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Impact of patient-prosthesis mismatch after transcatheter aortic valve-in-valve implantation in degenerated bioprostheses
被引:49
|作者:
Seiffert, Moritz
[1
]
Conradi, Lenard
[1
]
Baldus, Stephan
[2
]
Knap, Malgorzata
[2
]
Schirmer, Johannes
[1
]
Franzen, Olaf
[2
]
Koschyk, Dietmar
[2
]
Meinertz, Thomas
[2
]
Reichenspurner, Hermann
[1
]
Treede, Hendrik
[1
]
机构:
[1] Univ Heart Ctr Hamburg, Dept Cardiovasc Surg, D-20246 Hamburg, Germany
[2] Univ Heart Ctr Hamburg, Dept Gen & Intervent Cardiol, D-20246 Hamburg, Germany
来源:
关键词:
LONG-TERM SURVIVAL;
D O I:
10.1016/j.jtcvs.2011.11.004
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Objective: Transcatheter valve-in-valve implantation is evolving as an alternative to reoperative valve replacement in high-risk patients with degenerated bioprostheses. Nevertheless, hemodynamic performance is limited by the previously implanted xenograft. We report our experience with patient-prosthesis mismatch (PPM) after valve-in-valve implantation in the aortic position. Methods: Eleven patients (aged 79.3 +/- 6.1 years) received transapical implantation of a balloon-expandable pericardial heart valve into a degenerated bioprosthesis (size, 23.9 +/- 1.6 mm; range, 21-27 mm) in the aortic position. All patients were considered high risk for surgical valve replacement (logistic European System for Cardiac Operative Risk Evaluation, 31.8% +/- 24.1%). Severe PPM was defined as an indexed effective orifice area less than 0.65 cm(2)/m(2), determined by discharge echocardiography. Results: Severe PPM was evident in 5 patients (group 1) and absent in 6 patients (group 2). Mean transvalvular gradients decreased from 29.2 +/- 15.4 mm Hg before implantation to 21.2 +/- 9.7 mm Hg at discharge (group 1) and from 28.2 +/- 9.0 mm Hg before implantation to 15.2 +/- 6.5 mm Hg at discharge (group 2). Indexed effective orifice area increased from 0.5 +/- 0.1 cm(2)/m(2) to 0.6 +/- 0.1 cm(2)/m(2) and from 0.6 +/- 0.3 cm(2)/m(2) to 0.8 +/- 0.3 cm(2)/m(2). Aortic regurgitation decreased from grade 2.0 +/- 1.1 to 0.4 +/- 0.5 overall. No differences in New York Heart Association class improvement or survival during follow-up were observed. One patient required reoperation for symptomatic PPM 426 days after implantation. Conclusions: Valve-in-valve implantation can be performed in high-risk surgical patients to avoid reoperation. However, PPM frequently occurs, making adequate patient selection crucial. Small bioprostheses (<23 mm) should be avoided. Implantation into 23-mm xenografts can be recommended only for patients with a body surface area less than 1.8 m(2). Larger prostheses seem to carry a lower risk for PPM. Although no delay in clinical improvement was seen at short-term, 1 PPM-related surgical intervention raises concern regarding long-term performance. (J Thorac Cardiovasc Surg 2012;143:617-24)
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页码:617 / 624
页数:8
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