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dc.rights.licenseopenen_US
dc.contributor.authorDIAS MEIRELES, Vasco
dc.contributor.authorAIRAUD, Clémentine
dc.contributor.authorDEMAY, Elouan
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorCAZANAVE, Charles
hal.structure.identifierBiologie des maladies cardiovasculaires = Biology of Cardiovascular Diseases
dc.contributor.authorXUEREB, Fabien
dc.contributor.authorLAZARO, Pauline
dc.contributor.authorBACLE, Astrid
hal.structure.identifierBiologie des maladies cardiovasculaires = Biology of Cardiovascular Diseases
dc.contributor.authorLAHOUATI, Marin
dc.date.accessioned2025-03-04T12:54:55Z
dc.date.available2025-03-04T12:54:55Z
dc.date.issued2025-02-24
dc.identifier.issn1435-4373en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/205341
dc.description.abstractEnObese patients treated with daptomycin at 4 mg/kg have a 30% increased drug exposure, potentially raising the risk of adverse events (AEs) like rhabdomyolysis. Given limited data on the safety of higher doses (10 mg/kg) in this population, this study aimed to assess the safety of high-dose daptomycin in obese patients and to identify potential AEs risk factors. This multicenter, retrospective observational study was conducted from June 2021 to May 2022 using medical records. Patients with a BMI > 30 kg/m were classified as obese. AEs assessed included: CK elevation (> 5x upper limit of normal), severe elevation (> 10x upper limit), eosinophilic pneumonia, and elevated liver enzymes. Both univariate and multivariate analyses were conducted. A total of 1 303 patients were included: 970 non-obese and 333 Ob patients. These patients received an average daptomycin dose of 9.9 mg/kg based on actual body weight for an average treatment duration of 8.27 days. One-third of the patients had CK monitoring. AEs rates were 3.5% for the n-Ob group vs. 8.7% in the Ob group (p < 0.01). Ob patients had significantly higher CK levels (n-Ob, 9.5%; Ob, 20.3%; p = 0.001), and severe elevation (n-Ob, 5.2%; Ob, 10.9%; p = 0.03). Factors increasing AE risk included obesity, concomitant prescriptions of drugs with risk of rhabdomyolysis, eGFR 30-60 mL/min, and daptomycin duration (OR = 2.42; 4.34; 2.03 and 1.05, respectively, p < 0.001). On the opposite, consultation with an infectious disease specialist reduced risk (OR = 0.52, p = 0.024). This study highlights that obese patient has a significantly increased risk of AEs with high dose of daptomycin compared to non-obese patients. Adjusted body weight dosing may be considered to reduce AEs risk.
dc.language.isoENen_US
dc.title.enSafety of high-dose daptomycin in obese patients: a multicentric retrospective study.
dc.title.alternativeEur J Clin Microbiol Infect Disen_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1007/s10096-025-05065-0en_US
dc.subject.halSciences du Vivant [q-bio]/Médecine humaine et pathologieen_US
dc.identifier.pubmed39992533en_US
bordeaux.journalEuropean Journal of Clinical Microbiology and Infectious Diseasesen_US
bordeaux.hal.laboratoriesBiologie des maladies cardiovasculaires (BMC) - UMR 1034en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionINSERMen_US
bordeaux.institutionCNRS
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcepubmed
hal.identifierhal-04975983
hal.version1
hal.date.transferred2025-03-04T12:54:57Z
hal.popularnonen_US
hal.audienceInternationaleen_US
hal.exporttrue
workflow.import.sourcepubmed
dc.rights.ccPas de Licence CCen_US
bordeaux.COinSctx_ver=Z39.88-2004&amp;rft_val_fmt=info:ofi/fmt:kev:mtx:journal&amp;rft.jtitle=European%20Journal%20of%20Clinical%20Microbiology%20and%20Infectious%20Diseases&amp;rft.date=2025-02-24&amp;rft.eissn=1435-4373&amp;rft.issn=1435-4373&amp;rft.au=DIAS%20MEIRELES,%20Vasco&amp;AIRAUD,%20Cl%C3%A9mentine&amp;DEMAY,%20Elouan&amp;CAZANAVE,%20Charles&amp;XUEREB,%20Fabien&amp;rft.genre=article


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