Skip to textbook content
Doctor’s PassportTextbook
TopicsAll topics

Loading topic navigation…

Textbook navigation
TopicsAll topics

Loading topic navigation…

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.

Attention-deficit hyperactivity disorder

Paediatrics and child health · UK scope · Sources checked 27 Aug 2026 · Clinical review pending

RapidFull
!
Acute behavioural or treatment-related danger

ADHD itself is not an emergency, but acute psychosis or mania, suicidal intent, severe aggression, stimulant overdose and exertional cardiovascular symptoms require urgent assessment.

Action: Use ABCDE, obtain observations and capillary glucose, secure immediate safety and seek emergency paediatric, mental-health or poisons advice according to the presentation. Stop ADHD medication during an acute psychotic or manic episode and arrange specialist reassessment before any restart. Chest pain, collapse, sustained tachyarrhythmia or severe hypertension after a stimulant needs urgent cardiovascular assessment; do not attribute these findings to behaviour. Suspected overdose requires exact drug, formulation, amount and time, ECG and National Poisons Information Service or TOXBASE-guided care. Escalate suicidal intent or inability to maintain safety through the local urgent mental-health pathway and safeguarding procedures.

Synopsis

Recognise developmentally inappropriate inattention, hyperactivity and impulsivity, establish impairment across settings through specialist assessment, distinguish common mimics and coexisting needs, and use environmental, behavioural and medicine interventions safely in children and young people.

  • ADHD is a neurodevelopmental disorder: symptoms are developmentally inappropriate, began before age 12, persist, occur in at least 2 important settings and cause clear functional impairment.
  • Diagnosis is specialist and clinical. Rating scales support multi-informant assessment but neither a positive nor a negative score can independently diagnose or exclude ADHD.
  • Always assess sleep, hearing, vision, language, learning, autism, tics, anxiety, depression, trauma, epilepsy and the classroom environment; coexistence is common.
  • Under age 5, first-line treatment is an ADHD-focused group parent-training programme; medicine requires a second specialist opinion and persistent severe impairment.
  • From age 5, provide information, parent support and school environmental modifications before medicine; offer medication when significant impairment persists after these measures have been implemented and reviewed.
  • First-line medicine for children aged 5 years and over is methylphenidate. Age 5 use is off-label and remains specialist initiated.
  • After an adequate 6-week methylphenidate trial at an effective tolerated dose, switch to lisdexamfetamine when benefit remains insufficient.
  • Use dexamfetamine when lisdexamfetamine works but its longer effect is not tolerated; use atomoxetine or guanfacine when stimulants are not tolerated or separate adequate trials are ineffective.
  • Before medication record height, weight, pulse, blood pressure, cardiovascular history and current medicines; routine ECG is unnecessary without a clinical cardiac indication or interacting cardiac-risk medicine.
  • Monitor growth, pulse, blood pressure, sleep, appetite, mood, tics, seizures, adherence and diversion; review the continuing need for medicine at least annually.

Key red flags

Syncope on exertion, exertional chest pain, sudden-onset rapid regular palpitations, a murmur or a first-degree relative who died suddenly before age 40 requires cardiovascular opinion before ADHD medication.

Blood pressure persistently above the 95th centile for age and height requires paediatric hypertension assessment before or during treatment.

New hallucinations, delusions, marked mood elevation, severe agitation or suicidal thinking demands urgent mental-health review and medicine reassessment.

Developmental regression, seizures, focal neurological signs, episodic altered awareness or a major change from baseline is not explained by uncomplicated ADHD.

Severe sleepiness, loud snoring with witnessed apnoeas or profound insomnia can mimic or worsen inattention and needs a sleep-focused assessment.

Rapid weight loss, marked slowing of linear growth, persistent tachycardia or hypertension during medication requires dose review and specialist action.

Requests for early replacement prescriptions, sharing, selling or coercion around stimulants raise diversion and safeguarding risk.

Investigation priorities

01
Reference standard: specialist clinical diagnostic assessmentFirst stepReference standard

Integrate developmental and psychiatric history, symptom criteria, onset, persistence, multi-setting impairment, observation, collateral and differential diagnosis.

02
First-line: multi-informant history and collateralFirst line

Obtain concrete examples from child, caregivers and education, including strengths, impairment, age of onset, masking and environmental support.

Management branches

DiagnosisEstablish a persistent multi-setting pattern

Inattention, hyperactivity or impulsivity is causing concern.

  1. Screen immediately for acute risk, regression, seizures, sleep disorder, sensory loss, trauma and safeguarding concerns.
  2. Gather developmental history and concrete child, caregiver and education examples, then refer for specialist assessment when symptoms persist and impair function.
  3. Specialist confirms onset before age 12, presence in at least 2 settings, impairment and exclusion or recognition of alternative and coexisting conditions.

Key medicines

Methylphenidate immediate releaseChild 6–17 years: start 5 mg orally once or twice daily, increasing by 5–10 mg at weekly intervals; maximum 60 mg daily in divided doses. Space doses by about 4 hours. Age 5 use is specialist and off-label.Monitor appetite, growth, pulse, blood pressure, sleep, mood and tics. Avoid a late dose when it causes insomnia. It is a controlled drug: prescribe and store securely and assess misuse, diversion and school handling.
Methylphenidate modified release, approximately 12-hour tabletFor a suitable licensed formulation from age 6: start 18 mg orally each morning and increase by 18 mg at approximately weekly intervals; usual child maximum 54 mg daily. Follow the chosen product's SmPC.Release profiles differ between brands. Prescribe by brand, follow product-specific food instructions and do not crush. Do not switch blindly. Monitor stimulant effects, appetite, growth, sleep and cardiovascular observations.
Open full textbook →Answer 2 questions
Sources and review status6 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 attention deficit hyperactivity disorderUK diagnostic, baseline, non-pharmacological, medicine-sequence and monitoring recommendations.
  • BNFC treatment summary: attention deficit hyperactivity disorderCurrent UK paediatric treatment principles and medicine positioning.
  • BNFC methylphenidate hydrochlorideCurrent paediatric formulations, dosing, cautions and monitoring context.
  • BNFC lisdexamfetamine mesilateCurrent paediatric dosing, titration and prescribing safeguards.
  • BNFC atomoxetineWeight-banded dosing, adverse effects and safety information.
  • BNFC guanfacineWeight-banded prolonged-release dosing, tapering and cardiovascular monitoring.

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