PMID- 37059988 OWN - NLM STAT- MEDLINE DCOM- 20230419 LR - 20230419 IS - 1471-2334 (Electronic) IS - 1471-2334 (Linking) VI - 23 IP - 1 DP - 2023 Apr 14 TI - Omadacycline for treatment of acute bacterial infections: a meta-analysis of phase II/III trials. PG - 232 LID - 10.1186/s12879-023-08212-0 [doi] LID - 232 AB - OBJECTIVE: This study aims to assess the clinical efficacy and safety of omadacycline for the treatment of acute bacterial infections. METHODS: A search of PubMed, Embase, Cochrane Library, and Clinical Trials was conducted up to July 1, 2022. We included only randomized controlled trials (RCTs), in which omadacycline and other antibiotics were evaluated for treating acute bacterial infections in adults. The primary outcomes were clinical response and microbiological response, whereas the secondary outcome was the risk of adverse events (AEs). RESULTS: A total of seven RCTs involving 2841 patients with acute bacterial infection were included. Overall, our study illustrated that the clinical cure ratio of omadacycline was similar to the comparators in the treatment of acute bacterial infections (OR = 1.18, 95%CI = 0.96, 1.46, I(2) = 29%). Omadacycline had a microbiological eradication rate similar to comparators in the treatment of acute bacterial infections (OR = 1.02, 95%CI = 0.81, 1.29, I(2) = 42%). No statistical differences were observed between omadacycline and the comparators in terms of infection caused by Staphylococcus aureus (OR = 1.14, 95%CI = 0.80, 1.63, I(2) = 0%), methicillin-resistant S. aureus (MRSA, OR = 1.28, 95%CI = 0.73, 2.24, I(2) = 0%), methicillin-susceptible S. aureus (MSSA, OR = 1.12, 95%CI = 0.69, 1.81, I(2) = 0%), and Enterococcus faecalis (OR = 2.47, 95%CI = 0.36, 16.97, I(2) = 7%). A significant difference was found between omadacycline and the comparators for the risk of any AEs and treatment related AEs. The risk of discontinuation of the study drug due to an AEs was lower for omadacycline than for the comparators. CONCLUSION: Omadacycline is as good as comparators in terms of efficacy and tolerance in the treatment of acute bacterial infections in adult patients. Thus, omadacycline is an appropriate option for antibiotic therapy in adult patients with acute bacterial infections. CI - (c) 2023. The Author(s). FAU - Lin, Fei AU - Lin F AD - Department of Pharmacy, The First Affiliated Hospital of Chengdu Medical College, Chengdu, China. AD - Clinical Medical College, Chengdu Medical College, Chengdu, China. FAU - He, Rong AU - He R AD - Department of Respiratory and Critical Care Medicine, The First Affiliated Hospital of Chengdu Medical College, Chengdu, China. FAU - Yu, Bin AU - Yu B AD - Department of Pharmacy, Mianyang Central Hospital, Mianyang, China. FAU - Deng, Bowen AU - Deng B AD - Department of Pharmacy, The Sixth People's Hospital of Chengdu, Chengdu, China. FAU - Ling, Baodong AU - Ling B AD - School of Pharmacy, Chengdu Medical College, Chengdu, China. lingbaodong@cmc.edu.cn. FAU - Yuan, Mingyong AU - Yuan M AD - Clinical Medical College, Chengdu Medical College, Chengdu, China. yuanmingyong@cmc.edu.cn. AD - Outpatient Department, The First Affiliated Hospital of Chengdu Medical College, Chengdu, China. yuanmingyong@cmc.edu.cn. LA - eng PT - Journal Article PT - Meta-Analysis DEP - 20230414 PL - England TA - BMC Infect Dis JT - BMC infectious diseases JID - 100968551 RN - 0 (Anti-Bacterial Agents) RN - 090IP5RV8F (omadacycline) RN - 0 (Tetracyclines) SB - IM MH - Adult MH - Humans MH - Anti-Bacterial Agents/adverse effects MH - *Bacterial Infections/drug therapy MH - *Staphylococcal Infections/microbiology MH - Tetracyclines/adverse effects MH - Treatment Outcome MH - Clinical Trials, Phase II as Topic MH - Clinical Trials, Phase III as Topic PMC - PMC10105466 OTO - NOTNLM OT - Acute bacterial infections OT - Meta-analysis, Efficacy, Safety OT - Omadacycline COIS- All authors declare no conflict of interest. EDAT- 2023/04/15 06:00 MHDA- 2023/04/18 06:41 PMCR- 2023/04/14 CRDT- 2023/04/14 23:33 PHST- 2022/10/20 00:00 [received] PHST- 2023/04/01 00:00 [accepted] PHST- 2023/04/18 06:41 [medline] PHST- 2023/04/14 23:33 [entrez] PHST- 2023/04/15 06:00 [pubmed] PHST- 2023/04/14 00:00 [pmc-release] AID - 10.1186/s12879-023-08212-0 [pii] AID - 8212 [pii] AID - 10.1186/s12879-023-08212-0 [doi] PST - epublish SO - BMC Infect Dis. 2023 Apr 14;23(1):232. doi: 10.1186/s12879-023-08212-0.