International Journal of Infectious Diseases (Nov 2022)

Extended-spectrum antibiotics for community-acquired pneumonia with a low risk for drug-resistant pathogens

  • Hironori Kobayashi,
  • Yuichiro Shindo,
  • Daisuke Kobayashi,
  • Toshihiro Sakakibara,
  • Yasushi Murakami,
  • Mitsuaki Yagi,
  • Akinobu Matsuura,
  • Kenta Sato,
  • Kota Matsui,
  • Ryo Emoto,
  • Tetsuya Yagi,
  • Hideo Saka,
  • Shigeyuki Matsui,
  • Yoshinori Hasegawa

Journal volume & issue
Vol. 124
pp. 124 – 132

Abstract

Read online

Objectives: The potential hazards of extended-spectrum antibiotic therapy for patients with community-acquired pneumonia (CAP) with low risk for drug-resistant pathogens (DRPs) remain unclear; however, risk assessment for DRPs is essential to determine the initial antibiotics to be administered. The study objective was to assess the effect of unnecessary extended-spectrum therapy on the mortality of such patients. Methods: A post hoc analysis was conducted after a prospective multicenter observational study for CAP. Multivariable logistic regression analysis was performed to assess the effect of extended-spectrum therapy on 30-day mortality. Three sensitivity analyses, including propensity score analysis to confirm the robustness of findings, were also performed. Results: Among 750 patients with CAP, 416 with CAP with a low risk for DRPs were analyzed; of these, 257 underwent standard therapy and 159 underwent extended-spectrum therapy. The 30-day mortality was 3.9% and 13.8% in the standard and extended-spectrum therapy groups, respectively. Primary analysis revealed that extended-spectrum therapy was associated with increased 30-day mortality compared with standard therapy (adjusted odds ratio 2.82; 95% confidence interval 1.20-6.66). The results of the sensitivity analyses were consistent with those of the primary analysis. Conclusion: Physicians should assess the risk for DRPs when determining the empirical antibiotic therapy and should refrain from administering unnecessary extended-spectrum antibiotics for patients with CAP with a low risk for DRPs.

Keywords