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Organ Dysfunction in Children With Blood Culture-Proven Sepsis: Comparative Performance of Four Scores in a National Cohort Study.
Schlapbach, Luregn J; Goertz, Sabrina; Hagenbuch, Niels; Aubert, Blandine; Papis, Sebastien; Giannoni, Eric; Posfay-Barbe, Klara M; Stocker, Martin; Heininger, Ulrich; Bernhard-Stirnemann, Sara; Niederer-Loher, Anita; Kahlert, Christian R; Natalucci, Giancarlo; Relly, Christa; Riedel, Thomas; Aebi, Christoph; Berger, Christoph; Agyeman, Philipp K A.
Afiliação
  • Schlapbach LJ; Department of Intensive Care and Neonatology, and Children`s Research Center, University Children`s Hospital Zurich, Zurich, Switzerland.
  • Goertz S; Child Health Research Centre, University of Queensland, Brisbane, QLD, Australia.
  • Hagenbuch N; Division of Infectious Diseases, and Children's Research Center, University Children's Hospital Zurich, Zurich, Switzerland.
  • Aubert B; Department of Pediatrics, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.
  • Papis S; Clinic of Neonatology, Department Mother-Woman-Child, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.
  • Giannoni E; Pediatric Infectious Diseases Unit, Department of Woman, Child and Adolescent, Children's Hospital of Geneva, University Hospitals of Geneva and Faculty of Medicine, Geneva, Switzerland.
  • Posfay-Barbe KM; Clinic of Neonatology, Department Mother-Woman-Child, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.
  • Stocker M; Pediatric Infectious Diseases Unit, Department of Woman, Child and Adolescent, Children's Hospital of Geneva, University Hospitals of Geneva and Faculty of Medicine, Geneva, Switzerland.
  • Heininger U; Children's Hospital Lucerne, Lucerne, Switzerland.
  • Bernhard-Stirnemann S; Infectious Diseases and Vaccinology, University Children's Hospital Basel, Basel, Switzerland.
  • Niederer-Loher A; Children's Hospital Aarau, Aarau, Switzerland.
  • Kahlert CR; Children's Hospital of Eastern Switzerland, St. Gallen, Switzerland.
  • Natalucci G; Children's Hospital of Eastern Switzerland, St. Gallen, Switzerland.
  • Relly C; Department of Neonatology, University Hospital Zurich, Zurich, Switzerland.
  • Riedel T; Division of Infectious Diseases, and Children's Research Center, University Children's Hospital Zurich, Zurich, Switzerland.
  • Aebi C; Department of Pediatrics, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.
  • Berger C; Department of Pediatrics, Cantonal Hospital Graubuenden, Chur, Switzerland.
  • Agyeman PKA; Department of Pediatrics, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.
Pediatr Crit Care Med ; 25(3): e117-e128, 2024 Mar 01.
Article em En | MEDLINE | ID: mdl-37878412
ABSTRACT

OBJECTIVES:

Previous studies applying Sepsis-3 criteria to children were based on retrospective analyses of PICU cohorts. We aimed to compare organ dysfunction criteria in children with blood culture-proven sepsis, including emergency department, PICU, and ward patients, and to assess relevance of organ dysfunctions for mortality prediction.

DESIGN:

We have carried out a nonprespecified, secondary analysis of a prospective dataset collected from September 2011 to December 2015.

SETTING:

Emergency departments, wards, and PICUs in 10 tertiary children's hospitals in Switzerland. PATIENTS Children younger than 17 years old with blood culture-proven sepsis. We excluded preterm infants and term infants younger than 7 days old.

INTERVENTIONS:

None. MEASUREMENTS AND MAIN

RESULTS:

We compared the 2005 International Pediatric Sepsis Consensus Conference (IPSCC), Pediatric Logistic Organ Dysfunction-2 (PELOD-2), pediatric Sequential Organ Failure Assessment (pSOFA), and Pediatric Organ Dysfunction Information Update Mandate (PODIUM) scores, measured at blood culture sampling, to predict 30-day mortality. We analyzed 877 sepsis episodes in 807 children, with a 30-day mortality of 4.3%. Percentage with organ dysfunction ranged from 32.7% (IPSCC) to 55.3% (pSOFA). In adjusted analyses, the accuracy for identification of 30-day mortality was area under the curve (AUC) 0.87 (95% CI, 0.82-0.92) for IPSCC, 0.83 (0.76-0.89) for PELOD-2, 0.85 (0.78-0.92) for pSOFA, and 0.85 (0.78-0.91) for PODIUM. When restricting scores to neurologic, respiratory, and cardiovascular dysfunction, the adjusted AUC was 0.89 (0.84-0.94) for IPSCC, 0.85 (0.79-0.91) for PELOD-2, 0.87 (0.81-0.93) for pSOFA, and 0.88 (0.83-0.93) for PODIUM.

CONCLUSIONS:

IPSCC, PELOD-2, pSOFA, and PODIUM performed similarly to predict 30-day mortality. Simplified scores restricted to neurologic, respiratory, and cardiovascular dysfunction yielded comparable performance.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sepse / Insuficiência de Múltiplos Órgãos Limite: Adolescent / Child / Humans / Infant Idioma: En Revista: Pediatr Crit Care Med Assunto da revista: PEDIATRIA / TERAPIA INTENSIVA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Suíça

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sepse / Insuficiência de Múltiplos Órgãos Limite: Adolescent / Child / Humans / Infant Idioma: En Revista: Pediatr Crit Care Med Assunto da revista: PEDIATRIA / TERAPIA INTENSIVA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Suíça