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1.
Eur Respir J ; 32(3): 619-28, 2008 Sep.
Article in English | MEDLINE | ID: mdl-18448495

ABSTRACT

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.


Subject(s)
Hypertension, Pulmonary/complications , Hypertension, Pulmonary/drug therapy , Pulmonary Disease, Chronic Obstructive/complications , Sulfonamides/adverse effects , Vasodilator Agents/adverse effects , Aged , Bosentan , Double-Blind Method , Exercise Tolerance/drug effects , Female , Humans , Hypoxia , Male , Middle Aged , Pulmonary Disease, Chronic Obstructive/pathology , Quality of Life
2.
Eur J Vasc Endovasc Surg ; 34(4): 416-23, 2007 Oct.
Article in English | MEDLINE | ID: mdl-17689112

ABSTRACT

OBJECTIVES: We aimed to assess in vivo the long-term effects of percutaneous transluminal angioplasty (PTA) and endovascular brachytherapy (EVBT) on vessel wall by serial MRI. METHODS: Twenty patients with symptomatic stenosis of the femoropopliteal artery were randomly assigned to PTA (n=10) or PTA+EVBT (n=10, 14Gy by gamma-source). High-resolution MRI was performed prior, at 24-hours, 3-months, and 24-months after intervention. MRI data were analyzed by an independent, blinded observer. RESULTS: The effects of both procedures on vessel wall at 24-hours and 3-months have been reported. Despite similar percent decrease in lumen area between 3- and 24-months in both groups (-8% for PTA and -11% for PTA+EVBT), at 24-months lumen area gain compared to baseline was +30% in PTA versus +82% in PTA+EVBT (p<0.05). Total vessel area, which was increased at 24-hours and 3-months, returned to pre-treatment value in both groups. CONCLUSIONS: We demonstrated non-invasively that restenosis and inward remodeling after PTA are delayed by EVBT. At 24-months, patients treated with brachytherapy have larger lumen than those treated with PTA alone. The decrease in luminal and total vessel area between 3- and 24-months after EVBT indicates that the restenotic and remodeling process is not abolished but delayed with this therapy.


Subject(s)
Angioplasty, Balloon , Arteriosclerosis/therapy , Brachytherapy , Femoral Artery/pathology , Magnetic Resonance Imaging , Popliteal Artery/pathology , Aged , Arteriosclerosis/pathology , Female , Femoral Artery/radiation effects , Follow-Up Studies , Humans , Image Processing, Computer-Assisted , Male , Popliteal Artery/radiation effects , Recurrence
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