Pediatric Attention Deficit Hyperactivity Disorder Clinical Presentation

  • Author: Zainab P Contractor, MD; Chief Editor: Caroly Pataki, MD   more...
 
Updated: Jan 25, 2012
 

History

The DSM-IV criteria, in conjunction with a thorough clinical interview regarding daily functioning, are important in the diagnosis of attention deficit hyperactivity disorder (ADHD), previously termed attention deficit disorder (ADD). Of note, some of the DSM-IV criteria have been revised to reflect state-of-the-art knowledge, including data regarding ADHD (ADD) in girls and women. The clinician should also gather information that helps to identify any coexisting conditions.

History of present illness

All of the following DSM-IV criteria for ADHD (ADD) must be present:

  • Either the criteria for inattention or the criteria for hyperactivity/impulsivity must be met.
    • Inattention: At least 6 of the 9 symptoms of inattention listed below must have persisted for at least 6 months to a degree that is maladaptive and inconsistent with the patient's developmental level.
      1. Often fails to give close attention to details or makes careless mistakes in schoolwork, work, or 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 with instructions and often fails to finish schoolwork, chores, or duties in the workplace (not due to oppositional behavior or failure to understand instructions)
      5. Often has difficulty organizing tasks and activities
      6. Often avoids, dislikes, or is reluctant to engage in tasks that require sustained mental effort (eg, schoolwork, homework); often loses things necessary for tasks or activities (eg, school assignments, pencils, books, tools, toys)
      7. Often is easily distracted by extraneous stimuli (eg, toys, school assignments, pencils, books, tools)
      8. Often is forgetful in daily activities
    • Hyperactivity/impulsivity: At least 6 of the 9 symptoms of hyperactivity (symptoms 1-6) and impulsivity (symptoms 7-9) listed below have persisted for at least 6 months to a degree that is maladaptive and inconsistent with the patient's developmental level.
      1. Often fidgets with hands or feet or squirms in seat
      2. Often leaves seat in classroom or in other situations in which remaining seated is expected
      3. Often runs about or climbs excessively in situations in which it is inappropriate (in adolescents and adults, may be limited to subjective feelings of restlessness)
      4. Often has difficulty quietly playing or engaging in leisure activities
      5. Often on the go or often acts as if driven by a motor
      6. Often talks excessively
      7. Often blurts out answers before questions have been completed
      8. Often has difficulty awaiting turn
      9. Often interrupts or intrudes on others (eg, butts into conversations or games)
  • Some hyperactive-impulsive or inattentive symptoms that caused impairment are present before age 7 years
  • Symptoms must be present in 2 or more situations (eg, school, work, home).
  • The disturbance causes clinically significant distress or impairment in social, academic, or occupational function.
  • Behavior does not exclusively occur during the course of pervasive developmental disorder, premenstrual dysphoric disorder, schizophrenia, or other psychotic disorder. No mood disorder, anxiety dissociative disorder, or personality disorder accounts for the behavior.

Past medical history

  • Screen for the following medications or supplements that may have negative interactions with ADHD (ADD)-related medications:
    • Anticonvulsant agents
    • Antihypertensive agents
    • Caffeine-containing drugs
    • Pseudoephedrine
    • Ephedra
    • Monoamine oxidase inhibitors (MAOIs)
    • All medications known to be metabolized by means of the cytochrome P450 (CYP) 2D6 hepatic pathway (See the discussion about atomoxetine in the Medication section.)
  • Screening for medical concerns that may have negative interactions with ADHD (ADD) medications (Drugs of concern are shown in parentheses.)
    • Major arterial disease (stimulants)
    • Narrow-angle glaucoma (stimulants, imipramine, desipramine)
    • Heart disease (clonidine, desipramine, guanfacine, imipramine, stimulants)
    • Heart palpitations (stimulants)
    • Hepatic disease (atomoxetine)
    • Hypertension (stimulants, atomoxetine, bupropion)
    • Orthostasis (atomoxetine, bupropion, stimulants)
    • Pregnancy (all)
    • Renal disease (bupropion, clonidine)
    • Seizure disorder (bupropion, desipramine, imipramine)
    • Urinary retention or hesitancy (atomoxetine, bupropion, stimulants)
  • Approximately 30-50% of people with ADHD (ADD) have other significant psychiatric comorbidities. Consider screening patients for the following:

Family history

Inquire about a family history of ADHD (ADD) and of the coexistent conditions listed under History of present illness.

Social history

Inquire about the following:

  • Home and family interactions consistent with ADHD (ADD)
    • Disorganization of personal space is the norm.
    • Anger or rage reactions are prevalent.
    • The child usually seems most awake in the late evening.
    • Awakening the child for school causes major problems.
    • The child is often unable to complete what appear to be developmentally appropriate chores.
    • Homework organization and completion are often a problem.
    • High activity level is noted.
    • Completion of multistep directions is difficult.
    • Losing or forgetting material or conversations is observed.
  • Problems with the legal system
    • Arrests
    • Traffic tickets
    • Motor vehicle accidents
  • School performance
    • Report cards
    • Reprimands or notes sent home
    • Homework completion and/or turning homework in on time
    • Extracurricular activities
  • Family dysfunction
    • Drug abuse, alcohol abuse, or both
    • Parent(s) with ADHD (ADD)
    • Physical abuse
    • Sexual abuse
    • Recent death of loved one or friend
    • Severe chronic illness
    • Severe financial problems
  • Social skills
    • Friendships
    • Group cohesion
    • Strengths and interests
  • Pregnancy, potential for pregnancy, or safe-sex practices
    • Previous intercourse
    • Birth control
    • Condom use
  • Work performance
    • Type of work
    • Promptness
    • Overall work performance
  • Abuse of substances by patient or his or her friends (if the patient is an adolescent)
    • Alcohol
    • Caffeine
    • Marijuana
    • Other illicit drugs
    • Snorting stimulants
    • Prescription medications
    • Tobacco (eg, cigarettes, chewing tobacco, snuff)
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Physical

A focused physical examination is recommended if none has been performed within the last year or if suggested by history. Although a child or adolescent with ADHD (ADD) may exhibit few symptoms in a clinical setting, careful observation of behavior is important. The following should be included at onset of medication use and periodically to assess for medication-related negative effects:

  • Vital signs
    • Height
    • Weight
    • Blood pressure
    • Pulse
  • General appearance
    • Fidgeting
    • Impulse control
    • State of arousal
  • Mental status examination
    • Affect
    • Cognition
    • Speech patterns
    • Thought patterns
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Causes

At present, genetic loading appears to be the primary and perhaps only cause of ADHD (ADD). However, many environmental factors have been correlated with ADHD (ADD), and future research may prove these to be etiologic factors. Morbidity, as evidenced by signs and symptoms in people with ADHD (ADD), may be strongly correlated with the patient's home and school environments.

Genetic causes

Family, twin, adoption, and segregation analysis, as well as molecular genetic studies, show that ADHD (ADD) has a substantial genetic component. Molecular genetic studies have revealed several genes that appear to be associated with ADHD (ADD) because of their effect on dopamine receptors, dopamine transport, and dopamine beta-hydroxylase.

Research by the NIHM has shown that variants of the gene for catecho-O-methyltransferase (COMT) are associated with different levels of prefrontal dopamine activity. COMT metabolizes dopamine.

People with the val/val variant metabolize dopamine rapidly. Because fast metabolism of a substrate decreases the amount of substrate that is biologically available, these people have reduced prefrontal dopamine activity. This reduction, in turn, impairs prefrontal information processing.

Individuals with the val/met variant have fairly efficient prefrontal function.

Patients with the met/met variant have the most efficient prefrontal function. In fact, this variant results in an enzyme that is 3-4 times weaker than the product of the val/val variant.

Environmental causes

No environmental causes have been clearly identified. However, problems with pregnancy (including cigarette smoking during pregnancy) and/or delivery, head injuries, toxin exposure, heavy marijuana use beginning in early adolescence, marital or family dysfunction, and low social class have all been associated with ADHD (ADD).

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Contributor Information and Disclosures
Author

Zainab P Contractor, MD  Medical Director, The Affinity Center; Cincinnati, Ohio

Disclosure: Nothing to disclose.

Coauthor(s)

Christine A Mayhall, PhD  Clinical Psychologist, The Affinity Center

Christine A Mayhall, PhD is a member of the following medical societies: American Psychological Association

Disclosure: Nothing to disclose.

Specialty Editor Board

Chet Johnson, MD  Professor and Chair of Pediatrics, Associate Director, Developmental Pediatrician, Center for Child Health and Development, Shiefelbusch Institute for Life Span Studies, University of Kansas School of Medicine; LEND Director, University of Kansas Medical Center

Chet Johnson, MD is a member of the following medical societies: American Academy of Pediatrics

Disclosure: Nothing to disclose.

Mary L Windle, PharmD  Adjunct Associate Professor, University of Nebraska Medical Center College of Pharmacy; Editor-in-Chief, Medscape Drug Reference

Disclosure: Nothing to disclose.

Carrie Sylvester, MD, MPH  Senior Child and Adolescent Psychiatrist, Sound Mental Health

Carrie Sylvester, MD, MPH is a member of the following medical societies: American Academy of Child and Adolescent Psychiatry

Disclosure: Nothing to disclose.

Chief Editor

Caroly Pataki, MD  Professor of Clinical Psychiatry and Behavioral Sciences, Department of Psychiatry, Division Chair, Child and Adolescent Psychiatry, Keck School of Medicine of the University of Southern California

Caroly Pataki, MD is a member of the following medical societies: American Academy of Child and Adolescent Psychiatry, New York Academy of Sciences, and Physicians for Social Responsibility

Disclosure: Nothing to disclose.

Additional Contributors

The authors and editors of Medscape Reference gratefully acknowledge the contributions of previous author Susan Louisa Montauk, MD†,to the development and writing of this article.

References
  1. APA. Diagnostic and Statistical Manual of Mental Disorders. 4th ed. Washington, DC: American Psychiatric Association Press; 1994:78-85.

  2. Spinelli S, Joel S, Nelson TE, Vasa RA, Pekar JJ, Mostofsky SH. Different neural patterns are associated with trials preceding inhibitory errors in children with and without attention-deficit/hyperactivity disorder. J Am Acad Child Adolesc Psychiatry. Jul 2011;50(7):705-715.e3. [Medline].

  3. Ducharme S, Hudziak JJ, Botteron KN, Albaugh MD, Nguyen TV, Karama S, et al. Decreased regional cortical thickness and thinning rate are associated with inattention symptoms in healthy children. J Am Acad Child Adolesc Psychiatry. Jan 2012;51(1):18-27.e2. [Medline].

  4. Brown TE. Brown ADD Scales. San Antonio, TX: Psychological Corp; 1996:5-6.

  5. Nigg JT, Lewis K, Edinger T, Falk M. Meta-analysis of attention-deficit/hyperactivity disorder or attention-deficit/hyperactivity disorder symptoms, restriction diet, and synthetic food color additives. J Am Acad Child Adolesc Psychiatry. Jan 2012;51(1):86-97.e8. [Medline].

  6. [Best Evidence] Blader JC, Schooler NR, Jensen PS, Pliszka SR, Kafantaris V. Adjunctive divalproex versus placebo for children with ADHD and aggression refractory to stimulant monotherapy. Am J Psychiatry. Dec 2009;166(12):1392-401. [Medline].

  7. Habel LA, Cooper WO, Sox CM, et al. ADHD medications and risk of serious cardiovascular events in young and middle-aged adults. JAMA. Dec 28 2011;306(24):2673-83. [Medline].

  8. Wilens TE, Bukstein O, Brams M, Cutler AJ, Childress A, Rugino T, et al. A controlled trial of extended-release guanfacine and psychostimulants for attention-deficit/hyperactivity disorder. J Am Acad Child Adolesc Psychiatry. Jan 2012;51(1):74-85.e2. [Medline].

  9. Elia J, Ambrosini PJ, Rapoport JL. Treatment of attention-deficit-hyperactivity disorder. N Engl J Med. Mar 11 1999;340(10):780-8. [Medline].

  10. Hunt RD, Paguin A, Payton K. An update on assessment and treatment of complex attention-deficit hyperactivity disorder. Pediatr Ann. Mar 2001;30(3):162-72. [Medline].

  11. Johnson TM. Evaluating the hyperactive child in your office: is it ADHD?. Am Fam Physician. Jul 1997;56(1):155-60, 168-70. [Medline].

  12. Millichap JG. Etiologic classification of attention-deficit/hyperactivity disorder. Pediatrics. Feb 2008;121(2):e358-65. [Medline].

  13. Nadeau KG, Littman E, Quinn P. Understanding Girls With AD/HD. Springfield, MD: Advantage Books; 2000.

  14. Ramchandani P, Joughin C, Zwi M. Attention deficit hyperactivity disorder in children. Clin Evid. Jun 2002;262-71. [Medline].

  15. Rappley MD. Clinical practice. Attention deficit-hyperactivity disorder. N Engl J Med. Jan 13 2005;352(2):165-73. [Medline].

  16. Reeves G, Schweitzer J. Pharmacological management of attention-deficit hyperactivity disorder. Expert Opin Pharmacother. Jun 2004;5(6):1313-20. [Medline].

  17. Spencer TJ, Biederman J, Wilen T. Pharmacotherapy of ADHD with antidepressants. In: Barkley RS, ed. Attention Deficit Hyperactivity Disorder: A Handbook for Diagnosis and Treatment. 2nd ed. New York, NY: Guilford Press; 1998:552-63.

  18. Wolraich ML, ed. The Classification of Child and Adolescent Mental Diagnoses in Primary Care: Diagnostic and Statistical Manual for Primary Care (DSM-PC) Child. Elk Grove, IL: American Academy of Pediatrics; 1996.

  19. Wilens TE. Straight Talk about Psychiatric Medications for Kids. New York, NY: Guilford Press; 2002.

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Table 1. Pediatric Dosing of Stimulant Medications
MedicationInitial Pediatric DosePediatric Dosage Range and Maximum Dose*Common Pediatric Dose*Preparations
Methylphenidate immediate release (IR) (Ritalin, Methylin, generic)2.5-5 mg0.1-0.8 mg/kg/dose PO qd to 5 times/d; not to exceed 60 mg/d0.3-0.5 mg/kg/dose PO tid/qidAll preparations available as 5-mg, 10-mg, or 20-mg scored tabs; Methylin also available as 2.5-mg, 5-mg, or 10-mg chewable tab and PO solution (5 mg/5 mL and 10 mg/mL)
Methylphenidate sustained-release (SR) (Ritalin LA, Metadate CD)Convert from IR or use 10 mg.0.2-1.4 mg/kg/dose PO qd/tid; not to exceed 60 mg/d0.6-1 mg/kg/dose PO qd/bid10-mg, 20-mg, 30-mg, or 40-mg tabs (Metadate also has 50-mg and 60-mg tabs.); can be sprinkled into soft food (Do not cut, crush, or chew.)
Methylphenidate extended release (ER)‡ (Ritalin SR, Methylin ER, Metadate ER, generic SR)Convert from IR.0.2-1.4 mg/kg/dose PO qd/tid; not to exceed 60 mg/d0.6-1 mg/kg/dose PO qd/bid20-mg Spansules (Do not cut, crush, or chew.)
Methylphenidate OROS tablets (Concerta)Convert from IR or use 18 mg.0.3-2 mg/kg PO qd; not to exceed 54 mg/d0.8-1.6 mg/kg PO qd18-mg, 27-mg, 36-mg, and 54-mg tabs (Do not cut, crush, or chew.)
Methylphenidate transdermal patch (Daytrana)Convert from IR or use 10 mg (12.5 cm2 patch) released over 9 h and titrate up prn.0.3-2 mg/kg released over 9 h; not to exceed one 30-mg patch10-30 mg released over 9 h10-mg, 15-mg, 20-mg, 30-mg patches, applied to the hip
Dexmethylphenidate IR (Focalin)2.5-5-mg0.1-0.5 mg/kg/dose PO qd to qid; not to exceed 20 mg/d0.2-0.3 mg/kg/dose PO bid/tid2.5-mg, 5-mg, or 10-mg scored tabs (Do not cut, crush, or chew.)
Dexmethylphenidate extended release (Focalin-XR)5-10-mg0.2-1 mg/kg/dose PO qd to bid; not to exceed 20 mg/d0.4-0.6 mg/kg/dose PO qd/bid5-mg, 10-mg, or 20-mg scored tabs; can be sprinkled into soft food (Do not cut, crush, or chew.)
Dextroamphetamine (Dexedrine, Dextrostat)2.5-5 mg0.1-0.7 mg/kg/dose PO qd/qid; not to exceed 60 mg/d0.3-0.5 mg/kg/dose PO qd/tidDexedrine: 5-mg scored tabs; Dextrostat: 5-mg and 10-mg scored tabs
Dextroamphetamine Spansules (Dexedrine CR)5 mg0.1-0.75 mg/kg/dose PO qd/bid; not to exceed 60 mg/d0.3-0.6 mg/kg/dose PO qd/bid5-mg, 10-mg, or 15-mg Spansules; can be sprinkled into soft food (Do not cut, crush, or chew.)
Mixed amphetamine salts IR (Adderall, generic)2.5-5 mg0.1-0.7 mg/kg/dose PO qd/qid; not to exceed 40 mg/d0.3-0.5 mg/kg/dose PO tid/qid5-mg, 7.5-mg, 10-mg, 12.5-mg, 15-mg, 20-mg, or 30-mg scored tabs
Mixed amphetamine salt XR (Adderall-XR)Convert from IR or use 5-10 mg0.2-1.4 mg/kg/dose PO qd/tid



Not to exceed 30 mg/d



0.6-1 mg/kg/dose PO qd/bid5-mg, 10-mg, 15-mg, 20-mg, 25-mg, or 30-mg Spansules; can be sprinkled into soft food (Do not cut, crush, or chew.)
Lisdexamfetamine (Vyvanse)30 mg PO qam30-70 mg PO qamData limited (too early to tell)20-mg, 30-mg, 40-mg, 50-mg, 60-mg, or 70-mg caps (Swallow cap whole, sprinkle into soft food, or dissolve contents in glass of water and drink immediately.)
Note. In general, when the terms methylphenidate, Dexedrine, and Ritalin are used without abbreviations for extended-release preparations (eg, continuous release [CR], SR, osmotic-release oral system [OROS]), a short-acting, IR preparation is implied.



* Maximum pediatric dose suggested by the US Food and Drug Administration (FDA). Although some children benefit greatly from doses greater than these, benefit from use of either the lowest and highest ends of the dose range is uncommon.



†The methylphenidate patch contains a different total methylphenidate dose than the name implies because it is designed to last 12 hours (eg, 10-mg patch [patch size 12.5 cm2] delivers about 10 mg over 9 h [estimated delivery rate is 1.1 mg/h for this particular patch]). Delivery rate varies depending on patch size.



‡Many patients describe their experience with methylphenidate SR preparations as erratic and uncomfortable.



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