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侵入性通气重症监护病房患者黏液溶解剂和支气管扩张剂的预防性雾化(NEBULAE):一项随机对照试验的研究方案

Preventive nebulization of mucolytic agents and bronchodilating drugs in invasively ventilated intensive care unit patients (NEBULAE): study protocol for a randomized controlled trial.

作者信息

van der Hoeven Sophia M, Binnekade Jan M, de Borgie Corianne A J M, Bosch Frank H, Endeman Henrik, Horn Janneke, Juffermans Nicole P, van der Meer Nardo J M, Merkus Maruschka P, Moeniralam Hazra S, van Silfhout Bart, Slabbekoorn Mathilde, Stilma Willemke, Wijnhoven Jan Willem, Schultz Marcus J, Paulus Frederique

机构信息

Department of Intensive Care, Academic Medical Center, Meibergdreef 9, 1105 AZ, Amsterdam, The Netherlands.

Clinical Research Unit, Amsterdam, The Netherlands.

出版信息

Trials. 2015 Sep 2;16:389. doi: 10.1186/s13063-015-0865-0.

Abstract

BACKGROUND

Preventive nebulization of mucolytic agents and bronchodilating drugs is a strategy aimed at the prevention of sputum plugging, and therefore atelectasis and pneumonia, in intubated and ventilated intensive care unit (ICU) patients. The present trial aims to compare a strategy using the preventive nebulization of acetylcysteine and salbutamol with nebulization on indication in intubated and ventilated ICU patients.

METHODS/DESIGN: The preventive nebulization of mucolytic agents and bronchodilating drugs in invasively ventilated intensive care unit patients (NEBULAE) trial is a national multicenter open-label, two-armed, randomized controlled non-inferiority trial in the Netherlands. Nine hundred and fifty intubated and ventilated ICU patients with an anticipated duration of invasive ventilation of more than 24 hours will be randomly assigned to receive either a strategy consisting of preventive nebulization of acetylcysteine and salbutamol or a strategy consisting of nebulization of acetylcysteine and/or salbutamol on indication. The primary endpoint is the number of ventilator-free days and surviving on day 28. Secondary endpoints include ICU and hospital length of stay, ICU and hospital mortality, the occurrence of predefined pulmonary complications (acute respiratory distress syndrome, pneumonia, large atelectasis and pneumothorax), and the occurrence of predefined side effects of the intervention. Related healthcare costs will be estimated in a cost-benefit and budget-impact analysis.

DISCUSSION

The NEBULAE trial is the first randomized controlled trial powered to investigate whether preventive nebulization of acetylcysteine and salbutamol shortens the duration of ventilation in critically ill patients.

TRIAL REGISTRATION

NCT02159196, registered on 6 June 2014.

摘要

背景

对重症监护病房(ICU)中接受插管和机械通气的患者预防性雾化吸入黏液溶解剂和支气管扩张药物是一种旨在预防痰液堵塞,进而预防肺不张和肺炎的策略。本试验旨在比较在接受插管和机械通气的ICU患者中,使用乙酰半胱氨酸和沙丁胺醇预防性雾化与按需雾化的策略。

方法/设计:在有创机械通气的重症监护病房患者中进行的黏液溶解剂和支气管扩张药物预防性雾化(NEBULAE)试验是荷兰一项全国性多中心开放标签、双臂、随机对照非劣效性试验。950例预计有创通气时间超过24小时的接受插管和机械通气的ICU患者将被随机分配,以接受由乙酰半胱氨酸和沙丁胺醇预防性雾化组成的策略,或由按需雾化乙酰半胱氨酸和/或沙丁胺醇组成的策略。主要终点是无呼吸机天数和第28天存活情况。次要终点包括ICU和医院住院时间、ICU和医院死亡率、预定义肺部并发症(急性呼吸窘迫综合征、肺炎、大面积肺不张和气胸)的发生情况,以及干预措施预定义副作用的发生情况。将在成本效益和预算影响分析中估算相关医疗费用。

讨论

NEBULAE试验是首个有足够效力的随机对照试验,旨在研究乙酰半胱氨酸和沙丁胺醇预防性雾化是否能缩短重症患者的通气时间。

试验注册

NCT02159196,于2014年6月6日注册。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e73c/4557315/f75b96a5c4f7/13063_2015_865_Fig1_HTML.jpg

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