Hypercalcaemia Flashcards

1
Q

What is Hypercalcaemia

A

Calcium levels <2.6

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2
Q

At what point does hypercalcamia need to be treated

A

> 3.0

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3
Q

What should be done if calcium levels are >3.5

A

Requires urgent correction due to risk of dysrhythmia and coma

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4
Q

What categories can the causes of hypercalcaemia be put into

A

Parathyroid mediated
Non-Parathyroid mediated
Medications
Miscellaneous

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5
Q

What are the most common parathyroid mediated cause of hypercalcaemia

A

Primary hyperparathyroidism (sporadic) (most common)

Multiple endocrine neoplasia (MEN)

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6
Q

What is the most common Non-Parathyroid mediated causes of hypercalcaemia

A

Hypercalcaemia of malignancy

Vitamin D intoxication

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7
Q

When should you consider medicine as a cause of hypercalcaemia

A

Medicines should be considered of there is a slow rise in calcium

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8
Q

Whats the most common medicine that can cause hypercalcaemia

A

Thiazide diuretics

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9
Q

What are the clinical features of Hypercalcaemia

A

Polyuria
Polydipsia
nephrolithiasis

Anorexia
Nausea and vomitting

Muscle weakness

Decreased concentration

Shortning of QT interval

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10
Q

Why is the rate of calcium increase important

A

Hypercalcaemia is generally better tolerated if the rate of increase has been slow.

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11
Q

What investigations should you do for hypercalcaemia

A

PTH (most important)

U&Es 
Ca  
PO4  
Alk phos  
Myeloma screen  
Serum ACE 
Consider ECG
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12
Q

What is first line treatment for hypercalcemia

A

Rehydration – 0.9% Saline 4-6 litres over 24 hours – Monitor for fluid overload – Consider dialysis if severe renal failure

After rehydration, intravenous bisphosphonates (take couple of days to work) – Zolendronic acid 4mg over 15 mins – Give more slowly and consider dose reduction if renal impairment – Calcium will reach nadir at 2-4 days.

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13
Q

What is Primary hyperparathyroidism

A

Primary hyperparathyroidism is a condition in which one or more of the parathyroid glands makes too much PTH.

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14
Q

What is the epidemiology of Primary hyperparathyroidism

A

Female: male = 3:1

Incidence peaks 50-60 years

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15
Q

Whats the causes of Primary hyperparathyroidism

A

85% parathyroid adenoma
15% four gland hyperplasia
<1% MEN type 1 or 2A
<1% parathyroid carcinoma

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16
Q

Whats the presentation of Primary hyperparathyroidism

A

Usually asymptomatic

17
Q

What is the aim of investigations for

Primary hyperparathyroidism

A

To confirm diagnosis then find affects of hypercalcaemia

18
Q

What investigations should be carried out for Primary hyperparathyroidism

A

Ca,

PTH

U&Es: check renal function

Abdominal imaging: renal calculi

DEXA: osteoporosis

Spot urinary calcium/creatinine ratio

24 hour urinary calcium:

19
Q

Why do you do a Spot urinary calcium/creatinine ratio

A

To exclude Familial hypocalciuric hypercalcaemia … A RARE MIMIC

20
Q

What is the treatment for primary hyperparathyroidism

A

SURGICAL – definitive treatment. Curates 95% of people.

Medical

21
Q

What are indications for surgery primary hyperparathyroidism

A

Presence of symptoms due to hypercalcaemia

High serum calcium

Osteoporosis

Reduced GFR or presence of kidney stones

<50 years

22
Q

What is the medical management of primary hyperparathyroidism

A

Generous fluid intake (2-3 l/day)

Vitamin D replacement Cinacalcet

23
Q

What is Cinacalcet

A

Acts as a calcimetic and mimics the effect of calcium on the calcium sensing receptor on Chief cells, this leads to a fall in PTH and subsequently calcium levels) – expensive

24
Q

What is Familial hypocalciuric hypercalcaemia (FHH)

A

Autosomal dominant disorder of the calcium sensing receptor (runs in families)

25
How do you check for hypocalciuric hypercalcaemia (FHH)
It will present with Low urinary calcium levels (which should be high in primary hyperparathyroidism
26
What is multiple endocrine neoplasia
Autosomal dominoant conditions that present with a group of associated endorcrine conditions.
27
What should you think to suspect MEN type 1
Primary hyperparathyroidism Pancreatic Pituitary
28
What should you think to suspect MEN type 2
Medullary thyroid cancer | Phaeochromocytoma Primary hyperparathyroidism