Department of Pharmacy, Faculty of Science, National University of Singapore, Singapore.
Clin Ther. 2009;31 Pt 2:2379-86. doi: 10.1016/j.clinthera.2009.11.008.
Drug-drug interactions (DDIs) can lead to adverse clinical outcomes, particularly in oncology, because of the narrow therapeutic index of chemotherapeutic agents and because patients with cancer are at a high risk due to polypharmacy and age-related organ dysfunction. In a previously published study, drug profiles were developed based on primary and tertiary literature reviews for a list of clinically significant DDIs involving 28 oral anticancer agents (OAAs).
This study was based on a Delphi survey of oncology pharmacists; the survey results were used to develop a consensus list of clinically significant DDIs involving OAAs and nonanticancer agents.
In this study, the DDI profiles previously developed were updated, and the DDI pairs that were listed both in the 2009 Drug Interaction Facts (DIF) and the Thomson Micromedex DrugDex System compendia and that also met the predetermined criteria for clinical significance were selected for further evaluation. In a 2-round, electronically administered Delphi survey of oncology pharmacists, a 5-point Likert scale (1-5, where 1 = strongly agree and 5 = strongly disagree) was used to evaluate the DDI pairs based on 8 clinical aspects (clinical importance; irreversible morbidity and mortality; quality of data; quantity of data; patient's organ functions; comorbid conditions; awareness of interaction; and management burden). International pharmacists who specialized in oncology pharmacy practice and had > or =5 years of practice experience were eligible to participate.
Nine of the 23 surveyed pharmacists responded, giving a response rate of 39.1%. A total of 37 DDI pairs were selected from DIF and DrugDex and evaluated by the survey respondents, resulting in the identification, via consensus, of 12 clinically significant DDI pairs. The clinical aspects with the most DDIs that reached consensus of agreement were clinical importance (82.9%) and awareness of interaction (73.2%).
An expert panel identified 12 clinically significant DDIs involving OAAs.
药物-药物相互作用(DDI)可能导致不良临床结局,尤其是在肿瘤学领域,因为化疗药物的治疗指数较窄,而且癌症患者由于多种药物治疗和与年龄相关的器官功能障碍而处于高风险状态。在之前发表的一项研究中,根据初级和三级文献综述,为涉及 28 种口服抗癌药物(OAAs)的一组具有临床意义的 DDI 开发了药物特征。
本研究基于肿瘤学药师的 Delphi 调查;调查结果用于制定涉及 OAAs 和非抗癌药物的具有临床意义的 DDI 的共识清单。
在这项研究中,更新了之前开发的 DDI 特征,并选择了在 2009 年药物相互作用事实(DIF)和 Thomson Micromedex DrugDex 系统手册中列出且符合预定临床意义标准的 DDI 对进行进一步评估。在一项针对肿瘤学药师的两轮电子 Delphi 调查中,使用 5 分李克特量表(1-5,其中 1 表示非常同意,5 表示非常不同意)根据 8 个临床方面(临床重要性;不可逆的发病率和死亡率;数据质量;数据量;患者的器官功能;合并症;对相互作用的认识;以及管理负担)对 DDI 对进行评估。具有肿瘤学药学实践专业知识和 > 或 =5 年实践经验的国际药剂师有资格参加。
23 名调查药师中有 9 名做出了回应,回应率为 39.1%。从 DIF 和 DrugDex 中选择了 37 对 DDI 进行调查员评估,通过共识确定了 12 对具有临床意义的 DDI。通过共识达成一致意见的 DDI 中,临床方面最多的是临床重要性(82.9%)和对相互作用的认识(73.2%)。
一个专家小组确定了 12 种涉及 OAAs 的具有临床意义的 DDI。