TY - JOUR
T1 - Extended-spectrum antibiotics for community-acquired pneumonia with a low risk for drug-resistant pathogens
AU - Central Japan Lung Study Group
AU - Kobayashi, Hironori
AU - Shindo, Yuichiro
AU - Kobayashi, Daisuke
AU - Sakakibara, Toshihiro
AU - Murakami, Yasushi
AU - Yagi, Mitsuaki
AU - Matsuura, Akinobu
AU - Sato, Kenta
AU - Matsui, Kota
AU - Emoto, Ryo
AU - Yagi, Tetsuya
AU - Saka, Hideo
AU - Matsui, Shigeyuki
AU - Hasegawa, Yoshinori
N1 - Publisher Copyright:
© 2022 The Authors
PY - 2022/11
Y1 - 2022/11
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85140013437&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85140013437&partnerID=8YFLogxK
U2 - 10.1016/j.ijid.2022.09.015
DO - 10.1016/j.ijid.2022.09.015
M3 - Article
C2 - 36116670
AN - SCOPUS:85140013437
SN - 1201-9712
VL - 124
SP - 124
EP - 132
JO - International Journal of Infectious Diseases
JF - International Journal of Infectious Diseases
ER -