Feasibility of intentional bioprosthetic valve fracture in the tricuspid position

医学 三尖瓣 心脏病学 职位(财务) 断裂(地质) 内科学 财务 工程类 经济 岩土工程
作者
Jonathon A. Hagel,Chiao‐Yun Lin,Athar M. Qureshi,Daniel Tanase,Andreas Eicken,Jeffrey D. Zampi,Allison K. Cabalka,Jason H. Anderson,Shabana Shahanavaz
出处
期刊:Catheterization and Cardiovascular Interventions [Wiley]
卷期号:104 (3): 523-530
标识
DOI:10.1002/ccd.31168
摘要

Abstract Background Transcatheter 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. Aims Evaluate the feasibility of transcatheter tricuspid ViV replacement with fracture of the underlying BPV ring. Methods An 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. Results Ten 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. Conclusion Intentional 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.

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