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卡巴拉汀或加兰他敏治疗与尿失禁风险:一项荷兰数据库研究的结果

Treatment with rivastigmine or galantamine and risk of urinary incontinence: results from a Dutch database study.

作者信息

Kröger Edeltraut, Van Marum Rob, Souverein Patrick, Carmichael Pierre-Hugues, Egberts Toine

机构信息

Centre d'excellence sur le vieillissement de Québec, Centre de recherche du CHU de Québec, Québec, Canada; Utrecht University, Division of Pharmacoepidemiology and Pharmacotherapy, Utrecht Institute for Pharmaceutical Sciences, Utrecht, the Netherlands.

出版信息

Pharmacoepidemiol Drug Saf. 2015 Mar;24(3):276-85. doi: 10.1002/pds.3741. Epub 2015 Feb 4.

Abstract

BACKGROUND

Treatment of Alzheimer disease (AD) with cholinesterase inhibitors (ChEIs) may increase the risk of urinary incontinence (UI).

OBJECTIVE

To assess whether ChEI use was associated with the risk of UI among older patients with AD.

METHODS

A crossover cohort study using the PHARMO Record Linkage System included 10 years of data on drug dispensing histories for over two million Dutch residents. Included patients were aged 50 +, free of UI for the last 6 months, received a first ChEI prescription during the study period, had at least 12 months prior drug exposure history and one subsequent prescription of any drug. UI was defined as a first dispensing of a urinary spasmolytic or of incontinence products for at least 30 days. Cox regression with time-varying covariates and multivariate adjustment allowed assessing whether UI incidence was associated with ChEI exposure.

RESULTS

Among 3154 patients there were 657 UI cases during a mean follow-up of 5.1 years before a first ChEI dispensing, and 499 cases after ChEI initiation, during a mean follow-up of 2.0 years. Among the 2700 participants free of UI one year before ChEI initiation, the adjusted hazard ratio (HR) for UI was 1.13 (95% CI: 0.97-1.32) when periods with ChEI use were compared to periods without ChEI use. Sensitivity analyses may suggest an increased risk in the 1(st) month after ChEI initiation (HR: 1.72, p = 0.09) CONCLUSION: Worsening AD may increase incidence of UI, but no firm association between ChEI treatment and risk of UI could be shown from these data.

摘要

背景

使用胆碱酯酶抑制剂(ChEIs)治疗阿尔茨海默病(AD)可能会增加尿失禁(UI)的风险。

目的

评估在老年AD患者中使用ChEI是否与UI风险相关。

方法

一项使用PHARMO记录链接系统的交叉队列研究纳入了200多万荷兰居民10年的药物配药历史数据。纳入的患者年龄在50岁及以上,在过去6个月内无UI,在研究期间接受了第一张ChEI处方,有至少12个月的既往药物暴露史且后续有任何药物的一次处方。UI定义为首次配用尿路解痉药或失禁产品至少30天。采用具有时变协变量的Cox回归和多变量调整来评估UI发生率是否与ChEI暴露相关。

结果

在3154例患者中,在首次使用ChEI之前的平均5.1年随访期间有657例UI病例,在开始使用ChEI之后的平均2.0年随访期间有499例病例。在开始使用ChEI前一年无UI的2700名参与者中,将使用ChEI的时期与未使用ChEI的时期进行比较时,UI的调整后风险比(HR)为1.13(95%CI:0.97-1.32)。敏感性分析可能提示在开始使用ChEI后的第1个月风险增加(HR:1.72,p = 0.09)。结论:AD病情恶化可能会增加UI的发生率,但从这些数据中无法显示ChEI治疗与UI风险之间存在确切关联。

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