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Multicenter evaluation of a method to identify delayed diagnosis of diabetic ketoacidosis and sepsis in administrative data

  • Kenneth A. Michelson ORCID logo EMAIL logo , Richard G. Bachur , Andrea T. Cruz , Joseph A. Grubenhoff , Scott D. Reeves , Pradip P. Chaudhari , Michael C. Monuteaux , Arianna H. Dart and Jonathan A. Finkelstein
Published/Copyright: June 22, 2023

Abstract

Objectives

To derive a method of automated identification of delayed diagnosis of two serious pediatric conditions seen in the emergency department (ED): new-onset diabetic ketoacidosis (DKA) and sepsis.

Methods

Patients under 21 years old from five pediatric EDs were included if they had two encounters within 7 days, the second resulting in a diagnosis of DKA or sepsis. The main outcome was delayed diagnosis based on detailed health record review using a validated rubric. Using logistic regression, we derived a decision rule evaluating the likelihood of delayed diagnosis using only characteristics available in administrative data. Test characteristics at a maximal accuracy threshold were determined.

Results

Delayed diagnosis was present in 41/46 (89 %) of DKA patients seen twice within 7 days. Because of the high rate of delayed diagnosis, no characteristic we tested added predictive power beyond the presence of a revisit. For sepsis, 109/646 (17 %) of patients were deemed to have a delay in diagnosis. Fewer days between ED encounters was the most important characteristic associated with delayed diagnosis. In sepsis, our final model had a sensitivity for delayed diagnosis of 83.5 % (95 % confidence interval 75.2–89.9) and specificity of 61.3 % (95 % confidence interval 56.0–65.4).

Conclusions

Children with delayed diagnosis of DKA can be identified by having a revisit within 7 days. Many children with delayed diagnosis of sepsis may be identified using this approach with low specificity, indicating the need for manual case review.


Corresponding author: Kenneth A. Michelson, MD, MPH, Division of Emergency Medicine, Boston Children’s Hospital, 300 Longwood Ave, BCH 3066, Boston, MA 02115, USA, E-mail:

Award Identifier / Grant number: K08HS026503

Award Identifier / Grant number: N/A

  1. Research funding: Dr. Michelson received funding through award K08HS026503 from the Agency for Healthcare Research and Quality, and from the Boston Children’s Hospital Office of Faculty Development.

  2. Author contributions: All authors have accepted responsibility for the entire content of this manuscript and approved its submission.

  3. Competing interests: Authors state no conflict of interest.

  4. Informed consent: Not applicable.

  5. Ethical approval: This study was approved by each site’s Institutional Review Board and complied with the World Medical Association Declaration of Helsinki regarding ethical conduct of research involving human subjects.

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Supplementary Material

This article contains supplementary material (https://doi.org/10.1515/dx-2023-0019).


Received: 2023-02-16
Accepted: 2023-06-07
Published Online: 2023-06-22

© 2023 Walter de Gruyter GmbH, Berlin/Boston

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