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Endocrine Abstracts (2015) 39 EP21 | DOI: 10.1530/endoabs.39.EP21

BSPED2015 e-Posters Bone (9 abstracts)

Safe prescribing: vitamin D toxicity as a result of inadvertent overdose

Malathi Kurre , Priya Ramaswamy , Evelien Pease-Gevers & Jeremy Allgrove


Barts Health NHS Trust, London, UK.


Introduction: Prevalence of vitamin D deficiency is well recognised and public awareness is being raised to encourage intake of vitamin D supplements. Optimal serum concentration of 25OHD for bone and general health has not been established. Desirable serum concentration of 25OHD had been proposed as >75 nmol/l and levels above 500 nmol/l are deemed toxic. Guidance is available on tolerable upper limit of vitamin D intake by US Institute of Medicine.

Case report: A 4-year-old boy presented with a history of vomiting, polydipsia, polyuria, weight loss, and worsening constipation. He had been taking a number of holistic medications including vitamin D and calcium supplements to help with his autism. Corrected calcium at presentation was 4.08 mmol/l, with low PTH of 0.6 pmol/l and undetectably high 25OH vitamin D level on the standard assay. He was initially managed with hyperhydration, calcitonin, and furosemide. Calcium level dropped to 3.15 mmol/l, however, there was a rebound rise in calcium levels and he was treated with pamidronate infusions. After 12 days of treatment, calcium level came down to 2.18 mmol/l. Results obtained by diluting initial blood sample revealed a very high 25OH vitamin D level of 1890 nmol/l. Further investigations revealed a normal MRI brain and mild nephrocalcinosis on USS of kidneys.

On further exploration, we discovered that he was prescribed one drop a day of concentrated solution of colecalciferol containing 2000 IU/drop but the child was being given at least 1 ml a day for 4 months, which amounts to 40 000 IU/day.

Conclusion: Though vitamin D toxicity is a rare occurrence, it is mainly due to inadvertent use of very high doses of vitamin D. When prescribing concentrated solutions, the dosage and risks should be carefully explained.

Volume 39

43rd Meeting of the British Society for Paediatric Endocrinology and Diabetes

British Society for Paediatric Endocrinology and Diabetes 

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