直接口服抗凝剂和其他药物在肺栓塞患者中的药物-药物相互作用:来自lung genembolie Augsburg (LEA)的结果

IF 4 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Clinical Pharmacokinetics Pub Date : 2025-10-01 Epub Date: 2025-08-09 DOI:10.1007/s40262-025-01556-7
Klaus Peter Schmelzer, Dennis Freuer, Simone Fischer, Thomas M Berghaus, Jakob Linseisen, Christa Meisinger
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引用次数: 0

摘要

背景和目的:直接口服抗凝剂(DOACs)是目前公认的一类预防和治疗血栓的药物。到目前为止,评估肺栓塞(PE)患者DOACs与其他药物之间药物-药物相互作用(ddi)的真实数据的文献有限。本研究旨在研究PE患者的这些相互作用,以解决这一问题并改善患者护理。材料与方法:回顾性研究,患者出院时记录用药情况,3个月后复查。临床决策支持系统(AiDKlinik®Release 3.5)最初用于筛选ddi和药物相关问题。随后,将药物输入Lexicomp®,这是一个综合的药物相互作用数据库,以获得对鉴定的相互作用及其机制的详细科学解释和参考。采用二元logistic随机截距模型识别药物-抗凝相互作用的潜在危险因素。结果:纳入的477例PE患者中位数服用5种药物。药物-抗凝相互作用强烈依赖于服用药物的数量(P值< 0.001)。然而,这种关联是非线性的,导致更多药物的饱和效应。至少有一种药物-抗凝相互作用的优势比为0.40(95%可信区间0.17-0.96;P值= 0.040)。结论:ddi合并DOACs的可能性值得关注。通过了解最常见的相互作用、危险因素和避免策略,可以优化治疗的安全性和有效性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Drug-Drug Interactions Between Direct Oral Anticoagulants and Other Medications in Patients with Pulmonary Embolism: Results from the Lungenembolie Augsburg (LEA).

Background and aim: Direct oral anticoagulants (DOACs) are now a well-established class of medication for blood clot prevention and treatment. So far, literature evaluating real-world data on the drug-drug interactions (DDIs) between DOACs and other medications in patients with pulmonary embolism (PE) is limited. This study aims to investigate these interactions in patients with PE to address this and improve patient care.

Materials and methods: In a retrospective study, patients' medications were recorded upon hospital discharge and reviewed again 3 months later. A clinical decision support system (AiDKlinik® Release 3.5) was initially used to screen for DDIs and drug-related problems. Subsequently, medications were entered into Lexicomp®, a comprehensive drug interaction database, to gain detailed scientific explanations and references for the identified interactions and their mechanisms. Binary logistic random intercept models were used to identify potential risk factors of drug-anticoagulation interactions.

Results: The 477 included PE patients had a median intake of five drugs. Drug-anticoagulation interactions depended strongly on the number of medications taken (P value < 0.001). However, the association was non-linear, resulting in a saturation effect for a higher number of drugs. The odds ratio for having at least one drug-anticoagulation interaction was 0.40 (95% confidence interval 0.17-0.96; P value = 0.040) in patients with hypertension.

Conclusions: The potential for DDIs with DOACs represents a significant concern. By being aware of the most common interactions, risk factors and avoidance strategies, the safety and efficacy of therapy can be optimized.

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来源期刊
CiteScore
8.80
自引率
4.40%
发文量
86
审稿时长
6-12 weeks
期刊介绍: Clinical Pharmacokinetics promotes the continuing development of clinical pharmacokinetics and pharmacodynamics for the improvement of drug therapy, and for furthering postgraduate education in clinical pharmacology and therapeutics. Pharmacokinetics, the study of drug disposition in the body, is an integral part of drug development and rational use. Knowledge and application of pharmacokinetic principles leads to accelerated drug development, cost effective drug use and a reduced frequency of adverse effects and drug interactions.
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