Diagnosis of COPD
Diagnostic Criteria
COPD is diagnosed when post-bronchodilator spirometry demonstrates a FEV1/FVC ratio less than 0.70, confirming persistent airflow limitation that is not fully reversible. 1, 2
When to Suspect COPD
Consider COPD in any patient meeting these criteria:
- Age 40 years or older with chronic respiratory symptoms (dyspnea, chronic cough, sputum production, or recurrent respiratory infections) 1, 2
- Significant exposure history: tobacco smoking (particularly >40 pack-years), occupational dusts, or indoor/outdoor air pollution 1, 3
- Progressive dyspnea that worsens with exercise and persists throughout the day 2
- Wheezing during tidal breathing or recurrent lower respiratory tract infections, especially in winter 2
Clinical Predictors with High Diagnostic Value
The strongest clinical predictors that essentially confirm airflow obstruction include:
- Smoking history >55 pack-years combined with wheezing on auscultation and patient-reported wheezing (likelihood ratio 156) 4
- Combination of peak flow <350 L/min, diminished breath sounds, and smoking history ≥30 pack-years 3
- Smoking history >40 pack-years alone is the single best predictor 4, 3
Spirometry Requirements
Spirometry is mandatory to confirm the diagnosis and cannot be replaced by clinical assessment alone. 1, 2, 5
- Perform post-bronchodilator spirometry in all suspected cases 1, 2
- Diagnostic threshold: FEV1/FVC <0.70 after bronchodilator administration confirms COPD 1, 2, 4
- If initial FEV1/FVC is borderline (0.6-0.8), repeat spirometry to account for day-to-day variability 4
- Important caveat: The fixed ratio of 0.70 may overdiagnose COPD in patients >60 years and underdiagnose in those <45 years 4
Severity Classification
Classify COPD severity based on post-bronchodilator FEV1 percentage predicted (GOLD staging):
- Mild (GOLD 1): FEV1/FVC <0.7 and FEV1 ≥80% predicted 1, 2
- Moderate (GOLD 2): FEV1/FVC <0.7 and FEV1 50-80% predicted 1, 2
- Severe (GOLD 3): FEV1/FVC <0.7 and FEV1 30-50% predicted 1, 2
- Very Severe (GOLD 4): FEV1/FVC <0.7 and FEV1 <30% predicted 1, 2
Multidimensional Assessment for Treatment Planning
Beyond spirometry, assess these dimensions:
- Symptom burden: Use the modified Medical Research Council (mMRC) dyspnea scale (grades 0-4) or COPD Assessment Test 2, 6
- Exacerbation history: History of prior treated events is the best predictor of frequent exacerbations (≥2 per year) 2
- Hospitalization history: Prior hospitalization for COPD exacerbation indicates poor prognosis and increased mortality risk 2
- Comorbidities: Screen for lung cancer, cardiovascular disease, and other conditions 2
Physical Examination Findings
- Normal physical examination is common in early COPD 7
- As disease progresses, signs become apparent: measure respiratory rate, weight, height, and BMI in all patients 7
- Advanced disease shows nearly pathognomonic signs 7
Differential Diagnosis
Distinguish COPD from asthma:
- Asthma: Variable airflow limitation with marked spirometric improvement after bronchodilators or glucocorticosteroids, often associated with atopy 2
- COPD: Persistent airflow limitation (post-bronchodilator FEV1/FVC <0.70), typically develops after age 40 with significant smoking history 2
Indications for Specialist Referral
Refer to pulmonology for:
- Suspected severe COPD (FEV1 <30% predicted) 4
- Onset of cor pulmonale or assessment for oxygen therapy 4
- Age <40 years (to identify α1-antitrypsin deficiency) 4
- Uncertain diagnosis or symptoms disproportionate to lung function 4
- Bullous lung disease or frequent infections (to exclude bronchiectasis) 4
Common Diagnostic Pitfalls
- Do not rely on clinical assessment alone—spirometry is essential and cannot be bypassed 1, 5
- Avoid routine periodic spirometry after diagnosis—there is no evidence it improves outcomes or guides therapy modification; base treatment adjustments on symptoms, exacerbation frequency, and functional status 4
- Do not use spirometry to "motivate" smoking cessation—this strategy is ineffective 4
- COPD often develops decades before symptoms appear, with impaired lung growth during childhood/adolescence potentially contributing 1