André Noseda
Université libre de Bruxelles
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Featured researches published by André Noseda.
European Respiratory Journal | 1997
André Noseda; Jp Carpiaux; C Markstein; A Meyvaert; V. De Maertelaer
The purpose of this placebo-controlled, double-blind, randomized study was to assess the effect of nebulized morphine on dyspnoea perceived at rest by patients with advanced disease. Seventeen hospital in-patients with disabling dyspnoea received isotonic saline or morphine via nebulization for 10 min through a mouthpiece, combined with oxygen via nasal prongs. On four consecutive days, they were given one of the four following treatments in random order: saline with 2 L x min(-1) oxygen; 10 mg morphine with 2 L x min(-1) oxygen; 20 mg morphine with 2 L x min(-1) oxygen; and 10 mg morphine without oxygen (prongs fixed, no flow). Dyspnoea was assessed on a bipolar visual analogue scale (VAS) (-100% much more short of breath, +100% much less short of breath), and arterial oxygen saturation (Sa,O2) and respiratory frequency (fR) were recorded at the end of nebulization and 10 min later. In 14 subjects who completed the study, mean VAS ratings 10 min after the end of nebulization ranged +30 to +43%, with no significant difference between the four study days (VAS 20 mg morphine minus VAS saline, 95% confidence interval (95% CI) -6 to +8%). Sa,O2 significantly increased on the 3 days with supplemental oxygen, and remained stable on the zero flow day. Respiratory frequency significantly decreased on the 4 days, with a trend to correlation between VAS rating and parallel change in respiratory frequency (Spearmans rank correlation coefficient (r(s))=0.46; p=0.09). We conclude that the subjects benefited from saline or morphine via a placebo effect and/or a nonspecific effect, and that nebulized morphine had no specific effect on dyspnoea.
Lung | 1989
André Noseda; Jean Pierre Carpiaux; Thierry Prigogine; Jacqueline Schmerber
AbstractThis study was designed to investigate the reproducibility and clinical relevance of several lung function and exercise test indices in a sample of patients with stable severe chronic obstructive pulmonary disease (COPD).Twenty subjects (ages 67.8±2.0 years, forced expiratory volume in 1s, [FEV1] 39.7±2.8% predicted) receiving conventional medical therapy and pulmonary rehabilitation were tested 4 times at 1 month intervals. Testing procedures included lung function (inspiratory vital capacity [IVC], FEV1, plethysmographic functional residual capacity [FRC], specific conductance of the airways (sGaw), single breath transfer factor divided by the alveolar volume [TL/VA]); incremental, progressive, symptom-limited, cycle exercise (maximum work load [
Thorax | 1992
André Noseda; Jean Pierre Carpiaux; Jacqueline Schmerber; Jean Claude Yernault
Digestive Diseases and Sciences | 1987
André Noseda; Diamon Gangji; Michel Cremer
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European Respiratory Journal | 1994
André Noseda; Jean Pierre Carpiaux; Jacqueline Schmerber; F Valente; Jean Claude Yernault
Clinical Neurophysiology | 2007
Martine Dumont; Fabrice Jurysta; Jean Pol Lanquart; André Noseda; Philippe van de Borne; Paul Linkowski
max], maximum heart rate [HRmax], maximum ventilation [
Cancer Genetics and Cytogenetics | 1985
Diamon Gangji; André Noseda; Joseph Wybran; Alain Verhest
BMC Pulmonary Medicine | 2013
Fabrice Jurysta; Chantal Kempenaers; Jean Pol Lanquart; André Noseda; Philippe van de Borne; Paul Linkowski
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The American Journal of the Medical Sciences | 1985
André Noseda; Olivia Louis; Jean Mockel; Jean Claude Yernault
Sleep Medicine | 2009
André Noseda; S. André; V. Potmans; M. Kentos; V. De Maertelaer; G. Hoffmann
Emax], maximum oxygen uptake [