Acute Management of COPD Exacerbation
Immediately initiate combined short-acting bronchodilators (salbutamol 2.5–5 mg plus ipratropium 0.25–0.5 mg via nebulizer every 4–6 hours), oral prednisone 40 mg daily for exactly 5 days, controlled oxygen targeting SpO₂ 88–92%, and antibiotics for 5–7 days when sputum purulence is present with either increased dyspnea or sputum volume. 1
Immediate Bronchodilator Therapy
- Administer combined short-acting β₂-agonist (salbutamol 2.5–5 mg) with short-acting anticholinergic (ipratropium 0.25–0.5 mg) via nebulizer or metered-dose inhaler with spacer every 4–6 hours during the acute phase. 1
- This combination provides superior bronchodilation lasting 4–6 hours compared to either agent alone. 1
- For sicker hospitalized patients, nebulizers are preferred because they are easier to use and don't require coordination of 20+ inhalations needed to match nebulizer efficacy. 1
- Power nebulizers with compressed air, not oxygen, when hypercapnia is suspected, while delivering supplemental oxygen via low-flow nasal cannula (1–2 L/min) concurrently. 1
- Continue repeat dosing every 4–6 hours for 24–48 hours until clinical improvement occurs. 1
Systemic Corticosteroid Protocol
- Give oral prednisone 30–40 mg once daily for exactly 5 days starting immediately—this short course is as effective as 14-day regimens while reducing cumulative steroid exposure by more than 50%. 1
- Oral administration is equally effective to intravenous and should be the default route unless the patient cannot tolerate oral intake. 1
- Systemic corticosteroids improve lung function, oxygenation, shorten recovery time and hospitalization duration, and reduce treatment failure by over 50%. 1
- Do not continue corticosteroids beyond 5–7 days after the acute episode unless there is a separate indication for long-term treatment. 1
- Corticosteroids prevent hospitalization for subsequent exacerbations within the first 30 days but provide no benefit beyond this window. 1
Antibiotic Therapy Criteria and Selection
- Prescribe antibiotics for 5–7 days when the patient has increased sputum purulence plus either increased dyspnea or increased sputum volume (two of three cardinal symptoms with purulence being one). 1
- Antibiotic therapy reduces short-term mortality by approximately 77%, treatment failure by 53%, and sputum purulence by 44%. 1
- First-line antibiotic choices (based on local resistance patterns): 1
- Amoxicillin-clavulanate 875/125 mg orally twice daily
- Doxycycline 100 mg orally twice daily
- Azithromycin 500 mg day 1, then 250 mg daily for 4 days
- The most common causative organisms are Streptococcus pneumoniae, Haemophilus influenzae, and Moraxella catarrhalis. 1
- For the FDA-approved azithromycin regimen in COPD exacerbations, clinical cure rates at Day 21–24 were 85% with 3 days of azithromycin (500 mg once daily). 2
Controlled Oxygen Therapy
- Target oxygen saturation of 88–92% using controlled oxygen delivery (24–28% Venturi mask or 1–2 L/min nasal cannula) to correct life-threatening hypoxemia while minimizing CO₂ retention. 1
- Higher oxygen concentrations can aggravate hypercapnic respiratory failure and increase mortality in COPD patients. 1
- Obtain arterial blood gas within 60 minutes of initiating oxygen to assess for worsening hypercapnia (PaCO₂ > 45 mmHg) or acidosis (pH < 7.35). 1
- If initial ABG shows normal pH and PaCO₂, the SpO₂ target may be increased to 94–98% unless the patient has prior history of hypercapnic failure requiring NIV or usual stable saturation is < 94%. 1
- Repeat ABG at 30–60 minutes (or sooner if clinical deterioration) to detect rising PaCO₂ or falling pH. 1
Non-Invasive Ventilation for Respiratory Failure
- Initiate NIV immediately as first-line therapy when acute hypercapnic respiratory failure (PaCO₂ > 45 mmHg) with acidosis (pH < 7.35) persists for more than 30 minutes after standard medical management. 1
- NIV improves gas exchange, reduces work of breathing, decreases intubation rates by approximately 50%, shortens hospitalization duration, and improves survival. 1
- Success rates in appropriately selected patients are 80–85%. 1
- If pH falls below 7.26 with rising PaCO₂, prepare for immediate NIV. 1
Hospitalization Criteria
Admit to hospital or evaluate in emergency department for any of the following: 1
- Marked increase in dyspnea unresponsive to initial outpatient therapy
- Respiratory rate > 30 breaths/min
- Inability to eat or sleep because of respiratory symptoms
- New or worsening hypoxemia (SpO₂ < 90% on room air)
- New or worsening hypercapnia (PaCO₂ > 45 mmHg)
- Altered mental status or loss of alertness
- Persistent rhonchi after initial treatment requiring continued nebulization
- High-risk comorbidities (pneumonia, cardiac arrhythmia, heart failure, diabetes)
- Inability to care for oneself at home
Medications to Avoid
- Do not use intravenous methylxanthines (theophylline or aminophylline)—they increase side effects without added clinical benefit. 1
- Avoid cough suppressants during acute exacerbations, as productive cough is a necessary clearance mechanism. 3
- Do not use chest physiotherapy in acute COPD exacerbations—there is no evidence of benefit. 1
Discharge Planning and Follow-Up
- Schedule pulmonary rehabilitation within 3 weeks after discharge to reduce hospital readmissions and improve quality of life. 1
- Do not initiate pulmonary rehabilitation during hospitalization, as this increases mortality; wait until post-discharge. 1
- Continue or optimize long-acting bronchodilator therapy (LAMA, LABA, or combinations) before hospital discharge. 1
- Do not step down from triple therapy (LAMA/LABA/ICS) during or immediately after an exacerbation, as ICS withdrawal increases recurrent exacerbation risk. 1
- Verify proper inhaler technique at every visit, as improper use is a common cause of treatment failure. 1
- Provide intensive smoking cessation counseling with nicotine replacement therapy and behavioral intervention at every visit for current smokers. 1
Common Pitfalls to Avoid
- Never power nebulizers with oxygen in hypercapnic patients—use compressed air and provide supplemental oxygen separately via nasal cannula. 1
- Do not administer high-flow oxygen (> 28% FiO₂ or > 4 L/min) without arterial blood gas monitoring, as this can worsen hypercapnic respiratory failure and increase mortality. 1
- Do not delay NIV in patients with acute hypercapnic respiratory failure—immediate initiation is critical. 1
- Do not extend systemic corticosteroids beyond 5–7 days without a separate indication to avoid unnecessary steroid-related adverse effects. 1
- Do not reflexively prescribe antibiotics without assessing for the presence of at least two cardinal symptoms with purulence being one. 1