Key result
Potts shunt is linked to improved risk category in ~75% of pediatric PAH patients.
Why the study?
Does a CMR-guided multidisciplinary approach to Potts shunt improve clinical risk status and survival in children with Group 1 PAH?
Cohort (n=36)
No
Does a CMR-guided multidisciplinary approach to Potts shunt improve clinical risk status and survival in children with Group 1 PAH?
A CMR-guided multidisciplinary approach to Potts shunt in pediatric PAH improves risk status in 75% of patients, highlighting that intervention should occur before advanced right ventricular failure.
May support early CMR-guided Potts shunt in pediatric PAH; leaves open confirmation of survival benefit in randomized trials.
Rationale Potts shunt represents a strategy for children with refractory pulmonary arterial hypertension (PAH). Procedural timing remains undefined, and interventions may be associated with perioperative mortality and limited clinical benefit. Evidence integrating advanced imaging, multidisciplinary decision-making, and risk stratification is lacking.Objective: To evaluate the impact of a multidisciplinary approach and cardiac magnetic resonance imaging (CMR)-guided assessment on outcomes for Potts shunt in pediatric PAH, and investigate the association between timing of intervention, preoperative right ventricular (RV) function, and clinical improvement. Methods Prospective, single-center study of 36 consecutive Group 1 PAH children (median age 11.2 years) undergoing surgical (n = 20) or transcatheter (n = 16) Potts shunt. The primary endpoint was all-cause mortality or persistent high-risk status 6 months post-procedure. Logistic regression identified predictors of clinical improvement, and a pre-procedural risk score was developed to inform procedural timing. Measurements and Main Results Overall, 75% of patients improved in risk category (55.6% to low-risk, and 82% weaned off prostacyclin therapy). Preoperative RV dysfunction and increased RV volumes were associated with lower likelihood of clinical improvement. Delayed intervention correlated with diminished benefit and increased perioperative mortality (11.1% - limited to surgical patients early in the series). A six-parameter, CMR-based risk score demonstrated high discriminatory capacity (AUC 0.89) for predicting clinical improvement. Conclusions A multidisciplinary, CMR-guided approach enables optimized Potts timing, improved patient selection, and favorable clinical outcomes in children with PAH. Potts shunt should not be delayed until advanced right ventricular failure, and the proposed risk score may assist in guiding optimal intervention timing.
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Xu et al. (2026) conducted a cohort in Group 1 Pulmonary Arterial Hypertension (PAH) (n=36). Potts shunt (surgical or transcatheter) was evaluated on All-cause mortality or persistent high-risk status 6 months post-procedure. Potts shunt in pediatric pulmonary arterial hypertension improved risk category in 75% of patients, with a CMR-based risk score demonstrating high discriminatory capacity for improvement (AUC 0.89).
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