Addition of a Novel Qualitative Technique to Standard Quantitative Practices for Evaluation of Hazardous Drug Exposure in a Canadian Hospital Setting.

The Canadian journal of hospital pharmacy Pub Date : 2024-07-10 eCollection Date: 2024-01-01 DOI:10.4212/cjhp.3509
Raminder Grewal, Albert Karas, Sumit Goyal
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引用次数: 0

Abstract

Background: Current recommendations from regulatory authorities suggest quantitative surface sampling for detection of hazardous drugs at least once every 6 months. A more frequent and efficient process for hazardous drug testing might reduce the safety risks associated with exposure to these agents.

Objectives: The primary objective was to assess the findings of surface testing based on traditional quantitative sampling methods relative to the findings of qualitative surface sample testing with the BD HD Check system. The secondary objectives included assessment of the ease of integrating qualitative sampling into pharmacy protocols and identification of opportunities to enhance patient and staff education and safety.

Methods: Samples from 23 unique surfaces were tested concurrently once a month for 5 months using a quantitative surface sampling method and the qualitative BD HD Check system on adjacent 12 inch × 12 inch (30.5 cm × 30.5 cm) surface areas. The presence or absence of cyclophosphamide, methotrexate, and/or doxorubicin contamination was assessed by each of the 2 testing methods. The BD HD Check system was also assessed for ease of use and efficiency.

Results: Ten areas of contamination were identified over the 5-month period. Nine were detected by the BD HD Check system and one by the quantitative system. The BD HD Check system was easy to use, with results available in less than 10 minutes per area tested.

Conclusions: The BD HD Check system allows for more timely identification of surface contamination with hazardous drugs than the standard sampling protocol. The discrepancy in results between the 2 methods of hazardous drug surface sampling requires further investigation.

在标准定量评估方法的基础上增加一种新的定性技术,用于评估加拿大医院环境中的危险药物暴露。
背景:目前,监管机构建议至少每 6 个月进行一次定量表面采样以检测危险药物。更频繁、更高效的危险药物检测过程可能会降低接触这些制剂所带来的安全风险:主要目的是评估基于传统定量采样方法的表面检测结果与使用 BD HD Check 系统进行定性表面采样检测的结果。次要目标包括评估将定性采样纳入药房方案的难易程度,以及确定加强患者和员工教育与安全的机会:方法:使用定量表面取样方法和定性 BD HD Check 系统对相邻的 12 英寸×12 英寸(30.5 厘米×30.5 厘米)表面区域进行检测,每月一次,连续检测 5 个月,共检测 23 个独特表面的样本。这两种检测方法分别评估是否存在环磷酰胺、甲氨蝶呤和/或多柔比星污染。此外,还对 BD HD Check 系统的易用性和效率进行了评估:结果:5 个月期间共发现 10 个污染区域。结果:5 个月内发现了 10 个污染区,其中 9 个是 BD HD Check 系统检测到的,1 个是定量系统检测到的。BD HD Check 系统易于使用,每个区域的检测结果可在 10 分钟内得出:结论:与标准采样方案相比,BD HD Check 系统能更及时地识别危险药物的表面污染。两种危险药物表面采样方法的结果差异需要进一步调查。
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