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Professional Reference articles are designed for health professionals to use. They are written by UK doctors and based on research evidence, UK and European Guidelines. You may find one of our health articles more useful.

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Calcium has a vital role to play in the effective working of the majority of cells in the body and it is therefore important that the optimal level be maintained by the body. A reduction in serum calcium can stimulate parathyroid hormone (PTH) release which may then increase bone resorption, increase renal calcium reabsorption, and stimulate renal conversion of 25-hydroxyvitamin D3, to the active 1,25-dihydroxyvitamin D3, which then will increase intestinal calcium absorption. These mechanisms restore the serum calcium to normal and inhibit further production of PTH and 1,25-dihydroxyvitamin D3.[1]

The normal range for serum calcium is 2.25-2.5 mmol/L*. However, in hypercalcaemia, just over half the circulating calcium is protein bound and therefore the level of circulating protein, principally albumin, must also be taken into consideration in making this measurement. The level for serum calcium is frequently given by laboratories as both an uncorrected level and a corrected level which has allowed for changes in albumin levels. It is only the ionised (unbound) calcium which is physiologically important, taking part in cellular activities such as neuromuscular contraction, coagulation and other cellular activities.[2]

Elevated calcium concentrations have painful side-effects and are associated with significantly reduced quality of life and increased healthcare consumption.[3]

*The normal range is quoted for guidance only. Ranges may vary between laboratories or regions.

Correcting calcium levels

This will be done for you by the lab, but if not, as an approximation you could add 0.1 mmol/L to calcium concentration for every 4 g/L that albumin is below 40 g/L and a similar subtraction for raised albumin.

The 'correction' is only approximate and does not replace measurement of ionised calcium concentration. Take special care where the measured albumin is less than about 20 g/L because of the known inaccuracy of albumin measurement at low levels[4] .

  • Hypercalcaemia is an uncommon problem. Primary hyperparathyroidism is the most common cause. It affects mainly postmenopausal women.[5] The prevalence rate in the UK is around 1-7 per 1,000 adults, with an annual incidence of around 4-11 per 10,000 person-years in one Scottish study. [6]
  • Hypercalcaemia is the most frequently encountered endocrine/electrolyte disorder in malignancy-associated hospitalised patients. Its incidence is 15 per 100,000 person-years and it has been estimated that up to 20% of people with a malignancy wil be affected by hypercalcaemia at some point in the course of their illness.[7, 6]
  • The incidence in children is unknown but is thought to be less common than in adults.[7]

As effective calcium regulation is required for the healthy working of most cells in the body, a high level can produce a diverse collection of symptoms including:

Presentation of Hypercalcaemia

At levels <2.8 mmol/LAt levels <3.5 mmol/LAt levels >3.5 mmol/L

  • Polyuria and polydipsia
  • Dyspepsia - due to calcium-regulated release of gastrin
  • Depression
  • Mild cognitive impairment
All of the previous plus:

  • Muscle weakness
  • Constipation
  • Anorexia and nausea
  • Fatigue
All of the previous plus:
  • Abdominal pain
  • Vomiting
  • Dehydration
  • Lethargy
  • Cardiac arrhythmias, shortened QT interval
  • Coma
  • Pancreatitis

If the hypercalcaemia is long-standing, calcium may be deposited in soft tissues or may result in stone formation - eg, nephrocalcinosis, nephrolithiasis or chondrocalcinosis.

Causes of hypercalcaemia may be grouped into those secondary to raised PTH levels and those mediated by other factors. Primary hyperparathyroidism and malignancy are responsible for greater than 90% of all cases.[6]

PTH-mediated hypercalcaemia

Primary hyperparathyroidism is the most common cause of raised calcium levels, usually producing a mild hypercalcaemia.

Non-PTH-mediated hypercalcaemia[6]

  • Malignancy - the most common cause of non-PTH-mediated hypercalcaemia.
  • Granulomatous conditions - eg, sarcoidosis and tuberculosis.
  • Endocrine conditions - eg, thyrotoxicosis, phaeochromocytoma and primary adrenal insufficiency.
  • Drugs - eg, thiazide diuretics, vitamin D and vitamin A supplements.
  • Familial - eg, familial hypocalciuric hypercalcaemia.
  • Other - eg, prolonged immobilisation, calcium-alkali syndrome, AIDS.

Hypercalcaemia of malignancy can occur as a result of four different mechanisms: ectopic production of parathyroid hormone-related peptide by tumour cells, osteolytic hypercalcaemia, ectopic calcitriol (1,25-dihydroxyvitamin D), and ectopic PTH produced by tumour cells.[8]

Corrected calcium level - this will by definition be raised. Compared with the hypercalcaemia of malignancy, hyperparathyroidism tends to be associated with lower serum calcium levels (<3 mmol/L) and a longer duration of hypercalcaemia (more than six months).[9]

In the presence of a raised corrected calcium:[10, 6]

  • A raised albumin level in the presence of a raised urea indicates dehydration.
  • A raised albumin level in the presence of a normal urea suggests a cuffed specimen.
  • A normal alkaline phosphatase is indicative of myeloma (raised plasma protein), calcium-alkali syndrome (formerly milk-alkali syndrome),[11] thyrotoxicosis or sarcoidosis.
  • A raised alkaline phosphatase suggests bony metastases, sarcoidosis or thyrotoxicosis.
  • A raised calcitonin level is suggestive of B-cell lymphoma.

The following table may be helpful in interpreting laboratory results:

Interpreting Laboratory Values in Hypercalcaemia[10]
Condition Serum PhosphateSerum Alkaline Phosphatase Urine CalciumUrine Phosphate PTH
HyperparathyroidismLowNormal-highHigh (in 67% of patients)HighHigh
Vitamin D excessNormal-highLowHighHighLow
MalignancyOften lowHigh (except in haematological malignancy, when normal)VariableHighVariable
Granulomatous diseaseNormal-highNormal-highHighNormalLow
Calcium alkali syndromeNormal-highNormalNormalNormalLow
Familial hypocalciuric hypercalcaemiaNormal or lowNormalLow (<200 mg/day)NormalHigh

Interpreting PTH levels[6]

  • Raised PTH levels are suggestive of primary, secondary or tertiary hyperparathyroidism, or familial hypocalciuric hypercalcaemia.
  • Low PTH levels are seen in granulomatous disease, iatrogenic causes (eg, renal dialysis), adrenal insufficiency, thyrotoxicosis,and vitamin D intoxication.
  • The levels in malignancy may be low, normal or high.


  • Plain X-rays may show features indicative of bone abnormalities, such as demineralisation, bone cysts, pathological fractures or bony metastases.
  • Ultrasound scan, computerised tomography (CT) scan or intravenous pyelogram (IVP) may be required to detect abnormalities of the urogenital tract, such as calcification or stones.
  • Ultrasound or technetium scan of the parathyroid glands may be indicated if hypertrophy or adenoma is suspected.

This can be considered under the headings of the immediate management of acute hypercalcaemia and the longer-term management of the underlying condition. National Institute for Health and Care Excellence Clinical Knowledge Summaries (NICE CKS) recommend that GPs should refer all patients with non-acute hypercalcaemia to the appropriate specialist, depending on the suspected cause (or to an endocrinologist if no cause can be found).[6]

Acute hypercalcaemia[13]

Treatment should be initiated in hospital on the advice of a specialist and should include:

  • Increasing the circulating volume with 0.9% saline, helping to increase the urinary output of calcium.
  • A loop diuretic such as furosemide. This is occasionally used where there is fluid overload but it does not reduce serum calcium .
  • After rehydration, bisphosphonates (which act by reducing bone turnover) should be administered intravenously. Pamidronate and zolendronic acid are commonly used. Salmon calcitonin may also be given. It has fewer side-effects than bisphosphonates but is less effective in reducing hypercalcaemia.[14, 15]
  • Glucocorticoids are useful for hypercalcaemia due to vitamin D toxicity, sarcoidosis and lymphoma.[15]
  • Gallium was identified as a useful drug when it was found that patients with malignancy having gallium scans did not develop hypercalcaemia. It may be given intravenously to patients with malignant hypercalcaemia who do not respond to bisphosphonates.[16]
  • Cinacalcet hydrochloride is a calcimimetic (= mimicking the action of calcium) agent that effectively reduces parathyroid levels in patients with secondary hyperparathyroidism.[14]
  • Paricalcitol is also licensed for the prevention and treatment of secondary hyperparathyroidism associated with chronic kidney disease and kidney failure.[15]
  • Denosumab, a human monoclonal antibody, is licensed for the prevention of osteoporotic fractures but is also useful for patients with persistent or relapsed hypercalcaemia of malignancy.[17]
  • Patients with advanced underlying kidney disease and refractory severe hypercalcaemia should be considered for haemodialysis.[18]

Non-PTH-mediated hypercalcaemia

Treatment depends on the underlying condition.

PTH-mediated hypercalcaemia [6]

  • Asymptomatic patients may be treated conservatively with regular monitoring of bone density, renal function and serum and urinary calcium levels.
  • For symptomatic patients, dietary calcium should be reduced - eg, minimise the intake of dairy products and leafy vegetables.
  • Bed-bound patients should be mobilised if possible. Symptomatic patients will respond well to having the affected part of the parathyroid gland removed.
  • There is no consensus on the operative treatment of asymptomatic patients. In general, it tends to be reserved for patients who have impaired renal function, hypercalciuria, low bone mineral density or severe hypercalcaemia.[19]

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Further reading and references

  1. Goltzman D; Approach to Hypercalcemia. Endotext:, Inc. 2000-2016 Aug 8.

  2. Shane E et al; Hypercalcemia: Pathogenesis, Clinical Manifestations, Differential Diagnosis, and Management, American Bone and Mineral Research, 2006.

  3. Dalemo S, Eggertsen R, Hjerpe P, et al; Quality of life and health care consumption in primary care patients with elevated serum calcium concentrations in - a prospective, case control, study. BMC Fam Pract. 2014 May 515:84. doi: 10.1186/1471-2296-15-84.

  4. Biochemical Calculations; Sydpath

  5. Fraser WD; Hyperparathyroidism. Lancet. 2009 Jul 11374(9684):145-58.

  6. Hypercalcaemia; NICE CKS, August 2019 (UK access only)

  7. Lumachi F, Brunello A, Roma A, et al; Medical treatment of malignancy-associated hypercalcemia. Curr Med Chem. 200815(4):415-21.

  8. Malangone S, Campen CJ; Hypercalcemia of Malignancy. J Adv Pract Oncol. 2015 Nov-Dec6(6):586-92. Epub 2015 Nov 1.

  9. Assadi F; Hypercalcemia: an evidence-based approach to clinical cases. Iran J Kidney Dis. 2009 Apr3(2):71-9.

  10. Carroll MF, Schade DS; A practical approach to hypercalcemia. Am Fam Physician. 2003 May 167(9):1959-66.

  11. Patel AM, Adeseun GA, Goldfarb S; Calcium-alkali syndrome in the modern era. Nutrients. 2013 Nov 275(12):4880-93. doi: 10.3390/nu5124880.

  12. Cecchin D, Motta R, Zucchetta P, et al; Imaging studies in hypercalcemia. Curr Med Chem. 201118(23):3485-93.

  13. Emergency management of acute hypercalcaemia in adult patients; Society for Endocrinology, September 2016

  14. Clines GA; Mechanisms and treatment of hypercalcemia of malignancy. Curr Opin Endocrinol Diabetes Obes. 2011 Dec18(6):339-46. doi: 10.1097/MED.0b013e32834b4401.

  15. British National Formulary (BNF); NICE Evidence Services (UK access only)

  16. Leyland-Jones B; Treating cancer-related hypercalcemia with gallium nitrate. J Support Oncol. 2004 Nov-Dec2(6):509-16.

  17. Hu MI, Glezerman I, Leboulleux S, et al; Denosumab for patients with persistent or relapsed hypercalcemia of malignancy despite recent bisphosphonate treatment. J Natl Cancer Inst. 2013 Sep 18105(18):1417-20. doi: 10.1093/jnci/djt225. Epub 2013 Aug 29.

  18. Mirrakhimov AE; Hypercalcemia of Malignancy: An Update on Pathogenesis and Management. N Am J Med Sci. 2015 Nov7(11):483-93. doi: 10.4103/1947-2714.170600.

  19. Langdahl BL, Ralston SH; Diagnosis and management of primary hyperparathyroidism in Europe. QJM. 2012 Jun105(6):519-25. doi: 10.1093/qjmed/hcr225. Epub 2012 May 7.