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一项关于手动通气过程中逸出性医疗气溶胶在环境中释放的体外研究。

An in vitro investigation into the release of fugitive medical aerosols into the environment during manual ventilation.

机构信息

Aerogen, IDA Business Park, Dangan, Galway, Ireland.

School of Physics & Ryan Institute's Centre for Climate and Air Pollution Studies, National University of Ireland Galway, Galway, Ireland.

出版信息

J Hosp Infect. 2021 Feb;108:135-141. doi: 10.1016/j.jhin.2020.11.029. Epub 2020 Dec 6.

Abstract

BACKGROUND

During manual resuscitation, nebulizer therapy may be used to deliver therapeutics to patients in respiratory distress. However, the devices used to generate and deliver these medical aerosols have the potential to release these therapeutics into the local environment and expose caregivers to unwanted medical aerosols.

AIM

To quantify the levels of fugitive medical aerosol released into the environment during aerosol drug delivery using a manual resuscitation bag with and without filtration.

METHODS

Time-varying fugitive aerosol concentrations were measured using an aerodynamic particle sizer placed at a position designed to mimic a caregiver. Two nebulizer types were assessed, a vibrating mesh nebulizer and a jet nebulizer. The aerosol dose delivered to the simulated patient lung was also quantified.

FINDINGS

Filtration of the exhalation port of the manual resuscitation bag was seen to reduce fugitive medical aerosols to ambient levels for both nebulizer types. The vibrating mesh nebulizer delivered the greatest quantity of aerosol to the simulated adult patient (18.44 ± 1.03% versus 3.64 ± 0.26% with a jet nebulizer).

CONCLUSIONS

The results highlight the potential for exposure to fugitive medical aerosols released during the delivery of aerosol therapy with a manual resuscitation bag and also the potential for significant variation in patient lung dose depending on nebulizer type.

摘要

背景

在手动复苏过程中,可能会使用喷雾器疗法将治疗药物递送给呼吸困难的患者。然而,用于产生和输送这些医疗气溶胶的设备有可能将这些治疗药物释放到局部环境中,并使护理人员暴露于不必要的医疗气溶胶中。

目的

使用带有和不带有过滤装置的手动复苏袋来量化在气溶胶药物输送过程中释放到环境中的逸散性医疗气溶胶的水平。

方法

使用放置在模拟护理人员位置的空气动力学颗粒粒径仪来测量时变逸散性气溶胶浓度。评估了两种类型的喷雾器,一种是振动网式喷雾器,另一种是射流喷雾器。还定量了输送到模拟患者肺部的气溶胶剂量。

结果

过滤手动复苏袋的呼气端口被发现可将两种喷雾器类型的逸散性医疗气溶胶降低至环境水平。振动网式喷雾器向模拟成年患者输送的气溶胶量最大(18.44±1.03%,而射流喷雾器为 3.64±0.26%)。

结论

结果强调了在使用手动复苏袋输送气溶胶治疗时可能会暴露于逸散性医疗气溶胶的情况,以及根据喷雾器类型患者肺部剂量可能会有显著差异的情况。

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