Performance of newly developed add-on devices on aerosol delivery in noninvasive ventilated subjects.

IF 1.5 4区 医学 Q3 RESPIRATORY SYSTEM Experimental Lung Research Pub Date : 2024-01-01 Epub Date: 2024-10-23 DOI:10.1080/01902148.2024.2418555
Amal E Rashad, Yasmin M Madney, Ahmed M Abdelhaleem Ali, Mohammad F Mohammad, Fahad T Alsulami, Yousef Saeed Alqarni, Rania M Sarhan, Mohamed E A Abdelrahim
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Abstract

Background: Several techniques had been developed to generate aerosolized medications during noninvasive ventilation (NIV) using variable inhalation methods. This study hypothesized that large spacers were more efficient significantly than small spacers and adapters during NIV. Objective: The main objective of this study was to compare the performance of newly developed spacers with standard T-piece in NIV chronic obstructive pulmonary disease (COPD) subjects. Methods: Sixty COPD subjects requiring NIV were included in this study. A dual-limb circuit was used, and the mode of ventilator was set in spontaneous volume-controlled mode. Dual-limb ventilation circuit, consists of inspiratory-limb and expiratory-limb, is pressure and volume controlled in response to subject expiration providing relatively high resistance to expiratory flow. Two experimental sets were evaluated: the first was introducing two preliminary pressurized metered-dose inhalers (pMDI) puffs before the nebulization of 1 ml of a respirable solution of salbutamol by vibrating mesh nebulizer (VMN) using Minimhal and Combihaler. The second was to only nebulize 1 ml of salbutamol respirable solution by VMN using Combihaler, Minimhal, and standard T-piece. Two urine samples were collected after aerosol delivery: urine sample after 30 min. (USAL0.5) as an indicator of lung deposition and all urine pooled 24 h (USAL24) post-inhalation as an indicator of systemic absorption. The amount of salbutamol extracted from urine samples was assayed by high-performance liquid chromatography. Results: Minimhal + pMDI + VMN delivered a higher percentage of salbutamol 30 min post-inhalation than Minimhal + VMN (p < 0.001). Also, Combihaler + pMDI + VMN delivered a higher percentage of salbutamol 30 min post-inhalation than Combihaler + VMN (p < 0.001). Combihaler + VMN delivered a higher percentage of salbutamol 30 min and 24 h post-inhalation than both Minimhal + VMN and T-piece + VMN (p < 0.001). Standard T-piece delivered the lowest aerosol amount delivered to the lung compared to both spacers (p < 0.05). Conclusions: Introducing two pMDI puffs significantly improved aerosol delivery by both spacers. Combihaler significantly improves aerosol delivery more than Minimhal.

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新开发的附加装置在无创通气受试者气溶胶输送方面的性能。
背景:目前已开发出多种技术,可在无创通气(NIV)期间使用可变吸入方法产生气溶胶药物。本研究假设,在无创通气过程中,大型间隔器的效率明显高于小型间隔器和适配器。目标:本研究的主要目的是在慢性阻塞性肺病(COPD)患者进行无创通气时,比较新开发的垫片与标准 T 型垫片的性能。方法: 对 60 名需要 NIV 的 COPD 受试者进行测试:本研究共纳入 60 名需要 NIV 的 COPD 患者。使用双肢回路,呼吸机模式设定为自发容量控制模式。双肢通气回路由吸气肢和呼气肢组成,可根据受试者呼气情况进行压力和容量控制,为呼气流量提供相对较高的阻力。对两组实验进行了评估:第一组是在使用 Minimhal 和 Combihaler 通过振动网式雾化器(VMN)雾化 1 毫升沙丁胺醇可吸入溶液之前,先进行两次初步加压计量吸入器(pMDI)吸入。第二种方法是使用 Combihaler、Minimhal 和标准 T 型片,仅通过 VMN 雾化 1 毫升沙丁胺醇可吸入溶液。气雾剂给药后收集了两份尿样:30 分钟后的尿样(USAL0.5)和 30 分钟后的尿样(USAL0.6)。(USAL0.5)作为肺部沉积的指标,而吸入后 24 小时(USAL24)的所有尿液样本则作为全身吸收的指标。从尿液样本中提取的沙丁胺醇量采用高效液相色谱法进行测定。结果吸入后 30 分钟,吸入 Minimhal + pMDI + VMN 的沙丁胺醇比例高于吸入 Minimhal + VMN 的比例(p p p p 结论):引入两个 pMDI 粉扑可显著改善两种间隔器的气溶胶输送。Combihaler 比 Minimhal 更能明显改善气溶胶输送。
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来源期刊
Experimental Lung Research
Experimental Lung Research 医学-呼吸系统
CiteScore
3.80
自引率
0.00%
发文量
23
审稿时长
2 months
期刊介绍: Experimental Lung Research publishes original articles in all fields of respiratory tract anatomy, biology, developmental biology, toxicology, and pathology. Emphasis is placed on investigations concerned with molecular, biochemical, and cellular mechanisms of normal function, pathogenesis, and responses to injury. The journal publishes reports on important methodological advances on new experimental modes. Also published are invited reviews on important and timely research advances, as well as proceedings of specialized symposia. Authors can choose to publish gold open access in this journal.
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