COPD Exacerbation Treatment
For acute COPD exacerbations, immediately initiate short-acting beta-2 agonists (salbutamol 2.5-5 mg) combined with short-acting anticholinergics (ipratropium 0.25-0.5 mg) via nebulizer, systemic corticosteroids (prednisone 40 mg daily for exactly 5 days), and antibiotics (5-7 days) when the patient has increased sputum purulence plus either increased dyspnea or increased sputum volume. 1, 2
Immediate Bronchodilator Therapy
Combination therapy is superior to monotherapy for acute exacerbations:
- Administer salbutamol 2.5-5 mg plus ipratropium 0.25-0.5 mg via nebulizer immediately upon presentation 1, 2
- Nebulizers are preferred over metered-dose inhalers in hospitalized patients because they are easier to use and don't require coordination of 20+ inhalations needed to match nebulizer efficacy 2
- Repeat dosing every 4-6 hours during the acute phase (typically 24-48 hours) until clinical improvement occurs 1, 2
- The combination provides superior bronchodilation lasting 4-6 hours compared to either agent alone 1, 2
Important caveat: While ipratropium is widely used, the FDA label notes that ipratropium as a single agent has not been adequately studied for acute COPD exacerbations, and combination with beta-agonists has not been shown more effective than either drug alone in some studies 3. However, guideline consensus strongly supports combination therapy based on clinical experience and mechanistic rationale 1, 2.
Systemic Corticosteroid Protocol
The evidence for corticosteroids is robust and the dosing is specific:
- Give prednisone 40 mg orally once daily for exactly 5 days 1, 2
- Oral administration is equally effective to intravenous and should be the default route unless the patient cannot tolerate oral intake 1, 2
- A 5-day course is equally effective as 14-day courses but reduces cumulative steroid exposure by over 50% 2
- Corticosteroids improve lung function, oxygenation, shorten recovery time by 1-2 days, reduce treatment failure by over 50%, and prevent hospitalization for subsequent exacerbations within the first 30 days 1, 2
- Do not continue beyond 5-7 days after the acute episode unless there is a separate indication 1, 2
Antibiotic Therapy Decision Algorithm
Antibiotics should be prescribed based on specific clinical criteria:
- Give antibiotics for 5-7 days when the patient has all three cardinal symptoms (increased dyspnea, increased sputum volume, increased sputum purulence) OR two cardinal symptoms with increased sputum purulence as one of them 1, 2
- Antibiotics reduce short-term mortality by 77%, treatment failure by 53%, and sputum purulence by 44% 2
First-line antibiotic choices based on local resistance patterns: 1, 2
- Amoxicillin or amoxicillin/clavulanic acid
- Tetracycline derivatives (doxycycline)
- Macrolides (azithromycin) - particularly for patients with penicillin allergy
Common organisms: Streptococcus pneumoniae, Haemophilus influenzae, Moraxella catarrhalis, and viruses 2
The FDA label for azithromycin shows clinical success rates of 87-88% for acute bacterial exacerbations of chronic bronchitis when given 500 mg once daily for 3 days 4.
Oxygen Therapy Protocol
Controlled oxygen delivery is critical to avoid CO2 retention:
- Target oxygen saturation of 88-92% (not 94-98% as in other conditions) using controlled oxygen delivery 2
- Initial FiO2 should not exceed 28% via Venturi mask or 2 L/min via nasal cannulae until arterial blood gases are known 1
- Mandatory arterial blood gas measurement within 1 hour of initiating oxygen to assess for worsening hypercapnia and acidosis 1, 2
- The aim is to achieve PaO2 of at least 60 mmHg (8 kPa) or SpO2 ≥90% without causing respiratory acidosis 1
Respiratory Support for Severe Exacerbations
Noninvasive ventilation (NIV) should be initiated immediately for specific indications:
- Acute hypercapnic respiratory failure (pH <7.35 with elevated PaCO2) 1, 2
- Persistent hypoxemia despite oxygen therapy 2
- Severe dyspnea with respiratory muscle fatigue or use of accessory muscles 2
NIV benefits are substantial: 1, 2
- Improves gas exchange and reduces work of breathing
- Decreases intubation rates by approximately 50%
- Shortens hospitalization duration by 2-3 days
- Improves survival compared to standard medical therapy alone
NIV is less likely to succeed in: 2
- Confused or agitated patients
- Patients with large volumes of secretions
- Hemodynamic instability
Hospitalization Criteria
Admit patients with any of the following: 2
- Marked increase in symptom intensity requiring nebulization
- Severe underlying COPD (FEV1 <30% predicted)
- New physical signs (cyanosis, peripheral edema, altered mental status)
- Failure to respond to initial outpatient management within 24-48 hours
- Acute respiratory failure (pH <7.35, PaCO2 >45 mmHg with worsening)
- Significant comorbidities (heart failure, diabetes, renal failure)
- Frequent exacerbations (≥3 in past year)
- Older age (>65 years) with inability to care for self at home
- Diagnostic uncertainty
Discharge Planning and Prevention
Before discharge, implement the following: 2
- Continue or optimize long-acting bronchodilator therapy (LAMA/LABA or triple therapy if already on it) 2
- Do not step down from triple therapy during or immediately after exacerbation, as ICS withdrawal increases recurrent exacerbation risk 2
- Schedule pulmonary rehabilitation within 3 weeks after discharge (not during hospitalization, as this increases mortality) 2
- Provide intensive smoking cessation counseling with nicotine replacement therapy for current smokers 2
- Review and correct inhaler technique 2
- Schedule follow-up within 3-7 days to assess response 2
Common Pitfalls to Avoid
- Never use methylxanthines (theophylline) in acute exacerbations due to increased side effects without added benefit 1, 2
- Never continue systemic corticosteroids beyond 5-7 days for a single exacerbation 1, 2
- Never target normal oxygen saturations (94-98%) in COPD patients, as this increases risk of CO2 retention 1, 2
- Never delay NIV in patients with acute hypercapnic respiratory failure 2
- Never use chest physiotherapy in acute exacerbations, as there is no evidence of benefit 2