对美国医院不良药物事件监测实践的检查。

J P Juergens, S L Szeinbach
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引用次数: 0

摘要

不幸的是,受访者对ADE监测持消极态度和看法的原因并不完全清楚,因为它们通常与时间或人员限制无关。有迹象表明,不良的医疗记录文件是一个促成因素;然而,这一问题可以通过教育医生和护士了解获取和报告不良反应数据的重要性来解决。其他研究表明,医疗保健团队的所有成员都需要付出巨大的努力和勤奋才能始终如一地捕获ade。幸运的是,不幸的是,建立和维持一个有效的ADE监测计划的动机和至少最初的精力必须来自药房。最大的担忧是,许多药剂师对这个问题漠不关心,不投入必要的时间和精力来有效地获取和处理ADE信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An examination of adverse drug event monitoring practices in U.S. hospitals.

Unfortunately, the reasons for respondents' negative attitudes and perceptions toward ADE monitoring are not entirely clear because they generally are not related to time or staff constraints. There was some indication that poor medical record documentation was a contributing factor; however, this problem can be addressed through education of physicians and nurses as to the importance of capturing and reporting ADE data. Other research has demonstrated that substantial effort and diligence are required on the part of all members of the health care team to capture ADEs consistently. Fortunately or unfortunately--depending on the perspective--the motivation and at least the initial energy to establish and maintain an effective ADE monitoring program have to come from the pharmacy department. The greatest fear is that many pharmacists simply will be apathetic to the issue and not devote the time and energy necessary to capture and process ADE information effectively.

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