Azithromycin combination therapy for community-acquired pneumonia: propensity score analysis

Akihiro Ito1, Tadashi Ishida2, Hiromasa Tachibana2,3

  • 1Department of Respiratory Medicine, Ohara Healthcare Foundation, Kurashiki Central Hospital, Miwa 1-1-1, Kurashiki, Okayama, 710-8602, Japan. ai12306@kchnet.or.jp.

Scientific Reports
|December 6, 2019
PubMed

Insights

Adding azithromycin to β-lactam antibiotics for severe community-acquired pneumonia (CAP) patients not in the ICU significantly reduced 30-day mortality. This finding was specific to patients meeting Infectious Diseases Society of America/American Thoracic Society criteria.

Area of Science:

  • Infectious Diseases
  • Pulmonology
  • Clinical Pharmacology

Background:

  • Severe community-acquired pneumonia (CAP) management in non-intensive care units (ICU) often involves β-lactam monotherapy.
  • The role of adding macrolides, such as azithromycin, to β-lactam regimens for non-ICU CAP patients requires further clarification.

Purpose of the Study:

  • To evaluate the efficacy of adding azithromycin to β-lactam antibiotics in reducing 30-day mortality for hospitalized non-ICU patients with severe CAP.
  • To compare combination therapy versus β-lactam monotherapy using various severity classification criteria.

Main Methods:

  • Prospective cohort study of consecutive CAP patients hospitalized in non-ICU settings (October 2010 - November 2016).
  • Comparison of 30-day mortality between β-lactam/azithromycin combination and β-lactam monotherapy.
  • Patient stratification using CURB-65, Pneumonia Severity Index (PSI), and Infectious Diseases Society of America (IDSA)/American Thoracic Society (ATS) criteria.
  • Inverse probability of treatment weighting (IPTW) analysis to control for confounding factors.

Main Results:

  • Combination therapy did not significantly reduce 30-day mortality based on CURB-65 and PSI criteria.
  • However, based on IDSA/ATS criteria, azithromycin combination therapy significantly decreased 30-day mortality in severe CAP patients (OR 0.12).
  • No significant mortality reduction was observed for non-severe pneumonia patients using IDSA/ATS criteria (OR 1.85).
  • IPTW analysis confirmed these findings.

Conclusions:

  • Azithromycin combination therapy is associated with significantly reduced 30-day mortality in severe CAP patients who meet IDSA/ATS criteria.
  • The benefit of macrolide combination therapy may be criterion-dependent for non-ICU CAP patients.

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