Transfusion-Associated Delirium in Children: No Difference Between Short Storage Versus Standard Issue RBCs.


Journal

Critical care medicine
ISSN: 1530-0293
Titre abrégé: Crit Care Med
Pays: United States
ID NLM: 0355501

Informations de publication

Date de publication:
01 02 2022
Historique:
entrez: 31 1 2022
pubmed: 1 2 2022
medline: 1 3 2022
Statut: ppublish

Résumé

Primary objective is to determine if transfusion of short storage RBCs compared with standard issue RBCs reduced risk of delirium/coma in critically ill children. Secondary objective is to assess if RBC transfusion was independently associated with delirium/coma. This study was performed in two stages. First, we compared patients receiving either short storage or standard RBCs in a multi-institutional prospective randomized controlled trial. Then, we compared all transfused patients in the randomized controlled trial with a single-center cohort of nontransfused patients matched for confounders of delirium/coma. Twenty academic PICUs who participated in the Age of Transfused Blood in Critically Ill Children trial. Children 3 days to 16 years old who were transfused RBCs within the first 7 days of admission. Subjects were randomized to either short storage RBC study arm (defined as RBCs stored for up to seven days) or standard issue RBC study arm. In addition, subjects were screened for delirium prior to transfusion and every 12 hours after transfusion for up to 3 days. Primary outcome measure was development of delirium/coma within 3 days of initial transfusion. Additional outcome measures were dose-response relationship between volume of RBCs transfused and delirium/coma, and comparison of delirium/coma rates between transfused patients and individually matched nontransfused patients. We included 146 subjects in the stage I analysis; 69 were randomized to short storage RBCs and 77 to standard issue. There was no significant difference in delirium/coma development between study arms (79.5% vs 70.1%; p = 0.184). In the stage II analysis, adjusted odds for delirium in the transfused cohort was more than eight-fold higher than in the nontransfused matched cohort, even after controlling for hemoglobin (adjusted odds ratio, 8.9; CI, 2.8-28.4; p < 0.001). RBC transfusions (and not anemia) are independently associated with increased odds of subsequent delirium/coma. However, storage age of RBCs does not affect delirium risk.

Identifiants

pubmed: 35100190
doi: 10.1097/CCM.0000000000005393
pii: 00003246-202202000-00002
pmc: PMC8820396
mid: NIHMS1758841
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

173-182

Subventions

Organisme : NHLBI NIH HHS
ID : U01 HL116383
Pays : United States

Informations de copyright

Copyright © 2022 by the Society of Critical Care Medicine and Wolters Kluwer Health, Inc. All Rights Reserved.

Déclaration de conflit d'intérêts

Drs. Traube, Nellis, Avery, McQuillen, Fitzgerald, and Spinella received support for article research from the National Institutes of Health (NIH). Dr. Nellis’ institution received funding from the National Heart, Lung, and Blood Institute. Dr. McQuillen’s institution received funding from the National Institute of Child Health and Human Development. Dr. Fitzgerald’s institution received funding from the National Institute of Diabetes and Digestive and Kidney Diseases. Dr. Muszynski’s institution received funding from Washington University at St. Louis. Dr. Hanson’s institution received funding from the NIH. Dr. Lacroix’s institution received funding from the Canadian Institutes of Health Research. The remaining authors have disclosed that they do not have any potential conflicts of interest.

Références

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Auteurs

Chani Traube (C)

Division of Critical Care Medicine, Department of Pediatrics, Weill Cornell Medical College, New York, NY.

Marisa Tucci (M)

Department of Pediatrics, CHU Sainte-Justine, University of Montreal, Montreal, QC, Canada.

Marianne E Nellis (ME)

Division of Critical Care Medicine, Department of Pediatrics, Weill Cornell Medical College, New York, NY.

K Leslie Avery (KL)

Department of Pediatrics, University of Florida College of Medicine, Gainesville, FL.

Patrick S McQuillen (PS)

Department of Pediatrics, University of California San Francisco, San Francisco, CA.

Julie C Fitzgerald (JC)

Department of Anesthesiology and Critical Care, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA.

Jennifer A Muszynski (JA)

Division of Critical Care Medicine, Department of Pediatrics, Nationwide Children's Hospital, Columbus, OH.

Jill M Cholette (JM)

Department of Pediatrics, University of Rochester, Golisano Children's Hospital, Rochester, NY.

Adam J Schwarz (AJ)

Critical Care, CHOC Children's Hospital, Orange, CA.

Erika L Stalets (EL)

Division of Critical Care Medicine, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.
Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH.

Maureen A Quaid (MA)

Department of Pediatrics, Advocate Children's Hospital, Park Ridge, IL.

Sheila J Hanson (SJ)

Department of Pediatrics and Children's Wisconsin, Critical Care Section, Medical College of Wisconsin, Milwaukee, WI.

Jacques Lacroix (J)

Division of Pediatric Critical Care, Department of Pediatrics, CHU Sainte-Justine, Université de Montréal, Montréal, QC, Canada.

Ron W Reeder (RW)

Department of Pediatrics, University of Utah, Salt Lake City, UT.

Philip C Spinella (PC)

Division of Critical Care Medicine, Department of Pediatrics, Washington University School of Medicine, St. Louis, MO.

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