Effect of High-Dose Selenium on Postoperative Organ Dysfunction and Mortality in Cardiac Surgery Patients: The SUSTAIN CSX Randomized Clinical Trial.


Journal

JAMA surgery
ISSN: 2168-6262
Titre abrégé: JAMA Surg
Pays: United States
ID NLM: 101589553

Informations de publication

Date de publication:
01 03 2023
Historique:
pubmed: 12 1 2023
medline: 11 3 2023
entrez: 11 1 2023
Statut: ppublish

Résumé

Selenium contributes to antioxidative, anti-inflammatory, and immunomodulatory pathways, which may improve outcomes in patients at high risk of organ dysfunctions after cardiac surgery. To assess the ability of high-dose intravenous sodium selenite treatment to reduce postoperative organ dysfunction and mortality in cardiac surgery patients. This multicenter, randomized, double-blind, placebo-controlled trial took place at 23 sites in Germany and Canada from January 2015 to January 2021. Adult cardiac surgery patients with a European System for Cardiac Operative Risk Evaluation II score-predicted mortality of 5% or more or planned combined surgical procedures were randomized. Patients were randomly assigned (1:1) by a web-based system to receive either perioperative intravenous high-dose selenium supplementation of 2000 μg/L of sodium selenite prior to cardiopulmonary bypass, 2000 μg/L immediately postoperatively, and 1000 μg/L each day in intensive care for a maximum of 10 days or placebo. The primary end point was a composite of the numbers of days alive and free from organ dysfunction during the first 30 days following cardiac surgery. A total of 1416 adult cardiac surgery patients were analyzed (mean [SD] age, 68.2 [10.4] years; 1043 [74.8%] male). The median (IQR) predicted 30-day mortality by European System for Cardiac Operative Risk Evaluation II score was 8.7% (5.6%-14.9%), and most patients had combined coronary revascularization and valvular procedures. Selenium did not increase the number of persistent organ dysfunction-free and alive days over the first 30 postoperative days (median [IQR], 29 [28-30] vs 29 [28-30]; P = .45). The 30-day mortality rates were 4.2% in the selenium and 5.0% in the placebo group (odds ratio, 0.82; 95% CI, 0.50-1.36; P = .44). Safety outcomes did not differ between the groups. In high-risk cardiac surgery patients, perioperative administration of high-dose intravenous sodium selenite did not reduce morbidity or mortality. The present data do not support the routine perioperative use of selenium for patients undergoing cardiac surgery. ClinicalTrials.gov Identifier: NCT02002247.

Identifiants

pubmed: 36630120
pii: 2800335
doi: 10.1001/jamasurg.2022.6855
pmc: PMC9857635
doi:

Substances chimiques

Selenium H6241UJ22B
Sodium Selenite HIW548RQ3W
Anti-Inflammatory Agents 0

Banques de données

ClinicalTrials.gov
['NCT02002247']

Types de publication

Randomized Controlled Trial Multicenter Study Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

235-244

Investigateurs

Gregory Hare (G)
Michael Wa Chu (MW)
Pierre Voisine (P)
Francois Dagenais (F)
Eric Dumont (E)
Frédérique Jacques (F)
Eric Charbonneau (E)
Jean Perron (J)
Simone Lindau (S)
Roupen Hatzakorizan (R)
Assad Haneya (A)
Georg Trummer (G)
Angela Jareth (A)
Xuran Jiang (X)
Ellen Dresen (E)
Aileen Hill (A)

Auteurs

Christian Stoppe (C)

University of Ottawa Heart Institute, Ottawa, Ontario, Canada.

Bernard McDonald (B)

University of Ottawa Heart Institute, Ottawa, Ontario, Canada.

Patrick Meybohm (P)

Department of Anaesthesiology, Intensive Care, Emergency, and Pain Medicine, University Hospital Wuerzburg, Wuerzburg, Germany.

Kenneth B Christopher (KB)

Division of Renal Medicine, Brigham and Women's Hospital, Boston, Massachusetts.

Stephen Fremes (S)

Sunnybrook Research Institute, Toronto, Ontario, Canada.

Richard Whitlock (R)

Hamilton Health Sciences, Hamilton, Ontario, Canada.

Siamak Mohammadi (S)

Quebec Heart and Lung Institute, Laval University, Quebec City, Quebec, Canada.

Dimitri Kalavrouziotis (D)

Quebec Heart and Lung Institute, Laval University, Quebec City, Quebec, Canada.

Gunnar Elke (G)

University Hospital Schleswig-Holstein, Kiel, Germany.

Rolf Rossaint (R)

University Hospital Aachen, Aachen, Germany.

Philipp Helmer (P)

Department of Anaesthesiology, Intensive Care, Emergency, and Pain Medicine, University Hospital Wuerzburg, Wuerzburg, Germany.

Kai Zacharowski (K)

University Hospital Frankfurt, Frankfurt, Germany.

Ulf Günther (U)

Oldenburg Clinic, University of Oldenburg, Oldenburg, Germany.

Matteo Parotto (M)

Department of Anesthesiology and Pain Medicine, Toronto General Hospital, Toronto, Ontario, Canada.
Division of Critical Care Medicine, Department of Anesthesia and Interdepartmental University of Toronto, Toronto, Ontario, Canada.

Bernd Niemann (B)

University Hospital of Giessen, Giessen, Germany.

Andreas Böning (A)

University Hospital of Giessen, Giessen, Germany.

C David Mazer (CD)

Li Ka Shing Knowledge Institute, St Michael's Hospital, Toronto, Ontario, Canada.
Department of Anesthesiology and Pain Medicine, Department of Physiology, University of Toronto, Toronto, Ontario, Canada.

Philip M Jones (PM)

London Health Sciences Centre, London, Ontario, Canada.

Marion Ferner (M)

University Medical Center of the Johannes Gutenberg-University Mainz, Mainz, Germany.

Yoan Lamarche (Y)

Hôpital du Sacré-Coeur de Montréal, Montreal, Quebec, Canada.
Montreal Heart Institute, Montreal, Quebec, Canada.

Francois Lamontagne (F)

Hôpital Fleurimont (CHUS), Sherbrooke, Quebec, Canada.

Oliver J Liakopoulos (OJ)

Department of Cardiothoracic Surgery, Heart Center, University Hospital of Cologne, Cologne, Germany.

Matthew Cameron (M)

Jewish General Hospital, Montreal, Quebec, Canada.

Matthias Müller (M)

University Heart Center Freiburg Bad Krozingen, Bad Krozingen, Germany.

Alexander Zarbock (A)

University Hospital Münster, Münster, Germany.

Maria Wittmann (M)

University Hospital Bonn, Bonn, Germany.

Andreas Goetzenich (A)

University Hospital Aachen, Aachen, Germany.
now with Abiomed Europe GmbH, Aachen, Germany.

Erich Kilger (E)

Ludwig Maximilian University of Munich, Munich, Germany.

Lutz Schomburg (L)

Institute for Experimental Endocrinology, Charité-Universitätsmedizin Berlin, Berlin, Germany.

Andrew G Day (AG)

Clinical Evaluation Research Unit, Queen's University, Kingston, Ontario, Canada.

Daren K Heyland (DK)

Clinical Evaluation Research Unit, Queen's University, Kingston, Ontario, Canada.
Department of Critical Care Medicine, Queen's University, Kingston, Ontario, Canada.

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