Continuing Ketogenic Diet Therapy in Setting of Hypercalcemia

ObjectiveHypercalcemia is an uncommon, serious adverse effect of ketogenic diet therapy (KDT). This case highlights the management of hypercalcemia without discontinuing KDT.MethodsOur case study involves a retrospective chart analysis of one patient who developed hypercalcemia during KDT for seizure management.ResultsA 16-year-old male patient with cerebral palsy and intractable epilepsy acutely developed hypercalcemia after receiving KDT for 5 years. Despite hydration and discontinuation of calcium supplementation, hypercalcemia persisted. He was treated with pamidronate 0.3 mg/kg (dose renally adjusted) followed by 0.03 mg/kg intravenous zoledronate with reduction in serum calcium levels. KDT was continued.ConclusionsStandardized guidelines for managing hypercalcemia in adolescent patients with chronic KDT do not exist. More research is needed to guide management and monitoring while preserving seizure control with KDT.

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Publication Details

Journal
Journal of Child Neurology
Published
2026-07-30
DOI
https://doi.org/10.1177/08830738261464415
Primary Topic
Diet and metabolism studies
Type
article
Field-Weighted Citation Impact
0.00

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article

Continuing Ketogenic Diet Therapy in Setting of Hypercalcemia

Erik Allen Imel, Jackson Sawyer, Leslie Sarabia, Abby Wetzel et al.
Journal of Child Neurology
Diet and metabolism studies
article

Continuing Ketogenic Diet Therapy in Setting of Hypercalcemia

Erik Allen Imel, Jackson Sawyer, Leslie Sarabia, Abby Wetzel, Sofia Giannini, Sarah Isis Delima
article en

Abstract

ObjectiveHypercalcemia is an uncommon, serious adverse effect of ketogenic diet therapy (KDT). This case highlights the management of hypercalcemia without discontinuing KDT.MethodsOur case study involves a retrospective chart analysis of one patient who developed hypercalcemia during KDT for seizure management.ResultsA 16-year-old male patient with cerebral palsy and intractable epilepsy acutely developed hypercalcemia after receiving KDT for 5 years. Despite hydration and discontinuation of calcium supplementation, hypercalcemia persisted. He was treated with pamidronate 0.3 mg/kg (dose renally adjusted) followed by 0.03 mg/kg intravenous zoledronate with reduction in serum calcium levels. KDT was continued.ConclusionsStandardized guidelines for managing hypercalcemia in adolescent patients with chronic KDT do not exist. More research is needed to guide management and monitoring while preserving seizure control with KDT.

Journal of Child Neurology
Riley Hospital for Children (US), Indiana University School of Medicine, Indiana University (US)
School of Medicine, Indiana University
Good health and well-being
Openalex Percentile: Top 10%
Diet and metabolism studies
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