Management of ADHD in Adults
First-Line Pharmacological Treatment
Methylphenidate formulations (short-acting, intermediate-acting, or long-acting) or lisdexamfetamine are the recommended first-line pharmacological treatments for adults with ADHD, with long-acting formulations strongly preferred due to better adherence, lower abuse potential, and consistent symptom control throughout the day. 1, 2, 3
Stimulant Options and Dosing
Methylphenidate:
- Start at 30 mg once daily in the morning, titrate in 10-20 mg increments weekly up to maximum 70 mg/day 4
- Long-acting formulations provide 8-12 hours of coverage and are preferred over immediate-release (3-4 hours) 3
- Effective in 70-80% of patients with demonstrated superiority over placebo 2, 4
- Average effective dose is 20-30 mg daily, with maximum recommended dose of 60 mg when using divided dosing 2
Lisdexamfetamine:
- Start at 30 mg once daily in the morning, titrate in 20 mg increments weekly to target dose of 50-70 mg (maximum 70 mg) 4
- Prodrug formulation provides approximately 12 hours of coverage with minimal abuse potential compared to immediate-release amphetamines 3
- NICE guidelines recommend switching to lisdexamfetamine after a 6-week trial of methylphenidate at adequate dose without sufficient benefit 1
- Demonstrated significant placebo-adjusted improvement (18.6 points on ADHD-RS-IV) in controlled trials 4
Pre-Treatment Screening Requirements
Before initiating stimulant therapy, assess for: 4
- Cardiac disease: Obtain detailed personal and family history of sudden death, ventricular arrhythmia, structural cardiac abnormalities, cardiomyopathy, or coronary artery disease 1, 4
- Substance abuse history: Detailed drug and alcohol use history with consideration of urine drug screen, as stimulant prescribing in active substance abuse is contraindicated 5, 2
- Motor/verbal tics or Tourette's syndrome: Clinical evaluation before initiation 4
- Psychiatric comorbidities: Rule out bipolar disorder, severe anxiety, personality disorders, and assess baseline anxiety symptoms 5
Second-Line Non-Stimulant Options
Atomoxetine is the primary second-line option when stimulants fail after adequate optimization, are not tolerated, or are contraindicated. 1, 2
When to Use Non-Stimulants First-Line:
- Active substance use disorder 2
- Inadequate response or intolerable side effects to stimulants 2
- Comorbid severe tics or anxiety 2
- Patient preference or concerns about stimulant abuse potential 5, 1
- Night shift workers (atomoxetine provides 24-hour coverage without disrupting sleep-wake cycles) 2
Additional Non-Stimulant Options:
- Extended-release guanfacine (Intuniv): Effect size approximately 0.7, useful as monotherapy or adjunctive with stimulants 1, 2
- Extended-release clonidine (Kapvay): Can be administered before daytime sleep in night shift workers to leverage sedative effects 1, 2
- Bupropion and viloxazine: Additional alternatives though less extensively studied 2
Important caveat: Non-stimulants have smaller effect sizes compared to stimulants and require 2-12 weeks to achieve full therapeutic effect, whereas stimulants have immediate onset 2, 6
Concurrent Non-Pharmacological Interventions
Implement alongside medication, not as sequential steps: 1
- Psychoeducation: Improve understanding of ADHD symptoms, treatment expectations, and self-management strategies 1
- Cognitive Behavioral Therapy (CBT): Most extensively studied psychotherapy for adult ADHD, focusing on time management, organization, planning, and adaptive behavioral skills; increased effectiveness when combined with medication 2
- Mindfulness-Based Interventions: Emerging evidence for managing inattention, emotion regulation, executive function, and quality of life 2
- Recovery-focused care: Consider individual values, goals, and strengths in treatment planning 1
Monitoring Parameters
Regular Assessment Requirements:
- Vital signs: Blood pressure and pulse monitoring with each visit during titration, then periodically 2
- Core ADHD symptoms: Use standardized rating scales (ADHD-RS, Conners Adult ADHD Rating Scale, Brown ADD Scale) 5, 4
- Functional outcomes: Improvement in work performance, relationships, daily functioning 1, 4
- Comorbid anxiety tracking: Ensure anxiety is not worsening with stimulant use 2
- Substance abuse monitoring: Ongoing assessment for signs of medication misuse or diversion 5, 4
Common Adverse Effects to Monitor:
- Loss of appetite, insomnia, anxiety (most common with stimulants) 2
- Cardiovascular effects (elevated blood pressure, tachycardia) 2
- Potential for abuse, misuse, and addiction with stimulants 4
Treatment Algorithm
Confirm diagnosis using DSM criteria and structured assessment tools, with particular focus on childhood onset of symptoms 5, 1
Complete pre-treatment screening for cardiac disease, substance abuse, tics, and psychiatric comorbidities 4
Initiate long-acting methylphenidate OR lisdexamfetamine at 30 mg once daily in the morning 1, 4, 3
Titrate weekly in 10-20 mg increments (methylphenidate) or 20 mg increments (lisdexamfetamine) based on response and tolerability 4
If inadequate response after 6 weeks at adequate dose: Switch to the alternative stimulant (methylphenidate to lisdexamfetamine or vice versa) 1
If stimulants fail, not tolerated, or contraindicated: Switch to atomoxetine as primary second-line option 1, 2
Consider adjunctive therapy: Add guanfacine or clonidine if monotherapy insufficient 2
Implement concurrent CBT throughout pharmacological treatment for optimal outcomes 2
Special Populations
Comorbid anxiety: Stimulants are not contraindicated but require careful monitoring; they can indirectly reduce anxiety by improving executive function and reducing functional impairment 2
Substance use disorder: Non-stimulants (atomoxetine, guanfacine, clonidine) are strongly preferred; avoid stimulants in active substance abuse 5, 2
Medically ill patients: Consider lower starting doses (approximately half the standard ADHD dose) with slower titration 5