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Hypocalcaemia, also spelled hypocalcemia, is low calcium levels in the blood serum.[5] 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.[1][3][6] Mildly low levels that develop slowly often have no symptoms.[2][4] Otherwise symptoms may include numbness, muscle spasms, seizures, confusion, or cardiac arrest.[1][2]

Calcium within the periodic table
SymptomsNumbness, muscle spasms, seizures, confusion[1][2]
ComplicationsCardiac arrest.[1][2]
CausesHypoparathyroidism, vitamin D deficiency, kidney failure, pancreatitis, calcium channel blocker overdose, rhabdomyolysis, tumor lysis syndrome, bisphosphonates[1][2]
Diagnostic methodBlood serum < 2.1 mmol/L (corrected calcium or ionized calcium)[1][3][2]
TreatmentCalcium supplements, vitamin D, magnesium sulfate.[1][2]
Frequency~18% of people in hospital[4]

Common causes include hypoparathyroidism and vitamin D deficiency.[2] Others causes include kidney failure, pancreatitis, calcium channel blocker overdose, rhabdomyolysis, tumor lysis syndrome, and medications such as bisphosphonates.[1] Diagnosis should generally be confirmed with a corrected calcium or ionized calcium level.[2] Specific changes may be seen on an electrocardiogram (ECG).[1]

Initial treatment for severe disease is with intravenous calcium chloride and possibly magnesium sulfate.[1] Other treatments may include vitamin D, magnesium, and calcium supplements.[2] If due to hypoparathyroidism, hydrochlorothiazide, phosphate binders, and a low salt diet may also be recommended.[2] About 18% of people who are being treated in hospital have hypocalcemia.[4]


Signs and symptomsEdit


The neuromuscular symptoms of hypocalcemia are caused by a positive bathmotropic effect 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.[citation needed]

  • Petechiae which appear as on-off spots, then later become confluent, and appear as purpura (larger bruised areas, usually in dependent regions of the body).
  • Oral, perioral and acral paresthesias, tingling or 'pins and needles' sensation in and around the mouth and lips, and in the extremities of the hands and feet. This is often the earliest symptom of hypocalcaemia.
  • Carpopedal and generalized tetany (unrelieved and strong contractions of the hands, and in the large muscles of the rest of the body) are seen.
  • Latent tetany
  • Tendon reflexes are hyperactive
  • Life-threatening complications
  • Effects on cardiac output
  • ECG changes include the following:
    • Intermittent QT prolongation, or intermittent prolongation of the QTc (corrected QT interval) on the EKG (electrocardiogram) is noted. The implications of intermittent QTc prolongation predisposes to life-threatening cardiac electrical instability (and this is therefore a more critical condition than constant QTc prolongation). This type of electrical instability puts the patient at high risk of torsades de pointes, a specific type of ventricular tachycardia which appears on an EKG (or ECG) as something which looks a bit like a sine wave with a regularly increasing and decreasing amplitude. (Torsades de pointes can cause death, unless the patient can be medically or electrically cardioverted and returned to a normal cardiac rhythm.)


Hypoparathyroidism is a common cause of hypocalcemia. Calcium is tightly regulated by the parathyroid hormone (PTH). In response to low calcium levels, PTH induces the kidneys to reabsorb calcium, the kidneys to increase production of calcitriol (the active form of vitamin D) thereby increasing intestinal absorption of calcium, and the bones to release calcium. These actions lead to a re-balance in the blood calcium levels. 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 via parathyroidectomy or neck dissection for head and neck cancers. Hypoparathyroidism may also be due to autoimmune destruction of the glands.[citation needed]


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).[11]


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]).[12]


Management of this condition includes:[citation needed]

  • 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 alsoEdit


  1. ^ a b c d e f g h i j Soar, J; Perkins, GD; Abbas, G; Alfonzo, A; Barelli, A; Bierens, JJ; Brugger, H; Deakin, CD; Dunning, J; Georgiou, M; Handley, AJ; Lockey, DJ; Paal, P; Sandroni, C; Thies, KC; Zideman, DA; Nolan, JP (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.
  2. ^ a b c d e f g h i j k Fong, J; Khan, A (February 2012). "Hypocalcemia: updates in diagnosis and management for primary care". Canadian Family Physician. 58 (2): 158–62. PMC 3279267. PMID 22439169.
  3. ^ a b 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. ^ a b c Cooper, MS; Gittoes, NJ (7 June 2008). "Diagnosis and management of hypocalcaemia". BMJ (Clinical Research Ed.). 336 (7656): 1298–302. doi:10.1136/ PMC 2413335. PMID 18535072.
  5. ^ LeMone, Priscilla; Burke, Karen; Dwyer, Trudy; Levett-Jones, Tracy; Moxham, Lorna; Reid-Searl, Kerry (2015). Medical-Surgical Nursing. Pearson Higher Education AU. p. 237. ISBN 9781486014408. Archived from the original on 2016-10-02.
  6. ^ 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.
  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. Bibcode:1999PNAS...96.4154A. doi:10.1073/pnas.96.7.4154. PMC 22436. PMID 10097179.
  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. ^ Swaminathan, R. (2003). "Magnesium metabolism and its disorders". The Clinical Biochemist. Reviews. 24 (2): 47–66. ISSN 0159-8090. PMC 1855626. PMID 18568054.
  10. ^ Sheridan, R.L.; Ryan, C.M.; Quinby, W.C.; Blair, J.; Tompkins, R.G.; Burke, J.F. (1995). "Emergency management of major hydrofluoric acid exposures". Burns. 21 (1): 62–64. doi:10.1016/0305-4179(95)90785-x.
  11. ^ 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. PMC 3901605. PMID 24474951.
  12. ^ Fluids & Electrolytes: A 2-in-1 Reference for Nurses. Lippincott Williams & Wilkins. 2006. p. 122. ISBN 9781582554259. Archived from the original on 2017-03-19.

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