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Hospital Audit as a Useful Tool in the Process of Introducing Falsified Medicines Directive (FMD) into Hospital Pharmacy Settings?¢????A Pilot Study

机译:在将伪造药品指令(FMD)引入医院药房的过程中,医院审计是一种有用的工具-一项初步研究

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Background: Recently, the European Union has introduced the Falsified Medicines Directive (FMD). Additionally, in early 2016, a Delegated Act (DA) related to the FMD was published. The main objective of this study was to evaluate the usefulness of external audits in the context of implementing new regulations provided by the FMD in the secondary care environment. Methods: The external, in-person workflow audits were performed by an authentication company in three Polish hospital pharmacies. Each audit consisted of a combination of supervision (non-participant observation), secondary data analysis, and expert interviews with the use of an independently designed authorial Diagnostic Questionnaire. The questionnaire included information about hospital drug distribution procedures, data concerning drug usage, IT systems, medication order systems, the processes of medication dispensing, and the preparation and administration of hazardous drugs. Data analysis included a thorough examination of hospital documentation in regard to drug management. All data were subjected to qualitative analysis, with the aim of generating meaningful information through inductive inference. Results: Only one dispensing location in the Polish hospitals studied has the potential to be a primary authentication area. In the audited hospitals, an Automated Drug Dispensing System and unit dose were not identified during the study. Hospital wards contained an enclosed place within the department dedicated to drug storage under the direct supervision of senior nursing staff. An electronic order system was not available. In the largest center, unused medications are re-dispensed to different hospital departments, or may be sold to various institutions. Additionally, in one hospital pharmacy, pharmacists prepared parenteral nutrition and chemotherapeutic drugs for patients admitted to the hospital. Conclusions: External audits might prove beneficial in the course of introducing new regulations into everyday settings. However, such action should be provided before the final implementation of authentication services. To sum up, FMD can impact several hospital departments.
机译:背景:最近,欧盟引入了伪造药品指令(FMD)。此外,2016年初,发布了与FMD有关的授权法案(DA)。这项研究的主要目的是在二级保健环境中,在实施FMD提供的新法规的背景下,评估外部审计的有效性。方法:由一家认证公司在波兰的三家医院药房进行外部亲自工作流程审核。每次审核由监督(非参与者观察),辅助数据分析和专家访谈(结合使用独立设计的权威诊断调查表)组成。问卷包括有关医院药物分配程序的信息,有关药物使用情况的数据,IT系统,药物订购系统,药物分配过程以及危险药物的制备和管理。数据分析包括彻底检查有关药物管理的医院文件。所有数据都经过定性分析,目的是通过归纳推理产生有意义的信息。结果:在所研究的波兰医院中,只有一个配药地点有可能成为主要认证区域。在经审核的医院中,研究过程中未确定自动配药系统和单位剂量。医院病房在高级护理人员的直接监督下,在部门内设有一个专用于药品存储的封闭场所。电子订购系统不可用。在最大的中心,未使用的药物被重新分配到不同的医院部门,或者可以出售给各个机构。此外,在一家医院药房中,药剂师为入院的患者准备了肠胃外营养和化学治疗药物。结论:在将新法规引入日常环境的过程中,外部审计可能被证明是有益的。但是,应在最终实施身份验证服务之前提供此类操作。综上所述,口蹄疫可能会影响几个医院部门。

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