This handout is for attention-deficit/hyperactivity disorder (adhd) — chronic stepwise (aap 2019 pmid 31570648; apa 2024; nice ng87 2024; mta 16-yr hechtman pmid 30019501). Your care team identified this based on: inattention or hyperactivity-impulsivity symptoms with onset before age 12 yr in ≥ 2 settings (dsm-5-tr 2022 f90.x; aap 2019 pmid 31570648).
Other reasons your team may use this plan: academic decline (pediatric/adolescent) or occupational decline (adult) attributable to attention or hyperactivity-impulsivity symptoms (dsm-5-tr 2022; apa 2024); behavioral problems with oppositional or conduct features in pediatric — common adhd presentation with comorbid odd/cd ~ 30-50% (aap 2019; dsm-5-tr 2022); vanderbilt parent + teacher both ≥ 6/9 inattentive or hyperactive-impulsive symptoms with functional impairment in ≥ 2 settings (aap 2019 pmid 31570648).
Take these medications exactly as prescribed. Do not stop or change a dose without talking to your provider.
| Medication | Starting dose | How | When | What it does |
|---|---|---|---|---|
| methylphenidate | IR: 5 mg PO BID-TID; ER (Concerta): 18 mg PO daily AM; ER (Ritalin LA / Focalin XR): 10-20 mg PO daily AM; titrate weekly | PO | IR BID-TID; ER daily AM | Methylphenidate-class first-line per AAP 2019 PMID 31570648 (pediatric) and APA 2024 (adult); multiple formulations (IR / ER / patch / liquid); baseline HR + BP + weight + height + cardiac history + FH SCD < 35; no routine EKG in healthy children; growth velocity + appetite + sleep monitoring Q3-6 mo |
| amphetamine-dextroamphetamine | IR (Adderall): 5 mg PO BID; ER (Adderall XR): 5-10 mg PO daily AM; titrate weekly | PO | IR BID; ER daily AM | Amphetamine-class first-line per AAP 2019 PMID 31570648 (pediatric) and APA 2024 (adult); Schedule II controlled substance; informed consent on abuse / dependence / diversion risks; same baseline screen + monitoring as methylphenidate-class |
| lisdexamfetamine | 30 mg PO daily AM; titrate by 10-20 mg weekly | PO | once daily AM | Prodrug — lysine cleaved peripherally to active dexamfetamine; smoother PK; lower abuse liability than mixed amphetamine salts; same baseline screen + monitoring; also FDA-approved for moderate-severe BED (McElroy JAMA Psychiatry 2015 PMID 25587642 — dual indication if BED comorbid) |
Plan: ADHD stepwise pharmacotherapy ladder — Step 1 stimulant first-line (methylphenidate-class OR amphetamine-class for ≥ 6 yr; behavioral first-line for 4-5 yr) → Step 2 within-class switch → Step 3 cross-class switch → Step 4 non-stimulant (atomoxetine, viloxazine) → Step 5 augmentation (alpha-2 agonist guanfacine ER or clonidine ER) (AAP 2019 PMID 31570648; APA 2024; NICE NG87 2024)
Use these zones to know what to do based on how you feel.
Call 911 or go to the nearest emergency room right away if you have:
Continue treatment as long as functional benefit + no severe side effects; many continue lifelong; ADHD persists into adulthood ~50-65% per MTA 16-yr (Hechtman PMID 30019501); transition planning at age 17-18 with adult psychiatry handoff + written transition letter + medication-continuity plan + PCP handoff; relapse-prevention CBT for adult ADHD per Safren manual; ongoing comorbidity surveillance (MDD / anxiety / SUD / sleep / eating disorders)
Guideline: AAP Clinical Practice Guideline for ADHD in Children and Adolescents 2019 (Wolraich PMID 31570648) + APA Practice Guideline for Adult ADHD 2024 (verify publication — PMID NEEDS_SOURCE_REVIEW) + NICE NG87 Attention deficit hyperactivity disorder: diagnosis and management 2018 (last updated 2024) + MTA Cooperative Group 16-yr follow-up (Hechtman 2018 PMID 30019501)