Affiliation:
1. Center of Medicine Clinical Research, Department of Pharmacy, PLA General Hospital, Beijing, People’s Republic of China
Abstract
Abstract
Background
Complicated intra-abdominal infections (cIAIs) remain a leading cause of death in surgical wards, in which antibiotic treatment is crucial. We aimed to compare the efficacy and safety of novel β-lactam/β-lactamase inhibitors (BL/BLIs) in combination with metronidazole and carbapenems in the treatment of cIAIs.
Methods
A comprehensive search of randomized controlled trials (RCTs) was performed using Medline, Embase, and Cochrane Library, which compared the efficacy and safety of novel BL/BLIs and carbapenems for the treatment of cIAIs.
Results
Six RCTs consisting of 2254 patients were included. The meta-analysis showed that novel BL/BLIs in combination with metronidazole had a lower clinical success rate (risk difference [RD], –0.05; 95% CI, –0.07 to –0.02; I2 = 0%) and a lower microbiological success rate (RD, –0.04; 95% CI, –0.08 to –0.00; I2 = 0%). No difference was found between the 2 groups in incidence of adverse events (RD, 0.02; 95% CI, –0.01 to 0.06; I2 = 0%), serious adverse events (SAEs; RD, 0.01; 95% CI, –0.02 to 0.03; I2 = 0%), or mortality (RD, 0.01; 95% CI, –0.00 to 0.02). However, ceftazidime/avibactam had a higher risk of vomiting (RD, 0.03; 95% CI, 0.01 to 0.05; I2 = 47%), and the ceftolozane/tazobactam subgroup showed a higher incidence of SAEs (RD, 0.12; 95% CI, 0.01 to 0.03).
Conclusions
The efficacy of novel BL/BLIs in combination with metronidazole was not as high as that of carbapenems. Although no significant differences were found with respect to overall adverse events, SAEs, or mortality, the novel BL/BLIs has a higher risk of vomiting. We still need to be cautious about the clinical application of a new anti-infective combination.
Trial registration
PROSPERO ID: 42020166061.
Funder
National Natural Science Foundations of China
13th Five-Year Plan of National Major Science and Technology Projects
Publisher
Oxford University Press (OUP)
Subject
Infectious Diseases,Oncology
Cited by
4 articles.
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