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Updated: Jul 24, 2025

Evaluation of Right Ventricular Function in Experimental Models of Pulmonary Arterial Hypertension
Published on: June 27, 2025
Ventricular global function index is associated with clinical outcomes in pediatric pulmonary hypertension
Hieu T Ta1,2, Paul J Critser1,2, Michal Schäfer3
1Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
Insights
Global ventricular function index (GFI) shows prognostic value in pediatric pulmonary hypertension (PH). This cardiac magnetic resonance imaging (CMR) metric predicts adverse outcomes, offering an advantage over traditional measures in PH patients.
Area of Science:
- Cardiology
- Pediatric Medicine
- Medical Imaging
Background:
- Right ventricular (RV) metrics are crucial for prognostication in pulmonary hypertension (PH).
- A global ventricular function index (GFI) derived from cardiac magnetic resonance imaging (CMR) has shown predictive value for adverse outcomes in adults.
- GFI has not been previously evaluated in pediatric PH populations.
Purpose of the Study:
- To assess the feasibility of using GFI as a predictor of composite adverse outcome (CAO) in pediatric PH patients.
- To compare the predictive performance of GFI against traditional CMR-derived metrics.
Main Methods:
- Retrospective chart review of pediatric PH patients who underwent CMR between January 2005 and June 2021.
- Calculation of GFI (stroke volume divided by mean ventricular cavity and myocardial volume).
- Definition of CAO as death, lung transplant, Potts shunt, or parenteral prostacyclin initiation; analysis using Cox proportional hazards regression.
Main Results:
- The study included 89 pediatric PH patients; 24% experienced CAO.
- Patients with CAO had significantly higher indexed RV volumes and mass, but lower ejection fraction (EF) and GFI.
- Lower RV GFI (<43%) was associated with decreased event-free survival and increased CAO risk.
- Multivariable models showed GFI improved CAO prediction compared to ventricular volumes, mass, or EF.
Conclusions:
- RV GFI is a significant predictor of CAO in pediatric PH.
- GFI offers enhanced prognostic value compared to traditional CMR markers like RV EF.
- GFI is derived from readily available CMR data, requiring no additional post-processing, making it a potentially valuable clinical tool.
Background:
Multiple right ventricular (RV) metrics have prognostic value in pulmonary hypertension (PH). A cardiac magnetic resonance imaging (CMR) derived global ventricular function index (GFI) provided improved prediction of composite adverse outcome (CAO) in adults with atherosclerosis. GFI has not yet been explored in a PH population. We explored the feasibility of GFI as a predictor of CAO in a pediatric PH population.
Methods:
Two center retrospective chart review identified pediatric PH patients undergoing CMR from Jan 2005-June 2021. GFI, defined as the ratio of the stroke volume to the sum of mean ventricular cavity and myocardial volume, was calculated for each patient. CAO was defined as death, lung transplant, Potts shunt, or parenteral prostacyclin initiation after CMR. Cox proportional hazards regression was used to estimate associations and assess model performance between CMR parameters and CAO.
Results:
The cohort comprised 89 patients (54% female, 84% World Health Organization (WHO) Group 1; 70% WHO-FC ≤ 2; and 27% on parenteral prostacyclin). Median age at CMR was 12 years (IQR 8.1-17). Twenty-one (24%) patients experienced CAO during median follow up of 1.5 years. CAO cohort had higher indexed RV volumes (end systolic-145 vs 99 mL/m2, p = 0.003; end diastolic-89 vs 46 mL/m2, p = 0.004) and mass (37 vs 24 gm/m2, p = 0.003), but lower ejection fraction (EF) (42 vs 51%, p < 0.001) and GFI (40 vs 52%, p < 0.001). Higher indexed RV volumes (hazard ratios [HR] 1.01, CI 1.01-1.02), lower RV EF (HR 1.09, CI 1.05-1.12) and lower RV GFI (HR 1.09, CI 1.05-1.11) were associated with increased risk of CAO. In survival analysis, patients with RV GFI < 43% demonstrated decreased event-free survival and increased hazard of CAO compared to those with RV GFI ≥ 43%. In multivariable models, inclusion of GFI provided improved prediction of CAO compared to models incorporating ventricular volumes, mass or EF.
Conclusions:
RV GFI was associated with CAO in this cohort, and inclusion in multivariable models had increased predictive value compared to RVEF. GFI uses readily available CMR data without additional post-processing and may provide additional prognostic value in pediatric PH patients beyond traditional CMR markers.
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