{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,12,2]],"date-time":"2025-12-02T15:21:58Z","timestamp":1764688918643},"reference-count":39,"publisher":"Wiley","issue":"4","license":[{"start":{"date-parts":[[2013,5,25]],"date-time":"2013-05-25T00:00:00Z","timestamp":1369440000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Cathet Cardio Intervent"],"published-print":{"date-parts":[[2013,10]]},"abstract":"<jats:sec><jats:title>Objectives<\/jats:title><jats:p>To summarize our single Institution experience with staged total percutaneous management of aorto\u2010mitral pathology.<\/jats:p><\/jats:sec><jats:sec><jats:title>Background<\/jats:title><jats:p>Percutaneous treatment of aortic valve stenosis (AVS) and mitral valve regurgitation (MVR) has been recently proposed for patients at high surgical risk.<\/jats:p><\/jats:sec><jats:sec><jats:title>Methods<\/jats:title><jats:p>Data concerning consecutive patients undergoing percutaneous transcatheter AV implantation (TAVI) followed by MV repair with MitraClip\u00ae were prospectively collected and analyzed.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>From January 2010 to February 2012 a total of 254 patients were referred to undergo TAVI in our Institution. Seventeen (6.7%) had preoperative severe MVR that remained unchanged after TAVI. Due to exacerbation of symptoms 12 patients were subsequently submitted to MV repair with the MitraClip\u00ae device. Mean age was 79 years (72\u201386 years), median Ambler score was 30.1 (17.2\u201342.6) and EuroSCORE 22.3 (10.2\u201348.6). Procedural success rate was 100%. Postprocedural hospitalization was 7.1\u2009\u00b1\u20092.7 and 4.6\u2009\u00b1\u20090.9 days after TAVI and MV repair, respectively. Six months follow\u2010up echocardiography confirms improvement in LV\u2010EF (37.2\u2009\u00b1\u20099.9 vs. 43.5\u2009\u00b1\u200910.7, <jats:italic>P<\/jats:italic>\u2009&lt;\u20090.0001). No patient presents MVR exceeding grade I<jats:sup>+<\/jats:sup> or prosthetic aortic insufficiency\u2009&gt;\u2009I grade and all patients experienced an improvement in functional status.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusions<\/jats:title><jats:p>Percutaneous treatment of AVS and MVR is feasible and safe. A tailored approach should be considered to treat firstly the AVS and subsequently the MVR when severe MV dysfunction and symptoms persist. Short\u2010term durability of this combined percutaneous approach seems encouraging and justifies the economical burden to treat patients that have no other option. \u00a9 2013 Wiley Periodicals, Inc.<\/jats:p><\/jats:sec>","DOI":"10.1002\/ccd.24809","type":"journal-article","created":{"date-parts":[[2013,1,29]],"date-time":"2013-01-29T14:27:00Z","timestamp":1359469620000},"source":"Crossref","is-referenced-by-count":18,"title":["Staged total percutaneous treatment of aortic valve pathology and mitral regurgitation: Institutional experience"],"prefix":"10.1002","volume":"82","author":[{"given":"Stephan","family":"Kische","sequence":"first","affiliation":[{"name":"Medical Faculty, Department of Cardiology at University Hospital Rostock, Ernst-Heydemann-Str. 6 18057 Rostock Germany"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Giuseppe","family":"D'Ancona","sequence":"additional","affiliation":[{"name":"Medical Faculty, Department of Cardiology at University Hospital 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