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Educational draft · awaiting clinical reviewUse Rapid for revision, not patient-care decisions. Check current national and local guidance and the BNF or BNFC before acting.

ADHD in adults

Psychiatry · UK scope · Sources checked 27 Aug 2026 · Clinical review pending

RapidFull
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Acute activation is not routine ADHD

New severe agitation, sleeplessness, grandiosity, psychosis, chest pain, syncope, marked hypertension, suicidal intent or suspected stimulant toxicity demands urgent assessment for mania, psychosis, cardiovascular disease, overdose or substance-related harm.

Action: Assess ABCDE, observations, glucose, ECG and toxicology context as indicated, stop the next ADHD dose when a serious medicine-related event or acute psychotic or manic episode is suspected, and obtain emergency medical and mental-health advice.

Synopsis

Identify developmentally persistent attention, activity and impulse-regulation difficulties across settings, obtain specialist diagnosis, and deliver multimodal adult treatment with safe cardiovascular, psychiatric and diversion monitoring.

  • Adult ADHD is a neurodevelopmental disorder: impairing inattention and/or hyperactivity-impulsivity began in childhood, persist, occur in at least two important settings and are not better explained elsewhere.
  • Refer adults without a childhood diagnosis to a trained ADHD specialist when typical manifestations began during childhood, persisted and cause at least moderate impairment.
  • Diagnosis requires full clinical, developmental, psychiatric, physical and functional assessment with observer information when useful; rating scales cannot be the sole basis.
  • Assess sleep, mood, anxiety, autism, learning disability, trauma, substance use, epilepsy, brain injury and environmental demands because overlap and comorbidity are common.
  • Before medicine, record pulse, blood pressure, height and weight, cardiovascular history, current medicines, mental health and diversion risk; routine ECG is unnecessary without a clinical indication.
  • NICE offers lisdexamfetamine or methylphenidate as adult first-choice pharmacological options, with atomoxetine after intolerance or inadequate separate trials, alongside environmental modifications and information.
  • Monitor symptoms and function as well as adverse effects, pulse and blood pressure around dose changes and at least six-monthly, adult weight every six months, and treatment need at least yearly.

Key red flags

Symptoms that began only after head injury, substance use, mood episode, sleep disorder or another adult illness do not establish developmental ADHD and require an alternative-cause assessment.

Exertional syncope, cardiac-origin chest pain, sudden death in a first-degree relative under forty, congenital heart disease or a murmur prompts cardiovascular opinion before ADHD medication.

Current psychosis, mania, severe depression, suicide risk, uncontrolled substance use or safeguarding crisis changes treatment priority and may require same-day specialist care.

Rapid dose escalation, repeated lost prescriptions, early refill requests, intoxication or third-party demand raises diversion or misuse risk without automatically proving it.

Investigation priorities

01
Specialist developmental interviewFirst step

Confirm childhood onset, persistence, cross-setting symptoms, impairment and alternative explanations.

Management branches

ReferralConfirm developmental suspicion

Adult attention, restlessness or impulsivity suggests persistent childhood-onset ADHD with significant impairment.

  1. Document current examples, childhood evidence, affected settings, functional impact, strengths, sleep, substances, mental health and possible neurodevelopmental overlap.
  2. Refer for assessment by a professional trained in adult ADHD diagnosis rather than diagnosing solely from a screening score or medicine response.
  3. Address immediate suicide, psychosis, mania, intoxication, driving and safeguarding risks while useful organisational adjustments begin.

Key medicines

Lisdexamfetamine for adult ADHDUsing the current Elvanse SmPC, start 30 mg orally each morning; a 20 mg start may be used when appropriate. Increase by 10 mg or 20 mg at about weekly intervals to the lowest effective dose; maximum 70 mg once daily, reduced to no more than 50 mg daily in severe renal insufficiency with further reduction considered during dialysis. Do not divide a capsule dose, and avoid afternoon dosing because of insomnia. Stop if symptoms do not improve after appropriate dose adjustment over one month.Specialist initiation and titration are required. It is contraindicated with an MAOI or within 14 days, hyperthyroidism or thyrotoxicosis, an agitated state, symptomatic cardiovascular disease, advanced arteriosclerosis, moderate-to-severe hypertension, glaucoma or phaeochromocytoma. Monitor appetite, weight, sleep, mood, psychosis or mania, substances and diversion and check the current SmPC for interactions.
Concerta XL methylphenidate exampleFor adults new to this prolonged-release preparation, the current SmPC starts 18 mg orally once each morning and permits 18 mg increments at approximately weekly intervals according to response and tolerability, to a maximum 72 mg daily. Modified-release products are not automatically interchangeable; use the chosen product's instructions. Stop if symptoms do not improve after appropriate dose adjustment over one month.Specialist titration and controlled-drug governance apply. Concerta XL is contraindicated with an irreversible non-selective MAOI or within 14 days, glaucoma, phaeochromocytoma, hyperthyroidism or thyrotoxicosis; diagnosis or history of severe depression, anorexia nervosa or anorexic disorder, suicidal tendency, psychotic symptoms, severe mood disorder, mania, schizophrenia, psychopathic or borderline personality disorder; uncontrolled severe episodic type-I bipolar disorder; serious cardiovascular disease including severe hypertension, heart failure, arterial occlusive disease, angina, haemodynamically significant congenital heart disease, cardiomyopathy, myocardial infarction, potentially life-threatening arrhythmia or channelopathy; or cerebrovascular disease including aneurysm, vascular abnormality, vasculitis or stroke. Monitor pulse, blood pressure, weight, appetite, sleep, psychiatric change and misuse; swallow it whole and verify licensing and conversion before switching.
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Sources and review status4 sources · checked 27 Aug 2026 · clinical review pending+
Sources

Sources and review status

National guidance is shown before implementation-dependent detail. Typical adult dose examples remain subject to patient factors, contraindications and the live BNF or specialist protocol. Source check completed 27 Aug 2026; clinical approval remains outstanding.

  • NICE NG87 ADHD recommendationsAdult recognition, diagnosis, treatment sequence, baseline checks and monitoring.
  • Elvanse 30 mg Summary of Product CharacteristicsCurrent lisdexamfetamine adult regimen, administration, contraindications and safety.
  • Concerta XL 18 mg Summary of Product CharacteristicsPreparation-specific adult methylphenidate titration and monitoring.
  • Atomoxetine 100 mg Summary of Product CharacteristicsAdult atomoxetine dose, monitoring and safety information.

Editorial contact: Doctor’s Passport editorial team. Source-check date is separate from clinical approval. Report a content problem · Content changes

Authoring stateRapid draftClinical stateAwaiting reviewJurisdictionUnited Kingdom