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Identifying and Validating Pediatric Hospitalizations for MIS-C Through Administrative Data.
Auger, Katherine A; Hall, Matt; Arnold, Staci D; Bhumbra, Samina; Bryan, Mersine A; Hartley, David; Ivancie, Rebecca; Katragadda, Harita; Kazmier, Katie; Jacob, Seethal A; Jerardi, Karen E; Molloy, Matthew J; Parikh, Kavita; Schondelmeyer, Amanda C; Shah, Samir S; Brady, Patrick W.
Affiliation
  • Auger KA; Division of Hospital Medicine.
  • Hall M; James M. Anderson Center for Health Systems Excellence, Cincinnati Children's Hospital, Cincinnati, Ohio.
  • Arnold SD; Department of Pediatrics, University of Cincinnati School of Medicine, Cincinnati, Ohio.
  • Bhumbra S; Children's Hospital Association, Lenexa, Kansas.
  • Bryan MA; Department of Pediatrics, Emory University, Aflac Cancer and Blood Disorders Center at Children's Healthcare of Atlanta, Atlanta, Georgia.
  • Hartley D; Ryan White Center for Pediatric Infectious Disease and Global Health, Department of Pediatrics.
  • Ivancie R; Department of Pediatrics, University of Washington, Seattle, Washington.
  • Katragadda H; Seattle Children's Research Institute, Seattle, Washington.
  • Kazmier K; James M. Anderson Center for Health Systems Excellence, Cincinnati Children's Hospital, Cincinnati, Ohio.
  • Jacob SA; Department of Pediatrics, University of Cincinnati School of Medicine, Cincinnati, Ohio.
  • Jerardi KE; Department of Pediatrics, Stanford School of Medicine, Stanford, California.
  • Molloy MJ; Division of Pediatric Hospital Medicine.
  • Parikh K; Department of Pediatrics, UT Southwestern, Dallas, Texas.
  • Schondelmeyer AC; Department of Pediatrics, University of Washington, Seattle, Washington.
  • Shah SS; Division of Pediatric Hematology Oncology, Indiana University School of Medicine, Indianapolis, Indiana.
  • Brady PW; Division of Hospital Medicine.
Pediatrics ; 151(5)2023 05 01.
Article in En | MEDLINE | ID: mdl-37102310
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.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Medical Records / Hospitalization Type of study: Prognostic_studies Limits: Child / Humans Language: En Journal: Pediatrics Year: 2023 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Medical Records / Hospitalization Type of study: Prognostic_studies Limits: Child / Humans Language: En Journal: Pediatrics Year: 2023 Document type: Article