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长期药物治疗依从性的证据:随机对照试验的系统评价

Evidence for compliance with long-term medication: a systematic review of randomised controlled trials.

作者信息

King Michelle A, Pryce Rebecca L

机构信息

School of Pharmacy, Gold Coast Campus, Griffith University, Gold Coast, QLD, 4222, Australia,

出版信息

Int J Clin Pharm. 2014 Feb;36(1):128-35. doi: 10.1007/s11096-013-9893-6. Epub 2013 Nov 30.

DOI:10.1007/s11096-013-9893-6
PMID:24293307
Abstract

BACKGROUND

Pharmacists play a pivotal role in optimising medication use which often includes actions to maximise compliance with long-term medication. The best evidence to support medication use is derived from randomised controlled trials (RCTs). It is often assumed that 100 % compliance is required to obtain the outcomes identified in the trial. This assumption needs to be examined.

OBJECTIVE

To systematically review the reporting of compliance in RCTs of long-term medications.

METHOD

RCTs published in the New England Journal of Medicine, Journal of the American Medical Association, Lancet and BMJ in 2012, were reviewed to identify trials of medications for long-term use in adults. These trials were examined to evaluate the reporting of compliance.

MAIN OUTCOME MEASURES

The proportion of trials reporting compliance data, the methods used, and the proportion of trials using more than one method to determine compliance.

RESULTS

Of the 289 RCTs published in 2012, 25 assessed long-term medications in adults. Compliance was reported in 12 (48 %) studies and only 2 (8 %) studies used more than one method to measure compliance. Pill count was the most commonly reported method for measuring compliance, with patient reports and blood levels also being used.

CONCLUSION

The reporting of compliance in RCTs is poor and the methodology inconsistent. The methods used overestimate compliance. If compliance in a clinical trial is low, the evidence for the effectiveness and most importantly safety of the medication(s) is questionable. Two or more methods, one of which is standardised, should be used to measure compliance in clinical trials. The requirement to report compliance should be included in publication guidelines.

摘要

背景

药剂师在优化药物使用方面发挥着关键作用,这通常包括采取行动以最大程度地提高长期用药的依从性。支持药物使用的最佳证据来自随机对照试验(RCT)。人们通常认为,要获得试验中确定的结果需要100%的依从性。这一假设需要审视。

目的

系统评价长期药物随机对照试验中依从性的报告情况。

方法

对2012年发表在《新英格兰医学杂志》《美国医学会杂志》《柳叶刀》和《英国医学杂志》上的随机对照试验进行综述,以确定针对成人长期使用药物的试验。对这些试验进行审查以评估依从性的报告情况。

主要观察指标

报告依从性数据的试验比例、所使用的方法,以及使用不止一种方法确定依从性的试验比例。

结果

在2012年发表的289项随机对照试验中,有25项评估了成人长期使用的药物。12项(48%)研究报告了依从性,只有2项(8%)研究使用不止一种方法来衡量依从性。药片计数是最常报告的衡量依从性的方法,患者报告和血液水平也被使用。

结论

随机对照试验中依从性的报告情况不佳,方法也不一致。所使用的方法高估了依从性。如果临床试验中的依从性较低,那么药物有效性以及最重要的安全性的证据就值得怀疑。在临床试验中应使用两种或更多种方法来衡量依从性,其中一种应是标准化的。报告依从性的要求应纳入出版指南。

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