Revision Resources

Calcium Homeostasis – Clinical

July 31, 2016

Hypercalcaemia

Definitions

  • Normal serum corrected calcium = 2.1 – 2.6 mmol/L
  • Mild hypercalcaemia =  2.7 – 2.9 mmol/L
  • Moderate hypercalcaemia = 3.0 – 3.4 mmol/L
  • Severe hypercalcaemia =  greater than 3.4 mmol/L

Causes

  • primary hyperparathyroidism (most commonly due to a benign parathyroid adenoma)
  • familial hypocalciuric hypercalcaemia
  • sudden acidosis (resulting in release of bound calcium)
  • malignancy
  • sarcoidosis
  • chronic renal failure
  • thyrotoxicosis
  • pheochromocytoma
  • Addison’s disease
  • ingestion of excess calcium (milk-alkali syndrome) or vitamin D
  • drugs e.g. lithium, thiazide diuretics, theophylline toxicity
  • prolonged immobilisation
  • bone destruction usually by secondary deposits from malignancy or myeloma
  • hypermagnesaemia

The commonest causes of hypercalcaemia are primary hyperparathyroidism and hypercalcaemia of malignancy.

Clinical Features

  • STONES (renal calculi)
  • BONES (bone pain, fragile bones)
  • GROANS (lethargy, fatigue, generalised muscle weakness)
  • MOANS (constipation, abdominal pain, nausea/vomiting, pancreatitis, peptic ulcer)
  • THRONES (polyuria, polydipsia, dehydration, renal failure)
  • PSYCHIATRIC OVERTONES (confusion, depression, anxiety, hallucinations, insomnia)

ECG Changes

250px-Osborn_wave

By Jer5150 (.’) [GFDL or CC BY-SA 3.0], via Wikimedia Commons

Hypocalcaemia

Definitions

  • Normal serum corrected calcium = 2.2 – 2.6 mmol/L
  • Mild-moderate hypocalcaemia =  1.9 – 2.2 mmol/L
  • Severe hypocalcaemia = < 1.9 mmol/L

Causes

  • Hypoparathyroidism (e.g. DiGeorge syndrome, autoimmune, secondary to parathyroid or thyroid surgery, radiation or chemotoxic agents, infiltrative disease of the parathyroid glands or hypomagnesaemia) or pseudohypoparathyroidism (characterised by target organ resistance to PTH)
  • Acute pancreatitis
  • Renal failure
  • Vitamin D deficiency
  • Alkalosis or massive blood transfusion (due to increased intravascular ionised calcium binding)
  • Rhabdomyolysis or tumour lysis syndrome (due to extravascular calcium deposit)
  • Drugs e.g. bisphosphonates, fluoride poisoning, combination chemotherapy
  • Sepsis (due to impaired secretion of calcitriol and PTH, target organ resistance to PTH and increased lactate binding calcium in serum).

REMEMBER HARVARDS

The most common causes are hypoparathyroidism (frequently following surgery), vitamin D deficiency or abnormal vitamin D metabolism, chronic kidney disease and hypomagnesaemia.

Clinical Features

Patients with adjusted serum calcium > 1.9 are usually asymptomatic but many patients become symptomatic when levels are less than this.

Features of hypocalcaemia include:

  • carpopedal spasm in response to inflating a blood pressure cuff to above systolic BP (Trousseau’s sign)
  • twitching of the ipsilateral facial muscles in response to tapping on the facial nerve (Chvostek’s sign)
  • painful and fragile bones
  • numbness and paraesthesia in hands and feet
  • muscle cramps and spasms
  • myopathy
  • cardiac arrhythmias
  • cardiac failure
  • hypotension
  • prolonged QT interval
  • seizures
  • mood changes
  • cataracts

ECG Changes

  • Hypocalcaemia causes QTc prolongation primarily by prolonging the ST segment.
  • The T wave is typically left unchanged.
View Previous
| Website designed & hosted by Cyberfrog Design