Hypocalcemia & hypoparathyroidism Flashcards

1
Q

What is hypocalcemia?

A
  • serum calcium < 8.8 mg/dL with normal albumin

- ionized calcium < 4.45mg/dL

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2
Q

What are the causes of hypocalcemia post-op?

A
  • injury to parathyroid gland or its blood supply

- resection of parathyroid gland

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3
Q

What are the clinical features of hypocalcemia?

A
  • paresthesia
  • tetany
  • seizures
  • muscle cramps
  • muscle weakness
  • confusion
  • disorientation
  • Chvostek’s sign
  • Trousseau’s sign
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4
Q

How do u calculate the correction of calcium?

A

correct calcium = 0.8 x (normal albumin - patient’s albumin) + serum calcium

normal albumin = 3.4 - 5.4

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5
Q

When should a cAMP workup be ordered in hypocalcemia?

A

to differentiate between hypoparathyroidism & pseudo hypothyroidism
- elevated in hypoparathyroidism in response to PTH test

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6
Q

What will be seen on an ECG in case of hypocalcemia?

A

prolonged QT secondary to hypocalcemia -> ventricular arrhythmias

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7
Q

How is hypocalcemia treated?

A
  • maintain serum calcium in low normal range
    mild to moderate
  • oral calcium supplement (1-3g in 3 to 4 divided doses with meals) & vitamin D (calcitriol 0.5 twice a day)
  • calcium carbonate (40% elemental calcium)
  • calcium lactate (13%), calcium citrate (21%), calcium gluconate (9%)
  • patients with PPI or elderly -> calcium citrate
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8
Q

What increases the intestinal absorption of calcium?

A

Calcitriol
- short half-life -> 5 to 8 hours

Vitamin D3 (cholecalciferol) 
- longer half-life -> weeks to months 

increases phosphate absorption
- incase of severe hyperphosphatemia with vitamin D therapy -> give phosphate binders

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9
Q

What is the recommended magnesium replacement for low magnesium levels?

A
  • magnesium oxide 400mg BID -> could enhance calcemic recovery
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10
Q

How is severe hypocalcemia treated?

A

< 7.5 &/or severe symptoms

  • IV calcium
  • bolus -> 1 - 2g of calcium gluconate infused over 20 mins
  • calcium drip of 11g calcium gluconate in 1L 5% dextrose -> administered at 50mL/hr (IN PERSISTENT HYPOCALCEMIA)

as soon as patient is able too swallow -> higher doses of oral calcium (3 - 4g daily in 3 - 4 doses)

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11
Q

What is the goal of long term management of hypocalcemia?

A
  • maintain serum calcium within asymptomatic range
  • calcium + vitamin D + magnesium + thiazides

When calcium control is difficult
- give thiazide diuretics (>150mg/hr)

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12
Q

Albright hereditary osteodystrophy occurs due to?

A

Pseudohypothyroidism -> GNAS1 gene mutation

- short stature, round face, brachydactyly, obesity, & subcutaneous calcifications

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13
Q

What’s the disease variation is case of mother or father inheriting?

A

If from mother -> all signs of AHO + multiple hormone resistance
If from father -> AHO without resistance

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14
Q

How should PHP & iPPSD be treated?

A
  • maintain total & ionized calcium levels within reference range to suppress PTH levels
  • calcitriol, with oral calcium supplements
  • severe symptomatic hypocalcemia -> IV calcium
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