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延长QT间期药物的高风险使用频率。

Frequency of high-risk use of QT-prolonging medications.

作者信息

Allen LaPointe Nancy M, Curtis Lesley H, Chan K Arnold, Kramer Judith M, Lafata Jennifer Elston, Gurwitz Jerry H, Raebel Marsha A, Platt Richard

机构信息

Duke Center for Education and Research on Therapeutics, Duke Clinical Research Institute, Duke University Medical Center, Durham, NC 27715, USA.

出版信息

Pharmacoepidemiol Drug Saf. 2006 Jun;15(6):361-8. doi: 10.1002/pds.1155.

Abstract

PURPOSE

Prolongation of the QT interval has been associated with increased risk of torsades de pointes and death. Concurrent use of more than one QT-prolonging drug or a QT-prolonging drug with a drug that alters its pharmacokinetic profile is an important risk factor for adverse outcomes.

METHODS

Using a representative sample of 2 million health plan members from 10 health maintenance organizations with pharmacy benefits between January 1999 and July 2001, we identified potential drug interactions involving QT-prolonging medications. Prescription claims overlapping by at least 7 days for either 2 or more QT-prolonging drugs or a QT-prolonging drug with a drug that alters its clearance were considered potential drug interactions. We determined the number of drug interactions overall and the number of these interactions involving patients with other risk factors for torsades de pointes.

RESULTS

A total of 48 465 potential drug interactions were identified in 10 415 (4.6%) of the 228 550 patients with at least one prescription for a QT-prolonging drug. Amitriptyline was involved in 37 859 (78.1%) of the drug interactions. Of all potential drug interactions, 43 689 (90.1%) occurred in patients with at least one other risk factor for torsades de pointes, and 1053 (2.2%) were listed as a contraindicated combination in product labeling.

CONCLUSION

Potential drug interactions involving currently marketed QT-prolonging drugs occurred in 4.6% of patients who had a prescription for a QT-prolonging medication. The findings suggest several areas for targeted interventions to decrease the potential risk from QT-prolonging medications.

摘要

目的

QT间期延长与尖端扭转型室速及死亡风险增加相关。同时使用一种以上延长QT间期的药物,或一种延长QT间期的药物与另一种能改变其药代动力学特征的药物联用,是导致不良后果的重要危险因素。

方法

利用1999年1月至2001年7月期间来自10家提供药学福利的健康维护组织的200万健康计划成员的代表性样本,我们确定了涉及延长QT间期药物的潜在药物相互作用。两种或更多种延长QT间期的药物,或一种延长QT间期的药物与一种能改变其清除率的药物,其处方申请重叠至少7天,被视为潜在的药物相互作用。我们确定了总体药物相互作用的数量,以及这些相互作用中涉及有其他尖端扭转型室速危险因素患者的数量。

结果

在228550名至少有一张延长QT间期药物处方的患者中,有10415名(4.6%)患者共确定了48465种潜在药物相互作用。阿米替林参与了37859种(78.1%)药物相互作用。在所有潜在药物相互作用中,43689种(90.1%)发生在至少有一项其他尖端扭转型室速危险因素的患者中,1053种(2.2%)在产品标签中被列为禁忌组合。

结论

在有延长QT间期药物处方的患者中,4.6%发生了涉及目前上市的延长QT间期药物的潜在药物相互作用。研究结果提示了几个有针对性干预的领域,以降低延长QT间期药物的潜在风险。

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