Kinney Eric M, Vijapurapu Sandhya, Covvey Jordan R, Nemecek Branden D
West Virginia University Medicine, J.W. Ruby Memorial Hospital, Morgantown, West Virginia, USA.
Duquesne University School of Pharmacy, Pittsburgh, Pennsylvania, USA.
Pharmacotherapy. 2021 May;41(5):479-489. doi: 10.1002/phar.2520. Epub 2021 Apr 3.
Opioids are one of the most prescribed classes of analgesic medications. Their narrow therapeutic index and metabolism through cytochrome p450 (CYP) enzymes can result in a drug interaction when used concomitantly with rifamycins. In clinical scenarios where concurrent therapy with an opioid and a rifamycin occurs, there is no standardized guidance for managing the interaction. The objective of this review was to examine literature which evaluates the concomitant use of opioids and rifamycins with clinically relevant CYP-inducing properties. A systematic review following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) criteria was performed. PubMed, Scopus, and OVID Embase were queried for studies from database inception to January 2020 related to rifamycin and opioid medications. Only full-text, peer-reviewed, English language articles addressing clinical outcomes from concomitant rifamycin and opioid therapy were included. The review isolated 12 articles for data extraction from an original 2260 citations identified. Rifampin (11; 92%) and rifabutin (2; 17%) were the rifamycins studied along with seven different opioids. Decreased effect of opioids with concomitant rifampin therapy manifested as withdrawal in numerous patients on methadone and a decreased analgesic effect from tramadol, morphine, and, most notably, oxycodone. Only the combinations of rifampin with buccal fentanyl and rifabutin with buprenorphine and methadone were found to have no clinically measurable interaction. Available literature suggests that a decrease in opioid clinical effects is appreciated with concomitant rifamycin therapy. Further research is needed to focus on specific mitigation strategies beyond opioid agent selection, such as dosing adjustment recommendations.
阿片类药物是处方量最大的一类镇痛药。其治疗指数狭窄,且通过细胞色素P450(CYP)酶进行代谢,与利福霉素合用时可能会发生药物相互作用。在阿片类药物与利福霉素联合治疗的临床场景中,对于管理这种相互作用尚无标准化的指导。本综述的目的是研究评估具有临床相关CYP诱导特性的阿片类药物与利福霉素联合使用的文献。按照系统评价和Meta分析的首选报告项目(PRISMA)标准进行了系统评价。检索了PubMed、Scopus和OVID Embase数据库,以查找从数据库建立到2020年1月与利福霉素和阿片类药物相关的研究。仅纳入了涉及利福霉素与阿片类药物联合治疗临床结果的全文、经同行评审的英文文章。该综述从最初识别的2260篇文献中筛选出12篇进行数据提取。所研究的利福霉素包括利福平(11篇;92%)和利福布汀(2篇;17%),同时涉及七种不同的阿片类药物。利福平联合治疗使阿片类药物效果降低,表现为许多服用美沙酮的患者出现戒断症状,曲马多、吗啡尤其是羟考酮的镇痛效果降低。仅发现利福平与颊内芬太尼以及利福布汀与丁丙诺啡和美沙酮的组合没有临床可测的相互作用。现有文献表明,利福霉素联合治疗会使阿片类药物的临床效果降低。需要进一步研究关注除阿片类药物选择之外的具体缓解策略,如给药调整建议。