Infective Endocarditis After Surgical and Transcatheter Aortic Valve Replacement: A State of the Art Review

Author:

Alexis Sophia L.1ORCID,Malik Aaqib H.2ORCID,George Isaac3ORCID,Hahn Rebecca T.4ORCID,Khalique Omar K.4,Seetharam Karthik5,Bhatt Deepak L.6ORCID,Tang Gilbert H. L.1ORCID

Affiliation:

1. Department of Cardiovascular Surgery Mount Sinai Medical Center New York NY

2. Department of Medicine Westchester Medical Center Valhalla NY

3. Division of Cardiac Surgery Columbia University Medical Center New York NY

4. Division of Cardiology Columbia University Medical Center New York NY

5. Icahn School of Medicine at Mount Sinai New York NY

6. Brigham and Women’s Hospital Heart & Vascular Center Harvard Medical School Boston MA

Abstract

Abstract Prosthetic valve endocarditis (PVE) after surgical aortic valve replacement and transcatheter aortic valve replacement (TAVR) carries significant morbidity/mortality. Our review aims to compare incidence, predisposing factors, microbiology, diagnosis, management, and outcomes of PVE in surgical aortic valve replacement/TAVR patients. We searched PubMed and Embase to identify published studies from January 1, 2015 to March 13, 2020. Key words were indexed for original reports, clinical studies, and reviews. Reports were evaluated by 2 authors against a priori inclusion/exclusion criteria. Studies were included if they reported incidence and outcomes related to surgical aortic valve replacement/TAVR PVE and excluded if they were published pre‐2015 or included a small population. We followed the Cochrane methodology and Preferred Reporting Items for Systematic Reviews and Meta‐Analyses guidelines for all stages of the design and implementation. Study quality was based on the Newcastle‐Ottawa Scale. Thirty‐three studies with 311 to 41 025 patients contained relevant information. The majority found no significant difference in incidence of surgical aortic valve replacement/TAVR PVE (reported as 0.3%–1.2% per patient‐year versus 0.6%–3.4%), but there were key differences in pathogenesis. TAVR has a specific set of infection risks related to entry site, procedure, and device, including nonstandardized protocols for infection control, valve crimping injury, paravalvular leak, neo‐leaflet stress, intact/calcified native leaflets, and intracardiac hardware. With the expansion of TAVR to lower risk and younger patients, a better understanding of pathogenesis, patient presentation, and guideline‐directed treatment is paramount. When operative intervention is necessary, mortality remains high at 20% to 30%. Unique TAVR infection risks present opportunities for PVE prevention, therefore, further investigation is imperative.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

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