FFCP Endo Flashcards
(47 cards)
What is Waterhouse-Friedrichson syndrome?
hypoadrenalism caused by adrenal haemorrhage usually due to meningococcal infection
What might you see on blood test of someone with addison’s?
hypoglycaemia, hyponatraemia and hyperkalaemia
What is the investigation of choice for hypoadrenalism?
synacthen test - short synthetic ACTH. Cortisol measures at 9am then 30 and 60 minutes
How to treat Addisonian crisis?
0.9% saline in large volumes, IV hydrocortisone 100mg bolus stat then IM injections until patient able to take tablets
Sick day rules for addison’s?
glucocorticoid dose should be doubled and the fludrocortisone dose should stay the same
What are ACTH dependent causes of Cushing’s syndrome?
- Cushing’s disease - pituitary tumour secreting ACTH causing adrenal hyperplasia
- ectopic ACTH production most common being small cell lung cancer
First-line investigation for Cushing’s syndrome?
low dose dexamethasone suppression test - failure to suppress cortisol indicates Cushing’s syndrome
also 24 hour urinary free cortisol and late night salivary cortisol
How does high dose dexamethasone suppression test help to diagnose Cushing’s?
failure of the high dose to suppress cortisol suggests an ectopic sourse whilst suppression indicates a pituitary cause
Medical management of Cushing’s syndrome?
ketoconazole, metyrapone
What drug for treatment of symptoms of Grave’s disease?
beta blocker - propranolol
Anti thyroid drugs?
Carbimazole, propylthioruacil
What is a common cause of euvolemic hyponatraemia?
syndrome of inappropriate antidiuretic hormone secretion
What kind of hyponatremia does congestive heart failure cause?
hypervolaemic hyponatraemia
How do you confirm phaeochromocytoma?
24 hour urinary collection of metanephrines
How should you treat hypertension linked to phaeochromocytoma?
first alpha blockade (phenoxybenzamine), then beta blockade (if you do beta blocker first then unopposed alpha stimulation leads to hypertensive crisis)
Treatment of acute hypercalcaemia?
Aggressive rehydration (0.9% saline IV rapidly) and then consider bisphosphonate only when hydrated and calcium isnt falling
Investigations for acromegaly?
first line - serum IGF-1
If IGF1 raised then oral glucose tolerance test to confirm (there will be no suppression of GH)
What drug is ocreotide?
somatostatin analogue - directly inhibits release of growth homrone
What kind of drug is pegvisomant?
GH receptor antagonist - stops the action of growth hormone on the growth hormone receptor to reduce the production of IGF1
Stereotypical presentation of primary hyperaldosteronism?
hypertension, hypokalaemia and metabolic alkalosis. Might also have symptoms such as fatigue, muscle weakness and urination
Plasma renin in conn’s syndrome?
suppressed (whereas it would be elevated in secondary hyperaldosteronism).
This is bc aldosterone is overproduced independently of the RAAS system
Management of Conn’s?
Unilateral adrenal adenoma - surgery
Bilateral adrenal hyperplasia - aldosterone antagonist (eplerenone, spironolactone)
What familial endocrine neoplasia syndromes are associated with phaeochromocytoma?
Von Hippel Lindau disease
MEN 2
SDH mutation
Examples of alpha receptor blockers?
Doxazosin, phenoxybenzamine