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管腔大小和流速对经 Vapotherm 湿化高流量鼻导管系统输送雾化药物的影响。

Influences of cannula size and flow rate on aerosol drug delivery through the Vapotherm humidified high-flow nasal cannula system.

机构信息

Department of Anesthesiology and Critical Care Medicine, Nemours/Alfred I. duPont Hospital for Children, Wilmington, DE, USA.

出版信息

Pediatr Crit Care Med. 2013 Jun;14(5):e250-6. doi: 10.1097/PCC.0b013e31828a7f79.

Abstract

OBJECTIVE

We investigated the in vitro inspired dose and particle size distribution of albuterol delivered by a vibrating mesh nebulizer through the Vapotherm (Stevensville, MD) humidified high-flow nasal cannula system.

DESIGN

Albuterol (2.5 mg/3 mL) was delivered by an Aeroneb Solo (Aerogen, Galway, Ireland) nebulizer that was connected via adaptor proximal to the nasal cannula and downstream from the Vapotherm 2000i. Albuterol was collected onto an inspiratory filter mounted to a breath simulator programmed with age-appropriate breathing patterns. Particle sizing was completed by cascade impaction. Albuterol was quantified using ultraviolet spectrometry. Measurements were made using varying flow rates through infant, pediatric, and adult nasal cannulae.

SETTING

Aerosol research laboratory.

MEASUREMENTS AND MAIN RESULTS

The inspired dose (percent of nominal dose) for each cannula size and flow rate was 2.5%, 0.8%, 0.4%, and 0.2% for the adult cannula at 5, 10, 20, and 40 L/min, respectively; 1.2%, 0.6%, 0.1%, and 0.0% for the pediatric cannula at 3, 5, 10, and 20 L/min, respectively; and 0.6%, 0.6%, and 0.5% for the infant cannula at 3, 5, and 8 L/min, respectively. Most (62-80%) of the loaded albuterol dose accumulated within the adaptor. For each cannula size, there was a significant decrease in the inspired dose with increasing flow rates, p = 0.026 (infant), p = 0.001 (pediatric), and p < 0.001(adult). The inspired dose increased with increasing cannula size for 5, 10, and 20 L/min (p = 0.007, p < 0.001, and p = 0.005, respectively). The mass median aerodynamic diameter for all trials was less than 5 µm.

CONCLUSION

The amount of albuterol delivered with the Vapotherm system using this model was lower than the amount expected for a clinical response for the majority of flow rates and cannula size combinations. Further studies are needed before routine use of aerosolized albuterol through a Vapotherm high-flow system can be recommended.

摘要

目的

通过 Vapotherm(史蒂文斯维尔,MD)湿化高流量鼻插管系统,研究振动网孔雾化器输送的沙丁胺醇的体外吸入剂量和颗粒大小分布。

设计

沙丁胺醇(2.5 毫克/3 毫升)由 Aeroneb Solo(爱尔兰戈尔韦的 Aerogen)雾化器输送,该雾化器通过适配器连接在鼻插管的近端,位于 Vapotherm 2000i 的下游。沙丁胺醇被收集到安装在呼吸模拟器上的吸气过滤器上,呼吸模拟器按照年龄适当的呼吸模式编程。通过级联冲击完成颗粒尺寸测定。使用紫外线光谱法定量沙丁胺醇。使用不同的流速通过婴儿、儿科和成人鼻插管进行测量。

地点

气溶胶研究实验室。

测量和主要结果

对于每种插管尺寸和流速,成人插管在 5、10、20 和 40 L/min 时的吸入剂量(名义剂量的百分比)分别为 2.5%、0.8%、0.4%和 0.2%;儿科插管分别为 3、5、10 和 20 L/min 时为 1.2%、0.6%、0.1%和 0.0%;婴儿插管分别为 3、5 和 8 L/min 时为 0.6%、0.6%和 0.5%。加载的沙丁胺醇剂量的大部分(62-80%)积聚在适配器内。对于每种插管尺寸,随着流速的增加,吸入剂量显著降低,p = 0.026(婴儿),p = 0.001(儿科)和 p < 0.001(成人)。随着流速的增加,吸入剂量随着插管尺寸的增加而增加(p = 0.007,p < 0.001 和 p = 0.005)。所有试验的质量中值空气动力学直径均小于 5 µm。

结论

使用该模型的 Vapotherm 系统输送的沙丁胺醇量低于大多数流速和插管尺寸组合下预期的临床反应量。在推荐通过 Vapotherm 高流量系统常规使用雾化沙丁胺醇之前,需要进行进一步的研究。

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