Porat Daniel, Dahan Arik
Department of Clinical Pharmacology, School of Pharmacy, Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel.
Expert Rev Clin Pharmacol. 2025 Mar;18(3):101-108. doi: 10.1080/17512433.2025.2462093. Epub 2025 Feb 7.
Medication management after bariatric surgery is a major and complex challenge. The altered gastrointestinal anatomy/physiology post-surgery may impact oral drug absorption/pharmacokinetics, with potential clinical implications. Along with multiple studies/cases of impaired post-surgery drug absorption/pharmacokinetics, leading to potential treatment failure, reports of increased drug exposure, leading to post-bariatric safety issues and adverse effects risk, are also available; yet, this second scenario of increased post-surgery drug levels, is less familiar in practice.
In this article, we highlight and overview the literature reports of increased post-bariatric drug exposure and safety issues, and discuss the underlying relevant mechanisms. Finally, we provide clinical recommendations for managing this therapeutic challenge.
Around 25 drugs were found to exhibit post-bariatric enhanced pharmacokinetics and risk of adverse effects. Among them, toxicity with lithium treatment is well-established. Clear safety concerns were also raised for other drugs, including levothyroxine, atorvastatin, paracetamol and, importantly, immediate-release morphine. Cautious use, while closely monitoring clinical signs of toxicity, is advised for these drugs. Realizing the potentially altered post-bariatric pharmacokinetics of various drugs, and, in particular, the risk of increased exposure with related adverse effects, is essential for providing optimal pharmacological therapy and overall patient care to the growing bariatric population.
减肥手术后的药物管理是一项重大且复杂的挑战。手术后胃肠道解剖结构/生理功能的改变可能会影响口服药物的吸收/药代动力学,具有潜在的临床意义。除了多项关于术后药物吸收/药代动力学受损并导致潜在治疗失败的研究/病例外,也有关于药物暴露增加导致减肥后安全问题和不良反应风险的报道;然而,这种术后药物水平升高的第二种情况在实践中不太为人所熟知。
在本文中,我们重点介绍并概述了减肥后药物暴露增加和安全问题的文献报道,并讨论了潜在的相关机制。最后,我们提供了应对这一治疗挑战的临床建议。
发现约25种药物在减肥后表现出药代动力学增强和不良反应风险。其中,锂治疗的毒性已得到充分证实。其他药物也引发了明确的安全担忧,包括左甲状腺素、阿托伐他汀、对乙酰氨基酚,重要的是还有速释吗啡。建议谨慎使用这些药物,并密切监测毒性的临床体征。认识到减肥后各种药物潜在的药代动力学改变,尤其是暴露增加及相关不良反应的风险,对于为不断增长的减肥人群提供最佳药物治疗和整体患者护理至关重要。