Key result
Switching from bosentan to riociguat improves hemodynamics and exercise tolerance in idiopathic PAH.
Why the study?
In pulmonary arterial hypertension, guidelines mainly recommend sequential combination therapy after inadequate response to initial monotherapy, and switching between monotherapies targeting different molecular pathways has virtually no supporting data.
Case Report (n=1)
No
Answers are grounded in this paper and cite their sources.
Reveals improved hemodynamics and exercise capacity after switching from bosentan to riociguat in idiopathic pulmonary arterial hypertension, indicating an effective alternative strategy.
Pulmonary arterial hypertension (PAH) is a life-threatening disease characterized by progressive increase in pulmonary vascular resistance (PVR), higher pulmonary arteries mean pressure (mPAP), decrease in cardiac minute output (CMO) and other hemodynamic, functional and biochemical disorders. Existing PAH therapeutic algorithm, described in the European and Russian clinical guidelines, mainly suggest strategy of sequential combination therapy in the case of inadequate response to initial monotherapy. At this, switching from one PAH-specific drug to another is studied to a lesser extent. At the present similar approach (switching) has already been tested, for example, in switching from one endothelin receptor antagonist (ERA) to another, or from phosphodiesterase type 5 inhibitor (iPDE-5) to soluble guanylate cyclase stimulator (sGC). There are virtually no data about change of monotherapy when drugs target different molecular pathways of vascular tone regulation, in particular, in the pulmonary circulation vessels. This article describes clinical case of female patient with FC III pulmonary arterial hypertension (WHO) switched from therapy by endothelin-1 receptor antagonist (bosentan) to soluble guanylate cyclase stimulator (riociguat). Female, 37 years old, with verified by the right heart catheterization (RHC) diagnosis of idiopathic PAH (iPAH) received PAH-specific monotherapy of bosentan. Due to condition deterioration on the background of bosentan dose increase, medical conference decided to switch this patient to another class of PAH-specific therapy (sGC stimulator riociguat) with consequent follow-up. As a result of such approach positive changes in patient's condition, improvement of hemodynamic parameters, increased tolerance of physical exercise was demonstrated in comparison with previous therapy. This clinical case demonstrates safe and successful transfer from bosentan to riociguat in the patient with idiopathic PAH. Similar tactic for the change of therapy should be studied in further clinical trials.
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Devetyarova et al. (2018) conducted a case report in Idiopathic pulmonary arterial hypertension (WHO FC III) (n=1). Riociguat (switched from bosentan) vs. Previous bosentan monotherapy was evaluated on Clinical condition, hemodynamic parameters, and physical exercise tolerance. Switching from bosentan to riociguat in a 37-year-old female with WHO FC III idiopathic PAH safely improved clinical status, hemodynamic parameters, and exercise tolerance.
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