valve

The largest series with LOTUS Valve published so far

This work represents the UK experience with the second generation repositionable and retrievable valve Lotus (Boston Scientific, Natick, Massachusetts). &nbsp; It prospectively included 228 patients of mean age 81.4 ± 7.6 and a logistic EuroScore of 17.5 ± 12.4. &nbsp; From the total number of patients, 187 (82%) received the valve for aortic stenosis, 7<a href="https://solaci.org/en/2016/03/08/the-largest-series-with-lotus-valve-published-so-far/" title="Read more" >...</a>

One year outcomes of the new repositionable and retrievable valve

Original Title: 1-Year Outcomes with the Fully Repositionable and Retrievable Lotus Transcatheter Aortic Replacement Valve in 120 High-Risk Surgical Patients with Severe Aortic Stenosis Results of the REPRISE II Study. Reference: Ian T. Meredith et al. J Am Coll Cardiol Intv. 2016;9(4):376-384. &nbsp; This analysis represents the first report at one year of 120 patients enrolled<a href="https://solaci.org/en/2016/02/23/one-year-outcomes-of-the-new-repositionable-and-retrievable-valve/" title="Read more" >...</a>

Prótese Edwards Sapien XT e Medtronic Corevalve demonstram desempenho equivalente em 1 ano, em pacientes de alto risco submetidos a TAVI

Fundamentos: Existem poucos dados comparando diferentes pr&oacute;teses valvares (THV) utilizadas nos implantes percut&acirc;neos de valva a&oacute;rtica (TAVI), sendo que as pr&oacute;teses bal&atilde;o expans&iacute;veis parecem apresentar melhores resultados em rela&ccedil;&atilde;o &agrave;s bal&atilde;o-expans&iacute;veis. O objetivo do estudo foi comparar a performance hemodin&acirc;mica entre as pr&oacute;teses a&oacute;rticas Edwards Sapien XT (bal&atilde;o-expans&iacute;vel) e Medtronic CoreValve (auto-expans&iacute;vel) em pacientes de<a href="https://solaci.org/en/2015/06/24/protese-edwards-sapien-xt-e-medtronic-corevalve-demonstram-desempenho-equivalente-em-1-ano-em-pacientes-de-alto-risco-submetidos-a-tavi-2/" title="Read more" >...</a>

CoreValve Evolut R CE: Good results at 6 months of the new CoreValve repositionable

This study evaluated the safety and efficacy of the new repositionable self-expanding valve. The primary end point was all-cause mortality and stroke at 30 days. 60 patients were included and the possibility for reposition was used 22 times between 12 recaptures and 10 re-sheathed of the valve. All maneuvers were carried out successfully. A 30<a href="https://solaci.org/en/2015/06/24/corevalve-evolut-r-ce-good-results-at-6-months-of-the-new-corevalve-repositionable/" title="Read more" >...</a>

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