Riociguat in the Treatment of Pulmonary Arterial Hypertension

Arch Med Res. 2022 Jun;53(4):352-358. doi: 10.1016/j.arcmed.2022.04.001. Epub 2022 Apr 27.

Abstract

Pulmonary arterial hypertension (PAH) is a severe clinical condition that significantly affects patients' quality of life and survival. Since the emergence of prostanoids 45 years ago, different drugs acting on vasoconstriction/vasodilation mechanisms have been developed for the treatment of PAH. Current evidence shows that better results occur when combined therapy is initiated up-front with periodic and systematized evaluations for escalation and switching. Among these strategies, riociguat has a relevant role, supported by the results of several clinical studies. This document issues recommendations by a panel of experts who analysed and discussed the indications and limitations for riociguat in PAH in different institutions of the Mexican health system.

Keywords: Pulmonary arterial hypertension; Recommendations; Riociguat.

Publication types

  • Review
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Humans
  • Pulmonary Arterial Hypertension* / drug therapy
  • Pyrazoles / pharmacology
  • Pyrazoles / therapeutic use
  • Pyrimidines / pharmacology
  • Pyrimidines / therapeutic use
  • Quality of Life

Substances

  • Pyrazoles
  • Pyrimidines
  • riociguat