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ADHD
Attention-deficit/hyperactivity disorder
MODERATOR: DR.ASHUTOSH GUPTA
PRESENTATOR: DR. RAMASHANKAR
INTRODUCTION
It is a neuropsychiatric condition affecting pre-schoolers, children, adoles-
cents, and adults around the world.
Characterized by a pattern of
 Diminished sustained attention
 Increased impulsivity
 Hyperactivity .
Pooled data from various studies indicate that the world wide prevalence is
5.29%.
 5-10% in school going children
 2-6% in adolescents
 2% in adults
HISTORY
 ADHD first was described by in 1902 George Still.
 In 1920 this was termed as “minimal brain damage syndrome,”
 In 1960 the condition was renamed “minimal brain dysfunction.”
 ICD-9 and the DSM 2nd edition adopted the same descriptive term for the
condition— hyperkinetic syndrome of childhood.
 DSM3- attention deficit /hyperactivity disorder.
In ICD-10 it is named Hyperkinetic Disorder (HKD).
ADHD in parents and siblings of children with ADHD is 2 to 8 times greater
than in the general population.
 More prevalent in boys than in girls, ranging from 2:1 to as high as 9:1.
First-degree biological relatives are at high risk for developing ADHD as well
as other psychiatric disorders, including disruptive behavior disorders, anxiety
disorders, and depressive disorders.
 They are also at higher risk than the general population for learning disorders
and academic difficulties.
Parents show an increased incidence of substance use disorders.
AETIOLOGY
Largely genetic, with a heritability of approximately 75 percent.
Genetic Factors:
 The concordance rate among monozygotic twins ranges from 59 to 92 percent.
 In dizygotic twins ranges from 29 to 42 percent.
 First-degree relatives of children with ADHD have a 20 to 25 percent risk for
ADHD
Molecular Genetic:
Thyroid Receptor B Gene
Dopamine Type D2 Receptor Gene (DRD2)
Dopamine Transporter Gene (DAT1)
Dopamine 4 Receptor Gene (DRD4)
Neuroanatomical Aspects:
MRI, PET, SPECT, and functional MRI studies suggested decreased volume and
activity in prefrontal areas, anterior cingulate, globus pallidus, caudate,
thalamus, hippocampus, and cerebellum in children with ADHD.
PET Scan
ADHD vs. Normal
White, Red, Orange = higher glucose metabolism
Blue, Green, Purple = lower glucose metabolism
NORMAL ADHD
Neurotransmitters –
Dopamine System- very important
Noradrenergic System
Serotonin system- weak association
ADHD patients generally cannot activate prefrontal cortex areas appropriately
in response to cognitive tasks of attention and executive functioning. Some
studies suggest that this is because dopamine (DA) and norepinephrine (NE)
dysregulation in ADHD prevents the normal “tuning” of pyramidal neurons in
the prefrontal cortex.
Stimulant drugs bind strongly to DAT and compete with dopamine molecules at
the DAT site to prevent reuptake of dopamine back into the presynaptic axon for
metabolism.
Tricyclic antidepressants (TCAs) and atomoxetine are potent norepinephrine
reuptake inhibitors (NRIs), perhaps restoring a more normal ratio of epinephrine
and norepinephrine.
Neurophysiological Factors-
Showed significantly elevated beta activity on EEG
Environmental Factors-
 High lead exposure and maternal smoking have been associated with higher
rates of diagnosis of ADHD.
 Higher rates of ADHD are present in children who were born prematurely
and whose mothers were observed to have maternal infection during
pregnancy.
 Perinatal insult to the brain during early infancy caused by infection,
inflammation, and trauma may be contributing factors in the emergence of
ADHD symptoms.
DIAGNOSIS
DSM-5 Criteria
A. A persistent pattern of inattention and/or hyperactivity impulsivity that
interferes with functioning or development.
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).
A-1 Inattention
At least 6 symptoms for <17 years age group.
At least 5 symptoms for 17 years or more age group.
For at least 6 months duration.
1. Often fails to give close attention to details or makes careless mistakes in
schoolwork, at work, or during other activities
2. Often has difficulty sustaining attention in tasks or play activities
3. Often does not seem to listen when spoken to directly
4. Often does not follow through on instructions and fails to finish schoolwork,
chores, or duties in the workplace
5. Often has difficulty organizing tasks and activities
6. Often avoids, dislikes, or is reluctant to engage in tasks that require sustained
mental effort
7. Often loses things necessary for tasks or activities
8. Is often easily distracted by extraneous stimuli
9. Is often forgetful in daily activities.
A-2 Hyperactivity & Impulsivity
At least 6 symptoms for <17 years age group.
At least 5 symptoms for 17 years or more age group.
For at least 6 months duration.
1. Often fidgets with or taps hands or feet or squirms in seat
2. Often leaves seat in situations when remaining seated is expected
3. Often runs about or climbs in situations where it is inappropriate
4. Often unable to play or engage in leisure activities quietly
5. Is often “on the go,” acting as if “driven by a motor”
6. Often talks excessively
7. Often blurts out an answer before a question has been completed
8. Often has difficulty waiting his or her turn
9. Often interrupts or intrudes on others.
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).
SUBTYPE
Combined : If both Criterion A1 (inattention) and Criterion A2 (hyperactivity-
impulsivity) are met for the past 6 months.
Predominantly inattentive : If Criterion A1 (inattention) is only met for the past 6
months.
Predominantly hyperactive/impulsive : If Criterion A2 (hyperactivity- impulsivity)
is only met for the past 6 months.
ICD-10 Criteria
F-90
Hyperkinetic disorder always arise in first 5 years of life
IMPAIRED INATTENTION
OVERACTIVITY
Associated Features-Disinhibition in social relations, recklessness, impulsivity,
flouting of social rules.
DIFFERENTIAL DIAGNOSIS
OPPOSITIONAL DEFIANT DISORDER (ODD): A pattern of negative, hostile and
defiant behavior. Symptoms include frequent loss of temper, arguing (especially
with adults), refusal to obey rules, intentionally annoying others, blaming
others.
CONDUCT DISORDER (CD): A pattern of behavior that persistently violates the
basic rights of others or society’s rules. Behavior may include aggression toward
people and animals, destruction of property, deceitfulness or theft, or serious
rule violations.
DIFFERENTIAL DIAGNOSIS
 Mood Disorder
 Anxiety Disorder
 Bipolar disorder
 Personality disorder
 Sense organ deficits
 Autism
 Medication induced attention deficit
eg: bronchodilator, isoniazid, thyroid
 Substance abuse Learning Disability
 Epilepsy
 Thyroid abnormality
 Specific learning disorder
AUTISM ADHD
Both exhibit inattention, social dysfunction and difficult to
manage behavior.
 Has no great desire to be
social.
 Wants to be social. Feel sad,
confused on isolation
 Repetitive patterns of behavior
are present.
 Absent.
 Difficulty in communication is
present.
 There is no difficulty in
Communication
 Children show tantrums because of
inability to tolerate a change from
there expected course of event
 Due to impulsivity or poor self-
control.
ADHD RATING SCALE
Parent Rating Scales
 Conner's Parent Rating Scale
 Child Behavior Checklist
 Yale Children's Inventory Home
Situations Questionnaire
Teacher Rating Scales
 Conner's Teacher Rating Scale
 Child Behavior Checklist-Teacher Form
School Situations Questionnaire
 ADHD Comprehensive Teacher Rating
Scale (ACTReS)
 Swanson, Nolan and Pelham (SNAP-IV)
scale
 Vanderbilt ADHD Scale
 INCLEN – ADHD Diagnostic tool (Indian
adaptation)
TREATMENT
STIMULANT MEDICATION NON-STIMULANT MEDICATION
• Methylphenidate
• Dexmethylphenidate
• Dextroamphetamine
• lisdexamfetamine
Extended relase: OROS Technique
Osmotic controlled release extended
delivery system
• Atomoxetine
Black box warning: suicidal thought
• Tricyclic Anti-depressants:
Imipramine, Norimipramine &
Nortryptiline
• α2-Adrenergic Agents:
Clonidine, Guanfacine
• Non-TCA anti depressant:
Bupropion
STIMULANTS
Amphetamines and methylphenidates are two groups of stimulant medication
that have received U.S. Food and Drug Administration (FDA) approval for the
treatment of youth with ADHD.
These chemicals structurally resemble the catecholamine neurotransmitters
dopamine (DA) and norepinephrine (NE).
Improve vigilance and reaction time and reduce variability, short-term
memory, and learning of verbal and nonverbal material in children with ADHD.
Methylphenidate commonly used started 0.3-1 mg/kg tid and gradually
increased up to 60mg/day.
It reduce gross motor over activity, out-of-seat behavior, calling-out behavior in
the classroom, disruptiveness, impulsive behaviour.
Adverse Effects:
Common side effects include decreased appetite, weight loss, delayed onset of
sleep, headaches, stomach-aches, and increases in blood pressure and pulse.
Preschool children can experience increased irritability and crying.
Rebound :Rebound over activity, impulsivity, and inattention have been defined
as being more severe than reported at baseline off medication. They may occur
in the late afternoon or early evening.
long term side effect: reduce the rate of height and weight gains in developing
children with ADHD and it also increases substance use.
NONSTIMULANT
ATOMOXETINE HCl
 Norepinephrine reuptake inhibitor
 Well absorbed.
 ATX has been shown to reduce ADHD behaviors in children, adolescents, and
adults.
 Side effects-abdominal discomfort, decreased appetite, dizziness, vertigo
irritability and mood swings
 Metabolized by the cytochrome P450 (CYP) 2D6 hepatic enzyme system.
 DOSAGE-0.5-1.2mg/kg per day in children
TRICYCLIC ANTIDEPRESSANTS
 Imipramine, Nortriptyline, Amitriptyline have been found to be effective
 Lower dosages are required when compared to depression
 Side effects-Fatigue and sedation, Cholestatic jaundice, tachycardia, delirium,
weight gain, constipation, skin rash, lowered seizure threshold.
CVS S/E-Slowing of cardiac conduction, thus increasing PR and QRS intervals and
thus increase the risk of cardiac arrhythmia and thus heart block
BASELINE ECG SUGGESTED BEFORE STARTING MEDICATION
BUPROPION
 Non TCA anti-depressants
 Less effective than TCA or stimulants
 Starting dose for young adolescents is 75 mg twice a day to a maximum of 200
to 300 mg per day.
 S/E- fatigue, dry mouth, insomnia, headache, nausea, vomiting, tremor and
skin rash.
ALPHA ADRENERGIC ANTAGONISTS
 Clonidine and Guanfacine
 Decrease impulsivity and hyperactivity
 Clonidine used as alternative or adjunctive to Methylphenidate. Its sedative
effect counters insomniac effect of Methylphenidate.
 S/E-Daytime Sedation
Clonidine needs to be discontinued very slowly to prevent rebound adrenergic
over drive-Hypertension, agitation, headache chest pain, sleep disturbance
nausea and vomiting.
So never miss the dosage.
Clonidine should not be used in presence of preexisting cardiac problem.
Guanfacine is slightly less sedating than clonidine
PSYCHOSOCIAL TREATMENT OF
CHILDREN
This type of treatment includes different modalities, such as :
 Psychoeducation
 Academic organization skill teaching and remediation
 Parent training
 Behavior modification
 Cognitive–behavioral therapy (CBT)
 Social skills training
 Individual therapy.
Direct contingency management plus intensive behavior therapy have yielded
significant improvement.
These begin with psychoeducation about the course, risk factors, and long-
term outcomes of ADHD.
 Second, the parents are encouraged to attend more carefully to their child's
behavior, particularly when the child complies.
 Third, the parents are trained to use time out effectively.
 Fourth, the parents are instructed in establishing a contingency management
or token economy system at home. Then the parents learn how to manage
noncompliant behaviors in public settings.
 Finally, advances in prosocial behavior in school are supported by use of a
daily report card.
PROGNOSIS
 Course of ADHD is variable.
 Remission usually occurs between 12-20 years of age, unlikely before that.
 40-60% continue to be symptomatic through adolescence, 20-40% through
adulthood.
 Most cases get better as they grow. Hyperactivity usually stops by teenage.
Easy distractibility, mood swings, hot tempers & inability to complete tasks
persist.
 Those continue to have symptoms are vulnerable to antisocial behavior,
substance abuse, mood disorders & learning disorders.
MULTIMODAL TREATMENT STUDY OF
CHILDREN WITH ADHD (MTA STUDY)
 Supported by NIMH 1999
 A 14-month-long randomized clinical trial involving six clinical sites comparing
four treatment strategies
 More than 500 children was included
 Response on medication management, behavior therapy, combination of
medication and behavior therapy and community care are compared.
 All groups showed improvement over baseline; however, a combination of
medication management and behavior therapy led to greater reduction in
symptoms in children with ADHD.
ADULT MANIFESTATIONS OF ADHD
An approximate 2.5 % prevalence of ADHD in the population.
Utah Criteria for Adult Attention-Deficit/Hyperactivity Disorder (ADHD)
1. Retrospective childhood ADHD diagnosis
Narrow criterion: met DSM4 criteria in childhood by parent interview
Broad criterion: both 1 and 2 are met as reported by patient
a. Childhood hyperactivity
b. Childhood attention deficit
2. Adult characteristics: 5 additional symptoms including ongoing difficulties
with inattention and hyperactivity and at least 3 other symptoms
Inattention
Hyperactivity
Mood Lability
Irritability and hot temper
Impaired stress intolerance
Disorganization
Impulsivity
3. Exclusions: Not diagnosed in presence of severe depression, psychosis, or
severe personality disorder
Adults with ADHD demonstrate higher rates of learning disorders, anxiety
disorders, mood disorders, and substance use disorder compared with the
general population.
Treatment of ADHD in adults targets pharmacotherapy, mainly long-acting
stimulants, similar to that used with children and adolescents with ADHD.
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Adhd

  • 2. INTRODUCTION It is a neuropsychiatric condition affecting pre-schoolers, children, adoles- cents, and adults around the world. Characterized by a pattern of  Diminished sustained attention  Increased impulsivity  Hyperactivity .
  • 3. Pooled data from various studies indicate that the world wide prevalence is 5.29%.  5-10% in school going children  2-6% in adolescents  2% in adults
  • 4. HISTORY  ADHD first was described by in 1902 George Still.  In 1920 this was termed as “minimal brain damage syndrome,”  In 1960 the condition was renamed “minimal brain dysfunction.”  ICD-9 and the DSM 2nd edition adopted the same descriptive term for the condition— hyperkinetic syndrome of childhood.  DSM3- attention deficit /hyperactivity disorder. In ICD-10 it is named Hyperkinetic Disorder (HKD).
  • 5. ADHD in parents and siblings of children with ADHD is 2 to 8 times greater than in the general population.  More prevalent in boys than in girls, ranging from 2:1 to as high as 9:1.
  • 6. First-degree biological relatives are at high risk for developing ADHD as well as other psychiatric disorders, including disruptive behavior disorders, anxiety disorders, and depressive disorders.  They are also at higher risk than the general population for learning disorders and academic difficulties. Parents show an increased incidence of substance use disorders.
  • 7. AETIOLOGY Largely genetic, with a heritability of approximately 75 percent. Genetic Factors:  The concordance rate among monozygotic twins ranges from 59 to 92 percent.  In dizygotic twins ranges from 29 to 42 percent.  First-degree relatives of children with ADHD have a 20 to 25 percent risk for ADHD
  • 8. Molecular Genetic: Thyroid Receptor B Gene Dopamine Type D2 Receptor Gene (DRD2) Dopamine Transporter Gene (DAT1) Dopamine 4 Receptor Gene (DRD4)
  • 9. Neuroanatomical Aspects: MRI, PET, SPECT, and functional MRI studies suggested decreased volume and activity in prefrontal areas, anterior cingulate, globus pallidus, caudate, thalamus, hippocampus, and cerebellum in children with ADHD.
  • 10. PET Scan ADHD vs. Normal White, Red, Orange = higher glucose metabolism Blue, Green, Purple = lower glucose metabolism NORMAL ADHD
  • 11. Neurotransmitters – Dopamine System- very important Noradrenergic System Serotonin system- weak association ADHD patients generally cannot activate prefrontal cortex areas appropriately in response to cognitive tasks of attention and executive functioning. Some studies suggest that this is because dopamine (DA) and norepinephrine (NE) dysregulation in ADHD prevents the normal “tuning” of pyramidal neurons in the prefrontal cortex.
  • 12. Stimulant drugs bind strongly to DAT and compete with dopamine molecules at the DAT site to prevent reuptake of dopamine back into the presynaptic axon for metabolism. Tricyclic antidepressants (TCAs) and atomoxetine are potent norepinephrine reuptake inhibitors (NRIs), perhaps restoring a more normal ratio of epinephrine and norepinephrine.
  • 13. Neurophysiological Factors- Showed significantly elevated beta activity on EEG Environmental Factors-  High lead exposure and maternal smoking have been associated with higher rates of diagnosis of ADHD.  Higher rates of ADHD are present in children who were born prematurely and whose mothers were observed to have maternal infection during pregnancy.  Perinatal insult to the brain during early infancy caused by infection, inflammation, and trauma may be contributing factors in the emergence of ADHD symptoms.
  • 14. DIAGNOSIS DSM-5 Criteria A. A persistent pattern of inattention and/or hyperactivity impulsivity that interferes with functioning or development. 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).
  • 15. A-1 Inattention At least 6 symptoms for <17 years age group. At least 5 symptoms for 17 years or more age group. For at least 6 months duration. 1. Often fails to give close attention to details or makes careless mistakes in schoolwork, at work, or during other activities 2. Often has difficulty sustaining attention in tasks or play activities 3. Often does not seem to listen when spoken to directly 4. Often does not follow through on instructions and fails to finish schoolwork, chores, or duties in the workplace
  • 16. 5. Often has difficulty organizing tasks and activities 6. Often avoids, dislikes, or is reluctant to engage in tasks that require sustained mental effort 7. Often loses things necessary for tasks or activities 8. Is often easily distracted by extraneous stimuli 9. Is often forgetful in daily activities.
  • 17. A-2 Hyperactivity & Impulsivity At least 6 symptoms for <17 years age group. At least 5 symptoms for 17 years or more age group. For at least 6 months duration. 1. Often fidgets with or taps hands or feet or squirms in seat 2. Often leaves seat in situations when remaining seated is expected 3. Often runs about or climbs in situations where it is inappropriate 4. Often unable to play or engage in leisure activities quietly
  • 18. 5. Is often “on the go,” acting as if “driven by a motor” 6. Often talks excessively 7. Often blurts out an answer before a question has been completed 8. Often has difficulty waiting his or her turn 9. Often interrupts or intrudes on others.
  • 19. 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).
  • 20. SUBTYPE Combined : If both Criterion A1 (inattention) and Criterion A2 (hyperactivity- impulsivity) are met for the past 6 months. Predominantly inattentive : If Criterion A1 (inattention) is only met for the past 6 months. Predominantly hyperactive/impulsive : If Criterion A2 (hyperactivity- impulsivity) is only met for the past 6 months.
  • 21. ICD-10 Criteria F-90 Hyperkinetic disorder always arise in first 5 years of life IMPAIRED INATTENTION OVERACTIVITY Associated Features-Disinhibition in social relations, recklessness, impulsivity, flouting of social rules.
  • 22. DIFFERENTIAL DIAGNOSIS OPPOSITIONAL DEFIANT DISORDER (ODD): A pattern of negative, hostile and defiant behavior. Symptoms include frequent loss of temper, arguing (especially with adults), refusal to obey rules, intentionally annoying others, blaming others. CONDUCT DISORDER (CD): A pattern of behavior that persistently violates the basic rights of others or society’s rules. Behavior may include aggression toward people and animals, destruction of property, deceitfulness or theft, or serious rule violations.
  • 23. DIFFERENTIAL DIAGNOSIS  Mood Disorder  Anxiety Disorder  Bipolar disorder  Personality disorder  Sense organ deficits  Autism  Medication induced attention deficit eg: bronchodilator, isoniazid, thyroid  Substance abuse Learning Disability  Epilepsy  Thyroid abnormality  Specific learning disorder
  • 24. AUTISM ADHD Both exhibit inattention, social dysfunction and difficult to manage behavior.  Has no great desire to be social.  Wants to be social. Feel sad, confused on isolation  Repetitive patterns of behavior are present.  Absent.  Difficulty in communication is present.  There is no difficulty in Communication  Children show tantrums because of inability to tolerate a change from there expected course of event  Due to impulsivity or poor self- control.
  • 25.
  • 26. ADHD RATING SCALE Parent Rating Scales  Conner's Parent Rating Scale  Child Behavior Checklist  Yale Children's Inventory Home Situations Questionnaire Teacher Rating Scales  Conner's Teacher Rating Scale  Child Behavior Checklist-Teacher Form School Situations Questionnaire  ADHD Comprehensive Teacher Rating Scale (ACTReS)  Swanson, Nolan and Pelham (SNAP-IV) scale  Vanderbilt ADHD Scale  INCLEN – ADHD Diagnostic tool (Indian adaptation)
  • 27. TREATMENT STIMULANT MEDICATION NON-STIMULANT MEDICATION • Methylphenidate • Dexmethylphenidate • Dextroamphetamine • lisdexamfetamine Extended relase: OROS Technique Osmotic controlled release extended delivery system • Atomoxetine Black box warning: suicidal thought • Tricyclic Anti-depressants: Imipramine, Norimipramine & Nortryptiline • α2-Adrenergic Agents: Clonidine, Guanfacine • Non-TCA anti depressant: Bupropion
  • 28. STIMULANTS Amphetamines and methylphenidates are two groups of stimulant medication that have received U.S. Food and Drug Administration (FDA) approval for the treatment of youth with ADHD. These chemicals structurally resemble the catecholamine neurotransmitters dopamine (DA) and norepinephrine (NE). Improve vigilance and reaction time and reduce variability, short-term memory, and learning of verbal and nonverbal material in children with ADHD. Methylphenidate commonly used started 0.3-1 mg/kg tid and gradually increased up to 60mg/day.
  • 29. It reduce gross motor over activity, out-of-seat behavior, calling-out behavior in the classroom, disruptiveness, impulsive behaviour. Adverse Effects: Common side effects include decreased appetite, weight loss, delayed onset of sleep, headaches, stomach-aches, and increases in blood pressure and pulse. Preschool children can experience increased irritability and crying.
  • 30. Rebound :Rebound over activity, impulsivity, and inattention have been defined as being more severe than reported at baseline off medication. They may occur in the late afternoon or early evening. long term side effect: reduce the rate of height and weight gains in developing children with ADHD and it also increases substance use.
  • 31. NONSTIMULANT ATOMOXETINE HCl  Norepinephrine reuptake inhibitor  Well absorbed.  ATX has been shown to reduce ADHD behaviors in children, adolescents, and adults.  Side effects-abdominal discomfort, decreased appetite, dizziness, vertigo irritability and mood swings  Metabolized by the cytochrome P450 (CYP) 2D6 hepatic enzyme system.  DOSAGE-0.5-1.2mg/kg per day in children
  • 32. TRICYCLIC ANTIDEPRESSANTS  Imipramine, Nortriptyline, Amitriptyline have been found to be effective  Lower dosages are required when compared to depression  Side effects-Fatigue and sedation, Cholestatic jaundice, tachycardia, delirium, weight gain, constipation, skin rash, lowered seizure threshold. CVS S/E-Slowing of cardiac conduction, thus increasing PR and QRS intervals and thus increase the risk of cardiac arrhythmia and thus heart block BASELINE ECG SUGGESTED BEFORE STARTING MEDICATION
  • 33. BUPROPION  Non TCA anti-depressants  Less effective than TCA or stimulants  Starting dose for young adolescents is 75 mg twice a day to a maximum of 200 to 300 mg per day.  S/E- fatigue, dry mouth, insomnia, headache, nausea, vomiting, tremor and skin rash.
  • 34. ALPHA ADRENERGIC ANTAGONISTS  Clonidine and Guanfacine  Decrease impulsivity and hyperactivity  Clonidine used as alternative or adjunctive to Methylphenidate. Its sedative effect counters insomniac effect of Methylphenidate.  S/E-Daytime Sedation
  • 35. Clonidine needs to be discontinued very slowly to prevent rebound adrenergic over drive-Hypertension, agitation, headache chest pain, sleep disturbance nausea and vomiting. So never miss the dosage. Clonidine should not be used in presence of preexisting cardiac problem. Guanfacine is slightly less sedating than clonidine
  • 36. PSYCHOSOCIAL TREATMENT OF CHILDREN This type of treatment includes different modalities, such as :  Psychoeducation  Academic organization skill teaching and remediation  Parent training  Behavior modification  Cognitive–behavioral therapy (CBT)  Social skills training  Individual therapy.
  • 37. Direct contingency management plus intensive behavior therapy have yielded significant improvement. These begin with psychoeducation about the course, risk factors, and long- term outcomes of ADHD.  Second, the parents are encouraged to attend more carefully to their child's behavior, particularly when the child complies.
  • 38.  Third, the parents are trained to use time out effectively.  Fourth, the parents are instructed in establishing a contingency management or token economy system at home. Then the parents learn how to manage noncompliant behaviors in public settings.  Finally, advances in prosocial behavior in school are supported by use of a daily report card.
  • 39. PROGNOSIS  Course of ADHD is variable.  Remission usually occurs between 12-20 years of age, unlikely before that.  40-60% continue to be symptomatic through adolescence, 20-40% through adulthood.  Most cases get better as they grow. Hyperactivity usually stops by teenage. Easy distractibility, mood swings, hot tempers & inability to complete tasks persist.  Those continue to have symptoms are vulnerable to antisocial behavior, substance abuse, mood disorders & learning disorders.
  • 40. MULTIMODAL TREATMENT STUDY OF CHILDREN WITH ADHD (MTA STUDY)  Supported by NIMH 1999  A 14-month-long randomized clinical trial involving six clinical sites comparing four treatment strategies  More than 500 children was included  Response on medication management, behavior therapy, combination of medication and behavior therapy and community care are compared.  All groups showed improvement over baseline; however, a combination of medication management and behavior therapy led to greater reduction in symptoms in children with ADHD.
  • 41. ADULT MANIFESTATIONS OF ADHD An approximate 2.5 % prevalence of ADHD in the population. Utah Criteria for Adult Attention-Deficit/Hyperactivity Disorder (ADHD) 1. Retrospective childhood ADHD diagnosis Narrow criterion: met DSM4 criteria in childhood by parent interview Broad criterion: both 1 and 2 are met as reported by patient a. Childhood hyperactivity b. Childhood attention deficit
  • 42. 2. Adult characteristics: 5 additional symptoms including ongoing difficulties with inattention and hyperactivity and at least 3 other symptoms Inattention Hyperactivity Mood Lability Irritability and hot temper Impaired stress intolerance Disorganization Impulsivity 3. Exclusions: Not diagnosed in presence of severe depression, psychosis, or severe personality disorder
  • 43. Adults with ADHD demonstrate higher rates of learning disorders, anxiety disorders, mood disorders, and substance use disorder compared with the general population. Treatment of ADHD in adults targets pharmacotherapy, mainly long-acting stimulants, similar to that used with children and adolescents with ADHD.