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Predicting Adverse Outcomes for Shiga Toxin–Producing Escherichia coli Infections in Emergency Departments - 22/04/21

Doi : 10.1016/j.jpeds.2020.12.077 
Chu Yang Lin, BMedSci 1, Jianling Xie, MD, MPH 2, Stephen B. Freedman, MDCM, MSc 3, Ryan S. McKee, MD 4, David Schnadower, MD, MPH 5, Phillip I. Tarr, MD 6, Yaron Finkelstein, MD 7, Neil M. Desai, MBBCh 8, Roni D. Lane, MD 9, Kelly R. Bergmann, DO, MS 10, Ron L. Kaplan, MD 11, Selena Hariharan, MD, MHSA 5, Andrea T. Cruz, MD, MPH 12, Daniel M. Cohen, MD 13, Andrew Dixon, MD 14, Sriram Ramgopal, MD 15, Elizabeth C. Powell, MD, MPH 15, Jennifer Kilgar, MD 16, Kenneth A. Michelson, MD, MPH 17, Martin Bitzan, MD 18, 19, Kenneth Yen, MD, MS 20, Garth D. Meckler, MD, MSHS 21, Amy C. Plint, MD, MSc 22, Fran Balamuth, MD, PhD, MSCE 23, Stuart Bradin, DO 24, Serge Gouin, MDCM 25, April J. Kam, MD, MScPH 26, James A. Meltzer, MD, MS 27, Tracy E. Hunley, MD 28, Usha Avva, MD 29, Robert Porter, MD, MSc 30, Daniel M. Fein, MD 31, Jeffrey P. Louie, MD 32, Gillian A.M. Tarr, PhD 33,
on behalf of

Pediatric Emergency Research Canada (PERC) and Pediatric Emergency Medicine Collaborative Research Committee (PEMCRC) STEC Study Group

  List of additional members of the Pediatric Emergency Research Canada (PERC) and Pediatric Emergency Medicine Collaborative Research Committee (PEMCRC) STEC Study Group is available at www.jpeds.com (Appendix 1).
Annie Rominger, MD, Darcy Beer, MD, Christopher M. Pruitt, MD, Thomas J. Abramo, MD, Abigail Schuh, MD, John T. Kanegaye, MD, Nicholas E. Jones, MD

1 Faculty of Medicine and Dentistry, University of Alberta, Edmonton, Alberta, Canada 
2 Section of Pediatric Emergency Medicine, Department of Pediatric, Alberta Children's Hospital, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada 
3 Section of Pediatric Gastroenterology, Department of Pediatrics, Alberta Children's Hospital and Alberta Children's Hospital Research Institute, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada 
4 Section of Pediatric Emergency Medicine, Department of Pediatrics, University of Oklahoma Health Sciences Center, Oklahoma City, OK 
5 Division of Emergency Medicine, Cincinnati Children's Hospital Medical Center, and Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH 
6 Division of Gastroenterology, Hepatology, & Nutrition, Department of Pediatrics, Washington University in St Louis, School of Medicine, St Louis, MO 
7 Divisions of Emergency Medicine and Clinical Pharmacology & Toxicology, Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada 
8 Division of Pediatric Emergency Medicine, British Columbia Children's Hospital, Vancouver, British Columbia, Canada 
9 Division of Pediatric Emergency Medicine, University of Utah School of Medicine, Salt Lake City, UT 
10 Department of Emergency Medicine, Children's Minnesota, Minneapolis, MN 
11 Department of Pediatrics, Division of Emergency Medicine, University of Washington School of Medicine, Seattle Children's Hospital, Seattle, WA 
12 Pediatric Emergency Medicine and Pediatric Infectious Diseases, Baylor College of Medicine, Houston, TX 
13 Nationwide Children's Hospital & The Ohio State University, Columbus, OH 
14 University of Alberta, Stollery Children's Hospital, Women's and Children's Health Research Institute, Edmonton, Alberta, Canada 
15 Division of Emergency Medicine, Ann & Robert H. Lurie Children's Hospital of Chicago, Northwestern University Feinberg School of Medicine, Chicago, IL 
16 Department of Pediatrics, Schulich School of Medicine and Dentistry, London, Ontario, Canada 
17 Division of Emergency Medicine, Boston Children's Hospital, Boston, MA 
18 Division of Nephrology, Montreal Children's Hospital, McGill University Health Centre, Montreal, Canada 
19 Al Jalila Children's Hospital, Kidney Centre of Excellence, Dubai, United Arab Emirates 
20 Pediatric Emergency Medicine, Children's Medical Center, UT Southwestern, Dallas, TX 
21 Pediatrics and Emergency Medicine, University of British Columbia, Vancouver, British Columbia, Canada 
22 Departments of Pediatrics and Emergency Medicine, University of Ottawa and the Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada 
23 Department of Pediatrics, University of Pennsylvania Perelman School of Medicine, Division of Emergency Medicine, Children's Hospital of Philadelphia, Philadelphia, PA 
24 Children's Emergency Services, Department of Emergency Medicine, University of Michigan Medical School, Ann Arbor, MI 
25 Departments of Pediatric Emergency Medicine & Pediatrics, CHU Sainte-Justine, Universite de Montreal, Quebec, Canada 
26 Department of Pediatrics, McMaster Children's Hospital, McMaster University, Hamilton, Ontario, Canada 
27 Division of Emergency Medicine, Department of Pediatrics, Jacobi Medical Center, Bronx, NY 
28 Division of Pediatric Nephrology, Monroe Carell Jr Children's Hospital at Vanderbilt, Nashville, TN 
29 Department of Pediatrics, Joseph M. Sanzari Women and Children's Hospital, Hackensack University Medical Center, Hackensack, NJ 
30 Discipline of Pediatrics, Memorial University of Newfoundland, St John's, Newfoundland, Canada 
31 Division of Pediatric Emergency Medicine, Department of Pediatrics, Children's Hospital at Montefiore, Albert Einstein College of Medicine, Bronx, NY 
32 Division of Emergency Medicine, University of Minnesota, Masonic Children's Hospital, Minneapolis, MN 
33 Division of Environmental Health Sciences, University of Minnesota, Minneapolis, MN 

Reprint requests: Gillian A. M. Tarr, PhD, University of Minnesota, MMC 807, Room 1240, 420 Delaware St SE, Minneapolis, MN 55455University of MinnesotaMMC 807, Room 1240420 Delaware St SEMinneapolisMN55455

Abstract

Objective

To assess the performance of a hemolytic uremic syndrome (HUS) severity score among children with Shiga toxin-producing Escherichia coli (STEC) infections and HUS by stratifying them according to their risk of adverse events. The score has not been previously evaluated in a North American acute care setting.

Study design

We reviewed medical records of children <18 years old infected with STEC and treated in 1 of 38 participating emergency departments in North America between 2011 and 2015. The HUS severity score (hemoglobin [g/dL] plus 2-times serum creatinine [mg/dL]) was calculated using first available laboratory results. Children with scores >13 were designated as high-risk. We assessed score performance to predict severe adverse events (ie, dialysis, neurologic complication, respiratory failure, and death) using discrimination and net benefit (ie, threshold probability), with subgroup analyses by age and day-of-illness.

Results

A total of 167 children had HUS, of whom 92.8% (155/167) had relevant data to calculate the score; 60.6% (94/155) experienced a severe adverse event. Discrimination was acceptable overall (area under the curve 0.71, 95% CI 0.63-0.79) and better among children <5 years old (area under the curve 0.77, 95% CI 0.68-0.87). For children <5 years, greatest net benefit was achieved for a threshold probability >26%.

Conclusions

The HUS severity score was able to discriminate between high- and low-risk children <5 years old with STEC-associated HUS at a statistically acceptable level; however, it did not appear to provide clinical benefit at a meaningful risk threshold.

Le texte complet de cet article est disponible en PDF.

Keywords : hemolytic uremic syndrome, prognostic index, stx1, stx2

Abbreviations : AUC, DCA, ED, HUS, PEMCRC, PERC, STEC


Plan


 Affiliations, Funding and disclosure information is available at www.jpeds.com.


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Vol 232

P. 200 - mai 2021 Retour au numéro
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