Cranial Diabetes Insipidus Flashcards
1
Q
what causes it?
A
familial - very rare
- isolated in most cases
- DIDMOAD (DI, DM, optic atrophy, deaf)
acquired
- idiopathic in 50%
- trauma; road accidents, surgery, skull fracture
- tumour; sarcoid, ext irradiation, meningitis
2
Q
how is it diagnosed?
A
by the water deprivation test (NO water or 8-12 hrs)
check serum and urine osmolalities for 8hr and then 4 hr after giving IM DDAVP
if ur/serum osmol ratio>2 then it is normal, otherwise DI
if low and it improves after DDAVP then it is due to ‘cranial DI’ i.e. deficiency of DDAVP (anf not nephrogenic DI)
3
Q
how is it treated?
A
desmospray - nasally 10-60mcg/day
desmopressin oral tablets - 100-1000mcg per day
desmopressin injection - 1-2mcg IM per day e.g. emergency or post pituitary surgery