# A novel transcatheter tricuspid annuloplasty for severe tricuspid valve regurgitation via the K-clip™ system: early experience in China

**Authors:** Rongfeng Xu, Lijuan Chen, Xiaoli Zhang, Xiuxia Ding, Zhen Wang, Qitong Lu, Xiaoguo Zhang, Jiandong Ding, Genshan Ma

PMC · DOI: 10.3389/fcvm.2025.1598644 · Frontiers in Cardiovascular Medicine · 2025-10-01

## TL;DR

This study shows that the K-Clip™ system is a safe and effective new method for treating severe tricuspid valve regurgitation in high-risk patients.

## Contribution

The paper presents the first early clinical experience of the K-Clip™ system in China for transcatheter tricuspid repair.

## Key findings

- The K-Clip™ device was successfully implanted in all four patients with no major adverse events.
- Significant reductions in tricuspid regurgitation and improvements in quality of life were observed at 30 days.
- The procedure showed high success and safety, but larger trials are needed for long-term validation.

## Abstract

Patients who suffer from severe tricuspid regurgitation (TR) do not undergo standard care therapy because of the high surgical risk. As a result, safer and less invasive techniques are being sought after internationally. The objective of this study was to investigate the feasibility and safety of the K-Clip™ device, a novel interventional tricuspid annuloplasty system designed for transcatheter tricuspid repair that is positioned using ultrasound technology and fluoroscopy.

Four patients with severe symptomatic TR (3 with massive and 1 with torrential TR) and high surgical risk [STS score of 6.7 (5.6–11.1)] underwent tricuspid annular repair with the K-Clip™ device guided by echocardiography and fluoroscopy. Echocardiographic measurements [vena contracta width, regurgitant volume, effective regurgitant orifice area (EROA)], quality-of-life (QoL) measurements [NYHA functional class, Kansas City Cardiomyopathy Questionnaire score (KCCQ), and the 6-min walk test (6MWT)] were performed before the procedure and at the 30-day follow-up assessment.

The K-Clip™ device was successfully implanted in all four patients (2 patients with 2 clips each and 2 patients with 1 clip each). No procedural or 30-day major adverse events occurred. The TR was reduced by at least 1 grade in all patients. EROA (0.93 ± 0.40 mm2 VS 0.42 ± 0.11 mm2, p < 0.05), vena contracta width (17.95 ± 8.19 mm VS 7.48 ± 1.87 mm, p < 0.05) and regurgitant volume (97.00 ± 46.41 ml VS 43.50 ± 17.13 ml, p < 0.05) were obviously reduced at 30 days after the procedure. Significant improvements in the NYHA functional class, KCCQ score (37.58 ± 6.48 VS 58.55 ± 5.13, p < 0.01), and 6MWT (239.67 ± 31.64 m VS 402.67 ± 41.53 m, p < 0.05) outcome were observed at the 30-day follow-up visit.

This report on the early experience of transcatheter tricuspid repair with the K-Clip™ in China revealed notable clinical improvement, acceptable safety, and high procedural success. Larger prospective trials with extended follow-up periods are required to validate these encouraging preliminary findings and to clarify the effects of the K-Clip™ on clinical outcomes.

## Linked entities

- **Diseases:** tricuspid valve regurgitation (MONDO:0002870)

## Full-text entities

- **Diseases:** TR (MESH:D014262), Cardiomyopathy (MESH:D009202)
- **Chemicals:** K-Clip (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

31 references — full list in the complete paper: https://tomesphere.com/paper/PMC12521137/full.md

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Source: https://tomesphere.com/paper/PMC12521137