Hypercalcaemia (or Hypercalcemia) is an elevated calcium level in
the blood. (Normal range: 9-10.5 mg/dL or 2.2-2.6 mmol/L). It can be an asymptomatic laboratory
finding, but because an elevated calcium level is often indicative of other diseases, a diagnosis should be undertaken if it
persists. It can be due to excessive skeletal calcium release, increased intestinal calcium absorption, or decreased renal
calcium excretion.
Signs and symptoms
Hypercalcemia per se can result in fatigue, depression, confusion, anorexia, nausea, vomiting,
constipation, pancreatitis or increased urination "Bones, stones, groans, and psychic moans" is a saying which will help you remember the
signs and symptoms of hypercalcemia; if it is chronic it can result in urinary calculi (renal
stones or bladder stones). Abnormal heart rhythms can result, and
EKG findings of a short QT interval and a widened
T wave suggest hypercalcemia.
Symptoms are more common at high calcium levels (12.0 mg/dL or 3 mmol/l). Severe hypercalcemia (above 15-16 mg/dL or 3.75-4
mmol/l) is considered a medical emergency: at these levels, coma and cardiac arrest can result.
Causes
Treatments
The goal of therapy is to treat the hypercalcemia first and subsequently effort is directed to treat the underlying cause.
Initial therapy: fluids and diuretics
- hydration, increasing salt intake, and forced diuresis
- hydration is needed because many patients are dehydrated due to vomiting or renal defects in concentrating urine.
- increased salt intake also can increase body fluid volume as well as increasing urine sodium excretion, which further
increases urinary calcium excretion (In other words, calcium and sodium (salt) are handled in a similar way by the kidney.
Anything that causes increased sodium (salt) excretion by the kidney will, en passant, cause increased calcium excretion
by the kidney)
- after rehydration, a loop diuretic such as furosemide can be given to permit continued large volume intravenous salt and water replacement while
minimizing the risk of blood volume overload and thence pulmonary edema. In addition,
loop diuretics tend to depress renal calcium reabsorption thereby helping to lower blood
calcium levels
- can usually decrease serum calcium by 1-3 mg/dL within 24 h
- caution must be taken to prevent potassium or magnesium depletion
Additional therapy: bisphosphonates and calcitonin
- bisphosphonates are pyrophosphate analogues
with high affinity for bone, especially areas of high bone-turnover.
- they are taken up by osteoclasts and inhibit osteoclastic bone resorption
- current available drugs include (in order of potency): (1st gen) etidronate, (2nd
gen) tiludronate, IV pamidronate, alendronate, risedronate, and (3rd gen) zolendronate
- all patients with cancer-associated hypercalcemia should receive treatment with bisphosphonates since the 'first line' therapy (above) cannot be continued indefinitely nor is it without
risk. Further, even if the 'first line' therapy has been effective, it is a virtual certainty that the hypercalcemia will recur
in the patient with hypercalcemia of malignancy. Use of bisphoponates in such circumstances, then, becomes both therapeutic and
preventative
- patients in renal failure and hypercalcemia
should have a risk-benefit analysis before being given bisphosphonates, since they are
relatively contraindicated in renal failure.
- Calcitonin blocks bone resorption and also increases urinary calcium excretion by
inhibiting renal calcium reabsorption
- Usually used in life-threatening hypercalcemia along with rehydration, diuresis, and bisphosphonates
- Helps prevent recurrence of hypercalcemia
- Dose is 4 Units per kg via subcutaneous or intramuscular route every 12 hours, usually not continued indefinitely
Other therapies
- rarely used, or used in special circumstances
- plicamycin inhibits bone resorption (rarely used)
- gallium nitrate inhibits bone resprotion and changes structure of bone crystals (rarely
used)
- glucocorticoids increase urinary calcium excretion and decrease intestinal calcium
absorption
- dialysis usually used in severe hypercalcemia complicated by renal failure. Supplemental phosphate should be monitored and added if necessary
- phosphate therapy can correct the hypophosphatemia in the face of hypercalcemia and lower
serum calcium
See also
|
Metabolic pathology
/ Inborn error of metabolism (E70-90, 270-279) |
| Amino acid |
Aromatic
(Phenylketonuria, Alkaptonuria, Ochronosis, Tyrosinemia, Albinism,
Histidinemia) - Branched chain
(Maple syrup urine disease, Propionic
acidemia, Methylmalonic acidemia, Isovaleric acidemia, 3-Methylcrotonyl-CoA carboxylase deficiency) - Transport
(Cystinuria, Cystinosis, Hartnup disease, Fanconi syndrome, Oculocerebrorenal syndrome) - Sulfur (Homocystinuria, Cystathioninuria) - Urea cycle disorder (N-Acetylglutamate
synthase deficiency, Carbamoyl phosphate synthetase I
deficiency, Ornithine transcarbamylase deficiency,
Citrullinemia, Argininosuccinic
aciduria, Hyperammonemia) - Glutaric
acidemia type 1 - Sarcosinemia |
| Carbohydrate |
Lactose intolerance - Glycogen storage disease
(type I, type
II, type III, type IV, type V,
type VI, type
VII) - fructose metabolism (Fructose intolerance,
Fructose bisphosphatase deficiency, Essential fructosuria) - galactose metabolism (Galactosemia, Galactose-1-phosphate uridylyltransferase galactosemia,
Galactokinase deficiency) - other intestinal carbohydrate absorption
(Glucose-galactose malabsorption, Sucrose intolerance) - pyruvate metabolism and gluconeogenesis (PCD, PDHA) - Pentosuria - Renal glycosuria |
| Lipid
storage |
Sphingolipidoses/Gangliosidoses: GM2 gangliosidoses (Sandhoff disease, Tay-Sachs disease) - GM1 gangliosidoses - Mucolipidosis type IV - Gaucher's disease -
Niemann-Pick disease - Farber disease -
Fabry's disease - Metachromatic
leukodystrophy - Krabbe disease
Neuronal ceroid lipofuscinosis (Batten
disease) - Cerebrotendineous xanthomatosis - Cholesteryl ester storage disease (Wolman
disease) |
| Other lipid |
Lipoprotein/lipidemias:
Hyperlipidemia - Hypercholesterolemia -
Familial hypercholesterolemia - Xanthoma
- Combined hyperlipidemia - Lecithin cholesterol acyltransferase deficiency - Tangier disease - Abetalipoproteinemia
Fatty acid: Adrenoleukodystrophy - Carnitine (Primary, I, II) |
| Mineral |
Cu Wilson's
disease/Menkes disease - Fe Haemochromatosis - Zn Acrodermatitis
enteropathica - PO43− Hypophosphatemia/Hypophosphatasia - Mg2+
Hypermagnesemia/Hypomagnesemia -
Ca2+ Hypercalcaemia/Hypocalcaemia/Disorders of calcium
metabolism |
Fluid, electrolyte
and acid-base balance |
Electrolyte disturbance - Na+ Hypernatremia/Hyponatremia - Acidosis (Metabolic, Respiratory, Lactic) - Alkalosis (Metabolic, Respiratory) - Mixed disorder of acid-base
balance - H2O Dehydration/Hypervolemia - K+ Hypokalemia/Hyperkalemia - Cl− Hyperchloremia/Hypochloremia |
| Purine and pyrimidine |
Hyperuricemia -
Lesch-Nyhan syndrome - Xanthinuria |
| Porphyrin |
Acute intermittent, Gunther's, Cutanea tarda, Erythropoietic,
Hepatoerythropoietic, Hereditary copro-, Variegate |
| Bilirubin |
Unconjugated (Gilbert's syndrome, Crigler-Najjar syndrome) -
Conjugated (Dubin-Johnson syndrome, Rotor
syndrome) |
| Glycosaminoglycan |
Mucopolysaccharidosis - 1:Hurler/Hunter - 3:Sanfilippo - 4:Morquio - 6:Maroteaux-Lamy - 7:Sly |
| Glycoprotein |
Mucolipidosis -
I-cell disease - Pseudo-Hurler
polydystrophy - Aspartylglucosaminuria - Fucosidosis - Alpha-mannosidosis - Sialidosis |
| Other |
Alpha 1-antitrypsin deficiency - Cystic fibrosis
- Amyloidosis (Familial Mediterranean
fever) - Acatalasia |
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