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
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
235-244Investigateurs
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)