Notes
Notes
Introduction to Psychopathology
Normal development, common problems during the normal development phase, Etiology/Risk factors
of psychopathology
2. Classification of psychiatric disorders
Classification of psychiatric disorders in children and adolescents(ICD-10 & DSM-V), epidemiology,
3. Psychopathology of Childhood Disorders: Clinical Picture, assessment and intervention
Mental Retardation, Specific Learning Disorders (Reading disorder, Spelling Disorder, disorder of
written expression, Arithmetical Disorder), Pervasive Developmental Disorders (Autism, Asperger’s
Disorder, Rett’s Disorder, Childhood Disintegrative Disorder, PDD NOS), Specific Speech &
Language Disorders
4. Externalizing Disorders
Attention Deficit Hyperactivity Disorder (ADHD), Oppositional Defiant Disorders (ODD), Conduct
Disorder (CD), Alcohol and Substance Use Disorders, Juvenile Delinquency
5. Internalizing Disorders
Anxiety Disorder (Separation Anxiety Disorder, Social Phobia, Selective Mutism, Obsessive
Compulsive Disorders) Depressive Disorders, Suicide and Injurious Behavior
6. Other psychological disorders
Bipolar Affective Disorder, Psychotic Disorders, Eating Disorders, Bowel & Bladder Control
Disorders, Sleep and Movement Disorders, Obesity, Selective Mutism, Tourette’s & Tic Disorder,
Three major models used to understand psychopathology are the biological, psychological, and
sociocultural models. Each model offers a different perspective on the causes and treatment of mental
disorders, but a biopsychosocial approach is often considered the most comprehensive.
1. Biological Model: This model emphasizes the role of biological factors, including genetics, brain
chemistry, and the nervous system, in the development of psychopathology. It often suggests that
mental disorders can be treated with medication, electroconvulsive therapy, or other biological
interventions.
2. Psychological Model: This model focuses on psychological factors, such as learning, personality,
stress, and cognition, as contributors to psychopathology. It includes perspectives like
psychodynamic, behavioral, and cognitive-behavioral approaches, which emphasize the importance of
early life experiences, unconscious processes, and maladaptive thoughts and behaviors.
3. Sociocultural Model: This model highlights the influence of social, cultural, and environmental
factors, such as gender, race, ethnicity, and social support, in the development and expression of
psychopathology. It recognizes that individual behaviors and experiences are shaped by the broader
social context in which they occur.
Introduction
The Biopsychosocial model was first conceptualised by George Engel in 1977, suggesting that to
understand a person's medical condition it is not simply the biological factors to consider, but also the
psychological and social factors [1].
Bio (physiological pathology)
Psycho (thoughts emotions and behaviours such as psychological distress, fear/avoidance
beliefs, current coping methods and attribution)
Social (socio-economical, socio-environmental, and cultural factors suchs as work issues,
family circumstances and benefits/economics)
This model is commonly used in chronic pain with the view that the pain is a psychophysiological
behaviour pattern that cannot be categorised into biological, psychological, or social factors alone.
There are suggestions that physiotherapy should integrate psychological treatment to address all
components comprising the experience of chronic pain.
Physiotherapists must know how biopsychosocial factors interact in patients with chronic pain to
explain the perpetuation of this condition and use it as a basis for planning the intervention program.
The evidence has suggested a clinical biopsychosocial assessment for the physiotherapeutic
management of patients with chronic pain in order to understand and explain the predominant
mechanism of pain and psychosocial factors that may or may not be modified for the patient to
improve their condition.[4]
This clinical evaluation is carried out during the data collection at the patient's entrance. A practical
guide is proposed to take biopsychosocial data using the PSCEBSM (Pain–Somatic and medical
factors–Cognitive factors–Emotional factors–Behavioral factors–Social factors–Motivation) model.
P- Type of pain
Clinical identification and differentiation of the dominant pain mechanism:
nociceptive pain
neuropathic pain
non-neuropathic pain of central sensitization.
Using the following tools:
1. Classification criteria for differentiating predominant pain proposed by Nijs et al.
2. Widespread pain index/Body Diagram : ≥ 7 score suggesting generalized pain, therefore, non-
neuropathic pain of central sensitization
3. Central Sensitization Inventory (CSI) : 40 score suggesting non-neuropathic pain of central
sensitization
S- Somatic and medical factors
For physical therapist the physical examination is a very important part of his intervention - essential
to:
Be aware that some findings of clinical examinations such as
mobility, strength, neurodynamics, coordination, etc. could be altered because there is greater
sensitivity to mechanical stimulation and modified movement patterns in patients with non-
neuropathic pain of central sensitization.
Main goal in this stage is to evaluate the quality of movement, if the pattern of movement
causes the pain to persist and if there is kinesiofobia
Ask about current or previous health conditions, the disuse of body parts, changes in
movement patterns, exercise capacity, strength and muscle tone during movement, the action
of the drug in the CNS It is useful for data collection
C- Cognition / Perceptions
Both influence biologically on hypersensitivity in the brain by activating neuromatrix pain and also
influence the emotional and behavioral factors. :
1. Ask about perceptions: expectations of the intervention, expectations of the prognosis of their
pain, understanding of their situation and the strategies they have available to face their
situation, what the pain represents emotionally
2. Brief Illness Perception Questionnaire (Brief IPQ)
3. Pain Catastrophizing Scale (PCS)
E- Emotional factors
Ask if there is fear of specific movements, avoidance behaviors, psychological traumatic appearance
of pain, psychological problems at work, family, finances, society, etc. It is also suggested to use the
following scales:
1. State-Trait Anxiety Inventory (STAI)
2. Tampa-Scale of Kinesiophobia (TSK) and Fear Avoidence Belief Questionare
3. Injustice Experience Questionnaire (IEQ)
4. Patient Health Questionnaire-2 (PHQ-2), or Patient Health Questionnaire-9 (PHQ-9), or
Center of Epidemiologic Studies Depression Scale (CES-D)
B- Behavioral factors
Can lead to avoid activity or movement due to fear, which in turn is presented as physical inactivity or
disuse and, finally, disability. Therefore it is important to evaluate the behavior and adaptations that
the patient has made due to the pain.
S- Social factors
It refers to the social and environmental factors in which the patient develops, which could be useful
and supportive or harmful and stressful for the improvement of the patient's health condition. The data
collection can be divided as follows:
1. Housing or living situation
2. Social environment
3. Work
4. Relationship with the partner
5. Previous interventions
M- Motivation
Evaluating the motivation in the patient and his willingness to change is useful to modify his thoughts
regarding the relationship pain-kinesiophobia, pain-disability, and acceptance-catastrophism. For this
purpose, the following scale can be used:
1. Psychology Inflexibility in Pain Scale (PIPS)
o PIPS "evaluates components of psychological inflexibility (avoidance and fusion)" [5]
Clinical Contribution
The use of the biopsychosocial model as a clinical practice guide in physiotherapy allows the
physiotherapist to be aware of all the factors that influence the patient's state of health. In
addition, it allows laying the foundations of pain neuroscience education
The psychosocial factors the patient deals with can mean the intervention of other health
professionals besides the physiotherapist ie important to take into account the professional
limits, as well as the ethical principles that ensure the comprehensive management of the
patient.
The following videos emphasise the importance of using the biopsychosocial model to improve
patient functionality and the problem that currently exists for physiotherapists in the use of this
approach
The biopsychosocial and biomedical models offer distinct perspectives on understanding and
addressing health and illness.
Biomedical model
The biomedical model, which was historically prevalent, takes a reductionist approach by
focusing on biological factors and treating diseases through medical interventions. It sees
diseases as isolated physical abnormalities.
While this approach was once deemed sufficient, research within psychology and the social
sciences cast doubt on its effectiveness.
Biopsychosocial model
The biopsychosocial model adopts a holistic viewpoint, acknowledging the complex interplay
of biological, psychological, and social factors in shaping health and illness. It sees diseases
as outcomes of dynamic interactions among various dimensions. The model emphasizes the
interconnectedness of these dimensions, recognizing their mutual influence on an individual's
health.
The BPSM has been extended to consider additional holistic elements influencing the
perceived necessity for healthcare and the focus on health-related matters: Information,
Beliefs, and Conduct. Based on the model's dependence on perception, it has been considered
imperative to actively engage the individuals or communities whose requirements are being
addressed, regardless of whether the focus is on their health, education, employment,
housing, or any other needs. A key term in the biopsychosocial model is "syndemic" which
refers to a set of health problem factors that interact synergistically with each other ranging
from socioeconomic status to genetics.
Rothman, an American epidemiologist (1976, p. 588) defined a cause as “an event, condition or
characteristic without which the disease would not have occurred”. A risk factor can also be a cause
but all risk factors are not causes. A risk factor is the one that increases the chance of having a
particular condition. Let’s understand this with an example. Ishaan’s dietary habits are not good as it
includes sugary, fried and fatty foods; for the sake of simplicity, we will call it unhealthy diet and he is
also overweight. Arjun has the same diet (unhealthy diet) but he is not overweight as he compensates
for his calorie intake with his active lifestyle. Kabir has a healthy diet. His calorie intake is typical for
someone of his age group but he is also overweight. Kabir suffers from hypothyroidism which results
in slower metabolism that burns fewer calories. Here, we can clearly see that unhealthy diet is not
necessarily a reason behind being overweight. According to Rothman’s definition of a cause (as
mentioned above), we have to be sure that the condition wouldn’t have happened without this specific
factor. So, in Ishaan’s case we can say that his unhealthy diet led to him being overweight. However,
if we talk about the general condition, it might not be so clear. Unhealthy diet definitely increases the
chance of being overweight but if we look at it carefully we can see that what’s causing weight gain is
the difference between calories intake and calories burned. Since an unhealthy diet may increase the
calorie intake, it eventually may increase the chance of gaining too much weight. Thus, the term that
should be used here is “risk factor”.
Various terms can be used to specify the role a particular factor may play as an etiological or causal
factor in abnormal behaviour displayed by an individual. Some of these are described here.
Necessary cause can be understood as a condition that must exist for a disorder to occur. For
instance, general paresis (a degenerative brain disorder) cannot develop unless a person has
contracted syphilis previously. Many mental disorders do not appear to have a necessary
cause.
Sufficient cause is a condition that guarantees the occurrence of a disorder. For example,
hopelessness is understood to be a sufficient cause of depression or the fact that if
hopelessness occurs then depression will also occur. However, it is important to note here that
a sufficient cause may not be a necessary cause. So, we can say that hopelessness is not a
necessary cause of depression; there are other causes or causal factors as well that lead to
depression.
Contributory causes are the ones that increase the probability of the occurrence of a disorder
but they are neither necessary nor sufficient for the disorder to occur. For example, parental
rejection may increase the probability of a child having difficulty in dealing with close
intimate relationships later in life. Here, parental rejection is a contributory cause for
difficulties that the individual may develop later in life, but it is neither necessary nor
sufficient.
Another important consideration while understanding the causes is the time frame in which they
operate.
There are distal causal factors which occur relatively early in life but manifest their effects
after many years. For instance, if we take the above given example only, parental rejection or
loss of a parent early in life may become a distal contributory cause predisposing an
individual to depression later in life.
There are proximal causal factors which operate shortly before the occurrence of symptoms
of a particular disorder. For example, an event or a condition may prove too much for
someone, triggering the onset of a disorder; divorce could lead to depression.
A reinforcing contributory cause is the one that maintains the already occurring
maladaptive behaviour. For instance, some secondary gain like sympathy, relief from
unwanted responsibility due to illness could be some of the examples. Another interesting
example here could be that when a person has depression, their behaviour alienates them from
friends and family, which further enhances their sense of rejection reinforcing the existing
depression (Joiner & Timmons, 2009).
For most forms of psychopathology, we do not have an answer as to what is a necessary or a sufficient
cause behind them, but we do have a sound understanding of various contributory causes. We have a
fair understanding of proximal, distal and reinforcing causal factors as well but the picture is further
complicated by the fact that what is a proximal cause at one stage may also serve as a distal
contributory cause, predisposing the individual to a disorder in later life. For example, loss of a parent
can be a proximal cause for grief reaction of a child but may also serve as a distal contributory cause
for later if the child develops depression as an adult.
Another useful categorization is grouping them into predisposing, precipitating, and perpetuating
factors.
Predisposing factors are those that determine the vulnerability to other causes that are
present at the time of illness; something that puts the individual at risk of developing an
illness or a problem, for instance, genetic endowment, some birth trauma, psychological
factors during infancy or childhood.
Precipitating factors are the ones that occur shortly before the onset of a disorder, so they
trigger the onset of a problem. These can be physical (brain injury caused by accident) or
psychological (loss of a loved one) in nature, or even a combination of the two.
Perpetuating factors are the ones that maintain a disorder once it occurs. Understanding of
perpetuating factors plays an important role while deciding a line of treatment for the
individual.
Unit 2
Classification of psychiatric disorders
Classification of psychiatric disorders in children and adolescents(ICD-10 & DSM-V),
epidemiology
Psychiatric epidemiology is a field which studies the causes (etiology) of mental disorders
in society, as well as conceptualization and prevalence of mental illness. It is a subfield of the
more general epidemiology. It has roots in sociological studies of the early 20th century
In the context of the DSM-5-TR (Diagnostic and Statistical Manual of Mental Disorders, Fifth
Edition, Text Revision), epidemiology refers to the study of the distribution and determinants of
mental disorders in populations. It focuses on understanding the prevalence, incidence, risk factors,
and causes of mental disorders in specific groups of people. Essentially, it's about understanding how
and why mental disorders occur, who is affected, and how common they are.
Key Aspects of Epidemiology in DSM-5-TR:
Prevalence:
The proportion of a population that has a specific mental disorder at a given time.
Incidence:
The rate at which new cases of a mental disorder occur in a population over a specific period.
Risk Factors:
Sociodemographic, psychological, and biological factors that increase the likelihood of developing a
mental disorder.
Causes:
Understanding the underlying causes, including genetic, environmental, and behavioral factors, that
contribute to the development and maintenance of mental disorders.
Comorbidity:
The occurrence of multiple mental disorders in the same individual.
Treatment and Prevention:
Using epidemiological findings to inform the development and implementation of effective
prevention programs and treatments for mental disorders.
In epidemiology, incidence refers to the rate of new cases of a disease or condition occurring in a
population over a specific time period, while prevalence refers to the proportion of individuals in a
population who have a particular disease or condition at a specific point in time or over a specific
period.
Incidence:
Measures the risk of developing a new case of a disease.
Calculated by dividing the number of new cases by the total population at risk over a specific
time period.
Helps assess the rate at which new cases are appearing in a population.
Prevalence:
Reflects the total number of existing cases of a disease, both new and old, in a population at a
specific point in time.
Can be expressed as a percentage or as the number of cases per a certain population size (e.g.,
per 1,000 people).
Helps assess the burden of disease within a population.
Relationship between incidence and prevalence:
Prevalence is influenced by both incidence and the duration of the disease.
A higher incidence (more new cases) will tend to increase prevalence, as more people are
diagnosed with the condition.
A longer duration of the disease (people live longer with the condition) will also tend to
increase prevalence.
Conversely, a lower incidence or shorter disease duration will tend to decrease prevalence.
Prevalence
Prevalence looks at existing cases, while incidence looks at new cases.
In a population of 10,000 people, 500 persons are reported to be affected by a certain disease. So what
is the prevalence of this disease in this population?
The mathematical way to calculate this would be:
This formula will provide us with the information as a percentage. By dividing 500 by 10,000 and
multiplying the result by 100 (to make it a percentage), we find out that 5% of the population is
affected. So the prevalence of the disease in our population is 5%.
Rather than expressing prevalence as a percentage, we can also describe it as the number of people
affected in a standard sized population, for example 1,000 people. So instead we would calculate:
This means that for every 1,000 patients, 50 of them have the disease.
Prevalence is like describing a group photo:
How many people can you see there? That number is your population.
How many people share a certain feature (e.g. same hair colour)? This number is used to
calculate prevalence.
In epidemiology, we actually have three different ways to calculate the prevalence:
Point prevalence: The number of cases of a health event at a certain time. For example, in a
survey you would be asked if you are currently smoking.
Period prevalence: The number of cases of a health event in reference to a time period, often
12 months. For example, in a survey you would be asked if you have smoked during the past
12 months.
Lifetime prevalence: The number of cases of the health event in reference to the total
lifetime. For example, in a survey, you would be asked if you have ever smoked.
Incidence
HIV is nowadays a treatable infection with a normal life expectancy. This means that with stable
numbers of new cases, prevalence numbers will increase. Looking at the new cases (incidence)
provides a deeper understanding of what is going on.
In a population of 1,000 non-diseased persons, 28 were infected with HIV over two years of
observation. The incidence proportion is 28 cases per 1,000 persons, i.e. 2.8% over a two year period
or 14 cases per 1,000 person-years (incidence rate), because the incidence proportion (28 per 1,000) is
divided by the number of years
Unit 3
Psychopathology of Childhood Disorders: Clinical
Picture, assessment and intervention
Mental Retardation
Introduction
Intellectual disability is a condition that limits intelligence and disrupts abilities necessary for living
independently. Signs of this lifelong condition appear during childhood. Most people with this will
need some degree of assistance throughout their lives.
Support programs and educational offerings can help with managing symptoms and effects.
What is intellectual disability?
An intellectual disability is when limitations in your mental abilities affect intelligence, learning, and
everyday life skills. The effects of this can vary widely. Some people may experience minor effects
but still live independent lives. Others may have severe effects and need lifelong assistance and
support.
A common misconception is that intellectual disability is just a limitation on intelligence as assessed
by a simple IQ test. An IQ test is only one piece of information. Some people have an average or
above-average IQ but have trouble with other abilities necessary for everyday life.
Other people have lower-than-average IQs but also have skills and abilities that are strong enough that
they don’t meet the criteria for intellectual disability, or they meet criteria for a milder form of
intellectual disability than an IQ test indicates.
In the American Psychiatric Association’s Diagnostic and Statistical Manual of Mental Disorders,
fifth edition text revision (DSM-5-TR), the formal name for this condition is “intellectual
developmental disorder.” Although for many individuals, the exact cause of their intellectual disability
is unknown, many cases of intellectual disability happen because of differences in brain development.
Less commonly, they can develop because of brain damage from an illness, injury or other events
when a person is younger than 18 years old.
How common is intellectual disability?
Intellectual disability is uncommon but widespread. Worldwide, it affects 1% to 3% of children. It’s
slightly more common in men than in women.
DSM V TR
Diagnostic Criteria
Intellectual developmental disorder (intellectual disability) is a disorder with onset during the
developmental period that includes both intellectual and adaptive functioning deficits in conceptual,
social, and practical domains. The following three criteria must be met:
A. Deficits in intellectual functions, such as reasoning, problem solving, planning, abstract thinking,
judgment, academic learning, and learning from experience, confirmed by both clinical assessment
and individualized, standardized intelligence testing.
B. Deficits in adaptive functioning that result in failure to meet developmental and sociocultural
standards for personal independence and social responsibility. Without ongoing support, the adaptive
deficits limit functioning in one or more activities of daily life, such as communication, social
participation, and independent living, across multiple environments, such as home, school, work, and
community.
C. Onset of intellectual and adaptive deficits during the developmental period.
Note: The term intellectual developmental disorder is used to clarify its relationship with the WHO
ICD-11 classification system, which uses the term Disorders of Intellectual Development. The
equivalent term intellectual disability is placed in parentheses for continued use. The medical and
research literature use both terms, while intellectual disability is the term in common use by
educational and other professions, advocacy groups, and the lay public. In the United States, Public
Law 111-256 (Rosa’s Law) changed all references to “mental retardation” in federal laws to
“intellectual disability.”
Specify current severity (see Table 1):
F70 Mild
F71 Moderate
F72 Severe
F73 Profound
The diagnosis of intellectual developmental disorder is based on both clinical assessment and
standardized testing of intellectual functions, standardized neuropsychological tests, and
standardized tests of adaptive functioning.
Global Developmental Delay
F88
This diagnosis is reserved for individuals under the age of 5 years when the clinical severity level
cannot be reliably assessed during early childhood. This category is diagnosed when an individual
fails to meet expected developmental milestones in several areas of intellectual functioning and
applies to individuals who are unable to undergo systematic assessments of intellectual functioning,
including children who are too young to participate in standardized testing. This category requires
reassessment after a period of time.
ICD 10 criteria
What are the symptoms of intellectual disability?
The symptoms of intellectual disability revolve around difficulties in different skill sets, including
academic skills, social skills and domestic skills.
Intellectual disability affects:
Intelligence-related symptoms
“Intelligence” is the umbrella term for your ability to understand and interact with the world around
you. It goes beyond the traditional language and math skills an IQ test measures. Intelligence-related
symptoms of intellectual disability can mean you have any of the following:
Delayed or slowed learning of any kind (such as in school or from real-life experiences).
Slowed reading speed.
Difficulties with reasoning and logic.
Problems with judgment and critical thinking.
Trouble using problem-solving and planning abilities.
Distractibility and difficulty focusing.
Adaptive behaviours
Adaptive behaviours revolve around abilities and learned skills you need to live and support yourself
independently. Symptoms of adaptive behaviour-related limitations can mean you have any of the
following:
Slower learning of toilet training and self-care activities (bathing, dressing, etc.).
Slower social development.
Little or no fear or apprehension of new people (lack of “stranger danger” behaviours).
Needing help from parental figures or other caregivers with basic daily activities (bathing,
using the bathroom, etc.) past the expected age.
Difficulty learning how to do chores or other common tasks.
Trouble understanding concepts like time management or money.
Needing help managing healthcare appointments or medications.
Trouble understanding social boundaries.
Difficulty with or limited understanding of social interactions, including friendships and
romantic relationships.
What causes intellectual disability?
Intellectual disabilities can happen for many reasons. Experts also suspect that in many cases, there
are multiple causes and contributing factors. Causes and contributing factors can influence the
development of intellectual disability before or during birth or during the earliest years of childhood.
Prebirth causes or contributing factors include, but aren’t limited to, the following:
Genetics and inheritance. Many conditions that cause intellectual disability happen because
of genetic mutations. Some of these mutations can be passed from generation to generation.
Examples include Down syndrome, Fragile X syndrome or Prader-Willi syndrome.
Infections. Some infections — like toxoplasmosis and rubella — can disrupt fetal
development, resulting in conditions that can cause intellectual disability, such as cerebral
palsy.
Teratogens. These are substances that can disrupt fetal development. Examples include
alcohol, tobacco, certain medications, radiation exposure and more.
Medical conditions. Having certain medical conditions while pregnant can cause
developmental differences in a fetus. Those can later result in intellectual disability. Examples
include hormonal conditions like hypothyroidism.
Causes that can happen during birth include:
Lack of oxygen (hypoxia).
Premature birth.
Other types of brain injury during birth.
Causes that can happen during early childhood include:
Injuries or accidents. These can cause intellectual disability if they result in brain damage.
Toxic exposures. Heavy metals like lead and mercury can damage your brain and cause
intellectual disability.
Infections. Common infections that spread to your nervous system, such
as measles or meningitis, can cause intellectual disability.
Tumors or growths in the brain. This includes cancers and benign (noncancerous) growths.
Medical conditions. Seizures and various types of epilepsy, such as Lennox-Gastaut
syndrome, can cause brain damage. That can cause intellectual disability.
Introduction
Learning disabilities (disorders) affect how your child’s brain takes in and uses
information. There are multiple types, like dyslexia and nonverbal learning disorders.
Learning disabilities are manageable with interventions that can help your child learn
in a different way.
What is a learning disability?
Learning disabilities (LDs) affect how your brain processes information. This could include
how you:
Acquire (take in) information.
Organize information.
Retain information.
Understand information.
Use information.
LDs can involve verbal (words or speech) and/or nonverbal information. They typically affect
how you read, write and/or do math. They can range from mild to severe.
Learning disabilities don’t affect intelligence and are different from intellectual disabilities.
People with LDs have specific issues with learning. But they have an average or above-
average IQ (intelligence quotient).
Most people with an LD find out about it early in school. But some people don’t get a
diagnosis until adolescence or adulthood.
What’s the difference between a learning disability and a learning disorder?
Many people use “learning disability” and “learning disorder” interchangeably. But there are
technical differences:
Learning disorder: This is a diagnostic term. A licensed professional (like
a psychologist) diagnoses someone with a learning disorder based on certain criteria.
The Diagnostic and Statistical Manual of Mental Disorders (DSM-5-TR) defines
“learning disorder” and its criteria.
Learning disability: This is a legal term. A public school identifies a student with a
learning disability based on a variety of assessments and documentation. This may
result in legal rights, like the right to an individualized education plan (IEP). In the
U.S., the Individuals with Disabilities Education Act (IDEA) defines what a learning
disability is.
If your child qualifies for special education services, they’ll receive an Individualized
Education Program (IEP). This personalized education plan:
Lists academic goals for your child.
Specifies the services your child will receive.
Lists the specialists who’ll work with your child.
Some children require specialized learning in only one area while they continue to attend
regular classes. Other children may need separate, more intensive educational programs. As
required by U.S. law, children with LDs should participate as much as possible in classes
with their peers who don’t have LDs.
It may take time to find the best strategy for your child. Know that your diligence in helping
your child is worth it.
Outlook / Prognosis
What can I expect if my child has a learning disability?
Even though children don’t outgrow learning disabilities, they can learn to adapt and improve
their skills. Children who receive early diagnoses and interventions are more likely to
overcome challenges while maintaining a positive self-image.
They may also build on personal strengths that tend to come with learning disorders. For
example, people with dyslexia are often especially creative. Children with learning
disabilities can grow to become very productive and successful adults.
What are the complications of learning disabilities?
If your child has an LD, they may experience self-esteem issues or believe they aren’t
intelligent. They also have a higher risk of developing mental health conditions like anxiety
or depression.
Positive support from caregivers, teachers and friends can help your child overcome these
obstacles. But don’t hesitate to reach out to a mental health professional, as well.
In 2013, the DSM-5* changed the diagnostic criteria for Specific Learning Disorder (SLD) to
combine all three learning disorders (reading, mathematics, and written expression) into one
overarching diagnosis. Specific learning disorders (often referred to as a learning disorder or
learning disability, see note on terminology) are neurodevelopmental disorders that are
typically diagnosed in early school-aged children, although may not be recognized until
adulthood. They are characterized by a persistent impairment in at least one of three major
areas: reading, written expression, and/or math.
DSM V TR Criteria
Specific Learning Disorder
Diagnostic Criteria
A. Difficulties learning and using academic skills, as indicated by the presence of at least one
of the following symptoms that have persisted for at least 6 months, despite the provision of
interventions that target those difficulties:
1. Inaccurate or slow and effortful word reading (e.g., reads single words aloud incorrectly or
slowly and hesitantly, frequently guesses words, has difficulty sounding out words).
2. Difficulty understanding the meaning of what is read (e.g., may read text accurately but not
understand the sequence, relationships, inferences, or deeper meanings of what is read).
3. Difficulties with spelling (e.g., may add, omit, or substitute vowels or consonants).
4. Difficulties with written expression (e.g., makes multiple grammatical or punctuation
errors within sentences; employs poor paragraph organization; written expression of ideas
lacks clarity).
5. Difficulties mastering number sense, number facts, or calculation (e.g., has poor
understanding of numbers, their magnitude, and relationships; counts on fingers to add
single-digit numbers instead of recalling the math fact as peers do; gets lost in the midst of
arithmetic computation and may switch procedures).
6. Difficulties with mathematical reasoning (e.g., has severe difficulty applying mathematical
concepts, facts, or procedures to solve quantitative problems).
B. The affected academic skills are substantially and quantifiably below those expected for
the individual’s chronological age, and cause significant interference with academic or
occupational performance, or with activities of daily living, as confirmed by individually
administered standardized achievement measures and comprehensive clinical assessment. For
individuals age 17 years and older, a documented history of impairing learning difficulties
may be substituted for the standardized assessment.
C. The learning difficulties begin during school-age years but may not become fully manifest
until the demands for those affected academic skills exceed the individual’s limited capacities
(e.g., as in timed tests, reading or writing lengthy, complex reports for a tight deadline,
excessively heavy academic loads).
D. The learning difficulties are not better accounted for by intellectual disabilities,
uncorrected visual or auditory acuity, other mental or neurological disorders, psychosocial
adversity, lack of proficiency in the language of academic instruction, or inadequate
educational instruction.
Note: The four diagnostic criteria are to be met based on a clinical synthesis of the
individual’s history (developmental, medical, family, educational), school reports, and
psychoeducational assessment.
Coding note: Specify all academic domains and subskills that are impaired. When more than
one domain is impaired, each one should be coded individually according to the following
specifiers.
Specify if:
F81.0 With impairment in reading:
Word reading accuracy
Reading rate or fluency
Reading comprehension
Note: Dyslexia is an alternative term used to refer to a pattern of learning difficulties
characterized by problems with accurate or fluent word recognition, poor decoding, and poor
spelling abilities. If dyslexia is used to specify this particular pattern of difficulties, it is
important also to specify any additional difficulties that are present, such as difficulties with
reading comprehension or math reasoning.
F81.81 With impairment in written expression:
Spelling accuracy
Grammar and punctuation accuracy
Clarity or organization of written expression
F81.2 With impairment in mathematics:
Number sense
Memorization of arithmetic facts
Accurate or fluent calculation
Accurate math reasoning
Note: Dyscalculia is an alternative term used to refer to a pattern of difficulties characterized
by problems processing numerical information, learning arithmetic facts, and performing
accurate or fluent calculations. If dyscalculia is used to specify this particular pattern of
mathematic difficulties, it is important also to specify any additional difficulties that are
present, such as difficulties with math reasoning or word reasoning accuracy.
Specify current severity:
Mild: Some difficulties learning skills in one or two academic domains, but of mild enough
severity that the individual may be able to compensate or function well when provided with
appropriate accommodations or support services, especially during the school years.
Moderate: Marked difficulties learning skills in one or more academic domains, so that the
individual is unlikely to become proficient without some intervals of intensive and
specialized teaching during the school years. Some accommodations or supportive services at
least part of the day at school, in the workplace, or at home may be needed to complete
activities accurately and efficiently.
Severe: Severe difficulties learning skills, affecting several academic domains, so that the
individual is unlikely to learn those skills without ongoing intensive individualized and
specialized teaching for most of the school years. Even with an array of appropriate
accommodations or services at home, at school, or in the workplace, the individual may not
be able to complete all activities efficiently.
ICD 10 Criteria
F81.0 Specific reading disorder
The main feature of this disorder is a specific and significant impairment in the development
of reading skills, which is not solely accounted for by mental age, visual acuity problems, or
inadequate schooling. Reading comprehension skill, reading word recognition, oral reading
skill, and performance of tasks requiring reading may all be affected. Spelling difficulties are
frequently associated with specific reading disorder and often remain into adolescence even
after some progress in reading has been made. Children with specific reading disorder
frequently have a history of specific developmental disorders of speech and language, and
comprehensive assessment of current language functioning often reveals subtle
contemporaneous difficulties. In addition to academic failure, poor school attendance and
problems with social adjustment are frequent complications, particularly in the later
elementary and secondary school years. The condition is found in all known languages, but
there is uncertainty as to whether or not its frequency is affected by the nature of the language
and of the written script.
Diagnostic guidelines
The child's reading performance should be significantly below the level expected on the basis
of age, general intelligence, and school placement. Performance is best assessed by means of
an individually administered, standardized test of reading accuracy and comprehension. The
precise nature of the reading problem depends on the expected level of reading, and on the
language and script. However, in the early stages of learning an alphabetic script, there may
be difficulties in reciting the alphabet, in giving the correct names of letters, in giving simple
rhymes for words, and in analysing or categorizing sounds (in spite of normal auditory
acuity).
Later, there may be errors in oral reading skills such as shown by:
(a)omissions, substitutions, distortions, or additions of words or parts of words;
(b) slow reading rate;
(c)false starts, long hesitations or "loss of place" in text, and inaccurate phrasing; and
(d)reversals of words in sentences or of letters within words.
There may also be deficits in reading comprehension, as shown by, for example:
(e)an inability to recall facts read;
(f)inability to draw conclusions or inferences from material read; and
(g)use of general knowledge as background information rather than of information from a
particular story to answer questions about a story read.
In later childhood and in adult life, it is common for spelling difficulties to be more profound
than the reading deficits. It is characteristic that the spelling difficulties often involve
phonetic errors, and it seems that both the reading and spelling problems may derive in part
from an impairment in phonological analysis. Little is known about the nature or frequency
of spelling errors in children who have to read non-phonetic languages, and little is known
about the types of error in non-alphabetic scripts.
Specific developmental disorders of reading are commonly preceded by a history of disorders
in speech or language development. In other cases, children may pass language milestones at
the normal age but have difficulties in auditory processing as shown by problems in sound
categorization, in rhyming, and possibly by deficits in speech sound discrimination, auditory
sequential memory, and auditory association. In some cases, too, there may be problems in
visual processing (such as in letter discrimination); however, these are common among
children who are just beginning to learn to read and hence are probably not directly causally
related to the poor reading. Difficulties in attention, often associated with overactivity and
impulsivity, are also common. The precise pattern of developmental difficulties in the
preschool period varies considerably from child to child, as does their severity; nevertheless
such difficulties are usually (but not invariably) present.
Associated emotional and/or behavioural disturbances are also common during the school-
age period. Emotional problems are more common during the early school years, but conduct
disorders and hyperactivity syndromes are most likely to be present in later childhood and
adolescence. Low self-esteem is common and problems in school adjustment and in peer
relationships are also frequent.
Includes:
"backward reading"
developmental dyslexia
specific reading retardation
spelling difficulties associated with a reading disorder
Excludes:
acquired alexia and dyslexia (R48.0)
acquired reading difficulties secondary to emotional disturbance
(F93.-)
spelling disorder not associated with reading difficulties story read.
Diagnostic Criteria
A. Persistent deficits in social communication and social interaction across multiple contexts, as
manifested by all of the following, currently or by history (examples are illustrative, not exhaustive;
see text):
1. Deficits in social-emotional reciprocity, ranging, for example, from abnormal social approach and
failure of normal back-and-forth conversation; to reduced sharing of interests, emotions, or affect; to
failure to initiate or respond to social interactions.
2. Deficits in nonverbal communicative behaviours used for social interaction, ranging, for example,
from poorly integrated verbal and nonverbal communication; to abnormalities in eye contact and body
language or deficits in understanding and use of gestures; to a total lack of facial expressions and
nonverbal communication.
3. Deficits in developing, maintaining, and understanding relationships, ranging, for example, from
difficulties adjusting behavior to suit various social contexts; to difficulties in sharing imaginative
play or in making friends; to absence of interest in peers.
Complications
Because people with autism spectrum disorder often have a hard time interacting socially,
communicating or behaving, this can lead to problems with:
School and learning.
Getting a job.
Not being able to live on their own.
Being isolated socially.
Stress within the family.
Being a victim and being bullied.
What is pervasive developmental disorder (PDD)?
Pervasive developmental disorder was once a term used to describe a group of developmental delays
that affect social and communication skills. But now healthcare providers call it autism spectrum
disorder (ASD). This name change occurred in 2013, when the American Psychiatric Association
reclassified the four following conditions into one umbrella diagnosis in the DSM-5:
Autistic disorder.
Asperger’s syndrome.
Childhood disintegrative disorder.
Pervasive developmental disorder not otherwise specified (PDD-NOS).
Note: “Autism spectrum disorder” is the correct, updated term for “pervasive developmental
disorder.” But for this article, we’ll use both terms.
People with pervasive developmental disorder may experience a range of challenges, including:
Delays in language or communication.
Trouble adjusting to changes in their routines or surroundings.
Difficulty relating to others.
How common is pervasive developmental disorder?
Pervasive developmental disorder is the most common subtype of autism spectrum disorder, making
up about 47% of all ASD diagnoses.
Symptoms and Causes
What are the symptoms of pervasive developmental disorder?
The most common pervasive developmental disorder symptoms include difficulty with
communication and social interactions. Children with PDD may also:
Engage in repetitive behaviors like rocking or hand flapping.
Have difficulty expressing their thoughts through language.
Have a hard time with routine changes.
Avoid eye contact.
Have trouble engaging in conversation.
Have difficulty controlling their emotions.
Speak with a flat or high-pitched voice.
No two people with pervasive developmental disorder are the same. Symptoms can range from mild
to severe — and most people fall somewhere between the two ends of the spectrum.
What causes pervasive developmental disorder?
Researchers are still working to find a specific cause for pervasive development disorder. But it’s
likely there’s a combination of genetic and environmental factors rather than a single cause. Possible
factors include:
Genetics. Plenty of experts believe that genetics plays a major role in PDD. But they’re still
learning exactly how. Many people with pervasive developmental disorder have gene
mutations (changes). In fact, scientists have found more than 100 genes on different
chromosomes that contribute to autism spectrum disorder in some way. But it’s complex. Not
everyone with PDD has the same mutations in every gene. And some of these same mutations
appear in people without PDD. Currently, most researchers agree that specific genetic
mutations likely cause specific symptoms — or control how severe those symptoms become.
At the very least, these genetic mutations can increase your risk for PDD.
Environment. If you’re more prone to PDD because of a genetic mutation, then certain
situations or environments can further increase your chances of developing it. For instance, if
you have a specific genetic mutation, then getting an infection or coming into contact with a
certain toxin can cause PDD.
Biology. Researchers continue to examine biological factors that may increase your risk of
PDD. This includes conditions that affect your metabolism, immune system or certain areas
of your brain.
Pervasive developmental disorder risk factors
A risk factor is something that increases your chances of getting a certain condition. Experts have
identified some risk factors for PDD, including:
Having a sibling with PDD or another type of ASD.
Some genetic conditions like fragile X syndrome or Down syndrome.
Having biological parents who were at least 35 when you were born (advanced maternal age).
Low birth weight.
What are the complications of pervasive developmental disorder?
While every person with PDD has their own challenges, the severity of symptoms can vary widely.
Some children with PDD have typical language skills, while others may not speak at all. Your
healthcare provider can help determine what types of resources your child might need. Early diagnosis
and treatment can often reduce your child’s symptoms.
Diagnosis and Tests
How do healthcare providers diagnose pervasive developmental disorder?
There’s no lab test or medical exam that can diagnose pervasive developmental disorder. Instead,
healthcare providers observe a person’s behavior and look at their developmental history.
The American Academy of Pediatrics recommends that all children have screenings for autism
spectrum disorder when they’re 18 to 24 months of age. Most healthcare providers screen children
during routine developmental and wellness checkups. During these checkups, your provider will talk
and interact with your child. They’ll also ask you questions about how your child moves, behaves and
communicates at home.
While most diagnoses occur in early childhood, providers can also diagnose PDD and other types of
ASD in older children, teens and adults. If you think you or your child could have pervasive
developmental disorder or a related condition, talk to your healthcare provider. They can do an
evaluation or refer you to someone who specializes in ASD.
Management and Treatment
How do healthcare providers treat pervasive developmental disorder?
Healthcare providers use a variety of treatments to manage PDD, including:
Supportive therapies.
Medications.
Complementary medicine.
No two people are the same. What works for one may not work for another because each person has
specific and unique needs. Your healthcare provider will design a personalized approach to give help
and support where it’s needed most.
Supportive therapies
Supportive therapy is the mainstay treatment for pervasive developmental disorder. This can include
things like:
Speech therapy to help build communication and comprehension skills.
Occupational therapy to strengthen coordination and help you learn routine tasks like
bathing, getting dressed and brushing your teeth.
Physical therapy to develop motor skills and learn ways to exercise and increase stamina.
Applied behavioral analysis (ABA), a type of behavior therapy that aims to increase positive
behaviors and decrease negative ones.
Medications
There are no medications that treat PDD directly. But many people with pervasive developmental
disorder have attention-deficit/hyperactivity disorder (ADHD), anxiety, depression or other similar
conditions. In these cases, medications can help improve your overall quality of life.
Complementary medicine
Complementary medicine involves combining nontraditional approaches with traditional treatments.
This can include a wide range of things like:
Art therapy.
Music therapy.
Massage.
Acupuncture.
Yoga.
Meditation.
Your provider can help you find complementary therapies to enhance your overall health and
wellness.
What is Rett syndrome?
Rett syndrome is a rare genetic and neurological condition that primarily affects girls. A genetic
variant causes it and plays an important role in brain development. The condition leads to symptoms
that affect motor function, communication, and cognitive abilities.
For the first few months of your child’s life, they’ll develop and meet growth milestones as expected.
After 6 months, however, your child will lose the ability to perform previously learned skills . This
includes purposeful hand use and communication. Symptoms typically show up in stages as your
child gets older. Symptoms that affect your child’s development will stop getting worse (progressing)
with time. But they won’t go away. Your child will need care and support throughout their life.
Symptoms and Causes
Rett syndrome is a condition that affects your child’s movement and development.
Rett syndrome symptoms
Your child will develop as expected until about 6 months. The first signs of Rett syndrome
are developmental delays. These start when your child doesn’t reach expected milestones for their
age. Examples could include waving, walking, and speaking their first words.
As your child gets older, symptoms of developmental regression (loss of learned skills) become more
visible.
Symptoms that affect your child’s muscles, movement, and behaviour include:
Balance and coordination challenges (difficulty walking)
Difficulty speaking
Difficulty swallowing or chewing (can lead to trouble maintaining a healthy weight
or malnutrition)
Muscle weakness or spasticity
Problems performing familiar movements on command (apraxia)
Repeated hand movements like wringing, squeezing or clapping
Other symptoms of Rett syndrome include:
Difficulty sleeping
Gastrointestinal problems (reflux or constipation)
Intellectual disability
Irritability
Scoliosis
Slow growth
Life-threatening symptoms may include:
Breathing issues
Heartbeat irregularities
Seizures
Rett syndrome facial features
Children with Rett syndrome may have a small head size compared to the rest of their body
(microcephaly). This can make facial features look more pronounced. But, there aren’t identifiable
facial features for this condition.
Many symptoms of Rett syndrome overlap with another condition called Angelman syndrome. Some
common features include speech and communication impairment, developmental delay, seizures and
sleep disturbances. Facial feature changes are common with Angelman syndrome, like deep-set eyes,
a wide mouth and widely spaced teeth, for example. These features don’t happen with Rett syndrome.
Rett syndrome stages
This condition progresses in stages that happen as your child gets older. They might experience
different symptoms at each stage. Not all children go through every stage. For example, some people
with Rett syndrome are never able to walk.
Rett syndrome stages include:
Stage I, early onset, starts when your child is between 6 and 18 months. Your child’s
development slows, like delays in crawling or a lack of eye contact. Your child will have low
muscle tone and feeding challenges.
Stage II, the rapid progressive stage, usually occurs between ages 1 and 4 years. Your child
may lose some language skills and the use of their hands. They may constantly wring their
hands. Some children also experience behaviors that resemble autism spectrum disorder, like
a lack of interest in socializing.
Stage III, the plateau or pseudo-stationary stage, usually occurs between ages 2 and 10 years.
Your child’s symptoms from stage II may improve, like communication and motor skills.
They may show interest in socializing. Seizures are common.
Stage IV, or the late motor deterioration stage, may happen at any time after stage III. Your
child may lose walking skills and muscle strength. Your child should keep their
communication and thinking abilities.
Rett syndrome causes
A genetic variant of the MECP2 gene causes most cases of Rett syndrome. This gene provides
instructions to make the MECP2 protein. This protein holds the connection (synapse) between nerve
cells and helps your child’s brain function as expected.
Not all cases of Rett syndrome affect the MECP2 gene. Some gene variants (like deletions) or genetic
variants to other genes, like CDJK5 and FOXG1, can lead to atypical types. Some unidentified genes
can also cause symptoms.
The genetic change occurs spontaneously (randomly). It’s not usually inherited.
Rett syndrome in males
Rett syndrome almost always affects females. This is because the genetic change that causes it
happens on the X chromosome. You have two X chromosomes if you’re female.
Since males have one X chromosome and one Y chromosome, this condition rarely affects them. A
variant on a child’s only X chromosome can lead to miscarriage or death during early infancy due to
severe symptoms.
Healthcare providers identify this gene change in males as MECP2-related severe neonatal
encephalopathy. This condition can cause similar symptoms, like intellectual disability, seizures and
difficulty with movement.
Anxiety Disorders
Anxiety disorders are a group of mental disorders characterized by excessive and persistent fear or
anxiety that interferes with daily life. They can include conditions like generalized anxiety disorder
(GAD), panic disorder, social anxiety disorder, specific phobias, and more
Diagnostic Criteria
A. Developmentally inappropriate and excessive fear or anxiety concerning separation from those to
whom the individual is attached, as evidenced by at least three of the following:
1. Recurrent excessive distress when anticipating or experiencing separation from home or from
major attachment figures.
2. Persistent and excessive worry about losing major attachment figures or about possible harm to
them, such as illness, injury, disasters, or death.
3. Persistent and excessive worry about experiencing an untoward event (e.g., getting lost, being
kidnapped, having an accident, becoming ill) that causes separation from a major attachment figure.
4. Persistent reluctance or refusal to go out, away from home, to school, to work, o r elsewhere
because of fear of separation.
5. Persistent and excessive fear of or reluctance about being alone or without major attachment figures
at home or in other settings.
6. Persistent reluctance or refusal to sleep away from home or to go to sleep without being near a
major attachment figure.
7. Repeated nightmares involving the theme of separation.
8. Repeated complaints of physical symptoms (e.g., headaches, stomach-aches, nausea, vomiting)
when separation from major attachment figures occurs or is anticipated.
B. The fear, anxiety, or avoidance is persistent, lasting at least 4 weeks in children and adolescents and
typically 6 months or more in adults.
C. The disturbance causes clinically significant distress or impairment in social, academic,
occupational, or other important areas of functioning.
D. The disturbance is not better explained by another mental disorder, such as refusing to leave home
because of excessive resistance to change in autism spectrum disorder; delusions or hallucinations
concerning separation in psychotic disorders; refusal to go outside without a trusted companion in
agoraphobia; worries about ill health or other harm befalling significant others in generalized anxiety
disorder; or concerns about having an illness in illness anxiety disorder.
Associated Features
When separated from major attachment figures, children and adults with separation anxiety disorder
may exhibit social withdrawal, apathy, sadness, or difficulty concentrating on work or play.
Depending on their age, individuals may have fears of animals, monsters, the dark, muggers, burglars,
kidnappers, car accidents, plane travel, and other situations that are perceived as presenting danger to
the family or themselves. Some individuals become homesick and extremely uncomfortable when
away from home. Separation anxiety disorder in children may lead to school refusal, which in turn
may lead to academic difficulties and social isolation. When extremely upset at the prospect of
separation, children may show anger or occasionally aggression toward someone who is forcing
separation. When alone, especially in the evening or the dark, young children may report unusual
perceptual experiences (e.g., seeing people peering into their room, frightening creatures reaching for
them, feeling eyes staring at them). Children with this disorder may be described as demanding,
intrusive, and in need of constant attention, and, as adults, may appear dependent and overprotective
as parents. Adults with the disorder are likely to text or phone their major attachment figures
throughout the day and repeatedly check on their whereabouts. The individual’s excessive demands
often become a source of frustration for family members, leading to resentment and conflict within
the family.
Risk factors
A child may have an increased risk of developing separation anxiety disorder if they:
Experience the loss of someone close to them.
Go through a stressful situation like their parents getting divorced.
Switch schools or move to a new place.
Have a history of anxiety disorders in their biological family.
a family history of anxiety or depression
shy, timid personalities
low socioeconomic status
overprotective parents
a lack of appropriate parental interaction
problems dealing with kids their own age
Etiology
Genetic Factors
The majority of the patients who are diagnosed with separation anxiety disorder are found to have a
history of other psychiatric conditions themselves, or in their family. Therefore, researchers believe
separation anxiety disorder to be a heritable disorder and of genetic origin.
The first-degree relatives of patients with a history of mental illness are usually at a higher risk of
developing separation anxiety disorder, albeit the precise genetic trigger has not been identified yet.
Genetic and physiological
There is evidence that separation anxiety disorder may be heritable. Heritability was estimated at 73%
in a community sample of 6-year-old twins, with higher rates found in girls. Children with separation
anxiety disorder display particularly enhanced sensitivity to respiratory stimulation using CO2-
enriched air. Separation anxiety disorder also appears to aggregate in families.
Biological Factors
Similar to other psychiatric disorders, separation anxiety disorder also involves imbalances in
neurotransmitter levels. In the patients with separation anxiety disorder, the regulation mechanism that
controls the optimal level of such brain chemicals is impaired. Serotonin and norepinephrine levels
are believed to be majorly affected in such patients.
This results in poor central regulation of emotions, and amplified stress responses to low-level
triggers of danger.
Environmental Factors
While genetic and biological factors are believed to be the causal triggers of separation anxiety
disorder, environmental factors also form a major set of contributors. And unlike the above two,
environmental factors can be pinpointed relatively easily by closely observing the surroundings and
events of the patient’s life.
There exists a panoply of environmental stressors. The most basic one is an abrupt change in the
surroundings of a child who is prone to the disorder, such as, for example, the family moving to a new
city because of the parents’ work commitments. Having to adjust to a new dwelling, school,
neighborhood, and locality altogether can get too much for the child to handle.
Additionally, children may also “learn” anxious behavior from their parents or grandparents who are
over-protective and show excessive concern about their safety. They subconsciously imbibe a habit of
worrying extensively from the mere observation of their surroundings, and eventually fail to see
anything abnormal in that habit.
Stress and trauma are other important triggers of anxiety. Major losses such as the unexpected death
of a family member to whom the patient was closely attached can render the person very lonely and
traumatized. Separation from a caregiver, a close friend, or a pet may all have similar impacts with
varying severities according to the given situation. Partners with an emotionally interdependent
romantic relationship also find it really difficult to cope if faced with separation or divorce. The
extreme unfamiliarity with the new emotional space and unpreparedness to deal with the change can
contribute heavily to separation anxiety disorder.
Environmental
Separation anxiety disorder often develops after life stress, especially a loss (e.g., the death of a
relative or pet; an illness of the individual or a relative; a change of schools; parental divorce; a move
to a new neighborhood; immigration; a disaster that involved periods of separation from attachment
figures). Being bullied during childhood has been shown to be a risk factor for the development of
separation anxiety disorder. In young adults, other examples of life stress include leaving the parental
home, entering into a romantic relationship, and becoming a parent. A history of parental
overprotection and intrusiveness may be associated with separation anxiety disorder in both childhood
and adulthood.
Life events: If one has lost someone very close to them due to death, divorce, illness, moving,
etc., they may develop a separation anxiety disorder.
Family history: As genetics play a role in this disorder, having a family member with a
separation anxiety disorder or other anxiety-related condition, makes it more likely for an
individual to develop the same disorder
Introduction
Social anxiety disorder (formerly known as social phobia) is a mental health condition where
you experience intense and ongoing fear of being judged negatively and/or watched by
others. Social anxiety disorder (social phobia) is a medical condition that causes fear and
anxiety when you’re around people in social situations. People with social anxiety fear being
judged or watched by others. This disorder is treatable with talk therapy and medications such
as antidepressants.
If you have social anxiety disorder, you have anxiety or fear in specific or all social
situations, including:
Meeting new people.
Performing in front of people.
Taking or making phone calls.
Using public restrooms.
Asking for help in a restaurant, store or other public place.
Dating.
Answering a question in front of people.
Eating in front of people.
Participating in an interview.
A core feature of social anxiety disorder is that you’re afraid of being judged, rejected and/or
humiliated.
Who does social anxiety affect?
Social anxiety disorder is a common mental health condition that can affect anyone. Most
people who have social anxiety disorder experience symptoms before they’re 20 years
old. Females experience higher rates of social anxiety than males.
How common is social anxiety disorder?
Social anxiety disorder isn’t uncommon. Approximately 5% to 10% of people across the
world have social anxiety disorder. It’s the third most common mental health condition
behind substance use disorder and depression.
Diagnostic Criteria
A. Marked fear or anxiety about one or more social situations in which the individual is
exposed to possible scrutiny by others. Examples include social interactions (e.g., having a
conversation, meeting unfamiliar people), being observed (e.g., eating or drinking), and
performing in front of others (e.g., giving a speech).
Note: In children, the anxiety must occur in peer settings and not just during interactions with
adults.
B. The individual fears that he or she will act in a way or show anxiety symptoms that will be
negatively evaluated (i.e., will be humiliating or embarrassing; will lead to rejection or
offend others).
C. The social situations almost always provoke fear or anxiety.
Note: In children, the fear or anxiety may be expressed by crying, tantrums, freezing,
clinging, shrinking, or failing to speak in social situations.
D. The social situations are avoided or endured with intense fear or anxiety.
E. The fear or anxiety is out of proportion to the actual threat posed by the social situation
and to the sociocultural context.
F. The fear, anxiety, or avoidance is persistent, typically lasting for 6 months or more.
G. The fear, anxiety, or avoidance causes clinically significant distress or impairment in
social, occupational, or other important areas of functioning.
H. The fear, anxiety, or avoidance is not attributable to the physiological effects of a
substance (e.g., a drug of abuse, a medication) or another medical condition.
I. The fear, anxiety, or avoidance is not better explained by the symptoms of another mental
disorder, such as panic disorder, body dysmorphic disorder, or autism spectrum disorder.
J. If another medical condition (e.g., Parkinson’s disease, obesity, disfigurement from burns
or injury) is present, the fear, anxiety, or avoidance is clearly unrelated or is excessive.
Specify if:
Performance only: If the fear is restricted to speaking or performing in public.
ICD 10 criteria
Specifiers
Individuals with the performance only type of social anxiety disorder have performance fears
that are typically most impairing in their professional lives (e.g., musicians, dancers,
performers, athletes) or in roles that require regular public speaking. Performance fears may
also manifest in work, school, or academic settings in which regular public presentations are
required. Individuals with performance only social anxiety disorder do not fear or avoid non-
performance social situations.
Risk and Prognostic Factors
Temperamental- Underlying traits that predispose individuals to social anxiety disorder
include behavioral inhibition and fear of negative evaluation, as well as harm avoidance.
Personality traits consistently associated with social anxiety disorder are high negative
affectivity (neuroticism) and low extraversion.
Environmental- There is evidence that negative social experiences, particularly peer
victimization, are associated with the development of social anxiety disorder, although causal
pathways remain unknown. Childhood maltreatment and adversity are risk factors for social
anxiety disorder. Among African Americans and Caribbean Blacks in the United States,
everyday forms of ethnic discrimination and racism are associated with social anxiety
disorder.
Genetic and physiological - Traits predisposing individuals to social anxiety disorder, such
as behavioral inhibition, are strongly genetically influenced. The genetic influence is subject
to gene-environment interaction; that is, children with high behavioral inhibition are more
susceptible to environmental influences, such as socially anxious modeling by parents. Also,
social anxiety disorder is heritable. First-degree relatives have a two to six times greater
chance of having social anxiety disorder, and liability to the disorder involves the interplay of
disorder specific (e.g., fear of negative evaluation) and nonspecific (e.g., negative affectivity
[neuroticism]) genetic factors. Genetic contribution to social anxiety disorder has been found
to be higher for social anxiety disorder in children than social anxiety disorder in adults and
higher for social anxiety symptoms than a clinical diagnosis of social anxiety disorder.
Causes
Like many other mental health conditions, social anxiety disorder likely arises from a
complex interaction of biological and environmental factors. Possible causes include:
Inherited traits. Anxiety disorders tend to run in families. However, it isn't entirely
clear how much of this may be due to genetics and how much is due to learned
behavior.
Brain structure. A structure in the brain called the amygdala (uh-MIG-duh-luh) may
play a role in controlling the fear response. People who have an overactive amygdala
may have a heightened fear response, causing increased anxiety in social situations.
Environment. Social anxiety disorder may be a learned behaviour — some people
may develop significant anxiety after an unpleasant or embarrassing social situation.
Also, there may be an association between social anxiety disorder and parents who
either model anxious behaviour in social situations or are more controlling or
overprotective of their children.
What causes social anxiety disorder?
The exact cause of social anxiety disorder is unknown, but it may resultTrusted Source from
a combination of factors.
Physical, biological, and genetic factors likely play a role, according to scientists. Problems
with neurotransmitter systems may lead to imbalances in the hormones serotonin, dopamine,
and glutamate. These brain chemicals help regulate mood.
Environmental factors may contribute, but only as part of a complex interaction that also
involves biological and genetic features, some experts say.
Factors that may contribute include a history of:
emotional, physical, or other kinds of abuse
negative interactions with peers
overcontrolling parenting styles
having an insecure attachment style
Negative experiences may lead to a type of post-traumatic stress disorder (PTSD), where
social anxiety is a symptom.
Anxiety disorders can run in families, but it’s unclear whether this is due to genetic or
environmental factors.
Risk factors
Several factors can increase the risk of developing social anxiety disorder, including:
Family history. You're more likely to develop social anxiety disorder if your
biological parents or siblings have the condition.
Negative experiences. Children who experience teasing, bullying, rejection, ridicule
or humiliation may be more prone to social anxiety disorder. In addition, other
negative events in life, such as family conflict, trauma or abuse, may be associated
with this disorder.
Temperament. Children who are shy, timid, withdrawn or restrained when facing
new situations or people may be at greater risk.
New social or work demands. Social anxiety disorder symptoms typically start in the
teenage years, but meeting new people, giving a speech in public or making an
important work presentation may trigger symptoms for the first time.
Having an appearance or condition that draws attention. For example, facial
disfigurement, stuttering or tremors due to Parkinson's disease can increase feelings of
self-consciousness and may trigger social anxiety disorder in some people.
Complications
Left untreated, social anxiety disorder can control your life. Anxieties can interfere with
work, school, relationships or enjoyment of life. This disorder can cause:
Low self-esteem
Trouble being assertive
Negative self-talk
Hypersensitivity to criticism
Poor social skills
Isolation and difficult social relationships
Low academic and employment achievement
Substance abuse, such as drinking too much alcohol
Suicide or suicide attempts
Other anxiety disorders and certain other mental health disorders, particularly major
depressive disorder and substance abuse problems, often occur with social anxiety disorder.
Prevention
There's no way to predict what will cause someone to develop an anxiety disorder, but you
can take steps to reduce the impact of symptoms if you're anxious:
Get help early. Anxiety, like many other mental health conditions, can be harder to
treat if you wait.
Keep a journal. Keeping track of your personal life can help you and your mental
health professional identify what's causing you stress and what seems to help you feel
better.
Set priorities in your life. You can reduce anxiety by carefully managing your time
and energy. Make sure that you spend time doing things you enjoy.
Avoid unhealthy substance use. Alcohol and drug use and even caffeine or nicotine
use can cause or worsen anxiety. If you're addicted to any of these substances, quitting
can make you anxious. If you can't quit on your own, see your health care provider or
find a treatment program or support group to help you.
Cognitive behavioural therapy (CBT): CBT helps you learn new ways to manage anxiety,
for example, how to replace negative thoughts with positive ones.
Acceptance and commitment therapy (ACT): In ACT people learn to use mindfulness,
acceptance, and behavioural strategies to be more present and figure out how to live a value-
based life despite negative feelings.
Group therapy or a support group: This helps you learn social skills and techniques to
interact with people in social settings. Working in a group will help you see that you’re not
alone and enable role play of practical solutions.
Exposure therapy: In this type of therapy, a healthcare professional will help you gradually
face social situations rather than avoiding them
Medication
Medications can help improve your symptoms and help you function in your daily life.
Medications that can treat social anxiety disorder includeTrusted Source:
selective serotonin reuptake inhibitors (SSRIs) , such as paroxetine (Paxil)
and Sertraline (Zoloft)
selective norepinephrine reuptake inhibitors (SNRIs), for example, venlafaxine
(Effexor)
propanol
SSRIs and SNRIs can take several weeksTrusted Source to have an effect, but propanolol is a
short-acting drug that you can use when you need it.
You may start with a low dose and gradually increase your prescription to avoid side effects.
If you’re unhappy with one medication, the doctor may offer an alternative.
What medications are used to treat social anxiety disorder?
Antidepressants are effective for depression and anxiety disorders and are a frontline form of
treatment for social anxiety disorders. Anti-anxiety medications are typically used for shorter
periods of time. Blood pressure medication known as beta-blockers can be used for
symptoms of social anxiety disorder as well. Specific medications that are used to treat social
anxiety disorder include:
SSRIs (selective serotonin reuptake inhibitors): SSRIs are a type of antidepressant.
Common SSRIs used to treat social anxiety disorder include fluoxetine
(Prozac®), sertraline (Zoloft®), paroxetine, citalopram and escitalopram.
SNRIs (serotonin-norepinephrine reuptake inhibitors): SNRIs are another type of
antidepressant. Venlafaxine or duloxetine (Cymbalta®) are common SNRIs used to
treat social anxiety disorder.
Benzodiazepines: These medications are used for short periods of time, either while
the antidepressants start to work or used on-demand in situations that provoke anxiety.
They aren’t intended to be used for long periods. Lorazepam or alprazolam are
examples of benzodiazepines.
Beta-blockers: Some beta-blockers are used to treat or prevent physical symptoms of
anxiety, such as a fast heart rate. Propranolol or metoprolol are examples of beta-
blockers.
It could take time to figure out the best dosage and type of medication for you. Know that
starting the process of treating your social anxiety disorder brings you one step closer to
feeling better.
Selective Mutism
Introduction
Having selective mutism means some social situations cause so much fear or anxiety that you
find speaking difficult or impossible. This anxiety disorder usually starts in childhood, but the
effects can be lifelong. Identifying and treating this condition quickly improves its overall
outlook, especially during early childhood.
What is selective mutism?
Selective mutism (SM) is a mental health condition where you can’t talk in certain situations
because of fear or anxiety. It usually affects young children, but it can also affect adolescents
and adults.
This condition is more than being shy, bashful or timid. SM is an anxiety disorder. It can
overlap with other anxiety-related conditions and have lingering effects later in life.
Diagnostic Criteria
A. Consistent failure to speak in specific social situations in which there is an expectation for
speaking (e.g., at school) despite speaking in other situations.
B. The disturbance interferes with educational or occupational achievement or with social
communication.
C. The duration of the disturbance is at least 1 month (not limited to the first month of
school).
D. The failure to speak is not attributable to a lack of knowledge of, or comfort with, the
spoken language required in the social situation.
E. The disturbance is not better explained by a communication disorder (e.g., childhood-onset
fluency disorder) and does not occur exclusively during the course of autism spectrum
disorder, schizophrenia, or another psychotic disorder.
Diagnosis in children
A child can successfully overcome selective mutism if it's diagnosed at an early age
and appropriately managed.
It's important for selective mutism to be recognised early by families and schools so they can
work together to reduce a child's anxiety. Staff in early years settings and schools may receive
training so they're able to provide appropriate support.
If you suspect your child has selective mutism and help is not available, or there are
additional concerns – for example, the child struggles to understand instructions or follow
routines – speak to a GP and ask them to refer you to a local specialist service for a formal
diagnosis.
You can also contact a speech and language therapy clinic directly. Do not accept the opinion
that your child will grow out of it or they are "just shy".
Your GP or local integrated care board (ICB) should be able to give you the telephone
number of your nearest NHS speech and language therapy service or another specialist
service that can help in your area.
Your child may also need to see a mental health professional or school educational
psychologist.
The clinician may initially want to talk to you without your child present, so you can speak
freely about any anxieties you have about your child's development or behaviour.
They'll want to find out whether there's a history of anxiety disorders in the family, and
whether anything is causing distress, such as a disrupted routine or difficulty learning a
second language. They'll also look at behavioural characteristics and take a full medical
history.
A person with selective mutism may not be able to speak during their assessment, but the
clinician should be prepared for this and be willing to find another way to communicate.
For example, they may encourage a child with selective mutism to communicate through
their parents, or suggest that older children or adults write down their responses or use a
computer. They may watch the child playing or watch a video of them speaking in a
comfortable environment.
Diagnosis in adults
It's possible for adults to overcome selective mutism, although they may continue to
experience the psychological and practical effects of spending years without social interaction
or not being able to reach their academic or occupational potential.
Adults will ideally be seen by a mental health professional with access to support from a
speech and language therapist or another knowledgeable professional.
Diagnosis guidelines
Selective mutism is diagnosed according to specific guidelines. These include observations
about the person concerned as outlined:
they do not speak in specific situations, such as during school lessons or when they
can be overheard in public
they can speak normally in situations where they feel comfortable, such as when
they're alone with parents at home, or in their empty classroom or bedroom
their inability to speak to certain people has lasted for at least 1 month (2 months in a
new setting)
their inability to speak interferes with their ability to function in that setting
their inability to speak is not better explained by another behavioural, mental or
communication disorder
Associated difficulties
A child with selective mutism will often have other fears and social anxieties, and they may
also have additional speech and language difficulties.
They're often wary of doing anything that draws attention to them because they think that by
doing so, people will expect them to talk.
For example, a child may not do their best in class after seeing other children being asked to
read out good work, or they may be afraid to change their routine in case this provokes
comments or questions. Many have a general fear of making mistakes.
Accidents and urinary infections may result from being unable to ask to use the toilet and
holding on for hours at a time. School-aged children may avoid eating and drinking
throughout the day so they do not need to excuse themselves.
Children may have difficulty with homework assignments or certain topics because they're
unable to ask questions in class.
Teenagers may not develop independence because they're afraid to leave the house
unaccompanied. And adults may lack qualifications because they're unable to participate in
college life or subsequent interviews.
Selective mutism makes you talk less or feel unable to talk in situations where you aren’t
comfortable. Otherwise, you have no difficulty with talking.
What are the symptoms of selective mutism?
The “selective” in this condition’s name means it only happens in certain situations
(remember that it’s not a willful or deliberate choice not to talk). If you have SM, you have
no trouble talking in comfortable situations. However, you consistently find talking difficult
or impossible in uncomfortable situations.
The symptoms can take different forms. Some people are completely unable to talk (or nearly
so). Others may communicate less or in limited ways.
Total or near-total inability to communicate
This is going to great lengths to avoid communicating or avoiding it entirely. It can look like:
Feeling unable to speak. It can happen because you feel overwhelmed or paralyzed by
fear or anxiety. It can appear that you’re refusing to talk, but is an “autopilot”
response rather than a deliberate choice.
Tense or stiff posture, freezing or feeling unable to move.
A “deer in the headlights” or blank expression.
Avoiding eye contact.
Avoiding social interactions or not participating in them.
Not asking for things wanted or needed (such as a child in school not asking a teacher
if they can go to the bathroom, leading to daytime wetting).
Behaving disruptively (such as throwing temper tantrums) to avoid talking.
Nonverbal communication
Preferring to use widely understood sounds (such as “uh-uh” for “no” and “uh-huh”
for yes) or other noises instead of words.
Using nonverbal communication to avoid talking (such as writing responses or
pointing to things in a book).
Using gestures or other movements (such as facial expressions, pointing, miming, or
nodding or shaking your head) rather than words.
Minimal or reduced communication
Slowed responses.
Using single-word responses or very short sentences.
Mumbling, stuttering or whispering.
Changing one’s voice (speaking in a robot-like voice or changing one’s natural pitch
and tone).
Other symptoms[
Besides lack of speech, other common behaviors and characteristics displayed by selectively
mute people, according to Elisa Shipon-Blum's findings, include:
Shyness, social anxiety, fear of social embarrassment or social isolation and
withdrawal
Difficulty maintaining eye contact
Blank expression and reluctance to smile or incessant smiling
Difficulty expressing feelings, even to family members
Tendency to worry more than most people of the same age
Sensitivity to noise and crowds
On the flip side, there are some positive traits observed in many cases:
Above average intelligence, inquisitiveness, or perception
A strong sense of right and wrong
Creativity
Love for the arts
Empathy
Sensitivity for other people
What causes selective mutism?
Most children and adults with selective mutism are hypothesized to have an inherited
predisposition to anxiety. They often have inhibited temperaments, which is hypothesized to
be the result of over-excitability of the area of the brain called the amygdala.[16] This area
receives indications of possible threats and sets off the fight-or-flight response. Behavioral
inhibitions, or inhibited temperaments, encompass feelings of emotional distress and social
withdrawals. In a 2016 study,[17] the relationship between behavioral inhibition and selective
mutism was investigated. Children between the ages of three and 19 with lifetime selective
mutism, social phobia, internalizing behavior, and healthy controls were assessed using the
parent-rated Retrospective Infant Behavioral Inhibition (RIBI) questionnaire, consisting of 20
questions that addressed shyness and fear, as well as other subscales. The results indicated
behavioral inhibition does indeed predispose selective mutism. Corresponding with the
researchers’ hypothesis, children diagnosed with long-term selective mutism had a higher
behavioral inhibition score as an infant. This is indicative of the positive correlation between
behavioral inhibition and selective mutism.
Experts can’t fully explain why SM happens. However, they suspect several possible factors
may cause or contribute to it. These include:
Other mental health conditions
SM has strong connections to other mental health conditions. These aren’t necessarily causes.
They’re simply more likely to happen in people with SM. These conditions include:
Social anxiety disorder. This is extremely common in people who have SM. Experts
estimate that 75% to 100% of people with SM also have this.
Phobias.
Other anxiety disorders.
Autism spectrum disorder.
Separation anxiety.
Post-traumatic stress disorder (PTSD).
Family history or genetics
Anxiety disorders can run in families. People with SM are much more likely to have a first-
degree relative (a parent, sibling or child) with SM or another anxiety disorder.
Other communication disorders
Some children develop SM because of anxiety related to how they talk or how well they
understand others (like from auditory processing disorders or learning delays).
Children can also develop SM because of speech disorders (like stuttering or other forms
of fluency disorder). Some children develop SM because they don’t like their voice or feel
anxious about how they sound.
Social circumstances
Children with certain social factors or circumstances are more likely to develop SM. These
include:
Being bullied.
Traumatic events or abuse.
Family problems (such as emotional, verbal or physical violence in the home).
Immigrating to a place with a different primary language.
What are the complications of selective mutism?
SM can negatively affect your life in many ways. These can include:
Social difficulties, loneliness or isolation.
Developing other anxiety-related conditions or symptoms.
Impacts on academic achievement or work performance.
Diagnosis and Tests
How is selective mutism diagnosed?
A mental health provider, like a psychiatrist or psychologist, will usually diagnose SM. Other
providers, especially speech-language pathologists or speech therapists, may rule out other
conditions to help with the diagnosis.
A provider makes this diagnosis based on symptoms and behaviors. They’ll ask questions
about your (or your child’s) experiences and other factors that could contribute to this
condition.
Your provider will typically use screening questionnaires, checklists or other tools to help
determine if you meet the criteria. The American Psychiatric Association’s Diagnostic and
Statistical Manual of Mental Disorders, fifth edition text revision™(often referred to as “the
DSM-5®”) has five criteria that you must meet to receive a diagnosis of SM:
You consistently don’t talk in social situations where it’s expected, but have no
trouble talking in other situations.
Not talking affects your social, educational or work life, or any combination of the
three.
The inability to talk lasts longer than one month.
Not talking isn’t because you have trouble speaking or understanding the main
language others are using.
Your difficulty talking isn’t because of another communication disorder
like stuttering, and it isn’t only happening in connection with autism spectrum
disorder, schizophrenia spectrum disorders or other conditions that involve psychosis.
Management and Treatment
How is selective mutism treated, and is there a cure?
With treatment, it’s possible to reduce the severity and frequency of symptoms. With early
diagnosis and treatment, some people may see the symptoms vanish entirely.
The most common treatment approaches are:
Mental health therapy
Mental health therapy (especially cognitive behavioral therapy, or CBT) is generally the first
option. It’s also the most likely to help. Behavioral therapy helps you understand and cope
with anxiety and other distressing feelings that cause SM symptoms. It can also help with
modifying tantrums or other disruptive behaviors that can happen with SM.
For children, these forms of therapy should involve the people raising them, too. Parental
figures (including legal guardians or other loved ones) can contribute to the success of mental
health therapy.
Speech therapy
Speech therapy involves working with a speech therapist or another specialized healthcare
professional. It can be particularly helpful when SM happens with speech disorders.
Medications
Medications can be part of treatment for SM, especially if mental health or speech therapy
aren’t effective on their own.
The most common medications for treating SM are selective-serotonin reuptake inhibitors
(SSRIs). These mainly treat depression but can also treat anxiety-related disorders, including
SM. Other medications may also help. Your healthcare provider (or your child’s provider) can
tell you more about these and help you choose.
Complications/side effects of medications
Your healthcare provider is the best person to tell you about the possible side effects and
complications of the specific medication(s) you’re taking, and what you can do to limit or
avoid those effects.
Outlook / Prognosis
What can I expect if my child or I have SM?
In children, SM can affect how they do in school, socialize and make friends. It can also
cause children to avoid talking even when it’s important.
If you have SM as an adult, it can continue to have negative effects. SM can keep you from
making friends or developing relationships (social, work, romantic, etc.). It can also affect
how you do at school or at work.
How long does selective mutism last?
For many people, the symptoms seem to disappear by adulthood. The symptoms can still be
there, but shift and look more like another anxiety disorder (especially social anxiety
disorder).
What’s the outlook for selective mutism?
The outlook for SM is good overall, especially with early diagnosis and treatment. When
diagnosed and treated in early childhood, most people with SM can overcome or learn to
cope with it, so it doesn’t affect their lives as much (or at all).
When SM goes undetected or untreated, the outlook is less positive. It isn’t dangerous, but
the negative effects can be significant. People with SM often experience anxiety and
depression. Some struggle with social situations and feel lonely or isolated. It can also affect
their education, career and other important parts of their lives.
Treatment
[edit]
Contrary to popular belief, people with selective mutism do not necessarily improve with age.
[22]
Effective treatment is necessary for a child to develop properly. Without treatment,
selective mutism can contribute to chronic depression, further anxiety, and other social and
emotional problems.[23][24][25]
Consequently, treatment at an early age is important. If not addressed, selective mutism tends
to be self-reinforcing. Others may eventually expect an affected child to not speak and
therefore stop attempting to initiate verbal contact. Alternatively, they may pressure the child
to talk, increasing their anxiety levels in situations where speech is expected. Due to these
problems, a change of environment may be a viable consideration. However, changing school
is worth considering only if the alternative environment is highly supportive, otherwise a
whole new environment could also be a social shock for the individual or deprive them of any
friends or support they have currently. Regardless of the cause, increasing awareness and
ensuring an accommodating, supportive environment are the first steps towards effective
treatment. Most often affected children do not have to change schools or classes and have no
difficulty keeping up except on the communication and social front. Treatment in teenage or
adult years can be more difficult because the affected individual has become accustomed to
being mute, and lacks social skills to respond to social cues.[citation needed]
The exact treatment depends on the person's age, any comorbid mental illnesses, and a
number of other factors. For instance, stimulus fading is typically used with younger children
because older children and teenagers recognize the situation as an attempt to make them
speak, and older people with this condition and people with depression are more likely to
need medication.[26]
Like other disabilities, adequate accommodations are needed for those with the condition to
succeed at school, work, and in the home. In the United States, under the Individuals with
Disabilities Education Act (IDEA), a federal law, those with the disorder qualify for services
based upon the fact that they have an impairment that hinders their ability to speak, thus
disrupting their lives. This assistance is typically documented in the form of an Individualized
Education Program (IEP). Post-secondary accommodations are also available for people with
disabilities.[citation needed]
Under another law in the US, Section 504 of the Rehabilitation Act of 1973, public school
districts are required to provide a free, appropriate public education to every "qualified
handicapped person" residing within their jurisdiction. If the child is found to have
impairments that substantially limit a major life activity (in this case, learning), the education
agency has to decide what related aids or services are required to provide equal access to the
learning environment.[27]
Social Communication Anxiety Treatment (S-CAT) is a common treatment approach by
professionals and has proven to be successful. [28] S-CAT integrates components of behavioral-
therapy, cognitive-behavioral therapy (CBT), and an insight-oriented approach to increase
social communication and promote social confidence. Tactics such as systemic
desensitization, modeling, fading, and positive reinforcement enable individuals to develop
social engagement skills and begin to progress communicatively in a step-by-step manner.
There are many treatment plans that exist and it is recommended for families to do thorough
research before deciding on their treatment approach.[citation needed]
Self-modeling
[edit]
An affected child is brought into the classroom or the environment where the child will not
speak and is videotaped. First, the teacher or another adult prompts the child with questions
that likely will not be answered. A parent, or someone the child feels comfortable speaking to,
then replaces the prompter and asks the child the same questions, this time eliciting a verbal
response. The two videos of the conversations are then edited together to show the child
directly answering the questions posed by the teacher or other adult. This video is then shown
to the child over a series of several weeks, and every time the child sees themself verbally
answering the teacher/other adult, the tape is stopped and the child is given positive
reinforcement.[citation needed]
Such videos can also be shown to affected children's classmates to set an expectation in their
peers that they can speak. The classmates thereby learn the sound of the child's voice and,
albeit through editing, have the opportunity to see the child conversing with the teacher. [29][30]
Mystery motivators
[edit]
Mystery motivation is often paired with self-modeling. An envelope is placed in the child's
classroom in a visible place. On the envelope, the child's name is written along with a
question mark. Inside is an item that the child's parent has determined to be desirable to the
child. The child is told that when they ask for the envelope loudly enough for the teacher and
others in the classroom to hear, the child will receive the mystery motivator. The class is also
told of the expectation that the child ask for the envelope loudly enough that the class can
hear.[29][30][31]
Stimulus fading
[edit]
Affected subjects can be brought into a controlled environment with someone with whom
they are at ease and can communicate. Gradually, another person is introduced into the
situation. One example of stimulus fading is the sliding-in technique,[22] where a new person
is slowly brought into the talking group. This can take a long time for the first one or two
faded-in people but may become faster as the patient gets more comfortable with the
technique.
As an example, a child may be playing a board game with a family member in a classroom at
school. Gradually, the teacher is brought in to play as well. When the child adjusts to the
teacher's presence, then a peer is brought in to be a part of the game. Each person is only
brought in if the child continues to engage verbally and positively.[29][30][31]
Desensitization
[edit]
The subject communicates indirectly with a person to whom they are afraid to speak through
such means as email, instant messaging (text, audio or video), online chat, voice or video
recordings, and speaking or whispering to an intermediary in the presence of the target
person. This can make the subject more comfortable with the idea of communicating with this
person.
Shaping
[edit]
The subject is slowly encouraged to speak. The subject is reinforced first for interacting
nonverbally, then for saying certain sounds (such as the sound that each letter of the alphabet
makes) rather than words, then for whispering, and finally saying a word or more.[32]
Spacing
[edit]
Spacing is important to integrate, especially with self-modeling. Repeated and spaced out use
of interventions is shown to be the most helpful long-term for learning. Viewing videotapes
of self-modeling should be shown over a spaced out period of time of approximately 6 weeks.
[29][30][31]
Drug treatments
[edit]
Some practitioners believe there would be evidence indicating anxiolytics to be helpful in
treating children and adults with selective mutism, [33] to decrease anxiety levels and thereby
speed the process of therapy. Use of medication may end after nine to twelve months, once
the person has learned skills to cope with anxiety and has become more comfortable in social
situations.[citation needed] Medication is more often used for older children, teenagers, and adults
whose anxiety has led to depression and other problems.
Medication, when used, should never be considered the entire treatment for a person with
selective mutism. However, the reason why medication needs to be considered as a treatment
at all is because selective mutism is still prevalent, despite psychosocial efforts. But while on
medication, the person should still be in therapy to help them learn how to handle anxiety and
prepare them for life without medication, as medication is typically a short-term solution.
[citation needed]
Since selective mutism is categorized as an anxiety disorder, using similar medication to treat
either makes sense. Antidepressants have been used in addition to self-modeling and mystery
motivation to aid in the learning process. [further explanation needed][29][30] Furthermore, SSRIs in
particular have been used to treat selective mutism. In a systematic review, ten studies were
looked at which involved SSRI medications, and all reported medication was well tolerated.
[34]
In one of them, Black and Uhde (1994) conducted a double-blind, placebo-controlled
study investigating the effects of fluoxetine. By parent report, fluoxetine-treated children
showed significantly greater improvement than placebo-treated children. In another, Dummit
III et al. (1996) administered fluoxetine to 21 children for nine weeks and found that 76% of
the children had reduced or no symptoms by the end of the experiment. [35] This indicates that
fluoxetine is an SSRI that is indeed helpful in treating selective mutism.
Obsessive-Compulsive Disorder
Diagnostic Criteria
A. Presence of obsessions, compulsions, or both:
Obsessions are defined by (1) and (2):
1. Recurrent and persistent thoughts, urges, or images that are experienced, at some time
during the disturbance, as intrusive and unwanted, and that in most individuals cause marked
anxiety or distress.
2. The individual attempts to ignore or suppress such thoughts, urges, or images, or to
neutralize them with some other thought or action (i.e., by performing a compulsion).
Compulsions are defined by (1) and (2):
1. Repetitive behaviours (e.g., hand washing, ordering, checking) or mental acts (e.g.,
praying, counting, repeating words silently) that the individual feels driven to perform in
response to an obsession or according to rules that must be applied rigidly.
2. The behaviours or mental acts are aimed at preventing or reducing anxiety or distress, or
preventing some dreaded event or situation; however, these behaviors or mental acts are not
connected in a realistic way with what they are designed to neutralize or prevent, or are
clearly excessive.
Note: Young children may not be able to articulate the aims of these behaviors or mental acts.
B. The obsessions or compulsions are time-consuming (e.g., take more than 1 hour per
day) or cause clinically significant distress or impairment in social, occupational, or other
important areas of functioning.
C. The obsessive-compulsive symptoms are not attributable to the physiological effects of a
substance (e.g., a drug of abuse, a medication) or another medical condition.
D. The disturbance is not better explained by the symptoms of another mental disorder (e.g.,
excessive worries, as in generalized anxiety disorder; preoccupation with appearance, as in
body dysmorphic disorder; difficulty discarding or parting with possessions, as in hoarding
disorder; hair pulling, as in trichotillomania [hair-pulling disorder]; skin picking, as in
excoriation [skinpicking] disorder; stereotypies, as in stereotypic movement disorder;
ritualized eating behavior, as in eating disorders; preoccupation with substances or gambling,
as in substance-related and addictive disorders; preoccupation with having an illness, as in
illness anxiety disorder; sexual urges or fantasies, as in paraphilic disorders; impulses, as in
disruptive, impulse-control, and conduct disorders; guilty ruminations, as in major depressive
disorder; thought insertion or delusional preoccupations, as in schizophrenia spectrum and
other psychotic disorders; or repetitive patterns of behavior, as in autism spectrum disorder).
Specify if:
With good or fair insight: The individual recognizes that obsessive-compulsive disorder
beliefs are definitely or probably not true or that they may or may not be true.
With poor insight: The individual thinks obsessive-compulsive disorder beliefs are probably
true.
With absent insight/delusional beliefs: The individual is completely convinced that
obsessive-compulsive disorder beliefs are true.
Specify if:
Tic-related: The individual has a current or past history of a tic disorder.
Risk factors
Factors that may raise the risk of causing obsessive-compulsive disorder include:
Family history. Having parents or other family members with the disorder can raise
your risk of getting OCD.
Stressful life events. If you've gone through traumatic or stressful events, your risk
may increase. This reaction may cause the intrusive thoughts, rituals and emotional
distress seen in OCD.
Other mental health disorders. OCD may be related to other mental health disorders,
such as anxiety disorders, depression, substance abuse or tic disorders.
What causes OCD?
Researchers don’t know what exactly causes OCD. But they think several factors contribute
to its development, including:
Genetics: Studies show that people who have a first-degree relative (biological parent
or sibling) with OCD are at a higher risk for developing the condition. The risk
increases if the relative developed OCD as a child or teen.
Brain changes: Imaging studies have shown differences in the frontal cortex and
subcortical structures of the brain in people who have OCD. OCD is also associated
with other neurological conditions that affect similar areas of your brain,
including Parkinson’s disease, Tourette’s syndrome and epilepsy.
PANDAS syndrome: PANDAS is short for “pediatric autoimmune neuropsychiatric
disorders associated with streptococcal infections.” It describes a group of conditions
that can affect children who have had strep infections, such as strep throat or scarlet
fever. OCD is one of these conditions.
Childhood trauma: Some studies show an association between childhood trauma,
such as abuse or neglect, and the development of OCD.
Learning. Obsessive fears and compulsive behaviors can be learned from watching
family members or learning them over time.
Complications
Issues due to obsessive-compulsive disorder include:
Excessive time spent taking part in ritualistic behaviors.
Health issues, such as contact dermatitis from frequent hand-washing.
Having a hard time going to work or school or taking part in social activities.
Troubled relationships.
Poor quality of life.
Thoughts about suicide and behavior related to suicide.
Outlook / Prognosis
What is the prognosis of OCD?
The prognosis (outlook) of OCD can vary. OCD is often a lifelong condition that can wax
and wane.
People with OCD who receive appropriate treatment often experience increased quality of
life and improved social, school and/or work functioning.
If you don’t receive treatment, the cycle of obsessions and compulsions is more difficult to
break and treat, as structural changes in your brain take place. Because of this, it’s key to seek
medical care as soon as possible if you or your child experience symptoms.
Depressive Disorders
Introduction
Depression is a mood disorder that causes a persistent feeling of sadness and loss of interest.
Also called major depressive disorder or clinical depression, it affects how you feel, think and
behave and can lead to a variety of emotional and physical problems. You may have trouble
doing normal day-to-day activities, and sometimes you may feel as if life isn't worth living.
More than just a bout of the blues, depression isn't a weakness and you can't simply "snap
out" of it. Depression may require long-term treatment. But don't get discouraged. Most
people with depression feel better with medication, psychotherapy or both.
Depressive disorders include disruptive mood dysregulation disorder, major depressive
disorder (including major depressive episode), persistent depressive disorder, premenstrual
dysphoric disorder, substance/medication-induced depressive disorder, depressive disorder
due to another medical condition, other specified depressive disorder, and unspecified
depressive disorder. The common feature of all of these disorders is the presence of sad,
empty, or irritable mood, accompanied by related changes that significantly affect the
individual’s capacity to function (e.g., somatic and cognitive changes in major depressive
disorder and persistent depressive disorder). What differs among them are issues of duration,
timing, or presumed etiology.
Diagnostic Criteria
A. Severe recurrent temper outbursts manifested verbally (e.g., verbal rages) and/or
behaviourally (e.g., physical aggression toward people or property) that are grossly out of
proportion in intensity or duration to the situation or provocation.
B. The temper outbursts are inconsistent with the developmental level.
C. The temper outbursts occur, on average, three or more times per week.
D. The mood between temper outbursts is persistently irritable or angry most of the day,
nearly every day, and is observable by others (e.g., parents, teachers, peers).
E. Criteria A–D have been present for 12 or more months. Throughout that time, the
individual has not had a period lasting 3 or more consecutive months without all of the
symptoms in Criteria A–D.
F. Criteria A and D are present in at least two of three settings (i.e., at home, at school, with
peers) and are severe in at least one of these.
G. The diagnosis should not be made for the first time before age 6 years or after age 18
years.
H. By history or observation, the age at onset of Criteria A–E is before 10 years.
I. There has never been a distinct period lasting more than 1 day during which the full
symptom criteria, except duration, for a manic or hypomanic episode have been met.
Note: Developmentally appropriate mood elevation, such as occurs in the context of a highly
positive event or its anticipation, should not be considered as a symptom of mania or
hypomania.
J. The behaviours do not occur exclusively during an episode of major depressive disorder
and are not better explained by another mental disorder (e.g., autism spectrum disorder,
posttraumatic stress disorder, separation anxiety disorder, persistent depressive disorder).
Note: This diagnosis cannot coexist with oppositional defiant disorder, intermittent explosive
disorder, or bipolar disorder, though it can coexist with others, including major depressive
disorder, attention-deficit/hyperactivity disorder, conduct disorder, and substance use
disorders. Individuals whose symptoms meet criteria for both disruptive mood dysregulation
disorder and oppositional defiant disorder should only be given the diagnosis of disruptive
mood dysregulation disorder. If an individual has ever experienced a manic or hypomanic
episode, the diagnosis of disruptive mood dysregulation disorder should not be assigned.
K. The symptoms are not attributable to the physiological effects of a substance or another
medical or neurological condition.
Outlook / Prognosis
What is the prognosis for disruptive mood dysregulation disorder?
Children with DMDD can experience significant issues in school, at home and in social
relationships.
If left untreated, children with DMDD are at high risk of developing depression and/or
anxiety disorders in adulthood. Because of this, it’s important to seek help for your child as
soon as possible if they’re showing signs of DMDD.
Prevention
Can DMDD be prevented?
Although it might not be possible to prevent DMDD, recognizing and acting on symptoms
when they first appear can minimize distress to your child and family. It can also help prevent
many of the problems associated with the condition.
Living With
How can I help my child with disruptive mood dysregulation disorder?
If your child has disruptive mood dysregulation disorder, aside from getting them
professional care, you can help them and yourself in the following ways:
Learn as much as you can about DMDD: Talk to your child’s healthcare provider or
mental health professional. Ask questions about treatment options and new research
on DMDD.
Communicate regularly with your child’s healthcare provider: It’s important to work
closely with your child’s provider to make treatment decisions that are best for them.
Work with your child’s teacher or school counselor: Together, you can develop
strategies and accommodations that can help your child thrive in school.
Take a time-out or break when needed: If you’re about to make the conflict with your
child worse instead of better, take a break and step away. This also sets a good
example for your child. Support your child if they decide to take a break to prevent
escalating a negative situation.
Take care of yourself: Maintain interests and hobbies that you enjoy and manage
stress. Try to work with and gain support from the other adults who are interacting
with your child
There are several subtypes of major depressive disorder. Some of the most common subtypes
include:
Seasonal affective disorder (seasonal depression).
Prenatal depression and postpartum depression.
Atypical depression.
People with clinical depression often have other mental health conditions, such as:
Substance use disorder (dual diagnosis).
Panic disorder.
Social anxiety disorder.
Obsessive-compulsive disorder.
Diagnostic Criteria
A. Five (or more) of the following symptoms have been present during the same 2- week
period and represent a change from previous functioning; at least one of the symptoms is
either (1) depressed mood or (2) loss of interest or pleasure.
Note: Do not include symptoms that are clearly attributable to another medical condition.
1.Depressed mood most of the day, nearly every day, as indicated by either subjective report
(e.g., feels sad, empty, hopeless) or observation made by others (e.g., appears tearful).
(Note: In children and adolescents, can be irritable mood.)
2. Markedly diminished interest or pleasure in all, or almost all, activities most of the day,
nearly every day (as indicated by either subjective account or observation).
3. Significant weight loss when not dieting or weight gain (e.g., a change of more than 5% of
body weight in a month), or decrease or increase in appetite nearly every day.
(Note: In children, consider failure to make expected weight gain.)
4. Insomnia or hypersomnia nearly every day.
5. Psychomotor agitation or retardation nearly every day (observable by others, not merely
subjective feelings of restlessness or being slowed down).
6. Fatigue or loss of energy nearly every day.
7. Feelings of worthlessness or excessive or inappropriate guilt (which may be delusional)
nearly every day (not merely self-reproach or guilt about being sick).
8. Diminished ability to think or concentrate, or indecisiveness, nearly every day (either by
subjective account or as observed by others).
9. Recurrent thoughts of death (not just fear of dying), recurrent suicidal ideation without a
specific plan, or a suicide attempt or a specific plan for committing suicide.
B. The symptoms cause clinically significant distress or impairment in social, occupational,
or other important areas of functioning.
C. The episode is not attributable to the physiological effects of a substance or another
medical condition.
Note: Criteria A–C represent a major depressive episode.
Note: Responses to a significant loss (e.g., bereavement, financial ruin, losses from a natural
disaster, a serious medical illness or disability) may include the feelings of intense sadness,
rumination about the loss, insomnia, poor appetite, and weight loss noted in Criterion A,
which may resemble a depressive episode. Although such symptoms may be understandable
or considered appropriate to the loss, the presence of a major depressive episode in addition
to the normal response to a significant loss should also be carefully considered. This decision
inevitably requires the exercise of clinical judgment based on the individual’s history and the
cultural norms for the expression of distress in the context of loss.
D. At least one major depressive episode is not better explained by schizoaffective disorder
and is not superimposed on schizophrenia, schizophreniform disorder, delusional disorder, or
other specified and unspecified schizophrenia spectrum and other psychotic disorders.
E. There has never been a manic episode or a hypomanic episode.
Note: This exclusion does not apply if all of the manic-like or hypomanic-like episodes are
substance-induced or are attributable to the physiological effects of another medical
condition.
Types of depression
Symptoms caused by major depression can vary from person to person. To clarify the type of
depression you have, your doctor may add one or more specifiers. A specifier means that
you have depression with specific features, such as:
Anxious distress — depression with unusual restlessness or worry about possible
events or loss of control
Mixed features — simultaneous depression and mania, which includes elevated self-
esteem, talking too much and increased energy
Melancholic features — severe depression with lack of response to something that
used to bring pleasure and associated with early morning awakening, worsened mood
in the morning, major changes in appetite, and feelings of guilt, agitation or
sluggishness
Atypical features — depression that includes the ability to temporarily be cheered by
happy events, increased appetite, excessive need for sleep, sensitivity to rejection, and
a heavy feeling in the arms or legs
Psychotic features — depression accompanied by delusions or hallucinations, which
may involve personal inadequacy or other negative themes
Catatonia — depression that includes motor activity that involves either
uncontrollable and purposeless movement or fixed and inflexible posture
Peripartum onset — depression that occurs during pregnancy or in the weeks or
months after delivery (postpartum)
Seasonal pattern — depression related to changes in seasons and reduced exposure
to sunlight
Outlook / Prognosis
What is the prognosis of clinical depression (major depressive disorder)?
The prognosis (outlook) for clinical depression depends on a few factors, including:
Its severity.
If it’s treated or untreated.
If you have other mental health or medical conditions.
The prognosis is better in people who have mild episodes, seek treatment and have strong
support systems. The prognosis is worse in people who have other psychiatric or personality
disorders and who are 60 years or older when they’re diagnosed.
Untreated episodes of clinical depression (major depressive disorder) can last six to 12
months.
About two-thirds of people with clinical depression think about suicide. About 10% to 15%
of people with the condition die by suicide.
The good news is that clinical depression is one of the most treatable mental health
conditions. Approximately 80% to 90% of people with the condition who seek treatment
eventually respond well to treatment.
What are the possible complications of clinical depression?
Clinical depression (major depressive disorder) can greatly interfere with your daily
functioning and quality of life if it’s not treated.
People with clinical depression are at a high risk of developing anxiety disorders and
substance use disorders, which further increase their risk of suicide.
Depression can make underlying medical conditions worse or more difficult to manage, such
as:
Diabetes.
Hypertension (high blood pressure).
Chronic obstructive pulmonary disease (COPD).
Coronary artery disease.
People with clinical depression are also at high risk of developing self-destructive behavior as
a coping mechanism for their symptoms
Persistent depressive disorder (PDD)
Introduction
Persistent depressive disorder (PDD), formerly known as dysthymia or dysthymic disorder, is
mild or moderate depression that doesn’t go away. If you have persistent depressive disorder,
you may experience low mood, as well as other symptoms, occurring most days without
going away. Persistent depressive disorder (PDD) is a mild to moderate chronic depression. It
involves a sad or dark mood most of the day, on most days, for two years or more. PDD is
common and can happen to anyone at any age. The most effective treatment combines
medication, counseling, and healthy lifestyle choices.
Causes
The exact cause of persistent depressive disorder is not known. As with major depression, it
may involve more than one cause, such as:
Biological differences. People with persistent depressive disorder may have physical
changes in their brains. It's not clear how these changes affect the disorder, but they
may eventually help determine the causes.
Brain chemistry. Neurotransmitters are naturally occurring brain chemicals.
Research indicates that changes in neurotransmitters may play a large part in
depression and its treatment.
Inherited traits. Persistent depressive disorder appears to be more common in people
whose blood relatives also have the condition. Researchers are trying to find genes
that may be involved in causing depression.
Life events. As with major depression, traumatic events such as the loss of a loved
one, financial problems or a high level of stress can trigger persistent depressive
disorder in some people.
Risk factors
Persistent depressive disorder often begins early — in childhood, the teen years or young
adult life — and continues for a long time. Certain factors appear to increase the risk of
developing persistent depressive disorder, including:
Having a first-degree blood relative, such as a parent or sibling, with major depressive
disorder or other depressive disorders.
Traumatic or stressful life events, such as the loss of a loved one or major financial
problems.
Personality traits that include negativity, such as low self-esteem, being too dependent
or self-critical, or always thinking the worst will happen.
History of other mental health disorders, such as a personality disorder.
Diagnostic Criteria
This disorder represents a consolidation of DSM-IV-defined chronic major depressive
disorder and dysthymic disorder.
A. Depressed mood for most of the day, for more days than not, as indicated by either
subjective account or observation by others, for at least 2 years.
Note: In children and adolescents, mood can be irritable and duration must be at least 1 year.
B. Presence, while depressed, of two (or more) of the following:
1. Poor appetite or overeating.
2. Insomnia or hypersomnia.
3. Low energy or fatigue.
4. Low self-esteem.
5. Poor concentration or difficulty making decisions.
6. Feelings of hopelessness.
C. During the 2-year period (1 year for children or adolescents) of the disturbance, the
individual has never been without the symptoms in Criteria A and B for more than 2 months
at a time.
D. Criteria for a major depressive disorder may be continuously present for 2 years.
E. There has never been a manic episode or a hypomanic episode.
F. The disturbance is not better explained by a persistent schizoaffective disorder,
schizophrenia, delusional disorder, or other specified or unspecified schizophrenia spectrum
and other psychotic disorder.
G. The symptoms are not attributable to the physiological effects of a substance (e.g., a drug
of abuse, a medication) or another medical condition (e.g., hypothyroidism).
H. The symptoms cause clinically significant distress or impairment in social, occupational,
or other important areas of functioning.
Note: If criteria are sufficient for a diagnosis of a major depressive episode at any time during
the 2-year period of depressed mood, then a separate diagnosis of major depression should be
made in addition to the diagnosis of persistent depressive disorder along with the relevant
specifier (e.g., with intermittent major depressive episodes, with current episode).
Specify if:
With anxious distress (pp. 210–211)
With atypical features (p. 212)
Specify if:
In partial remission (p. 214)
In full remission (p. 214)
Specify if:
Early onset: If onset is before age 21 years.
Late onset: If onset is at age 21 years or older.
Specify if (for most recent 2 years of persistent depressive disorder):
With pure dysthymic syndrome: Full criteria for a major depressive episode have not been
met in at least the preceding 2 years.
With persistent major depressive episode: Full criteria for a major depressive episode have
been met throughout the preceding 2-year period
With intermittent major depressive episodes, with current episode: Full criteria for a
major depressive episode are currently met, but there have been periods of at least 8 weeks in
at least the preceding 2 years with symptoms below the threshold for a full major depressive
episode.
With intermittent major depressive episodes, without current episode: Full criteria for a
major depressive episode are not currently met, but there has been one or more major
depressive episodes in at least the preceding 2 years.
Specify current severity:
Mild (p. 214)
Moderate (p. 214)
Severe (p. 214)
Unit 4
Externalizing Disorders
Attention Deficit Hyperactivity Disorder (ADHD), Oppositional Defiant Disorders (ODD),
Conduct Disorder (CD), Alcohol and Substance Use Disorders, Juvenile Delinquency
Diagnostic Criteria
A. A persistent pattern of inattention and/or hyperactivity-impulsivity that interferes with
functioning or development, as characterized by (1) and/or (2):
1. Inattention: Six (or more) of the following symptoms have persisted for at least 6 months
to a degree that is inconsistent with developmental level and that negatively impacts directly
on social and academic/occupational activities:
Note: The symptoms are not solely a manifestation of oppositional behavior, defiance,
hostility, or failure to understand tasks or instructions. For older adolescents and adults (age
17 and older), at least five symptoms are required.
a. Often fails to give close attention to details or makes careless mistakes in schoolwork, at
work, or during other activities (e.g., overlooks or misses details, work is inaccurate).
b. Often has difficulty sustaining attention in tasks or play activities (e.g., has difficulty
remaining focused during lectures, conversations, or lengthy reading).
c. Often does not seem to listen when spoken to directly (e.g., mind seems elsewhere, even in
the absence of any obvious distraction).
d. Often does not follow through on instructions and fails to finish schoolwork, chores, or
duties in the workplace (e.g., starts tasks but quickly loses focus and is easily sidetracked).
e. Often has difficulty organizing tasks and activities (e.g., difficulty managing sequential
tasks; difficulty keeping materials and belongings in order; messy, disorganized work; has
poor time management; fails to meet deadlines).
f. Often avoids, dislikes, or is reluctant to engage in tasks that require sustained mental effort
(e.g., schoolwork or homework; for older adolescents and adults, preparing reports,
completing forms, reviewing lengthy papers).
g. Often loses things necessary for tasks or activities (e.g., school materials, pencils, books,
tools, wallets, keys, paperwork, eyeglasses, mobile telephones).
h. Is often easily distracted by extraneous stimuli (for older adolescents and adults, may
include unrelated thoughts).
i. Is often forgetful in daily activities (e.g., doing chores, running errands; for older
adolescents and adults, returning calls, paying bills, keeping appointments).
2. Hyperactivity and impulsivity: Six (or more) of the following symptoms have persisted
for at least 6 months to a degree that is inconsistent with developmental level and that
negatively impacts directly on social and academic/occupational activities:
Note: The symptoms are not solely a manifestation of oppositional behavior, defiance,
hostility, or a failure to understand tasks or instructions. For older adolescents and adults (age
17 and older), at least five symptoms are required.
a. Often fidgets with or taps hands or feet or squirms in seat.
b. Often leaves seat in situations when remaining seated is expected (e.g., leaves his or her
place in the classroom, in the office or other workplace, or in other situations that require
remaining in place).
c. Often runs about or climbs in situations where it is inappropriate. (Note: In adolescents or
adults, may be limited to feeling restless.)
d. Often unable to play or engage in leisure activities quietly.
e. Is often “on the go,” acting as if “driven by a motor” (e.g., is unable to be or uncomfortable
being still for extended time, as in restaurants, meetings; may be experienced by others as
being restless or difficult to keep up with).
f. Often talks excessively.
g. Often blurts out an answer before a question has been completed (e.g., completes people’s
sentences; cannot wait for turn in conversation).
h. Often has difficulty waiting his or her turn (e.g., while waiting in line).
i. Often interrupts or intrudes on others (e.g., butts into conversations, games, or activities;
may start using other people’s things without asking or receiving permission; for adolescents
and adults, may intrude into or take over what others are doing).
B. Several inattentive or hyperactive-impulsive symptoms were present prior to age 12 years.
C. Several inattentive or hyperactive-impulsive symptoms are present in two or more settings
(e.g., at home, school, or work; with friends or relatives; in other activities).
D. There is clear evidence that the symptoms interfere with, or reduce the quality of, social,
academic, or occupational functioning.
E. The symptoms do not occur exclusively during the course of schizophrenia or another
psychotic disorder and are not better explained by another mental disorder (e.g., mood
disorder, anxiety disorder, dissociative disorder, personality disorder, substance intoxication
or withdrawal).
Specify whether:
F90.2 Combined presentation: If both Criterion A1 (inattention) and Criterion
A2 (hyperactivity-impulsivity) are met for the past 6 months.
F90.0 Predominantly inattentive presentation: If Criterion A1 (inattention) is met but
Criterion A2 (hyperactivity-impulsivity) is not met for the past 6 months.
F90.1 Predominantly hyperactive/impulsive presentation: If Criterion A2 (hyperactivity-
impulsivity) is met and Criterion A1 (inattention) is not met for the past 6 months.
Specify if:
In partial remission: When full criteria were previously met, fewer than the full criteria have
been met for the past 6 months, and the symptoms still result in impairment in social,
academic, or occupational functioning.
Specify current severity:
Mild: Few, if any, symptoms in excess of those required to make the diagnosis are present,
and symptoms result in no more than minor impairments in social or occupational
functioning.
Moderate: Symptoms or functional impairment between “mild” and “severe” are present.
Severe: Many symptoms in excess of those required to make the diagnosis, or several
symptoms that are particularly severe, are present, or the symptoms result in marked
impairment in social or occupational functioning.
Associated Features
Delays in language, motor, or social development are not specific to ADHD but often
co-occur.
Emotional dysregulation or emotional impulsivity commonly occurs in children and
adults with ADHD.
Individuals with ADHD self-report and are described by others as being quick to
anger, easily frustrated, and overreactive emotionally.
Even in the absence of a specific learning disorder, academic or work performance is
often impaired.
Individuals with ADHD may exhibit neurocognitive deficits in a variety of areas,
including working memory, set shifting, reaction time variability, response inhibition,
vigilance, and planning/organization, although these tests are not sufficiently sensitive
or specific to serve as diagnostic indices.
Although ADHD is not associated with specific physical features, rates of minor
physical anomalies (e.g., hypertelorism, highly arched palate, low-set ears) may be
elevated. Subtle motor delays and other neurological soft signs may occur. (Note that
marked co-occurring clumsiness and motor delays should be coded separately [e.g.,
developmental coordination disorder].)
Children with neurodevelopmental disorders with a known cause (e.g., fragile X
syndrome, 22q11 deletion syndrome) may often also have symptoms of inattention
and impulsivity/hyperactivity; they should receive an ADHD diagnosis if their
symptoms meet the full criteria for the disorder.
Prevalence
Population surveys suggest that ADHD occurs worldwide in about 7.2% of children;
however, cross-national prevalence ranges widely, from 0.1% to 10.2% of children
and adolescents. Prevalence is higher in special populations such as foster children or
correctional settings. In a cross-national meta-analysis, ADHD occurred in 2.5% of
adults.
ADHD types
There are four types of ADHD that healthcare providers diagnose in children and adults:
Inattentive ADHD. This involves difficulty focusing, finishing tasks and staying
organized. With this type, you have few or no hyperactivity symptoms.
Hyperactive-impulsive ADHD. This involves difficulty sitting still or having “quiet
time.” You have excess energy and are extremely talkative. You may also interrupt
others and act without thinking it through first. You may show less obvious trouble
with paying attention.
Combined presentation. This is the most common type of ADHD, and it’s what most
people associate with the condition. You have many inattentive
symptoms and hyperactive-impulsive symptoms.
Unspecified presentation. This is when you have severe symptoms that interfere
with daily life, but your symptoms don’t meet the official criteria for the types listed
above. In this case, providers assign “unspecified ADHD” as the diagnosis.
Providers also use the terms mild, moderate and severe to describe how much symptoms
affect your daily life.
Diagnosis of ADHD
Clinical criteria based on the DSM -5-TR
ADHD causes
ADHD is genetic. This means your child is born with certain gene changes that cause
differences in their brain development (neurodivergence). Often, the gene changes that cause
ADHD are passed down within biological families. Kids with ADHD commonly have
biological parents or siblings with the condition.
Researchers continue to look into how ADHD affects the brain. Here’s what we know so far.
With ADHD, the frontal lobe of your child’s brain is wired in a way that makes it harder for
them to use directed attention. Directed attention is the ability to focus on something you
don’t find very interesting.
We use directed attention to plan, multitask and solve problems (executive functions). It can
take a lot of energy to use directed attention, especially when there are other, more interesting
things around us.
If your child has ADHD, it takes even more energy than usual to direct their attention to
things they have to do. That means after a long day at school, your child might resist doing a
task that otherwise seems simple — like hanging up their coat or backpack. The attention it
requires to do these “basic” chores is simply not available to them.
On the other hand, your child is better than most neurotypical kids at using automatic
attention. This is the type of attention we use to focus on something we’re interested in. It
allows for something called hyperfocus, or the ability to “get in the zone” and do something
for hours on end. Your child might use hyperfocus to become really good at a hobby or game
or to reach certain goals.
Causes
While the exact cause of ADHD is not clear, research efforts continue. Factors that may be
involved in the development of ADHD include:
Genetics. ADHD can run in families, and studies indicate that genes may play a role.
Environment. Certain environmental factors also may increase risk, such as lead
exposure as a child.
Problems during development. Problems with the central nervous system at key
moments in development may play a role.
Risk factors
Experts believe that some people have genes that predispose them to ADHD. In other words,
the genes make ADHD a possibility for that person. But then, certain environmental
factors tip the scales and cause ADHD to develop.
Environmental risk factors include:
Exposure to certain toxins during fetal development, including tobacco, alcohol
or lead
Low birth weight (the lower the weight, the higher the risk)
Preterm birth
Environmental - Very low birth weight and degree of prematurity convey a greater
risk for ADHD; the more extreme the low weight, the greater the risk. Prenatal
exposure to smoking is associated with ADHD even after controlling for parental
psychiatric history and socioeconomic status. A minority of cases may be related to
reactions to aspects of diet. Neurotoxin exposure (e.g., lead), infections (e.g.,
encephalitis), and alcohol exposure in utero have been correlated with subsequent
ADHD, but it is not known whether these associations are causal.
Genetic and physiological- The heritability of ADHD is approximately 74%. Large-
scale genome-wide association studies (GWAS) have identified a number of loci
enriched in evolutionarily constrained genomic regions and loss-of-function genes as
well as around brain-expressed regulatory regions. There is no single gene for ADHD
Visual and hearing impairments, metabolic abnormalities, and nutritional deficiencies
should be considered as possible influences on ADHD symptoms. ADHD is elevated
in individuals with idiopathic epilepsy
Risk factors
Risk of ADHD may increase if:
You have blood relatives, such as a parent or sibling, with ADHD or another mental
health disorder
Your mother smoked, drank alcohol or used drugs during pregnancy
As a child, you were exposed to environmental toxins — such as lead, found mainly
in paint and pipes in older buildings
You were born prematurely
Treatment of ADHD
Behavioral therapy
ADHD behavior therapy: Children with ADHD often benefit from behavior therapy,
social skills training, parent skills training and counseling, which may be provided by
a psychiatrist, psychologist, social worker or other mental health professional. Some
children with ADHD may also have other conditions such as an anxiety disorder or
depression. In these cases, counseling may help both ADHD and the coexisting
problem. Examples of therapy include:
- Behavior therapy. Teachers and parents can learn behavior-changing strategies,
such as token reward systems and timeouts, for dealing with difficult situations.
- Social skills training. This can help children learn appropriate social behaviors.
- Parenting skills training. This can help parents develop ways to understand and
guide their child's behavior.
- Psychotherapy. This allows older children with ADHD to talk about issues that
bother them, explore negative behavior patterns and learn ways to deal with their
symptoms.
- Family therapy. Family therapy can help parents and siblings deal with the stress of
living with someone who has ADHD.
Stimulant medications:
- Currently, stimulant drugs (psychostimulants) are the most commonly prescribed
medications for ADHD. Stimulants appear to boost and balance levels of brain
chemicals called neurotransmitters. These medications help improve the signs and
symptoms of inattention and hyperactivity — sometimes effectively in a short period
of time.
- Examples include:
Amphetamines. These include dextroamphetamine (Dexedrine),
dextroamphetamine-amphetamine (Adderall XR, Mydayis) and
lisdexamfetamine (Vyvanse).
Methylphenidates. These include methylphenidate (Concerta, Ritalin, others)
and dexmethylphenidate (Focalin).
- Stimulant drugs are available in short-acting and long-acting forms. A long-acting
patch of methylphenidate (Daytrana) is available that can be worn on the hip.
- The right dose varies from child to child, so it may take some time to find the correct
dose. And the dose may need to be adjusted if significant side effects occur or as your
child matures. Ask your doctor about possible side effects of stimulants.
Outlook / Prognosis
How long does ADHD last?
ADHD doesn’t go away but doesn’t have to be an impairing condition. You can’t outgrow it,
but treatment can help manage your symptoms. Thanks to effective treatments, some people
don’t show impairment from ADHD symptoms once they’ve reached adulthood. But for
others, symptoms still affect their daily life. Providers tailor care to each individual’s needs.
Prognosis for ADHD
Traditional classrooms and academic activities often exacerbate symptoms and signs in
children with untreated or inadequately treated ADHD. Social and emotional adjustment
problems may be persistent. Poor acceptance by peers and loneliness tend to increase with
age and with the obvious display of symptoms. Substance abuse may result if ADHD is not
identified and adequately treated because many adolescents and adults with ADHD self-
medicate with both legal (eg, caffeine) and illegal (eg, cocaine, amphetamines) substances.
Although hyperactivity symptoms and signs tend to diminish with age, adolescents and adults
may display residual difficulties. Predictors of poor outcomes in adolescence and adulthood
include
Coexisting low intelligence
Aggressiveness
Social and interpersonal problems
Parental mental or behavioral health disorders
Problems in adolescence and adulthood manifest predominantly as academic failure, low self-
esteem, and difficulty learning appropriate social behavior. Adolescents and adults who have
predominantly impulsive ADHD may have an increased incidence of personality trait
disorders and antisocial behavior; many continue to display impulsivity, restlessness, and
poor social skills. People with ADHD seem to adjust better to work than to academic and
home situations, particularly if they can find jobs that do not require intense attention to
perform.
Oppositional defiant disorder
Introduction
Oppositional defiant disorder (ODD) is a condition in which your child displays a pattern of
uncooperative, defiant and angry behavior toward people in authority. Oppositional defiant
disorder (ODD) is a behavior condition in which your child displays a continuing pattern of
uncooperative, defiant and sometimes hostile behavior toward people in authority. This
behavior often disrupts your child’s normal daily functioning, including relationships and
activities within their family and at school. ODD is treatable with psychotherapy and parent
management training.
It’s common for children — especially those two to three years old and in their early teens —
to be oppositional or defiant of authority once in a while. They might express their defiance
by arguing, disobeying or talking back to adults, including their parents or teachers. When
this behavior lasts longer than six months and goes beyond what’s usual for your child’s age,
it might suggest that they have ODD.
The majority of children and teens who have ODD also have at least one other mental health
condition, including:
Attention-deficit hyperactivity/disorder (ADHD).
Anxiety disorders, including obsessive-compulsive disorder (OCD).
Learning differences.
Mood disorders, such as depression.
Impulse control disorders.
About 30% of children with ODD develop a more serious behavior condition called conduct
disorder. ODD behaviors can continue into adulthood if ODD isn’t properly diagnosed and
treated.
What’s the difference between ODD and ADHD?
Approximately 40% of children with attention-deficit/hyperactivity disorder (ADHD) also
have oppositional defiant disorder or a related conduct disorder. While these two conditions
commonly occur together, they’re distinct conditions.
ODD is related to a child’s conduct and how they interact with their parents, siblings,
teachers and friends. ADHD is a neurodevelopmental disorder that causes a person to be
easily distracted, disorganized and excessively restless.
Who does oppositional defiant disorder affect?
ODD most commonly affects children and teenagers, but it can also affect adults. It most
commonly begins by age 8.
Some children outgrow ODD or receive proper treatment for it, while others continue to have
symptoms through adulthood.
Boys are more likely to have ODD in their younger years than girls. But teenagers are
affected equally.
Your child is more likely to develop ODD if they have the following risk factors:
A history of child abuse or neglect.
A parent or caregiver who has a mood disorder or who has substance or alcohol use
disorders.
Exposure to violence.
Inconsistent discipline and lack of adult supervision.
Instability in their family, such as divorce, moving to different houses often and
changing schools frequently.
Financial problems in their family.
Parents who have or have had ODD, attention-deficit/hyperactivity disorder (ADHD)
or behavioral problems.
Researchers estimate that oppositional defiant disorder affects 2% to 11% of children. This
range is so wide because some children may be misdiagnosed as having conduct disorder,
and teenagers, as a population, are often underdiagnosed.
Diagnostic Criteria
A. A pattern of angry/irritable mood, argumentative/defiant behavior, or vindictiveness
lasting at least 6 months as evidenced by at least four symptoms from any of the following
categories, and exhibited during interaction with at least one individual who is not a sibling.
Angry/Irritable Mood
1. Often loses temper.
2. Is often touchy or easily annoyed.
3. Is often angry and resentful.
Argumentative/Defiant Behavior
4. Often argues with authority figures or, for children and adolescents, with adults.
5. Often actively defies or refuses to comply with requests from authority figures or with
rules.
6. Often deliberately annoys others.
7. Often blames others for his or her mistakes or misbehavior.
Vindictiveness
8. Has been spiteful or vindictive at least twice within the past 6 months.
Note: The persistence and frequency of these behaviors should be used to distinguish a
behavior that is within normal limits from a behavior that is symptomatic. For children
younger than 5 years, the behavior should occur on most days for a period of at least 6
months unless otherwise noted (Criterion A8). For individuals 5 years or older, the behavior
should occur at least once per week for at least 6 months, unless otherwise noted (Criterion
A8). While these frequency criteria provide guidance on a minimal level of frequency to
define symptoms, other factors should also be considered, such as whether the frequency and
intensity of the behaviors are outside a range that is normative for the individual’s
developmental level, gender, and culture.
B. The disturbance in behavior is associated with distress in the individual or others in his or
her immediate social context (e.g., family, peer group, work colleagues), or it impacts
negatively on social, educational, occupational, or other important areas of functioning.
C. The behaviors do not occur exclusively during the course of a psychotic, substance use,
depressive, or bipolar disorder. Also, the criteria are not met for disruptive mood
dysregulation disorder.
Specify current severity:
Mild: Symptoms are confined to only one setting (e.g., at home, at school, at
work, with peers).
Moderate: Some symptoms are present in at least two settings.
Severe: Some symptoms are present in three or more settings.
Specifiers
It is not uncommon for individuals with oppositional defiant disorder to show symptoms only
at home and only with family members. However, the pervasiveness of the symptoms is an
indicator of the severity of the disorder.
What causes oppositional defiant disorder (ODD)?
Researchers believe that the cause of oppositional defiant disorder is a complex combination
of biological, genetic and environmental factors:
Genetic factors: Research suggests that genetics account for about 50% of the
development of ODD. Many children and teens with ODD have close family
members with mental health conditions, including mood disorders, anxiety disorders
and personality disorders. Further, many children and teens with ODD also have other
mental health conditions, such as ADHD, learning differences, or depression and
anxiety disorder, which suggests a genetic link between the conditions.
Biological factors: Some studies suggest that changes to certain areas of your brain
can lead to behavior disorders. In addition, ODD has been linked to issues with
certain neurotransmitters, which help nerve cells in your brain communicate with each
other. If these chemicals are out of balance or not working properly, messages might
not make it through your brain correctly, leading to symptoms.
Environmental factors: Having a chaotic family life, childhood maltreatment and
inconsistent parenting can all contribute to the development of ODD. In addition, peer
rejection, deviant peer groups, poverty, neighborhood violence and other unstable
social or economic factors may contribute to the development of ODD.
Risk factors
Oppositional defiant disorder is a complex problem. Possible risk factors for ODD include:
Temperament — a child who has a temperament that includes difficulty managing
emotions, such as reacting with strong emotions to situations or having trouble
tolerating frustration.
Parenting issues — a child who experiences abuse or neglect, harsh or inconsistent
discipline, or a lack of proper supervision.
Other family issues — a child who lives with parent or family relationships that are
unstable or has a parent with a mental health condition or substance use disorder.
Environment — problem behaviors that are reinforced through attention from peers
and inconsistent discipline from other authority figures, such as teachers.
Complications
Children and teenagers with oppositional defiant disorder may have trouble at home with
parents and siblings, in school with teachers, and at work with supervisors and other authority
figures. Children and teens with ODD may struggle to make and keep friends and
relationships.
ODD also may lead to other problems, such as:
Poor school and work performance.
Antisocial behavior.
Legal problems.
Impulse control problems.
Substance use disorder.
Suicide.
Many children and teens with ODD also have other mental health conditions, such as:
Attention-deficit/hyperactivity disorder (ADHD).
Conduct disorder.
Depression.
Anxiety disorders.
Learning and communication disorders.
Treating these other mental health conditions may help reduce ODD symptoms. It may be
difficult to treat ODD if these other conditions are not evaluated and treated appropriately.
Most symptoms seen in children and teens with ODD also happen at times in other children
without it. This is very true for children around ages 2 or 3, or during the teen years. Many
children tend to disobey, argue with parents, or defy authority. They may often behave this
way when they are tired, hungry, or upset. But in children and teens with ODD, these
symptoms happen more often and are more severe. They also interfere with learning and
school adjustment. And in some cases, they disrupt the child’s relationships with others.
Symptoms of ODD may include:
Having frequent temper tantrums
Arguing a lot with adults
Refusing to do what an adult asks
Always questioning rules and refusing to follow rules
Doing things to annoy or upset others, including adults
Blaming others for the child’s own misbehaviors or mistakes
Being easily annoyed by others
Often having an angry attitude
Speaking harshly or unkindly
Seeking revenge or being vindictive
ODD can be mild, moderate, or severe:
Mild ODD. The symptoms occur only in 1 setting (home or school).
Moderate ODD. The symptoms are seen in at least 2 settings (home and school).
Severe ODD. The symptoms occur in 3 or more settings (for instance at home or
school, with peers, or in public).
Many of these symptoms can be caused by other mental health problems. Make sure your
child sees a healthcare provider for a diagnosis.
How is ODD diagnosed in a child?
If you see symptoms of ODD in your child or teen, get a diagnosis right away. Early
treatment can often prevent future problems.
Before a mental health referral is made, your child's healthcare provider will want to rule out
any other health problems. Once this is done, a child psychiatrist or qualified mental health
expert can diagnose ODD. They will talk with you and your child's teachers about your
child’s behavior. They may also watch your child. In some cases, your child may need mental
health testing.
For a child to be diagnosed with ODD, symptoms must be present for at least 6 months. A
certain number of symptoms must also be present and observed during interactions with at
least 1 person who is not a sibling. The criteria used for children younger than age 5 is
slightly different. Providers will also figure out if your child's behavior is outside a range of
normal behaviors expected for their developmental level, culture, and gender.
Extreme defiance can also occur because of certain situations. And it can be a sign of an
undiagnosed learning disability. So it's important that all possibilities are looked at closely
before making a diagnosis.
How is ODD treated in a child?
Early treatment can often prevent future problems. Treatment will depend on your child’s
symptoms, age, and health. It will also depend on how bad the ODD is.
Children with ODD may need to try different therapists and types of therapies before they
find what works for them. Coordination between healthcare providers, family, and school is
key to treatment success. Treatment may include:
Cognitive-behavioral therapy. A child learns to better solve problems and
communicate. They also learn how to control impulses and anger.
Family therapy. This therapy helps make changes in the family. It improves
communication skills and family interactions. Having a child with ODD can be very
hard for parents. It can also cause problems for siblings. Parents and siblings need
support and understanding.
Peer group therapy. A child learns better social skills.
Medicines. These are not often used to treat ODD. But a child may need them for
other symptoms or disorders, such as ADHD or anxiety disorders.
Conduct Disorder (CD)
Introduction
Conduct disorder (CD) is a mental health condition that involves a consistent pattern of
aggressive and disobedient behaviours. It affects children and teens and is treatable with
various forms of psychotherapy (talk therapy).
Conduct disorder (CD) is a mental health condition that affects children and teens that’s
characterized by a consistent pattern of aggressive behaviours and actions that harm the well-
being of others. Children with conduct disorder also often violate rules and societal norms.
Conduct disorder lies on a spectrum of disruptive behavioural disorders, which also
includes oppositional defiant disorder (ODD). In some cases, ODD leads to CD.
Conduct disorder often occurs alongside other psychiatric conditions, including:
Depression.
Attention-deficit/hyperactivity disorder (ADHD).
Learning disorders.
What is the difference between conduct disorder and personality disorders?
A personality disorder is a mental health condition that involves long-lasting, disruptive
patterns of thinking, behavior, mood and relating to others. Most personality disorders begin
in the teen years when personality further develops and matures. As a result, almost all people
diagnosed with personality disorders are above the age of 18.
One exception to this is antisocial personality disorder (ASPD) — approximately 80% of
people with this disorder will have started to show symptoms by the age of 11.
There’s not much difference between conduct disorder (CD) and ASPD, but CD is typically
diagnosed in children. If an adult meets the criteria for both conditions, then a mental health
professional would give them a diagnosis of ASPD instead of CD.
Who does conduct disorder affect?
Conduct disorder affects children and adolescents. It can have early onset before age 10, but
commonly develops in adolescence (between ages 10 years to 19 years).
The condition is more common in male children than female children. The average age of
presentation is 10 years to 12 years in males and 14 years to 16 years in females.
How common is conduct disorder?
Conduct disorder affects anywhere between 2% and 10% of children and adolescents in the
United States.
Types of conduct disorder
There are three types of conduct disorder. They’re categorized according to the age at which
symptoms of the disorder first occur:
Childhood onset occurs when the signs of conduct disorder appear before age 10.
Adolescent onset occurs when the signs of conduct disorder appear during the teen
years.
Unspecified onset means the age at which conduct disorder first occurs is unknown.
Some children will be diagnosed with conduct disorder with limited prosocial emotions.
Children with this specific conduct disorder are often described as callous and unemotional.
Diagnostic Criteria
A. A repetitive and persistent pattern of behaviour in which the basic rights of others or major age-appropriate
societal norms or rules are violated, as manifested by the presence of at least three of the following 15 criteria in
the past 12 months from any of the categories below, with at least one criterion present in the past 6 months:
3. Has used a weapon that can cause serious physical harm to others (e.g., a bat, brick, broken bottle, knife,
gun).
6. Has stolen while confronting a victim (e.g., mugging, purse snatching, extortion, armed robbery).
Destruction of Property
8. Has deliberately engaged in fire setting with the intention of causing serious damage.
Deceitfulness or Theft
11. Often lies to obtain goods or favors or to avoid obligations (i.e., “cons” others).
12. Has stolen items of nontrivial value without confronting a victim (e.g., shoplifting, but without breaking and
entering; forgery).
13. Often stays out at night despite parental prohibitions, beginning before age 13 years.
14. Has run away from home overnight at least twice while living in the parental or parental surrogate home, or
once without returning for a lengthy period.
C. If the individual is age 18 years or older, criteria are not met for antisocial personality disorder.
Specify whether:
F91.1 Childhood-onset type: Individuals show at least one symptom characteristic of conduct disorder prior to
age 10 years.
F91.2 Adolescent-onset type: Individuals show no symptom characteristic of conduct disorder prior to age 10
years.
F91.9 Unspecified onset: Criteria for a diagnosis of conduct disorder are met, but there is not enough
information available to determine whether the onset of the first symptom was before or after age 10 years.
Specify if:
With limited prosocial emotions: To qualify for this specifier, an individual must have displayed at least two of
the following characteristics persistently over at least 12 months and in multiple relationships and settings.
These characteristics reflect the individual’s typical pattern of interpersonal and emotional functioning over this
period and not just occasional occurrences in some situations. Thus, to assess the criteria for the specifier,
multiple information sources are necessary. In addition to the individual’s self-report, it is necessary to consider
reports by others who have known the individual for extended periods of time (e.g., parents, teachers, co-
workers, extended family members, peers).
Lack of remorse or guilt: Does not feel bad or guilty when he or she does something wrong (exclude remorse
when expressed only when caught and/or facing punishment). The individual shows a general lack of concern
about the negative consequences of his or her actions. For example, the individual is not remorseful after hurting
someone or does not care about the consequences of breaking rules.
Callous—lack of empathy: Disregards and is unconcerned about the feelings of others. The individual is
described as cold and uncaring. The individual appears more concerned about the effects of his or her actions on
himself or herself, rather than their effects on others, even when they result in substantial harm to others.
Unconcerned about performance: Does not show concern about poor/problematic performance at school, at
work, or in other important activities. The individual does not put forth the effort necessary to perform well,
even when expectations are clear, and typically blames others for his or her poor performance.
Shallow or deficient affect: Does not express feelings or show emotions to others, except in ways that seem
shallow, insincere, or superficial (e.g., actions contradict the emotion displayed; can turn emotions “on” or “off”
quickly) or when emotional expressions are used for gain (e.g., emotions displayed to manipulate or intimidate
others).
Mild: Few if any conduct problems in excess of those required to make the diagnosis are present, and conduct
problems cause relatively minor harm to others (e.g., lying, truancy, staying out after dark without permission,
other rule breaking).
Moderate: The number of conduct problems and the effect on others are intermediate between those specified
in “mild” and those in “severe” (e.g., stealing without confronting a victim, vandalism).
Severe: Many conduct problems in excess of those required to make the diagnosis are present, or conduct
problems cause considerable harm to others (e.g., forced sex, physical cruelty, use of a weapon, stealing while
confronting a victim, breaking and entering).
Subtypes
Three subtypes of conduct disorder are provided based on the age at onset of the disorder. Both childhood-onset
and adolescent-onset subtypes can occur in a mild, moderate, or severe form. An unspecified-onset subtype is
designated when there is insufficient information to determine age at onset.
In childhood-onset conduct disorder, individuals are usually male, have disturbed peer relationships, may have
had oppositional defiant disorder during early childhood, and usually have symptoms that meet full criteria for
conduct disorder prior to puberty. Individuals with the childhood-onset type may be more likely to display
aggression toward others than individuals with the adolescent-onset type. Many children with this subtype also
have concurrent attentiondeficit/ hyperactivity disorder (ADHD) or other neurodevelopmental difficulties.
Individuals with childhood-onset type are more likely to have persistent conduct disorder into adulthood than
are those with adolescent-onset type. Individuals with adolescent-onset conduct disorder tend to have more
normative peer relationships (although they often display conduct problems in the company of others).
Specifiers
A minority of individuals with conduct disorder exhibit characteristics that qualify for the “with limited
prosocial emotions” specifier. The indicators of this specifier are those that have often been labeled as callous
and unemotional traits in research. Other personality features, such as thrill seeking, fearlessness, and
insensitivity to punishment, may also distinguish those with characteristics described in the specifier. Individuals
with characteristics described in this specifier may be more likely than other individuals with conduct disorder
to engage in aggression that is planned for instrumental gain. Individuals with conduct disorder of any subtype
or any level of severity can have characteristics that qualify for the specifier “with limited prosocial emotions,”
although individuals with the specifier are more likely to have childhood-onset type and a severity specifier
rating of severe.
Although the validity of self-report to assess the presence of the specifier has been supported in some research
contexts, individuals with conduct disorder with this specifier may not readily admit to the traits in a clinical
interview. Thus, to assess the criteria for the specifier, multiple information sources are necessary. Also, because
the indicators of the specifier are characteristics that reflect the individual’s typical pattern of interpersonal and
emotional functioning, it is important to consider reports by others who have known the individual for extended
periods of time and across relationships and settings (e.g., parents, teachers, co-workers, extended family
members, peers).
Associated Features
Especially in ambiguous situations, aggressive individuals with conduct disorder frequently misperceive the
intentions of others as more hostile and threatening than is the case and respond with aggression that they then
feel is reasonable and justified. Personality features of trait negative emotionality and poor self-control,
including poor frustration tolerance, irritability, temper outbursts, suspiciousness, insensitivity to punishment,
thrill seeking, and recklessness, frequently co-occur with conduct disorder. Substance misuse is often an
associated feature, particularly in adolescent girls.
What Causes Conduct Disorder in Children?
Many factors seem to contribute to this disorder. Research has found that children and teens with conduct
disorder seem to have an impairment in the frontal lobe of the brain. This interferes with their ability to plan,
avoid harm, and learn from negative experiences.
In addition, these factors seem to put children and teens at a higher risk to develop conduct disorder:
Biological parents diagnosed with ADHD, alcohol use disorder, depression, bipolar disorder, or
schizophrenia.
Poor nutrition.
Living in poverty.
Maternal psychopathology.
Exposure to violence.
Peer delinquency.
Researchers aren’t sure what exactly causes conduct disorder (CD), but they think it’s a complex combination of
genetic/biological and environmental factors.
Genetic/biological factors:
Various studies show that certain characteristics of CD can be inherited, including antisocial behavior,
impulsivity, temperament, aggression and insensitivity to punishment.
Traumatic brain injury, seizures and neurological damage can contribute to aggression.
Parents of adolescents with CD often have engaged in substance use and antisocial behaviors. They’re
also frequently diagnosed with ADHD, mood disorders, schizophrenia or antisocial personality
disorder.
A home environment that lacks structure and adequate supervision with frequent conflicts between
parents can lead to maladaptive behavior in children, which can lead to CD.
Children exposed to frequent domestic violence are more likely to develop CD.
Living in low social and economic environments with overcrowding and unemployment leads to
economic and social stress with a lack of adequate parenting. CD affects more children living in low
economic environments than not.
Availability of drugs and increased crime in a child’s neighborhood increases their risk of developing
CD.
It’s important to note that conduct disorder can occur in children from high-functioning, healthy families.
The exact cause of conduct disorder is not known, but it is believed that a combination of biological, genetic,
environmental, psychological, and social factors play a role.
Biological: Some studies suggest that defects or injuries to certain areas of the brain can lead to
behavior disorders. Conduct disorder has been linked to particular brain regions involved in regulating
behavior, impulse control, and emotion. Conduct disorder symptoms may occur if nerve cell circuits
along these brain regions do not work properly. Further, many children and teens with conduct disorder
also have other mental illnesses, such as attention-deficit/hyperactivity disorder (ADHD), learning
disorders, depression, substance abuse, or an anxiety disorder, which may contribute to the symptoms
of conduct disorder.
Genetics: Many children and teens with conduct disorder have close family members with mental
illnesses, including mood disorders, anxiety disorders, substance use disorders, and personality
disorders. This suggests that a vulnerability to conduct disorder may be at least partially inherited.
Environmental: Factors such as a dysfunctional family life, childhood abuse, traumatic experiences, a
family history of substance abuse, and inconsistent discipline by parents may contribute to the
development of conduct disorder.
Psychological: Some experts believe that conduct disorders can reflect problems with moral awareness
(notably, lack of guilt and remorse) and deficits in cognitive processing.
Social: Low socioeconomic status and not being accepted by their peers appear to be risk factors for
the development of conduct disorder.
Parenting styles significantly impact the development of conduct disorder, with harsh, inconsistent, and
neglectful parenting styles being linked to higher levels of conduct problems. Specifically, authoritarian
parenting, characterized by strict rules and limited responsiveness, has been associated with negative behavioral
outcomes like conduct disorders, while authoritative parenting, which combines high expectations with warmth
and support, can help reduce these issues.
Elaboration:
Harsh or Punitive Parenting: This involves using overly strict rules, harsh punishments, and
limited responsiveness to the child's needs. This can lead to feelings of resentment, fear, and a
lack of trust, potentially contributing to behavioral problems.
Inconsistent Parenting: Erratic disciplinary practices, where rules are not consistently
enforced, can confuse children and make them feel unsure of what is expected.
Authoritative Parenting: This style balances high expectations with responsiveness, warmth,
and support. It involves clear rules and expectations, but also provides a sense of
understanding and empathy. This can lead to children feeling secure and empowered, which
promotes prosocial behaviors.
Responsive Parenting: This involves being attentive to a child's needs, providing emotional
support, and fostering positive interactions.
Usually, disruptive behaviors stop during early adulthood, but in about one third of cases, they persist. Many of
these cases meet the criteria for antisocial personality disorder. Early onset is associated with a poorer
prognosis.
Some children and adolescents subsequently develop mood or anxiety disorders, somatic symptom or related
disorders, substance-related disorders, or early adult–onset psychotic disorders. Children and adolescents with
conduct disorder tend to have higher rates of physical and other psychiatric disorders.
The prognosis (outlook) for conduct disorder depends on how early the condition developed and if it was
treated.
Usually, the disruptive behaviors of conduct stop during early adulthood, but in about one-third of cases, they
continue. Many of these cases meet the criteria for antisocial personality disorder.
Early onset of the condition (before 10 years of age) is associated with a poorer prognosis and is strongly
associated with a significant decline in school performance.
Some children and adolescents with conduct disorder develop other mental health conditions, including:
Depression and bipolar disorder may also develop in the teen years and early adulthood. Suicidal ideation can be
a complication of these conditions. It’s important to get your child immediate medical care if they’re talking
about or threatening suicide.
Psychotherapy
Treating comorbid disorders with medications and psychotherapy may improve self-esteem and self-control and
ultimately improve control of conduct disorder. Medications may include stimulants, mood stabilizers, and
atypical antipsychotics, especially short-term use of risperidone.
Moralization and dire admonitions are ineffective and should be avoided. Individual psychotherapy, including
cognitive therapy and behavior modification, may help. Often, seriously disturbed children and adolescents must
be placed in residential centers where their behavior can be managed appropriately, thus separating them from
the environment that may contribute to their aberrant behavior.
Therapies include:
Parent management training: The goal of this therapy is to train the child’s parents to set consistent
discipline with proper rewarding of positive behaviors.
Psychotherapy: “Psychotherapy” is a term for a variety of treatment techniques that aim to help a
person identify and change troubling emotions, thoughts and behaviors. Working with a mental health
professional can provide support, education and guidance to the person and their family. Psychotherapy
for conduct disorder usually needs to target family life and school with a focus on improving family
dynamics, academic functioning and improving your child’s behavior in the context of various
environments.
Anger management training: The goal of anger management is to reduce both your child’s emotional
feelings and the physiological arousal that anger causes. You can’t get rid of or totally avoid the things
or people that make them angry, so anger management training teaches your child how to control their
reactions.
Individual psychotherapy, such as cognitive behavioral therapy: Individual therapy for a child with
conduct disorder focuses on developing problem-solving skills, strengthening relationships by
resolving conflicts and learning skills to decline negative influences in their environment.
Community-based treatment: This treatment involves therapeutic schools and residential treatment
centers that can provide a structured program to reduce disruptive behaviors.
Healthcare providers typically don’t use medication to directly treat conduct disorder, but as other mental health
conditions often occur alongside conduct disorder, your child may benefit from medication to manage these
conditions.
Treatment will depend on your child’s symptoms, age, and general health. It will also depend on how severe the
condition is.
Cognitive-behavioral therapy. A child learns how to better solve problems, communicate, and handle
stress. He or she also learns how to control impulses and anger.
Family therapy. This therapy helps make changes in the family. It improves communication skills and
family interactions.
Peer group therapy. A child develops better social and interpersonal skills.
Medicines. These are not often used to treat conduct disorder. But a child may need them for other
symptoms or disorders, such as ADHD.
Experts don’t know exactly why some children develop conduct disorder. Things such as a traumatic
experience, social problems, and biological factors may be involved. To reduce the risk for this disorder, parents
can learn positive parenting strategies. This can help to create a closer parent-child relationship. It can also
create a safe and stable home life for the child.
Early treatment for your child can often prevent future problems. Here are things you can do to help your child:
Tell others about your child’s conduct disorder. Work with your healthcare provider and schools to
develop a treatment plan.
Reach out for support. Being in touch with other parents who have a child with conduct disorder may
be helpful. If you feel overwhelmed or stressed out, talk with your healthcare provider about a support
group for caregivers of children with conduct disorder.
Unit 6
Other psychological disorders
1. Genetic Factors:
Family History: Bipolar disorder is more common in people with a genetic predisposition.
People with a family history of bipolar disorder have a higher risk of developing the disorder.
If a parent has bipolar disorder, the child is more likely to develop the disorder.
Genetic Predisposition: Genetic factors can affect chemical imbalances in the brain. Research
shows that people with bipolar disorder may have certain genetic variations.
2. Biochemical Factors:
Brain Chemistry: Bipolar disorder is associated with an imbalance of chemicals in the brain
called neurotransmitters (such as serotonin, dopamine, norepinephrine). These chemicals
regulate mood, energy levels and thought processes. Disturbances in the balance of these
substances can cause extreme mood swings.
Changes in Brain Structure: Some studies show that people with bipolar disorder have
changes in brain structure and function. In particular, structural changes in brain regions such
as the frontal lobe, hippocampus and amygdala can lead to problems in regulating emotional
responses.
3. Environmental Factors:
Stressful Life Events: Although bipolar disorder can occur with a genetic predisposition,
often stressful life events can trigger the disorder. Major life changes, traumatic events,
losses, family problems or financial difficulties can initiate or worsen symptoms of bipolar
disorder.
Traumas: Traumatic events in childhood, such as physical, sexual or emotional abuse, can
increase the risk of bipolar disorder. Post-traumatic stress disorder (PTSD) and other mental
health problems may also play a role in the development of this disorder.
4. Hormonal Changes:
Impact of Hormones: It is thought that hormonal changes can trigger symptoms of bipolar
disorder, especially in women. Hormonal fluctuations such as pregnancy, the postpartum
period and menopause can lead to the onset of this disorder or exacerbate symptoms.
Bipolar Disorder
Bipolar disorder (formerly known as manic-depressive illness or manic depression) is a
lifelong mood disorder and mental health condition that causes intense shifts in mood, energy
levels, thinking patterns and behavior. These shifts can last for hours, days, weeks or months
and interrupt your ability to carry out day-to-day tasks.
There are a few types of bipolar disorder, which involve experiencing significant fluctuations
in mood referred to as hypomanic/manic and depressive episodes. However, people with
bipolar disorder aren’t always in a hypomanic/manic or depressive state. They also
experience periods of normal mood, known as euthymia.
Bipolar I Disorder
For a diagnosis of bipolar I disorder, it is necessary to meet the following criteria for a manic
episode. The manic episode may have been preceded by and may be followed by hypomanic
or major depressive episodes.
Manic Episode
A. A distinct period of abnormally and persistently elevated, expansive, or irritable mood and
abnormally and persistently increased activity or energy, lasting at least 1 week and present
most of the day, nearly every day (or any duration if hospitalization is necessary).
B. During the period of mood disturbance and increased energy or activity, three (or more) of
the following symptoms (four if the mood is only irritable) are present to a significant degree
and represent a noticeable change from usual behaviour:
1. Inflated self-esteem or grandiosity.
2. Decreased need for sleep (e.g., feels rested after only 3 hours of sleep).
3. More talkative than usual or pressure to keep talking.
4. Flight of ideas or subjective experience that thoughts are racing.
5. Distractibility (i.e., attention too easily drawn to unimportant or irrelevant external
stimuli), as reported or observed.
6. Increase in goal-directed activity (either socially, at work or school, or sexually) or
psychomotor agitation (i.e., purposeless non-goal-directed activity).
7. Excessive involvement in activities that have a high potential for painful consequences
(e.g., engaging in unrestrained buying sprees, sexual indiscretions, or foolish business
investments).
C. The mood disturbance is sufficiently severe to cause marked impairment in social or
occupational functioning or to necessitate hospitalization to prevent harm to self or others, or
there are psychotic features.
D. The episode is not attributable to the physiological effects of a substance (e.g., a drug of
abuse, a medication, other treatment) or another medical condition.
Note: A full manic episode that emerges during antidepressant treatment (e.g., medication,
electroconvulsive therapy) but persists at a fully syndromal level beyond the physiological
effect of that treatment is sufficient evidence for a manic episode and, therefore, a bipolar I
diagnosis.
Note: Criteria A–D constitute a manic episode. At least one lifetime manic episode is
required for the diagnosis of bipolar I disorder.
Hypomanic Episode
A. A distinct period of abnormally and persistently elevated, expansive, or irritable mood and
abnormally and persistently increased activity or energy, lasting at least 4 consecutive days
and present most of the day, nearly every day.
B. During the period of mood disturbance and increased energy and activity, three (or more)
of the following symptoms (four if the mood is only irritable) have persisted, represent a
noticeable change from usual behavior, and have been present to a significant degree:
1. Inflated self-esteem or grandiosity.
2. Decreased need for sleep (e.g., feels rested after only 3 hours of sleep).
3. More talkative than usual or pressure to keep talking.
4. Flight of ideas or subjective experience that thoughts are racing.
5. Distractibility (i.e., attention too easily drawn to unimportant or irrelevant external
stimuli), as reported or observed.
6. Increase in goal-directed activity (either socially, at work or school, or sexually) or
psychomotor agitation.
7. Excessive involvement in activities that have a high potential for painful consequences
(e.g., engaging in unrestrained buying sprees, sexual indiscretions, or foolish business
investments).
C. The episode is associated with an unequivocal change in functioning that is
uncharacteristic of the individual when not symptomatic.
D. The disturbance in mood and the change in functioning are observable by others.
E. The episode is not severe enough to cause marked impairment in social or occupational
functioning or to necessitate hospitalization. If there are psychotic features, the episode is, by
definition, manic.
F. The episode is not attributable to the physiological effects of a substance (e.g., a drug of
abuse, a medication, other treatment) or another medical condition.
Note: A full hypomanic episode that emerges during antidepressant treatment (e.g.,
medication, electroconvulsive therapy) but persists at a fully syndromal level beyond the
physiological effect of that treatment is sufficient evidence for a hypomanic episode
diagnosis. However, caution is indicated so that one or two symptoms (particularly increased
irritability, edginess, or agitation following antidepressant use) are not taken as sufficient for
diagnosis of a hypomanic episode, nor necessarily indicative of a bipolar diathesis.
Note: Criteria A–F constitute a hypomanic episode. Hypomanic episodes are common in
bipolar I disorder but are not required for the diagnosis of bipolar I disorder.
Major Depressive Episode
A. Five (or more) of the following symptoms have been present during the same 2- week
period and represent a change from previous functioning; at least one of the symptoms is
either (1) depressed mood or (2) loss of interest or pleasure.
Note: Do not include symptoms that are clearly attributable to another medical condition.
1. Depressed mood most of the day, nearly every day, as indicated by either subjective report
(e.g., feels sad, empty, or hopeless) or observation made by others (e.g., appears tearful).
(Note: In children and adolescents, can be irritable mood.)
2. Markedly diminished interest or pleasure in all, or almost all, activities most of the day,
nearly every day (as indicated by either subjective account or observation).
3. Significant weight loss when not dieting or weight gain (e.g., a change of more than 5% of
body weight in a month), or decrease or increase in appetite nearly every day. (Note: In
children, consider failure to make expected weight gain.)
4. Insomnia or hypersomnia nearly every day.
5. Psychomotor agitation or retardation nearly every day (observable by others, not merely
subjective feelings of restlessness or being slowed down).
6. Fatigue or loss of energy nearly every day.
7. Feelings of worthlessness or excessive or inappropriate guilt (which may be delusional)
nearly every day (not merely self-reproach or guilt about being sick).
8. Diminished ability to think or concentrate, or indecisiveness, nearly every day (either by
subjective account or as observed by others).
9. Recurrent thoughts of death (not just fear of dying), recurrent suicidal ideation without a
specific plan, or a suicide attempt or a specific plan for committing suicide.
B. The symptoms cause clinically significant distress or impairment in social, occupational,
or other important areas of functioning.
C. The episode is not attributable to the physiological effects of a substance or another
medical condition.
Note: Criteria A–C constitute a major depressive episode. Major depressive episodes are
common in bipolar I disorder but are not required for the diagnosis of bipolar I disorder.
Note: Responses to a significant loss (e.g., bereavement, financial ruin, losses from a natural
disaster, a serious medical illness or disability) may include the feelings of intense sadness,
rumination about the loss, insomnia, poor appetite, and weight loss noted in Criterion A,
which may resemble a depressive episode. Although such symptoms may be understandable
or considered appropriate to the loss, the presence of a major depressive episode in addition
to the normal response to a significant loss should also be carefully considered. This decision
inevitably requires the exercise of clinical judgment based on the individual’s history and the
cultural norms for the expression of distress in the context of loss.1
Bipolar I Disorder
A. Criteria have been met for at least one manic episode (Criteria A–D under “Manic
Episode” above).
B. At least one manic episode is not better explained by schizoaffective disorder and is not
superimposed on schizophrenia, schizophreniform disorder, delusional disorder, or other
specified or unspecified schizophrenia spectrum and other psychotic disorder.
Coding and Recording Procedures
The diagnostic code for bipolar I disorder is based on type of current or most recent episode
and its status with respect to current severity, presence of psychotic features, and remission
status. Current severity and psychotic features are only indicated if full criteria are currently
met for a manic or major depressive episode. Remission specifiers are only indicated if the
full criteria are not currently met for a manic, hypomanic, or major depressive episode. Codes
are as follows:
Associated Features
During a manic episode, individuals often do not perceive that they are ill or in need of
treatment and vehemently resist efforts to be treated. Individuals may change their dress,
makeup, or personal appearance to a more sexually suggestive or flamboyant style. Some
perceive a sharper sense of smell, hearing, or vision. Gambling and antisocial behaviours may
accompany the manic episode. Mood may shift very rapidly to anger or depression; some
individuals may become hostile and physically threatening to others and, when delusional,
become physically assaultive or suicidal. Serious consequences of a manic episode (e.g.,
involuntary hospitalization, difficulties with the law, serious financial difficulties) often result
from poor judgment, loss of insight, and hyperactivity. Depressive symptoms occur in some
35% of manic episodes (see “with mixed features” specifier, p. 170), and mixed features are
associated with poorer outcome and increased suicide attempts. Bipolar I disorder is also
associated with significant decrements in quality of life and well-being.
Trait-like features associated with the diagnosis include hyperthymic, depressive,
cyclothymic, anxious, and irritable temperaments, sleep and circadian rhythm disturbances,
reward sensitivity, and creativity. Having a first-degree relative with bipolar disorder
increases the risk of diagnosis approximately 10-fold.
Bipolar II Disorder
Diagnostic Criteria
For a diagnosis of bipolar II disorder, it is necessary to meet the following criteria for a
current or past hypomanic episode and the following criteria for a current or past major
depressive episode:
Hypomanic Episode
A. A distinct period of abnormally and persistently elevated, expansive, or irritable mood and
abnormally and persistently increased activity or energy, lasting at least 4 consecutive days
and present most of the day, nearly every day.
B. During the period of mood disturbance and increased energy and activity, three (or more)
of the following symptoms have persisted (four if the mood is only irritable), represent a
noticeable change from usual behavior, and have been present to a significant degree:
1. Inflated self-esteem or grandiosity.
2. Decreased need for sleep (e.g., feels rested after only 3 hours of sleep).
3. More talkative than usual or pressure to keep talking.
4. Flight of ideas or subjective experience that thoughts are racing.
5. Distractibility (i.e., attention too easily drawn to unimportant or irrelevant external
stimuli), as reported or observed.
6. Increase in goal-directed activity (either socially, at work or school, or sexually) or
psychomotor agitation.
7. Excessive involvement in activities that have a high potential for painful consequences
(e.g., engaging in unrestrained buying sprees, sexual indiscretions, or foolish business
investments).
C. The episode is associated with an unequivocal change in functioning that is
uncharacteristic of the individual when not symptomatic.
D. The disturbance in mood and the change in functioning are observable by others.
E. The episode is not severe enough to cause marked impairment in social or occupational
functioning or to necessitate hospitalization. If there are psychotic features, the episode is, by
definition, manic.
F. The episode is not attributable to the physiological effects of a substance (e.g., a drug of
abuse, a medication, other treatment) or another medical condition.
Note: A full hypomanic episode that emerges during antidepressant treatment (e.g.,
medication, electroconvulsive therapy) but persists at a fully syndromal level beyond the
physiological effect of that treatment is sufficient evidence for a hypomanic episode
diagnosis. However, caution is indicated so that one or two symptoms (particularly increased
irritability, edginess, or agitation following antidepressant use) are not taken as sufficient for
diagnosis of a hypomanic episode, nor necessarily indicative of a bipolar diathesis.
Major Depressive Episode
A. Five (or more) of the following symptoms have been present during the same 2- week
period and represent a change from previous functioning; at least one of the symptoms is
either (1) depressed mood or (2) loss of interest or pleasure.
Note: Do not include symptoms that are clearly attributable to a medical condition.
1.Depressed mood most of the day, nearly every day, as indicated by either subjective report
(e.g., feels sad, empty, or hopeless) or observation made by others (e.g., appears tearful).
(Note: In children and adolescents, can be irritable mood.)
2. Markedly diminished interest or pleasure in all, or almost all, activities most of the day,
nearly every day (as indicated by either subjective account or observation).
3. Significant weight loss when not dieting or weight gain (e.g., a change of more than 5% of
body weight in a month), or decrease or increase in appetite nearly every day. (Note: In
children, consider failure to make expected weight gain.)
4. Insomnia or hypersomnia nearly every day.
5. Psychomotor agitation or retardation nearly every day (observable by others, not merely
subjective feelings of restlessness or being slowed down).
6. Fatigue or loss of energy nearly every day.
7. Feelings of worthlessness or excessive or inappropriate guilt (which may be delusional)
nearly every day (not merely self-reproach or guilt about being sick).
8. Diminished ability to think or concentrate, or indecisiveness, nearly every day (either by
subjective account or as observed by others).
9. Recurrent thoughts of death (not just fear of dying), recurrent suicidal ideation without a
specific plan, or a suicide attempt or a specific plan for committing suicide.
B. The symptoms cause clinically significant distress or impairment in social, occupational,
or other important areas of functioning.
C. The episode is not attributable to the physiological effects of a substance or another
medical condition.
Note: Criteria A–C constitute a major depressive episode.
Note: Responses to a significant loss (e.g., bereavement, financial ruin, losses from a natural
disaster, a serious medical illness or disability) may include the feelings of intense sadness,
rumination about the loss, insomnia, poor appetite, and weight loss noted in Criterion A,
which may resemble a depressive episode. Although such symptoms may be understandable
or considered appropriate to the loss, the presence of a major depressive episode in addition
to the normal response to a significant loss should be carefully considered. This decision
inevitably requires the exercise of clinical judgment based on the individual’s history and the
cultural norms for the expression of distress in the context of loss.
Bipolar II Disorder
A. Criteria have been met for at least one hypomanic episode (Criteria A–F under
“Hypomanic Episode” above) and at least one major depressive episode (Criteria A–C under
“Major Depressive Episode” above).
B. There has never been a manic episode.
C. At least one hypomanic episode and at least one major depressive episode are not better
explained by schizoaffective disorder and are not superimposed on schizophrenia,
schizophreniform disorder, delusional disorder, or other specified or unspecified
schizophrenia spectrum and other psychotic disorder.
D. The symptoms of depression or the unpredictability caused by frequent alternation
between periods of depression and hypomania causes clinically significant distress or
impairment in social, occupational, or other important areas of functioning.
Coding and Recording Procedures
Bipolar II disorder has one diagnostic code: F31.81. Its status with respect to current severity,
presence of psychotic features, course, and other specifiers cannot be coded but should be
indicated in writing (e.g., F31.81 bipolar II disorder, current episode depressed, moderate
severity, with mixed features; F31.81 bipolar II disorder, most recent episode depressed, in
partial remission).
Specify current or most recent episode:
Hypomanic
Depressed
If current episode is hypomanic (or most recent episode if bipolar II disorder is in partial or
full remission):
In recording the diagnosis, terms should be listed in the following order: bipolar II disorder,
current or most recent episode hypomanic, in partial remission/in full remission (p. 175) (if
full criteria for a hypomanic episode are not currently met), plus any of the following
hypomanic episode specifiers that are applicable.
Note: The specifiers “with rapid cycling” and “with seasonal pattern” describe the pattern of
mood episodes.
Specify if:
With anxious distress (p. 169–170)
With mixed features (pp. 170–171)
With rapid cycling (p. 171)
With peripartum onset (pp. 173–174)
With seasonal pattern (pp. 174–175)
If current episode is depressed (or most recent episode if bipolar II disorder is in partial or
full remission):
In recording the diagnosis, terms should be listed in the following order: bipolar II disorder,
current or most recent episode depressed, mild/moderate/severe (if full criteria for a major
depressive episode are currently met), in partial remission/in full remission (if full criteria for
a major depressive episode are not currently met) (p. 175), plus any of the following major
depressive episode specifiers that are applicable.
Note: The specifiers “with rapid cycling” and “with seasonal pattern” describe the pattern of
mood episodes.
Specify if:
With anxious distress (pp. 169–170)
With mixed features (pp. 170–171)
With rapid cycling (p. 171)
With melancholic features (pp. 171–172)
With atypical features (pp. 172–173)
With mood-congruent psychotic features (p. 173)
With mood-incongruent psychotic features (p. 173)
With catatonia (p. 173). Coding note: Use additional code F06.1.
With peripartum onset (pp. 172–174)
With seasonal pattern (pp. 174–175)
Specify course if full criteria for a mood episode are not currently met:
In partial remission (p. 175)
In full remission (p. 175)
Specify severity if full criteria for a major depressive episode are currently met:
Mild (p. 175)
Moderate (p. 175)
Severe (p. 175)
Cyclothymic Disorder
Diagnostic Criteria
A. For at least 2 years (at least 1 year in children and adolescents) there have been numerous
periods with hypomanic symptoms that do not meet criteria for a hypomanic episode and
numerous periods with depressive symptoms that do not meet criteria for a major depressive
episode.
B. During the above 2-year period (1 year in children and adolescents), Criterion A symptoms
have been present for at least half the time and the individual has not been without the
symptoms for more than 2 months at a time.
C. Criteria for a major depressive, manic, or hypomanic episode have never been met.
D. The symptoms in Criterion A are not better explained by schizoaffective disorder,
schizophrenia, schizophreniform disorder, delusional disorder, or other specified or
unspecified schizophrenia spectrum and other psychotic disorder.
E. The symptoms are not attributable to the physiological effects of a substance (e.g., a drug
of abuse, a medication) or another medical condition (e.g., hyperthyroidism).
F. The symptoms cause clinically significant distress or impairment in social, occupational, or
other important areas of functioning.
Specify if:
With anxious distress (see pp. 169–170)
Psychotic Disorders
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and-adolescents/schizophrenia-in-children-and-adolescents