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Medication Errors Associated With Adverse Drug Reactions in Iran (2015-2017): A P-Method Approach

机译:与伊朗药物不良反应相关的用药错误(2015-2017年):P方法

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摘要

Medication errors are the second most common cause of adverse patient safety incidents and the single most common preventable cause of adverse events in medical practice. Given the high human fatalities and financial burden of medication errors for healthcare systems worldwide, reducing their occurrence is a global priority. Therefore, appropriate policies to reduce medication errors, using national data and valid statistics are required. The primary objective of this study was to provide a national ‘characteristic profile’ of medication error-associated adverse drug reactions (ADRs), which are also known as preventable ADRs (pADRs). A retrospective study of pADR reports submitted to the national pharmacovigilance center (PCV) within Iran’s Food and Drug Administration was conducted over a 2-year period (2015-2017). Preventability Method (P-Method), which is a standardized tool developed and recommended by the World Health Organization (WHO), was used for preventability assessment. The results of the analyses revealed that while the number of pADRs increased from year one to two (601 to 630), their proportion out of all ADRs per year decreased (7.32% to 6.44%). The percentage of pADRs was higher in females (61.01%) and adults (83.27%), and the highest number of reports were received by nurses (71.57%). Having ‘a documented hypersensitivity to an administered drug or drug class’ was the most common preventable factor in both years (61.23% and 54.29% respectively), and ‘anti-infectives used systemically’ were the medication class which primarily contributed to both serious (53.29%) and non-serious pADRs (39.19%). The specific characteristics of medication errors associated with ADRs from this study, especially the preventable criteria which led to theiroccurrence, can help devise more specific preventative policies.
机译:药物错误是造成患者安全不良事件的第二大最常见原因,也是医疗实践中最常见的可预防的不良事件。鉴于全世界医疗系统的高人员死亡人数和药物错误造成的经济负担,减少错误的发生是全球优先事项。因此,需要采取适当的政策来减少用药错误,使用国家数据和有效统计数据。这项研究的主要目的是提供与药物错误相关的不良药物不良反应(ADR)的全国性“特征”,也称为可预防的ADR(pADR)。在两年(2015年至2017年)期间,对提交给伊朗食品药品监督管理局国家药物警戒中心(PCV)的pADR报告进行了回顾性研究。预防性方法(P-Method)是由世界卫生组织(WHO)开发和推荐的标准化工具,用于预防性评估。分析结果表明,虽然pADR的数量从第一年增加到第二年(601到630),但它们在每年所有ADR中的比例却下降了(7.32%至6.44%)。女性(61.01%)和成年人(83.27%)的pADR百分比较高,护士收到的报告数量最高(71.57%)。在过去的两年中,“对所用药物或药物类别有超敏反应”是最常见的可预防因素(分别为61.23%和54.29%),而“系统使用抗感染药”是导致这两种情况严重的主要原因( 53.29%)和非严重的pADR(39.19%)。这项研究中与ADR相关的用药错误的具体特征,尤其是导致其发生的可预防标准发生,可以帮助制定更具体的预防政策。

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