Tricuspid Structural Valve Deterioration Treated with a Transcatheter Valve-in-Valve Implantation: A Single-Center Prospective Registry

被引:1
作者
Pravda, Nili Schamroth [1 ,2 ]
Assa, Hana Vaknin [1 ,2 ]
Levi, Amos [1 ,2 ]
Witberg, Guy [1 ,2 ]
Shapira, Yaron [1 ,2 ]
Vaturi, Mordechai [1 ,2 ]
Orvin, Katia [1 ,2 ]
Barkan, Yeela Talmor [1 ,2 ]
Hamdan, Ashraf [1 ,2 ]
Mishaev, Raffael [2 ]
Sharoni, Ram [2 ,3 ]
Perl, Leor [1 ,2 ]
Sagie, Alexander [1 ,2 ]
Kornowski, Ran [1 ,2 ]
Codner, Pablo [1 ,2 ]
机构
[1] Rabin Med Ctr, Dept Cardiol, IL-4941492 Petah Tiqwa, Israel
[2] Tel Aviv Univ, Fac Med, IL-6423906 Tel Aviv, Israel
[3] Rabin Med Ctr, Cardiothorac Surg Dept, IL-4941492 Petah Tiqwa, Israel
关键词
tricuspid valve; structural valve deterioration; valve-in-valve; transcatheter; outcomes; OUTCOMES; SURGERY;
D O I
10.3390/jcm11092667
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The valve-in-valve (ViV) technique is an emerging alternative for the treatment of bioprosthetic structural valve deterioration (SVD) in the tricuspid position. We report on the outcomes of patients treated by a transcatheter tricuspid valve-in-valve (TT-ViV) implantation for symptomatic SVD in the tricuspid position during the years 2010-2019 at our center. Three main outcomes were examined during the follow-up period: TT-ViV hemodynamic data per echocardiography, mortality and NYHA functional class. Our cohort consisted of 12 patients with a mean age 65.4 +/- 11.9 years, 83.3% male. The mean time from initial valve intervention to TT-ViV was 17.4 +/- 8.7 years. The indications for TT-ViV were varied (41.7% for predominant regurgitation, 33.3% for predominant stenosis and 25.0% with a mixed pathology). All patients were treated with a balloon-expandable device. The mean follow-up was 3.4 +/- 1.3 years. Tricuspid regurgitation was >= moderate in 57.2% of patients prior to the procedure and this decreased to 0% following the procedure. The mean transtricuspid valve gradients mildly decreased from the mean pre-procedural values of 9.0 mmHg to 7.0 mmHg at one month following the procedure (p = 0.36). Mortality at one year was 8.0% (95% CI 0-23). At the baseline, 4 patients (33.3%) were in NYHA functional class III/IV; this was reduced to 2 patients (18.2%) at the one year follow-up and both were in NYHA III. The TT-ViV procedure offered a safe, feasible and less invasive treatment option for patients with SVD in our detailed cohort.
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