Revisiting Post-ICU Admission Fluid Balance Across Pediatric Sepsis Mortality Risk Strata: A Secondary Analysis of a Prospective Observational Cohort Study.

acute kidney injury biomarkers critical illness fluid overload positive fluid balance post-ICU admission fluid balance sepsis septic shock

Journal

Critical care explorations
ISSN: 2639-8028
Titre abrégé: Crit Care Explor
Pays: United States
ID NLM: 101746347

Informations de publication

Date de publication:
Jan 2024
Historique:
medline: 18 1 2024
pubmed: 18 1 2024
entrez: 18 1 2024
Statut: epublish

Résumé

Post-ICU admission cumulative positive fluid balance (PFB) is associated with increased mortality among critically ill patients. We sought to test whether this risk varied across biomarker-based risk strata upon adjusting for illness severity, presence of severe acute kidney injury (acute kidney injury), and use of continuous renal replacement therapy (CRRT) in pediatric septic shock. Ongoing multicenter prospective observational cohort. Thirteen PICUs in the United States (2003-2023). Six hundred and eighty-one children with septic shock. None. Cumulative percent PFB between days 1 and 7 (days 1-7 %PFB) was determined. Primary outcome of interest was complicated course defined as death or persistence of greater than or equal to two organ dysfunctions by day 7. Pediatric Sepsis Biomarker Risk Model (PERSEVERE)-II biomarkers were used to assign mortality probability and categorize patients into high mortality ( Our data demonstrate the influence of cumulative %PFB on the risk of complicated course in pediatric septic shock. Contrary to our previous report, this risk was largely driven by patients categorized as having a high mortality risk based on PERSEVERE-II biomarkers. Incorporation of such prognostic enrichment tools in randomized trials of restrictive fluid management or early initiation of de-escalation strategies may inform targeted application of such interventions among at-risk patients.

Identifiants

pubmed: 38234587
doi: 10.1097/CCE.0000000000001027
pmc: PMC10793970
doi:

Types de publication

Journal Article

Langues

eng

Pagination

e1027

Informations de copyright

Copyright © 2024 The Authors. Published by Wolters Kluwer Health, Inc. on behalf of the Society of Critical Care Medicine.

Déclaration de conflit d'intérêts

Dr. Atreya and Cincinnati Children’s Hospital (CCHMC) hold a provisional patent for a unified biomarker model—PERSEVERENCE that incorporates Pediatric Sepsis Biomarker Risk Model (PERSEVERE) and endothelial dysfunction markers to predict the risk of multiple organ dysfunctions in sepsis. Dr. Atreya received funding through the Cincinnati Children’s Research Foundation (CCRF) Procter-Scholar Award. Dr. Stanski and CCHMC hold a provisional patent for the use of PERSEVERE biomarkers in sepsis-associated acute kidney injury. Dr. Stanski is supported by the National Center for Advancing Translational Sciences of the National Institutes of Health (NIH) (KL2TR001426). Dr. Atreya, Dr. Stanski, and CCHMC hold a provisional patent for PERSEVERENCE sepsis-associated acute kidney injury model to identify high-risk patients for microvascular modulating therapies. Dr. Fitzgerald, Dr. Weiss, Dr. Haileselassie, Dr. Quasney, and Dr. Alder received funding from the NIH.

Auteurs

Mihir R Atreya (MR)

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

Natalie Z Cvijanovich (NZ)

Department of Pediatrics, UCSF Benioff Children's Hospital Oakland, Oakland, CA.

Julie C Fitzgerald (JC)

Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA.

Scott L Weiss (SL)

Department of Pediatrics, Nemours Children's Hospital, Wilmington, DE.

Michael T Bigham (MT)

Department of Pediatrics, Akron Children's Hospital, Akron, OH.

Parag N Jain (PN)

Department of Pediatrics, Texas Children's Hospital and Baylor College of Medicine, Houston, TX.

Kamal Abulebda (K)

Department of Pediatrics, Riley Hospital for Children, Indianapolis, IN.

Riad Lutfi (R)

Department of Pediatrics, Riley Hospital for Children, Indianapolis, IN.

Jeffrey Nowak (J)

Department of Pediatrics, Children's Hospital and Clinics of Minnesota, Minneapolis, MN.

Neal J Thomas (NJ)

Department of Pediatrics, Penn State Hershey Children's Hospital, Hershey, PA.

Torrey Baines (T)

Department of Pediatrics, University of Florida Health Shands Children's Hospital, Gainesville, FL.

Michael Quasney (M)

Department of Pediatrics, CS Mott Children's Hospital at the University of Michigan, Ann Arbor, MI.

Bereketeab Haileselassie (B)

Department of Pediatrics, Lucile Packard Children's Hospital Stanford, Palo Alto, CA.

Rashmi Sahay (R)

Division of Biostatistics and Epidemiology, Cincinnati Children's Hospital Medical Center Cincinnati, Cincinnati, OH.

Bin Zhang (B)

Division of Biostatistics and Epidemiology, Cincinnati Children's Hospital Medical Center Cincinnati, Cincinnati, OH.

Matthew N Alder (MN)

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

Natalja L Stanski (NL)

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

Stuart L Goldstein (SL)

Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH.
Division of Nephrology, Cincinnati Children's Hospital Medical Center and Cincinnati Children's Research Foundation, Cincinnati, OH.

Classifications MeSH