Chronic thromboembolic pulmonary hypertension: Medical treatment


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Ozsu S., Cinarka H.

PULMONARY CIRCULATION, vol.3, no.2, pp.341-344, 2013 (Journal Indexed in SCI) identifier identifier identifier

  • Publication Type: Article / Review
  • Volume: 3 Issue: 2
  • Publication Date: 2013
  • Doi Number: 10.4103/2045-8932.114761
  • Title of Journal : PULMONARY CIRCULATION
  • Page Numbers: pp.341-344

Abstract

Chronic thromboembolic pulmonary hypertension (CTEPH) is responsible for significant levels of morbidity and mortality. The estimated cumulative incidence of CTEPH is 2-4% among patients presenting with acute pulmonary thromboembolism. Currently, at the time of CTEPH diagnosis, 37.9% of the patients in an international registry were receiving at least one pulmonary arterial hypertension ( PAH)-targeted therapy. Advanced medical therapy is considered in patients with inoperable disease, as a bridge to pulmonary endarterectomy or in those with persistent or recurrent pulmonary hypertension. PAH-specific medical therapies include endothelin receptor antagonists, phosphodiesterase inhibitors, and prostacyclin analogues. The present article will focus on recent developments in the pharmacological treatment of CTEPH.