Parathyroid Disorders: Hyperparathyroidism & Hypoparathyroidism – Anesthetic Relevance


I.  Overview of Parathyroid Function

  • The parathyroid glands (usually 4) are located posterior to the thyroid.
  • They regulate calcium and phosphate homeostasis via parathyroid hormone (PTH).

Actions of PTH:

Organ

Effect

Bone

Stimulates osteoclasts bone resorption Ca²

Kidney

Ca² reabsorption, phosphate reabsorption, activates 1α-hydroxylase (vitamin D activation)

Gut (via calcitriol)

Ca² and phosphate absorption


 Normal Calcium Physiology

  • Total serum calcium: 8.5–10.5 mg/dL
    • Ionized (free): ~50% (active form) normal: 1.1–1.3 mmol/L
    • Protein-bound (mostly to albumin): ~40%
    • Complexed (with phosphate, citrate): ~10%

📌 Only ionized calcium is physiologically active – important for muscle contraction, nerve conduction, coagulation, enzyme function.

Factors Influencing Calcium Levels

  • pH: Alkalosis more calcium binds to albumin ionized Ca²⁺
  • Albumin: Low albumin low total Ca²⁺ but normal ionized Ca²⁺
  • Citrate (e.g., in massive transfusion): Binds calcium hypocalcemia
  • Magnesium: Deficiency impairs PTH secondary hypocalcemia


II. Hyperparathyroidism (HPT)

A. Types

Type

Features

Primary HPT

Parathyroid adenoma (85%), hyperplasia, carcinoma

Secondary HPT

CKD calcitriol & chronic hypocalcemia PTH

Tertiary HPT

Long-standing secondary HPT autonomous PTH secretion



B. Clinical Features

  • Bones – Bone pain, fractures (osteitis fibrosa cystica)
  • Stones – Nephrolithiasis, nephrocalcinosis
  • Groans – Abdominal pain, pancreatitis, peptic ulcers, constipation
  • Moans – Fatigue, depression, cognitive dysfunction
  • Short QT interval on ECG


C. Investigations

  • Serum Ca²⁺ (ionized and total)
  • Serum phosphate
  • PTH
  • Elevated alkaline phosphatase (with bone turnover)
  • Imaging: Sestamibi scan, USG, 4D-CT (for localization)


III. Hypoparathyroidism

A. Causes

Type

Causes

Postsurgical

Most common: post-thyroidectomy/parathyroidectomy

Autoimmune

Autoimmune polyglandular syndromes

Genetic

DiGeorge syndrome, familial

Other

Radiation, infiltrative diseases (hemochromatosis, Wilson’s)



B. Clinical Features

  • Neuromuscular excitability: Tetany, cramps, perioral numbness, carpopedal spasm
  • Chvostek’s sign, Trousseau’s sign
  • Laryngospasm, seizures
  • QT prolongation arrhythmias
  • Cataracts, dry skin, brittle nails (chronic cases)


C. Labs

  • Total and ionized Ca²⁺
  • Serum phosphate
  • or inappropriately normal PTH
  • Normal to low magnesium


IV. 🔶 Anesthetic Implications of Parathyroid Disorders


A. Preoperative Evaluation

🔹 Hyperparathyroidism

  • Correct hypercalcemia (hydrate, loop diuretics, bisphosphonates)
  • Evaluate renal function (stones, nephrocalcinosis)
  • Assess bone status, fractures
  • Baseline ECG (QT shortening, arrhythmias)
  • Check electrolytes (Ca²⁺, Mg²⁺, phosphate)

🔹 Hypoparathyroidism

  • Correct hypocalcemia, magnesium
  • Evaluate for seizures, laryngospasm, prolonged QT
  • Avoid alkalosis ( ionized Ca²⁺)
  • Ensure recent labs: ionized Ca²⁺, phosphate, Mg²⁺


B. Intraoperative Management

Concern

Hyperparathyroidism

Hypoparathyroidism

Airway

Possible difficult airway in MEN syndrome or hyperplasia

Risk of laryngospasm

Fluid management

Hydration crucial

Care with fluids to prevent dilutional hypocalcemia

Calcium status

Monitor ionized Ca² continuously if possible

Continuous monitoring required

Arrhythmias

Short QT, brady- or tachyarrhythmias

Prolonged QT, torsades risk

Neuromuscular blockade

sensitivity to NMBs

sensitivity to NMBs

Transfusions

Citrate in PRBCs chelates calcium worse hypocalcemia

Can precipitate tetany; Ca² supplementation needed

Ventilation

Avoid hyperventilation (alkalosis ionized Ca²)

Same; maintain normocapnia

ECG Monitoring

QT interval shortening

QT prolongation

Cardiac Contractility

Increases initially

 Decreases

Other

Coagulation (impaired clotting cascade)

Nephrogenic DI



C. Postoperative Considerations

🔹 Post-Parathyroidectomy

  • “Hungry bone syndrome”: Sudden drop in Ca²⁺ due to bone remineralization
    Symptoms: hypocalcemia, tetany, arrhythmias
    Management: aggressive calcium and vitamin D supplementation
  • Monitor for laryngospasm, seizures
  • Observe for hypomagnesemia, hypophosphatemia

🔹 Hypoparathyroid Patients

  • Continue oral calcium, calcitriol
  • ICU monitoring for unstable ionized calcium
  • Watch for respiratory complications (e.g., laryngospasm)


VI. Viva/MCQ Pearls

  • Most common cause of hypoparathyroidism: Post-surgical
  • Classic sign of acute hypocalcemia: Trousseau’s sign
  • Calcium level at which tetany occurs: Ionized Ca²⁺ < 0.9 mmol/L
  • Hungry bone syndrome: Post-parathyroidectomy hypocalcemia
  • QT interval in hypercalcemia: Shortened
  • PTH effect on phosphate: due to renal excretion
  • Calcium gluconate vs. calcium chloride: Gluconate preferred for peripheral IV