The incidence of cerebral edema in pediatric patients with diabetic ketoacidosis: a retrospective study
- PMID: 40205526
- PMCID: PMC11983962
- DOI: 10.1186/s13104-025-07237-9
The incidence of cerebral edema in pediatric patients with diabetic ketoacidosis: a retrospective study
Abstract
Objective: Cerebral edema is a severe and potentially fatal complication of diabetic ketoacidosis (DKA), particularly in pediatric patients. Despite its clinical significance, limited data exist on its incidence and associated risk factors in resource-limited settings. This study aimed to determine the incidence of cerebral edema in pediatric patients with DKA and investigate potential contributing factors. This retrospective study analyzed data from 270 pediatric DKA patients admitted to the Children's Medical Center Hospital, Tehran, between March 2018 and March 2020. Patients aged 1 day to 18 years were included based on standard DKA diagnostic criteria (blood glucose > 250 mg/dL, pH < 7.3, bicarbonate < 18 mEq/L, and ketonemia/ketonuria). Patients with incomplete records or pre-existing neurological conditions were excluded. The statistical analyses included independent t-tests and Fisher's exact tests.
Results: The incidence of cerebral edema was 6.67%. Elevated blood glucose levels at admission were significantly associated with cerebral edema (P = 0.01), suggesting a potential role in its pathophysiology. Additionally, a strong correlation was observed between cerebral edema and ICU admission (P < 0.001), indicating a more severe disease course. The results suggest that early glucose control and neurological monitoring are critical for preventing adverse outcomes such as cerebral edema in pediatric DKA patients.
Keywords: Cerebral edema; Diabetic ketoacidosis; Hyperglycemia; Pediatric.
© 2025. The Author(s).
Conflict of interest statement
Declarations. Ethics approval and consent to participate: Ethical approval for this study was obtained from the Ethics Committee of Tehran University of Medical Sciences (Approval No. IR.TUMS.CHMC.REC.1399.035). The research was conducted in compliance with the ethical guidelines set forth in the Declaration of Helsinki. Due to the retrospective nature of the study, informed consent to participate was not obtained from the participants. The need for informed consent was waived by the Ethics Committee, as the study involved the use of anonymized patient data collected as part of routine clinical care, with no identifying information recorded. All patient data were anonymized to maintain confidentiality. Consent for publication: Not applicable. Competing interests: The authors declare no competing interests. Clinical trial number: Not applicable.
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