Clinical outcomes after implantation of a sutureless aortic bioprosthesis with concomitant mitral valve surgery: the SURE-AVR registry

Author:

Baghai MaxORCID, ,Glauber Mattia,Fontaine Raphael,Castillo Jose Cuenca,Walker Antony H.,Livi Ugolino,Montiel José,Royse Alistair,Bisleri Gianluigi,Pacini Davide,Argano Vincenzo,Roumy Aurelien,Asimakopoulos George,Solinas Marco

Abstract

Abstract Background Early treatment of aortic valve stenosis is recommended in eligible symptomatic patients with severe aortic valve stenosis who would otherwise have a poor prognosis. The sutureless aortic valve bioprosthesis offers an alternative to standard aortic valve replacement with a sutured valve, but limited data are available in patients who have undergone multiple valve procedures involving the new, sutureless technology. We sought to investigate outcomes in high operative risk patients with previous or concomitant valve surgery who were implanted with a sutureless valve. Methods SURE-AVR is an ongoing, prospective, multinational registry of patients undergoing aortic valve replacement. In-hospital and post-discharge outcomes up to 5 years were collected. Results The study population comprised 78 patients (mean ± SD: age 73.6 ± 7.6 years, logistic EuroSCORE 18.0 ± 17.5) enrolled at 13 sites who presented for concomitant or previous mitral valve repair (n = 45) or replacement (n = 33), with or without additional concomitant procedures, and were implanted with a sutureless valve. Mean ± SD overall aortic cross-clamp time was 109 ± 41 min and cardiopulmonary bypass time was 152 ± 49 min. Mean ± SD aortic pressure gradients decreased from 37.6 ± 17.7 mmHg preoperatively to 13.0 ± 5.7 mmHg at hospital discharge, and peak aortic pressure gradient from 61.5 ± 28.7 to 23.4 ± 10.6 mmHg. Early events included 1 death, 1 transient ischaemic attack, and 1 bleed (all 1.3%); a permanent pacemaker implantation was required in 6 patients (7.7%), and 2 reoperations (not valve related) (2.6%) took place. Over a median follow-up of 55.5 months (Q1 13.4, Q3 68.6), 12 patients died (6 cardiovascular and 6 non-cardiovascular, both 2.1% per patient-year). Five-year survival was 81.3%. Late paravalvular leak occurred in 2 patients (0.7% per patient-year) and permanent pacemaker implantation was required in 3 patients (0.1% per patient-year). There was no apparent rise in mean or peak aortic pressure gradient over the study. Conclusions These results suggest that the sutureless implant is a technically feasible procedure during mitral surgery and is associated with good clinical outcomes.

Funder

LivaNova

Publisher

Springer Science and Business Media LLC

Subject

Cardiology and Cardiovascular Medicine,General Medicine,Surgery,Pulmonary and Respiratory Medicine

Cited by 6 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Sutureless Valves, a “Wireless” Option for Patients With Aortic Valve Disease;Journal of the American College of Cardiology;2024-07

2. The Perceval Sutureless Bioprosthetic Aortic Valve: Evolution of Surgical Valve Technology;Innovations: Technology and Techniques in Cardiothoracic and Vascular Surgery;2024-03

3. The 10 Commandments of Perceval Implantation;Innovations: Technology and Techniques in Cardiothoracic and Vascular Surgery;2023-07

4. The 7 Pillars for Perceval Implantation With Mitral Valve Repair or Replacement;Innovations: Technology and Techniques in Cardiothoracic and Vascular Surgery;2023-07

5. Perceval valve intermediate outcomes: a systematic review and meta-analysis at 5-year follow-up;Journal of Cardiothoracic Surgery;2023-04-11

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