Skip to main content
Case Reports in Endocrinology logoLink to Case Reports in Endocrinology
. 2021 Jul 30;2021:3286274. doi: 10.1155/2021/3286274

Vitamin D Intoxication and Nephrocalcinosis in a Young Breastfed Infant

Abdullah Al-Kandari 1,, Hussain Sadeq 1, Rita Alfattal 1, Maryam AlRashid 2, Mayra Alsaeid 3
PMCID: PMC8349280  PMID: 34373793

Abstract

Numerous studies were performed assessing the benefits and side effects of vitamin D. Vitamin D helps in regulating the calcium and phosphate metabolism leading to a healthy mineral and bone development. Vitamin D intoxication is an uncommon event that leads to hypercalcemia which can be associated with both immediate and late morbidities that can cause severe renal complications. Here, we present a case of a 4-month-old girl with a history of decreased feed and activity due hypercalcemia and high vitamin D level, which led to nephrocalcinosis. The patient received IV fluids, IV diuretics, methylprednisolone, and bisphosphonate in order to normalize the calcium level in blood. With clear verbal and written instructions for the dosage and administration of vitamin D supplements, as well as clear warnings of the potential risks of overdose, vitamin D intoxication could be an easily avoidable condition.

1. Introduction

In the past decade, several studies focusing on the benefits of vitamin D have been reported [15]. Vitamin D is an essential hormone in the human body that regulates calcium homeostasis and prevents the development of rickets [68]. Vitamin D intoxication is an uncommon event that leads to hypercalcemia, which is associated with both immediate and late morbidities that can cause severe renal complications [915]. Recently, there have been several case reports of vitamin D toxicity in very young infants due to vitamin D overdose [10, 12]. The present case study reports an infant who developed acute hypercalcemia and nephrocalcinosis after prolonged administration of an overdose of over-the-counter vitamin D supplements by the mother. Over-the-counter drugs are safe when used properly as directed by the pharmacist; however, misuse or miscommunication can lead to a rare devastating consequence, such as our report.

2. Case Presentation

A 4-month-old girl was brought to the emergency department with a history of lethargy, decreased feeding, and constipation for more than a month. On examination, the patient exhibited signs of moderate dehydration such as dry skin, poor skin turgor, and decreased urine output although initial vital signs were within normal limit (heart rate was 122 beats per minute, respiratory rate was 38 respiration per minute, and blood pressure was 90/60 mmHg). Routine investigations performed in the emergency department identified a high corrected calcium level (5.60 mmol/L; normal range: 2.25–2.75). Upon further questioning of the parents, it became apparent that the girl had been receiving an excessive dose of vitamin D supplementation. The patient had been receiving a full 1 mL dropper of an over-the-counter vitamin D supplement (1 mL dose equal to 5000 IU) three times a day on a daily basis, for a one-month period, instead of the intended dose of three drops once per day (three drops dose equals to 400 IU). Parents are highly educated with excellent socioeconomic status; however, miscommunication with the pharmacist regarding the dosage led to this mistake. This unfortunate event led the patient to present with vitamin D intoxication, with the blood test for vitamin 25-hydroxyvitamin D (25(OH)D) levels showing a level of 350 nmol/L (critical level: >250 nmol/L).

The infant was admitted to a general pediatric ward for further management of calcium and vitamin D levels. She was put on intravenous (IV) fluids containing normal saline and dextrose at rate of 28 ml/hour, which equals to 150 ml/kg/day. She also received 1 mg/kg furosemide IV divided into three doses per day along with the 3-day IV course of 0.3 mg/kg methylprednisolone once daily. Furthermore, the patient was fed with low calcium formula milk (Nutricia™ Kindergen).

As part of the routine assessment of hypercalcemia and vitamin D toxicity, various laboratory and radiological investigations were performed to assess the extent of the toxicity on the patient's renal system. Both serum creatinine and urea were normal upon admission, 32 umol/L (normal range: 11–34 umol/L) and 5.9 mmol/L (normal range: 1.8–6.4 mmol/L), respectively. Urine analysis was performed as well and showed no abnormal parameters. However, urine calcium (mmol/L) to urine creatinine (mmol/L) ratio was significantly abnormal (6.17; normal range: 0.08–0.57). Additionally, an abdominal ultrasound was performed, showing evidence of nephrocalcinosis (Figure 1).

Figure 1.

Figure 1

Ultrasound image of patient's right kidney showing echogenic medullary pyramids suggestive of nephrocalcinosis.

Furosemide (1 mg/kg/dose three times per day) was replaced with thiazide (1 mg/kg/dose twice per day) on day 3 of admission, and potassium citrate (1 mmol dose three times per day) was administered to reduce the risk of exacerbating the existing nephrocalcinosis.

The rate of reduction of the corrected calcium level was unsatisfactory, as on day 4 of admission, the level remained high at 4.17 mmol/L. At this point, bisphosphonate therapy was initiated, with two doses given (first dose of 0.5 mg/kg and second dose of 1 mg/kg).

On day 9 of admission, the corrected calcium level was 3.44 mmol/L, and the clinical condition of the patient had improved in terms of feeding and physical activity level. At the point of discharge after 10 days in the hospital, the patient's corrected calcium level had reduced to 2.96 mmol/L. The patient was discharged with a prescription of low calcium milk formula and potassium citrate (0.5 mmol three times per day). Furthermore, follow-up appointments with an endocrinologist and nephrologist were also given. Summary of daily laboratory results is gathered and presented in Table 1.

Table 1.

Summary of daily laboratory results during patient's hospital stay.

Day/lab. Ca (mmol/L), NR: 2.25–2.75 PO4 (mmol/L), NR: 0.81–2.26 BUN (mmol/L), NR: 1.8–6.4 Cr (umol/L), NR: 11–34 Urine Ca : Cr ratio, NR: 0.08–0.57
Day 1 5.60 1.28 5.9 32 6.17
Day 2 4.69 1.23 4.8 28 9.83
Day 3 4.42 1.05 2.9 29
Day 4 4.17 1.28 2.2 29
Day 5 4.33 1.22 1.9 33 2.58
Day 6 3.92 1.20 1.6 30
Day 7 4.19 1.30 2.6 31
Day 8 4.14 1.12 2.8 31
Day 9 3.44 0.85 1.0 24 2.71
Day 10 2.96 0.84 <0.8 26

NR, normal range.

3. Discussion

Although breastfeeding remains the best source of infant nutrition, breast milk can lack adequate amounts of vitamin D [10, 16]. The American Academy of Pediatrics (AAP) recommends the provision of vitamin D supplements to any breastfed infant to avoid the risk of developing nutritional vitamin D deficiency, also known as nutritional rickets [10]. Guidelines issued by the AAP and the National Academy of Sciences indicate that all breastfeeding and nonbreastfeeding infants who drink <500 ml per day should receive 20 IU of vitamin D supplement per day [17]. Over-the-counter vitamin D supplements are easily and readily available [18]. The inappropriate administration of high doses of vitamin D in infants are typically provided by families for complaints such as delayed teething, late walking, and knock-knee gait [9]. Without appropriate instructions on dosing and administration, a significant risk of vitamin D toxicity exists [13, 18]. The Endocrine Society states that vitamin D toxicity is defined as 25(OH)D concentrations exceeding 375 nmol/L [19], with levels above this toxic threshold associated with the onset of hypercalcemia [1921]. Signs and symptoms of vitamin D intoxication are directly related to the effects of hypercalcemia [17, 20, 22], including decreased oral intake, nausea, vomiting, constipation, weakness, lethargy, and generalized malaise [17, 20, 21]. Hypercalcemia and vitamin D toxicity can lead to serious complications including renal failure, hypertension, and nephrocalcinosis [17, 23, 24]. Medullary nephrocalcinosis can be detected by ultrasound [9]. Nephrocalcinosis is a common pathological condition, characterized by hypercalciuria and/or hypercalcemia, with only 10% of cases caused by vitamin D intoxication [9]. Treatment for vitamin D toxicity usually involves removal of the exogenous source, intravenous fluid hydration, diuretics, a low-calcium diet, the administration of steroids, bisphosphonate therapy, and sometimes, renal dialysis [6, 2325].

4. Conclusions and Recommendations

With clear verbal and written instructions for the dosage and administration of vitamin D supplements, as well as clear warnings of the potential risks of overdose, vitamin D intoxication could be an easily avoidable condition. Parents should also be advised to carefully read the instructions provided for any over-the-counter vitamin D supplements. Moreover, the inclusion of proper medication reconciliation with each visit to a pediatric clinic could help parents to avoid this type of mistake.

Acknowledgments

The authors' thank and convey their best regards to the Pediatrics Department of Amiri Hospital's nurses and to the parents of the patient.

Conflicts of Interest

The authors declare that they have no conflicts of interest.

References

  • 1.Vogiatzi M. G., Jacobson-Dickman E., DeBoer M. D. Vitamin D supplementation and risk of toxicity in pediatrics: a review of current literature. The Journal of Clinical Endocrinology and Metabolism. 2014;99(4):1132–1141. doi: 10.1210/jc.2013-3655. [DOI] [PubMed] [Google Scholar]
  • 2.Kimball S., Fuleihan G. E.-H., Vieth R. Vitamin D: a growing perspective. Critical Reviews in Clinical Laboratory Sciences. 2008;45(4):339–414. doi: 10.1080/10408360802165295. [DOI] [PubMed] [Google Scholar]
  • 3.Holick M. F. The D-lightful vitamin D for child health. JPEN. Journal of Parenteral and Enteral Nutrition. 2012;36(1 Suppl):9s–19s. doi: 10.1177/0148607111430189. [DOI] [PubMed] [Google Scholar]
  • 4.Alshahrani F., Aljohani N. Vitamin D: deficiency, sufficiency and toxicity. Nutrients. 2013;5(9):3605–3616. doi: 10.3390/nu5093605. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Pandita K. K., Razdan S., Kudyar R. P., Beigh A., Kuchay S., Banday T. “Excess good can be dangerous”. A case series of iatrogenic symptomatic hypercalcemia due to hypervitaminosis D. Clinical Cases in Mineral and Bone Metabolism. 2012;9(2):p. 118. [PMC free article] [PubMed] [Google Scholar]
  • 6.Chatterjee M., Speiser P. W. Pamidronate treatment of hypercalcemia caused by vitamin D toxicity. Journal of Pediatric Endocrinology and Metabolism. 2007;20(11):1241–1248. doi: 10.1515/jpem.2007.20.11.1241. [DOI] [PubMed] [Google Scholar]
  • 7.Jazayeri M., Moradi Y., Rasti A., Nakhjavani M., Kamali M., Baradaran H. R. Prevalence of vitamin D deficiency in healthy Iranian children: a systematic review and meta-analysis. Medical Journal of the Islamic Republic of Iran. 2018;32:p. 83. doi: 10.14196/mjiri.32.83. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Makariou S., Liberopoulos E. N., Elisaf M., Challa A. Novel roles of vitamin D in disease: what is new in 2011? European Journal of Internal Medicine. 2011;22(4):355–362. doi: 10.1016/j.ejim.2011.04.012. [DOI] [PubMed] [Google Scholar]
  • 9.Talarico V., Barreca M, Galiano R, Galati M. C, Raiola G. Vitamin D and risk for vitamin A intoxication in an 18-month-old boy. Case Reports in Pediatrics. 2016;2016 doi: 10.1155/2016/1395718.1395718 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Bilbao N. A. Vitamin D toxicity in young breastfed infants: report of 2 cases. Global Pediatric Health. 2017;4 doi: 10.1177/2333794X17731695.2333794x17731695 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Kaptein S., Risselada A. J., Boerma E. C., Egbers P. H. M., Nieboer P. Life-threatening complications of vitamin D intoxication due to over-the-counter supplements. Clinical Toxicology. 2010;48(5):460–462. doi: 10.3109/15563650.2010.486382. [DOI] [PubMed] [Google Scholar]
  • 12.Araki T., Holick M. F., Alfonso B. D., et al. Vitamin D intoxication with severe hypercalcemia due to manufacturing and labeling errors of two dietary supplements made in the United States. The Journal of Clinical Endocrinology & Metabolism. 2011;96(12):3603–3608. doi: 10.1210/jc.2011-1443. [DOI] [PubMed] [Google Scholar]
  • 13.Anık A., Çatlı G., Abacı A., Dizdarer C., Böber E. Acute vitamin D intoxication possibly due to faulty production of a multivitamin preparation. Journal of Clinical Research in Pediatric Endocrinology. 2013;5(2):136–9. doi: 10.4274/Jcrpe.896. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Kaur P., Mishra S. K., Mithal A. Vitamin D toxicity resulting from overzealous correction of vitamin D deficiency. Clinical Endocrinology. 2015;83(3):327–331. doi: 10.1111/cen.12836. [DOI] [PubMed] [Google Scholar]
  • 15.Bell D. A., Crooke M. J., Hay N., Glendenning P. Prolonged vitamin D intoxication: presentation, pathogenesis and progress. Internal Medicine Journal. 2013;43(10):1148–1150. doi: 10.1111/imj.12269. [DOI] [PubMed] [Google Scholar]
  • 16.Dawodu A., Tsang R. C. Maternal vitamin D status: effect on milk vitamin D content and vitamin D status of breastfeeding infants. Advances in Nutrition. 2012;3(3):353–361. doi: 10.3945/an.111.000950. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Barrueto F. Acute vitamin D intoxication in a child. Pediatrics. 2005;116(3):e453–e456. doi: 10.1542/peds.2004-2580. [DOI] [PubMed] [Google Scholar]
  • 18.Taylor P. N., Davies J. S. A review of the growing risk of vitamin D toxicity from inappropriate practice. British Journal of Clinical Pharmacology. 2018;84(6):1121–1127. doi: 10.1111/bcp.13573. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Holick M. F., Binkley N. C., Bischoff-Ferrari H. A., et al. Evaluation, treatment, and prevention of vitamin D deficiency: an Endocrine Society clinical practice guideline. The Journal of Clinical Endocrinology and Metabolism. 2011;96(7):1911–1930. doi: 10.1210/jc.2011-0385. [DOI] [PubMed] [Google Scholar]
  • 20.Marcinowska-Suchowierska E., Kupisz-Urbańska M., Łukaszkiewicz J., Płudowski P., Jones G. Vitamin D toxicity-A clinical perspective. Frontiers in Endocrinology. 2018;9:p. 550. doi: 10.3389/fendo.2018.00550. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Cusano N. E., Thys-Jacobs S., Bilezikian J. P. Vitamin D. Elsevier; 2018. Hypercalcemia due to vitamin D toxicity; pp. 507–526. [DOI] [Google Scholar]
  • 22.Guerra V., Vieira Neto O. M., Laurindo A. F., Paula F. J., Moysés Neto M. Hypercalcemia and renal function impairment associated with vitamin D toxicity: case report. Jornal brasileiro de nefrologia : ’orgao oficial de Sociedades Brasileira e Latino-Americana de Nefrologia. 2016;38(4):466–469. doi: 10.5935/0101-2800.20160074. [DOI] [PubMed] [Google Scholar]
  • 23.Nimesh M. An unsuspected pharmacological vitamin D toxicity in a child and its brief review of literature. Toxicol Int. 2015;22:167–169. doi: 10.4103/0971-6580.172284. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Çağlar A., Tuğçe Çağlar H. Vitamin D intoxication due to misuse: 5 year experience. Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 2021;28(3):222–225. doi: 10.1016/j.arcped.2020.12.009. [DOI] [PubMed] [Google Scholar]
  • 25.Conti G., Chirico V, Lacquaniti A, et al. Vitamin D intoxication in two brothers: be careful with dietary supplements. Journal of Pediatric Endocrinology & Metabolism : JPEM. 2014;27(7-8):763–767. doi: 10.1515/jpem-2013-0220. [DOI] [PubMed] [Google Scholar]

Articles from Case Reports in Endocrinology are provided here courtesy of Wiley

RESOURCES