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Hypocalcaemia is low calcium levels in the blood serum.[1] The normal range is 2.1–2.6 mmol/L (8.8–10.7 mg/dl, 4.3–5.2 mEq/L) with levels less than 2.1 mmol/l defined as hypocalcemia.[2][3][4] Mildly low levels that develop slowly often have no symptoms.[5][6] Otherwise symptoms may include numbness, muscle spasms, seizures, confusion, or cardiac arrest.[2][5]

Common causes include hypoparathyroidism and vitamin D deficiency.[5] Others causes include kidney failure, pancreatitis, calcium channel blocker overdose, rhabdomyolysis, tumor lysis syndrome, and medications such as bisphosphonates.[2] Diagnosis should generally be confirmed with a corrected calcium or ionized calcium level.[5] Specific changes may be seen on an electrocardiogram (ECG).[2]

Initial treatment for severe disease is with intravenous calcium chloride and possibly magnesium sulfate.[2] Other treatments may include vitamin D, magnesium, and calcium supplements.[5] If due to hypoparathyroidism, hydrochlorothiazide, phosphate binders, and a low salt diet may also be recommended.[5] About 18% of people who are being treated in hospital have hypocalcemia.[6]

Signs and symptoms[edit]


The neuromuscular symptoms of hypocalcemia are caused by a positive bathmotropic effect (i.e. increased responsiveness) due to the decreased interaction of calcium with sodium channels. Since calcium blocks sodium channels and inhibits depolarization of nerve and muscle fibers, reduced calcium lowers the threshold for depolarization.[7] The symptoms can be recalled by the mnemonic "CATs go numb" - convulsions, arrhythmias, tetany, and numbness in the hands and feet and around the mouth.


Hypoparathyroidism is a common cause of hypocalcemia.[9] Calcium is tightly regulated by the parathyroid hormone (PTH). In response to low calcium levels, PTH levels rise, and conversely if there are high calcium levels then PTH secretion declines.[10] However, in the setting of absent, decreased, or ineffective PTH hormone, the body loses this regulatory function, and hypocalcemia ensues. Hypoparathyroidism is commonly due to surgical destruction of the parathyroid glands.[9] Hypoparathyroidism may also be due to autoimmune problem.[11][12] Some causes of hypocalcaemia are as follows:

  • Gain of function mutations of the calcium-sensing receptor
  • Foscarnet use
  • Loop diuretic use
  • Crohn disease
  • High level of lactic acid in the blood
  • Pseudohypoparathyroidism


Physiologically, blood calcium is tightly regulated within a narrow range for proper cellular processes. Calcium in the blood exists in three primary states: bound to proteins (mainly albumin), bound to anions such as phosphate and citrate, and as free (unbound) ionized calcium. Only the ionized calcium is physiologically active. Normal blood calcium level is between 8.5 to 10.5 mg/dL (2.12 to 2.62 mmol/L) and that of ionized calcium is 4.65 to 5.25 mg/dL (1.16 to 1.31 mmol/L).[18]


An ECG of a person with hypocalcemia

Because a significant portion of calcium is bound to albumin, any alteration in the level of albumin will affect the measured level of calcium. A corrected calcium level based on the albumin level is: Corrected calcium (mg/dL) = measured total Ca (mg/dL) + 0.8 * (4.0 - serum albumin [g/dL]).[19]


  • Intravenous calcium gluconate 10% can be administered, or if the hypocalcaemia is severe, calcium chloride is given instead. This is only appropriate if the hypocalcemia is acute and has occurred over a relatively short time frame. But if the hypocalcemia has been severe and chronic, then this regimen can be fatal, because there is a degree of acclimatization that occurs. The neuromuscular excitability, cardiac electrical instability, and associated symptoms are then not cured or relieved by prompt administration of corrective doses of calcium, but rather exacerbated. Such rapid administration of calcium would result in effective over correction – symptoms of hypercalcemia would follow.
  • However, in either circumstance, maintenance doses of both calcium and vitamin-D (often as 1,25-(OH)2-D3, i.e. calcitriol) are often necessary to prevent further decline

See also[edit]


  1. LeMone, Priscilla; Burke, Karen; Dwyer, Trudy; Levett-Jones, Tracy; Moxham, Lorna; Reid-Searl, Kerry (2015) (in en). Medical-Surgical Nursing. Pearson Higher Education AU. p. 237. ISBN 9781486014408. 
  2. 2.0 2.1 2.2 2.3 2.4 Soar, J; Perkins, GD; Abbas, G; Alfonzo, A; Barelli, A; Bierens, JJ; Brugger, H; Deakin, CD et al. (October 2010). "European Resuscitation Council Guidelines for Resuscitation 2010 Section 8. Cardiac arrest in special circumstances: Electrolyte abnormalities, poisoning, drowning, accidental hypothermia, hyperthermia, asthma, anaphylaxis, cardiac surgery, trauma, pregnancy, electrocution.". Resuscitation 81 (10): 1400–33. doi:10.1016/j.resuscitation.2010.08.015. PMID 20956045. 
  3. Pathy, M.S. John (2006). "Appendix 1: Conversion of SI Units to Standard Units". Principles and practice of geriatric medicine. 2 (4. ed.). Chichester [u.a.]: Wiley. p. Appendix. doi:10.1002/047009057X.app01. ISBN 9780470090558. 
  4. Minisola, S; Pepe, J; Piemonte, S; Cipriani, C (2 June 2015). "The diagnosis and management of hypercalcaemia". BMJ (Clinical Research Ed.) 350: h2723. doi:10.1136/bmj.h2723. PMID 26037642. 
  5. 5.0 5.1 5.2 5.3 5.4 5.5 Fong, J; Khan, A (February 2012). "Hypocalcemia: updates in diagnosis and management for primary care". Canadian Family Physician 58 (2): 158–62. PMID 22439169. 
  6. 6.0 6.1 Cooper, MS; Gittoes, NJ (7 June 2008). "Diagnosis and management of hypocalcaemia". BMJ (Clinical Research Ed.) 336 (7656): 1298–302. doi:10.1136/ PMID 18535072. 
  7. Armstrong, C. M.; Cota, Gabriel (1999). "Calcium block of Na+ channels and its effect on closing rate". Proceedings of the National Academy of Sciences of the United States of America 96 (7): 4154–4157. doi:10.1073/pnas.96.7.4154. PMID 10097179. Bibcode1999PNAS...96.4154A. 
  8. Durlach, J; Bac, P; Durlach, V; Bara, M; Guiet-Bara, A (June 1997). "Neurotic, neuromuscular and autonomic nervous form of magnesium imbalance". Magnesium Research 10 (2): 169–95. PMID 9368238. 
  9. 9.0 9.1 Nussey, S. S.; Whitehead, S. A. (2013-04-08). Endocrinology: An Integrated Approach. CRC Press. p. 194. ISBN 9780203450437. 
  10. Bijlani, R. L.; Manjunatha, S. (2010-11-26). Understanding Medical Physiology: A Textbook for Medical Students. Jaypee Brothers Publishers. p. 465. ISBN 9789380704814. 
  11. "Hypoparathyroidism. Parathyroid symptoms and disease | Patient". Retrieved 2015-09-05. 
  12. "Hypoparathyroidism" (in en-US). "These cases may be called autoimmune hypoparathyroidism and develop when the body’s own immune system mistakenly attacks parathyroid tissue and leads to the loss of the secretion of parathyroid hormone." 
  13. 13.0 13.1 13.2 Metheny, Norma (2012). Fluid and electrolyte balance : nursing considerations (5th ed.). Sudbury, MA: Jones & Bartlett Learning. p. 93. ISBN 978-0-7637-8164-4. Retrieved 4 September 2015. 
  14. 14.0 14.1 14.2 14.3 Helms, Richard (2006). Textbook of therapeutics : drug and disease management (8. ed.). Philadelphia, Pa. [u.a.]: Lippincott Williams & Wilkins. p. 1035. ISBN 978-0-7817-5734-8. Retrieved 4 September 2015. 
  15. 15.0 15.1 15.2 15.3 15.4 15.5 Fong, Jeremy; Khan, Aliya (2012). "Hypocalcemia: updates in diagnosis and management for primary care". Canadian Family Physician 58 (2): 158–62. PMID 22439169. 
  16. Hall, edited by Patrick T. Murray, Hugh R. Brady, Jesse B. (2006). Intensive care in nephrology. London: Taylor & Francis. p. 129. ISBN 978-0-203-02482-9. Retrieved 4 September 2015. 
  17. MedlinePlus Encyclopedia Hypocalcemia - infants
  18. Siyam, Fadi F.; Klachko, David M. (2013). "What Is Hypercalcemia? The Importance of Fasting Samples". Cardiorenal Medicine 3 (4): 232–238. doi:10.1159/000355526. ISSN 1664-3828. PMID 24474951. 
  19. (in en) Fluids & Electrolytes: A 2-in-1 Reference for Nurses. Lippincott Williams & Wilkins. 2006. p. 122. ISBN 9781582554259. 

External links[edit]

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