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使用带储雾罐的软雾吸入器和压力定量吸入器经口鼻及气管造口给药

Oronasal and Tracheostomy Delivery of Soft Mist and Pressurized Metered-Dose Inhalers With Valved Holding Chamber.

作者信息

Berlinski Ariel, Cooper Brandy

机构信息

Pulmonology Section, Department of Pediatrics, University of Arkansas for Medical Sciences and the Pediatric Aerosol Research Laboratory, Arkansas Children's Hospital Research Institute, Little Rock, Arkansas.

College of Pharmacy, University of Arkansas for Medical Sciences, Little Rock, Arkansas.

出版信息

Respir Care. 2016 Jul;61(7):913-9. doi: 10.4187/respcare.04575. Epub 2016 Mar 22.

Abstract

BACKGROUND

Some pediatric tracheostomized patients who receive inhaled drugs undergo decannulation, and it is unknown whether the dose has to be adjusted. Pressurized metered-dose inhalers (pMDIs) and soft mist inhalers (SMIs) used with valved holding chambers (VHCs) made of non-electrostatic material are available. We hypothesized that using an SMI and changing the delivery route from tracheostomy to oronasal would increase lung dose.

METHODS

Four units of a metallic VHC were studied with albuterol hydrofluoroalkane (pMDI) and albuterol/ipratropium bromide with an SMI using an anatomically correct in vitro model of a 5-y-old spontaneously breathing tracheostomized child. The drug was captured in a filter and was termed lung dose. We tested breathing patterns with tidal volumes of 50, 155, and 300 mL. A mask and a special adapter were used as interfaces for oronasal and tracheostomy delivery, respectively. Spectrophotometry (276 nm) was used to determine albuterol concentration.

RESULTS

The use of SMI resulted in a higher lung dose than the pMDI for all tested conditions except delivery through tracheostomy with tidal volume of 155 mL (P = .69). Switching from oronasal to tracheostomy delivery increased the lung dose for all tested conditions except for the pMDI with the 300-mL tidal volume (P = .83). The use of SMI resulted in higher deposition in the tracheostomy tube than the pMDI.

CONCLUSIONS

In general, an SMI delivers a higher lung dose than a pMDI when using a metallic spacer during oronasal and tracheostomy route with the latter providing a higher lung dose.

摘要

背景

一些接受吸入药物治疗的小儿气管切开患者会进行拔管,而剂量是否需要调整尚不清楚。现已有与由非静电材料制成的带阀储物罐(VHC)配合使用的压力定量吸入器(pMDI)和软雾吸入器(SMI)。我们推测,使用SMI并将给药途径从气管切开改为口鼻吸入会增加肺部药物剂量。

方法

使用一个5岁自主呼吸的气管切开儿童的解剖学正确体外模型,对四个金属VHC装置进行了研究,分别使用沙丁胺醇氢氟烷烃(pMDI)以及与SMI配合使用的沙丁胺醇/异丙托溴铵。药物被捕获在过滤器中,称为肺部药物剂量。我们测试了潮气量为50、155和300 mL时的呼吸模式。分别使用面罩和特殊适配器作为口鼻吸入和气管切开给药的接口。采用分光光度法(276 nm)测定沙丁胺醇浓度。

结果

在除潮气量为155 mL经气管切开给药外的所有测试条件下,使用SMI时的肺部药物剂量均高于pMDI(P = 0.69)。在除潮气量为300 mL的pMDI外的所有测试条件下,从口鼻吸入改为气管切开给药均增加了肺部药物剂量(P = 0.83)。使用SMI时在气管切开管中的沉积高于pMDI。

结论

一般来说,在口鼻吸入和气管切开途径中使用金属储物罐时,SMI的肺部药物剂量高于pMDI,而气管切开途径的肺部药物剂量更高。

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