Bogaard Leonie, Tsoi Kayan, van de Steeg Bas, Brandon Esther F A, Geers Lisanne, van Herwaarden Margreet, Jansman Frank, Maas Dominique, Monster-Simons Margje, Ong David S Y, Borgsteede Sander D
Department Clinical Decision Support, Health Base Foundation, Houten, Netherlands.
Department of Clinical Pharmacy, Canisius Wilhelmina Hospital, Nijmegen, Netherlands.
Front Pharmacol. 2024 Sep 30;15:1412692. doi: 10.3389/fphar.2024.1412692. eCollection 2024.
Drug-drug interactions (DDIs) may influence the effectiveness and safety of medication treatment, which may require additional monitoring, dose adjustment or avoidance of certain drugs. DDIs involving P-glycoprotein (P-gp) affect many drugs, but current official product information is often insufficient to guide the management of these DDIs in clinical practice. The aim of this paper is to describe a protocol to assess DDIs involving P-gp and to develop and implement practice recommendations for clinically relevant P-gp-mediated DDIs that affect clinical outcomes through changes in systemic drug exposure.
A combined literature review and expert opinion approach will be used according to the following seven steps: set up an expert panel (step 1), establish core concepts and definitions (step 2), select potential P-gp-modulators (i.e., P-gp-inducers and -inhibitors) and P-gp-substrates to be evaluated (step 3), select and extract evidence-based data, and present findings in standardized assessment reports (step 4), discuss and adopt classifications and practice recommendations with the expert panel (step 5), publish and integrate information and alerts in clinical decision support systems (CDSS) (step 6), (re)assessments of DDIs and potential new DDIs when new information is available or when initiated by healthcare providers (step 7).
The expert panel will classify potential P-gp-modulators and -substrates as clinically relevant P-gp-inducer, -inhibitor and/or -substrate and draw conclusions about which combinations of classified modulators and substrates will lead to clinically relevant DDIs. This may include the extrapolation of conclusions for DDIs where limited or no data are available, based on the pharmacological characteristics of these drugs. For (potential) DDIs that are considered to be clinically relevant, practice recommendations will be developed.
This protocol describes a standardized, evidence- and expert opinion-based assessment of P-gp-mediated DDIs that affect clinical outcomes. This approach will generate alerts with practice recommendations for clinically relevant DDIs and transparent rationales for DDIs that are considered to be irrelevant. These recommendations will improve individual patient care by supporting healthcare professionals to make consistent decisions on how to manage P-gp mediated DDIs.
药物相互作用(DDIs)可能会影响药物治疗的有效性和安全性,这可能需要额外的监测、剂量调整或避免使用某些药物。涉及P-糖蛋白(P-gp)的药物相互作用会影响许多药物,但目前的官方产品信息往往不足以指导临床实践中这些药物相互作用的管理。本文的目的是描述一种评估涉及P-gp的药物相互作用的方案,并针对通过全身药物暴露变化影响临床结局的临床相关P-gp介导的药物相互作用制定并实施实践建议。
将根据以下七个步骤采用文献综述和专家意见相结合的方法:组建专家小组(步骤1),确立核心概念和定义(步骤2),选择潜在的P-gp调节剂(即P-gp诱导剂和抑制剂)以及待评估的P-gp底物(步骤3),选择并提取基于证据的数据,并在标准化评估报告中呈现结果(步骤4),与专家小组讨论并采用分类和实践建议(步骤5),在临床决策支持系统(CDSS)中发布并整合信息和警示(步骤6),当有新信息可用或由医疗保健提供者发起时,对药物相互作用和潜在的新药物相互作用进行(重新)评估(步骤7)。
专家小组将把潜在的P-gp调节剂和底物分类为临床相关的P-gp诱导剂、抑制剂和/或底物,并就分类的调节剂和底物的哪些组合会导致临床相关的药物相互作用得出结论。这可能包括根据这些药物的药理学特性,对有限或无数据的药物相互作用的结论进行外推。对于被认为具有临床相关性的(潜在)药物相互作用,将制定实践建议。
本方案描述了一种基于证据和专家意见的标准化评估,用于评估影响临床结局的P-gp介导的药物相互作用。这种方法将为临床相关的药物相互作用生成带有实践建议的警示,并为被认为不相关的药物相互作用提供透明的理由。这些建议将通过支持医疗保健专业人员就如何管理P-gp介导的药物相互作用做出一致决策,来改善个体患者的护理。