医学
肥胖低通气综合征
减肥
物理疗法
随机对照试验
肺康复
体质指数
康复
肥胖
生活质量(医疗保健)
通气不足
外科
内科学
呼吸系统
护理部
作者
Swapna Mandal,E. Suh,Rachel Elizabeth Harding,Anna Vaughan-France,Michelle Ramsay,Bronwen Connolly,Danielle E. Bear,Helen MacLaughlin,Sharlene A. Greenwood,Michael I. Polkey,Mark Elliott,Tao Chen,Abdel Douiri,John Moxham,Patrick B. Murphy,Nicholas Hart
出处
期刊:Thorax
[BMJ]
日期:2017-09-29
卷期号:73 (1): 62-69
被引量:48
标识
DOI:10.1136/thoraxjnl-2016-209826
摘要
Background Respiratory management of obesity hypoventilation syndrome (OHS) focusses on the control of sleep-disordered breathing rather than the treatment of obesity. Currently, there are no data from randomised trials of weight loss targeted rehabilitation programmes for patients with OHS. Intervention A 3-month multimodal hybrid inpatient–outpatient motivation, exercise and nutrition rehabilitation programme, in addition to non invasive ventilation (NIV), would result in greater per cent weight loss compared with standard care. Methods A single-centre pilot randomised controlled trial allocated patients to either standard care or standard care plus rehabilitation. Primary outcome was per cent weight loss at 12 months with secondary exploratory outcomes of weight loss, exercise capacity and health-related quality of life (HRQOL) at the end of the rehabilitation programme to assess the intervention effect. Results Thirty-seven patients (11 male, 59.8±12.7 years) with a body mass index of 51.1±7.7 kg/m 2 were randomised. At 12 months, there was no between-group difference in per cent weight loss (mean difference −5.9% (95% CI −14.4% to 2.7%; p=0.17)). At 3 months, there was a greater per cent weight loss (mean difference −5% (95% CI −8.3% to −1.4%; p=0.007)), increased exercise capacity (6 min walk test 60 m (95% CI 29.5 to 214.5) vs 20 m (95% CI 11.5 to 81.3); p=0.036) and HRQL (mean difference SF-36 general health score (10 (95% CI 5 to 21.3) vs 0 (95% CI −5 to 10); p=0.02)) in the rehabilitation group. Conclusion In patients with OHS, a 3-month comprehensive rehabilitation programme, in addition to NIV, resulted in improved weight loss, exercise capacity and QOL at the end of the rehabilitation period, but these effects were not demonstrated at 12 months, in part, due to the limited retention of patients at 12 months. Trial registration number Pre-results; NCT01483716 .
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