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Early, Persistent Lymphopenia Is Associated With Prolonged Multiple Organ Failure and Mortality in Septic Children.
Podd, Bradley S; Banks, Russell K; Reeder, Ron; Telford, Russell; Holubkov, Richard; Carcillo, Joseph; Berg, Robert A; Wessel, David; Pollack, Murray M; Meert, Kathleen; Hall, Mark; Newth, Christopher; Lin, John C; Doctor, Allan; Shanley, Tom; Cornell, Tim; Harrison, Rick E; Zuppa, Athena F; Sward, Katherine; Dean, J Michael; Randolph, Adrienne G.
Afiliação
  • Podd BS; Division of Pediatric Critical Care Medicine, Department of Critical Care Medicine, Children's Hospital of Pittsburgh, Center for Critical Care Nephrology and Clinical Research Investigation and Systems Modeling of Acute Illness Center, University of Pittsburgh, Pittsburgh, PA.
  • Banks RK; Department of Pediatrics, University of Pittsburgh, Pittsburgh, PA.
  • Reeder R; Department of Pediatrics, University of Utah, Salt Lake City, UT.
  • Telford R; Department of Pediatrics, University of Utah, Salt Lake City, UT.
  • Holubkov R; Department of Statistics, Carnegie Mellon University, Pittsburgh, PA.
  • Carcillo J; Department of Pediatrics, University of Utah, Salt Lake City, UT.
  • Berg RA; Division of Pediatric Critical Care Medicine, Department of Critical Care Medicine, Children's Hospital of Pittsburgh, Center for Critical Care Nephrology and Clinical Research Investigation and Systems Modeling of Acute Illness Center, University of Pittsburgh, Pittsburgh, PA.
  • Wessel D; Department of Pediatrics, University of Pittsburgh, Pittsburgh, PA.
  • Pollack MM; Department of Anesthesiology, Children's Hospital of Philadelphia, Philadelphia, PA.
  • Meert K; Division of Critical Care Medicine, Department of Pediatrics, Children's National Hospital, Washington, DC.
  • Hall M; Division of Critical Care Medicine, Department of Pediatrics, Children's National Hospital, Washington, DC.
  • Newth C; Division of Critical Care Medicine, Department of Pediatrics, Children's Hospital of Michigan, Detroit, MI.
  • Lin JC; Department of Pediatrics, Central Michigan University, Mt. Pleasant, MI.
  • Doctor A; Division of Critical Care Medicine, Department of Pediatrics, The Research Institute at Nationwide Children's Hospital Immune Surveillance Laboratory, and Nationwide Children's Hospital, Columbus, OH.
  • Shanley T; Division of Pediatric Critical Care Medicine, Department of Anesthesiology and Pediatrics, Children's Hospital Los Angeles, Los Angeles, CA.
  • Cornell T; Division of Critical Care Medicine, Department of Pediatrics, St. Louis Children's Hospital, St. Louis, MO.
  • Harrison RE; Division of Critical Care Medicine, Department of Pediatrics, St. Louis Children's Hospital, St. Louis, MO.
  • Zuppa AF; Division of Critical Care Medicine, Department of Pediatrics, C. S. Mott Children's Hospital, Ann Arbor, MI.
  • Sward K; Division of Critical Care Medicine, Department of Pediatrics, C. S. Mott Children's Hospital, Ann Arbor, MI.
  • Dean JM; Division of Critical Care Medicine, Department of Pediatrics, Mattel Children's Hospital at University of California Los Angeles, Los Angeles, CA.
  • Randolph AG; Department of Anesthesiology, Children's Hospital of Philadelphia, Philadelphia, PA.
Crit Care Med ; 51(12): 1766-1776, 2023 Dec 01.
Article em En | MEDLINE | ID: mdl-37462434
ABSTRACT

OBJECTIVES:

Sepsis-associated immune suppression correlates with poor outcomes. Adult trials are evaluating immune support therapies. Limited data exist to support consideration of immunomodulation in pediatric sepsis. We tested the hypothesis that early, persistent lymphopenia predicts worse outcomes in pediatric severe sepsis.

DESIGN:

Observational cohort comparing children with severe sepsis and early, persistent lymphopenia (absolute lymphocyte count < 1,000 cells/µL on 2 d between study days 0-5) to children without. The composite outcome was prolonged multiple organ dysfunction syndrome (MODS, organ dysfunction beyond day 7) or PICU mortality.

SETTING:

Nine PICUs in the National Institutes of Health Collaborative Pediatric Critical Care Research Network between 2015 and 2017. PATIENTS Children with severe sepsis and indwelling arterial and/or central venous catheters.

INTERVENTIONS:

Blood sampling and clinical data analysis. MEASUREMENTS AND MAIN

RESULTS:

Among 401 pediatric patients with severe sepsis, 152 (38%) had persistent lymphopenia. These patients were older, had higher illness severity, and were more likely to have underlying comorbidities including solid organ transplant or malignancy. Persistent lymphopenia was associated with the composite outcome prolonged MODS or PICU mortality (66/152, 43% vs 45/249, 18%; p < 0.01) and its components prolonged MODS (59/152 [39%] vs 43/249 [17%]), and PICU mortality (32/152, 21% vs 12/249, 5%; p < 0.01) versus children without. After adjusting for baseline factors at enrollment, the presence of persistent lymphopenia was associated with an odds ratio of 2.98 (95% CI [1.85-4.02]; p < 0.01) for the composite outcome. Lymphocyte count trajectories showed that patients with persistent lymphopenia generally did not recover lymphocyte counts during the study, had lower nadir whole blood tumor necrosis factor-α response to lipopolysaccharide stimulation, and higher maximal inflammatory markers (C-reactive protein and ferritin) during days 0-3 ( p < 0.01).

CONCLUSIONS:

Children with severe sepsis and persistent lymphopenia are at risk of prolonged MODS or PICU mortality. This evidence supports testing therapies for pediatric severe sepsis patients risk-stratified by early, persistent lymphopenia.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sepse / Linfopenia Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Adult / Child / Humans / Infant Idioma: En Revista: Crit Care Med Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sepse / Linfopenia Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Adult / Child / Humans / Infant Idioma: En Revista: Crit Care Med Ano de publicação: 2023 Tipo de documento: Article