Vandael E, De WuLf I, Foulon V
J Pharm Belg. 2016 Dec(4):14-23.
Introduction Community pharmacists have an important role in the management of drug-drug interactions (DD). One of the interactions that can lead to serious adverse drug events, more specifically Torsade de Pointes and sudden cardiac death, are DDI with risk of CT-prolongation. Many drugs from different therapeutic classes have been linked with the risk of QT-prolongation (as listed in the QT-drug lists of CredibleMeds]. Moreover, patient-specific risk factors should be taken into account. This leads to a complex risk estimation of QT-prolongation for each patient. Aim The aim of this study is to investigate the prevalence of DDI and the management of these interactions in community pharmacies, with special attention for DDI with a risk of QT-prolongation. Method This epidemiological study is based on data of an interuniversity, observational study in 534 Belgian community pharmacies with a last-year pharmacy student (November 2012 - March 2013), in which all drug-related problems (DRP) and associated interventions of the pharmacist were registered for drugs on prescription. In this study, all DRP that were registered as a DDI were selected. The evidence for these DD was verified in four information sources (DelphiCare, Medscape, Drugs.com, handbook 'Commentaren Medicatiebewaking'). Finally, an in-depth analysis was performed for DDI with risk of QT-prolongation. QT-prolonging drugs were identified with the QT-drug lists of CredibleMeds. Results In total, 64.962 prescriptions and 15.952 DRP were registered in the interuniversity study, of which 1858 DRP (11.6%) described as a DDI that was confirmed in at least one of the information sources. Of these interactions, 223 [12.0%] were linked with a risk of QT- prolongation. The majority of the concerned drugs are situated in list 1 of CredibleMeds (known risk of Torsade de Pointes). In 69 CT-prolonging DDI, two drugs of list 1 were involved. The most frequent QT-prolonging DDI was between escitalopram and quetiapine (N=11J. In 69.5% of the QT-prolonging DDI, an intervention was performed by the community pharmacist. In 47.8% of these interventions, the DDI was discussed with the patient. In 28.3% of the QT-prolonging DDI, the pharmacist contacted the physician. However, the proposed intervention was often considered unnecessary by the physician (42.9%). In only 4.5% of the interventions, the involved CT-prolonging drug was replaced by an alternative. Conclusion DDI represent an important part of the DRP in community pharmacies, including DDI with a risk of CT-prolongation (12% of the interactions). In the majority of the QT-prolonging DDI, at least one QT-prolonging drug of list 1 of CredibleMeds [known risk of Torsade de Pointes) was involved. In only 4.5% of the interventions, the involved QT-prolonging drug was replaced by an alternative.
引言
社区药剂师在药物相互作用(DDI)的管理中发挥着重要作用。其中一种可能导致严重药物不良事件,尤其是尖端扭转型室速和心源性猝死的相互作用,是具有QT间期延长风险的药物相互作用。许多来自不同治疗类别的药物都与QT间期延长风险有关(如可信药物QT药物列表中所列)。此外,还应考虑患者特定的风险因素。这导致对每个患者的QT间期延长风险进行复杂的评估。
目的
本研究的目的是调查社区药房中药物相互作用的发生率以及对这些相互作用的管理,特别关注具有QT间期延长风险的药物相互作用。
方法
这项流行病学研究基于一项在534家比利时社区药房进行的跨大学观察性研究数据,研究对象为最后一年的药学专业学生(2012年11月 - 2013年3月),其中所有与药物相关的问题(DRP)以及药剂师针对处方药的相关干预措施均被记录。在本研究中,所有被登记为药物相互作用的DRP都被选中。这些药物相互作用的证据在四个信息来源(DelphiCare、Medscape、Drugs.com、《药物监测评论》手册)中得到验证。最后,对具有QT间期延长风险的药物相互作用进行了深入分析。通过可信药物的QT药物列表识别出延长QT间期的药物。
结果
在跨大学研究中总共记录了64962张处方和15952个DRP,其中1858个DRP(11.6%)被描述为药物相互作用,且在至少一个信息来源中得到证实。在这些相互作用中,223个(12.0%)与QT间期延长风险相关。大多数相关药物位于可信药物列表1中(已知有尖端扭转型室速风险)。在69例QT间期延长的药物相互作用中,涉及列表1中的两种药物。最常见的QT间期延长药物相互作用是艾司西酞普兰与喹硫平之间的相互作用(N = 11)。在69.5%的QT间期延长药物相互作用中,社区药剂师进行了干预。在这些干预措施中,47.8%的情况下与患者讨论了药物相互作用。在28.3%的QT间期延长药物相互作用中,药剂师联系了医生。然而,医生通常认为所提议的干预措施不必要(42.9%)。在仅4.5%的干预措施中,将涉及的延长QT间期的药物替换为替代药物。
结论
药物相互作用是社区药房中DRP的重要组成部分,包括具有QT间期延长风险的药物相互作用(占相互作用的12%)。在大多数QT间期延长的药物相互作用中,涉及可信药物列表1中至少一种已知有尖端扭转型室速风险的延长QT间期的药物。在仅4.5%的干预措施中,将涉及的延长QT间期的药物替换为替代药物。