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[网状雾化器能否改善院前雾化治疗?对模拟院前呼吸窘迫急诊患者的体外研究]

[Can mesh nebulizers improve prehospital aerosol therapy? An in vitro study on simulated prehospital emergency patients suffering from respiratory distress].

作者信息

Otto M, Kropp Y, Kummer L, Thiel M, Tsagogiorgas C

机构信息

Klinik für Anästhesiologie und Operative Intensivmedizin, Universitätsmedizin Mannheim, Medizinische Fakultät Mannheim, Universität Heidelberg, Theodor-Kutzer-Ufer 1-3, 68167, Mannheim, Deutschland.

Klinik für Anästhesiologie, Universitätsklinikum Heidelberg, Heidelberg, Deutschland.

出版信息

Anaesthesiologie. 2022 Oct;71(10):758-766. doi: 10.1007/s00101-022-01183-y. Epub 2022 Aug 17.

Abstract

BACKGROUND

Nebulizers used to treat prehospital emergency patients should provide a high output efficiency to achieve a fast onset of therapeutic drug effects while remaining unaffected by the presence of supplementary oxygen flow or the patient's breathing pattern. On the other hand, nebulizer performance is directly influenced by differences in device design, gas flow and patients' breathing patterns. Several studies from emergency departments were able to demonstrate an improvement in patient outcome when using a mesh nebulizer instead of a jet nebulizer. Data or bench studies regarding prehospital care are non-existent.

OBJECTIVE

The aim of the present in vitro study was to evaluate which type of aerosol generator would best address the requirements of a prehospital adult emergency patient suffering from respiratory distress.

MATERIAL AND METHODS

We evaluated the performance of a jet nebulizer (Cirrus™ 2, Intersurgical®) and two mesh nebulizers (Aerogen Solo® with USB controller, Aerogen Limited and M‑Neb® mobile, NEBU-TEC International med. Produkte Eike Kern GmbH) with the possibility of portable operation in an in vitro model of a spontaneously breathing adult emergency patient. One physiological and three pathological breathing patterns (distressed breathing pattern as well as stable and acute exacerbated chronic obstructive pulmonary disease) were simulated. Nebulizer output and salbutamol lung deposition were measured at different oxygen flow rates using a face mask as the delivery interface.

RESULTS

The mesh nebulizers produced a significantly higher aerosol output when compared to the jet nebulizer. The M‑Neb® mobile was able to significantly exceed the output of the Aerogen Solo®. Oxygen flow had the largest influence on the output of the jet nebulizer but hardly affected the mesh nebulizers. After a nebulization time of 10 min the M‑Neb® mobile also achieved the highest total salbutamol lung deposition (P < 0.001). Aerosol drug deposition was therefore mainly determined by the nebulizer's drug output per unit time. The deposition could not be improved using a spacer but was strongly influenced by the simulated emergency patients' breathing pattern.

CONCLUSION

The use of mesh nebulizers might have the potential to improve the aerosol therapy of prehospital emergency patients. In general, mesh nebulizers seem to be superior to jet nebulizers regarding aerosol output per unit time and total lung deposition. The present data suggest that aerosol output and drug deposition to the collection filter in this simulated setting are closely connected and crucial for total salbutamol deposition, as the deposition could not be improved by adding a spacer. Aerosol drug deposition in simulated emergency patients' lungs is therefore mainly determined by the nebulizer's drug output per unit time. The level of oxygen flow used had the largest influence on the output of the jet nebulizer but hardly affected the output of the tested mesh nebulizers. Mesh nebulizers could therefore enable a demand-adapted oxygen therapy due to their consistent performance despite the presence of oxygen flow. A high respiratory rate was associated with a high drug deposition, which is clinically desirable in the treatment of patients in respiratory distress; however, drug underdosing must also be expected in the treatment of bradypneic patients. Further clinical studies must prove whether our findings also apply to the treatment of real prehospital emergency patients.

摘要

背景

用于治疗院前急诊患者的雾化器应具备高输出效率,以便迅速产生治疗药物效果,同时不受补充氧气流量或患者呼吸模式的影响。另一方面,雾化器的性能直接受设备设计、气流和患者呼吸模式差异的影响。急诊科的多项研究表明,使用网状雾化器而非喷射雾化器可改善患者预后。目前尚无关于院前急救的相关数据或实验台研究。

目的

本体外研究旨在评估哪种类型的气溶胶发生器最能满足患有呼吸窘迫的院前成年急诊患者的需求。

材料与方法

我们在一个模拟自主呼吸成年急诊患者的体外模型中,评估了一款喷射雾化器(Cirrus™ 2,Intersurgical®)和两款网状雾化器(配备USB控制器的Aerogen Solo®,Aerogen Limited;以及M-Neb® mobile,NEBU-TEC International med. Produkte Eike Kern GmbH)的便携操作性能。模拟了一种生理呼吸模式和三种病理呼吸模式(窘迫呼吸模式以及稳定期和急性加重期慢性阻塞性肺疾病)。使用面罩作为输送接口,在不同氧气流量下测量雾化器输出和沙丁胺醇肺部沉积量。

结果

与喷射雾化器相比,网状雾化器产生的气溶胶输出量显著更高。M-Neb® mobile的输出量明显超过Aerogen Solo®。氧气流量对喷射雾化器的输出影响最大,但对网状雾化器影响很小。雾化10分钟后,M-Neb® mobile的沙丁胺醇肺部总沉积量也最高(P < 0.001)。因此,气溶胶药物沉积主要取决于雾化器的单位时间药物输出量。使用间隔器并不能改善沉积情况,但模拟急诊患者的呼吸模式对其有很大影响。

结论

使用网状雾化器可能有改善院前急诊患者气溶胶治疗的潜力。总体而言,在单位时间气溶胶输出量和肺部总沉积量方面,网状雾化器似乎优于喷射雾化器。目前的数据表明,在这种模拟环境中,气溶胶输出和收集过滤器上的药物沉积与沙丁胺醇总沉积密切相关且至关重要,因为添加间隔器并不能改善沉积情况。因此,模拟急诊患者肺部的气溶胶药物沉积主要取决于雾化器的单位时间药物输出量。所用氧气流量水平对喷射雾化器的输出影响最大,但对测试的网状雾化器输出影响很小。因此,尽管存在氧气流,网状雾化器因其性能一致,可实现按需调整的氧气治疗。高呼吸频率与高药物沉积相关,这在治疗呼吸窘迫患者时临床上是理想的;然而,在治疗呼吸过缓患者时也可能预期会出现药物剂量不足的情况。进一步的临床研究必须证明我们的发现是否也适用于实际院前急诊患者的治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75e2/9525251/8276a353d764/101_2022_1183_Fig1_HTML.jpg

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