Borgonje Paula E, Wibier Lisa, Noordman Patrick, Woerdenbag Herman J, Gareb Bahez
Department of Clinical Pharmacy, Meander Medical Centre, Maatweg 3, 3813 TZ Amersfoort, The Netherlands.
Apotheek A15, Buys Ballotstraat 2, 4207 HT Gorinchem, The Netherlands.
Pharmacy (Basel). 2022 Aug 23;10(5):101. doi: 10.3390/pharmacy10050101.
In the compounding facilities of hospital pharmacies, extemporaneous preparations for parenteral administration are produced using aseptic handling. The designated environment for this practice is a clean area, such as a laminar airflow (LAF) cabinet placed in a classified cleanroom complying with good manufacturing practices (GMP) and International Organization for Standardization (ISO) 14644-1 guidelines. The European GMP Annex 1 (Revision 2020) and United States Pharmacopeia (USP) <797> monograph state that airflow visualization studies (“smoke” studies) should be performed to substantiate the cleanroom and LAF cabinet performance and their qualification status. Even though smoke studies are required by these guidelines, current literature does not describe detailed practical protocols and acceptance criteria. The objective of this study was to develop and implement a practical smoke study protocol to ensure compliance with aseptic handling guidelines in hospital pharmacies. First, a literature search was performed to collect information about smoke study protocols and acceptance criteria. Subsequently, a smoke study protocol was developed for a downflow and crossflow LAF cabinet as well as for grade C/B cleanroom areas. As a proof of concept, the smoke study protocol for the downflow LAF cabinet was executed in the at-rest and in-operation states. Video recordings of the smoke studies were analyzed to assess the performance of the cabinet. Finally, the video recordings obtained from the smoke studies were used in a training program for hospital pharmacy operators, which showed that smoke studies might aid in operators’ aseptic handling awareness. To the best of our knowledge, the present study provides for the first time a practical approach for the development of smoke study protocols in a hospital pharmacy setting and shows potential for training operators, process optimization, and continuous quality improvement.
在医院药房的配制设施中,通过无菌操作制备用于肠胃外给药的临时制剂。进行这种操作的指定环境是一个洁净区域,例如放置在符合良好生产规范(GMP)和国际标准化组织(ISO)14644-1指南的分级洁净室内的层流通风柜(LAF)。欧洲GMP附录1(2020年修订版)和美国药典(USP)<797>专论指出,应进行气流可视化研究(“烟雾”研究),以证实洁净室和层流通风柜的性能及其合格状态。尽管这些指南要求进行烟雾研究,但当前文献并未描述详细的实际方案和验收标准。本研究的目的是制定并实施一项实际的烟雾研究方案,以确保医院药房符合无菌操作指南。首先,进行文献检索以收集有关烟雾研究方案和验收标准的信息。随后,针对垂直流和水平流层流通风柜以及C/B级洁净室区域制定了烟雾研究方案。作为概念验证,在静止状态和运行状态下对垂直流层流通风柜的烟雾研究方案进行了执行。对烟雾研究的视频记录进行分析,以评估通风柜的性能。最后,从烟雾研究中获得的视频记录被用于医院药房操作人员的培训计划,结果表明烟雾研究可能有助于提高操作人员的无菌操作意识。据我们所知,本研究首次提供了一种在医院药房环境中制定烟雾研究方案的实际方法,并显示出在培训操作人员、优化流程和持续质量改进方面的潜力。