Key result
Transapical mitral valve repair using the Mitralstitch system was safe and feasible, with 100% of patients (10/10) achieving safety and efficacy endpoints at 1-month follow-up.
Why the study?
Conventional mitral valve repair surgery requires cardiopulmonary bypass and carries significant morbidity and risks, whereas transapical beating-heart mitral valve repair using artificial chordae implantation could reduce surgical morbidity.
Does transapical artificial chordae implantation using the Mitralstitch system safely reduce mitral regurgitation in patients with severe degenerative MR?
Does transapical artificial chordae implantation using the Mitralstitch system safely reduce mitral regurgitation in patients with severe degenerative MR?
This first-in-human study demonstrates the initial safety and feasibility of the Mitralstitch system for transapical beating-heart mitral valve repair in patients with severe degenerative mitral regurgitation.
Transapical beating-heart chordal repair may reduce morbidity in degenerative MR; leaves open safety and durability pending prospective trials.
Background Severe mitral regurgitation (MR) is associated with progressive heart failure and impairment of survival. Degenerative MR accounts for most MV repair surgeries. Conventional mitral valve repair surgery requires cardiopulmonary bypass and is associated with significant morbidity and risks. Transapical beating‐heart mitral valve repair by artificial chordae implantation with transesophageal echocardiography (TEE) guidance has the potential to significantly reduce surgical morbidity. We report the first‐in‐human experience of degenerative MR repair using a novel artificial chordae implantation device (Mitralstitch TM system). Methods Ten patients with severe MR underwent transapical artificial chordae implantation using MitralstitchTM system. The procedure was performed through a small left thoracotomy under general anesthesia and TEE guidance. Patients underwent transthoracic echocardiography and other assessments during the follow‐up. Results All 10 patients with an average age of 63.7 ± 9.6 years successfully received transapical artificial chordae implantation. Their MR reduced from severe to none or trace in five patients, mild in five patients before discharge. Five patients received one artificial chordal implantation, four patients received two, and one patient received three and edge‐to‐edge repair by locking two of them. The safety and efficacy endpoint were achieved in all patients at 1‐month follow‐up. At 1‐year follow‐up, six patients had mild MR, three patients had moderate MR, one patient had recurrence of severe MR and underwent surgical repair. Conclusions The results of this first‐in‐human study show safety and feasibility of transapical mitral valve repair using MitralStitch system. Patient selection and technical refinement are crucial to improve the outcomes.
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Wang et al. (2022) studied Severe mitral regurgitation (n=10). Transapical artificial chordae implantation (Mitralstitch system) was evaluated on Safety and efficacy at 1-month follow-up. Transapical mitral valve repair using the Mitralstitch system was safe and feasible, with 100% of patients (10/10) achieving safety and efficacy endpoints at 1-month follow-up.
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