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Contemporary suprasternal transcatheter aortic valve replacement: A multicenter experience using a simple, reliable alternative access approach
Author(s) -
Eudailey Kyle W.,
Olds Anna,
Lewis Clifton T.,
Nazif Tamim N.,
Vahl Torsten,
Khalique Omar K.,
Hahn Rebecca T.,
Bapat Vinayak,
Borger Michael A.,
Leon Martin B.,
Ahmed Mustafa I.,
Kodali Susheel,
George Isaac
Publication year - 2020
Publication title -
catheterization and cardiovascular interventions
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.988
H-Index - 116
eISSN - 1522-726X
pISSN - 1522-1946
DOI - 10.1002/ccd.28460
Subject(s) - medicine , valve replacement , single center , aortic valve , surgery , cohort , cardiology , stenosis
Objectives To describe outcomes after suprasternal (SS) transcatheter aortic valve replacement (TAVR) as a new alternative access approach. Background There still remains a cohort of the TAVR population who are not suitable for a transfemoral (TF) approach. SS‐TAVR is a safe and effective alternative to TF‐TAVR and has now become our preferred alternative access route. Methods We retrospectively reviewed all patients from New York Presbyterian Hospital, Columbia University Medical Center and Princeton Baptist Medical Center who underwent SS‐TAVR from 2015 to July 2018. A total of 84 patients were included in the study. Results Technical success was achieved in all cases. Thirty‐day survival was 98.8% ( n = 83). There were minimal complications. Most notably, there were no transient ischemic attacks or strokes (0%, n = 0). Reexploration for bleeding was 3.6% ( n = 3), and major bleeding was 1.7% ( n = 1). We also achieved satisfactory results with a mean aortic valve gradient of 6.07 ± 3.79 mmHg and an aortic valve area of 2.21 ± 0.51 cm 2 . No patients had anything more than mild paravalvular leak. The mean length of stay (LOS) in the intensive care unit was 1.42 ± 1.23 days, and hospital LOS was 4.20 ± 3.29 days. Conclusions SS access for TAVR is an extremely important technique to have in any valve team's alternative access armamentarium. This technique can be safely and reliably reproduced with any standard hybrid operating room setup and no additional equipment, and it can be used with any commercially available valve system. In the current experience, minimal complications and excellent early term results were obtained.