Pulmonary
Dyspnea and cough drive most pulmonary vignettes. The trick: distinguish obstructive (asthma, COPD) from restrictive (fibrosis, neuromuscular) from vascular (PE, pulmonary HTN) from infectious (pneumonia, TB).
Chief complaints
Vignettes enter through one of these doors. Each complaint lays out the full differential, marks the can't-miss diagnoses, and tells you the next right action for each.
Dyspnea (pulmonary)
Acute vs chronic is the first fork. Then hypoxic vs not.
Acute: PE, pneumothorax, pulmonary edema, asthma or COPD exacerbation, pneumonia, anaphylaxis, DKA. Chronic: COPD, asthma, ILD, pulmonary HTN, HF, obesity hypoventilation, anemia. The workup pattern: SpO2, CXR, ABG, BNP, D-dimer as indicated.
| Diagnosis | Key features / clues | Next step |
|---|---|---|
| Pulmonary embolism | Pleuritic pain, tachycardia, hypoxia, unilateral leg swelling. Risk factors: immobility, malignancy, OCP, pregnancy, prior VTE. | Wells → D-dimer if low, CT-PA if intermediate/high · anticoagulate |
| Tension pneumothorax | Sudden, unilateral absent breath sounds, tracheal deviation away, hypotension. | Needle decompression 2nd ICS MCL before imaging |
| Cardiogenic pulmonary edema | Orthopnea, bilateral crackles, S3, JVD, edema. | Furosemide · O2 · BiPAP · nitrates if hypertensive |
| Anaphylaxis | Rapid onset, stridor, wheezing, urticaria, hypotension after exposure. | IM epinephrine 0.3–0.5 mg lateral thigh · repeat Q5 min PRN |
| Asthma exacerbation | Wheezing, prolonged expiration, accessory muscle use, prior asthma history. | SABA + ipratropium nebs · systemic steroids · magnesium if severe · intubate if exhausted or silent chest |
| COPD exacerbation | Increased dyspnea, cough, sputum purulence in known COPD. | SABA/SAMA · steroids (prednisone 40 mg × 5 days) · antibiotics if ≥ 2 cardinal features |
| Pneumonia | Fever, productive cough, focal crackles, consolidation on CXR. | CURB-65 or PSI for disposition · empiric antibiotics |
Cough
Duration splits the differential: acute (< 3 wk), subacute (3–8 wk), chronic (> 8 wk).
Acute: URI, bronchitis, pneumonia, PE, heart failure. Subacute: post-infectious, pertussis. Chronic: the big three are upper airway cough syndrome (postnasal drip), asthma, and GERD. Also consider ACEi, smoking, bronchiectasis, TB, lung cancer, and ILD.
| Diagnosis | Key features / clues | Next step |
|---|---|---|
| Community-acquired pneumonia | Fever, productive cough, consolidation on CXR. | CURB-65 · outpatient: amoxicillin or doxycycline · inpatient: ceftriaxone + azithromycin |
| Lung cancer | Smoker > 20 pack-years, chronic cough, hemoptysis, weight loss. | CXR → CT chest · biopsy |
| Tuberculosis | Chronic cough, hemoptysis, night sweats, weight loss, TB exposure or endemic country. | AFB smear × 3, sputum culture, NAAT · CXR (upper lobe cavitary) · isolate |
| Upper airway cough syndrome | Postnasal drip, throat clearing, cobblestoning. | First-generation antihistamine trial |
| Asthma / cough-variant | Nocturnal cough, wheezing, atopy, diurnal variation. | Spirometry with bronchodilator response · methacholine challenge if normal |
| GERD | Postprandial, nocturnal, heartburn may or may not be present. | Empiric PPI × 8 weeks |
| ACE inhibitor cough | Dry cough developing weeks to months after starting ACEi. | Switch to ARB |
Hemoptysis
Massive (> 600 mL/24h) kills by asphyxiation, not exsanguination. Position bleeding side down.
The big differential: bronchitis, bronchiectasis, TB, lung cancer, PE with infarction, vasculitis (GPA, anti-GBM), pulmonary edema (pink frothy). Always confirm it's truly pulmonary (not GI or nasopharyngeal).
| Diagnosis | Key features / clues | Next step |
|---|---|---|
| Massive hemoptysis | > 600 mL/24h or hemodynamically unstable. | Protect airway (intubate if needed) · position bleeding side DOWN · bronchoscopy · embolization |
| Lung cancer | Smoker, weight loss, chronic cough. | CT chest · biopsy |
| Tuberculosis | Night sweats, weight loss, exposure. | AFB × 3 · isolate |
| PE with infarction | Pleuritic pain, VTE risk factors, often small-volume hemoptysis. | CT-PA |
| Bronchiectasis | Chronic purulent sputum, recurrent infections, clubbing, cystic changes on CT. | CT chest · sputum culture · antibiotics |
| Goodpasture / GPA | Hemoptysis + hematuria + pulmonary-renal syndrome. | Anti-GBM, ANCA · renal biopsy · plasmapheresis + steroids + cyclophosphamide |
Disease deep dives
Once you've identified the likely diagnosis from the chief complaint, these pages give you the presentation, workup, management, and exam pearls in depth.
Asthma
Reversible airway obstruction. Step therapy from SABA alone to biologics. Exacerbation management is the exam's favorite.
Episodic wheeze, cough, dyspnea, chest tightness. Triggers: allergens, cold, exercise, URI, aspirin. Atopic history common.
- Spirometry. FEV1/FVC < 0.7 with ≥ 12% improvement after bronchodilator is diagnostic.
- Methacholine challenge. If spirometry is normal but clinical suspicion remains. > 20% FEV1 drop is positive.
- Peak flow. For monitoring, not diagnosis.
- FeNO. Elevated in eosinophilic asthma, useful to identify biologic candidates.
- Step 1, intermittent. PRN ICS-formoterol (preferred, GINA) or SABA PRN.
- Step 2, mild persistent. Low-dose ICS + PRN SABA, OR ICS-formoterol as needed.
- Steps 3–4, moderate. Low-to-medium dose ICS + LABA, as maintenance and reliever therapy (MART).
- Step 5, severe. High-dose ICS-LABA + tiotropium or biologic. Biologic choice by phenotype: anti-IgE (omalizumab), anti-IL-5 (mepolizumab, benralizumab), anti-IL-4R (dupilumab).
- Exacerbation. Albuterol + ipratropium nebs Q20 min × 3, oral or IV steroids, O2 to SpO2 ≥ 92%. IV magnesium if severe. Intubate for silent chest, altered mental status, rising CO2.
COPD
Irreversible obstruction from smoking (usually). The workhorse: staging, exacerbation, and when to give oxygen.
Chronic cough, sputum, dyspnea. Smoker > 20 pack-years. Barrel chest, pursed-lip breathing, decreased breath sounds, prolonged expiration.
- Spirometry. Post-bronchodilator FEV1/FVC < 0.7 is diagnostic.
- GOLD staging. GOLD 1 (FEV1 ≥ 80%), 2 (50–79%), 3 (30–49%), 4 (< 30%). Symptoms and exacerbation history now drive therapy (ABE groups).
- Alpha-1 antitrypsin. If young, non-smoker, or basilar emphysema.
- All patients. Smoking cessation (only intervention that slows progression), vaccines (flu, pneumococcal, COVID, RSV, Tdap), pulmonary rehab.
- Group A (low sx, low risk). Bronchodilator (LABA or LAMA).
- Group B (high sx, low risk). LABA + LAMA.
- Group E (high exacerbation). LABA + LAMA ± ICS (ICS if eosinophils ≥ 300 or asthma overlap).
- Long-term oxygen. PaO2 ≤ 55 or SaO2 ≤ 88% at rest, OR ≤ 59/89 with cor pulmonale or polycythemia. The only intervention besides cessation that improves survival.
- Exacerbation. Short-acting bronchodilators, oral or IV steroids (prednisone 40 mg × 5 days), antibiotics if ≥ 2 of increased dyspnea, sputum volume, or purulence. BiPAP if pH < 7.35 and PCO2 > 45.
Pulmonary Embolism
Clot in the pulmonary artery. Diagnosis is about pretest probability. Treatment tiers by hemodynamic stability.
Dyspnea, pleuritic pain, tachycardia, hypoxia. Risk factors: immobility, malignancy, pregnancy, OCPs, prior VTE, inherited thrombophilia, recent surgery.
- Wells score. PE likely (> 4) vs unlikely (≤ 4). Drives next step.
- D-dimer. Only useful if Wells ≤ 4 and no other high-risk features. Age-adjusted cutoff: age × 10 in patients > 50 years.
- CT-PA. First-line imaging. Sensitive and specific.
- V/Q scan. If CT contrast is contraindicated (pregnancy, severe renal dysfunction, contrast anaphylaxis).
- Echo. For risk stratification. RV strain predicts mortality.
- Massive PE (hemodynamic instability). Systemic thrombolysis (tPA 100 mg over 2 hours). Surgical or catheter embolectomy if thrombolytics are contraindicated.
- Submassive (RV dysfunction, elevated troponin, stable BP). Heparin. Consider catheter-directed thrombolysis.
- Low-risk PE. DOAC (apixaban or rivaroxaban) as outpatient if feasible.
- Duration. Provoked by transient factor: 3 months. Unprovoked or malignancy: indefinite. Consider thrombophilia workup only if it would change management.
- IVC filter. Only if anticoagulation is contraindicated or there is recurrent PE despite adequate anticoagulation.
Pneumonia
CAP vs HAP vs VAP vs aspiration. Pathogen and severity drive antibiotic choice and disposition.
Fever, productive cough, pleuritic pain, dyspnea. Exam: focal crackles, bronchial breath sounds, egophony, dullness to percussion. CXR shows infiltrate.
- CXR. Lobar (bacterial, Strep pneumo), interstitial (viral, atypical), cavitary (TB, Staph, anaerobes, fungal).
- CURB-65. Confusion, Urea > 20, RR ≥ 30, BP < 90/60, age ≥ 65. Outpatient 0–1, inpatient 2, ICU ≥ 3.
- Blood cultures. Before antibiotics if hospitalized.
- Sputum Gram stain and culture. If severe or suspected resistant pathogen.
- Urinary antigen. Strep pneumo, Legionella (if severe).
- CAP outpatient, healthy. Amoxicillin, doxycycline, or macrolide (resistance limits macrolides).
- CAP outpatient, comorbidities. Amox-clav or cefpodoxime PLUS macrolide or doxycycline, OR respiratory fluoroquinolone (levofloxacin, moxifloxacin).
- CAP inpatient, non-ICU. Ceftriaxone + azithromycin, OR respiratory fluoroquinolone.
- CAP ICU. Ceftriaxone + azithromycin. Add anti-MRSA and anti-pseudomonal coverage if risk factors are present.
- HAP/VAP. Broad-spectrum: pip-tazo or cefepime + vancomycin. Tailor to local antibiogram.
- Aspiration. Ampicillin-sulbactam or clindamycin (anaerobic coverage). RLL if upright; posterior segment of upper lobe or superior segment of lower lobe if supine.