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急性四肢瘫后阻塞性睡眠呼吸暂停的自动滴定持续气道正压通气治疗(COSAQ):一项随机对照试验的研究方案。

Auto-titrating continuous positive airway pressure treatment for obstructive sleep apnoea after acute quadriplegia (COSAQ): study protocol for a randomized controlled trial.

机构信息

Institute for Breathing and Sleep, Austin Hospital, Melbourne, Australia.

出版信息

Trials. 2013 Jun 19;14:181. doi: 10.1186/1745-6215-14-181.

Abstract

BACKGROUND

Quadriplegia is a severe, catastrophic injury that predominantly affects people early in life, resulting in lifelong physical disability. Obstructive sleep apnoea is a direct consequence of quadriplegia and is associated with neurocognitive deficits, sleepiness and reduced quality of life. The usual treatment for sleep apnoea is nasal continuous positive airway pressure (CPAP); however, this is poorly tolerated in quadriplegia. To encourage patients to use this therapy, we have to demonstrate that the benefits outweigh the inconvenience. We therefore propose a prospective, multinational randomized controlled trial of three months of CPAP for obstructive sleep apnoea after acute quadriplegia.

METHODS/DESIGN: Specialist spinal cord injury centres across Australia, New Zealand, the UK and Canada will recruit medically stable individuals who have sustained a (new) traumatic quadriplegia (complete or incomplete second cervical to first thoracic level lesions). Participants will be screened for obstructive sleep apnoea using full, portable sleep studies. Those with an apnoea hypopnoea index greater than 10 per hour will proceed to an initial three-night trial of CPAP. Those who can tolerate CPAP for at least 4 hours on at least one night of the initial trial will be randomized to either usual care or a 3-month period of auto-titrating CPAP. The primary hypothesis is that nocturnal CPAP will improve neuropsychological functioning more than usual care alone. The secondary hypothesis is that the magnitude of improvement of neuropsychological function will be predicted by the severity of baseline sleepiness measures, sleep fragmentation and sleep apnoea. Neuropsychological tests and full polysomnography will be performed at baseline and 3 months with interim measures of sleepiness and symptoms of autonomic dysfunction measured weekly. Spirometry will be performed monthly. Neuropsychological tests will be administered by blinded assessors. Recruitment commenced in July 2009.

DISCUSSION

The results of this trial will demonstrate the effect of nocturnal CPAP treatment of obstructive sleep apnoea in acute quadriplegia. If CPAP can improve neurocognitive function after injury, it is likely that rehabilitation and subsequent community participation will be substantially improved for this group of predominantly young and severely physically disabled people.

TRIAL REGISTRATION

Australian New Zealand Clinical Trial Registry ACTRN12605000799651.

摘要

背景

四肢瘫痪是一种严重的灾难性损伤,主要影响生命早期的人群,导致终身身体残疾。阻塞性睡眠呼吸暂停是四肢瘫痪的直接后果,与神经认知缺陷、嗜睡和生活质量降低有关。阻塞性睡眠呼吸暂停的常用治疗方法是持续气道正压通气(CPAP);然而,在四肢瘫痪中,这种方法的耐受性很差。为了鼓励患者使用这种治疗方法,我们必须证明其益处大于不便之处。因此,我们提出了一项针对急性四肢瘫痪后三个月 CPAP 治疗阻塞性睡眠呼吸暂停的前瞻性、多国随机对照试验。

方法/设计:澳大利亚、新西兰、英国和加拿大的专业脊髓损伤中心将招募医疗稳定的新创伤性四肢瘫痪(第二颈椎至第一胸椎水平完全或不完全损伤)患者。参与者将通过全面、便携式睡眠研究筛查阻塞性睡眠呼吸暂停。呼吸暂停低通气指数大于 10 次/小时的患者将进行初始三晚 CPAP 试验。那些能够在初始试验至少一晚耐受 CPAP 至少 4 小时的患者将被随机分配到常规治疗或为期 3 个月的自动滴定 CPAP 组。主要假设是夜间 CPAP 将改善神经心理学功能,优于单独常规治疗。次要假设是神经心理学功能改善的幅度将通过基线嗜睡程度、睡眠片段化和睡眠呼吸暂停的严重程度来预测。神经心理学测试和全夜睡眠图将在基线和 3 个月时进行,每周进行一次嗜睡和自主神经功能障碍症状的中间测量。每月进行一次肺功能检查。神经心理学测试将由盲法评估者进行。招募于 2009 年 7 月开始。

讨论

该试验的结果将证明急性四肢瘫痪中夜间 CPAP 治疗阻塞性睡眠呼吸暂停的效果。如果 CPAP 能改善损伤后的神经认知功能,那么这群主要是年轻且身体严重残疾的人,他们的康复和随后的社区参与度很可能会得到实质性的提高。

试验注册

澳大利亚新西兰临床试验注册 ACTRN12605000799651。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/236d/3706386/e04f4a9d248d/1745-6215-14-181-1.jpg

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