Clin Med - Parathyroid (Carlozzi) Flashcards

1
Q

Identify the symptoms consistent with hyperparathyroidism

A
  • Stones: renal stones, polyuria, polydipsia, uremia
  • Bones: osteitis fibrosa, radiologic osteoporosis, osteomalacia - MC phalanges or distal clavicles
  • Abdominal Groans: constipation, nausea, vomiting, peptic ulcer, pancreatitis
  • Psychic Moans: lethargy, fatigue, depression, memory loss, psychosis, personality change, confusion, coma
  • Short QT interval
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2
Q

Outline the medical therapy of primary hyperparathyroidism

A
  • Usually managed surgically
  • Observation reserved for patients with comorbid conditions who can’t tolerate surgery or for very elderly patients who may die of another cause
  • In postmenopausal women: estrogen supplements and alendronate may help with bone density
  • Those who go through parathyroidectomy should be monitored with metabolic panels and assessment of bone mass
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3
Q

Explain the role of using a parathyroid hormone level to determine the cause of hypercalcemia

A

•Intact PTH can differentiate hyperparathyroidism induced hypercalcemia from other forms of hypercalcemia

  • if PTH high, then cause for hypercalcemia is hyperparathyroidism
  • if PTH suppressed, then other etiologies must be investigated
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4
Q

What does the term “hungry bone syndrome” mean?

A

marked hypocalcemia and hypophosphatemia can occur in those with long-standing hyperparathyroidism and extensive bone resorption

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5
Q

Explain the manifestations of hungry bone syndrome

A
  • Rebound uptake of calcium and phosphorus by bones that have been starved from hyperparathyroidism results in postop hypocalcemia
  • usually seen in pts with elevated preoperative alk phos
  • Will have low phosphorus (high in surgical hypoparathyroidism), elevated PTH, and low mg
  • can be associated with severe and diffuse bone pain
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6
Q

What is the treatment of hungry bone syndrome?

A

If pt is symptomatic, use IV calcium.

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7
Q

Outline the monitoring parameters for post-surgical parathyroidectomy patient.

A
  • Serum calcium monitored several weeks after surgery until levels stabilized
  • Calcium/PTH checked 6 months post-op to exclude persistent hyperparathyroidism
  • If treated with oral calcium/vitamin D, IV calcium used for severe/symptomatic hypocalcemia
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8
Q

Parathyroidectomy 1+ gland versus 4-gland removal.

A

When 1+ parathyroid gland identified/preserved - parathyroid hormone level usually return to normal and 4-gland removal can lead to permanent hypoparathyroidism

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9
Q

Identify the symptoms consistent with hypoparathyroidism

A
  • Paresthesia
  • Hyperirritability
  • Fatigue
  • Anxiety
  • Mood swings/personality disturbances
  • Seizures
  • Hoarseness
  • Wheezing/dyspnea
  • Muscle cramps, diaphoresis, biliary colic
  • Hypomagnesemia, hypokalemia, alkalosis - worsen signs/sx of hypocalcemia
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10
Q

Describe the iatrogenic cause of hypoparathyroidism

A
  • Excision of all parathyroid glands through surgery in treatment of thyroid, laryngeal or other neck malignancy
  • Repeated neck explorations for primary hyperparathyroidism caused by parathyroid adenoma may also cause it
  • Extensive irradiation of face, neck mediastinum - can cause destruction of all 4 parathyroid glands
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11
Q

Lab workup of hypoparathyroidism

-PTH hormone

A

•Low concentration with concomitant low calcium level in primary hypoparathyroidism

  • Would be elevated as result of resistance to PTH from mutations in PTH receptor system: if pseudohypoparathyroidism
  • Low, with high calcium levels in secondary hypoparathyroidism
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12
Q

Lab workup of hypoparathyroidism

-calcium

A

•Total calcium level cannot be interpreted without protein/albumin levels

  • Hypoalbuminemia can cause low overall calcium levels: for every 1mg/dL drop in serum albumin below 4.0, add 0.8mg/dL to the calcium
  • Alkalosis causes ionized calcium to bind to albumin more strongly: causes decrease in ionized calcium
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13
Q

Lab workup of hypoparathyroidism

-vitamin D

A

Important to exclude vitamin D deficiency as cause of hypocalcemia

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14
Q

Lab workup of hypoparathyroidism

-serum magnesium

A

Hypomagnesemia may cause PTH deficiency and hypocalcemia: exclude in patient with primary hypoparathyroidism

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15
Q

Lab workup of hypoparathyroidism

-serum phosphorus

A

In absence of PTH, phosphorus levels in blood may rise

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16
Q

Outline the monitoring parameters for patient with chronic hypocalcemia

A
  • Serum calcium, phosphorus, creatinine: weekly-monthly during initial phase and twice yearly after treatment stabilization
  • F/u evaluations: every 1-2 weeks during initial phase and every 3-6 months after treatment stabilization
  • Urinary calcium: twice yearly
  • Ophthalmoscopic exam: yearly