Medical Journal Digest

Asthma Diagnosis and Treatment in UK Primary Care 2026: What the BTS/NICE/SIGN Guideline (NG245) Changed

4 min read By Dr Tim Hamilton, Consultant in Palliative Medicine, NHS Wales

Asthma Diagnosis and Treatment in UK Primary Care 2026: What the BTS/NICE/SIGN Guideline (NG245) Changed

In November 2024, the British Thoracic Society, NICE, and SIGN published a single joint asthma guideline — NG245 — replacing three separate sets of advice that had drifted apart for years. Two changes stand out for primary care, and both are large: how asthma is diagnosed, and what the reliever inhaler now contains.

This post covers what changed and what it means at the appointment level in 2026. It is written for UK GPs, GP registrars, practice nurses, GP pharmacists, and trainees. The guideline and the BNF remain the authoritative references; this post summarises and links, it does not substitute for clinical judgement.

Diagnosis now leads with inflammation

The old reflex was to reach for spirometry first. NG245 reorders the pathway around markers of eosinophilic airway inflammation.

For adults aged 16 and over with a suggestive history, the first step is a blood eosinophil count or a FeNO measurement. If the eosinophil count is above the laboratory reference range, or FeNO is 50 ppb or more, asthma can be diagnosed at that point. Where those are not diagnostic, testing continues in sequence — bronchodilator reversibility, peak expiratory flow variability, and, if still unresolved, a bronchial challenge.

The principle underneath is worth stating: no single test is a gold standard. Spirometry with reversibility has high specificity but low sensitivity in adults; peak flow variability is specific but insensitive; FeNO is specific but loses sensitivity in smokers and in obesity. The pathway is built to be followed in order, not cherry-picked — a negative early test does not rule asthma out, it moves you to the next test.

For primary care, the practical question this raises is access. A pathway that leads with FeNO and eosinophils depends on those tests being available, and that availability is uneven. Knowing your local route to FeNO is now part of being able to diagnose asthma to guideline standard.

The reliever has changed

The bigger shift for day-to-day prescribing is the end of the SABA-only reliever for people aged 12 and over.

The evidence is hard to argue with: over-reliance on a short-acting beta agonist, without an inhaled corticosteroid, is associated with worse outcomes — and it was a recurring theme in the National Review of Asthma Deaths. NG245 responds by putting an anti-inflammatory component into the reliever itself.

AIR — anti-inflammatory reliever. For people aged 12 and over with infrequent symptoms, starting therapy is now a low-dose inhaled corticosteroid/formoterol inhaler taken as needed, rather than a SABA alone. One as-needed inhaler delivers both treatment and relief.

MART — maintenance and reliever therapy. For more persistent symptoms, the step up is a single inhaled corticosteroid/formoterol inhaler used both as regular maintenance and as the reliever. The patient carries one device, not two. The economic analysis behind the guideline found AIR and MART to be more effective and less costly than the traditional inhaled corticosteroid plus separate SABA approach.

From November 2025, a budesonide/formoterol dry powder inhaler was also licensed for MART in children aged 6 to 11, extending the approach to younger children. The age-specific pathways differ, so the guideline should be consulted directly for the under-16 and under-12 detail.

What this means for practice

Two pieces of work follow from the guideline, and neither needs a new clinic.

The first is inhaler review. Patients still on a SABA-only reliever are the priority cohort — a search for high SABA issue without a preventer surfaces them quickly, and each is a conversation about switching to an anti-inflammatory reliever. The second is diagnostic discipline: a documented, sequential pathway rather than a single test, and a clear local route to FeNO so that diagnosis is not stalled by access.

The reliever-in-the-pocket habit is decades old. Changing it is the patient-facing work the guideline creates — and it is where the outcome benefit actually sits.

A note on what this post is — and is not

This is a guideline summary for awareness. It is not a substitute for NICE NG245, the BNF, or local prescribing and diagnostic policy. The age-specific pathways, test cut-offs, and licensed products should be confirmed against the guideline and the BNF before applying them. Clinical decisions remain the responsibility of the treating clinician.

The Monday Clinical Brief publishes weekly summaries of the most important new papers and guideline updates across 31 UK medical specialties — including guideline changes like this one. We surface them, summarise them, and link to them, so practice-changing material does not get missed in a busy clinical week.

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Frequently Asked Questions

What is the first diagnostic test for asthma under the 2024 BTS/NICE/SIGN guideline?

For people aged 16 and over with a history suggestive of asthma, NG245 starts with a marker of eosinophilic airway inflammation: a blood eosinophil count or a fractional exhaled nitric oxide (FeNO) measurement. If the eosinophil count is above the laboratory reference range, or the FeNO level is 50 ppb or more, asthma can be diagnosed. If those are not diagnostic, testing proceeds sequentially to bronchodilator reversibility, peak flow variability, and bronchial challenge. No single test is treated as a gold standard.

What is AIR (anti-inflammatory reliever) therapy?

AIR is the use of a low-dose inhaled corticosteroid/formoterol combination inhaler taken as needed for symptom relief, rather than a short-acting beta agonist (SABA) alone. It delivers both anti-inflammatory treatment and bronchodilation in a single as-needed inhaler. For people aged 12 and over with infrequent symptoms, NG245 positions AIR as starting therapy, replacing the old SABA-only step.

What is MART and when is it used?

MART — maintenance and reliever therapy — uses a single inhaled corticosteroid/formoterol inhaler as both regular maintenance treatment and the as-needed reliever. It is the step up from AIR for people with more persistent symptoms, and it keeps the patient on one inhaler rather than separate preventer and reliever devices. The BNF and the guideline hold the specific products and doses licensed for MART.

Is SABA-only treatment still recommended for asthma?

No. NG245 moves away from short-acting beta agonist (SABA) reliever therapy used on its own, reflecting strong evidence that SABA over-reliance without inhaled corticosteroid is associated with poorer outcomes. The reliever now carries an anti-inflammatory component. Reviewing and switching patients still on SABA-only inhalers is one of the practical priorities the guideline creates.

Has anything changed for children?

Yes. From November 2025, a budesonide/formoterol dry powder inhaler (100 micrograms/6 micrograms per actuation) was licensed for MART in children aged 6 to 11, extending the anti-inflammatory reliever approach to younger children. The diagnostic pathway and treatment steps differ by age group, so the guideline itself should be consulted for the under-16 and under-12 pathways.

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Dr Tim Hamilton · Consultant in Palliative Medicine, NHS Wales

Dr Tim Hamilton is a Consultant in Palliative Medicine in NHS Wales and the founder of The Monday Clinical Brief. He built MCB to help busy UK clinicians keep up with the literature across 31 specialties.