Introduction of EUBIS standards to upgrade inspections of blood establishments to improve the safety of blood transfusion: The Polish experience.

IF 1.5 4区 医学 Q3 HEMATOLOGY Transfusion Medicine Pub Date : 2023-12-01 Epub Date: 2023-09-21 DOI:10.1111/tme.13007
Elżbieta Lachert, Jolanta Antoniewicz-Papis, Agata Mikołowska, Jolanta Kubis, Zbigniew M Szczepiorkowski, Magdalena Łętowska
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Abstract

Background and objectives: The competent authority (CA) responsible for external inspections of Polish blood establishments (BEs) and supervision of the quality system is the Institute of Haematology and Transfusion Medicine (IHTM). Before the implementation of the European Blood Inspection System (EuBIS) classification of non-compliance, the IHTM inspections were conducted according to national guidelines and the non-compliance-related recommendations were based on the inspectors' own experience and interpretation of the observed problems. Since 2009, IHTM inspections were already performed according to EuBIS guidelines. The study assessed the impact of the EuBIS classification on the IHTM recommendations. We assumed that the implementation of consistent assessment criteria contributed to the upgrading of the quality of BE inspections.

Materials and methods: BE-inspection protocols; 30 from 2009 to 2010 and 61 from 2016 to 2019. Non-compliance-related recommendations were classified according to the seriousness of non-compliances (critical, major, other significant, and observation) and also to the area of BE activity (documentation, organisation of work, qualification and validation, pathway from donor qualification to blood component-issue, quality control of blood components, adverse events and reactions).

Results: The recommendations mostly referred to document-keeping and work organisation and were distributed as follows: 2009-2 critical (others unclassified), 2010-1-13 major, 4-25 other significant and 1-7 suggestions, 2016-2019-3-9 critical, 90-196 major, and 157-297 other significant as well as 14-22 suggestions.

Conclusion: Polish BEs still require: integrated document management, analysis of IHTM recommendations, implementation of corrective and preventive measures and personnel training in identifying similar non-compliances in other procedures.

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引入EUBIS标准以升级血液机构的检查,以提高输血安全性:波兰的经验。
背景和目标:负责波兰血液机构外部检查和质量体系监督的主管机构是血液学和输血医学研究所。在实施欧洲血液检查系统(EuBIS)的不合规分类之前,IHTM检查是根据国家指南进行的,与不合规相关的建议是基于检查员自己的经验和对观察到的问题的解释。自2009年以来,IHTM已根据欧洲清算银行的指导方针进行了检查。该研究评估了EuBIS分类对IHTM建议的影响。我们认为,实施一致的评估标准有助于提高BE检查的质量。材料和方法:BE检验协议;2009年至2010年为30人,2016年至2019年为61人。根据不合规的严重性(关键、重大、其他重大和观察)以及BE活动的领域(文件、工作组织、资格和验证、从捐献者资格到血液成分问题的途径、血液成分的质量控制、不良事件和反应)对不合规相关建议进行分类建议主要涉及文件保存和工作组织,分布如下:2009-2关键(其他未分类),2010-1-13主要,4-25其他重要和1-7建议,2016-2019-3-9关键,90-196主要,157-297其他重要和14-22建议。结论:波兰BEs仍然需要:综合文件管理、IHTM建议分析、纠正和预防措施的实施以及人员培训,以识别其他程序中的类似不符合项。
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来源期刊
Transfusion Medicine
Transfusion Medicine 医学-血液学
CiteScore
2.70
自引率
0.00%
发文量
96
审稿时长
6-12 weeks
期刊介绍: Transfusion Medicine publishes articles on transfusion medicine in its widest context, including blood transfusion practice (blood procurement, pharmaceutical, clinical, scientific, computing and documentary aspects), immunohaematology, immunogenetics, histocompatibility, medico-legal applications, and related molecular biology and biotechnology. In addition to original articles, which may include brief communications and case reports, the journal contains a regular educational section (based on invited reviews and state-of-the-art reports), technical section (including quality assurance and current practice guidelines), leading articles, letters to the editor, occasional historical articles and signed book reviews. Some lectures from Society meetings that are likely to be of general interest to readers of the Journal may be published at the discretion of the Editor and subject to the availability of space in the Journal.
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