草药/膳食补充剂-药物相互作用的日常评估:一项初步研究。

Joao Victor Souza-Peres, Kimberly Flores, Bethany Umloff, Michelle Heinan, Paul Herscu, Mary Beth Babos
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引用次数: 0

摘要

缺乏可靠的信息阻碍了临床医生对可疑的草药相互作用的评估。这项初步研究是一项基于调查的研究,旨在从草药医生、有执照的卫生保健提供者和非专业人员的角度对草药与药物相互作用的现实经验进行描述性分析。报告的膳食补充剂与药物的相互作用是根据最常被引用的资源来评估潜在的补充剂与药物的相互作用。使用大多数临床医生可用的工具进行歧化分析,使用来自美国联邦不良事件报告系统(FAERS)和美国食品安全和应用营养中心(CFSAN)不良事件报告系统(CAERS)的数据。该研究的次要目的包括探讨受访者使用膳食补充剂的原因,并对受访者对膳食补充剂与药物相互作用的看法进行定性分析。虽然补充药物相互作用的报告与常用的补充药物相互作用评价资源和通过FAERS进行的歧化分析的一致性很低,但使用CAERS数据的一致性很高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Everyday Evaluation of Herb/Dietary Supplement-Drug Interaction: A Pilot Study.

Everyday Evaluation of Herb/Dietary Supplement-Drug Interaction: A Pilot Study.

Everyday Evaluation of Herb/Dietary Supplement-Drug Interaction: A Pilot Study.

Everyday Evaluation of Herb/Dietary Supplement-Drug Interaction: A Pilot Study.

A lack of reliable information hinders the clinician evaluation of suspected herb-drug interactions. This pilot study was a survey-based study conceived as a descriptive analysis of real-life experiences with herb-drug interaction from the perspective of herbalists, licensed health-care providers, and lay persons. Reported dietary supplement-drug interactions were evaluated against the resources most commonly cited for the evaluation of potential supplement-drug interactions. Disproportionality analyses were performed using tools available to most clinicians using data from the U.S. Federal Adverse Event Reporting System (FAERS) and the US Center for Food Safety and Applied Nutrition (CFSAN) Adverse Event Reporting System (CAERS). Secondary aims of the study included exploration of the reasons for respondent use of dietary supplements and qualitative analysis of respondent's perceptions of dietary supplement-drug interaction. While agreement among reported supplement-drug interactions with commonly cited resources for supplement-drug interaction evaluation and via disproportionality analyses through FAERS was low, agreement using data from CAERS was high.

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