Asthma (Chronic)

NICE guideline [NG245] Asthma: diagnosis, monitoring and chronic asthma management (BTS, NICE, SIGN). Published: 27 Nov 2024

Background information

Asthma: Asthma is a chronic respiratory condition characterised by chronic airway inflammation and airway hyper-responsiveness to variable triggers, presenting with recurrent symptoms such as wheeze, breathlessness, chest tightness, and cough. It is defined by variable expiratory airflow limitation that is typically reversible, either spontaneously or with treatment. [Ref]

Atopy: Genetic predisposition to produce immunoglobulin E (IgE) antibodies in response to common environmental allergens, leading to an increased risk of developing immediate-type hypersensitivity reactions and clinical syndromes such as atopic dermatitis, allergic rhinitis, and asthma (collectively known as the atopic triad). [Ref]

Prevalence: ~ 6.5% of the UK population >6 yrs 

Age of onset: typically in childhood / young adults 

Sex:
  • ♂ > ♀ in <18 yrs 
  • ♀ > ♂ in >18 yrs

Associated comorbidities [Ref]
  • Atopic disorders: allergic rhinitis, atopic dermatitis, chronic rhinosinusitis
  • GORD
  • Obesity / OSA 
  • Allergic bronchopulmonary aspergillosis (ABPA)

Cause/Pathogenesis
  • Multifactorial → Combination of genetic factors, Immune dysregulation (esp. type 2 inflammation), environmental exposures → Chronic airway inflammation & hyperresponsiveness → Asthma symptoms [REF]

Risk factors (developing asthma / persistent symptoms)
  • Genetic / Host-related 
    • Personal / family history of atopy 
    • Perinatal factors: preterm birth, low birth weight 
    • Overweight / Obesity
 
  • Environmental / Lifestyle Exposure
    • Smoking: Active/passive (including e-cigarettes)
    • Allergens (if sensitised): House dust mites, pets, pollens, moulds, foods
    • Other exposures: Air pollution, noxious chemicals, fungal spores 

Known Triggers (of asthma symptoms / exacerbations)
  • Viral URTIs 
  • Exercise 
  • Anxiety or strong emotions (i.e, laughter/crying) 
  • Weather changes 
  • Drugs 
    • Beta-blockers
    • Aspirin
    • NSAIDs
  • Occupational triggers → Occupational asthma 
    • Most commonly: Airborne allergic sensitisation to flour dust or Isocyanates

  • Acute exacerbations (asthma attacks)
    • Leading cause of asthma-related morbidity & mortality. [Ref] 
  • Respiratory complications
    • Acute: pneumomediastinum, pneumothorax, pneumonia, hypercapnic respiratory failure 
    • Chronic (esp poorly controlled asthma): airway remodelling →  fixed/persistent airflow limitation that is NOT fully reversible (spontaneously or with bronchodilator therapy)

  • Childhood-onset asthma (<18 yrs) 
    • Mild asthma (with infrequent wheezing) → often remits by adolescence 
    • Severe asthma (with frequent wheezing) → more likely to persist into adulthood 
    • Risk factors for persistence: atopy, parental asthma, later symptom onset, wheeze unrelated to viral infections, maternal/passive smoking
  • Adult-onset asthma (≥18 yrs)
    • Generally poorer prognosis than childhood-onset asthma [Ref] 

Investigation and Diagnosis Guidelines

Apart from a structured clinical history, specifically check for:
  • Cough / breathlessness / chest tightness / reported wheeze / noisy breathing
  • Any triggers that worsen symptoms
  • Personal / family history of asthma or allergic rhinitis

Possible examination findings:
  • Expiratory polyphonic wheeze
 

It is uncommon for a patient with stable asthma to present with a wheeze. It is more common when the patient is experiencing an exacerbation.

Even if the examination is normal, the person may still have asthma.

The choice of test and interpretation depends on the age group.
 

1 positive test result from ANY of the following is sufficient to diagnose asthma (on top of clinical suspicion).
 
  Object tests Positive test result
1st line FeNO
OR
Blood eosinophil count
FeNO ≥50 ppb
OR
↑ Blood eosinophil count  
2nd line Spirometry with BDRBronchodilator reversibility (preferred)
 
 Post-bronchodilator FEV1 improvement by:
  • ≥12% and ≥200mL from baseline OR 
  • ≥10% of predicted normal FEV1
Alternative: PEFPeak expiratory flow for 2 weeks (twice daily) PEF variability ≥20%
3rd line Bronchial challenge test Bronchial hyperresponsiveness

1 positive test result from ANY of the following is sufficient to diagnose asthma (on top of clinical suspicion).
 
  Object tests Positive test result
1st line FeNO FeNO ≥35 ppb
2nd line Spirometry with BDRBronchodilator reversibility (preferred)

 
 Post-bronchodilator FEV1 improvement by:
  • ≥12% from baseline OR
  • ≥10% of predicted normal FEV1
Alternative: PEFPeak expiratory flow for 2 weeks (twice daily) PEF variability ≥20%
3rd line Skin prick test for house dust mite

OR

Total IgE AND Blood eosinophil count
Sensitive to house dust mite OR

↑ total IgE AND ↑ Blood eosinophil count (>0.5)

**Exclude asthma if not sensitive to house dust mite OR total IgE not raised.

DO NOT perform object tests in <5 y/o, as it is difficult and there are no good reference standards.

If asthma is suspected clinically:
  • Initiate treatment (see below)
  • Review regularly
  • If symptoms persist when they reach 5 y/o → attempt objective tests

If a child is unable to perform objective tests when they are aged 5:
  • Re-attempt tests every 6 to 12 months
  • Refer for specialist assessment if the child's asthma is not responding to treatment

 

In children under 5 years old, it can be difficult to distinguish asthma from viral-induced wheeze, which many children outgrow. Definitive diagnosis is often deferred until the child is older and able to perform objective tests.

Asthma in young children may present less typically, with episodic cough and breathlessness, often triggered by viral infections and more noticeable at night.

Management Guidelines

It is important to recognise the definition of uncontrolled asthma, defined by ANY of the following:

  • Any exacerbation requiring oral steroids
  • Using reliever inhaler ≥3 days / week
  • Night time waking ≥1 day / week

 

Features of uncontrolled asthma should always prompt assessment for poor adherence, incorrect inhaler technique, or inadequate treatment.

Step up the treatment when asthma is not controlled:
 

Step 1 Start AIR therapy with (budesonide/formoterol inhaler as needed)
Step 2 Change to low-dose MART (low-dose ICS/formoterol inhaler)
Step 3 Change to moderate-dose MART (moderate-dose ICS/formoterol inhaler)
Step 4 Check FeNO and blood eosinophil count:
  • Either raised → refer to specialist
  • None raised → 8-12 weeks trial of adding LTRA or LAMA to moderate-dose MART
 
Subsequent steps
If asthma controlled → continue
If inadequate control → trial the other option
If not controlled after trials of both → refer to specialist

If patient is highly symptomatic or there are severe exacerbations upon first diagnosis → offer low-dose MART as step 1 (then consider stepping down afterwards).

 

At step 4 of the NICE asthma guidelines, FeNO and blood eosinophil count are used to identify persistent type 2 (eosinophilic) inflammation in resistant asthma. Elevated levels indicate likely benefit from intensified anti-inflammatory therapy (high-dose ICS) or biologics, while low levels suggest alternative causes of poor control (e.g., non-eosinophilic asthma, non-adherence, comorbidities).


Anti-inflammatory reliever (AIR) therapy
  • Reliever Therapy
    • Involves a combined ICS/formoterol inhaler used as needed  
    • Only licensed product: budesonide/formoterol inhaler 
Maintenance and reliever therapy (MART)
  • Reliever and maintenance therapy
  • Involves a combined ICS/formoterol inhaler used daily and as needed 
  
  

AIR and MART essentially involve the same type of inhaler (ICS/formoterol) but are used differently:

  • AIR to be used as needed (reliever inhaler)
  • MART to be used as needed and daily (reliever and maintenance inhaler).

SABA monotherapy is no longer recommended

If patient is using low-dose ICS + SABA as needed OR MART:
  • Step down to AIR therapy (low-dose ICS/formoterol combination inhaler as needed)

The table below gives summary guidance on how to transfer patients on other treatment pathways (including older guidance) to the current guidance.
 
 
Existing Treatment  New Recommendations
SABA as needed Switch to AIR as needed 
Maintenance therapy including low-dose ICS  Switch to low-dose MART 
Maintenance therapy including moderate-dose ICS  Switch to moderate-dose MART 
Maintenance therapy including high-dose ICS  Refer to respiratory specialist  

Consider the following for an 8-12 week trial:
  • Maintenance therapy: paediatric low-dose ICS twice daily AND 
  • Reliever therapy: SABA as needed

If symptoms resolve during the trial → consider stopping the treatment after 8-12 weeks

For more details, see below for NICE’s algorithm.

Pregnancy 
  • Adequate asthma control is vital in pregnancy; asthma review is recommended during early pregnancy and postpartum
  • The following can be safely taken during pregnancy: 
    • SABA and LABA 
    • ICS 
    • Oral theophyllines 
    • Oral corticosteroids (to treat exacerbations) 
  • NICE recommends that LTRA and LAMA should not be stopped if required to maintain adequate control

Breastfeeding 
  • Medications can be used as normal, in line with recommendations in the BNF 

After starting or adjusting medicines for asthma, review the response to treatment in 8 to 12 weeks

Check FeNO level when asthma is uncontrolled, ↑ FeNO may indicate:
  • Poor adherence to treatment, or
  • Need to increase dose of ICS

Complete control of asthma: (all must be present)
  • No daytime symptoms
  • No nighttime waking due to asthma
  • No reliever inhaler use
  • No asthma attacks
  • No limitations on activity
  • Normal lung function – FEV1 and/or PEF >80% predicted or best
  • Minimal side effects from treatment

Check:
  • Time off work / asthma due to asthma
  • Usage of reliever inhaler
  • Number of oral corticosteroid courses
  • Any presentation to emergency department / hospital admission due to asthma

Consider the following:
  • Asthma Control Questionnaire / Asthma Control Test / Childhood Asthma Control Test
  • FeNO – at review + before and after changing asthma therapy

DO NOT use regular PEF monitoring

Suspect occupational asthma in:
  • Adult-onset asthma
  • Poorly controlled established asthma
  • Reappearance of childhood asthma

Screen occupational asthma with:
  • Are symptoms the same / better / worse on days away from work
  • Are symptoms the same / better / worse on time away from work, longer than usual breaks, at weekends, or between shifts

If occupational asthma is suspected → refer to occupational asthma specialist for serial PEFPeak expiratory flow.

References

Author: Adams Lau, Maansi Shah
Reviewer: Konstantinos Mantonanakis 
Last Edited: 12/05/25