Transcatheter Treatment of Degenerated Bioprosthetic Valves: Patients Characteristics, Procedural Details and Outcomes - A Multicenter Israeli Registry

Uri Landes 1 Amit Segev 2 Israel Barbash 2 Yaron Almagor 3 Haim Danenberg 4 Ronen Jaffe 5 Ram Sharony 6 Katia Orvin 1 Amos Levi 1 Abid Assali 1 Hana Vaknin-Assa 1 Nader Khader 5 Ashraf Hamdan 1 Yaron Shapira 1 Ehud Raanani 2 Alexander Sagie 1 Victor Guetta 2 Ran Kornowski 1
1Department of Cardiology, Rabin Medical Center, Petach Tikva and Sackler Faculty of Medicine, Tel Aviv University
2Leviev Heart Center, Sheba Medical Center
3Department of Cardiology, Shaare Zedek Medical Center
4Department of Cardiology, Hadassah Medical Center
5Department of Cardiology, Carmel Medical Center
6Department of Cardiothoracic Surgery, Rabin Medical Center, Petach Tikva and Sackler Faculty of Medicine, Tel Aviv University

Background:
Transcatheter Valve-in-Valve implantation (ViV) is a less invasive approach to treat patients with bioprosthetic valve deterioration at high risk for redo-surgery. This is the largest registry reporting on ViV experience in Israel.

Methods:
A datasheet was circulated to multiple Israeli centers involved in ViV. Data from participating centers were collected, analyzed and reported in-line with VARC-2 recommendations.

Results:
Between March-2010 and Nov-2016, along with a linear growth in procedural volume, a total of 132 patients underwent ViV in the 5 partaking centers: age 77 [SD, 13] years; 38% men; median Society-of-Thoracic-Surgeons (STS) score 6.1 [IQR, 4.1; 10.4] %. Throughout the years there was a shift to treat patients at lower STS-score (9.7% to 7.1%, p<0.01). Follow-up continued up-to 6.5 years [median 2.5 (IQR, 1.1; 3.8) years]. Procedures were performed in the aortic (70%) [mean age 77±12 years, STS-score: 7.8±5.4%], mitral (23%) [mean age 76±12 years, STS-score: 9.5±6.5%], tricuspid (5%) [mean age 69±5.9 years, STS-score: 3.8±1.2%], and combined (2%) positions. Aortic-VIV were performed via the trans-femoral, trans-apical and trans-axillary routes in 92.5%, 2.5% and 5%; respectively, and using self-expandable (94%) or balloon-expandable (6%) devices. Mitral-VIV were performed via the trans-apical route (97.5%) and using balloon-expandable (SXT, 93.5%; S3, 6.5%) devices. The composite end-point of device success rate was 97%, and 30-days stroke rate was 0.9%. Baseline NYHA functional-class was III/IV in most (87%) patients, enhanced to I/II in the majority (91%, at 1-month), and kept well stable in long-term follow-up. Survival rates for all-VIV patients was: 94.5% (30-days), 92%% (1-year), and 75% (3-years).

Conclusions:
The ViV intervention in 5 Israeli TAVI centers is being used to treat a wide range of degenerated surgical valves in different positions. It is safe, effective and expanding. The implications on surgical vs. ViV strategy as optimal management of patients at lower-risk needs further investigation.

Uri Landes
Uri Landes
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