Endo Flashcards
4 causes of hypovolaemic hyponatraemia with low urine sodium (<20)
- normal kidney function
a) vomiting
b) diarrhoea
c) trauma
d) burns
3 causes of hypovolaemic hyponatraemia with high urine sodium (>20)
- renal loss
a) Addison’s
b) diuretics
d) renal failure (CKD)
3 causes of hypervolaemic hyponatraemia
a) heart failure
b) nephrotic syndrome
c) liver failure
causes of euvolaemic hyponatraemia with high urine sodium (>20)
SIADH
causes of euvolaemic hyponatraemia with normal urine sodium
- hypothyroidism
what is pseudohyponatraemia
low sodium with high/normal serum osmolarity
causes of pseudohyponatraemia
normal serum osmo:
- hyperlipidaemia, hyperproteinaemia
high serum osmo:
- hyperglycaemia, mannitol
causes of SIADH
a) drugs: SSRIs, sulphonylurea, PPI
b) chest: small cell cancer, TB
c) neuro: infection, SAH
management of SIADH
fluid restriction + vaptans
effect of pituitary tumour on visual field
bitemporal hemianopia
management of hypervolaemic hyponatraemia
fluid restriction + furosemide
management of hypovolaemic hyponatraemia
slow infusion of saline
complication of untreated hyponatraemia
cerebral oedema
complications of rapid correction of hyponatraemia
osmotic demyelination syndrome (locked in syndrome)
3 causes of hypernatraemia
- dehydration
- diabetes insipidus
- Conn’s, Cushing’s
complications of rapid correction of hypernatraemia
cerebral oedema
HPG axis in prolactinoma
i) too much prolactin stops kisspeptin in
hypothalamus
ii) less GnRH
iii) less LH & FSH
-> dopamine stops prolactin
what are other causes of raised prolactin
- pregnancy
- PCOS
- metoclopramide
prolactinoma presentation in men
low libido
erectile dysfunction
infertility
gynaecomastia
headache
bitemporal hemianopia
prolactinoma presentation in women
low libido
amenorrhoea
infertility
galactorrhoea
headache
bitemporal hemianopia
prolactinoma investigations
i) urine beta HCG
ii) high prolactin > 6000
iii) low LH & FSh
iv) pituitary MRI
prolactinoma treatment
i) cabergoline (dopamine agonist)
ii) surgery only if cabergoline fails
acromegaly presentation
coarse facial features
big hands
prognathism
headaches
bitemporal hemianopia
sweating
acromegaly investigations
i) plasma IGF-1
ii) oral glucose tolerance test (diagnostic)
- GH rises instead of falling
iii) pituitary MRI
acromegaly management
i) transsphenoidal surgery
ii) octreotide if inoperable
- also dopamine agonists
acromegaly complications
diabetes
hypertension
cardiomyopathy
pseudogout
what is Addison’s
autoimmune adrenal gland destruction
presentation of Addison’s
hyperpigmentation
weakness
vomiting
weight loss
salt craving
electrolytes in Addison’s
hyponatraemia
hyperkalaemia
metabolic acidosis
hypoglycaemia
diagnostic test for Addison’s
short synACTHen test
how to investigate secondary hypocortisolism (low ACTH)
insulin induced hypoglycaemia
- normal should make ACTH