Nocturnal non-invasive nasal ventilation in stable hypercapnic COPD: a randomised controlled trial

被引:302
|
作者
McEvoy, R. D. [1 ,2 ]
Pierce, R. J. [3 ]
Hillman, D. [4 ]
Esterman, A. [5 ]
Ellis, E. E. [6 ]
Catcheside, P. G. [1 ,2 ]
O'Donoghue, F. J. [1 ,2 ,3 ]
Barnes, D. J. [7 ]
Grunstein, R. R. [7 ]
机构
[1] Repatriat Gen Hosp, Adelaide Inst Sleep Hlth, Daw Pk, SA 5000, Australia
[2] Flinders Univ S Australia, Adelaide, SA, Australia
[3] Austin Hosp, Inst Breathing & Sleep, Heidelberg, Vic 3084, Australia
[4] Queen Elizabeth II Med Ctr, WA Sleep Disorders Res Inst, Nedlands, WA, Australia
[5] Univ S Australia, Sch Nursing & Midwifery, Adelaide, SA 5001, Australia
[6] Univ Sydney, Fac Hlth Sci, Sch Physiotherapy, Sydney, NSW 2006, Australia
[7] Royal Prince Alfred Hosp, Sleep Res Grp, Woolcock Inst, Sydney, NSW, Australia
基金
英国医学研究理事会;
关键词
OBSTRUCTIVE PULMONARY-DISEASE; POSITIVE-PRESSURE VENTILATION; OXYGEN-THERAPY; CHEST-WALL; SLEEP; HYPOVENTILATION; MULTICENTER; PREVALENCE; SURVIVAL; SUPPORT;
D O I
10.1136/thx.2008.108274
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Background: Sleep hypoventilation has been proposed as a cause of progressive hypercapnic respiratory failure and death in patients with severe chronic obstructive pulmonary disease (COPD). A study was undertaken to determine the effects of nocturnal non-invasive bi-level pressure support ventilation (NIV) on survival, lung function and quality of life in patients with severe hypercapnic COPD. Method: A multicentre, open-label, randomised controlled trial of NIV plus long-term oxygen therapy (LTOT) versus LTOT alone was performed in four Australian University Hospital sleep/respiratory medicine departments in patients with severe stable smoking-related COPD (forced expiratory volume in 1 s (FEV1.0) to <1.5 litres or <50% predicted and ratio of FEV1.0 to forced vital capacity (FVC) <60% with awake arterial carbon dioxide tension (Paco(2)) >46 mm Hg and on LTOT for at least 3 months) and age <80 years. Patients with sleep apnoea (apnoea-hypopnoea index >20/h) or morbid obesity (body mass index >40) were excluded. Outcome measures were survival, spirometry, arterial blood gases, polysomnography, general and disease-specific quality of life and mood. Results: 144 patients were randomised (72 to NIV + LTOT and 72 to LTOT alone). NIV improved sleep quality and sleep-related hypercapnia acutely, and patients complied well with therapy (mean (SD) nightly use 4.5 (3.2) h). Compared with LTOT alone, NIV (mean follow-up 2.21 years, range 0.01-5.59) showed an improvement in survival with the adjusted but not the unadjusted Cox model (adjusted hazard ratio (HR) 0.63, 95% CI 0.40 to 0.99, p = 0.045; unadjusted HR 0.82, 95% CI 0.53 to 1.25, p = NS). FEV1.0 and Paco(2) measured at 6 and 12 months were not different between groups. Patients assigned to NIV + LTOT had reduced general and mental health and vigour. Conclusions: Nocturnal NIV in stable oxygen-dependent patients with hypercapnic COPD may improve survival, but this appears to be at the cost of worsening quality of life.
引用
收藏
页码:561 / 566
页数:6
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