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Management and outcomes in secondary diabetes among pediatric patients hospitalized with hemophagocytic lymphohistiocytosis

  • Cintya Schweisberger , Nila Palaniappan , Nicole M. Wood , Lauren E. Amos and Kelsee Halpin ORCID logo EMAIL logo

Abstract

Objectives

Hemophagocytic lymphohistiocytosis (HLH) is a life-threatening disorder marked by massive cytokine release from macrophage and T-cell activation. Hallmarks include fever, splenomegaly, cytopenias, hypertriglyceridemia, hypofibrinogemia, and elevations in ferritin and soluble IL-2 receptor. Given the association of HLH with inflammation and glucocorticoid therapy, the development of hyperglycemia is not unexpected. Descriptions of the prevalence of secondary diabetes in youth diagnosed with HLH are lacking.

Methods

Retrospective review from 2010 through 2019 of hospitalized youth 0–21 years diagnosed with HLH. The primary outcome of interest was the development of secondary diabetes, defined as a serum glucose 200 mg/dL or higher necessitating insulin therapy.

Results

Of 28 patients with HLH, 36 % (n=10) developed secondary diabetes. The only risk factor associated with secondary diabetes was an infectious cause of HLH (60 % vs. 27.8 %, p 0.041). Intravenous regular insulin was used in 80 % of patients with a mean duration of 9.5 days (2–24 days). Most (70 %) needed insulin within 5 days of starting steroids. Stays in the ICU were longer (median 20 vs. 3 days, p 0.007) and intubation more likely (90 vs. 45 %, p 0.041) among those with secondary diabetes. Mortality was high (16–30 %) regardless of insulin use (p 0.634).

Conclusions

One-third of hospitalized pediatric patients with HLH developed secondary diabetes requiring insulin therapy. Insulin is typically started within 5 days of initiating steroids, limited to IV infusions, and often is not needed by discharge. Secondary diabetes was associated with longer ICU stays and heightened risk of intubation.


Corresponding author: Kelsee Halpin, MD, MPH, Division of Endocrinology and Diabetes, Children’s Mercy Kansas City, 3101 Broadway Blvd. Suite 900, Kansas City, MO 64111, USA; and University of Missouri-Kansas City School of Medicine, Kansas City, MO, USA, E-mail:

Acknowledgments

We would like to acknowledge Mary Verner whose expertise in data retrieval was vital to successful study completion.

  1. Research funding: None declared.

  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: The study was approved by the Children’s Mercy Kansas City Institutional Review Board including a waiver of the need for informed consent/assent due to the retrospective nature of the research.

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Received: 2023-05-09
Accepted: 2023-05-23
Published Online: 2023-06-05
Published in Print: 2023-07-26

© 2023 Walter de Gruyter GmbH, Berlin/Boston

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