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International Consensus Criteria for Pediatric Sepsis and Septic Shock.
Schlapbach, Luregn J; Watson, R Scott; Sorce, Lauren R; Argent, Andrew C; Menon, Kusum; Hall, Mark W; Akech, Samuel; Albers, David J; Alpern, Elizabeth R; Balamuth, Fran; Bembea, Melania; Biban, Paolo; Carrol, Enitan D; Chiotos, Kathleen; Chisti, Mohammod Jobayer; DeWitt, Peter E; Evans, Idris; Flauzino de Oliveira, Cláudio; Horvat, Christopher M; Inwald, David; Ishimine, Paul; Jaramillo-Bustamante, Juan Camilo; Levin, Michael; Lodha, Rakesh; Martin, Blake; Nadel, Simon; Nakagawa, Satoshi; Peters, Mark J; Randolph, Adrienne G; Ranjit, Suchitra; Rebull, Margaret N; Russell, Seth; Scott, Halden F; de Souza, Daniela Carla; Tissieres, Pierre; Weiss, Scott L; Wiens, Matthew O; Wynn, James L; Kissoon, Niranjan; Zimmerman, Jerry J; Sanchez-Pinto, L Nelson; Bennett, Tellen D.
Affiliation
  • Schlapbach LJ; Department of Intensive Care and Neonatology, and Children's Research Center, University Children's Hospital Zurich, University of Zurich, Zurich, Switzerland.
  • Watson RS; Child Health Research Centre, University of Queensland, Brisbane, Australia.
  • Sorce LR; Department of Pediatrics, University of Washington, Seattle.
  • Argent AC; Seattle Children's Research Institute and Pediatric Critical Care, Seattle Children's, Seattle, Washington.
  • Menon K; Ann & Robert H. Lurie Children's Hospital, Chicago, Illinois.
  • Hall MW; Department of Pediatrics, Northwestern University Feinberg School of Medicine, Chicago, Illinois.
  • Akech S; Department of Paediatrics and Child Health, Red Cross War Memorial Children's Hospital, Cape Town, South Africa.
  • Albers DJ; University of Cape Town, Cape Town, South Africa.
  • Alpern ER; Department of Pediatrics, Children's Hospital of Eastern Ontario, Canada.
  • Balamuth F; University of Ottawa, Ontario, Canada.
  • Bembea M; Division of Critical Care Medicine, Nationwide Children's Hospital, Columbus, Ohio.
  • Biban P; The Ohio State University College of Medicine, Columbus, Ohio.
  • Carrol ED; Kenya Medical Research Institute (KEMRI)-Wellcome Trust Research Programme, Nairobi, Kenya.
  • Chiotos K; Departments of Biomedical Informatics, Bioengineering, Biostatistics and Informatics, University of Colorado School of Medicine, Aurora.
  • Chisti MJ; Department of Biomedical Informatics, Columbia University, New York, New York.
  • DeWitt PE; Ann & Robert H. Lurie Children's Hospital, Chicago, Illinois.
  • Evans I; Department of Pediatrics, Division of Emergency Medicine, Northwestern University Feinberg School of Medicine, Chicago, Illinois.
  • Flauzino de Oliveira C; Department of Pediatrics, University of Pennsylvania, Perelman School of Medicine, Philadelphia.
  • Horvat CM; Division of Emergency Medicine, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
  • Inwald D; Department of Anesthesiology and Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Ishimine P; Pediatric Intensive Care Unit, Verona University Hospital, Verona, Italy.
  • Jaramillo-Bustamante JC; University of Liverpool, Department of Clinical Infection, Microbiology and Immunology, Institute of Infection, Veterinary and Ecological Sciences, Liverpool, United Kingdom.
  • Levin M; Department of Anesthesiology and Critical Care, Perelman School of Medicine at the University of Pennsylvania, Philadelphia.
  • Lodha R; Divisions of Critical Care Medicine and Infectious Diseases, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
  • Martin B; Intensive Care Unit, Dhaka Hospital, Nutrition Research Division, International Centre for Diarrhoeal Disease Research, Bangladesh (icddr,b), Dhaka, Bangladesh.
  • Nadel S; Department of Biomedical Informatics, University of Colorado School of Medicine, Aurora.
  • Nakagawa S; Department of Critical Care Medicine, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
  • Peters MJ; Clinical Research, Investigation, and Systems Modeling of Acute Illness (CRISMA) Center, Pittsburgh, Pennsylvania.
  • Randolph AG; AMIB-Associação de Medicina Intensiva Brasileira, São Paulo, Brazil.
  • Ranjit S; LASI-Latin American Institute of Sepsis, São Paulo, Brazil.
  • Rebull MN; Department of Critical Care Medicine, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
  • Russell S; Clinical Research, Investigation, and Systems Modeling of Acute Illness (CRISMA) Center, Pittsburgh, Pennsylvania.
  • Scott HF; Paediatric Intensive Care, Cambridge University Hospitals NHS Foundation Trust, Cambridge, United Kingdom.
  • de Souza DC; Departments of Emergency Medicine and Pediatrics, University of California, San Diego School of Medicine, La Jolla.
  • Tissieres P; PICU Hospital General de Medellín "Luz Castro de Gutiérrez" and Hospital Pablo Tobón Uribe, Medellín, Colombia.
  • Weiss SL; Red Colaborativa Pediátrica de Latinoamérica (LARed Network).
  • Wiens MO; Section of Paediatric Infectious Diseases, Department of Infectious Diseases, Imperial College London, London, United Kingdom.
  • Wynn JL; Department of Paediatrics, St Mary's Hospital, Imperial College Healthcare NHS Trust, London, United Kingdom.
  • Kissoon N; Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, India.
  • Zimmerman JJ; Departments of Biomedical Informatics and Pediatrics (Division of Critical Care Medicine), University of Colorado School of Medicine and Pediatric Intensive Care Unit, Children's Hospital Colorado, Aurora.
  • Sanchez-Pinto LN; Pediatric Intensive Care Unit, Children's Hospital Colorado, Aurora.
  • Bennett TD; Paediatric Intensive Care, St Mary's Hospital, London, United Kingdom.
JAMA ; 331(8): 665-674, 2024 02 27.
Article in En | MEDLINE | ID: mdl-38245889
ABSTRACT
Importance Sepsis is a leading cause of death among children worldwide. Current pediatric-specific criteria for sepsis were published in 2005 based on expert opinion. In 2016, the Third International Consensus Definitions for Sepsis and Septic Shock (Sepsis-3) defined sepsis as life-threatening organ dysfunction caused by a dysregulated host response to infection, but it excluded children.

Objective:

To update and evaluate criteria for sepsis and septic shock in children. Evidence Review The Society of Critical Care Medicine (SCCM) convened a task force of 35 pediatric experts in critical care, emergency medicine, infectious diseases, general pediatrics, nursing, public health, and neonatology from 6 continents. Using evidence from an international survey, systematic review and meta-analysis, and a new organ dysfunction score developed based on more than 3 million electronic health record encounters from 10 sites on 4 continents, a modified Delphi consensus process was employed to develop criteria.

Findings:

Based on survey data, most pediatric clinicians used sepsis to refer to infection with life-threatening organ dysfunction, which differed from prior pediatric sepsis criteria that used systemic inflammatory response syndrome (SIRS) criteria, which have poor predictive properties, and included the redundant term, severe sepsis. The SCCM task force recommends that sepsis in children be identified by a Phoenix Sepsis Score of at least 2 points in children with suspected infection, which indicates potentially life-threatening dysfunction of the respiratory, cardiovascular, coagulation, and/or neurological systems. Children with a Phoenix Sepsis Score of at least 2 points had in-hospital mortality of 7.1% in higher-resource settings and 28.5% in lower-resource settings, more than 8 times that of children with suspected infection not meeting these criteria. Mortality was higher in children who had organ dysfunction in at least 1 of 4-respiratory, cardiovascular, coagulation, and/or neurological-organ systems that was not the primary site of infection. Septic shock was defined as children with sepsis who had cardiovascular dysfunction, indicated by at least 1 cardiovascular point in the Phoenix Sepsis Score, which included severe hypotension for age, blood lactate exceeding 5 mmol/L, or need for vasoactive medication. Children with septic shock had an in-hospital mortality rate of 10.8% and 33.5% in higher- and lower-resource settings, respectively. Conclusions and Relevance The Phoenix sepsis criteria for sepsis and septic shock in children were derived and validated by the international SCCM Pediatric Sepsis Definition Task Force using a large international database and survey, systematic review and meta-analysis, and modified Delphi consensus approach. A Phoenix Sepsis Score of at least 2 identified potentially life-threatening organ dysfunction in children younger than 18 years with infection, and its use has the potential to improve clinical care, epidemiological assessment, and research in pediatric sepsis and septic shock around the world.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Shock, Septic / Sepsis Type of study: Prognostic_studies Limits: Child / Humans Language: En Journal: JAMA Year: 2024 Document type: Article Affiliation country: Switzerland

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Shock, Septic / Sepsis Type of study: Prognostic_studies Limits: Child / Humans Language: En Journal: JAMA Year: 2024 Document type: Article Affiliation country: Switzerland
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