Diagnosing Asthma in Children Aged 5-16 Years
Do not diagnose asthma based on symptoms alone—the European Respiratory Society strongly recommends using a combination of objective tests including spirometry, bronchodilator reversibility testing, and fractional exhaled nitric oxide (FeNO) as first-line diagnostic tools, requiring at least two abnormal test results to confirm the diagnosis. 1, 2
Why Objective Testing is Essential
Misdiagnosis of asthma in children is alarmingly common, with over-diagnosis leading to unnecessary corticosteroid treatment and associated side effects, while under-diagnosis results in preventable morbidity, poor quality of life, and increased mortality. 1 Respiratory symptoms in children are frequently nonspecific and often represent viral respiratory tract infections rather than asthma. 1
Step 1: Clinical Assessment (But Don't Stop Here)
Key Symptoms to Document
- Wheeze is the most diagnostically useful symptom, with sensitivity of 55-86% and specificity of 64-90% for asthma. 2
- Cough and breathing difficulty are nonspecific and should never be used alone to diagnose asthma. 2
- Document symptom patterns including frequency, triggers, and response to previous treatments. 2
Critical Pitfall
Physicians correctly diagnose asthma based on clinical examination alone only 63-74% of the time, and symptoms correlate poorly with actual airway obstruction in one-third to one-half of patients. 3 This is why you must proceed to objective testing. 1
Step 2: First-Line Objective Testing (All Three Tests)
Spirometry
- Measure FEV1 and FEV1/FVC ratio. 2
- Abnormal results: FEV1 or FEV1/FVC less than lower limit of normal (LLN) and/or <80% predicted. 2
- Important: Normal spirometry does NOT exclude asthma, and abnormal spirometry alone does NOT confirm it. 2
Bronchodilator Reversibility (BDR) Testing
- Perform BDR testing even if spirometry is normal when clinical suspicion is high. 2
- A positive BDR indicates reversible airflow obstruction characteristic of asthma. 2
Fractional Exhaled Nitric Oxide (FeNO)
- Perform FeNO testing before spirometry. 2
- Cut-off: ≥25 ppb is considered elevated. 2
- Elevated FeNO suggests eosinophilic airway inflammation. 2
Step 3: Diagnostic Decision-Making
Confirm Asthma Diagnosis When:
At least two objective test results are abnormal, such as:
- Abnormal spirometry PLUS positive BDR, OR
- Abnormal spirometry PLUS elevated FeNO, OR
- Positive BDR PLUS elevated FeNO 2
When Diagnosis Remains Unclear:
- Consider peak expiratory flow rate (PEFR) variability with 2 weeks of twice-daily measurements; variability >12% suggests asthma. 2
- Use watchful waiting when initial tests are normal but clinical suspicion remains high, and repeat testing when the child is symptomatic. 2
Critical Pitfalls to Avoid
Never Diagnose Based On:
- Symptoms alone—this results in misdiagnosis in many children. 1, 2
- A single abnormal objective test—at least two abnormal results are required. 1
- Treatment response alone—do not diagnose asthma based solely on improvement after a trial of preventer medication. 2
Consider Alternative Diagnoses:
Before confirming asthma, rule out conditions that mimic it, including foreign body aspiration, vocal cord dysfunction, vascular rings, laryngotracheomalacia, enlarged lymph nodes, or tumors. 4 In younger children, consider cystic fibrosis and other congenital conditions. 5, 6
Age-Specific Considerations
These evidence-based recommendations specifically apply to children aged 5-16 years. 1, 2 Diagnosis in children under 5 years is particularly challenging due to difficulty obtaining objective lung function measurements and requires a different approach. 4, 6
The Bottom Line
The diagnostic algorithm requires:
- Clinical assessment documenting wheeze and symptom patterns
- All three first-line objective tests: spirometry, BDR, and FeNO
- At least two abnormal test results to confirm diagnosis
- Additional testing (PEFR variability) or watchful waiting if diagnosis remains unclear 2
This systematic approach prevents both over-diagnosis (avoiding unnecessary corticosteroid exposure) and under-diagnosis (preventing morbidity and mortality), directly improving quality of life outcomes. 1