrenia can be divided into five groups (this division is not used in ICD-10). Positive symptoms (i.e., those that a healthy person does not have and that stand out upon their appearance) include (1) delusions, i.e., "a set of morbid ideas, reasoning, and conclusions that take possession of the patient's consciousness, distort reality, and are not amenable to external correction" (Bleikher V. M., 1983)—typically, delusions are built around ideas of influence, persecution, and a special mission; (2) hallucinations, i.e., perceptual distortions, typically voices commenting on the patient's behavior, discussing them, and localized either outside or inside the body, especially in the head; (3) catatonic symptoms (freezing, bizarre postures, walking in circles, agitation or stupor, vocalizations); (4) agitation (fussing excitement and inner tension); (5) behavioral and speech disturbances. Positive symptoms are hypothesized to be associated with abnormalities in mesolimbic neural networks. Negative symptoms (i.e., the result of a deficit in normally intact functions) are represented by (1) poverty of speech, (2) blunting and a limited range of emotions, (3) decreased social contacts, passivity, (4) stereotypy in thinking and difficulties in abstracting, (5) attention impairments, decreased motivation, and anhedonia. They are much harder to notice in children than positive psychotic symptoms, but careful observation reveals content and lexical impoverishment of speech, limited non-verbal communicative responses, restricted eye contact with the interlocutor, neglect of one's own appearance and grooming, sometimes including personal hygiene. Parents and close relatives usually notice changes in interests, loss of motivation for studies, sports, and hobbies, and avoidance of social contacts. Negative symptoms may appear earlier than positive ones, serving as peculiar harbingers of psychosis. Their emergence is hypothesized to be linked to dysfunctions in the prefrontal cortex. Cognitive symptoms are associated with executive dysfunction (memory and intelligence in schizophrenia patients, except for those with very early onset, are usually preserved), i.e., with goal-setting, planning, attention allocation, evaluation and monitoring of completed actions, and modulation of one's behavior based on indirect social cues. Cognitive symptoms are likely mediated by the dorsolateral prefrontal cortex. Affective symptoms include anxiety, tension, feelings of guilt, unease, and irritability. They result from dysfunction in the ventromedial prefrontal cortex. Aggression manifests as verbal, non-verbal, physical impact directed at inanimate objects, animals, people, including oneself, and is typically associated with the content of hallucinatory and delusional symptoms. In younger schizophrenia patients, aggression and auto-aggression may be unpredictable and spontaneous, posing a high degree of danger to themselves and others. Aggression manifestations are associated with neurotransmitter metabolism disturbances in the amygdala and orbitofrontal cortex.

Treatment for schizophrenia is typically prolonged and comprehensive. The scientific literature describes a few cases of practical recovery confirmed by long-term follow-up. However, as a rule, such an outcome is difficult to achieve. Many patients with schizophrenia, despite ongoing treatment, become disabled due to their mental disorder. Therefore, the goal of treatment becomes achieving stable remission and preventing the desocialization of patients.

In the treatment of schizophrenia in children, pharmacotherapy occupies a leading place. Productive symptoms are managed with neuroleptics (antipsychotics), some of which are likely capable of alleviating negative symptoms as well; however, negative symptoms in schizophrenia are characterized by persistence and worsen as the disease progresses, whereas positive symptoms can usually be controlled. Along with antipsychotics, antidepressants (for depressive affective symptoms), anxiolytics (for anxiety states), and mood stabilizers are used. Antiparkinsonian medications are used to prevent side effects of neuroleptic drugs. Shock therapy methods (electroconvulsive therapy, insulin coma therapy) are not used in the treatment of children. Prescribing treatment for schizophrenia is strictly the prerogative of a psychiatrist.

The most crucial component of successful schizophrenia therapy is the socialization of patients. If a patient's mental state allows them to study or work, such an opportunity should not be neglected. After acute conditions are resolved, psychotherapeutic support, including cognitive behavioral therapy and family therapy, is indicated for all patients. Family and friends' support and the engagement of patients in social relationships are of great importance for achieving therapeutic success in schizophrenia.

Information for patients (older children)

Schizophrenia is a mental disorder that disrupts a person's perception of reality. It can cause hallucinations, delusions, thought disorders, learning difficulties, and an unwillingness to socialize with others.

In its early stages, schizophrenia may resemble typical adolescent behavior: withdrawal, abandonment of hobbies, and loss of contact with friends. However, there are important differences: no new interests replace the old ones, processing information (especially academic) becomes difficult, and profound apathy toward one's life takes over the personality. Concurrently, positive symptoms develop: hallucinations and delusions. Hallucinations in schizophrenia can be auditory or visual. Auditory hallucinations resemble a "voice" sounding inside the patient's head. In schizophrenia, the patient understands that the "voice" is heard only by them. Delusions typically involve the conviction that one is being persecuted or that others want to harm them, and these individuals can be complete strangers or even mystical entities (e.g., demons).

To the patient, the "voices" are beyond their control, "arise on their own," and can interfere with the thought process and voluntary actions. "Voices" in schizophrenia are not a mystery to science. In fact, they are the person's own thoughts that, due to the mental disorder, are perceived as external influence. Today, the most likely cause is considered to be dysfunction of subcortical brain nuclei responsible for recognizing whether external stimuli are one's own or external.

The difficulty in recognizing hallucinations and delusions for the patient themselves lies in a reduced insight into their condition. This means the patient does not view what is happening as unusual: they take the emerging hallucinations for granted and do not rationally evaluate their delusions.

Schizophrenia is also characterized by volitional disorders. Externally, this manifests as an unwillingness to do anything, neglect of personal hygiene, and lack of initiative. Volitional disorders are dangerous because the patient may commit dangerous acts under the influence of hallucinations—up to and including suicide, because "the voice commanded it."

If schizophrenia is suspected, one should definitely consult a psychiatrist. The goal of treatment is to reintegrate the patient into society so they can lead a full life. Antipsychotics (also known as neuroleptics) are used to treat schizophrenia. Their efficacy has been proven in numerous scientific studies. Antipsychotics are prescribed for a long period—at least 1 year—and treatment may be continued at the discretion of the attending physician. Antipsychotics are the most effective therapy for schizophrenia, suppressing delusions and hallucinations and normalizing the patient's thought processes. People with schizophrenia who receive treatment can study and work. To achieve this, it is important to купировать acute symptoms.

The state in which a patient's hallucinations have ceased, delusions have resolved, and thinking has normalized is called remission. Once achieved, psychotherapeutic methods can be introduced, primarily cognitive behavioral therapy.

Cases where schizophrenia symptoms resolve without treatment are extremely rare. It is strongly discouraged to neglect medical care or refuse medication. Untreated schizophrenia leads to disability in the vast성이 of cases.

Appendix G. Assessment Scales, Questionnaires, and Other Evaluation Tools

Appendix G1. Positive and Negative Syndrome Scale.

Russian title - Positive and Negative Syndrome Scale (PANSS).

Original title - Positive and Negative Syndrome Scale — PANSS

Source - Kay S.R, Fiszbein A, Opler L.A. The positive and negative syndrome scale (PANSS) for schizophrenia. 1987. Schizophr Bull. 13 (2): 261-76. doi:10.1093/schbul/13.2.261

Type (underline):

- rating scale

- index

- questionnaire

- other (specify)

Purpose: The Positive and Negative Syndrome Scale is used to assess the mental state of patients with schizophrenia and to evaluate changes in their condition over time, particularly during treatment.

Content (template):

Assessment is based on the severity of positive and negative symptoms. The positive symptoms assessed are: (1) delusions, (2) conceptual disorganization, (3) hallucinatory behavior, (4) excitement, (5) grandiosity, (6) suspiciousness/persecution, (7) hostility. The negative symptoms assessed are: (1) blunted affect, (2) emotional withdrawal, (3) poor rapport, (4) passive/apathetic social withdrawal, (5) difficulty in abstract thinking, (6) lack of spontaneity and flow of conversation, (7) stereotyped thinking. Along with positive and negative symptoms, the scale assesses general psychopathological syndromes: (1) somatic concern, (2) anxiety, (3) guilt feelings, (4) tension, (5) mannerisms and posturing, (6) depression, (7) motor retardation, (8) uncooperativeness, (9) unusual thought content, (10) disorientation, (11) attention deficit, (12) lack of judgment and insight, (13) disturbance of volition, (14) poor impulse control, (15) preoccupation, (16) active social avoidance.

Assessment domains and criteria:

Positive Syndrome Scale (P)

P1. Delusions

Unfounded, unrealistic, and idiosyncratic beliefs. Severity is rated based on the thought content expressed in the interview and its impact on social relations and patient behavior.

1. Absent: the patient's condition does not meet the definition of the traits.

2. Very mild: questionable pathology; evaluated signs may be at the upper limit of normal.

3. Mild: presence of one or two vague, poorly structured, and unstable delusions that do not impair the patient's thinking, behavior, or relationships with others.

4. Moderate: kaleidoscopic alternation of multiple poorly structured and unstable delusions, or the presence of several well-structured ideas that occasionally affect the patient's thinking, relationships with others, and behavior.

5. Marked: presence of numerous, well-structured, and persistent delusions that periodically affect the patient's thinking, social relationships, and behavior.

6. Severe: presence of a complex of structured, often

systematized, persistent delusions that noticeably impair the thought process, the patient's relationships with others, and their behavior.

7. Extreme: presence of a persistent complex of numerous or detailed systematized delusions that significantly impact the main aspects of the patient's life, leading to inappropriate actions that in some cases pose a danger to the patient and others.

P 2. Thought disorders

Disorganization of the thought process characterized by a breakdown in the goal-directed flow of thoughts, i.e., overinclusiveness (circumstantiality), rambling (rezonerstvo), derailment, amorphousness of associations, inconsistency, paralogical thinking, or "thought blocking" (sperrung). Severity is assessed based on the state of the cognitive-speech process during the interview.

1. Absent: the patient's condition does not meet the definition of the disorder.

2. Very mild: questionable pathology; evaluated signs may be at the upper limit of normal.

3. Mild: thinking is circumstantial, overelaborate, paralogical, or characterized by derailment. The patient experiences some difficulty when attempting to concentrate on a single thought; random associations may appear if the physician persists.

4. Moderate: during brief, simple communication, the ability to concentrate on specific thoughts is preserved; however, with the slightest pressure or in more complex situations, thinking becomes more amorphous (vague) and lacking in goal-directedness.

5. Marked: the patient almost always experiences difficulty in organizing a goal-directed flow of thoughts, manifested as derailment, inconsistency, and vagueness of thinking even in the absence of external pressure.

6. Severe: cognitive activity is severely disrupted; inconsistency and incoherence of thinking are observed almost constantly.

7. Extreme: incoherence of thinking reaches the level of word salad (incoherence). There is pronounced loosening of associative ties, leading to a complete loss of the ability to communicate, up to "schizophasia" or mutism.

P 3. Hallucinations

Statements or behavior indicating perception without a corresponding external stimulus. Pathological perception may occur in the auditory, visual, olfactory, or somatic modalities. Severity is assessed based on verbal reports or external manifestations during the interview, as well as information obtained from medical staff or relatives.

1. Absent: the patient's condition does not meet the definition of the disorder.

2. Very mild: questionable pathology; evaluated signs may be at the upper limit of normal.

3. Mild: one or two rare but distinct hallucinations, or several vague pathological perceptions that do not affect the patient's thinking or behavior.

4. Moderate: frequent but non-continuous hallucinations; the patient's thinking and behavior are mildly impaired.

5. Marked: frequent hallucinations involving sometimes more than one sensory modality and markedly disrupting thinking and/or behavior. Delusional interpretation of hallucinatory experiences with corresponding emotional and verbal accompaniment is possible.

6. Severe: practically continuous hallucinations that substantially impair the patient's thinking and behavior; perceptual disturbances are experienced as real-life events with corresponding emotional and verbal reactions that severely impede the patient's adaptive capacities.

7. Extreme: the patient's personality is almost entirely engulfed by hallucinations, which essentially dictate the direction of their thinking and behavior. Hallucinations are accompanied by persistent delusional interpretation, verbal and behavioral reactions, which implies, among other things, complete subordination to imperative hallucinations.

P4. Excitement

Hyperactivity manifested by increased motor function, heightened sensitivity to external stimuli, elevated level of arousal (hypervigilance), and excessively labile mood. Severity is assessed by behavior during the interview, as well as information obtained from medical staff and relatives.

1. Absent: the patient's condition does not meet the definition of the disorder.

2. Very mild: questionable pathology; evaluated signs may be at the upper limit of normal.

3. Mild: the patient is somewhat agitated and the level of arousal is elevated, but clearly defined episodes of excitement or excessive mood lability are absent. Speech may be accelerated.

4. Moderate: evident agitation, increased irritability, acceleration of speech and motor activity are noted during the interview. Episodes of intense excitement may occasionally be observed.

5. Marked: substantial hyperactivity or frequent episodes of motor excitation. The patient finds it difficult to sit quietly in one place for more than a few minutes.

6. Severe: the patient is extremely agitated throughout the entire interview, attention is scattered; sleep and eating may be impaired.

7. Extreme: extreme agitation of the patient prevents normal eating, disrupts sleep, and impairs interpersonal relationships.

Acceleration of speech and increased motor excitation can lead to speech incoherence, confusion, and exhaustion.

P5. Grandiosity

Inflated self-esteem and an unjustified conviction of superiority, including ideas of possessing special abilities, wealth, knowledge, fame, power, or moral righteousness. Severity is assessed by the content of thoughts revealed in the interview with the physician and their reflection in the patient's behavior.

1. Absent: the patient's condition does not meet the definition of the disorder.

2. Very mild: questionable pathology; evaluated signs may be at the upper limit of normal.

3. Mild: some expansiveness and boastfulness are noted. Clearly elaborated grandiose ideas are not detected.

4. Moderate: the patient asserts superiority over others and maintains an inflated self-image; poorly elaborated delusions of special status or abilities may be present, which, however, do not dictate the patient's behavior.

5. Marked: clearly elaborated ideas of outstanding abilities, power, or exceptional status, which influence the patient's attitude toward others but do not manifest in their behavior.

6. Severe: clearly elaborated delusions of superiority in multiple domains simultaneously (wealth, knowledge, fame, etc.) manifest not only in statements but also in relationships with others, as well as in certain actions.

7. Extreme: thinking, interpersonal relationships, and behavior are almost entirely determined by multiple delusions of extraordinary abilities, wealth, knowledge, fame, power, and/or moral virtues, which may acquire an absurd content.

P6. Suspiciousness / Persecution

Unfounded or exaggerated ideas of persecution, manifested by wariness, distrust, suspicious vigilance, or a more overt conviction of hostility from others. Severity is assessed by the content of thoughts expressed during the interview and their impact on the patient's behavior.

1. Absent: the patient's condition does not meet the definition of the disorder.

2. Very mild: questionable pathology; evaluated signs may be at the upper limit of normal.

3. Mild: the patient displays wariness or even overt distrust, but impairments in thought processes, behavior, and interpersonal relationships are practically absent.

4. Moderate: distrust is pronounced enough to hinder the interview with the physician and affect the patient's behavior; nevertheless, persecutory delusions are absent. On the other hand, some patients may exhibit poorly elaborated persecutory delusions that do not affect social relationships.

5. Marked: distrust is so intense that it leads to the disruption of relationships with others. Elaborated persecutory delusions may be present that little alter the nature of interpersonal relationships or the patient's behavior.

6. Severe: elaborated persecutory delusions that tend to expand and systematize, having a substantial impact on the patient's relationships with others.

7. Extreme: a complex of systematized persecutory delusions that almost entirely determines the patient's train of thought, social relationships, and behavior.

P7. Hostility

Verbal or other manifestations of anger and antagonism, including sarcasm, passive-aggressive behavior, threats, and overt assault. Severity is assessed by behavior during the interview and information obtained from medical staff and relatives.

1. Absent: the patient's condition does not meet the definition of the disorder.

2. Very mild: questionable pathology; evaluated signs may be at the upper limit of normal.

3. Mild: indirect or covert manifestations of anger, e.g., sarcasm, disrespect, hostile remarks, episodes of irritability.

4. Moderate: overt hostility, rapid

irritability, and direct manifestations of anger and resentment.

5. Marked: the patient is extremely irritable, occasionally resorting to verbal insults and threats.

6. Severe: contact with the patient is difficult due to verbal insults and threats, which also significantly disrupts relationships with others. The patient may be bellicose and prone to destruction, but does not commit physical assaults on people.

7. Extreme: marked anger with virtually complete lack of contact with the physician and others, or episodes of physical assault on people.

Negative Syndromes (N)

N1. Blunted Affect

Reduced emotionality, expressed as a decrease in facial expressiveness, inability to display feelings, and communicative gesturing. Severity is assessed by observing the physical manifestations of the patient's vital tone and emotionality during the interview.

1. Absent: the patient's condition does not meet the definition of the disorder.

2. Very mild: questionable pathology; evaluated signs may be at the upper limit of normal.

3. Mild: facial expressions and communicative gestures appear strained, forced, artificial, or impoverished.

4. Moderate: a reduction in the range of facial expressiveness and gesturing determines a characteristic "bored" (expressionless) appearance.

5. Marked: affect is usually "blunted" (flattened), facial expressions are scanty, gesturing is impoverished.

6. Severe: pronounced affect blunting and deficiency of emotional reactions are observed most of the time. Extremely strong uncontrolled affective outbursts in the form of excitement, fits of rage, or motiveless laughter are occasionally possible.

7. Extreme: facial modulations and communicative gestures are practically absent. Facial expression is persistently indifferent or frozen.

N2. Emotional Withdrawal

Lack of interest in life events, participation in them, and a sense of emotional involvement in them. Severity is assessed by information obtained from medical staff and relatives, as well as by observing the patient's behavior during the interview.

1. Absent: the patient's condition does not meet the definition of the disorder.

2. Very mild: questionable pathology; evaluated signs may be at the upper limit of normal.

3. Mild: the patient is usually low in initiative and may occasionally show weak interest in surrounding events.

4. Moderate: the patient generally emotionally disengages from the influence of the environment and its demands, but with active encouragement can be engaged in more active activities.

5. Marked: the patient exhibits distinct emotional detachment from surrounding people and ongoing events and does not respond to any attempts at activation from the outside. They appear reserved, compliant, aimless, and at times can be engaged in at least brief communication and arouse interest in their own needs.

6. Severe: marked indifference to the surroundings and lack of emotional reactions manifest in a sharp reduction of verbal communication with people and neglect of personal needs, thus requiring the organization of special supervision and care for the patient.

7. Extreme severity: due to profound indifference to the environment and lack of emotional experiences, the patient appears almost completely detached, uncommunicative, and indifferent to their own needs.

N3. Difficulties in communication (poor contact, uncommunicativeness)

Lack of openness and frankness in conversations with people, empathy, interest, or involvement with the interlocutor, manifested by difficulty in establishing interpersonal contacts and a reduction in the volume of verbal and non-verbal communication. The severity is assessed by the patient's behavior and attitude toward the physician during the interview.

1. Absent: the patient's condition does not meet the definition of the disorder.

2. Very mild: questionable pathology; evaluated signs may be at the upper limit of normal.

3. Mild severity: some artificiality, stiffness, and grandiloquence are felt when communicating with the patient. The patient's speech lacks emotional depth and is often impersonal and pedantic in nature.

4. Moderate severity: the patient generally appears alienated, keeps a distance from the interlocutor, answers questions mechanically, and their actions express boredom or a lack of interest in the conversation.

5. Marked severity: obvious alienation and lack of interest on the part of the patient in the conversation significantly impede productive contact with them. The patient tries to avoid eye contact with the interlocutor.

6. Severe severity: the patient is extremely indifferent to the environment, keeps a distance from the interlocutor, avoids eye contact, and cannot sustain a return gaze. Answers are monosyllabic and superficial. Attempts at non-verbal contact remain practically unanswered.

7. Extreme severity: the patient cannot be engaged in conversation, appears completely indifferent, and persistently avoids verbal and non-verbal contact with the physician.

N4. Passively apathetic social withdrawal

Decreased interest and initiative in social relationships due to passivity, apathy, loss of energy, and volitional drives, leading to reduced sociability and neglect of daily activities. Severity is assessed based on information about the patient's social behavior obtained from medical staff and relatives.

1. Absent: the patient's condition does not meet the definition of the disorder.

2. Very mild: questionable pathology; evaluated signs may be at the upper limit of normal.

3. Mild severity: occasionally shows interest in social communication, but has little initiative. Enters into contact with other people only upon the latter's initiative.

4. Moderate severity: participates passively, mechanically, and without interest in most social relationships, trying to stay in the background.

5. Marked severity: takes passive participation in a very narrow circle of social contacts, showing practically no interest in them or initiative. Spends little time communicating with other people.

6. Severe severity: the patient is apathetic most of the time, tends toward self-isolation, very rarely shows any social activity, and at times neglects their own needs. Enters into social contacts only occasionally.

7. Extreme severity: the patient is profoundly apathetic, socially isolated, neglects their own needs, and ceases to care for themselves.

N5. Impairment of abstract thinking

Disorder of abstract-symbolic thinking, manifested by difficulty in classification and generalization, as well as the inability to move away from concrete or egocentric ways of solving problems. Severity is assessed by responses to questions about the semantic commonality of objects or concepts, interpretation of proverbs, and the predominance of concrete thinking over abstract thinking during the conversation.

1. Absent: the patient's condition does not meet the definition of the disorder.

2. Very mild: questionable pathology; evaluated signs may be at the upper limit of normal.

3. Mild severity: a tendency to give a literal or personal interpretation of complex proverbs is noted. Difficulties are possible when interpreting abstract or distantly related conceptual interpretations.

4. Moderate severity: the patient frequently resorts to concrete thinking, experiences difficulties in interpreting most proverbs and some abstract concepts, as well as in identifying the most characteristic feature and functional phenomenon of an object or item.

5. Marked severity: thinking is predominantly concrete; the patient experiences difficulties in interpreting most proverbs and concepts.

6. Severe severity: the patient is unable to understand the abstract meaning of any of the proposed proverbs or figurative expressions, and classifies only the most elementary concepts by functional similarity. Thinking is completely unproductive or limited to the ability to identify characteristic features, determine functional purpose, or idiosyncratic interpretations.

7. Extreme severity: only concrete thinking remains in the patient, with a complete lack of understanding of proverbs, common metaphors and comparisons, or simple concepts; the ability to classify objects and phenomena even on the basis of the most characteristic features and functional properties disappears. This score can also be used to assess patients with whom conversation is practically impossible due to severely impaired cognitive activity.

N6. Impairment of spontaneity and flow of speech

Difficulty in normal verbal communication due to apathy, a sense of defenselessness, decreased volitional drives, or thought disorders, manifested by a disturbance in the fluency of speech and the productivity of verbal contact. A score is given based on the severity of these signs during the interview with the physician.

1. Absent: the patient's condition does not meet the definition of the disorder.

2. Very mild: questionable pathology; evaluated signs may be at the upper limit of normal.

3. Mild severity: the patient is uninitiative during the conversation, their answers are usually brief and devoid of details, and direct and leading questions must be asked to obtain information.

4. Moderate severity: the patient's speech lacks fluency, is uneven or intermittent. Leading questions often have to be asked to obtain the required information.

5. Marked severity: the conversation clearly suffers from a lack of spontaneity and frankness on the part of the patient; answers to questions consist of one or two short sentences.

6. Severe severity: the patient's answers are reduced to a few words or short phrases aimed at terminating the conversation or sharply reducing the volume of communication with the physician (e.g., "I don't know", "I can't talk about this"). As a result, the conversation is severely hampered and unproductive.

7. Extreme severity: the patient's speech is generally reduced to occasional utterances; conversation with them is impossible.

N7. Stereotyped thinking

Impairment of fluency, spontaneity, and flexibility of thinking, manifested by rigidity, repetitiveness, or banality of thoughts. Severity is assessed by the nature of the cognitive process during the interview.

1. Absent: the patient's condition does not meet the definition of the disorder.

2. Very mild: questionable pathology; evaluated signs may be at the upper limit of normal.

3. Mild severity: some rigidity of attitudes and ideas is revealed. The patient may refuse to consider alternative viewpoints or experience difficulty in switching from one thought to another.

4. Moderate severity: the conversation constantly returns to the same topic, and the patient has difficulty switching to another topic.

5. Marked severity: the rigidity and stereotypy of thinking are so pronounced that the conversation, despite the physician's opposition, is limited to two or three prevailing topics.

6. Severe severity: uncontrolled repetition of demands, statements, individual thoughts, or questions, which significantly complicates the conversation.

7. Extreme severity: constantly repeated ideas or individual phrases dominate the patient's thinking, behavior, and speech, leading to inadequacy and a sharp limitation of contact with the physician.

Scale of General Psychopathological Syndromes (G)

G1. Somatic concern

Complaints about physical health or the conviction of having a somatic disease or disorder, which can range from a vague feeling of illness to distinct delusions of a fatal somatic disease. Severity is assessed based on the patient's statements during the interview with the physician.

1. Absent: the patient's condition does not meet the definition of the disorder.

2. Very mild: questionable pathology; evaluated signs may be at the upper limit of normal.

3. Mild severity: noticeable concern about one's health or physical condition, manifested in occasional questions and the desire to receive support from the physician.

4. Moderate severity: complaints of poor health or disorders of individual body functions. However, there is no delusional conviction. The condition is amenable to psychotherapeutic intervention.

5. Marked severity: the patient frequently or constantly complains of a physical illness or bodily dysfunction. One or two delusional ideas on this topic may be noted, which do not entirely determine the patient's thoughts and behavior.

6. Severe severity: the patient is sufficiently preoccupied with one or more delusional ideas of physical illness or organic lesion of various bodily functions. However, there is no complete envelopment of the personality, including its affective sphere, by delusional ideas. The physician has difficulty distracting the patient from these thoughts.

7. Extreme severity: numerous and frequently manifested delusional ideas of somatic illness or several delusional ideas of a catastrophic outcome of the disease, completely absorbing the patient's thoughts and feelings.

G2. Anxiety

Subjective experience of nervousness, anxiety, apprehension, or tension, ranging from excessive concern about the present or future to panic reactions. Severity is assessed based on information obtained from the patient during the interview and corresponding physical manifestations.

1. Absent: the patient's condition does not meet the definition of the disorder.

2. Very mild: questionable pathology; evaluated signs may be at the upper limit of normal.

3. Mild: The patient expresses some concern, excessive worry, or apprehension, which is not accompanied by any somatic or behavioral reactions.

4. Moderate: The patient reports increased nervousness and anxiety accompanied by mild physical signs, such as fine hand tremor or sweating.

5. Severe: The patient reports anxiety accompanied by somatic and behavioral reactions, such as noticeable tension, impaired concentration, palpitations, and sleep disturbances.

6. Very severe: A nearly constant subjective experience of fear accompanied by phobias, marked anxiety, and various somatic manifestations.

7. Extreme: The patient's life is significantly disrupted by a nearly constant feeling of anxiety, which may occasionally escalate into panic attacks.

03. Guilt feelings

Feelings of remorse or self-blame regarding past real or imaginary misdeeds. Severity is assessed based on the patient's reports of guilt and the degree to which it affects their thinking and behavior.

1. Absent: the patient's condition does not meet the definition of the disorder.

2. Very mild: questionable pathology; evaluated signs may be at the upper limit of normal.

3. Mild: Targeted questioning reveals a vague sense of guilt and self-blame regarding a minor misdeed, which, however, does not heavily preoccupy the patient.

4. Moderate: The patient expresses clear concern about a real misdeed, which does not, however, affect their behavior; full cognitive preoccupation with these thoughts is not observed.

5. Severe: The patient experiences intense guilt with ideas of self-deprecation or punishment. The feeling of guilt may be related to the development of delusional psychosis, may occur spontaneously, may serve as a source of preoccupation and/or depressed mood, and does not lessen after talking with the physician.

6. Very severe: Ideas of guilt reach delusional proportions and are accompanied by feelings of hopelessness and worthlessness. The patient is convinced that they will be severely punished for their misdeeds and may view ongoing events as such a punishment.

7. Extreme: The patient's entire lifestyle is subjugated by the unshakable idea of their own guilt. They believe they deserve the harshest punishment, up to and including life imprisonment, torture, and/or death. Suicidal thoughts or a tendency to attribute problems faced by others to their own past actions may also occur simultaneously.

04. Tension

External manifestations of fear, anxiety, and agitation, such as stiffness in conversation, tremor, sweating, and motor restlessness (akathisia). Severity is assessed during the interview based on the patient's statements and corresponding physical signs of mental tension.

1. Absent: the patient's condition does not meet the definition of the disorder.

2. Very mild: Questionable pathology; assessed indicators may be at the upper limit of normal.

3. Mild: The patient's posture and movements indicate a mild degree of agitation (e.g., some stiffness of movement, transient akathisia, tendency to change posture, fine and rapid hand tremor).

4. Moderate: Distinct manifestations of increased nervousness in the form of fidgetiness, hand tremor, sweating, and nervous mannerisms.

5. Severe: Marked tension with a wide variety of manifestations (e.g., nervous shivering, profuse sweating, and motor restlessness) while maintaining generally normal behavior during the interview.

6. Very severe: The degree of tension is such that it interferes with normal communication. For example, the patient may exhibit constant fidgetiness, inability to sit in one place for long, or accelerated breathing.

7. Extreme: The patient's condition is close to panic. Marked acceleration of motor activity, continuous pacing, or running around the room is observed. The patient cannot remain in one place for more than a minute, making conversation impossible.

05. Mannerisms and posturing

Unnatural movements and/or postures that give the patient's behavior an awkward, dysplastic, or eccentric character. Severity is assessed by observing the physical manifestations of the disorder during the interview, as well as from information obtained from relatives and medical staff.

1. Absent: the patient's condition does not meet the definition of the disorder.

2. Very mild: Questionable pathology. Assessed signs may be at the upper limit of normal.

3. Mild: Some awkwardness of movement or slight rigidity in postures.

4. Moderate: Noticeable awkwardness or dysplastic (fragmented) movements; the patient may assume unnatural postures for a short time.

5. Severe: The patient occasionally makes strange, ritual-like movements or freezes in unnatural, distorted postures for fairly long periods of time.

6. Very severe: Frequent repetitions of eccentric, "ritualistic" movements, mannerisms, or stereotyped movements; freezing in unnatural postures may be observed for prolonged periods.

7. Extreme: Normal functioning is severely impaired due to the patient's nearly constant performance of ritualistic or stereotyped movements, pronounced mannerisms, or prolonged freezing in unnatural postures.

06. Depression

Experience of sadness, despondency, helplessness, and pessimism. Severity is assessed based on the patient's reports of their mood during the interview and corresponding changes in interpersonal relationships and behavior.

1. Absent: the patient's condition does not meet the definition of the disorder.

2. Very mild: questionable pathology; evaluated signs may be at the upper limit of normal.

3. Mild: Subjective feelings of sadness and depressed mood are elicited only upon targeted questioning; appearance and behavior remain unchanged.

4. Moderate: Distinct experiences of sadness and hopelessness, which the patient may mention on their own initiative, but which do not significantly affect the patient's behavior and social relationships. Psychotherapeutic correction of the condition is possible.

5. Severe: Clearly depressed mood with experiences of sadness, pessimism, loss of life interests, psychomotor retardation, and some sleep and appetite disturbances. Not amenable to psychotherapeutic correction.

6. Very severe: Deeply depressed mood with persistent experiences of hopelessness and personal worthlessness; the patient occasionally weeps, accompanied by significant deterioration in sleep and appetite, decreased motor activity, loss of life interests, and possible lapses in self-care.

7. Extreme: Depressive experiences significantly impair the patient's functioning. Marked somatovegetative disorders, psychomotor retardation, loss of all social interests, lapses in self-care, and impaired concentration are observed. The patient weeps frequently; depressive or nihilistic delusions, as well as suicidal thoughts and tendencies, may develop.

07. Motor retardation

Decreased motor activity manifested by slowed movements and speech, sluggish reactions to stimuli, and reduced physical tone. Severity is assessed both by behavior during illness and from reports by medical staff and relatives.

1. Absent: the patient's condition does not meet the definition of the disorder.

2. Very mild: questionable pathology; evaluated signs may be at the upper limit of normal.

3. Mild: Mild, but noticeable slowing of movements and speech. Some reduction in productivity during conversation and gesturing may occur.

4. Moderate: The patient's movements are clearly slowed, speech may be unproductive, the patient takes a long time to answer questions, long pauses appear in conversation, and speech rate is reduced.

5. Severe: Motor activity is markedly reduced, making communication with the patient unproductive and interfering with the performance of social and professional duties. The patient sits or lies down for long periods.

6. Very severe: Movements are extremely slowed; motor and speech activity are minimal. The patient spends entire days sitting or lying around aimlessly.

7. Extreme: The patient is almost completely immobile and responds poorly to external stimuli.

08. Uncooperativeness (refusal to cooperate, poor sociability)

Active refusal to cooperate and follow instructions from the physician, medical staff, or relatives, which may be associated with mistrust, defense mechanisms, stubborness, negativism, defiance of authority, hostility, or belligerence. Severity is assessed based on behavior during the interview, as well as information obtained from medical staff and relatives.

1. Absent: the patient's condition does not meet the definition of the disorder.

2. Very mild: questionable pathology; evaluated signs may be at the upper limit of normal.

3. Mild: The patient complies with requirements while expressing displeasure, impatience, or a sarcastic attitude. Tries to avoid discussing undesirable topics.

4. Moderate: At times, the patient openly refuses to follow basic rules of communal living, such as making the bed, following the daily schedule, etc.; may exhibit hostile, negativistic defense reactions, which, however, in most cases do not preclude the possibility of reaching an agreement.

5. Severe: The patient frequently violates communal living rules; those around characterize them as an "outcast" or as someone with a severely impaired ability to communicate. During the interview, they are irritable or withdrawn and try to avoid answering many questions.

6. Very severe: The patient strongly resists cooperation and rapport-building, exhibits active negativism, and is sometimes belligerent. They refuse to follow most communal living rules and often do not wish to converse with the physician.

7. Extreme: Active resistance significantly hinders the performance of almost all major social functions. A complete refusal to participate in any social activity is possible, including personal hygiene rules, conversations with relatives or medical staff. Even a brief dialogue with the physician is difficult.

09. Unusual thought content

Thinking characterized by the presence of strange, fantastic, or eccentric thoughts, varying in content from atypical or detached from life to distorted, unnatural, or clearly absurd. Severity is assessed based on the content of thoughts expressed by the patient during the interview.

1. Absent: the patient's condition does not meet the definition of the disorder.

2. Very mild: questionable pathology; evaluated signs may be at the upper limit of normal.

3. Mild: Somewhat strange or idiosyncratic (non-conventional) thought content, or the use of familiar ideas in an unusual context.

4. Moderate: Frequent distortion of thoughts, sometimes reaching the level of eccentric ones.

5. Severe: The patient expresses many strange and fantastic thoughts (e.g., believes they are the adopted son of a king or that they just escaped death), and sometimes clearly absurd ones (e.g., that they have hundreds of children, receive radio signals from space through a dental filling).

6. Very severe: The patient expresses numerous illogical and absurd thoughts (e.g., that they have three heads, that they are an alien from another planet).

7. Extreme: Thinking is overloaded with absurd, eccentric, and fantastic ideas.

010. Disorientation

Loss of awareness of one's relationship to reality, including place, time, and people around, due to confusion or detachment from reality. Severity is assessed based on a targeted interview with the patient.

1. Absent: the patient's condition does not meet the definition of the disorder.

2. Very mild: questionable pathology; evaluated signs may be at the upper limit of normal.

3. Mild: General orientation is largely preserved; the patient experiences difficulties with certain specific questions. For example, they may know where they live but get the exact address wrong; recognize medical staff by face but not know what they do; know the month but confuse the days of the week or err by at least two days in dates. Sometimes a narrowing of the patient's knowledge base may be noted: they may be oriented in their immediate environment, but not beyond it. For example, the patient knows the staff they have to deal with, but does not know the names of political figures.

4. Moderate: The patient does not always recognize people and correctly name the place or time of stay. For example, they may know they are in a hospital, but not know its name; know the name of the city, but not the names of the region, district, or street; know the name of the attending physician, but not the names of many other staff members; can name the year and season, but are confused about the month.

5. Severe: The patient recognizes people with great difficulty, has a very vague idea of their whereabouts, and most people around them seem unfamiliar. They can more or less correctly name the year, but do not know the current month, day of the week, or even the season.

6. Very severe: The patient practically fails to recognize people and does not know the time and place of their location. For example, they have no idea where they are, are off by more than a year in determining the time, and can barely name one or two people who have been around them recently.

7. Extreme: The patient has completely lost orientation regarding people, place, and time; is completely oblivious to or incorrectly pictures their location and the current year, and fails to recognize the closest people: parents, spouse, friends, or the attending physician.

011. Attention impairment

Disorder of goal-directed attention, manifested by a lack of concentration, increased distractibility, difficulties in focusing, maintaining, or switching attention to new objects. Severity is assessed based on observation of the patient throughout the interview.

1. Absent: the patient's condition does not meet the definition of the disorder.

2. Very mild: questionable pathology; evaluated signs may be at the upper limit of normal.

3. Mild: Limited ability to concentrate, manifested by some distractibility or waning attention toward the end of the interview.

4. Moderate: The interview with the patient is difficult due to increased distractibility, difficulty focusing on a given topic for long periods, or conversely, quickly switching to new topics.

5. Severe: Communication with the patient is seriously impaired due to poor concentration, frequent distractibility, and/or poor ability to switch to other topics.

6. Very severe: The patient's attention can be engaged only briefly or with great difficulty due to frequent distraction by internal experiences or extraneous external stimuli.

7. Extreme: Attention is so impaired that even a brief conversation becomes impossible.

012. Impaired insight

Inadequate understanding of one's mental state and current life situation, manifested by the inability to recognize the presence of a disease or its symptoms in the past and present, denial of the need for hospitalization or psychiatric treatment, making decisions without sufficient consideration of their consequences, and building unrealistic plans for the future. Severity is assessed by the content of thoughts expressed by the patient during the interview.

1. Absent: The patient's condition does not fit the description of the disorder.

2. Very mild: questionable pathology; evaluated signs may be at the upper limit of normal.

3. Mild: The patient acknowledges the presence of a mental disorder, but underestimates its severity, the need for treatment, or prevention. The ability to adequately plan future actions may be impaired.

4. Moderate: The patient has only a vague or distant idea of their illness. At times they may deny its presence or fail to understand what the main symptoms of the illness are, such as delusions, thought disorders, suspiciousness, or social alienation. The patient may acknowledge the need for treatment only for clinical manifestations such as anxiety, tension, or sleep disturbances.

5. Severe: The patient acknowledges the presence of a mental disorder in the past, but not in the present. When questioned, they may point to the presence of certain non-existent or irrelevant symptoms, showing a tendency to misinterpret them or even elaborate them delusionally. The need for psychiatric treatment is usually denied.

6. Very severe: Does not consider themselves mentally ill; denies the presence of any psychiatric symptoms in both the past and the present, while formally agreeing to hospitalization and treatment, yet failing to understand their meaning and necessity.

7. Extreme: The patient completely denies the presence of a mental illness in both the past and the present; interprets hospitalization and treatment through delusional mechanisms (e.g., as punishment for misdeeds, as actions of persecutors, etc.). Consequently, the patient usually refuses to cooperate with medical staff, tries to avoid taking medications, and fails to comply with the treatment regimen.

013. Volitional disorder

Impairment of volitional initiative, the ability to achieve set goals and control one's thoughts, behavior, movements, and speech. Severity is assessed based on the patient's statements and behavior during the interview.

1. Absent: The patient's condition does not fit the description of the disorder.

2. Very mild: questionable pathology; evaluated signs may be at the upper limit of normal.

3. Mild: Some indecisiveness appears in the patient's speech and thoughts, which practically does not affect communication and behavior.

4. Moderate: The patient is frequently ambivalent; experiences difficulties in decision-making. The interview with the patient is somewhat difficult due to the scattered nature of their thoughts.

5. Marked severity: volitional impairments affect both the patient's thinking and behavior; pronounced indecisiveness is observed, which hampers spontaneous motor and speech activity, as well as impedes the establishment of social relationships.

6. Severe impairment: volitional disorders hinder the performance of even the simplest automatic actions, such as dressing and self-care; distinct speech disorders are noted.

7. Extreme severity: virtually complete absence of volitional acts, manifested as psychomotor retardation up to complete immobility and/or mutism.

014. Impairment of impulse control (aggressiveness)

Impairment in the regulation and control of internal drives, leading to unexpected, unmodulated, voluntary, and non-target-directed discharges of tension and emotions without regard for potential consequences. Severity is assessed based on behavior during the interview and information from medical staff and relatives.

1. Absent: The patient's condition does not fit the description of the disorder.

2. Very mild: questionable pathology; evaluated signs may be at the upper limit of normal.

3. Mild severity: under stress or when desires are unfulfilled, the patient is easily irritated or upset, but rarely acts impulsively in accordance with their experiences.

4. Moderate severity: the patient becomes wrathful and prone to verbal attacks at the slightest provocation, occasionally resorting to threats. One or two episodes of physical resistance or a tendency toward destructive actions may be noted.

5. Marked severity: periodic impulsive outbursts are observed, accompanied by insults, property damage, or threats of physical violence. One or two episodes of attacking people may occur, necessitating patient isolation, physical restraints, or other calming measures.

6. Severe impairment: frequent impulsive (uncontrolled) outbursts of aggressiveness are observed; the patient constantly threatens, makes demands, or destroys surrounding objects without a clear understanding of the consequences of these actions. The patient exhibits a distinct tendency toward violent acts, including assaults motivated by sexual drive. Behavior may be driven by compliance with imperative hallucinations.

7. Extreme severity: the patient makes continuous attempts to attack people with the intent to kill or rape, and is prone to self-harm. At the same time, they exhibit extreme cruelty. Due to the inability to control dangerous impulses, the patient requires constant monitoring, isolation, or physical restraint.

015. Preoccupation with internal experiences

Preoccupation with internal experiences, thoughts, feelings, or autistic fantasies, leading to impaired adaptation and orientation in the surrounding environment. Severity is assessed based on the patient's responses and behavior during the interview.

1. Absent: The patient's condition does not fit the description of the disorder.

2. Very mild: questionable pathology; evaluated signs may be at the upper limit of normal.

3. Mild severity: excessive preoccupation with one's needs and problems, manifested in persistent attempts to steer the conversation toward topics of concern to the patient, with a lack of interest in other issues.

4. Moderate severity: at times, the patient appears self-absorbed, engrossed in daydreams or experiences, which somewhat hinders the conversation with them.

5. Marked severity: the patient is engrossed in autistic fantasies or internal experiences, which affects their behavior and significantly impairs social and communicative activity. Sometimes the patient sits with a blank stare, whispers and/or talks to themselves, and performs stereotyped movements.

6. Severe impairment: the patient is almost completely absorbed by their internal experiences, which significantly impairs concentration, participation in conversation, and orientation in the environment. The patient often smiles or laughs at something, whispers, and talks to themselves.

7. Extreme severity: complete preoccupation with internal experiences, accompanied by a sharp decline in adaptation. The patient's behavior is entirely subordinated to hallucinations, and they pay little attention to surrounding people and the environment.

016. Active social withdrawal

Reduction in social activity stemming from groundless fear, hostile or suspicious attitudes. Severity is assessed based on information regarding the patient's social activity obtained from medical staff or relatives.

1. Absent: The patient's condition does not fit the description of the disorder.

2. Very mild: questionable pathology; evaluated signs may be at the upper limit of normal.

3. Mild severity: the patient feels awkward in the presence of other people and prefers to spend time alone, although they exhibit social activity when necessary.

4. Moderate severity: the patient is reluctant to enter into social contacts, requires constant encouragement, and may abruptly terminate them upon the emergence of anxiety, suspicion, or hostile attitudes.

5. Marked severity: the patient refuses most social contacts with fear or anger, despite attempts by others to engage them. They spend most of their time alone to no purpose.

6. Severe impairment: due to intense fear, hostile or suspicious attitudes, the patient exhibits only the most necessary social activity. When initiative is shown by others, the patient displays a clear desire to avoid contacts and generally tries to stay away from people.

7. Extreme severity: the patient cannot be engaged in social relationships due to severe fear, hostility, or persecutory delusions. They strive by all means to avoid contacts and remain in complete isolation.

Key (interpretation): using this scale measures the degree of impairment in the aforementioned categories across three subscales, taking into account the child's age. The nature of expected impairments is described within the diagnostic material itself. Assessments include: (1) severity of positive symptoms on the Positive Syndrome Scale (7 items); (2) severity of negative symptoms on the Negative Syndrome Scale (7 items); (3) composite index (positive symptom scores minus negative symptom scores); (4) severity of other mental disorders on the General Psychopathology Scale (16 items); (5) risk of potential aggression (3 additional items along with anamnestic data).

Comment: abroad, completion of the scale is typically performed by psychologists, which is why the Structured Clinical Interview for Positive and Negative Syndrome Scale (PANSS) has been developed (Opler L.A., Kay S.R., Lindenmayer J.P., Fiszbein A., 1999). In routine clinical practice, an experienced specialist performs the rating automatically during the clinical interview with the patient.

Explanations: the scale should be used dynamically; the recommended interval for re-administering the scale is 7–10 days.

Appendix G2. Personal and Social Performance Scale.

Russian title - Personal and Social Performance Scale.

Original title - Personal and Social Performance scale (PSP)

Source - Morosini P.L., Magliano L., Brambilla L., Ugolini S., Pioli R. Development, reliability and acceptability of a new version of the DSM-IV Social and Occupational Functioning Assessment Scale (SOFAS) to assess routine social functioning. Acta Psychiatrica Scandinavica 2000. 101: 323-329

Type (underline):

- rating scale

- index

- questionnaire

- other (specify)

Purpose: The Personal and Social Performance Scale is used to assess the ability to learn and acquire speech skills, evaluate relationships with loved ones and others, assess self-care skills development, evaluate agitation and aggressive behavior—including during ongoing treatment—and assess treatment efficacy as well as during the creation and implementation of an individual psychological correction and medical rehabilitation plan.

Content (template):

An assessment in 4 main domains of functioning is used, taking into account the child's age:

Domains of functioning:

(a) ability to learn and acquire speech skills;

(b) relationships with loved ones and others;

(c) self-care;

(d) agitation and aggressive behavior.

Criteria for domains a–d:

Domain (a): categories (assessment is carried out by a psychiatrist or medical psychologist)

- The absence of problems in the learning ability domain in children was characterized by the successful acquisition of key subject-practical activity skills appropriate for the given age. As a rule, such children attended a regular kindergarten group, studied under a general school education curriculum, or could be placed in such institutions.

- Mild severity of impairments in this domain was characterized by fluctuations in work capacity, deterioration of concentration under load, and certain difficulties when engaging in goal-directed activities. Children in this group needed to exert more effort to master the material, but they were able to cope with it without outside help.

- Marked difficulties manifested as an uneven pace of intellectual activity, decreased academic performance, rapid fatiguability, distractibility, and a restricted range of interests. Some patients exhibited age-inappropriate speech sound production disorders. Children continued to study under general educational standards, but often required additional specialist support: tutors, psychologists, speech therapists.

- Significant impairments in this area were characterized by a progressive delay in intellectual development, a marked lag behind peers, immaturity or overvalued interests, and difficulty switching attention. Phrasal speech disorders, and difficulties in acquiring reading and writing skills were observed. These children were recommended additional specialist support, as well as age-appropriate specialized educational conditions: attendance in a developmental delay group, individual education, or transfer to a curriculum for children with mental retardation.

- Severe learning impairments implied the presence of cognitive deficit accompanied by pronounced thought disorders specific to this disease. Marked speech underdevelopment was noted. Preschool children attended developmental delay groups or remained unorganized. School-age children were educated according to correctional programs for individuals with mild mental retardation.

- Very severe maladaptation in this area was characterized by a profound cognitive defect; often, speech skills were absent, or speech did not serve a communicative function. School-age children from this group studied under an auxiliary program for individuals with severe mental retardation or remained unorganized; in isolated cases, they were placed in psychoneurological residential facilities.

Domain (b): categories (evaluated by a psychiatrist or medical psychologist)

- Evaluation based on the criterion of relationships with loved ones and others was performed as follows: the absence of problems in this area was characterized by emotional attachment to loved ones, active communicative interaction, a desire to expand one's social circle, the ability to understand emotions and non-verbal cues of others (taking age into account), and the establishment of friendships. Children eagerly communicated within a peer group and adapted well to the collective.

- Mild impairments were distinguished by emotional flatness, a certain formality in communication with others, and selectivity and superficiality of contacts.

- Marked impairments were characterized by a restricted range of contacts, difficulty or inability in establishing friendships, a desire for solitude, a preference for activities involving mechanisms rather than people, difficulty adapting to a new collective, and avoidance of group or class attendance.

- Significantly pronounced difficulties were observed in children distinguished by emotional flattening, egocentrism, difficulty in recognizing and using non-verbal cues in communication while preserving expressive speech, an active desire for solitude, restriction of contacts to family members, fears, hostility, or lack of interest in other children. Significant difficulties in functioning within a collective were noted.

- Severe impairments in this area implied underdevelopment of emotional responsivity ranging up to indifference toward loved ones, or pronounced symbiotic attachment to the mother, difficulty in differentiating between "friend or foe", and selective responsivity to directed speech.

- Very severe impairments were characterized by a lack of response to directed speech, active withdrawal from contact with any people, monotony of emotional responses, and detachment from surroundings.

Domain (c): categories (evaluated by a psychiatrist or medical psychologist)

- The norm for the acquisition of self-care skills for children aged 3-4 years is the ability to use cutlery and the potty, and independently put on and take off clothes; for 6-7 years, the ability to tie shoelaces, button clothes, and independently perform hygiene procedures; for 8-10 years, the ability to look after one's belongings, prepare simple dishes, and count change; from 10-11 years, the ability to make purchases in a store, clean the house, and use basic household appliances.

- Mild impairments in this area were characterized by minor difficulties in performing basic skills (skills were acquired according to age).

- Marked impairments were characterized by clumsiness and difficulty in executing skills (despite timely skill development). Significant impairments were observed in children who required adult guidance for self-care; skills were acquired according to age but were performed partially or in a distorted manner.

- Severe impairments implied the acquisition of skills at a younger age level; in daily life and self-care, adult assistance was required in most situations.

- Very severe impairments were observed in children who were completely incapable of self-care and required the constant presence of an adult.

Domain (d): categories (evaluated by a psychiatrist or medical psychologist)

- The absence of agitation and aggressive behavior was considered the norm.

- Mild criteria included withdrawal, coarseness, demonstrative behavior, and active complaints about others.

- Marked criteria included boundary issues in behavior, insolence, and manifestations of negativism.

- Significantly pronounced manifestations included: profanity directed at others, property damage, and socially unacceptable behavior (taking age into account).

- Severe manifestations included: verbal threats directed at others, aggression toward others and/or autoaggression, without the intention to inflict serious physical harm.

- Very severe criteria included targeted aggressive acts aimed at inflicting serious physical harm, or chaotic non-targeted aggression and autoaggression.

Key (interpretation): this scale measures the degree of difficulty in 4 main functional domains, taking into account the child's age. The level of functional impairment is assessed by the severity of difficulties experienced by the patient over the past 7 days. Based on the clinical assessment, the interval corresponding to the level of social functioning is selected: (in points)

- 100-91 points: Full functioning in all four main domains. The patient's positive qualities are highly appreciated by others, they successfully cope with everyday problems, and their interests and activities are diverse.

- 90-81 points: Good level of functioning in all four main domains, with only those problems or difficulties encountered by all people.

- 80-71 points: Minor difficulties in one or more domains a-c.

- 70-61 points: Marked, but not reaching a significant level, difficulties in one or more domains a-c, or minor problems in domain d.

- 60-51 points: Significant difficulties in one of the domains a-c, or marked problems in domain d.

- 50-41 points: Significant difficulties in two or more domains a-c, or severe difficulties in one of the domains a-c, with or without marked problems in domain d.

- 40-31 points: Severe difficulties in one domain and significant difficulties in at least one of the domains a-c, or significant problems in domain d.

- 30-21 points: Severe difficulties in two domains a-c, or severe problems in domain d, with or without impairments in domains a-c.

- 20-11 points: Severe impairments in all domains a-d, or very severe problems in domain d, with or without impairments in the main domains a-c. If the patient responds to external stimuli, they fall into the 20-16 points interval; if not, into the 15-11 points interval.

- 10-1 points: A-spontaneity combined with gross behavioral disturbances without danger to the patient's life (scores 6-10) or with danger to the patient's life, e.g., threat of death due to starvation, dehydration, infections, inability to assess a dangerous situation (scores 5-1).

Explanations: the scale should be used dynamically; the recommended interval for re-administering the scale is 7–10 days.

Scales and calculators from this guideline

Dopamine calculatorCalculation of dopamine infusion rate (mcg/kg/min → ml/h) with automaticMoCA — score calculationMontreal Cognitive Assessment: sum of scores by section

If you practice in the specialty of psychiatry

ClinRevs Pro690 ₽ per month · cancel anytime

Clinical calculators and scalesRisk calculation, dosing, and scoring using scales from clinical guidelines — online, no registration required.

Open calculators

Answers based on Russian clinical guidelines right inside ChatGPT and Claude Connect the WhiteCoat Pro connector, and the assistant will answer according to the "Schizophrenia" guideline and other active Russian Ministry of Health clinical guidelines with a reference to the section rather than retelling foreign guidelines. Address: mcp.pervoklassno.ru/mcp. How to configure ChatGPT, Claude, Gemini, and Perplexity for Russian clinical guidelines

Subscribe in 2 minutes

AI Research DigestEvery morning — fresh PubMed articles in your specialty: translation, AI analysis, and link to the original. Reads in four minutes.

Subscribe for 990 ₽

Related clinical guidelines