Long-term therapy with endothelin-1 antagonist for pulmonary hypertension secondary to systemic sclerosis

Lilach Shalev, Pnina Langevitz, Gisele Zandman-Goddard

Research output: Contribution to journalArticlepeer-review

Abstract

Pulmonary hypertension in systemic sclerosis appears in up to 35% of patients, is characterized by increased pulmonary artery resistance, and carries a poorer prognosis than in patients with other causes of pulmonary hypertension. The recommended therapy for stage III disease, based on clinical trials and by the Israeli Ministry of Health for 2006, includes bosentan (Tracleer), an endothelin-1 antagonist. This is a case report of a patient with severe pulmonary hypertension secondary to systemic sclerosis where therapy with prostacyclins was contraindicated due to the development of congestive heart failure and severe atherosclerosis. The patient responded well to bosentan monotherapy for 4 years until his death.

Original languageEnglish
Pages (from-to)287-289
Number of pages3
JournalHarefuah
Volume147
Issue number4
StatePublished - Apr 2008
Externally publishedYes

Keywords

  • Bosentan
  • Endothelin-1 antagonist
  • Pulmonary hypertension
  • Systemic sclerosis

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