McNamara Renae J, Epsley Charlotte, Coren Esther, McKeough Zoe J
Departments of Physiotherapy and Respiratory Medicine, Prince of Wales Hospital, Barker Street, Randwick, NSW, Australia, 2031.
Cochrane Database Syst Rev. 2017 Dec 19;12(12):CD012296. doi: 10.1002/14651858.CD012296.pub2.
Singing is a complex physical activity dependent on the use of the lungs for air supply to regulate airflow and create large lung volumes. In singing, exhalation is active and requires active diaphragm contraction and good posture. Chronic obstructive pulmonary disease (COPD) is a progressive, chronic lung disease characterised by airflow obstruction. Singing is an activity with potential to improve health outcomes in people with COPD.
To determine the effect of singing on health-related quality of life and dyspnoea in people with COPD.
We identified trials from the Cochrane Airways Specialised Register, ClinicalTrials.gov, the World Health Organization trials portal and PEDro, from their inception to August 2017. We also reviewed reference lists of all primary studies and review articles for additional references.
We included randomised controlled trials in people with stable COPD, in which structured supervised singing training of at least four sessions over four weeks' total duration was performed. The singing could be performed individually or as part of a group (choir) facilitated by a singing leader. Studies were included if they compared: 1) singing versus no intervention (usual care) or another control intervention; or 2) singing plus pulmonary rehabilitation versus pulmonary rehabilitation alone.
Two review authors independently screened and selected trials for inclusion, extracted outcome data and assessed risk of bias. We contacted authors of trials for missing data. We calculated mean differences (MDs) using a random-effects model. We were only able to analyse data for the comparison of singing versus no intervention or a control group.
Three studies (a total of 112 participants) were included. All studies randomised participants to a singing group or a control group. The comparison groups included a film workshop, handcraft work, and no intervention. The frequency of the singing intervention in the studies ranged from 1 to 2 times a week over a 6 to 24 week period. The duration of each singing session was 60 minutes.All studies included participants diagnosed with COPD with a mean age ranging from 67 to 72 years and a mean forced expiratory volume in one second (FEV) ranging from 37% to 64% of predicted values. The sample size of included studies was small (33 to 43 participants) and overall study quality was low to very low. Blinding of personnel and participants was not possible due to the physical nature of the intervention, and selection and reporting bias was present in two studies.For the primary outcome of health-related quality of life, there was no statistically significant improvement in the St George's Respiratory Questionnaire total score (mean difference (MD) -0.82, 95% confidence interval (CI) -4.67 to 3.02, 2 studies, n = 58, low-quality evidence). However, there was a statistically significant improvement in the SF-36 Physical Component Summary (PCS) score favouring the singing group (MD 12.64, 95% CI 5.50 to 19.77, 2 studies, n = 52, low-quality evidence). Only one study reported results for the other primary outcome of dyspnoea, in which the mean improvement in Baseline Dyspnoea Index (BDI) score favouring the singing group was not statistically significant (MD 0.40, 95% CI -0.65 to 1.45, 1 study, n = 30, very low-quality evidence).No studies examined any long-term outcomes and no adverse events or side effects were reported.
AUTHORS' CONCLUSIONS: There is low to very low-quality evidence that singing is safe for people with COPD and improves physical health (as measured by the SF-36 physical component score), but not dyspnoea or respiratory-specific quality of life. The evidence is limited due to the low number of studies and the small sample size of each study. No evidence exists examining the long-term effect of singing for people with COPD. The absence of studies examining singing performed in conjunction with pulmonary rehabilitation precludes the formulation of conclusions about the effects of singing in this context. More randomised controlled trials with larger sample sizes and long-term follow-up, and trials examining the effect of singing in addition to pulmonary rehabilitation, are required to determine the effect of singing on health-related quality of life and dyspnoea in people with COPD.
唱歌是一项复杂的身体活动,依赖肺部提供空气以调节气流并产生较大的肺容量。在唱歌过程中,呼气是主动的,需要膈肌主动收缩并保持良好姿势。慢性阻塞性肺疾病(COPD)是一种以气流受限为特征的进行性慢性肺部疾病。唱歌是一项有可能改善COPD患者健康状况的活动。
确定唱歌对COPD患者健康相关生活质量和呼吸困难的影响。
我们从Cochrane Airways专业注册库、ClinicalTrials.gov、世界卫生组织试验平台和PEDro中检索自创建至2017年8月的试验。我们还查阅了所有原始研究和综述文章的参考文献列表以获取更多参考文献。
我们纳入了稳定期COPD患者的随机对照试验,试验中进行了为期四周、至少四个疗程的结构化监督唱歌训练。唱歌可以单独进行,也可以在唱歌指导者的协助下作为团体(唱诗班)活动的一部分进行。纳入的研究需比较:1)唱歌与无干预(常规护理)或其他对照干预;或2)唱歌加肺康复与单纯肺康复。
两位综述作者独立筛选并选择纳入试验,提取结局数据并评估偏倚风险。我们与试验作者联系获取缺失数据。我们使用随机效应模型计算平均差(MD)。我们仅能分析唱歌与无干预或对照组比较的数据。
纳入三项研究(共112名参与者)。所有研究均将参与者随机分为唱歌组或对照组。比较组包括电影工作坊、手工制作和无干预。研究中唱歌干预的频率为每周1至2次,为期6至24周。每次唱歌课程时长为60分钟。所有研究纳入的参与者均被诊断为COPD,平均年龄在67至72岁之间,一秒用力呼气容积(FEV)平均为预测值的37%至64%。纳入研究的样本量较小(33至43名参与者),总体研究质量低至极低。由于干预的物理性质,无法对人员和参与者进行盲法,两项研究存在选择和报告偏倚。对于健康相关生活质量这一主要结局,圣乔治呼吸问卷总分无统计学显著改善(平均差(MD)-0.82,95%置信区间(CI)-4.67至3.02,2项研究,n = 58,低质量证据)。然而,SF-36身体成分总结(PCS)评分在唱歌组有统计学显著改善(MD 12.64,95%CI 5.50至19.77,2项研究,n = 52,低质量证据)。仅一项研究报告了呼吸困难另一主要结局的结果,其中唱歌组基线呼吸困难指数(BDI)评分的平均改善无统计学显著意义(MD 0.40,95%CI -0.65至1.45,1项研究,n = 30,极低质量证据)。没有研究考察任何长期结局,也未报告不良事件或副作用。
证据质量低至极低,表明唱歌对COPD患者安全且可改善身体健康(以SF-36身体成分评分衡量),但不能改善呼吸困难或呼吸特异性生活质量。由于研究数量少且每项研究样本量小,证据有限。尚无证据考察唱歌对COPD患者的长期影响。缺乏考察唱歌与肺康复联合效果的研究,无法得出唱歌在此背景下效果的结论。需要更多样本量更大、有长期随访的随机对照试验,以及考察唱歌除肺康复之外效果的试验,以确定唱歌对COPD患者健康相关生活质量和呼吸困难的影响。