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老年单纯性尿路感染女性中喹诺酮类药物与延长QT间期药物相互作用的描述

A Description of QT-Interval Prolonging Drug Interactions with Fluoroquinolones in Older Women with Uncomplicated Urinary Tract Infections.

作者信息

Trenaman Shanna C, von Maltzahn Maia, Stewart Samuel Alan, Tamim Hala, Sketris Ingrid, Black Emily

机构信息

College of Pharmacy, Faculty of Health, Dalhousie University, Halifax, NS.

Geriatric Medicine, Nova Scotia Health, Halifax, NS.

出版信息

Can Geriatr J. 2025 Sep 3;28(3):228-234. doi: 10.5770/cgj.28.835. eCollection 2025 Sep.

Abstract

BACKGROUND

Fluoroquinolone (FQ) antibiotics are associated with QT-interval prolongation and Torsades de Pointes (TdP). Female sex, older age, and other QT-interval prolonging medications further increase risk for TdP. Our aim was to describe QT-interval prolonging drug interactions when FQs were dispensed to women who resided in long-term care (LTC) for uncomplicated urinary tract infections (UTIs).

METHODS

This retrospective cohort study used administrative health data from the Nova Scotia Seniors' Pharmacare program from January 2005 through March 2020. The cohort included women residing in LTC dispensed a FQ antibiotic within five days of a diagnostic code for an uncomplicated UTI in physician billing data. Additional drug dispensations were collected 30 and 90 days after the FQ to identify drug interactions that resulted in potentially increased QT-interval prolongation risk. Drug interactions were described. A Mann-Kendall trend test assessed the change in the frequency of FQ-drug interactions over the study period.

RESULTS

Annual dispensation of FQs ranged from 12-28% of antibiotic dispensations for presumed uncomplicated UTI. The proportion of FQ dispensations associated with a QT-interval prolonging drug interaction increased over time (=.00007). Within 30 days of the FQ dispensation, the most common drug interactions identified were: furosemide (n=702, 20.3% of FQ-drug interactions), citalopram (n=566, 16.4% of FQ-drug interactions), and trazodone (n=461, 13.3% of FQ-drug interactions).

CONCLUSIONS

An increasing proportion of women dispensed a FQ for uncomplicated UTI experienced a potential QT-interval prolonging drug interaction over the study period. When prescribing FQs to older women, addressing potentially modifiable risk factors for TdP, and monitoring closely, is warranted.

摘要

背景

氟喹诺酮(FQ)类抗生素与QT间期延长及尖端扭转型室速(TdP)有关。女性、老年以及其他可延长QT间期的药物会进一步增加TdP的风险。我们的目的是描述在为长期护理(LTC)机构中患有单纯性尿路感染(UTI)的女性开具FQ类药物时,药物间延长QT间期的相互作用情况。

方法

这项回顾性队列研究使用了2005年1月至2020年3月新斯科舍省老年人药物护理项目的行政健康数据。该队列包括在医生计费数据中因单纯性UTI诊断代码而在五天内开具了FQ类抗生素的LTC机构女性居民。在开具FQ类药物30天和90天后收集额外的药物配给信息,以识别导致QT间期延长风险可能增加的药物相互作用。对药物相互作用进行了描述。采用Mann-Kendall趋势检验评估研究期间FQ类药物相互作用频率的变化。

结果

在假定为单纯性UTI的抗生素配给中,FQ类药物的年配给量占12%-28%。与QT间期延长药物相互作用相关的FQ类药物配给比例随时间增加(P=.00007)。在开具FQ类药物的30天内,识别出的最常见药物相互作用为:呋塞米(n=702,占FQ类药物相互作用的20.3%)、西酞普兰(n=五百六十六,占FQ类药物相互作用的16.4%)和曲唑酮(n=461,占FQ类药物相互作用的13.3%)。

结论

在研究期间,为单纯性UTI开具FQ类药物的女性中,经历潜在QT间期延长药物相互作用的比例不断增加。在为老年女性开具FQ类药物时,有必要考虑并处理TdP的潜在可改变风险因素,并密切监测。

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