Evidence map›Paper›PMID 38234587›Full record

ArticleCritical care explorations2024

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

Mihir R Atreya, Natalie Z Cvijanovich, Julie C Fitzgerald, Scott L Weiss, Michael T Bigham, Parag N Jain, Kamal Abulebda, Riad Lutfi, Jeffrey Nowak, Neal J Thomas and 8 more

Open access · goldAbstract read
In one paragraph

Article in Critical care explorations, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.4field-weighted citation impact, top 41% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

18 authors at 6 institutions in 1 country.

Mihir R AtreyaDivision of Critical Care Medicine, Cincinnati Children's Hospital Medical Center Cincinnati, Cincinnati, OH.
Natalie Z CvijanovichDepartment of Pediatrics, UCSF Benioff Children's Hospital Oakland, Oakland, CA.
Julie C FitzgeraldDepartment of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA.
Scott L WeissDepartment of Pediatrics, Nemours Children's Hospital, Wilmington, DE.
Michael T BighamDepartment of Pediatrics, Akron Children's Hospital, Akron, OH.
Parag N JainDepartment of Pediatrics, Texas Children's Hospital and Baylor College of Medicine, Houston, TX.
Kamal AbulebdaDepartment of Pediatrics, Riley Hospital for Children, Indianapolis, IN.
Riad LutfiDepartment of Pediatrics, Riley Hospital for Children, Indianapolis, IN.
Jeffrey NowakDepartment of Pediatrics, Children's Hospital and Clinics of Minnesota, Minneapolis, MN.
Neal J ThomasDepartment of Pediatrics, Penn State Hershey Children's Hospital, Hershey, PA.
Torrey BainesDepartment of Pediatrics, University of Florida Health Shands Children's Hospital, Gainesville, FL.
Michael QuasneyDepartment of Pediatrics, CS Mott Children's Hospital at the University of Michigan, Ann Arbor, MI.
Bereketeab HaileselassieDepartment of Pediatrics, Lucile Packard Children's Hospital Stanford, Palo Alto, CA.
Rashmi SahayDivision of Biostatistics and Epidemiology, Cincinnati Children's Hospital Medical Center Cincinnati, Cincinnati, OH.
Bin ZhangDivision of Biostatistics and Epidemiology, Cincinnati Children's Hospital Medical Center Cincinnati, Cincinnati, OH.
Matthew N AlderDivision of Critical Care Medicine, Cincinnati Children's Hospital Medical Center Cincinnati, Cincinnati, OH.
Natalja L StanskiDivision of Critical Care Medicine, Cincinnati Children's Hospital Medical Center Cincinnati, Cincinnati, OH.
Stuart L GoldsteinDepartment of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH.
University of Cincinnati Medical Center · USAkron Children's Hospital · USChildren's Hospital of Philadelphia · USPenn State Milton S. Hershey Medical Center · USTexas Children's Hospital · USUCSF Benioff Children's Hospital · US

Funding

KL2 Training ProgramKL2TR001426 · NCATS · UNIVERSITY OF CINCINNATI · PI ZELLER, MARGARET H · 2015 to 2024
$6.8M
Supplement for MIRA award_Wong_2021R35GM126943 · NIGMS · CINCINNATI CHILDRENS HOSP MED CTR · PI ALDER, MATTHEW N · 2018 to 2022
$2.7M
Pediatric septic acute kidney injury: personalizing antibiotic dosing through understanding acute kidney injury risk factors and biomarker profilesK23DK119463 · NIDDK · CHILDREN'S HOSP OF PHILADELPHIA · PI FITZGERALD, JULIE C. HOLLOWS · 2020 to 2024
$810k
Developing a Precision Medicine Approach to Pediatric Sepsis-Associated Acute Kidney Injury: Identification of Unique Subphenotypes and Strategies for Bedside ImplementationK23GM151444 · NIGMS · CINCINNATI CHILDRENS HOSP MED CTR · PI Natalja L. Stanski · 2023 to 2026
$769k
NCATS NIH HHS KL2 TR001426NIDDK NIH HHS K23 DK119463NIGMS NIH HHS K23 GM151444NIGMS NIH HHS R35 GM126943
6 · The paper itself

Abstract

objectivesPost-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.

designOngoing multicenter prospective observational cohort.

settingThirteen PICUs in the United States (2003-2023). PATIENTS: Six hundred and eighty-one children with septic shock.

interventionsNone. MEASUREMENTS AND MAIN

resultsCumulative 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 (

conclusionsOur 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.

Indexed as

acute kidney injurybiomarkerscritical illnessfluid overloadpositive fluid balancepost-ICU admission fluid balancesepsisseptic shock

Identifiers

PMID38234587
PMCPMC10793970
OpenAlexW4390903829

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.