接受多个临床科室处方的门诊患者中与 CYP3A4 相关的潜在药物相互作用的特征。

IF 1.2 Q4 PHARMACOLOGY & PHARMACY Journal of Pharmaceutical Health Care and Sciences Pub Date : 2024-08-05 DOI:10.1186/s40780-024-00368-4
Rina Matsuoka, Shinsuke Akagi, Tomohiro Konishi, Masashi Kondo, Hideki Matsubara, Shohei Yamamoto, Keiji Izushi, Yuichi Tasaka
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引用次数: 0

摘要

背景:药物相互作用(DDI)会增加药物不良反应(ADR)的发生率。在之前的一份报告中,我们发现在服用六种或六种以上药物的患者中,一张处方中由相同的 CYP 分子种类引起的潜在 DDI 的发生率超过 90%,并且 CYP3A4 对临床实践中潜在 DDI 数量的增加有显著影响。然而,导致多个临床科室处方中潜在 DDIs 数量增加的因素仍然不甚明了:这项观察性研究在日本冈山县的 5 家药房进行。研究对象包括 2022 年 4 月 11 日至 2022 年 4 月 24 日期间在这些药房就诊的患者,但不包括仅持有来自单一临床科室处方的患者。进行了分层分析,以根据服用药物的数量确定与 CYP3A4 相关的潜在 DDI 的发生率。此外,还使用多元线性回归分析确定了与 CYP3A4 相关潜在 DDIs 所涉药物数量增加相关的因素。在这项研究中,按临床科室细分的处方数据中包含两种或两种以上药物的潜在 DDIs 被用作对照数据:本研究共纳入了 372 名接受多个临床科室处方的门诊患者。导致 CYP3A4 相关潜在 DDI 的药物数量随着临床科室数量的增加而增加。值得注意的是,与按临床科室细分的处方相比,在服用少于六种药物的病例中,来自多个临床科室的处方出现 CYP3A4 相关潜在 DDI 的频率更高。多元回归分析表明,"心血管药物"、"影响中枢神经系统的药物 "和 "泌尿生殖和肛门器官药物 "是增加 CYP3A4 相关潜在 DDIs 的三大药物类别:总之,这些结果突出表明,对于接受多个临床科室处方的门诊患者,即使服用的药物数量少于六种,也必须对处方药物采取统一的管理策略,并持续监测 ADRs。
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Characteristics of CYP3A4-related potential drug-drug interactions in outpatients receiving prescriptions from multiple clinical departments.

Background: Drug-drug interactions (DDIs) increase the incidence of adverse drug reactions (ADRs). In a previous report, we revealed that the incidence of potential DDIs due to the same CYP molecular species in one prescription exceeds 90% among patients taking six or more drugs and that CYP3A4 markedly influences the increase in the number of potential DDIs in clinical practice. However, the factors contributing to an increased number of potential DDIs in prescriptions from multiple clinical departments remain poorly clarified.

Methods: This observational study was performed at five pharmacies in Okayama Prefecture, Japan. Patients who visited these pharmacies from 11 April 2022 to 24 April 2022 were included, except those who had prescriptions only from a single clinical department. A stratified analysis was performed to determine the incidence of CYP3A4-related potential DDIs according to the number of drugs taken. Additionally, factors associated with an increase in the number of drugs involved in CYP3A4-related potential DDIs were identified using multiple linear regression analysis. In this study, potential DDIs for the prescription data subdivided by clinical department, containing two or more drugs, were used as control data.

Results: Overall, 372 outpatients who received prescriptions from multiple clinical departments were included in the current study. The number of drugs contributing to CYP3A4-related potential DDIs increased with an increase in the number of clinical departments. Notably, in cases taking fewer than six drugs, prescriptions from multiple clinical departments had a higher frequency of CYP3A4-related potential DDIs than those in prescriptions subdivided by clinical department. Multiple regression analysis identified "Cardiovascular agents", "Agents affecting central nervous system", and "Urogenital and anal organ agents" as the top three drug classes that increase CYP3A4-related potential DDIs.

Conclusion: Collectively, these results highlight the importance of a unified management strategy for prescribed drugs and continuous monitoring of ADRs in outpatients receiving prescriptions from multiple clinical departments even if the number of drugs taken is less than six.

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CiteScore
1.80
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0.00%
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29
审稿时长
8 weeks
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