TY - JOUR
T1 - Transcatheter Pulmonary Valve Replacement With the Sapien Prosthesis
AU - Shahanavaz, Shabana
AU - Zahn, Evan M.
AU - Levi, Daniel S.
AU - Aboulhousn, Jamil A.
AU - Hascoet, Sebastien
AU - Qureshi, Athar M.
AU - Porras, Diego
AU - Morgan, Gareth J.
AU - Bauser Heaton, Holly
AU - Martin, Mary Hunt
AU - Keeshan, Britton
AU - Asnes, Jeremy D.
AU - Kenny, Damien
AU - Ringewald, Jeremy M.
AU - Zablah, Jenny E.
AU - Ivy, Margaret
AU - Morray, Brian H.
AU - Torres, Alejandro J.
AU - Berman, Darren P.
AU - Gillespie, Matthew J.
AU - Chaszczewski, Kasey
AU - Zampi, Jeffrey D.
AU - Walsh, Kevin P.
AU - Julien, Plessis
AU - Goldstein, Bryan H.
AU - Sathanandam, Shyam K.
AU - Karsenty, Clement
AU - Balzer, David T.
AU - McElhinney, Doff B.
N1 - Publisher Copyright:
© 2020 American College of Cardiology Foundation
PY - 2020/12/15
Y1 - 2020/12/15
N2 - Background: There are limited published data focused on outcomes of transcatheter pulmonary valve replacement (TPVR) with either a Sapien XT or Sapien 3 (S3) valve. Objectives: This study sought to report short-term outcomes in a large cohort of patients who underwent TPVR with either a Sapien XT or S3 valve. Methods: Data were entered retrospectively into a multicenter registry for patients who underwent attempted TPVR with a Sapien XT or S3 valve. Patient-related, procedural, and short-term outcomes data were characterized overall and according to type of right ventricular outflow tract (RVOT) anatomy. Results: Twenty-three centers enrolled a total of 774 patients: 397 (51%) with a native/patched RVOT; 183 (24%) with a conduit; and 194 (25%) with a bioprosthetic valve. The S3 was used in 78% of patients, and the XT was used in 22%, with most patients receiving a 29-mm (39%) or 26-mm (34%) valve. The implant was technically successful in 754 (97.4%) patients. Serious adverse events were reported in 67 patients (10%), with no difference between RVOT anatomy groups. Fourteen patients underwent urgent surgery. Nine patients had a second valve implanted. Among patients with available data, tricuspid valve injury was documented in 11 (1.7%), and 9 others (1.3%) had new moderate or severe regurgitation 2 grades higher than pre-implantation, for 20 (3.0%) total patients with tricuspid valve complications. Valve function at discharge was excellent in most patients, but 58 (8.5%) had moderate or greater pulmonary regurgitation or maximum Doppler gradients >40 mm Hg. During limited follow-up (n = 349; median: 12 months), 9 patients were diagnosed with endocarditis, and 17 additional patients underwent surgical valve replacement or valve-in-valve TPVR. Conclusions: Acute outcomes after TPVR with balloon-expandable valves were generally excellent in all types of RVOT. Additional data and longer follow-up will be necessary to gain insight into these issues.
AB - Background: There are limited published data focused on outcomes of transcatheter pulmonary valve replacement (TPVR) with either a Sapien XT or Sapien 3 (S3) valve. Objectives: This study sought to report short-term outcomes in a large cohort of patients who underwent TPVR with either a Sapien XT or S3 valve. Methods: Data were entered retrospectively into a multicenter registry for patients who underwent attempted TPVR with a Sapien XT or S3 valve. Patient-related, procedural, and short-term outcomes data were characterized overall and according to type of right ventricular outflow tract (RVOT) anatomy. Results: Twenty-three centers enrolled a total of 774 patients: 397 (51%) with a native/patched RVOT; 183 (24%) with a conduit; and 194 (25%) with a bioprosthetic valve. The S3 was used in 78% of patients, and the XT was used in 22%, with most patients receiving a 29-mm (39%) or 26-mm (34%) valve. The implant was technically successful in 754 (97.4%) patients. Serious adverse events were reported in 67 patients (10%), with no difference between RVOT anatomy groups. Fourteen patients underwent urgent surgery. Nine patients had a second valve implanted. Among patients with available data, tricuspid valve injury was documented in 11 (1.7%), and 9 others (1.3%) had new moderate or severe regurgitation 2 grades higher than pre-implantation, for 20 (3.0%) total patients with tricuspid valve complications. Valve function at discharge was excellent in most patients, but 58 (8.5%) had moderate or greater pulmonary regurgitation or maximum Doppler gradients >40 mm Hg. During limited follow-up (n = 349; median: 12 months), 9 patients were diagnosed with endocarditis, and 17 additional patients underwent surgical valve replacement or valve-in-valve TPVR. Conclusions: Acute outcomes after TPVR with balloon-expandable valves were generally excellent in all types of RVOT. Additional data and longer follow-up will be necessary to gain insight into these issues.
KW - Sapien S3
KW - Sapien XT
KW - tetralogy of Fallot
UR - http://www.scopus.com/inward/record.url?scp=85097440248&partnerID=8YFLogxK
U2 - 10.1016/j.jacc.2020.10.041
DO - 10.1016/j.jacc.2020.10.041
M3 - Article
C2 - 33303074
AN - SCOPUS:85097440248
SN - 0735-1097
VL - 76
SP - 2847
EP - 2858
JO - Journal of the American College of Cardiology
JF - Journal of the American College of Cardiology
IS - 24
ER -