Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/58766
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Type: Journal article
Title: Nocturnal non-invasive nasal ventilation in stable hypercapnic COPD: a randomised controlled trial
Author: McEvoy, R.
Pierce, R.
Hillman, D.
Esterman, A.
Ellis, E.
Catcheside, P.
O'Donoghue, F.
Barnes, D.
Grunstein, R.
Citation: Thorax, 2009; 64(7):561-566
Publisher: British Med Journal Publ Group
Issue Date: 2009
ISSN: 0040-6376
1468-3296
Statement of
Responsibility: 
R D McEvoy, R J Pierce, D Hillman, A Esterman, E E Ellis, P G Catcheside, F J O’Donoghue, D J Barnes, R R Grunstein, on behalf of the Australian trial of noninvasive Ventilation in Chronic Airflow Limitation (AVCAL) Study Group
Abstract: 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) ,1.5 litres or ,50% predicted and ratio of FEV1.0 to forced vital capacity (FVC) ,60% with awake arterial carbon dioxide tension (PaCO2) .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 PaCO2 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.
Keywords: Australian trial of non-invasive Ventilation in Chronic Airflow Limitation (AVCAL) Study Group
Humans
Pulmonary Disease, Chronic Obstructive
Hypercapnia
Carbon Dioxide
Forced Expiratory Volume
Treatment Outcome
Positive-Pressure Respiration
Survival Analysis
Affect
Partial Pressure
Quality of Life
Aged
Female
Male
Rights: Copyright status unknown
DOI: 10.1136/thx.2008.108274
Published version: http://dx.doi.org/10.1136/thx.2008.108274
Appears in Collections:Aurora harvest 5
Molecular and Biomedical Science publications

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