Hypocalcemia & hypoparathyroidism Flashcards
What is hypocalcemia?
- serum calcium < 8.8 mg/dL with normal albumin
- ionized calcium < 4.45mg/dL
What are the causes of hypocalcemia post-op?
- injury to parathyroid gland or its blood supply
- resection of parathyroid gland
What are the clinical features of hypocalcemia?
- paresthesia
- tetany
- seizures
- muscle cramps
- muscle weakness
- confusion
- disorientation
- Chvostek’s sign
- Trousseau’s sign
How do u calculate the correction of calcium?
correct calcium = 0.8 x (normal albumin - patient’s albumin) + serum calcium
normal albumin = 3.4 - 5.4
When should a cAMP workup be ordered in hypocalcemia?
to differentiate between hypoparathyroidism & pseudo hypothyroidism
- elevated in hypoparathyroidism in response to PTH test
What will be seen on an ECG in case of hypocalcemia?
prolonged QT secondary to hypocalcemia -> ventricular arrhythmias
How is hypocalcemia treated?
- 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
What increases the intestinal absorption of calcium?
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
What is the recommended magnesium replacement for low magnesium levels?
- magnesium oxide 400mg BID -> could enhance calcemic recovery
How is severe hypocalcemia treated?
< 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)
What is the goal of long term management of hypocalcemia?
- maintain serum calcium within asymptomatic range
- calcium + vitamin D + magnesium + thiazides
When calcium control is difficult
- give thiazide diuretics (>150mg/hr)
Albright hereditary osteodystrophy occurs due to?
Pseudohypothyroidism -> GNAS1 gene mutation
- short stature, round face, brachydactyly, obesity, & subcutaneous calcifications
What’s the disease variation is case of mother or father inheriting?
If from mother -> all signs of AHO + multiple hormone resistance
If from father -> AHO without resistance
How should PHP & iPPSD be treated?
- maintain total & ionized calcium levels within reference range to suppress PTH levels
- calcitriol, with oral calcium supplements
- severe symptomatic hypocalcemia -> IV calcium