Parathyroid disorders - Endo Flashcards
Physio Overview
- Calcium and Phosphate Homeostasis
- 3 sites: intestine, kidney, bone
- 3 hormones: parathyroid hormone (PTH), calcitonin, calcitriol (active Vitamin D)
PTH
↑ renal Ca reabsorption, ↓ renal phos reabsorption, ↑ bone Ca and phos resorption (overall increased Ca and decreased phos levels)
Calcitonin (from thyroid)
↓ renal Ca and phos reabsorption (weak), ↓ bone Ca resorption
Calcitriol (aVitD)
↑ intestinal Ca absorption, ↑ renal Ca and phos reabsorption, ↑ bone Ca and phos resorption during hypocalcemia
- PTH ↑ serum Ca and ↓ serum phos
- Calcitonin ↓ serum Ca (“it tones down Ca”)
- aVitD ↑ serum Ca
- PTH and Calcitonin are opposites
- ↑ PTH = ↑ Ca and ↓ phos
normal interplay
hypocalcemia stimulates
- ↑ PTH, which ↑ bone Ca resorption , ↑ renal Ca reabsorption and ↑ renal aVitD production
- ↑ aVitD ↑ intestinal Ca absorption
hypercalcemia stimulates
-↓ PTH, which ↓ bone Ca resorption (↑ bone mineralization), ↓renal Ca reabsorption (↑ renal Ca secretion) and ↓ renal aVitD production (which ↓ intestinal Ca absorption)
- too much PTH = hypercalcemia, hypophosphatemia
- too little PTH = hypocalcemia, hyperphosphatemia
HYPERPARATHYROIDISM
Epidemiology
-1-4/1000, mc in >70yo Females, 10% familial
Etiology
- 1⁰ : 80% parathyroid adenoma, 20% hyperplasia, <1% carcinoma
- 2⁰ - the body normally responding to hypocalcemia, as in a Malabsorption Syndrome with subsequent 2⁰ hyperparathyroidism
1⁰: nl or ↑ PTH ↑ Ca
2⁰: ↑ PTH nl or ↓ Ca
HYPERPARATHYROIDISM - pathophys
Physio
- Increase serum calcium concentration
- ↑ renal Ca reabsorption, ↓ renal phos reabsorption, ↑ bone Ca and phos resorption
Pathophysio
- ↑ PTH = hypercalcemia because more Ca is reabsorbed in the kidneys and more is leeched out of the bone = demineralization -> fx or bone cysts (osteitis fibrosa cystica)
- ↑ PTH = so much Ca ends up in the glomerular filtrate, that the kidneys can’t keep up reabsorbing it = hypercalciuria -> nephrolithiasis
- ↑ PTH = less kidney phos reabsorption = more phos into the urine = hyperphosphaturia and nl/hypophosphatemia
HYPERPARATHYROIDISM - s/s
S/S
- hyperPTH is the mcc of hypercalcemia
- hyperCa usually found incidentally on routine chem panels
- mild hyperCa may be silent or have so little symptoms that they are only found on specific history questioning
- mild hyperCa = measured Ca < 12mg/dL, symptomatic hyperCa = measured Ca >12mg/dL
- hyperCa = adjusted total Ca >10.5 mg/dL
- adjusted Ca = corrected Ca = measured Ca + [0.8 x (4.0 - serum albumin)]
hypercalcemia symptoms = “Bones, Stones, (abdominal) Groans, (psychiatric) Moans, (fatigue) Overtones”
- bones: more trabecular/less cortical bone (thin cortex on XR), low bone density/demineralization -> bone pain and tenderness, arthralgias, fxs
- stones: calcium nephrolithiasis
- groans: abdominal pain (N/V/D/C)
- moans: depression, cognitive impairment (memory loss), psychosis, stupor…
- overtones: malaise, fatigue
- others: polyuria/polydipsia (hypercalciuria), cardiac (arrhythmias, heart block, HTN, athero progression), PUD, pancreatitis, neuro (paresthesias, weakness)
HYPERPARATHYROIDISM - w/u, tx
W/U
- measured serum Ca, albumin, phosphate
- spot urinary Ca
- PTH assay
- bone density
- imaging not usually necessary unless planning surgery (dx is based on labs)
Tx
- if asymptomatic: monitor, keep active, drink adequate fluids, avoid immobilization, avoid thiazides and high doses of VitA and Ca-containing antacids, biannual serum Ca and albumin, annual BUN/Cr and urine Ca, bone density q2y
- if symptomatic (especially if kidney stones or bone disease): surgical parathyroidectomy
HYPOPARATHYROIDISM
Etiology
- congenital
- acquired: post thyroidectomy or parathyroidectomies
- autoimmune: associated with other endocrinopathies
- associated with heavy metal disease (Wilson’s Dz = copper; Hemochromatosis = iron)
- concomitant with Mg deficiency
HYPOPARATHYROIDISM - pathophys
Physio
-↑ renal Ca reabsorption, ↓ renal phos reabsorption, ↑ bone Ca and phos resorption
Pathophysio
- ↓ PTH = ↓ renal Ca reabsorption = ↑ Ca excretion = hypocalcemia and hypercalciuria
- ↓ PTH = more kidney phos reabsorption = less into the urine = hyperphosphatemia
HYPOPARATHYROIDISM - s/s
hypocalcemia
- tetany, cramps, carpopedal spasm
- altered mental status, convulsions
- stridor
- perioral and distal extremity paresthesias
- Chvostek Sign: tapping on the facial n. gives facial m. contraction
- Trousseau phenomenon: carpal/digital spasm on inflating a BP cuff
HYPOPARATHYROIDISM - w/u, tx
W/U
- measured Ca and albumin to get corrected Ca
- PTH assay
- EKG prolonged QT interval, T wave
Tx
-acute tetany with stridor may require emergency treatment: intubation, IV CaGluconate, PO Ca and VitD and Mg
-goal is serum Ca 8-8.5 mg/dL
i-f mild/asymptomatic, monitoring
-if chronic/symptomatic, then mainly po Ca and VitD
-recombinant PTH/teriparatide/Forteo, but very expensive
-monitor with serum Ca and spot urine Ca to keep at <30mg/dL