Y2 ENDOCRINE TESTS Flashcards

1
Q

to investigate if adrenal insufficiency?

A

short synacthen test

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2
Q

how do you perform a short synacthen test?

A
  • measure plasma cortisol
    before test.

–> IV/IM ACTH

  • measure plasma 30 minutes after.
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3
Q

what is a normal ACTH baseline?

A

> 250nmol/L

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4
Q

what should cortisol be normally after ACTH injection

A

> 550nmol/L

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5
Q

what will happen in the synacthen test if the patient has adrenal insufficiency?

A

cortisol will remain low despite ACTH injection.

Should not rise above >550nmol/L after 30 min or increase by >200nmol/L.

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6
Q

what will happen to levels in the synacthen test if the patient has adrenal insufficiency?

A
  • very high ACTH.
  • low cortisol.
  • high renin.
  • low aldosterone.
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7
Q

how do you diagnose cushing’s?

A
  1. overnight dexamethasone suppression test.
  2. 24hour urinary free cortisol.
  3. late night salivary cortisol.
  4. low dose dexamethasone suppression test.

repeat to confirm.

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8
Q

what results of an overnight dexamethasone test will be seen in Cushing’s?

A

plasma cortisol >50nmol/L.

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9
Q

what results of a 24 hour urine free cortisol will be seen in Cushing’s?

A

elevation

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10
Q

what results of a low dose dexamethasone suppression test would indicate cushing’s?

A

no suppression.

if there is suppression it suggests another cause e.g. depression, obesity, alcohol abuse.

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11
Q

following a failure of cortisol to suppress after a low dose dexamethasone suppression test, what would be the next step?

A

imaging/investigation for pituitary adenoma or ectopic source of ACTH.

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12
Q

test to diagnose primary aldosteronism?

A

aldosteron to renin ratio.

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13
Q

if suspicion of primary aldosteronism and ARR is raised, what is the next step?

A

saline suppression test

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14
Q

what confirms primary aldosteronism?

A

failure of plasma aldosterone to suppress by >50% with 2 litres of saline

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15
Q

how do you confirm subtype of primary aldosteronism?

A
  • adrenal CT to check for adenoma or bilateral adrenal hyperplasia.

?- adrenal vein sampling to confirm adenoma is true source of excess aldosterone - only sometimes check?

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16
Q

how do you diagnose congenital adrenal hyperplasia?

A

basal or stimulated 17-OH progesterone.

17
Q

how do you investigate phaeochromocytoma initially?

A
  • urinary 24 hour catecholamines or metanephrins.
  • plasma catecholamine (ideally when symptomatic).

note it is episodic catecholamine secretion therefore urine and plasma levels may be normal.

18
Q

how do you confirm phaeochromocytoma once catecholamine excess has been established?

A

MRI scan (abdo. or whole body).

  • MIBG
  • PET
19
Q

when might phaeochromocytoma levels of catecholamine be low?

A
  • if malignant or extra-adrenal as they are less efficient at catecholamine synthesis.
  • catecholamine excretion is episodic.
20
Q

investigation of hypercalcaemia?

A

PTH

21
Q

Low/normal albumin +
- suppressed PTH
- high phosphate
suggests?

A

bone pathology

22
Q

Low/normal albumin +

  • high/normal PTH
  • low/normal phosphate
  • reduced urine Ca2+ suggests?
A

familial hypocalciuric hypercalcaemia (FHH)

23
Q

Low/normal albumin +

  • high/normal PTH
  • low/normal phosphate
  • increased urine Ca2+ suggests?
A

primary or tertiary hyperparathyroidism

24
Q
  • hypercalcaemia
  • raised albumin
  • raised urea
    suggests?
A

dehydration

25
Q
Low/normal albumin +
- suppressed PTH
- high phosphate 
\+ high alk. phosphatase (ALP)
suggests?
A
  • bone mets
  • sarcoidosis
  • thyrotoxicosis
26
Q
Low/normal albumin +
- suppressed PTH
- high phosphate 
\+ low alk. phosphatase (ALP)
suggests?
A
  • myeloma.
  • vit. D excess
  • mild alkali syndrome (thyrotoxicosis, sarcoidosis, raised HCO3)
27
Q
  • hypercalcaemia
  • raised ALP
  • suppressed PTH
    suggests?
A

malignancy

28
Q

how do you diagnose hypercalcaemia of malignancy?

A
  • x-ray, CT, MRI

- isotope bone scan

29
Q

how do you image the parathyroid glands?

A

sestamibi scan

30
Q
  • raised PTH

- raised Ca2+

A

primary or tertiary hyperparathyroidism

31
Q
  • low Ca2+

- raised PTH

A

secondary hyperparathroidism

32
Q

how do you diagnose Paget’s disease?

A
  • x-ray
  • isotope bone scan shows distribution across body
  • raised ALP and normal liver function test