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Revista médica de Chile

versão impressa ISSN 0034-9887

Resumo

HERRERA, Sebastián et al. Survival of patients with pulmonary arterial hypertension after the advent of specific pulmonary vasodilator therapies. Rev. méd. Chile [online]. 2016, vol.144, n.7, pp.829-836. ISSN 0034-9887.  http://dx.doi.org/10.4067/S0034-98872016000700002.

Background: Pulmonary arterial hypertension (PAH) is a rare and progressive disease. Long-term survival remains poor despite of advances in specific vasodilator therapy. Aim: To describe the survival rate in a cohort of PAH patients in two referral centers in Chile. Patients and Methods: One hundred fifteen patients aged 43 ± 15.6 years (85% females) with PAH qualified for this study. Their median pulmonary artery pressure was 55.4 ± 14 mmHg and their six minutes walking capacity was 368 ± 119 m. They were followed for 58 ± 0.4 months and their actual survival rates were compared with the estimated survival using the equation proposed by the French registry of PAH. Results: One, two and three year survival rates were 97, 94 and 89%, respectively. The observed survival rates were greater than the estimated survival. Conclusions: The improvement in survival rates observed in this cohort of patients is similar to what has been described in literature.

Palavras-chave : Follow-Up Studies; Hypertension, Pulmonary; Registries; Survival rate.

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