Rationale and design of the ELEANOR trial early aortic valve surgery versus watchful waiting strategy in severe asymptomatic aortic regurgitation, ACRONYM: ELEANOR
Radka Kočková,
Jan Vojáček,
Helena Bedáňová,
Petr Fila,
Ivo Skalský,
Daniela Žáková,
Michal Klán,
Barbora Míková,
Karel Mědílek,
Martin Tuna,
Monika Fialová,
Radka Dvořáková,
Zuzana Hlubocká,
Roman Panovský,
Kryštof Slabý,
Elayne Kelen de Oliveira,
Filip Casselman,
Martin Pěnička
Affiliations
Radka Kočková
Na Homolce Hospital, Prague, Czech Republic; Charles University, Faculty of Medicine in Hradec Králové, Hradec Králové, Czech Republic; Corresponding author. Center for Congenital Heart Disease in Adults, Na Homolce Hospital, Cardiothoracic Surgery Department, Roentgenova 37/2, Prague, 15030, Czech Republic.
Jan Vojáček
Charles University, Faculty of Medicine in Hradec Králové, Hradec Králové, Czech Republic; University Hospital Hradec Králové, Hradec Králové, Czech Republic
Helena Bedáňová
Centre of Cardiovascular Surgery and Transplantation, Brno, Czech Republic
Petr Fila
Centre of Cardiovascular Surgery and Transplantation, Brno, Czech Republic; Faculty of Medicine, Masaryk University, Brno, Czech Republic
Ivo Skalský
Na Homolce Hospital, Prague, Czech Republic
Daniela Žáková
Centre of Cardiovascular Surgery and Transplantation, Brno, Czech Republic
Michal Klán
Na Homolce Hospital, Prague, Czech Republic
Barbora Míková
Na Homolce Hospital, Prague, Czech Republic
Karel Mědílek
Charles University, Faculty of Medicine in Hradec Králové, Hradec Králové, Czech Republic; University Hospital Hradec Králové, Hradec Králové, Czech Republic
Martin Tuna
Charles University, Faculty of Medicine in Hradec Králové, Hradec Králové, Czech Republic; University Hospital Hradec Králové, Hradec Králové, Czech Republic
Monika Fialová
University Hospital Hradec Králové, Hradec Králové, Czech Republic
Radka Dvořáková
University Hospital Hradec Králové, Hradec Králové, Czech Republic
Zuzana Hlubocká
2nd Department of Internal Cardiovascular Medicine, General University Hospital in Prague, First Faculty of Medicine, Charles University, Czech Republic
Roman Panovský
International Clinical Research Center, St. Anne's University Hospital Brno, Brno, Czech Republic; 1st Department of Internal, Brno, Czech Republic Medicine/Cardioangiology at St. Anne's University Hospital, Brno, Czech Republic
Kryštof Slabý
Department of Rehabilitation and Sports Medicine, Second Faculty of Medicine, Charles University in Prague, Czech Republic
Elayne Kelen de Oliveira
CardioPaTh PhD Program, Department of Advanced Biomedical Sciences, Federico II University, Naples, Italy; Cardiovascular Center OLV Clinic Aalst, Belgium
Background: The optimal treatment of patients with severe symptomatic aortic regurgitation (AR) is state-of-the-art surgery. Asymptomatic patients with advanced left ventricular (LV) dilatation and/or impaired ejection fraction should undergo surgical treatment, but there is no guidelines consensus on cut-off values for this recommendation. Multimodality imaging has brought new tools for the accurate selection of asymptomatic patients at risk of early clinical deterioration, however, prospective and randomized data are pending. Cardiac magnetic resonance (CMR)-derived AR quantification along with LV remodeling assessment appears to be the most accurate tool for a selection of such patients at risk. Trial design: The objective of our prospective and multicenter study is to determine whether patients at risk of early clinical deterioration as per CMR assessment will benefit from early surgical treatment. The study is designed as a superiority trial to demonstrate that early surgical treatment is safe and more effective than the standard treatment. A total of 217 asymptomatic patients with severe AR, but without current guidelines-based surgical indication, will be enrolled across all centers. We expect 24 % of patients identified as high clinical risk and therefore eligible for 1:1 randomization to early surgical treatment within 3 months or a watchful waiting strategy. Follow-up will be annual. We expect a complete restoration of LV size and function along with improved quality of life and physical performance in a short-term follow-up of 12 months. The primary endpoint will be a composite safety and efficacy with all criteria mandatory: 15 % or larger reduction of baseline CMR-derived LV end-diastolic volume index, LV ejection fraction >50 %, and no major adverse cardiovascular events. The annual follow-up will continue for a minimum of 4 years until the required number of endpoints is achieved to show a statistically significant difference in cardiovascular morbidity and mortality in early surgically treated patients. Conclusion: The ELEANOR trial is the first multicenter randomized controlled study to compare early surgical treatment with a watchful waiting strategy in asymptomatic patients with chronic severe AR at high risk of early clinical deterioration as per CMR assessment but without guidelines-based indications for surgical treatment.