Northern Ireland Public Health Laboratory, Department of Bacteriology, Belfast City Hospital, Belfast, Northern Ireland, United Kingdom.
School of Biomedical Sciences, Ulster University, Coleraine, Northern Ireland, United Kingdom.
Respir Care. 2020 Oct;65(10):1443-1450. doi: 10.4187/respcare.07362. Epub 2020 Mar 24.
Nebulizer therapy is an important treatment component for patients with cystic fibrosis (CF). Nebulizer manufacturers' guidelines advocate thorough nebulizer drying after washing. The aim of this study, therefore, was to examine the microbiology associated with nebulizer drying, particularly related to control, and to examine microbiologically non-adherence to the recommended drying procedures.
Four aspects of nebulizer drying were examined in 3 common nebulizers, including examination of the drying profile, improvement to the drying profile of assembled nebulizers, survival of in tap water and in tap water plus 0.5% (v/v) dishwashing detergent, and the effect of drying of in tap water and tap water plus residual sputum (1%v/v, 10%v/v). Microbiologic examination was performed by using (5 clinical CF strains plus 1 National Collection of Type Cultures Reference strain).
There were differences in the time to complete dryness between disassembled and fully assembled nebulizers. Vigorous repeated shaking was unable to drive off all residual water on assembled nebulizers. counts did not decrease significantly in either tap water or in tap water plus detergent after 24 h storage at ambient temperature. In contrast, all organisms were killed when nebulizers were dried for 24 h, even when contaminated with 1% and 10% sputum. Dishwashing detergent did not demonstrate any antibacterial activity.
This study demonstrated that nebulizer drying, if applied properly, had the ability to reduce counts of to non-detectable levels. Equally, this study showed that, if the device was not dried thoroughly and moisture remained, then the device was able to support the survival of at high numbers, which constituted an infection risk to the patient with CF. This information may help educate and inform the patient with CF about the importance of proper nebulizer drying for control to improve patient awareness and safety.
雾化器治疗是囊性纤维化(CF)患者的重要治疗组成部分。雾化器制造商的指南主张在清洗后彻底干燥雾化器。因此,本研究的目的是检查与雾化器干燥相关的微生物学,特别是与控制相关的微生物学,并检查不遵守推荐干燥程序的微生物学情况。
在 3 种常见的雾化器中检查了雾化器干燥的 4 个方面,包括检查干燥曲线、改善组装好的雾化器的干燥曲线、在自来水和自来水加 0.5%(v/v)洗碗液中的存活情况,以及在自来水中干燥和自来水加残留痰(1%v/v、10%v/v)对 的影响。微生物学检查使用(5 株临床 CF 菌株加 1 株国家类型培养物参考菌株)进行。
拆卸和组装好的雾化器完全干燥所需的时间存在差异。剧烈反复摇晃无法去除组装好的雾化器上的所有残留水分。在环境温度下储存 24 小时后,自来水中的 计数没有显著下降,即使在加入洗碗液后也是如此。相比之下,即使雾化器受到 1%和 10%痰液的污染,干燥 24 小时后所有 生物均被杀死。洗碗液没有表现出任何抗菌活性。
本研究表明,正确应用雾化器干燥能够将 的数量减少到无法检测的水平。同样,本研究表明,如果设备没有彻底干燥并且仍有水分存在,则设备能够以高数量支持 的存活,这对 CF 患者构成了感染风险。这些信息可能有助于教育和告知 CF 患者适当的雾化器干燥对于 控制的重要性,以提高患者的意识和安全性。