Eur Respir J 2004; 23:825-831
Copyright ©ERS Journals Ltd 2004
Long-acting inhaled anticholinergic therapy improves sleeping oxygen saturation in COPD
W.T. McNicholas1,
P.M.A. Calverley3,
A. Lee4 and
J.C. Edwards2 on behalf of the Tiotropium Sleep Study in COPD Investigators
1 St. Vincent's University Hospital, Elm Park, and 2 Boehringer Ingelheim Ireland Ltd, Dublin, Ireland. 3 University Hospital Aintree, Liverpool, and 4 Boehringer Ingelheim Ltd, Bracknell, UK
CORRESPONDENCE: W.T. McNicholas, Dept of Respiratory Medicine, St. Vincent's University Hospital, Elm Park, Dublin 4, Ireland. Fax: 353 12697949. E-mail: walter.mcnicholas@ucd.ie
Keywords: Chronic obstructive pulmonary disease, randomised controlled trial, sleep-disordered breathing, tiotropium bromide
Received: July 24, 2003
Accepted March 15, 2004
This study was entirely supported by a grant from Boehringer Ingelheim Ltd.
Oxygen desaturation occurs during sleep in severe chronic obstructive pulmonary disease (COPD), especially during rapid eye movement (REM) sleep, due to hypoventilation and ventilation-perfusion mismatching, but the possible contribution of airflow limitation is unclear.
In a randomised, placebo-controlled, double-blind study of severe, stable COPD patients, the authors compared 4 weeks treatment with a long-acting inhaled anticholinergic agent (tiotropium), taken in the morning (tiotropium-AM), or in the evening (tiotropium-PM), on sleeping arterial oxygen saturation (Sa,O2) and sleep quality. Overnight polysomnography was performed at baseline and after 4 weeks treatment. A total of 95 patients with awake resting arterial oxygen tension 9.98 kPa (75 mmHg) were randomised, with a mean age of 66.4 yrs and mean forced expiratory volume in one second (FEV1) of 32% predicted.
A total of 80 patients completed the study, of which 56 fulfilled the polysomnographic criterion of at least 2 h sleep in both sleep study nights and represent the group analysed. Tiotropium significantly improved spirometry compared with placebo. Both tiotropium-AM and tiotropium-PM groups had higher Sa,O2 during REM than placebo (+2.41% and +2.42%, respectively, and both pooled and tiotropium-PM groups had higher Sa,O2 during total sleep time (+2.49% and +3.06%, respectively). End-of-treatment FEV1 correlated with Sa,O2 during REM sleep, however, tiotropium did not change sleep quality.
Sustained anticholinergic blockade improves sleeping arterial oxygen saturation without affecting sleep quality.
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Copyright © 2004 by the European Respiratory Society.
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