Identifying and Validating Pediatric Hospitalizations for MIS-C Through Administrative Data

Author:

Auger Katherine A.123,Hall Matt4,Arnold Staci D.5,Bhumbra Samina6,Bryan Mersine A.78,Hartley David23,Ivancie Rebecca9,Katragadda Harita1011,Kazmier Katie7,Jacob Seethal A.12,Jerardi Karen E.13,Molloy Matthew J.1,Parikh Kavita1314,Schondelmeyer Amanda C.123,Shah Samir S.13,Brady Patrick W.123

Affiliation:

1. aDivision of Hospital Medicine

2. bJames M. Anderson Center for Health Systems Excellence, Cincinnati Children’s Hospital, Cincinnati, Ohio

3. cDepartment of Pediatrics, University of Cincinnati School of Medicine, Cincinnati, Ohio

4. dChildren’s Hospital Association, Lenexa, Kansas

5. eDepartment of Pediatrics, Emory University, Aflac Cancer and Blood Disorders Center at Children’s Healthcare of Atlanta, Atlanta, Georgia

6. fRyan White Center for Pediatric Infectious Disease and Global Health, Department of Pediatrics

7. gDepartment of Pediatrics, University of Washington, Seattle, Washington

8. hSeattle Children’s Research Institute, Seattle, Washington

9. iDepartment of Pediatrics, Stanford School of Medicine, Stanford, California

10. jDivision of Pediatric Hospital Medicine

11. kDepartment of Pediatrics, UT Southwestern, Dallas, Texas

12. lDivision of Pediatric Hematology Oncology, Indiana University School of Medicine, Indianapolis, Indiana

13. mDivision of Hospital Medicine, Children’s National Hospital, Washington, District of Columbia

14. nGeorge Washington University School of Health Sciences, Washington, District of Columbia

Abstract

BACKGROUND Individual children’s hospitals care for a small number of patients with multisystem inflammatory syndrome in children (MIS-C). Administrative databases offer an opportunity to conduct generalizable research; however, identifying patients with MIS-C is challenging. METHODS We developed and validated algorithms to identify MIS-C hospitalizations in administrative databases. We developed 10 approaches using diagnostic codes and medication billing data and applied them to the Pediatric Health Information System from January 2020 to August 2021. We reviewed medical records at 7 geographically diverse hospitals to compare potential cases of MIS-C identified by algorithms to each participating hospital’s list of patients with MIS-C (used for public health reporting). RESULTS The sites had 245 hospitalizations for MIS-C in 2020 and 358 additional MIS-C hospitalizations through August 2021. One algorithm for the identification of cases in 2020 had a sensitivity of 82%, a low false positive rate of 22%, and a positive predictive value (PPV) of 78%. For hospitalizations in 2021, the sensitivity of the MIS-C diagnosis code was 98% with 84% PPV. CONCLUSION We developed high-sensitivity algorithms to use for epidemiologic research and high-PPV algorithms for comparative effectiveness research. Accurate algorithms to identify MIS-C hospitalizations can facilitate important research for understanding this novel entity as it evolves during new waves.

Publisher

American Academy of Pediatrics (AAP)

Subject

Pediatrics, Perinatology and Child Health

Reference31 articles.

1. Centers for Disease Control and Prevention . Multisystem inflammatory syndrome (MIS-C). Available at: https://www.cdc.gov/mis-c/index.html. Accessed February 24, 2021

2. Clinical characteristics of 58 children with a pediatric inflammatory multisystem syndrome temporally associated with SARS-CoV-2;Whittaker;JAMA,2020

3. Multisystem inflammatory syndrome in children: an international survey;Bautista-Rodriguez;Pediatrics,2021

4. Multisystem inflammatory syndrome in infants <12 months of age, United States, May 2020-January 2021;Godfred-Cato;Pediatr Infect Dis J,2021

5. Multisystem inflammatory syndrome in children-United States, February 2020-July 2021;Miller;Clin Infect Dis,2022

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