Parathyroid Disease Flashcards

1
Q

What is hyperparathyroidism?

A

Excessive release of PTH

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2
Q

What is the feedback mechanism for the parathyroid gland?

A

Aim ↑Ca2+ & ↓Phos
Parathyroid detects low level of extracellular Ca2+
Releases PTH
Bones: Leads to bone resorption
Kidneys: Reabsorption of Ca2+ & excretion of PO4-, ↑Calcitriol (active vit D)
Intestine: ↑Ca2+ absorption

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3
Q

What is diffusible & non-diffusible Ca2+?

A

D: Free ionised (Muscle contraction, neuronal action, hormone secretion, coagulation)
ND: Bound to -ve charge proteins (Albumin, not involved in cellular processes)

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4
Q

What is primary hyperparathyroidism?

A

Parathyroid gland releases PTH independent of extracellular Ca2+ levels
Stimulates osteoclast to break down bones
↑bowel + ↑renal reabsorption of Ca2+
Bloods: ↑Ca + ↑PTH + ↓PO4

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5
Q

What does primary hyperparathyroidism lead to?

A

Hypercalcaemia

Hypophosphataemia

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6
Q

What are the causes of primary hyperparathyroidism?

A

80% Parathyroid adenoma
Hyperplasia
Parathyroid carcinoma

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7
Q

What does hypercalcaemia do to muscle contractions?

A

↓slows muscle contraction, diminishes neuron firing

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8
Q

What are the severities of hyperparathyroidism?

A

Mild: Ca <2.8
Mod: Ca<3.5
Severe: >3.5
ALSO APPLIES TO HYPERCA OF MALIGNANCY

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9
Q

What are the different Sx for the different severities of hyperparathyroidism?

A

MILD: Polyuria, polydipsia, dehydration, dyspepsia, mild cognitive impairment
MOD: Mild Sx, muscle weakness, constipation, anorexia, renal stones, fatigue
SEVERE: Prev Sx, abdo & bone pain, N&V, arrhythmia, confusion, fits, coma

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10
Q

How is hyperparathyroidism investigated?

A
BP: HTN
Bloods: U&amp;E (↑PTH, ↑Ca2+, ↓PO4), LFTs (↑ALP)
24hr urinary Ca2+
ECG: Short QT interval
DEXA Scan: Osteoporosis
Biopsy: ?Carcinoma
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11
Q

How is hyperparathyroidism managed?

A

MILD:

1) Fluids
2) Vit D/Cholecalciferol
3) Cinacalcet
4) Parathyroidectomy: <50yo, end organ damage, creatinine clearance <60 if asymptomatic

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12
Q

What drugs should be avoided in hyperparathyroidism?

A

Thiazides

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13
Q

What are the complications of hyperparathyroidism?

A

Osteoporosis
Pancreatitis
Osteitis fibrosa cystica
Nephrocalcinosis

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14
Q

What diagnosis needs to be ruled out in parathyroid issues?

A

Malignancy- Parathyroid produced by SCLC mimics PTH

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15
Q

What is secondary hyperparathyroidism?

A

Parathyroid gland hyperplasia

Leads to the release of excess PTH in response to chronic hypoCa

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16
Q

What are the causes of secondary hyperparathyroidism?

A

CKD (common)

Chronic lack of calcitrol (↓Vit D/ lack of sunlight)

17
Q

What are the Sx of hypocalcaemia?

A
Tetany: Twitching, spasms, cramps
Perioral paraesthesia
Trousseau (BP cuff on = cramp)
Chvostek's sign: Tap parotid = facial twitch
ALL SEEN IN HYPOPARATHYROIDISM
18
Q

How is secondary hyperparathyroidism investigated?

A
Bloods:
↑PTH
↓Ca2+
↑Phosph
↓Vitamin D
19
Q

How is secondary hyperparathyroidism managed?

A

Correct cause

Cinacalcet if PTH >85

20
Q

What is tertiary hyperparathyroidism?

A
Prolonged 2o hyperPTH
Develop primary
Release PTH independent of Ca2+ levels
HYPERCALCAEMIA
↑Ca2+ +  ↑↑PTH
21
Q

What are the complications of secondary hyperparathyroidism?

A

Renal osteodystrophy- due to excess bone resorption

Calcification in blood & soft tissue- ↑phosphate stick to Ca2+ in vessels = calcification

22
Q

What is hypercalcaemia of malignancy?

A
Tumours produce GF
Transforms GFa into PTH
Leads to bone resorption 
Releases Ca2+ into blood
Also renal tubular Ca2+ reabsorption
Also GI Ca2+ absorption
23
Q

What are the most common malignant causes of hyperCa?

A
Lung cancer
Breast
Myeloma
Renal cell
Lymphoma
Head &amp; neck cancers
24
Q

How is hypercalcaemia of malignancy treated?

A

1) IV Fluids: 0.9% NaCl 3-4L/day
2) Bisphosphonates: IV infusion Zolindronic acid/ Pamidronate IF Ca2+ >3
3) Corticosteroids (Sarcoidosis)
4) Calcitonin: If symptomatic + Ca2+ >4

25
Q

Describe how bisphosphonates should be taken?

A

Given post re-hydration
Tablet w/lots of water
Sat up/standing
On empty stomach (30mins before)

26
Q

What are the SE of bisphosphonates?

A

Acute: Fever, myalgia, arthralgia
GI: Reflux, oesophagitis, ulcers
Atypical fractures
Osteonecrosis of the jaw

27
Q

How is hypoparathyroidism managed?

A

Primary & Pseudo: Ca2+ = Alfacalcidol supplements

Secondary:

28
Q

What are the causes of hypoparathyroidism?

A

Primary: ↓PTH due to gland failure– AI or Di George synd
Secondary: RT, surgery (para)thyroidectomy, hypoMg
PseudohypoPTH: Failure of target cell response to PTH
PseudopseudohypoPTH: Morphological Sx of pseudo but normal biochemistry.

29
Q

What are the investigations for hypoparathyroidism?

A
Bloods:
Exclude other causes of hypoCa
Primary= ↓Ca ↑Phos, ↓PTH, normal ALP
PseudohypoPTH = ↓Ca ↑Phos ↑/(N) PTH
U+Es: Exclude CKD 
Vitamin D3: Exclude vit.D def  
ECG: Prolonged QT
Urinary cAMP &amp; PO4- post-PTH infusion: ∆ pseudohypoPTH
30
Q

What are the causes of hypercalcaemia?

A
Malignancy
Hyperparathyroidism
Sarcoidosis
Vit D intoxication
Drugs: Thiazides
31
Q

How is primary hyperparathyroidism diagnosed?

A

Adjusted Ca↑ PTH↑ ↑urinary Ca >2.5
U&E normal
NOT on Li or thiazide

32
Q

What are the causes of raised PTH?

A

Renal failure
Vit D deficiency
Renal hypercalciuria
Drugs (Lithium, thiazides)