Initial Dosage of Dexmethylphenidate for ADHD
For pediatric patients (ages 6-17 years) new to methylphenidate, start dexmethylphenidate extended-release at 5 mg once daily in the morning; for adults, start at 10 mg once daily in the morning. 1
Starting Doses Based on Prior Medication History
Patients New to Methylphenidate
- Pediatric patients (6-17 years): Begin with 5 mg once daily in the morning 1
- Adults: Begin with 10 mg once daily in the morning 1
- Administer with or without food 1
Patients Currently on Methylphenidate
- Conversion rule: Dexmethylphenidate dose should be half (1/2) the current total daily dose of methylphenidate 1
- This reflects that dexmethylphenidate contains only the active d-threo-enantiomer, requiring approximately half the dose of racemic methylphenidate for equivalent efficacy 2, 3
Patients Currently on Dexmethylphenidate Immediate-Release
- Direct conversion: Give the same total daily dose using the extended-release formulation 1
- The extended-release formulation mimics two doses of immediate-release given 4 hours apart 2, 3
Titration Protocol
Dose Escalation Schedule
- Pediatric patients: Increase in 5 mg increments weekly based on symptom response and tolerability 1
- Adults: Increase in 10 mg increments weekly based on symptom response and tolerability 1
- Continue titration until optimal symptom control is achieved or side effects emerge 4, 1
Maximum Recommended Doses
Monitoring During Titration
Systematic Assessment Requirements
- Obtain standardized ADHD rating scales from teachers and parents for children before each dose increase 4, 5
- For adults, collect symptom ratings from the patient and significant others 4, 5
- These ratings can be obtained through phone contact between visits to guide titration decisions 4
- Monitor blood pressure, pulse, height, and weight at each visit 5, 6
Follow-Up Schedule
- Maintain weekly contact (by telephone or in-person) during initial titration 6
- Titration typically requires 2-4 weeks to reach optimal dosing 6
- After stabilization, schedule follow-up appointments at least monthly 5, 6
Administration Options
Capsule Administration
- Capsules may be swallowed whole 1
- Alternative for patients unable to swallow: Open capsule and sprinkle entire contents on applesauce 1
- This flexibility avoids the need for midday dosing at school, a significant practical advantage 2
Duration of Action Considerations
Pharmacokinetic Profile
- Single dose provides bimodal release mimicking two immediate-release doses given 4 hours apart 2, 3
- Efficacy demonstrated from 0.5 hours post-dose up to 11-12 hours after administration 2
- Rapid onset allows symptom control throughout the school day without midday dosing 2
Critical Pitfalls to Avoid
Dosing Errors
- Do not use weight-adjusted dosing: Fixed-dose titration using whole pills reflects standard practice and avoids the impracticality of cutting unscored tablets 4
- Avoid starting too high: Beginning at excessive doses leads to unnecessary side effects and decreased medication adherence 6
- Do not exceed maximum doses: If 30 mg/day (pediatric) or 40 mg/day (adult) fails to control symptoms, consider switching to a different stimulant class rather than exceeding recommended limits 5
Monitoring Failures
- Systematically assess side effects: Specifically query about insomnia, decreased appetite, headaches, irritability, and social withdrawal at each contact 4, 6
- Do not rely solely on subjective reports: Use validated, standardized rating scales to objectively measure improvement 4, 5
- Monitor cardiovascular parameters: Stimulants can increase blood pressure and heart rate; regular monitoring is essential 5, 6, 1
Premature Treatment Changes
- Do not switch medication classes prematurely: Ensure the patient has reached the maximum recommended dose before concluding treatment failure 5
- Titrate slowly with small children: Take care to increase doses gradually in younger or smaller patients to minimize side effects 4
When to Stop Dose Escalation
Response Criteria
- Stop increasing when adequate symptom control is achieved based on standardized rating scales 4, 5
- Stop if troublesome side effects emerge that outweigh therapeutic benefits 4, 1
- Consider treatment response successful if patient shows "much" or "very much" improved on Clinical Global Impression scale 5