Dd for copd
| Feature | COPD | Asthma |
|---|---|---|
| Onset | Usually >40 yrs, insidious | Often childhood/young adult |
| Smoking history | Almost always present | Not required |
| Airflow obstruction | Incompletely reversible | Largely reversible (≥12% & 200 mL post-bronchodilator) |
| Symptoms | Persistent, progressive | Variable, episodic |
| Atopy / family history | Uncommon | Common |
| Eosinophilia | Uncommon | Common |
| DLCO | Reduced (especially emphysema) | Normal |
| Pathology | CD8+ T cells, neutrophils; mild basement membrane thickening | CD4+ T cells, eosinophils; marked basement membrane thickening (~20% thicker than COPD) |
Note: Asthma-COPD Overlap (ACO) exists — many patients diagnosed with asthma actually have COPD or a mixed picture. (Tintinalli's Emergency Medicine)
| Condition | Distinguishing Features |
|---|---|
| Pleural effusion | Dullness to percussion, absent breath sounds; CXR/US confirms |
| Malignancy | Unexplained weight loss, hemoptysis, new mass on imaging; lung cancer risk increased with COPD |
| Cardiac arrhythmia | Palpitations, ECG diagnosis; COPD increases risk of AF |
| Pericardial effusion | Muffled heart sounds, JVD, hypotension; echocardiography |
| Metabolic acidosis | Tachypnea + dyspnea without primary pulmonary cause; ABG shows ↓pH, ↓HCO₃⁻, compensatory hyperventilation |
| α₁-Antitrypsin deficiency | COPD onset <45 yrs or non-smoker; panacinar emphysema, basilar predominance; measure serum AAT |
| ILD / Pulmonary fibrosis | Restrictive pattern (↓FVC, normal FEV1/FVC), bibasilar fine crackles ("velcro"), honeycombing on HRCT |
| Sarcoidosis | Hilar adenopathy, non-caseating granulomas; biopsy |
| Tracheobronchopathia osteoplastica | Bony nodules in airways on bronchoscopy/CT; rare |