Development and Implementation of an Ultraviolet-Dye-Based Qualification Procedure for Hand Washing and Disinfection to Improve Quality Assurance of Pharmacy Preparations and Compounding, Especially in Cleanrooms: A Pilot Study.

IF 2 Q3 PHARMACOLOGY & PHARMACY Pharmacy Pub Date : 2024-04-25 DOI:10.3390/pharmacy12030073
Catharina W J Knol, Paul H Stob, Herman J Woerdenbag
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Abstract

Even though, nowadays, most medicines are manufactured industrially, patients may have medical needs that can only be met by a tailor-made approach. This requires the availability of pharmacy preparations made under Good Manufacturing Practice (GMP) conditions. An efficient hand hygiene practice is essential herewith, especially if sterile products that are prepared in a cleanroom are concerned. The effectiveness of hand washing and hand disinfection procedures greatly relies on adequate training. We carried out an observational cross-sectional pilot study aimed at optimizing hand hygiene training with objective and measurable quality assessments using an ultraviolet (UV) dye. Practical acceptance criteria for qualifying personnel through this method were set and evaluated. In total, 25 GMP-qualified cleanroom operators washed and disinfected their hands with UV dye hand wash lotion and UV dye hand alcohol, respectively. To obtain a proof-of-concept, the results were judged based on adherence to the WHO six-step protocol and associated acceptance criteria. Commonly missed areas were brought to light, and the influence of procedure duration was investigated. UV-dye-based assessments appeared to be more valuable in hand disinfection than in hand washing. In both procedures, the back of the hands and the thumbs were frequently missed. This underpins the need for enhanced and repeated education on hand washing and disinfection. Additionally, a dry skin gave rise to extra cleaning challenges. From this pharmacy practice pilot study with a focus on pharmaceutical product care, it may be concluded that the application of UV-dye-based assessments offers valuable insights for pharmacists to optimize hand hygiene, thereby increasing the safety of tailor-made medicines and on-site preparations.

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开发和实施基于紫外线-染料的洗手和消毒资格鉴定程序,以提高药物制剂和复方制剂的质量保证,尤其是在洁净室中:试点研究。
尽管如今大多数药品都是工业化生产的,但病人的医疗需求可能只能通过量身定制的方法来满足。这就需要有在药品生产质量管理规范(GMP)条件下生产的药剂。因此,有效的手部卫生操作至关重要,尤其是在洁净室中配制的无菌产品。洗手和手部消毒程序的有效性在很大程度上取决于充分的培训。我们开展了一项观察性横断面试点研究,旨在通过使用紫外线(UV)染料进行客观、可测量的质量评估,优化手部卫生培训。我们制定并评估了通过这种方法鉴定人员资格的实用验收标准。共有 25 名通过 GMP 认证的洁净室操作人员分别使用紫外线染料洗手液和紫外线染料洗手酒精进行了洗手和消毒。为获得概念验证,根据世界卫生组织的六步方案和相关验收标准对结果进行了评判。常见的遗漏区域被揭示出来,程序持续时间的影响也得到了研究。与洗手相比,基于紫外线染料的评估似乎对手部消毒更有价值。在这两种程序中,手背和大拇指经常被遗漏。这说明有必要加强和反复开展洗手和消毒教育。此外,皮肤干燥也给清洁工作带来了额外的挑战。从这项以药品护理为重点的药房实践试点研究中可以得出结论,应用基于紫外线染料的评估为药剂师优化手部卫生提供了宝贵的见解,从而提高了定制药品和现场制剂的安全性。
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来源期刊
Pharmacy
Pharmacy PHARMACOLOGY & PHARMACY-
自引率
9.10%
发文量
141
审稿时长
11 weeks
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