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振动筛网技术的可靠性。

Reliability of Vibrating Mesh Technology.

作者信息

Gowda Ashwin A, Cuccia Ann D, Smaldone Gerald C

机构信息

Division of Pulmonary, Critical Care and Sleep Medicine, Department of Medicine, State University of New York at Stony Brook, Stony Brook, New York

Respiratory Care Program, School of Health, Technology and Management, State University of New York at Stony Brook, Stony Brook, New York. Departmental funds were used to support this study. The authors have disclosed no conflicts of interest.

出版信息

Respir Care. 2017 Jan;62(1):65-69. doi: 10.4187/respcare.04702. Epub 2016 Nov 15.

Abstract

BACKGROUND

For delivery of inhaled aerosols, vibrating mesh systems are more efficient than jet nebulizers are and do not require added gas flow. We assessed the reliability of a vibrating mesh nebulizer (Aerogen Solo, Aerogen Ltd, Galway Ireland) suitable for use in mechanical ventilation.

METHODS

An initial observational study was performed with 6 nebulizers to determine run time and efficiency using normal saline and distilled water. Nebulizers were run until cessation of aerosol production was noted, with residual volume and run time recorded. Three controllers were used to assess the impact of the controller on nebulizer function. Following the observational study, a more detailed experimental protocol was performed using 20 nebulizers. For this analysis, 2 controllers were used, and time to cessation of aerosol production was noted. Gravimetric techniques were used to measure residual volume. Total nebulization time and residual volume were recorded. Failure was defined as premature cessation of aerosol production represented by residual volume of > 10% of the nebulizer charge.

RESULTS

In the initial observational protocol, an unexpected sporadic failure rate was noted of 25% in 55 experimental runs. In the experimental protocol, a failure rate was noted of 30% in 40 experimental runs. Failed runs in the experimental protocol exhibited a wide range of retained volume averaging ± SD 36 ± 21.3% compared with 3.2 ± 1.5% (P = .001) in successful runs. Small but significant differences existed in nebulization time between controllers.

CONCLUSIONS

Aerogen Solo nebulization was often randomly interrupted with a wide range of retained volumes.

摘要

背景

对于吸入气雾剂的输送,振动筛网系统比喷射雾化器更高效,且不需要额外的气流。我们评估了一种适用于机械通气的振动筛网雾化器(Aerogen Solo,爱尔兰戈尔韦的Aerogen有限公司)的可靠性。

方法

使用6个雾化器进行了一项初始观察性研究,以确定使用生理盐水和蒸馏水时的运行时间和效率。运行雾化器直至观察到气溶胶产生停止,记录剩余体积和运行时间。使用三个控制器来评估控制器对雾化器功能的影响。在观察性研究之后,使用20个雾化器进行了更详细的实验方案。对于该分析,使用了2个控制器,并记录气溶胶产生停止的时间。采用重量法测量剩余体积。记录总雾化时间和剩余体积。失败定义为气溶胶产生过早停止,以剩余体积大于雾化器装药量的10%为代表。

结果

在初始观察方案中,在55次实验运行中意外发现散发性故障率为25%。在实验方案中,在40次实验运行中发现故障率为30%。实验方案中的失败运行表现出广泛的残留体积范围,平均±标准差为36±21.3%,而成功运行中的残留体积为3.2±1.5%(P = .001)。不同控制器之间的雾化时间存在微小但显著的差异。

结论

Aerogen Solo雾化经常随机中断,残留体积范围广泛。

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