Sheers Nicole L, O'Sullivan Rachel, Howard Mark E, Berlowitz David J
Department of Respiratory and Sleep Medicine, Austin Health, Heidelberg, VIC, Australia.
Institute for Breathing and Sleep, Heidelberg, VIC, Australia.
Front Rehabil Sci. 2023 Jul 26;4:1164628. doi: 10.3389/fresc.2023.1164628. eCollection 2023.
Respiratory muscle weakness results in substantial discomfort, disability, and ultimately death in many neuromuscular diseases. Respiratory system impairment manifests as shallow breathing, poor cough and associated difficulty clearing mucus, respiratory tract infections, hypoventilation, sleep-disordered breathing, and chronic ventilatory failure. Ventilatory support (i.e., non-invasive ventilation) is an established and key treatment for the latter. As survival outcomes improve for people living with many neuromuscular diseases, there is a shift towards more proactive and preventative chronic disease multidisciplinary care models that aim to manage symptoms, improve morbidity, and reduce mortality. Clinical care guidelines typically recommend therapies to improve cough effectiveness and mobilise mucus, with the aim of averting acute respiratory compromise or respiratory tract infections. Moreover, preventing recurrent infective episodes may prevent secondary parenchymal pathology and further lung function decline. Regular use of techniques that augment lung volume has similarly been recommended (volume recruitment). It has been speculated that enhancing lung inflation in people with respiratory muscle weakness when well may improve respiratory system "flexibility", mitigate restrictive chest wall disease, and slow lung volume decline. Unfortunately, clinical care guidelines are based largely on clinical rationale and consensus opinion rather than level A evidence. This narrative review outlines the physiological changes that occur in people with neuromuscular disease and how these changes impact on breathing, cough, and respiratory tract infections. The biological rationale for lung volume recruitment is provided, and the clinical trials that examine the immediate, short-term, and longer-term outcomes of lung volume recruitment in paediatric and adult neuromuscular diseases are presented and the results synthesised.
呼吸肌无力在许多神经肌肉疾病中会导致严重不适、残疾,最终导致死亡。呼吸系统损害表现为呼吸浅、咳嗽无力以及相关的排痰困难、呼吸道感染、通气不足、睡眠呼吸障碍和慢性呼吸衰竭。通气支持(即无创通气)是治疗后者的既定关键疗法。随着许多神经肌肉疾病患者的生存结局得到改善,护理模式正朝着更积极主动的慢性疾病多学科护理模式转变,旨在控制症状、改善发病率并降低死亡率。临床护理指南通常推荐改善咳嗽效果和促进痰液排出的疗法,以避免急性呼吸功能不全或呼吸道感染。此外,预防反复感染发作可防止继发性肺实质病变和进一步的肺功能下降。同样也推荐定期使用增加肺容量的技术(肺容量募集)。据推测,在呼吸肌无力患者病情稳定时增加肺膨胀可能会改善呼吸系统的“灵活性”,减轻胸廓限制性疾病,并减缓肺容量下降。不幸的是,临床护理指南很大程度上基于临床理论和共识意见,而非A级证据。本叙述性综述概述了神经肌肉疾病患者发生的生理变化,以及这些变化如何影响呼吸、咳嗽和呼吸道感染。阐述了肺容量募集的生物学原理,并介绍了在儿童和成人神经肌肉疾病中研究肺容量募集的即时、短期和长期结果的临床试验,并对结果进行了综合分析。