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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.

Childhood asthma diagnosis and stepwise treatment

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

RapidFull
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Acute asthma attack

Breathlessness preventing speech or feeding, saturation below 92%, silent chest, cyanosis, exhaustion, altered consciousness or poor respiratory effort requires immediate acute-asthma treatment rather than completion of diagnostic tests.

Action: Give oxygen to target 94–98%, inhaled salbutamol by oxygen-driven nebuliser or repeated metered-dose inhaler and spacer according to severity, add ipratropium and systemic corticosteroid for severe disease, call senior paediatric help and transfer to hospital. Do not sedate; escalate early for life-threatening features.

Synopsis

Diagnose variable airflow obstruction with age-appropriate objective evidence, separate preschool wheeze and mimics, assess future attack risk as well as current symptoms, and use the current BTS, NICE and SIGN age-specific inhaled-corticosteroid pathways with technique, adherence and environmental review before escalation.

  • Asthma is variable respiratory symptoms with variable expiratory airflow limitation. Typical patterns are wheeze, breathlessness, chest tightness or cough that vary over time and with exercise, viral infection, allergens, cold air or night.
  • Do not diagnose from symptoms alone in a child able to test. Record objective evidence and the basis for diagnosis; examination may be normal between episodes.
  • Age 5–16 first objective test: FeNO. A value at least 35 ppb confirms asthma in a compatible history; inhaled corticosteroid can suppress FeNO and make testing falsely normal.
  • If FeNO is not raised or unavailable, perform spirometry with bronchodilator reversibility. An FEV1 rise at least 12% from baseline, or at least 10% of predicted normal FEV1, supports diagnosis.
  • If spirometry is delayed, twice-daily peak flow for 2 weeks supports diagnosis when amplitude percentage mean variability is at least 20%. Persistent doubt requires allergy/eosinophil assessment then paediatric specialist review and possible bronchial challenge.
  • Under age 5 there is no reliable reference test. Use a clinical phenotype, exclude alternatives, trial treatment when indicated and retry objective testing every 6–12 months once feasible.
  • Before every step up, check diagnosis, inhaler and spacer technique, adherence, dose actually dispensed, smoke or vape exposure, allergen triggers and comorbidity.
  • Age 5–11 first-line maintenance is twice-daily paediatric low-dose inhaled corticosteroid plus short-acting beta2 agonist as needed.
  • If uncontrolled at age 5–11 and able to use it, consider paediatric low-dose MART, then moderate-dose MART. Licensing is device and age specific; current NICE notes only one 100/6 microgram budesonide/formoterol dry-powder inhaler licensed for MART age 6–11 in November 2025.
  • If unable to manage MART, consider an 8–12 week montelukast trial, stopping if ineffective; then step to low-dose and moderate-dose ICS/LABA plus SABA. Discuss the MHRA warning about neuropsychiatric reactions.
  • Under 5 with interval symptoms or severe recurrent episodes: trial twice-daily low-dose ICS plus SABA for 8–12 weeks. Stop and reassess response; add an LTRA trial only after technique, adherence and environment review, and refer when uncontrolled.
  • Give a personalised written action plan, spacer education and regular review. Step down after sustained control, one change at a time, while retaining an anti-inflammatory strategy and monitoring attacks.

Key red flags

Silent chest, cyanosis, altered consciousness, exhaustion, hypotension or poor respiratory effort indicates life-threatening asthma.

Stridor, drooling, sudden choking, unilateral signs or no response to bronchodilator suggests upper-airway obstruction or foreign body rather than asthma.

Persistent wet cough, clubbing, faltering growth, recurrent focal pneumonia or neonatal symptoms suggests cystic fibrosis, bronchiectasis or structural disease.

Previous intensive-care ventilation, recent severe attack, excessive reliever use and poor inhaled-corticosteroid adherence predict future fatal or near-fatal attacks.

Symptoms only with feeds, recurrent aspiration, cardiac signs or fixed monophonic wheeze requires an alternative pathway.

Adolescent smoking or vaping, psychosocial distress, medicine access and deliberate underuse must be assessed confidentially and without blame.

Investigation priorities

01
First-line age 5–16: fractional exhaled nitric oxideFirst stepFirst line

Identify type-2 airway inflammation within a suggestive history.

Management branches

DiagnoseBuild objective confirmation

A child aged at least 5 years has a suggestive variable symptom history.

  1. Treat urgent symptoms first and obtain FeNO before ICS where feasible.
  2. If unconfirmed, proceed through spirometry reversibility, peak-flow variability and allergy/eosinophil steps.
  3. Refer for specialist opinion and challenge when doubt remains rather than applying an unsupported label.

Key medicines

Paediatric low-dose inhaled corticosteroidUse a licensed age-appropriate ICS and the current BTS, NICE and SIGN paediatric dose table, generally twice daily for children 5–11; under 5 use an 8–12 week twice-daily low-dose trial when indicated.Dose equivalence varies by molecule and device. Teach spacer use and mouth rinsing, monitor height and total steroid burden, and use the lowest effective dose after stable control.
MontelukastAge 6 months–5 years: 4 mg orally at night; age 6–14 years: 5 mg at night; age 15 years and over: 10 mg at night. For asthma step-up, use an 8–12 week monitored trial and stop if ineffective.Discuss MHRA neuropsychiatric warnings, including sleep, mood, behaviour and suicidal symptoms. Reassess benefit explicitly and do not continue an ineffective trial.
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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 NG245 asthma recommendationsJoint BTS, NICE and SIGN diagnosis, objective thresholds and age-specific treatment sequence.
  • NICE NG245 inhaled corticosteroid dose guideCurrent paediatric low, moderate and high ICS dose categories by medicine and device.
  • MHRA montelukast neuropsychiatric reactionsCurrent warnings and counselling requirements.
  • Asthma and Lung UK inhaler techniqueUK device-specific technique resources for patients and clinicians.

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