Hypocalcaemia

Hypocalcemia
Synonyms	Hypocalcemia
Calcium within the periodic table
Specialty	Endocrinology
Symptoms	Numbness, muscle spasms, seizures, confusion[1][2]
Complications	Cardiac arrest.[1][2]
Causes	Hypoparathyroidism, vitamin D deficiency, kidney failure, pancreatitis, calcium channel blocker overdose, rhabdomyolysis, tumor lysis syndrome, bisphosphonates[1][2]
Diagnostic method	Blood serum < 2.1 mmol/L (corrected calcium or ionized calcium)[1][3][2]
Treatment	Calcium supplements, vitamin D, magnesium sulfate.[1][2]
Frequency	~18% of people in hospital[4]

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]

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. If due to hypoparathyroidism, hydrochlorothiazide, phosphate binders, and a low salt diet may also be recommended.^[2] About 18% of people who are in hospital have hypocalcemia.^[4]

Signs and symptoms

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/parasthesias in the hands and feet and around the mouth.

• 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
  • Trousseau sign of latent tetany (eliciting carpal spasm by inflating the blood pressure cuff and maintaining the cuff pressure above systolic)
  • Chvostek's sign (tapping of the inferior portion of the cheekbone will produce facial spasms)^[8]
• Tendon reflexes are hyperactive
• Life-threatening complications
  • Laryngospasm
  • Cardiac arrhythmias
• Effects on cardiac output
  • Negative chronotropic effect, or a decrease in heart rate.
  • Negative inotropic effect, or a decrease in contractility
• 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.)

Causes

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.

• Eating disorders
• Prolonged vomiting (e.g. with a viral illness)
• Exposure to mercury, including infantile acrodynia
• Excessive dietary magnesium, as with supplementation.
• Excessive dietary zinc, as with supplementation (causes rapid hypocalcemia).
• Prolonged use of medications/laxatives containing magnesium
• Chelation therapy for metal exposure, particularly EDTA
• Osteoporosis treatment or preventive agents, such as bisphosphonates and denosumab.
• Agents for the treatment of hypercalcemia, such as Calcitonin.
• Chronic kidney failure
• Absent active vitamin D
  • Decreased dietary intake
  • Decreased sun exposure
  • Defective Vitamin D metabolism
    • Anticonvulsant therapy
    • Vitamin-D dependent rickets, type I
• Ineffective active vitamin D
  • Intestinal malabsorption
  • Vitamin-D dependent rickets, type II
• Pseudohypoparathyroidism
• Severe acute hyperphosphataemia
• Tumour lysis syndrome
• Acute kidney failure
  • Rhabdomyolysis (initial stage)
• Exposure to hydrofluoric acid
• As a complication of pancreatitis
• Alkalosis, often caused by hyperventilation
  • As blood plasma hydrogen ion concentration decreases, caused by respiratory or metabolic alkalosis, the concentration of freely ionized calcium, the biologically active component of blood calcium, decreases. Because a portion of both hydrogen ions and calcium are bound to serum albumin, when blood becomes alkalotic, the bound hydrogen ions dissociate from albumin, freeing up the albumin to bind with more calcium and thereby decreasing the freely ionized portion of total serum calcium. For every 0.1 increase in pH, ionized calcium decreases by about 0.05 mmol/L. This hypocalcaemia related to alkalosis is partially responsible for the cerebral vasoconstriction that causes the lightheadedness, fainting, and paraesthesia often seen with hyperventilation.
  • Tetany may also be seen with this condition.
• Neonatal hypocalcemia
  • Very low birth weight (less than 1500 grams)
  • Gestational age less than 32 weeks

Mechanism

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).

Diagnosis

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]).^[9] Another way to determine the calcium level is to measure directly the ionized calcium level.

Management

• 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

• Calcium metabolism
• Hypercalcaemia
• Milk fever (hypocalcemia in animals)
• Calcium deficiency (plant disorder)
• Hypomagnesemia with secondary hypocalcemia

References

External links