The pharmacokinetics of antibiotics in patients with obesity: a systematic review and consensus guidelines for dose adjustments
- PMID: 40383125
- DOI: 10.1016/S1473-3099(25)00155-0
The pharmacokinetics of antibiotics in patients with obesity: a systematic review and consensus guidelines for dose adjustments
Abstract
Obesity can cause physiological changes resulting in antibiotic pharmacokinetic alterations and suboptimal drug exposures. This systematic review aimed to summarise the available evidence on this topic and provide guidance for dose adjustment of antibiotics in adult (age ≥18 years) patients with obesity (BMI >30 kg/m2). We searched PubMed, Embase, and CENTRAL databases to find relevant studies published between database inception and Dec 30, 2023. We initially identified 6113 studies, which became 4654 studies after duplicate removal, and 128 studies were included in the final review. β-lactam antibiotics were most commonly studied (57 studies), followed by the group of glycopeptides, lipoglycopeptides, and oxazolidinones (45 studies). The certainty of evidence was low or very low for all antibiotics and a meta-analysis was not possible due to the heterogeneity of study populations and methods. Obesity modestly alters the pharmacokinetics of β-lactam antibiotics, but evidence does not support routine dose adjustments. For aminoglycosides and glycopeptides, the impact of obesity on pharmacokinetics is evident and weight-based dosing is recommended. Data are sparse for other antibiotic classes and research needs are described. In the absence of robust pharmacokinetic data, therapeutic drug monitoring can be used to guide individualised dosing.
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Conflict of interest statement
Declaration of interests MH has received payment or honoraria from Gilead Sciences, Pfizer, MSD, Shionogi, and Insmed. CK has received grants from AbbVie, AstraZeneca, Boehringer Ingelheim, Roche, Merck, Novo Nordisk, and Sanofi for the PharMetrX PhD programme. JLK has received grants from AbbVie, bioMérieux, Merck, Pfizer, Shionogi, Entasis Therapeutics, VenatoRx, and Melinta; and has received payment or honoraria from Abbvie and Shionogi. EIN has received grants from Roche and is a member of the scientific advisory board for Gradientech. MPP has received consulting fees from Wolters Kluwer and iDi Pac. MZ has received grants from Pfizer, Novavax, and Shionogi; and has received consulting fees from Delta4, Janssen Pharmaceuticals, Sandoz, Shionogi, AOP Orphan, AstraZeneca, Theralia, InfectoPharm, and BioVersys. JAR has received grants from Qpex Biopharma, Pfizer, and bioMérieux; and has received payment or honoraria from Qpex Biopharma, Gilead, Advanz Pharma, Pfizer, and Sandoz. All other authors declare no competing interests.
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