Thirty-Day Outcome of Transcatheter Aortic Valve Implantation With the Edwards SAPIEN XT Prosthesis via the Transiliofemoral Approach : Japanese Single-Center Experience
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- Fuku Yasushi
- Department of Cardiology, Kurashiki Central Hospital
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- Goto Tsuyoshi
- Department of Cardiology, Kurashiki Central Hospital
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- Komiya Tatsuhiko
- Departments of Cardiovascular Surgery, Kurashiki Central Hospital
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- Sakaguchi Genichi
- Department of Cardiovascular Surgery, Shizuoka Prefectural General Hospital
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- Shimamoto Takeshi
- Departments of Cardiovascular Surgery, Kurashiki Central Hospital
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- Maruo Takeshi
- Department of Cardiology, Kurashiki Central Hospital
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- Hasegawa Daiji
- Department of Cardiology, Kurashiki Central Hospital
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- Otsuru Suguru
- Department of Cardiology, Kurashiki Central Hospital
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- Saito Naoki
- Department of Cardiology, Yokohama General Hospital
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- Hyodo Yusuke
- Department of Cardiology, Kurashiki Central Hospital
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- Ueno Go
- Departments of Cardiovascular Surgery, Kurashiki Central Hospital
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- Kadota Kazushige
- Department of Cardiology, Kurashiki Central Hospital
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- Mitsudo Kazuaki
- Department of Cardiology, Kurashiki Central Hospital
書誌事項
- タイトル別名
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- Thirty-Day Outcome of Transcatheter Aortic Valve Implantation With the Edwards SAPIEN XT Prosthesis via the Transiliofemoral Approach
- – Japanese Single-Center Experience –
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Background: Few data exist on the results of transcatheter aortic valve implantation (TAVI) via the transfemoral approach in small slightly built Japanese patients with severe aortic stenosis who are ineligible or at high-risk for conventional surgical aortic valve replacement (SAVR). Therefore, the purpose was to investigate the early outcomes of TAVI using the transiliofemoral approach in Japan. Methods and Results: Between June 2010 and June 2013, 21 consecutive patients (mean age, 81.0 years; 81.0% female) underwent TAVI with Edwards SAPIEN XT valves using the transiliofemoral approach. The mean body surface area was 1.44±0.15m2. The device success rate was 90.5%. Although 2 patients did not meet the echocardiographic criteria for device success, no failure to deliver and deploy a valve occurred. The mean effective aortic valve area increased from 0.54±0.12cm2 at baseline to 1.46±0.29cm2 after the procedure (P<0.001), and the mean aortic transvalvular pressure gradient decreased from 51.0±15.6 at baseline to 11.2±3.6 after the procedure (P<0.001). The 30-day mortality and combined safety endpoint rates were 0% and 4.8%, respectively. All patients achieved New York Heart Association functional class I or II at 30 days. Conclusions: Early outcome of TAVI with the Edwards-SAPIEN XT valve via the transiliofemoral approach at Kurashiki Central Hospital is satisfactory for patients who are ineligible or at high risk for SAVR. (Circ J 2014; 78: 1357–1363)<br>
収録刊行物
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- Circulation Journal
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Circulation Journal 78 (6), 1357-1363, 2014
一般社団法人 日本循環器学会
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詳細情報 詳細情報について
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- CRID
- 1390282680084385792
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- NII論文ID
- 130003391113
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- NII書誌ID
- AA11591968
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- COI
- 1:STN:280:DC%2BC2crpvFChsg%3D%3D
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- ISSN
- 13474820
- 13469843
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- NDL書誌ID
- 025461973
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- PubMed
- 24694765
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- 本文言語コード
- en
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- データソース種別
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- JaLC
- NDL
- Crossref
- PubMed
- CiNii Articles
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- 使用不可