Treatment of ADHD Symptoms
For elementary school-aged children (6-11 years), FDA-approved stimulant medications (methylphenidate or amphetamines) should be prescribed as first-line treatment, with behavioral therapy strongly recommended as well, preferably both together. 1
Treatment Algorithm by Age Group
Preschool-Aged Children (4-5 years)
- Behavioral therapy administered by parents and/or teachers is the mandatory first-line treatment before considering any medication 1
- Methylphenidate may be prescribed only if behavioral interventions fail to provide significant improvement AND there is moderate-to-severe continuing functional impairment 1
- The risks of starting medication at this early age must be weighed against the harm of delaying treatment, particularly in areas where evidence-based behavioral treatments are unavailable 1
Elementary School-Aged Children (6-11 years)
- Stimulant medications (methylphenidate and amphetamines) have the strongest evidence (Quality A) and should be prescribed as first-line pharmacological treatment 1
- Parent- and/or teacher-administered behavioral therapy should be implemented concurrently (Quality B evidence) 1
- The hierarchy of medication efficacy is: stimulants > atomoxetine > extended-release guanfacine > extended-release clonidine 1
- If methylphenidate fails after adequate dosing and duration, lisdexamfetamine should be the next option before considering non-stimulants 1
Adolescents (12-18 years)
- FDA-approved medications should be prescribed with the adolescent's assent (Quality A evidence) 1
- Behavioral therapy may be prescribed but has weaker evidence (Quality C) in this age group 1
- Screen for substance use symptoms before initiating treatment; if active substance use is identified, refer to a subspecialist 1
- Monitor closely for medication diversion, as this is a particular concern in adolescents 1
Medication Specifics
Stimulants (First-Line)
- Mechanism: Inhibit reuptake (and promote release in amphetamines) of dopamine and norepinephrine 1
- Effect size: Approximately 1.0, representing medium-to-large clinical benefit 1
- Onset: Rapid treatment effects within days 1
- Formulations: Available in short-acting and various long-acting preparations; extended-release formulations improve adherence and reduce rebound symptoms 1
- Common adverse effects: Decreased appetite, sleep disturbances, increased blood pressure and pulse, headaches 1
- Monitoring required: Height, weight, heart rate, blood pressure at each follow-up visit 2
Atomoxetine (Second-Line)
- Dosing for children/adolescents ≤70 kg: Start at 0.5 mg/kg/day, increase after minimum 3 days to target of 1.2 mg/kg/day (maximum 1.4 mg/kg or 100 mg, whichever is less) 3
- Dosing for children/adolescents >70 kg and adults: Start at 40 mg/day, increase after minimum 3 days to target of 80 mg/day (maximum 100 mg) 3
- Effect size: Approximately 0.7, smaller than stimulants 1
- Onset: 6-12 weeks until full effects are observed 1
- Advantages: "Around-the-clock" effects, uncontrolled substance, preferred first-line option when comorbid substance use disorders, disruptive behavior disorders, or tic/Tourette's disorder exist 1
- Black box warning: Monitor for suicidality and clinical worsening 1, 3
Alpha-2 Agonists (Extended-Release Guanfacine, Clonidine)
- Effect size: Smaller than stimulants 1
- Onset: 2-4 weeks for full effects 1
- Advantages: "Around-the-clock" effects, uncontrolled substance, preferred when comorbid sleep disorder, substance use disorder, disruptive behavior disorders, or tic/Tourette's disorder 1
- Common adverse effects: Somnolence/sedation (frequent), fatigue, hypotension 1
- Administration: Evening dosing preferable due to sedation; clonidine requires twice-daily dosing 1
Behavioral Therapy Components
Evidence-Based Interventions
- Parent training programs teach strategies to prevent and respond to problematic behaviors like interrupting, aggression, and non-compliance 1
- Classroom management interventions implemented by teachers 1
- Social skills training through repeated practice with performance feedback 1
- Daily report cards and point systems for school-based management 1
- Benefits of behavioral therapy persist after treatment ends, unlike medication effects which cease upon discontinuation 1
Critical Management Principles
Chronic Disease Model
- ADHD must be recognized as a chronic condition requiring ongoing follow-up and management 1
- Periodic reevaluation of long-term medication usefulness is mandatory 3
- Adjustment and changes to the treatment regimen are the rule, not the exception, due to symptom changes, psychosocial situation changes, and normal development (e.g., weight gain) 1
School Integration
- The school environment, program, or placement is a fundamental part of any treatment plan 1
- Children may be eligible for services under a 504 Rehabilitation Act Plan or special education IEP under "other health impairment" designation 1
- Strong family-school partnerships enhance treatment effectiveness 1
Combination Therapy Benefits
- Combined medication and behavioral therapy allows for lower stimulant dosages, potentially reducing adverse effects 1
- Combination treatment shows greater improvements in academic and conduct measures, particularly when ADHD is comorbid with anxiety or in lower socioeconomic environments 1
- Parents and teachers report significantly higher satisfaction with combined therapy 1
Common Pitfalls to Avoid
Diagnostic Errors
- Do not use EEG or neuroimaging routinely for ADHD diagnosis in non-specialized settings 1
- Inappropriate diagnosis and stimulant use by non-specialized providers is a documented concern 1
- Always confirm DSM-5 criteria are met with documented impairment in multiple settings before initiating treatment 1
Medication Management Errors
- Do not prescribe medication for children whose symptoms fail to meet DSM-5 criteria for ADHD 1
- Anticholinergics should not be used routinely for preventing extrapyramidal side effects if antipsychotics are considered 1
- Screen for bipolar disorder, mania, or hypomania (personal or family history) before starting atomoxetine 3
- In hepatic insufficiency, reduce atomoxetine dose to 50% (moderate impairment) or 25% (severe impairment) of normal 3