Key Points
            - Use the highest‑yield diagnostic test early; do not let testing delay time‑critical therapy.
- Set objective targets and reassess frequently.
- Plan definitive source control or disease‑specific therapy when indicated; document follow‑up and patient education.
                                        Algorithm
            - Controlled O2 to SpO2 88–92% and bronchodilators; add steroids.
- Add antibiotics if criteria met; evaluate for NIV based on gas exchange.
- Address triggers and discharge plan (inhalers, action plan, smoking cessation).
                                        Clinical Synopsis & Reasoning
            Treat acute COPD exacerbations with short‑acting bronchodilators (SABA/SAMA), systemic corticosteroids (e.g., prednisone 40 mg daily ×5 days), and antibiotics when increased sputum purulence/volume and dyspnea are present. Use controlled O2 (SpO2 88–92%) and early NIV for hypercapnic respiratory failure.
                                        Treatment Strategy & Disposition
            Stabilize ABCs. Initiate guideline‑concordant first‑line therapy with precise dosing and continuous monitoring. Escalate to advanced/procedural interventions based on explicit failure criteria. Define ICU, step‑down, and ward disposition triggers; involve specialty teams early.
                                        Epidemiology / Risk Factors
            - Risk varies by comorbidity and precipitants; see citations for condition‑specific data.
                                        Investigations
            
              
                | Test | Role / Rationale | Typical Findings | Notes | 
|---|
                
                  | ABG/VBG and pulse oximetry | Assessment | Hypercapnia and hypoxemia | Guide NIV/O2 | 
| CXR and viral/bacterial testing as indicated | Etiology | Exclude pneumonia/PE/COVID | — | 
| ECG, BMP (K+, Mg2+) | Safety | β‑agonist effects; diuretic use | — | 
                
              
             
                                        High-Risk & Disposition Triggers
            
              
                | Trigger | Why it matters | Action | 
|---|
                
                  | Severe dyspnea, RR >30, or accessory muscle use | Impending failure | NIV early; consider ICU | 
| pH <7.25 or rising PaCO2 | Ventilatory failure | Escalate NIV/intubation | 
| Refractory hypoxemia or arrhythmias | Instability | Intubate; ICU | 
| Pneumonia, CHF, or PE trigger | Worse outcomes | Broaden workup/treatment | 
| Frequent exacerbations or poor support | Safety | Admit; arrange follow-up | 
                
              
             
                                        Pharmacology
            
              
                | Medication/Intervention | Mechanism | Onset | Role in Therapy | Limitations | 
|---|
                
                  | Albuterol + Ipratropium nebulized q4–6 h | Bronchodilation | Minutes | First‑line | — | 
| Prednisone 40 mg PO daily ×5 days (or IV methylprednisolone) | Anti‑inflammatory | Hours‑days | Short course effective | — | 
| Azithromycin or Amoxicillin‑clavulanate (selected) | Antibiotics | Days | If purulence + symptoms | Local resistance patterns | 
| NIV (BiPAP) if pH ≤7.35 or PaCO2 high | Ventilatory support | Minutes | Reduces intubation/mortality | Contraindications apply | 
                
              
             
                                        Prognosis / Complications
            - Outcome depends on timeliness of diagnosis and definitive therapy; monitor for complications.
                                        Patient Education / Counseling
            - Provide red‑flag education, adherence guidance, and explicit return precautions; arrange timely specialty follow‑up.
                  
        
                  References
                      - GOLD COPD report — Link