Skip to main content

Corticosteroids and pediatric septic shock outcomes: a risk stratified analysis.

Publication ,  Journal Article
Atkinson, SJ; Cvijanovich, NZ; Thomas, NJ; Allen, GL; Anas, N; Bigham, MT; Hall, M; Freishtat, RJ; Sen, A; Meyer, K; Checchia, PA; Shanley, TP ...
Published in: PLoS One
2014

BACKGROUND: The potential benefits of corticosteroids for septic shock may depend on initial mortality risk. OBJECTIVE: We determined associations between corticosteroids and outcomes in children with septic shock who were stratified by initial mortality risk. METHODS: We conducted a retrospective analysis of an ongoing, multi-center pediatric septic shock clinical and biological database. Using a validated biomarker-based stratification tool (PERSEVERE), 496 subjects were stratified into three initial mortality risk strata (low, intermediate, and high). Subjects receiving corticosteroids during the initial 7 days of admission (n = 252) were compared to subjects who did not receive corticosteroids (n = 244). Logistic regression was used to model the effects of corticosteroids on 28-day mortality and complicated course, defined as death within 28 days or persistence of two or more organ failures at 7 days. RESULTS: Subjects who received corticosteroids had greater organ failure burden, higher illness severity, higher mortality, and a greater requirement for vasoactive medications, compared to subjects who did not receive corticosteroids. PERSEVERE-based mortality risk did not differ between the two groups. For the entire cohort, corticosteroids were associated with increased risk of mortality (OR 2.3, 95% CI 1.3-4.0, p = 0.004) and a complicated course (OR 1.7, 95% CI 1.1-2.5, p = 0.012). Within each PERSEVERE-based stratum, corticosteroid administration was not associated with improved outcomes. Similarly, corticosteroid administration was not associated with improved outcomes among patients with no comorbidities, nor in groups of patients stratified by PRISM. CONCLUSIONS: Risk stratified analysis failed to demonstrate any benefit from corticosteroids in this pediatric septic shock cohort.

Duke Scholars

Altmetric Attention Stats
Dimensions Citation Stats

Published In

PLoS One

DOI

EISSN

1932-6203

Publication Date

2014

Volume

9

Issue

11

Start / End Page

e112702

Location

United States

Related Subject Headings

  • Treatment Outcome
  • Shock, Septic
  • Risk Factors
  • Male
  • Logistic Models
  • Humans
  • General Science & Technology
  • Female
  • Comorbidity
  • Child, Preschool
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Atkinson, S. J., Cvijanovich, N. Z., Thomas, N. J., Allen, G. L., Anas, N., Bigham, M. T., … Wong, H. R. (2014). Corticosteroids and pediatric septic shock outcomes: a risk stratified analysis. PLoS One, 9(11), e112702. https://doi.org/10.1371/journal.pone.0112702
Atkinson, Sarah J., Natalie Z. Cvijanovich, Neal J. Thomas, Geoffrey L. Allen, Nick Anas, Michael T. Bigham, Mark Hall, et al. “Corticosteroids and pediatric septic shock outcomes: a risk stratified analysis.PLoS One 9, no. 11 (2014): e112702. https://doi.org/10.1371/journal.pone.0112702.
Atkinson SJ, Cvijanovich NZ, Thomas NJ, Allen GL, Anas N, Bigham MT, et al. Corticosteroids and pediatric septic shock outcomes: a risk stratified analysis. PLoS One. 2014;9(11):e112702.
Atkinson, Sarah J., et al. “Corticosteroids and pediatric septic shock outcomes: a risk stratified analysis.PLoS One, vol. 9, no. 11, 2014, p. e112702. Pubmed, doi:10.1371/journal.pone.0112702.
Atkinson SJ, Cvijanovich NZ, Thomas NJ, Allen GL, Anas N, Bigham MT, Hall M, Freishtat RJ, Sen A, Meyer K, Checchia PA, Shanley TP, Nowak J, Quasney M, Weiss SL, Banschbach S, Beckman E, Howard K, Frank E, Harmon K, Lahni P, Lindsell CJ, Wong HR. Corticosteroids and pediatric septic shock outcomes: a risk stratified analysis. PLoS One. 2014;9(11):e112702.

Published In

PLoS One

DOI

EISSN

1932-6203

Publication Date

2014

Volume

9

Issue

11

Start / End Page

e112702

Location

United States

Related Subject Headings

  • Treatment Outcome
  • Shock, Septic
  • Risk Factors
  • Male
  • Logistic Models
  • Humans
  • General Science & Technology
  • Female
  • Comorbidity
  • Child, Preschool