Zakrzewski-Jakubiak Hubert, Doan Julie, Lamoureux Pamela, Singh Dharmender, Turgeon Jacques, Tannenbaum Cara
Université de Montréal, Québec, Canada.
Am J Geriatr Pharmacother. 2011 Dec;9(6):461-70. doi: 10.1016/j.amjopharm.2011.09.006. Epub 2011 Oct 22.
Polypharmacy increases the risk of cytochrome P450-based drug-drug interactions (CYP450-DDIs), leading to decreased therapeutic efficacy or increased drug toxicity.
The aims of this study were to investigate the utility of a new CYP450-DDI software, InterMED-Rx, in aiding pharmacists in detecting CYP450-DDIs in hospitalized elderly patients and to ascertain pharmacists' agreement on how to intervene for each CYP450-DDI.
A consensus panel of geriatric pharmacists first established guidelines for managing clinically relevant pharmacokinetic CYP450-DDIs. A prospective study was then conducted of patients newly admitted to a geriatric hospital whose pharmaceutical profile underwent analysis with InterMED-Rx. Rates and types of interventions were recorded.
Pharmacists' interrater agreement on how to manage CYP450-DDIs was initially only moderate (Cohen's κ, 0.51; 95% CI, 0.39-0.62), but improved subsequent to deliberation (Cohen's κ, 0.79; 95% CI, 0.70-0.88). Persistent disagreement involved interactions between 2 drugs with similar affinities for the same cytochrome. One hundred patients with polypharmacy (≥5 medications) aged 82.3 years (range, 65-96), with a mean (SD) of 12.2 (4.1) drugs (range, 5-27) were recruited for the prospective study. Eighty percent of patients had at least 1 CYP450 DDI detected with InterMED-Rx. A total of 238 CYP450-DDIs were identified involving CYP3A4 (70.2%), CYP2D6 (22.7%), and CYP2C9 (3.4%) substrates or inhibitors. Nineteen percent of patients received immediate medication adjustment, and 39% required follow-up of clinical signs, symptoms, and laboratory tests to determine whether future modification was needed. More than one half (56%) of all patients who required clinical follow-up had further medication adjustment prior to discharge.
Use of the InterMED-Rx software identified elderly patients at risk for pharmacokinetic interactions and facilitated interventions aimed at reducing adverse drug events. Although consensus can be reached among pharmacists on how to intervene for many CYP450-DDI scenarios, certain situations allow for multiple intervention strategies.
多重用药会增加基于细胞色素P450的药物相互作用(CYP450-DDIs)的风险,导致治疗效果降低或药物毒性增加。
本研究旨在探讨一种新型CYP450-DDI软件InterMED-Rx在协助药剂师检测住院老年患者CYP450-DDIs方面的效用,并确定药剂师对于如何针对每种CYP450-DDI进行干预的共识。
老年药剂师共识小组首先制定了管理临床相关药代动力学CYP450-DDIs的指南。随后对一家老年医院新入院患者进行前瞻性研究,使用InterMED-Rx对其用药情况进行分析。记录干预的发生率和类型。
药剂师在如何管理CYP450-DDIs方面的评分者间一致性最初仅为中等(Cohen's κ,0.51;95%CI,0.39-0.62),但经过讨论后有所改善(Cohen's κ,0.79;95%CI,0.70-0.88)。持续存在分歧的情况涉及对同一细胞色素具有相似亲和力的两种药物之间的相互作用。招募了100名多重用药(≥5种药物)的患者,年龄82.3岁(范围65-96岁),平均(标准差)服用12.2(4.1)种药物(范围5-27种)进行前瞻性研究。80%的患者通过InterMED-Rx检测到至少1种CYP450 DDI。共识别出238例CYP450-DDIs,涉及CYP3A4(70.2%)、CYP2D6(22.7%)和CYP2C9(3.4%)的底物或抑制剂。19%的患者立即进行了药物调整,39%的患者需要对临床体征、症状和实验室检查进行随访,以确定是否需要未来调整。所有需要临床随访的患者中,超过一半(56%)在出院前进行了进一步的药物调整。
使用InterMED-Rx软件可识别有药代动力学相互作用风险的老年患者,并促进旨在减少药物不良事件的干预措施。虽然药剂师在如何针对许多CYP450-DDI情况进行干预方面可以达成共识,但某些情况允许采用多种干预策略。