Efficacy and safety of novel glycopeptides versus vancomycin for the treatment of gram-positive bacterial infections including methicillin resistant Staphylococcus aureus: A systematic review and meta-analysis

dc.contributor.authorJame, Wissal
dc.contributor.authorBasgut, Bilgen
dc.contributor.authorAbdi, Abdikarim
dc.contributor.pubmedID34843561en_US
dc.date.accessioned2022-06-16T13:10:05Z
dc.date.available2022-06-16T13:10:05Z
dc.date.issued2021
dc.description.abstractObjective To compare between current evidence of novel glycopeptides against vancomycin for the treatment of gram-positive bacterial infections. Methodology A systematic review and meta-analysis was done. Major databases were searched for eligible randomized control trials that assessed clinical success, microbiological success and safety profile of novel glycopeptides versus vancomycin for infections caused by gram-positive bacteria. Results This meta-analysis included eleven trials (7289 participants) comparing telavancin, dalbavancin and oritavancin with vancomycin. No differences were detected between novel glycopeptides and vancomycin for the treatment of skin and soft tissue infections (SSTIs) among modified intent-to-treat patients (OR: 1.04, CI: 0.92-1.17) as well as within the clinically evaluable patients (OR: 1.09, CI: 0.91-1.30). Data analysed from SSTIs, HAP and bacteremia studies on telavancin showed insignificant high clinical response in microbiologically evaluable patients infected with methicillin resistant Staphylococcus aureus (MRSA) (OR: 1.57, CI: 0.94-2.62, p: 0.08) and in the eradication of MRSA (OR: 1.39, CI: 0.99-1.96, P:0.06). Dalbavancin was non-inferior to vancomycin for the treatment of osteomyelitis in a phase II trial, while it was superior to vancomycin for the treatment of bacteremia in a phase II trial. Data analysed from all trials showed similar rates of all-cause mortality between compared antibiotics groups (OR: 0.67, CI: 0.11-4.03). Telavancin was significantly related with higher adverse events (OR: 1.24, CI: 1.07-1.44, P: <0.01) while dalbavancin and oritavancin were associated with significant fewer adverse events (OR: 0.73, CI: 0.57-0.94, p: 0.01; OR: 0.72, CI: 0.59-0.89, p: <0.01 respectively). Conclusion Efficacy and safety profiles of both dalbavancin and oritavancin were the same as vancomycin in the treatment of gram-positive bacterial infections in different clinical settings, while telavancin might be an effective alternative to vancomycin in MRSA infections, but caution is required during its clinical use due to the high risk of adverse events, especially nephrotoxicity.en_US
dc.identifier.issn1932-6203en_US
dc.identifier.issue11en_US
dc.identifier.scopus2-s2.0-85120379164en_US
dc.identifier.urihttps://journals.plos.org/plosone/article?id=10.1371/journal.pone.0260539
dc.identifier.urihttp://hdl.handle.net/11727/7051
dc.identifier.volume16en_US
dc.identifier.wos000752076100098en_US
dc.language.isoengen_US
dc.relation.isversionof10.1371/journal.pone.0260539en_US
dc.relation.journalPLOS ONEen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectSKIN-STRUCTURE INFECTIONSen_US
dc.subjectSOFT-TISSUE INFECTIONSen_US
dc.subjectHOSPITAL-ACQUIRED PNEUMONIAen_US
dc.subjectSINGLE-DOSE ORITAVANCINen_US
dc.subjectONCE-WEEKLY DALBAVANCINen_US
dc.subjectCOMPLICATED SKINen_US
dc.subjectSTANDARD THERAPYen_US
dc.subjectTELAVANCINen_US
dc.subjectANTIBIOTICSen_US
dc.subjectTRIALSen_US
dc.titleEfficacy and safety of novel glycopeptides versus vancomycin for the treatment of gram-positive bacterial infections including methicillin resistant Staphylococcus aureus: A systematic review and meta-analysisen_US
dc.typereviewen_US

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