Transseptal or Transapical Transcatheter Valve-in-Valve Implantation Versus Redo Surgical Replacement for Degenerated Mitral Bioprostheses
Gomes Nicz, P. F.; Marchi, M. F. d. S.; Barbosa Ribeiro, H.; Machado, F. C.; Sampaio, R. O.; Palma da Fonseca, J. H. d. A.; De Arruda, J. a.; Falcao, C. H. E.; Prudente, M. L.; Vahle, V. d. A.; Okino, A. A.; de Oliveira, M. A. P.; Deininger, M. O.; Portela, A. L. F.; Cristovao, S. A. B.; Bernardes, R. d. C.; Falcao, B. d. A. A.; de Campos Martins, E. C.; de Sao Thiago, L. E. K.; Dourado Oliveira, A. D.; Souza, F. S. d. F.; Pessoa de Melo, E. F.; Botelho da Silva, A. C.; de Paula, J. E. T.; Filho, E. M.; Mandil, A.; Viana, M. S.; Sarmento-Leite, R.; Gomes, W. F.; Bezerra, C. G.; de Souza, A. J.
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BackgroundBioprosthetic mitral valve degeneration can be problematic as redo surgical mitral valve replacement (Redo-SMVR) is associated with a high morbidity and mortality. Valve-in-valve transcatheter mitral valve replacement (TMVR) has emerged as an alternative for high-risk patients, but comparative data is lacking. ObjectivesWe aimed to evaluate the outcomes of Redo-SMVR vs. TMVR, using either transapical (TA) or transseptal (TS) approach. Methods and ResultsA total of 415 patients (69% rheumatic) were included between January 2014 to May 2023 (Redo-SMVR=239; TA-TMVR=84; TS-TMVR=92). Patients in the Redo-SMVR group were younger (51.7{+/-}12.3, 64.3{+/-}10.5, 73.7{+/-}10.9, respectively for Redo, TA and TS; p<0.001) with a lower median STS score (2.9 [1.7 - 5.1], 6.6 [3.9-10.5], 6.5 [4.2-10.0]; p<0.001). 30-day mortality was significantly higher for both Redo-SMVR and TA-TMVR vs. TS-TMVR (14.2%, 15.5%, 4.3%; p=0.030) and procedural success was lower (52.5%, 64.9%, 88%; p<0.001). There was no difference in terms of 1-year mortality rate across the groups (Log-rank p=0.222). Reduced preprocedural left ventricular ejection fraction, higher right ventricular systolic pressure (RVSP), and the presence of coronary artery disease were independently associated with 30-day mortality, while transseptal approach was protective. At 1-year follow-up, the predictors of mortality remained consistent, with significant tricuspid regurgitation replacing RVSP (all with p<0.05). ConclusionsIn high-risk patients with dysfunctional mitral bioprosthesis and most with rheumatic etiology, TS-TMVR was associated with higher procedural success and better short-term outcomes, including all-cause mortality, despite higher risk characteristics. In the mid-term follow-up, there were no significant differences in mortality across the groups.
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