ERJ
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Published online before print April 30, 2008, 10.1183/09031936.00011308
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Google Scholar
Right arrow Articles by Stolz, D.
Right arrow Articles by Tamm, M.
PubMed
Right arrow PubMed Citation
Right arrow Articles by Stolz, D.
Right arrow Articles by Tamm, M.
Eur Respir J 2008; 32:619-628
Copyright ©ERS Journals Ltd 2008

A randomised, controlled trial of bosentan in severe COPD

D. Stolz1,2, H. Rasch3, A. Linka4, M. Di Valentino5, A. Meyer1, M. Brutsche1 and M. Tamm1

1 Clinic of Pneumology and Pulmonary Cell Research, 3 Divisions of Nuclear Medicine and 5 Cardiology, University Hospital Basel, Basel, and 4 Division of Cardiology State Hospital, Winterthur, Switzerland. 2 Harvard School of Public Health, Boston, MA, USA.

CORRESPONDENCE: D. Stolz, Clinic of Pulmonary Medicine and Respiratory Cell Research, University Hospital Basel, Petersgraben 4, CH-4031 Basel, Switzerland. Fax: 41 612654587. E-mail: dstolz{at}uhbs.ch

Keywords: Endothelin-receptor antagonist, exercise capacity, pulmonary hypertension, treatment

Received: January 23, 2008
Accepted April 14, 2008

Pulmonary hypertension during exercise is common in severe chronic obstructive pulmonary disease (COPD). It was hypothesised that the use of the endothelin-receptor antagonist bosentan can improve cardiopulmonary haemodynamics during exercise, thus increasing exercise tolerance in patients with severe COPD.

In the present double-blind, placebo-controlled study, 30 patients with severe or very severe COPD were randomly assigned in a 2:1 ratio to receive either bosentan or placebo for 12 weeks. The primary end-point was change in the 6-min walking distance. Secondary end-points included changes in health-related quality of life, lung function, cardiac haemodynamics, maximal oxygen uptake and pulmonary perfusion patterns.

Compared with placebo, patients treated with bosentan during 12 weeks showed no significant improvement in exercise capacity as measured by the 6-min walking distance (mean±SD 331±123 versus 329±94 m). There was no change in lung function, pulmonary arterial pressure, maximal oxygen uptake or regional pulmonary perfusion pattern. In contrast, arterial oxygen pressure dropped, the alveolar–arterial gradient increased and quality of life deteriorated significantly in patients assigned bosentan.

The oral administration of the endothelin receptor antagonist bosentan not only failed to improve exercise capacity but also deteriorated hypoxaemia and functional status in severe chronic obstructive pulmonary disease patients without severe pulmonary hypertension at rest.




This article has been cited by other articles:


Home page
Eur Respir JHome page
A. Chaouat, R. Naeije, and E. Weitzenblum
Pulmonary hypertension in COPD
Eur. Respir. J., November 1, 2008; 32(5): 1371 - 1385.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2008 by the European Respiratory Society.