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Transition from Parenteral Prostacyclin Therapy to Oral Selexipag in Pulmonary Arterial Hypertension: a Single Center, Case Series

E. Mims

David Poch

Demosthenes Papamatheakis

Timothy Fernandes

Sandra Lombardi

Luis Santana

Nick Kim


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Conference: 2017 PH Professional Network Symposium

Release Date: 10.06.2017

Presentation Type: Abstracts

File Download: 2017 PHPN Abstract 1002

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Abstract presented at the 2017 PH Professional Network Symposium held in Bethesda, Md on October 5-7, 2017


Review all patients with PAH on IV or SC therapy that were transition to selexipag in our institution.


We reviewed all patients with PAH on IV or SC therapy that transitioned to selexipag therapy in our institution. Rationale for transition was highly individualized and included patient preference, history of complications related to ongoing IV or SC treatment and hemodynamic/clinical profile. NYHA function class (FC) was assessed before and after transition to selexipag; 8 patients in the cohort had follow-up hemodynamics by the time of presentation.


Nine (64%) patients were on IV epoprostenol and five patients on SC treprostinil prior to transition.

Duration of parenteral therapy prior to transition ranged from 9-62 months (mean 30.1 ± 18.3 months).

The majority of patients were female (86%) and over the age of 50 (mean 55.6 ± 11 years).

All patients were on background PAH therapy. Eight on combined ERA/NO-pathway medications. Five patients on NO-pathway alone and one patient on ERA alone.

Average time between transitioning to selexipag and functional class assessment was 6.6 months.

Eleven (79%) of the 14 patients maintained their NYHA FC after transitioning to selexipag.

Two patients had worsening of FC after transitioning. One of these patients required re-initiation of parenteral therapy.

One patient with scleroderma and clinical features of PVOD transitioned to selexipag for difficulty maintaining IV therapy without option of lung transplantation. She was functional class IV prior to transition – and had clinical worsening due to right heart failure and died under hospice care.


The transition from chronic parenteral prostacyclin therapy to oral selexipag is feasible but requires careful individualized consideration with close monitoring during and after the transition period.