Feasibility of intentional bioprosthetic valve fracture in the tricuspid position

Author:

Hagel Jonathon A.12ORCID,Lin C. Huie3,Qureshi Athar M.4ORCID,Tanase Daniel5ORCID,Eicken Andreas5,Zampi Jeffrey D.2ORCID,Cabalka Allison K.6ORCID,Anderson Jason6ORCID,Shahanavaz Shabana1

Affiliation:

1. The Heart Institute, Cincinnati Children's Hospital University of Cincinnati Cincinnati Ohio USA

2. University of Michigan, C.S. Mott Children's Hospital Ann Arbor Michigan USA

3. Houston Methodist DeBakey Heart and Vascular Center Houston Texas USA

4. Lillie Frank Abercrombie Section of Cardiology Texas Children's Hospital, Baylor College of Medicine Houston Texas USA

5. Department of Pediatric Cardiology and Congenital Heart Defects Deutsches Herzzentrum München, DHM Munich Germany

6. Mayo Clinic College of Medicine, Department of Pediatrics Division of Structural Heart Disease Rochester Now York USA

Abstract

AbstractBackgroundTranscatheter tricuspid valve‐in‐valve (ViV) replacement has yielded good hemodynamic outcomes in the treatment of dysfunctional bioprosthetic valves (BPVs). Intentional fracture of certain rigid BPV frames, if feasible, allows a larger implanted valve when compared with implant into an unfractured BPV. There remains limited data on the feasibility of tricuspid valve frame fracture.AimsEvaluate the feasibility of transcatheter tricuspid ViV replacement with fracture of the underlying BPV ring.MethodsAn international multicenter registry of tricuspid ViV replacement with intentional tricuspid valve frame fracture was created. Demographic data along with procedural characteristics, outcomes, and follow‐up data were collected. Comparison was made to the pre‐ and post‐ViV replacement with fracture of the tricuspid valve frame conditions.ResultsTen patients from six centers were included with a median age and weight of 29 years and 67.3 kg respectively. Tricuspid valve frame fracture was performed using a median balloon diameter 3 mm (IQR 3–5) larger than the true inner diameter (ID). The final ID was a mean of 1.5 mm (95% CI: 0.35, 2.64: p < 0.05), and median 1.1 mm (0.5, 2.1) larger than the reported true ID of the surgical BPV after ViV replacement. The mean tricuspid inflow gradient by echocardiogram decreased by 6.65 mmHg (95% CI: 4.14, 9.15: p < 0.001). All procedures were without complication, specifically there was no heart block, pericardial effusion, or right coronary disruption.ConclusionIntentional tricuspid valve frame fracture with tricuspid ViV replacement is feasible and can increase the valve orifice potentially reducing the risk of ViV patient prosthesis mismatch and is not associated with significant complications.

Publisher

Wiley

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