4.6 Article

Transcatheter Aortic Valve Replacement for the Treatment of Pure Native Aortic Valve Regurgitation A Systematic Review

Journal

JACC-CARDIOVASCULAR INTERVENTIONS
Volume 9, Issue 22, Pages 2308-2317

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.jcin.2016.08.049

Keywords

meta-analysis; pure native aortic regurgitation; systematic review; transcatheter aortic valve replacement

Funding

  1. Veronesi Foundation
  2. Abbott
  3. Biotronik
  4. Boston Scientific
  5. Edwards Lifesciences
  6. Medtronic
  7. Medicines Company
  8. St. Jude Medical
  9. AstraZeneca
  10. Eli Lilly
  11. Abbott Vascular
  12. Bayer
  13. Biosensors

Ask authors/readers for more resources

OBJECTIVES This study sought to summarize available evidence on transcatheter aortic valve replacement (TAVR) for the treatment of native pure aortic regurgitation (AR). BACKGROUND Surgical aortic valve replacement (SAVR) is the gold standard for the treatment of AR. However, case series of high-risk patients undergoing TAVR for native pure AR were reported. METHODS We systematically searched Medline, Embase, and Scopus for reports of at least 5 patients with native pure AR undergoing TAVR. Patients' and procedural characteristics were summarized. The primary outcome of interest was all-cause mortality. Pooled estimates were calculated using a random-effects meta-analysis. The study protocol was registered in PROSPERO (CRD42016038422). RESULTS Thirteen reports including 237 patients were included in the analysis. Self-expandable prostheses were used in 79% of patients, whereas 21% of the patients were treated with a balloon-expandable valve. Device success ranged between 74% and 100%. Seventeen patients (7%) required the implantation of a second valve. Conversion to SAVR was reported in 6 (2.5%) cases. The rate of all-cause mortality at 30 days amounted to 7% (95% confidence interval [CI]: 3% to 13%; I-2 = 37%). Cerebrovascular events were rare (0%, 95% CI: 0% to 1%; I-2 = 0); major bleeding and vascular complications occurred in 2% (95% CI: 0% to 7%; I-2 = 41%), and 3% (95% CI: 1% to 7%; I-2 = 0%), respectively. Permanent pacemaker implantation was required in 11% of patients (95% CI: 5% to 19%; I-2 = 50%). The rate of moderate or severe post-procedural AR amounted to 9% (95% CI: 0% to 28%; I-2 = 90%). CONCLUSIONS Among selected patients with native pure AR deemed at high risk for SAVR, TAVR is technically feasible and associated with an acceptable risk of early mortality. (C) 2016 by the American College of Cardiology Foundation.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available