Key result
Anatomy-guided PTPV achieves ~100% biventricular repair and survival in suitable PAIVS and critical PS.
Why the study?
Pulmonary atresia with intact ventricular septum and critical pulmonary stenosis span a spectrum of right ventricular hypoplasia in which the optimal initial management pathway remains uncertain.
Does an anatomy-guided percutaneous transcatheter pulmonary valvuloplasty (PTPV)-first strategy achieve biventricular circulation and favorable mid-term survival in infants with pulmonary atresia with intact ventricular septum or critical pulmonary stenosis?
Cohort (n=21)
No
Does an anatomy-guided percutaneous transcatheter pulmonary valvuloplasty (PTPV)-first strategy achieve biventricular circulation and favorable mid-term survival in infants with pulmonary atresia with intact ventricular septum or critical pulmonary stenosis?
Answers are grounded in this paper and cite their sources.
An anatomy-guided PTPV-first strategy based on a tripartite RV and absence of major sinusoidal communications enables staged RV recruitment and achieves biventricular circulation with 100% mid-term survival in selected infants with PAIVS and cPS.
Pulmonary atresia with intact ventricular septum (PAIVS) and critical pulmonary stenosis (cPS) span a spectrum of right ventricular hypoplasia in which the optimal initial pathway remains uncertain. We describe mid-term outcomes of an anatomy-guided percutaneous transcatheter pulmonary valvuloplasty (PTPV)-first strategy. We retrospectively reviewed 24 patients treated invasively from 2007 through 2025; three lacked measurable right ventricular end-diastolic volume (RVEDV) and were excluded, leaving an analytic cohort of 21 patients (PAIVS, n = 9; cPS, n = 12). Fifteen patients with a tripartite right ventricle and no major sinusoidal communication underwent PTPV first; six with an absent outlet component or major sinusoidal communication entered a single-ventricle pathway. All 15 PTPV-first patients achieved biventricular circulation; all three PAIVS patients in this group required subsequent, elective surgical right ventricular decompression, consistent with staged rather than failed decompression. All six single-ventricle patients completed Fontan circulation, and no PTPV-first patient required one-and-a-half ventricular repair or crossed over to Fontan. All 21 patients were alive after a median follow-up of 8 years [interquartile range, 6–11]. One patient with borderline RVEDV and tricuspid valve Z-score developed protein-losing enteropathy 11 years after Fontan completion. PTPV-first patients tended to have higher RVEDV and less negative tricuspid valve Z-scores than single-ventricle patients, reflecting selection criteria rather than validated thresholds. PTPV first permitted staged right ventricular recruitment and biventricular circulation with favorable mid-term outcomes, with surgical decompression as an effective subsequent step. Given the small, retrospective, single-center design, these findings are hypothesis-generating and warrant prospective reassessment of borderline right ventricles.
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Sano et al. (2026) conducted a cohort in Pulmonary atresia with intact ventricular septum (PAIVS) or critical pulmonary stenosis (cPS) (n=21). Anatomy-guided percutaneous transcatheter pulmonary valvuloplasty (PTPV)-first strategy vs. Single-ventricle pathway culminating in Fontan circulation (for patients with an absent RV outlet component or major sinusoidal communication) was evaluated on Achievement of biventricular circulation (BVR). An anatomy-guided PTPV-first strategy achieved biventricular circulation in 100% (15/15) of anatomically suitable PAIVS/cPS patients with 100% survival over a median 8-year follow-up.
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