Shock Severity Modifies Associations Between RBC Transfusion in the First 48 Hours of Sepsis Onset and the Duration of Organ Dysfunction in Critically Ill Septic Children.


Journal

Pediatric critical care medicine : a journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies
ISSN: 1529-7535
Titre abrégé: Pediatr Crit Care Med
Pays: United States
ID NLM: 100954653

Informations de publication

Date de publication:
08 2020
Historique:
pubmed: 21 3 2020
medline: 7 1 2021
entrez: 21 3 2020
Statut: ppublish

Résumé

To test the hypothesis that early RBC transfusion is associated with duration of organ dysfunction in critically ill septic children. Secondary analysis of a single-center prospective observational study. Multivariable negative binomial regression was used to determine relationships between RBC transfusion within 48 hours of sepsis onset and number of days in 14 with organ dysfunction, or with multiple organ dysfunction syndrome. A PICU at a quaternary care children's hospital. Children less than 18 years old with severe sepsis/septic shock by consensus criteria were included. Patients with RBC transfusion prior to sepsis onset and those on extracorporeal membrane oxygenation support within 48 hours of sepsis onset were excluded. None. Ninety-four patients were included. Median age was 6 years (0-13 yr); 61% were male. Seventy-eight percentage had septic shock, and 41 (44%) were transfused RBC within 48 hours of sepsis onset (early RBC transfusion). On multivariable analyses, early RBC transfusion was independently associated with 44% greater organ dysfunction days (adjusted relative risk, 1.44 [1.04-2.]; p = 0.03), although risk differed by severity of illness (interaction p = 0.004) and by shock severity (interaction p = 0.04 for Vasoactive Inotrope Score and 0.03 for shock index). Relative risks for multiple organ dysfunction syndrome days varied by shock severity (interaction p = 0.008 for Vasoactive Inotrope Score and 0.01 for shock index). Risks associated with early RBC transfusion were highest for the children with the lowest shock severities. In agreement with previous studies, early RBC transfusion was independently associated with longer duration of organ dysfunction. Ours is among the first studies to document different transfusion-associated risks based on clinically available measures of shock severity, demonstrating greater transfusion-associated risks in children with less severe shock. Larger multicenter studies to verify these interaction effects are essential to plan much-needed RBC transfusion trials for critically ill septic children.

Identifiants

pubmed: 32195902
doi: 10.1097/PCC.0000000000002338
pii: 00130478-202008000-00022
doi:

Types de publication

Journal Article Observational Study Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

e475-e484

Subventions

Organisme : NHLBI NIH HHS
ID : K08 HL123925
Pays : United States
Organisme : NICHD NIH HHS
ID : UG1 HD083170
Pays : United States

Commentaires et corrections

Type : CommentIn

Références

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Auteurs

Lara S Srouji (LS)

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

Melissa Moore-Clingenpeel (M)

Division of Critical Care Medicine, Nationwide Children's Hospital, Columbus, OH.
Biostatistics Resource at Nationwide Children's Hospital, Columbus, OH.

Josey Hensley (J)

Center for Clinical and Translational Research, Abigail Wexner Research Institute at Nationwide Children's Hospital, Columbus, OH.

Lisa Steele (L)

Center for Clinical and Translational Research, Abigail Wexner Research Institute at Nationwide Children's Hospital, Columbus, OH.

Kristin Greathouse (K)

Center for Clinical and Translational Research, Abigail Wexner Research Institute at Nationwide Children's Hospital, Columbus, OH.

Larissa Anglim (L)

Center for Clinical and Translational Research, Abigail Wexner Research Institute at Nationwide Children's Hospital, Columbus, OH.

Lisa Hanson-Huber (L)

Center for Clinical and Translational Research, Abigail Wexner Research Institute at Nationwide Children's Hospital, Columbus, OH.

Jyotsna Nateri (J)

Center for Clinical and Translational Research, Abigail Wexner Research Institute at Nationwide Children's Hospital, Columbus, OH.

Kathleen Nicol (K)

Department of Pathology, Nationwide Children's Hospital, Columbus, OH.

Mark W Hall (MW)

Division of Critical Care Medicine, Nationwide Children's Hospital, Columbus, OH.
Center for Clinical and Translational Research, Abigail Wexner Research Institute at Nationwide Children's Hospital, Columbus, OH.

Octavio Ramilo (O)

Center for Clinical and Translational Research, Abigail Wexner Research Institute at Nationwide Children's Hospital, Columbus, OH.
Division of Pediatric Infectious Diseases, Nationwide Children's Hospital, Columbus, OH.

Jennifer A Muszynski (JA)

Division of Critical Care Medicine, Nationwide Children's Hospital, Columbus, OH.
Center for Clinical and Translational Research, Abigail Wexner Research Institute at Nationwide Children's Hospital, Columbus, OH.

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