How to Start Methylphenidate for ADHD
Begin methylphenidate at 5 mg twice daily (after breakfast and lunch) for pediatric patients aged 6 years and older, or 5-10 mg in the morning after breakfast for adults, then increase by 5-10 mg weekly based on response and tolerability until symptoms improve or side effects emerge. 1, 2, 3, 4
Pre-Treatment Assessment Requirements
Before initiating methylphenidate, complete the following screening:
- Cardiovascular evaluation: Assess baseline blood pressure, pulse, and screen for symptomatic cardiovascular disease, structural cardiac abnormalities, cardiomyopathy, serious arrhythmias, or coronary artery disease—stimulants are contraindicated in patients with these conditions 2, 4
- Substance use screening: Evaluate current or past substance abuse, as this represents a relative contraindication requiring close supervision 2
- Psychiatric screening: Screen for risk factors for developing manic episodes or psychotic symptoms before starting treatment 4
- Family history: Obtain family history of sudden death, repeated fainting, or arrhythmias 2
- Tic assessment: Evaluate family history and clinically assess for tics or Tourette's syndrome 4
Initial Dosing Protocol
Pediatric Patients (6 Years and Older)
- Starting dose: 5 mg twice daily, administered after breakfast and lunch 1, 3, 4
- Optional third dose: May add an after-school dose to help with homework and social activities 1
- Titration schedule: Increase by 5-10 mg weekly until symptoms improve or side effects emerge 1, 3, 4
- Maximum dose: 60 mg/day total; daily dosage above 60 mg is not recommended 1, 4
Adult Patients
- Starting dose: 5-10 mg once daily in the morning after breakfast 2, 3
- Titration schedule: Increase by 5-10 mg increments weekly based on response and tolerability 2, 3
- Dosing frequency: Administer in divided doses 2-3 times daily, preferably 30-45 minutes before meals 4
- Average maintenance dose: 20-30 mg daily 4
- Maximum dose: 60-72 mg/day depending on formulation 2, 4
Titration Strategy: Fixed-Dose Method
The American Academy of Child and Adolescent Psychiatry recommends using a fixed-dose, escalating stepwise-titration method rather than weight-adjusted dosing:
- Use whole or half pills during titration to avoid pill fragments of unknown strength 1
- Increase total daily doses through the 10-60 mg range until the patient shows improvement or troublesome side effects 1
- Titrate slowly with small children and stop or reverse the dose increase when side effects occur 1
- No reliable predictors exist for individual response—pretreatment characteristics do not reliably predict who will respond 1
Monitoring During Titration
Assessment Schedule
- Follow-up frequency: Schedule appointments at least monthly until symptoms stabilize 2, 3
- Rating scales: Obtain standardized ADHD rating scales from teachers and parents (for children) or from patient and significant other (for adults) before each dose increase 1, 3
- Vital signs: Monitor blood pressure and pulse at each visit 2, 3
Target Outcomes to Assess
- Therapeutic response: Assess improvement in core ADHD symptoms (inattention, hyperactivity, impulsivity) using validated rating scales 1, 3
- Adverse effects: Systematically query for decreased appetite, insomnia, headaches, irritability, social withdrawal, agitation, jitteriness, and gastrointestinal symptoms 1, 5
- Cardiovascular effects: Monitor for increased blood pressure, heart rate, palpitations, and arrhythmias 1, 4
- Weight: Track weight in pediatric patients due to risk of growth suppression 4
Timing and Administration Considerations
- Administer early in the day to minimize insomnia—typically after breakfast and lunch 1
- Adjust timing of end-of-day dose to minimize side effects such as reduced appetite at dinner and delayed sleep onset 1
- Peak plasma concentration occurs within 1-3 hours, with behavioral effects lasting approximately 4 hours for immediate-release formulations 6
- Consider long-acting formulations for maintenance treatment to improve adherence and provide 8-12 hours of symptom control 2, 6
When to Stop Titration
- Stop increasing the dose when:
Critical Pitfalls to Avoid
- Do not start at excessively high doses—this increases adverse effects and reduces adherence; begin conservatively, especially in older patients who may have increased sensitivity 2
- Do not use weight-adjusted dosing—standard methylphenidate tablets are unscored, making fractional doses impractical and resulting in pill fragments of unknown strength 1
- Do not titrate too rapidly—allow a minimum of one week between dose adjustments to properly evaluate response 2, 3
- Do not rely on plasma concentrations—behavioral responses are highly variable, and assessment of plasma concentrations is not clinically useful 6
- Do not prematurely switch medication classes—if response is inadequate at lower doses, continue titrating to maximum recommended dose before switching 3
Alternative Strategies if Methylphenidate Fails
- Switch to alternative stimulant: If maximum dose (60 mg/day) does not adequately control symptoms, switch to a different stimulant class such as amphetamine formulations, which have a different mechanism of action 2, 3
- Consider non-stimulants: Reserve atomoxetine or alpha-2 agonists (guanfacine) as second-line options only after maximizing stimulant trials 2, 3
Special Population Considerations
- Older adults: Use more conservative titration, increasing by 5 mg every 2 weeks instead of weekly due to age-related increased sensitivity to both therapeutic and adverse effects 3
- Patients with comorbid anxiety or depression: Note that methylphenidate may alleviate these symptoms in addition to ADHD symptoms 7
- Patients with substance use history: Exercise caution and close supervision, though methylphenidate has pharmacokinetic properties that reduce abuse potential compared with drugs like cocaine 1