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Our approach to empiric antibacterial treatment of COPD exacerbations in outpatients*

Our approach to empiric antibacterial treatment of COPD exacerbations in outpatients*
Prompt and appropriate antibiotic use has been associated with improved clinical outcomes in patients with moderate to severe COPD exacerbations. Empiric regimens are designed to target the most likely pathogens (Haemophilus influenzae, Moraxella catarrhalis, and Streptococcus pneumoniae) and should be broadened to target drug-resistant pathogens and difficult-to-eradicate pathogens (eg, macrolide-resistant S. pneumoniae, nontypeable strains of H. influenzae) in those at risk for poor outcomes. Coverage for Pseudomonas is indicated in patients with risk factors for infection with this pathogen. All patients should be evaluated for clinical response in approximately 72 hours, and sputum Gram stain and culture should be considered for those who fail to response to empiric treatment. Modifications to this approach may be needed for patients with a history of colonization or infection with drug-resistant pathogens (including Pseudomonas) or when a specific pathogen is suspected.

COPD: chronic obstructive pulmonary disease; FEV1: forced expiratory volume in 1 second.

* Antiviral therapy for influenza is also indicated for exacerbations triggered by influenza infection.

¶ Suspicion for other cardiopulmonary disorders (heart failure, pneumothorax) and more severe infections (eg, pneumonia) should be absent for the diagnosis of an acute COPD exacerbation.

Δ Age alone is not a strict risk factor but should be considered as additive to other risk factors.

Selection among antibiotic choices is based on local microbial sensitivity patterns, patient comorbidities, prior infecting organisms, potential adverse events and drug interactions, and also provider and patient preferences. In particularly, modifications to this regimen may be needed for patients with a history of drug-resistant Pseudomonas based on severity of illness, degree of suspicion for Pseudomonas, and prior susceptibility profiles of pseudomonal isolates.

§ If recent antibiotic exposure (eg, within the past 3 months), select an antibiotic from a different class than the most recent agent used.

¥ Trimethoprim-sulfamethoxazole is a reasonable alternative when macrolides and cephalosporins cannot be used due to allergy, potential adverse effects, or availability.

‡ Some experts add amoxicillin or another agent with better activity against S. pneumoniae to ciprofloxacin for broader empiric treatment.

† Because fluoroquinolone resistance is prevalent among Pseudomonas aeruginosa strains, we obtain a sputum Gram stain and culture with susceptibility testing for these patients to help guide subsequent management decisions. For most other outpatients, obtaining a sputum culture is not needed unless the patient fails to respond to empiric treatment.

** Levofloxacin has lesser activity against Pseudomonas than ciprofloxacin but has greater activity against S. pneumoniae and M. catarrhalis is thus a reasonable alternative to ciprofloxacin for patients who are at increased risk of Pseudomonas infection but lack microbiologic evidence of Pseudomonas infection or colonization.
References:
  1. Sethi S, Murphy TF. Acute exacerbations of chronic bronchitis: New developments concerning microbiology and pathophysiology--impact on approaches to risk stratification and therapy. Infect Dis Clin N Am 2004; 18:861.
  2. Sethi S, Anzueto A, Miravitlles M, et al. Determinants of bacteriological outcomes in exacerbations of chronic obstructive pulmonary disease. Infection 2016; 44:65.
  3. Gallego M, Pomares X, Espasa M, et al. Pseudomonas aeruginosa isolates in severe chronic obstructive pulmonary disease: characterization and risk factors. BMC Pulm Med 2014; 14:103.
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