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重症监护病房中的逃逸气溶胶:一篇叙述性综述。

Fugitive aerosols in the intensive care unit: a narrative review.

作者信息

O'Toole Ciarraí, Joyce Mary, McGrath James A, O'Sullivan Andrew, Byrne Miriam A, MacLoughlin Ronan

机构信息

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

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

出版信息

Ann Transl Med. 2021 Apr;9(7):592. doi: 10.21037/atm-20-2280.

Abstract

The risk of unintended inhalation of fugitive aerosols is becoming a topic of increasing interest in the healthcare arena. These fugitive aerosols may be bioaerosols, generated by the patient themselves through cough or sneeze, or they may be therapeutic medical aerosols, generated by therapeutic medical aerosol generators with the intent of delivery to a specific patient's respiratory tract. This review focus' on therapeutic aerosols in the intensive care unit (ICU) only, those typically generated by nebulisers. In the intensive care environment, patients are generally in receipt of ventilatory support, and the literature suggests that these different support interventions influence fugitive therapeutic medical aerosol emissions in a variety of ways. Predominant ventilatory support interventions include, but are not limited to, invasive mechanical ventilation (MV), non-invasive mechanical ventilation (NIV), high flow nasal therapy (HFNT), and supplemental oxygen delivery in spontaneously breathing patients. Further, factors such as nebuliser type, patient interface, patient breathing pattern, nebuliser position in the patient breathing circuit and medication formulation characteristics also have been shown to exert influence on aerosol concentrations and distance from the source. Here we present the state of the art knowledge in this, as yet, poorly described field of research, and identify the key risks, and subsequently, opportunities to mitigate the risks of unintended exposure of both patients and bystanders during and for periods following the administration of therapeutic aerosols.

摘要

意外吸入逸散性气雾剂的风险正成为医疗保健领域日益关注的话题。这些逸散性气雾剂可能是生物气雾剂,由患者自身咳嗽或打喷嚏产生,也可能是治疗性医用气雾剂,由治疗性医用气雾剂发生器产生,旨在输送到特定患者的呼吸道。本综述仅关注重症监护病房(ICU)中的治疗性气雾剂,通常由雾化器产生。在重症监护环境中,患者通常接受通气支持,文献表明这些不同的支持干预措施会以多种方式影响逸散性治疗性医用气雾剂的排放。主要的通气支持干预措施包括但不限于有创机械通气(MV)、无创机械通气(NIV)、高流量鼻导管治疗(HFNT)以及为自主呼吸患者提供补充氧气。此外,雾化器类型、患者接口、患者呼吸模式、雾化器在患者呼吸回路中的位置以及药物制剂特性等因素也已被证明会对气雾剂浓度和离源距离产生影响。在此,我们介绍这个迄今描述甚少的研究领域的最新知识,并确定关键风险,以及随后在治疗性气雾剂给药期间及之后降低患者和旁观者意外暴露风险的机会。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b67/8105852/aa7cca528f35/atm-09-07-592-f1.jpg

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