Long-Term Clinical and Echocardiographic Outcomes Following the Ross Procedure

Author:

Notenboom Maximiliaan L.1,Melina Giovanni2,Veen Kevin M.1,De Robertis Fabio3,Coppola Giuditta3,De Siena Paolo3,Navarra Emiliano M.2,Gaer Jullien3,Ibrahim Michael E. K.4,El-Hamamsy Ismail5,Takkenberg Johanna J. M.1,Yacoub Magdi H.67

Affiliation:

1. Department of Cardiothoracic Surgery, Erasmus University Medical Center, Rotterdam, the Netherlands

2. Department of Cardiac Surgery, Sant’Andrea Hospital, Sapienza University of Rome, Rome, Italy

3. Department of Cardiothoracic Surgery and Transplantation, Royal Brompton & Harefield Hospitals, Guy’s and St Thomas’ NHS Foundation Trust, London, United Kingdom

4. Division of Cardiovascular Surgery, University of Pennsylvania, Philadelphia

5. Department of Cardiovascular Surgery, The Mount Sinai Hospital, Icahn School of Medicine at Mount Sinai, New York, New York

6. National Heart and Lung Institute, Imperial College London, London, United Kingdom

7. Cardiac Surgery Department, Aswan Heart Centre, Magdi Yacoub Foundation, Aswan, Egypt

Abstract

ImportanceThe Ross procedure as treatment for adults with aortic valve disease (AVD) has been the subject of renewed interest.ObjectiveTo evaluate the long-term clinical and echocardiographic outcomes following the Ross procedure for the treatment of adults with AVD.Design, Setting, and ParticipantsThis post hoc analysis of a randomized clinical trial included adult patients (age <69 years) who underwent a Ross procedure for the treatment of AVD, including those with active endocarditis, rheumatic AVD, decreased ejection fraction, and previous cardiac surgery. The trial, conducted from September 1, 1994, to May 31, 2001, compared homograft root replacement with the Ross procedure at a single center. Data after 2010 were collected retrospectively in November and December 2022.ExposureRoss procedure.Main Outcomes and MeasuresThe primary end point was long-term survival among patients who underwent the Ross procedure compared with that in the age-, country of origin– and sex-matched general population. Secondary end points were freedom from any reintervention, autograft reintervention, or homograft reintervention and time-related valve function, autograft diameter, and functional status.ResultsThis study included 108 adults (92 [85%] male) with a median age of 38 years (range, 19-66 years). Median duration of clinical follow-up was 24.1 years (IQR, 22.6-26.1 years; 2488 patient-years), with 98% follow-up completeness. Of these patients, 9 (8%) had active endocarditis and 45 (42%) underwent reoperations. The main hemodynamic lesion was stenosis in 30 (28%) and regurgitation in 49 (45%). There was 1 perioperative death (0.9%). Twenty-five year survival was 83.0% (95% CI, 75.5%-91.2%), representing a relative survival of 99.1% (95% CI, 91.8%-100%) compared with the general population (83.7%). At 25 years, freedom from any reintervention was 71.1% (95% CI, 61.6%-82.0%); from autograft reintervention, 80.3% (95% CI, 71.9%-89.6%); and from homograft reintervention, 86.3% (95% CI, 79.0%-94.3%). Thirty-day mortality after the first Ross-related reintervention was 0% and after all Ross-related reinterventions was 3.8% (n = 1); 10-year survival after reoperation was 96.2% (95% CI, 89.0%-100%).Conclusions and RelevanceThis study found that the Ross procedure provided excellent survival into the third decade postoperatively that was comparable to that in the general population. Long-term freedom from reintervention demonstrated that the Ross procedure may be a durable substitute into late adulthood, showing a delayed but progressive functional decline.Trial Registrationisrctn.org Identifier: ISRCTN03530985

Publisher

American Medical Association (AMA)

Subject

Cardiology and Cardiovascular Medicine

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