PMID- 33120768 OWN - NLM STAT- MEDLINE DCOM- 20201119 LR - 20221005 IS - 1536-5964 (Electronic) IS - 0025-7974 (Print) IS - 0025-7974 (Linking) VI - 99 IP - 43 DP - 2020 Oct 23 TI - Carbapenems versus alternative beta-lactams monotherapy or in combination for febrile neutropenia: Systematic review and meta-analysis of randomized controlled trial. PG - e22725 LID - 10.1097/MD.0000000000022725 [doi] LID - e22725 AB - BACKGROUND: Febrile neutropenia (FN) in cancer patients can be life threatening and require the timely antimicrobial agents treatment. METHODS: To compare the effectiveness and safety of carbapenems versus beta-lactams for FN. PubMed, Medline (Ovid SP), Cochrane CENTRAL, and Embase were searched up to March 2019. FN in patients due to undergoing chemotherapy and treated with carbapenems and beta-lactams were included. Odds ratio (OR) and 95% confidence interval (CI) were estimated. RESULTS: Fifty randomized controlled trials (RCTs) studies involving 10,995 participants were included. Carbapenems were more likely to experience treatment success without modification (OR = 1.34, 95% CI = 1.24-1.46) compared with beta-lactams. Meropenem (OR = 1.36, 95% CI = 1.18-1.56; OR = 1.24, 95% CI = 1.01-1.53), imipenem/cilastatin (OR = 1.40, 95% CI = 1.19-1.65; OR = 1.31, 95% CI = 1.04-1.67) showed higher effectiveness from that by beta-lactams monotherapy or in combination with aminoglycoside, respectively. Carbapenems-aminoglycoside combination therapy does not provide an advantage over carbapenems alone. Meropenem showed similar risk of adverse events (AEs) versus beta-lactams. Imipenem/cilastatin was related to higher risk of AEs compared with beta-lactams. There was no significant difference between carbapenems and beta-lactams monotherapy or in combination. CONCLUSION: Meropenem and imipenem/cilastatin monotherapy appears to be available treatment for FN compared with beta-lactams. Imipenem/cilastatin was related to higher risk of AEs. Balancing the evidence for drug efficacy and side effects, meropenem monotherapy appears to be available treatment for FN. Individual centers should select the best matching therapy regimens according to local epidemiology and susceptibility patterns. FAU - Tang, Xiuge AU - Tang X AD - Department of Cardiovascular Medicine. FAU - Chen, Lingyuan AU - Chen L AD - Department of Pharmacy. FAU - Li, Yan AU - Li Y AD - Department of Pharmacy. FAU - Jiang, Junsong AU - Jiang J AD - Department of Reproductive Medicine, The People's Hospital of Hechi, Hechi, China. FAU - Li, Xianshu AU - Li X AD - Department of Pharmacy. FAU - Liang, Xueyan AU - Liang X AD - Department of Pharmacy. LA - eng PT - Comparative Study PT - Journal Article PT - Meta-Analysis PT - Systematic Review PL - United States TA - Medicine (Baltimore) JT - Medicine JID - 2985248R RN - 0 (Anti-Bacterial Agents) RN - 0 (Carbapenems) RN - 0 (beta-Lactams) SB - IM MH - Anti-Bacterial Agents/*administration & dosage MH - Carbapenems/*administration & dosage MH - Drug Therapy, Combination MH - Febrile Neutropenia/*drug therapy MH - Humans MH - *Randomized Controlled Trials as Topic MH - beta-Lactams/*administration & dosage PMC - PMC7581108 COIS- The authors have no conflicts of interest to disclose. EDAT- 2020/10/31 06:00 MHDA- 2020/11/20 06:00 PMCR- 2020/10/23 CRDT- 2020/10/30 01:01 PHST- 2020/10/30 01:01 [entrez] PHST- 2020/10/31 06:00 [pubmed] PHST- 2020/11/20 06:00 [medline] PHST- 2020/10/23 00:00 [pmc-release] AID - 00005792-202010230-00044 [pii] AID - MD-D-19-10269 [pii] AID - 10.1097/MD.0000000000022725 [doi] PST - ppublish SO - Medicine (Baltimore). 2020 Oct 23;99(43):e22725. doi: 10.1097/MD.0000000000022725.