Buckberg versus Del Nido in isolated aortic valve replacement: a prospective, two-centre, randomized trial.

0 CARDIAC & CARDIOVASCULAR SYSTEMS
Manel Tauron-Ferrer, Elena Roselló-Díez, Christian Muñoz-Guijosa, Constanza Fernández-DeVinzenzi, José Montiel, Sandra Casellas, Ángela Irabien-Ortiz, Laura Corominas-García, César Piedra, Ignasi Julià, Claudio Fernández, Virginia Cegarra, Nerea Guadalupe, Marta Molina, Juan F Tabilo, Carla Gotsens-Asenjo, Cristina Sobre, Víctor Gomez, Elisabet Berastegui, Antonino J Ginel
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引用次数: 0

Abstract

Objectives: Interest in Del Nido solution is increasing in adult cardiac surgery. This study compared Del Nido with Buckberg cardioplegia in patients undergoing isolated aortic valve replacement.

Methods: A prospective, two-centre, randomized trial was conducted from July 2019 to August 2023, with adult patients undergoing first-time isolated aortic valve replacement, and were randomized to receive Buckberg (n = 159) or Del Nido (n = 152) solution. Primary end-point was Creatine Kinase and ultrasensitive Troponin T postoperative peak level.

Results: A total of 311 patients were recruited. Total cardioplegia volume was higher in Del Nido group (1000 ml vs 374.5 ml, P < 0.001). No differences were observed in peak Creatine Kinase or Troponin T levels (422 vs 407 U/L and 282 vs 258 ng/L for Buckberg and Del Nido, respectively) or during postoperative days 1-5. After cross-clamp removal, patients in Del Nido group showed higher rates of spontaneous rhythm (66.7% vs 43.1%, P < 0.001) and less ventricular fibrillation requiring defibrillation (23.6% vs 49.7%, P < 0.001). Peak intraoperative glucose levels (128 mg/dl vs 198 mg/dl, P < 0.001) and insulin administration (18.1% vs 51.0%, P < 0.001) were lower in the Del Nido group. No other differences were found.

Conclusions: No differences between Del Nido and Buckberg solutions were detected. Del Nido presents better intraoperative glycaemic control, higher spontaneous rhythm, less ventricular fibrillation requiring defibrillation after cross-clamp removal, and more comfortable surgical workflow due to less re-dose interruptions.

Clinical registration number: EU-CTR number: 2018-002701-59.

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