首页> 外文期刊>PLoS One >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
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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

机译:药物评估工具的开发与验证,以评估在科威特后急性冠状动脉综合征患者冠心病中的冠心病中的二次预防依据依据依据依据

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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 (MAT STEMI and MAT NSTEACS ). 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 CVR0.54 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 MAT STEMI and MAT NSTEACS consisted of eighteen and twelve medication-related criteria, respectively. Face validity resulted in dividing each MAT into five dimensions. In the MAT STEMI , 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 MAT NSTEACS , 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 MAT STEMI and MAT NSTEACS 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. MAT STEMI and MAT NSTEACS were developed and validated to be utilized for optimizing medication therapy management and improving therapeutic interventions.
机译:估计心血管疾病估计导致科威特所有死亡率的46%。基于证据的临床实践的目的导致了对药物评估工具(垫子)设计的兴趣增加,以确定与基于证据的实践的偏差,最终提供一致的标准规定的基础。本研究旨在使用国际准则提取的质量标准开发和验证垫子,以评估急性冠状动脉综合征(Stemi或NSTEACS的患者冠心病二次预防的处方实践。审查了国际指南以开发两垫( STEMI和MAT NSTEACS)。开发工具的面部和内容有效性与三位垫专家和十三名心脏病学术。使用了两种定量方法来确定内容有效性:(i)内容有效性比(CVR)和CVR值的平均值;(ii)物品级(I-CVI)的内容有效性指数,以及工具的比例级(S-CVI / AVE),具有平均方法。具有CVR <0.54和I-CVI的标准淘汰。最终,在66名患者的记录中进行了两种垫子的可行性测试,作为试点研究。最初的发达的席位和垫NSTEAC组成了十八和十二种药物相关的标准,RE观察。面部有效性导致将每个垫分为五个维度。在掩模STEMI中,三个标准具有CVR值& 0.54和i-cvis& 70%。消除了两个标准,保留了一个标准。这导致了十六条标准,平均CVR 0.85和S-CVI / AVE 92.3%。在Mat NSTEAC中,消除了一个标准。这导致11个平均CVR 0.93和S-CVI / AVE的标准96.5%。 STEMI和MAT NSTEAS的整体粘附评分分别为64.1%(95%CI:57.8-69.9%)和62.0%(95%CI:53.4-69.9%)。它被认为是两个垫子的中间粘附。 STEMI和MAT NSTEACS开发并验证,可用于优化药物治疗管理和改善治疗干预措施。

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