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ORIGINAL ARTICLE |
1 Service de Pneumologie et Réanimation Respiratoire, Université Paris-Sud 11, Centre National de Reference de l'Hypertension Arterielle Pulmonaire, Institut Paris-Sud Cytokines, Hôpital Antoine- Béclère, Clamart, France; and Service de Pneumologie et Réanimation, CHU Larrey, Toulouse, France
2 Service de Pneumologie et Réanimation Respiratoire, Université Paris-Sud 11, Centre National de Reference de l'Hypertension Arterielle Pulmonaire, Institut Paris-Sud Cytokines, Hôpital Antoine- Béclère, Clamart, France
3 Service de Pneumologie et Réanimation, CHU Larrey, Toulouse, France
| Abstract |
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Bosentan has proven 4-month efficacy in patients with human immunodeficiency virus-associated pulmonary arterial hypertension (PAH-HIV). Here, we describe the long-term outcome of unselected PAH-HIV patients treated with first-line bosentan.
Data were analysed for 59 consecutive WHO functional class II-IV PAH-HIV patients treated with first-line bosentan between May 2002 and July 2007. HIV status, 6-minute walk distance and haemodynamics were assessed at baseline, after 4 months, and every 6–12 months thereafter.
After 4 months, 6-minute walk distance increased from 358±98 to 435±89m and pulmonary vascular resistance decreased from 737±328 to 476±302 dyn·s·cm-5. At last evaluation, 29±15 months, 6-minute walk distance remained stable and pulmonary vascular resistance decreased further to 444±356 dyn·s·cm-5. Haemodynamics normalised in 10 patients. At their last evaluation, these 10 patients were in WHO functional class I, with a 6-minute walk distance of 532±52m. Overall survival estimates were 93%, 86% and 66% at 1, 2 and 3 years, respectively. Bosentan was safe when combined with highly-active antiretroviral therapy with no negative impact on HIV-infection control.
Our data confirm long-term benefits of bosentan therapy in PAH-HIV patients with improvements in symptoms, 6-minute walk distance and haemodynamics, and with favourable overall survival.
Keywords: Bosentan, endothelin, human immunodeficiency virus, hypertension, pulmonary
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