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开发和验证药物评估工具,以评估科威特急性冠脉综合征后患者二级预防冠心病的处方依从性是否符合循证指南。

Development and validation of medication assessment tools to evaluate prescribing adherence to evidence-based guidelines for secondary prevention of coronary heart disease in post-acute coronary syndromes patients in Kuwait.

机构信息

Department of Pharmacy Practice, Faculty of Pharmacy, Kuwait University, Jabriya, Kuwait.

出版信息

PLoS One. 2020 Nov 30;15(11):e0241633. doi: 10.1371/journal.pone.0241633. eCollection 2020.

Abstract

Cardiovascular diseases are estimated to cause 46% of all mortalities in Kuwait. The aim of evidence-based clinical practice has led to an increased interest in the design of medication assessment tools (MATs) to identify deviations from evidence-based practice, and eventually provide the basis of consistent standardized prescribing. This study was designed to develop and validate MATs using quality standards extracted from international guidelines to evaluate prescribing practices in secondary prevention of coronary heart disease in patients with post-acute coronary syndrome (STEMI or NSTEACS]. International guidelines were reviewed to develop two MATs (MATSTEMI and MATNSTEACS). Face and content validity of the developed tools was performed with three MAT experts and thirteen cardiologists. Two quantitative approaches were used to determine content validity: (i) Content Validity Ratio (CVR) and the average of CVR values; and (ii) Content validity index at item level (I-CVI) and scale-level of the tool (S-CVI/Ave) with the average approach. Criteria with a CVR<0.54 and I-CVI <70% were eliminated. Ultimately, feasibility testing of both MATs was performed on 66 patients' records as a pilot study. The initial developed MATSTEMI and MATNSTEACS consisted of eighteen and twelve medication-related criteria, respectively. Face validity resulted in dividing each MAT into five dimensions. In the MATSTEMI, three criteria had CVR values < 0.54 and I-CVIs < 70%. Two criteria were eliminated and one was retained. This resulted in sixteen criteria with average CVR 0.85 and S-CVI/Ave 92.3%. In the MATNSTEACS, one criterion was eliminated. This resulted in eleven criteria with average CVR 0.93 and S-CVI/Ave 96.5%. The overall adherence scores to the MATSTEMI and MATNSTEACS were 64.1% (95% CI: 57.8-69.9%) and 62.0% (95% CI: 53.4-69.9%), respectively. It was judged as intermediate adherence for both MATs. MATSTEMI and MATNSTEACS were developed and validated to be utilized for optimizing medication therapy management and improving therapeutic interventions.

摘要

在科威特,心血管疾病估计导致了 46%的总死亡率。循证临床实践的目的导致人们对药物评估工具 (MAT) 的设计越来越感兴趣,以确定与循证实践的偏差,并最终为一致的标准化处方提供依据。本研究旨在使用从国际指南中提取的质量标准来开发和验证 MAT,以评估急性冠脉综合征后 (STEMI 或 NSTEACS) 患者冠心病二级预防中的处方实践。回顾了国际指南,以开发两种 MAT (MATSTEMI 和 MATNSTEACS)。通过三位 MAT 专家和十三位心脏病专家对开发的工具进行了表面效度和内容效度评估。采用两种定量方法来确定内容效度:(i)内容效度比 (CVR) 和 CVR 值的平均值;以及 (ii) 工具的项目水平内容效度指数 (I-CVI) 和工具的平均水平内容效度指数 (S-CVI/Ave)。CVR<0.54 和 I-CVI<70%的标准被删除。最终,对这两种 MAT 进行了 66 例患者记录的可行性测试,作为一项试点研究。最初开发的 MATSTEMI 和 MATNSTEACS 分别包含十八个和十二个与药物相关的标准。表面效度将每个 MAT 分为五个维度。在 MATSTEMI 中,有三个标准的 CVR 值<0.54,I-CVI<70%。删除了两个标准,保留了一个标准。结果是 16 个标准的平均 CVR 为 0.85,S-CVI/Ave 为 92.3%。在 MATNSTEACS 中,删除了一个标准。结果是 11 个标准的平均 CVR 为 0.93,S-CVI/Ave 为 96.5%。MATSTEMI 和 MATNSTEACS 的总体依从评分分别为 64.1%(95%CI:57.8-69.9%)和 62.0%(95%CI:53.4-69.9%)。这两种 MAT 的判断结果为中等依从性。已经开发并验证了 MATSTEMI 和 MATNSTEACS,以用于优化药物治疗管理和改善治疗干预。

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