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Reference Point

Asthma

A clinical reference for UK primary care

Last reviewed 4 May 2026 · Next review August 2026

Around 5.4 million people in the UK live with asthma. The annual asthma death toll has risen by nearly a quarter since the 2014 National Review of Asthma Deaths (NRAD), with an average of around 1,500 deaths each year in recent data and four deaths per day.1

In November 2024, NICE, BTS and SIGN published the first joint asthma guideline. NG244 is the pathway document; NG245 contains the full diagnostic and management recommendations. The most significant change for primary care is the diagnostic pathway in adults: blood eosinophil count or fractional exhaled nitric oxide (FeNO) is now first-line, with spirometry second-line.2,3

NRAD identified key risk factors for asthma death that remain central to risk-stratified care: overuse of short-acting beta-2 agonist (SABA) inhalers, underuse of inhaled corticosteroids (ICS), and inadequate follow-up after emergency presentations.1,3

Asthma diagnosis

Objective tests for diagnosing asthma

Per NG245, eosinophils or fractional exhaled nitric oxide (FeNO) are first-line, with spirometry second-line. Recommendations differ for adults and children aged 5 to 16.3

Adults: first-line

Eosinophils above lab reference range, or FeNO u226550 ppb

NG245 recommendation 1.2.1. Measure blood eosinophil count or FeNO level in adults with a history suggestive of asthma.3

Adults: second-line if not confirmed

BDR: FEV1 increase u226512% AND u2265200 ml

NG245 recommendation 1.2.2. Bronchodilator reversibility (BDR) with spirometry, post-bronchodilator vs pre-bronchodilator value.3

Children 5 to 16: first-line

FeNO u226535 ppb

NG245 recommendation 1.2.5. Measure FeNO level in children with a history suggestive of asthma.3

Children 5 to 16: second-line

BDR: FEV1 increase u226512%

NG245 recommendation 1.2.6. If FeNO is not raised or unavailable, measure bronchodilator reversibility with spirometry.3

If spirometry unavailable or delayed

Peak expiratory flow (PEF) twice daily for 2 weeks

NG245 recommendations 1.2.3 and 1.2.7. PEF variability supports diagnosis if spirometry is not accessible.3

Children under 5

Clinical judgement

NG245 section 1.3. Objective tests are not reliable in this age group; diagnosis is based on clinical features.3

If asthma is suspected but not confirmed

Per NG245 recommendations 1.2.4 and 1.2.8: if asthma is not confirmed by initial tests but still suspected on clinical grounds, refer for specialist tests. In children, also measure total IgE and blood eosinophil count.3

Risk stratification

Risk factors for poor asthma outcomes

SABA over-use

More than 2 inhalers per year

NG245 lists over-use of short-acting beta-2 agonist inhalers (more than 2 per year) as a risk factor for poor outcomes. NRAD identified SABA over-use as a key indicator of poorly controlled asthma.1,3

Oral corticosteroid use

u22652 courses per year

NG245 identifies needing 2 or more courses of oral corticosteroids per year as a risk factor for poor outcomes.3

Emergency presentations

u22652 ED visits or any admission

NG245 lists 2 or more visits to an emergency department, or any hospital admission for asthma, as a risk factor for poor outcomes.3

Adherence

Non-adherence to medicines

NG245 includes non-adherence to medicines as a risk factor. NRAD identified underuse of preventer inhalers as a key risk factor for asthma death.1,3

Annual review

Monitoring asthma control

Per NG245 recommendation 1.5.1, check the following at every review.3

01

Symptoms

Ask about current asthma symptoms

02

Time off work or school

Due to asthma

03

Reliever use

Including check of prescription record

04

Oral corticosteroid courses

Number in past year

05

Hospital or ED attendance

Any admissions or emergency visits

06

Validated questionnaire

Consider ACQ, ACT, or Childhood ACT

Referral pathways

Specialist asthma care

Per NG245 recommendation 1.7.5: refer adults with asthma not controlled on moderate-dose MART if FeNO or eosinophils are raised. Per 1.7.6: refer if not controlled on moderate-dose MART despite trials of an LTRA and a LAMA.3

Suspected occupational asthma

Per NG245 section 1.4 and the BTS/SIGN guidance: refer for specialist assessment if occupational exposure is suspected.3

Diagnosis not confirmed but suspected

Per NG245 recommendations 1.2.4 and 1.2.8: refer for specialist tests if asthma is not confirmed by initial objective testing but still clinically suspected.3

Acute severe asthma

Same-day emergency assessment for features of acute severe or life-threatening asthma, per the BTS/SIGN management of acute asthma section retained in NG244.2

Pregnancy

Per NG245 section 1.12: women with asthma who are pregnant or planning pregnancy should be managed in line with the specific pregnancy and breastfeeding recommendations.3

Find all NICE updates relevant to primary care

View NICE Guidelines

This reference point is intended for UK Healthcare Professionals only. Content reports established clinical knowledge and current NICE guidance. It is not a substitute for clinical judgement or for the original guidelines. Last reviewed 4 May 2026.

References

All sources verified at last review. Where primary literature is cited, original peer-reviewed publications are linked.

  1. 1.Asthma + Lung UK. Asthma care is in crisis - charity sounds the siren as asthma death toll rises. Press release, 24 April 2024.
  2. 2.National Institute for Health and Care Excellence. Asthma pathway (BTS, NICE, SIGN). NICE guideline NG244. Published 27 November 2024.
  3. 3.National Institute for Health and Care Excellence. Asthma: diagnosis, monitoring and chronic asthma management (BTS, NICE, SIGN). NICE guideline NG245. Published 27 November 2024.

Medical Disclaimer: The content on Medicine Central is intended solely for registered UK healthcare professionals and is provided for educational and informational purposes only. It does not constitute medical advice, clinical guidance, or a substitute for professional clinical judgment. Always refer to current NICE guidelines, local formularies, and your own clinical assessment when making patient care decisions. Medicine Central accepts no liability for any loss, harm, or damage arising from reliance on the information provided. Content is reviewed periodically but may not reflect the most recent evidence or guideline updates. This site is not intended for use by patients or the general public.

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