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首页> 外文期刊>The annals of pharmacotherapy >Proposal of Standardization to Assess Adherence With Medication Records: Methodology Matters
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Proposal of Standardization to Assess Adherence With Medication Records: Methodology Matters

机译:关于药物记录依从性评估的标准化提案:方法学问题

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摘要

Background: Medication adherence is the process by which patients take their medication as prescribed and is an umbrella term that encompasses all aspects of medication use patterns. Ambiguous terminology has emerged to describe a deviation from prescribed regimen, forcing the European ABC Project to define 3 phases of medication use: initiation, implementation, and discontinuation. However, different measures of medication adherence using medication records are currently available that do not always distinguish between these phases. The literature is lacking standardization and operationalization of the assessment methods. Objective: To propose a harmonization of standards as well as definitions of distinct measures and their operationalization to quantify adherence to medication from medication records. Methods: Group discussions and consensus process among all coauthors. The propositions were generated using the authors' experiences and views in the field of adherence, informed by theory. Results: The concepts of adherence measures within the new taxonomy were harmonized, and the standards necessary for the operationalization of adherence measures from medication records are proposed. Besides percentages and time-to values, the addition of a dichotomous value for the reinitiation of treatment is proposed. Methodological issues are listed that should be disclosed in studies on adherence. Conclusions: The possible impact of the measures in adherence research is discussed. By doing this, the results of future adherence research should gain in accuracy. Finally, studies will become more transparent, enabling comparison between studies.
机译:背景:药物依从性是患者按照处方服用药物的过程,是涵盖药物使用模式各个方面的总称。出现了模棱两可的术语来描述偏离处方方案的情况,这迫使欧洲ABC项目定义了药物使用的三个阶段:开始,实施和停用。然而,目前有使用药物记录的药物依从性的不同度量,这些度量不能总是区分这些阶段。文献缺乏评估方法的标准化和可操作性。目的:提出标准的统一以及不同措施的定义及其可操作性,以量化用药记录中对药物的依从性。方法:所有共同作者之间进行小组讨论和达成共识。这些命题是根据作者在依从性领域的经验和观点得出的,并从理论上得到了启发。结果:统一了新分类法中的依从性措施概念,并提出了根据药物记录实施依从性措施所需的标准。除了百分比和达到时间的值外,还建议增加一个二分值以重新开始治疗。列出了在依从性研究中应披露的方法论问题。结论:讨论了这些措施对依从性研究的可能影响。通过这样做,将来的依从性研究的结果应获得准确性。最后,研究将变得更加透明,从而可以进行研究之间的比较。

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