Section: Endocrine Sub-section: Parathyroid

Signs/Symptoms of Hypocalcaemia

  • Acute manifestations
    • Tetany
    • Seizures
  • Also get
    • Cardiac abnormalities
    • Papilloedema
    • Psychiatric – emotional instability, anxiety, depression
    • Fatigue
    • Hyperirritability

Tetany

  • Uncommon unless Ca2+ < 1.1mmol/L
  • Due to peripheral neuromuscular irritability
    • Hyperexcitable peripheral neurons
    • NB: Synergism with alkalosis
  • Mild symptoms can cause anxiety, hyperventilation, exacerbation of symptoms
  • Symptoms
    • Mild
      • Perioral numbness, peripheral paraesthesia, cramps
    • Severe
      • Carpopedal spasm, laryngospasm, seizures
    • Classic Findings
      • Trousseau’s sign (most specific)
        • Induction of carpal spasm by inflating BP cuff over systolic for 3 mins
        • Can also induce voluntarily with hyperventilation after cuff removal
      • Chvostek’s sign
        • Contraction of ipsilateral facial muscles by tapping on facial nerve just anterior to the ear
        • Can range from lip twitching to full spasm of all facial muscles
          • Can be present in 10% of normal people as well
      • NB: Both may be negative in patients with hypocalcaemia

Seizures

  • Can be only presenting symptom
  • If in absence of tetany may be due to low CSF Ca2+ rather than serum Ca2+
  • Can get
    • Generalized tonic-clonic
    • Generalized absence
    • Focal seizures

Cardiovascular effects

  • Decreased myocardial performance or CHF
  • Myocardial dysfunction reversible with Ca2+
  • Mechanism undefined
    • ? Ca2+ role in excitation-contraction coupling
    • Prolonged Q-T interval
    • Can get arrhythmias – but rare
    • Most severely can get Torsades-de-pointes
      • But less common than hypokalaemia or hypomagnesaemia

Treatment

  • IV Ca2+ replacement if:
    • Symptomatic (Tetany, seizures, carpopedal spasm)
    • Prolonged Q-T
    • Or if Ca2+ < 1.9mmol/L
    • Rapid infusion
      • 1 or 2 g Calcium Gluconate in 50mL normal saline over 10-20mins
      • Followed by continued slow infusion
        • 10% Calcium Gluconate or 10% Calcium Chloride in normal saline (50mL/hr)
  • Treat concurrent hypomagnesaemia
    • For mild/chronic cases
    • PO supplementation (Calcium Carbonate)
    • Don’t forget Vit D supplementation if required

Hypoparathyroidism

  • Inadequate PTH secretion leads to
    • Hypocalcaemia
    • Hyperphosphataemia
  • Most commonly a result of damage to normal glands
    • Post surgical or after reimplantation
  • Can also be
    • Congenital
    • Pseudohypoparathyroidism

Congenital Hypoparathyroidism

  • Extremely rare causes of hypoparathyroidism
    • Born without adequate parathyroid tissue (e.g. DiGeorge syndrome)
      • Caused by microdeletions occurring in chromosome region 22q11.2
      • Features vary widely and include:
        • Congenital heart defects
        • Defects in the palate
        • Facial anomalies
        • Recurrent infections
        • Learning disabilities
    • Hypoparathyroidism secondary to maternal hyperparathyroidism
      • Hyperparathyroidism during pregnancy associated with foetal complications in 80% of cases
    • Maternal hypercalcaemia results in suppression of foetal parathyroid glands > Foetal hypocalcaemia
      • Intrauterine growth retardation
      • Preterm delivery
      • Low birth rate
      • Foetal death
    • Most cases of neonatal hypoparathyroidism are transient
      • Respond to Ca2+ supplementation

Pseudohypoparathyroidism

  • Rare metabolic condition
  • Have low serum Ca2+ and hyperphosphataemia
    • PTH is appropriately elevated because of the hypocalcaemia
    • But body fails to respond to PTH
  • Linked to a dysfunction of the Gsα subunit of G proteins (3 types)
  • Type 1a (Albright Hereditary Osteodystrophy)
    • Characteristic phenotypic appearance
    • Short fourth and fifth metacarpals and a rounded facies
    • Associated with thyroid-stimulating hormone resistance
  • Type 1b
    • Biochemically similar but lacks the phenotypic appearance
    • Associated with a methylation defect
  • Type 2
    • Occur downstream of type 1a or 1b
    • A normal cAMP response to PTH stimulation occurs, despite the inherent abnormality in calcium regulation