Background: Percutaneous pulmonary valve implantation (PPVI) is an increasingly practiced treatment
option for patients with right ventricular outflow tract (RVOT) dysfunction. After
encouraging results with the Edwards Sapien and XT valves in the pulmonary position,
Edwards’ latest modification, the Sapien 3 valve is available for clinical PPVI trials.
Objectives: This study aimed to review procedural data and early outcomes for the Sapien 3 valves
(Edwards Lifesciences, Irvine, California, United States) for PPVI.
Methods: We performed a multicenter, retrospective, observational registry analysis of patients
who underwent PPVI with the Edwards Sapien 3 transcatheter heart valve between 2015
and 2017 in five centers in Germany.
Results: A total of 46 patients could be enrolled (mean weight 56.8 ± 26.9 kg, min. 11.8,
max. 114 kg). The majority had tetralogy of Fallot as underlying diagnosis (48%),
and a Contegra conduit as the most common RVOT configuration pre-PPVI (34.8%). However,
pulmonary insufficiency or both, insufficiency ≥ moderate and stenosis ≥ 20 mm Hg
were the leading indications for PPVI (78.3%). Most procedures were two-stage procedures
(82.6%) with 100% prestenting. Valve sizes were 20 mm (n = 1), 23 mm (n = 15), 26 mm (n = 18), and 29 mm (n = 12). Procedural success rate was high (95.6%) with a low frequency of periprocedural
complications (4.3%): In two patients, surgical pulmonary valve implantation had to
be performed after balloon rupture during (one-stage) PPVI procedure.
Follow-up data were available up to 24-month post-PPVI. NYHA class improved in all
patients (93.3% were at NYHA I). The rate of patients with moderate/severe pulmonary
regurgitation decreased from 74% at baseline to 0% after PPVI, and the calculated
peak systolic gradient for all patients decreased from 24.2 (SD ± 20.9) mm Hg to 7.1
mm Hg (SD ± 5.0). There were no episodes of endocarditis, no thromboses, and no stent
fractures documented.
Conclusion: The Edwards Sapien 3 valve is a viable option for PPVI in patients with conduits,
native pulmonary valves, or transannular patches. Continued data collection is necessary
to verify long-term results.
