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Updated: Feb 14, 2026

Evaluation of Right Ventricular Function in Experimental Models of Pulmonary Arterial Hypertension
Published on: June 27, 2025
Right ventricular function mirrors clinical improvement with use of prostacyclin analogues in pediatric pulmonary
Rachel K Hopper1, Yan Wang1, Valerie DeMatteo1
11 24349 Division of Cardiology, Department of Pediatrics, The Children's Hospital of Philadelphia and Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA.
Insights
Prostacyclin analogues improved right ventricular (RV) function in children with pulmonary hypertension (PH). Echocardiography showed early and sustained improvements in RV strain and function, alongside better clinical markers of PH severity.
Area of Science:
- Pediatric Cardiology
- Pulmonology
- Cardiovascular Imaging
Background:
- Pediatric pulmonary hypertension (PH) leads to significant right ventricular (RV) failure, morbidity, and mortality.
- RV dysfunction is a key factor in the progression and outcomes of pediatric PH.
Purpose of the Study:
- To evaluate the impact of prostacyclin analogues on RV function in pediatric PH patients.
- To assess changes in echocardiographic parameters and clinical markers of PH severity following prostacyclin analogue treatment.
Main Methods:
- Retrospective cohort study of 49 children with PH treated with epoprostenol or treprostinil (2001-2015).
- Echocardiograms (including TAPSE and RV global longitudinal strain) and clinical data collected at baseline and 1-12 months post-treatment.
- Blinded analysis of echocardiographic measurements.
Main Results:
- Prostacyclin analogues significantly improved TAPSE (P=0.007), RV strain (P<0.001), and qualitative RV function (P=0.037).
- Improvements were observed in BNP levels (P<0.001), functional class (P=0.047), and 6-minute walk distance (P=0.001).
- Early improvements in TAPSE and RV strain were noted, suggesting a rapid therapeutic effect.
Conclusions:
- Prostacyclin analogues are associated with early and sustained improvement in RV function in children with PH.
- RV strain emerges as a sensitive echocardiographic marker for assessing RV function in pediatric PH.
- Treatment with prostacyclin analogues positively impacts both echocardiographic and clinical indicators of PH severity in children.
Abstract:
Pulmonary hypertension (PH) causes significant morbidity and mortality in children due to right ventricular (RV) failure. We sought to determine the effect of prostacyclin analogues on RV function assessed by echocardiography in children with PH. We conducted a retrospective cohort study of children with PH treated with a prostacyclin analogue (epoprostenol or treprostinil) between January 2001 and August 2015 at our center. Data were collected before initiation of treatment (baseline) and at 1-3 and 6-12 months after. Protocolized echocardiogram measurements including tricuspid annular plane systolic excursion (TAPSE) and RV global longitudinal strain were made with blinding to clinical information. Forty-nine individuals (65% female), aged 0-29 years at the time of prostacyclin initiation were included. Disease types included pulmonary arterial hypertension (idiopathic [35%], heritable [2%], and congenital heart disease-associated [18%]), developmental lung disease (43%), and chronic thromboembolic PH (2%). Participants received intravenous (IV) epoprostenol (14%) and IV/subcutaneous (SQ) (67%) or inhaled (18%) treprostinil. Over the study period, prostacyclin analogues were associated with improvement in TAPSE ( P = 0.007), RV strain ( P < 0.001), and qualitative RV function ( P = 0.037) by echocardiogram, and BNP ( P < 0.001), functional class ( P = 0.047) and 6-min walk distance ( P = 0.001). TAPSE and strain improved at early follow up ( P = 0.05 and P = 0.002, respectively) despite minimal RV pressure change. In children with PH, prostacyclin analogues are associated with an early and sustained improvement in RV function measured as TAPSE and strain as well as clinical markers of PH severity. RV strain may be a sensitive marker of RV function in this population.
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