Pituitary Flashcards
Which hypothalamic hormones stimulate what pituitary hormones
GHRH- GH GnRH- LH and FSH TRH- TSH and Prolactin Dopamine- inhibits prolactin CRH- ACTH
Contraindications to the CPFT
- Ischaemic heart disease
- Epilepsy
- Untreated hypothyroidism (impairs the GH and cortisol response)
Summary of CPFT
- Fast patient overnight, ensure good IV access, weigh patient
- Mix into 5ml syringe: insulin dose (0.15 units/kg), TRH 200mcg, LHRH 100mcg - give IV
- Bloods: basal thyroxine plus glucose, cortisol, GH, LH, FSH, TSH, prolactin every 30min for
1 hour- Glucose, cortisol, GH up to 2 hours - Replacements: urgent hydrocortisone, T4, oestrogen, GH
Interpretation of Insulin aspect of CPFT
Insulin should cause hypo - <2.2mmol/L- therefore increasing ACTH and GH
oAdequate cortisol response=↑greater than 170nmol/l to above 500nmol/l.
o Adequate GH response=↑greater than 6mcg/L
Interpretation of TRH aspect of CPFT
Should raise TSH and prolactin (usually dopamine inhibits prolactin but if hypothyroid prolactin is high due to lack of neg feedback)
o The normal result is a TSH rise to>5mU/l (30 min value>60 min value)
o Hyperthyroidism=TSH remains suppressed
o Hypothyroidism=exaggerated response.
GnRH interpretation of CFPT
Should increase LH/FSH
Peak around 30/60 mins
LH should > 10 U/l and FSH should > 2 U/l.
An inadequate response=possible early indication of hypopituitarism.
Gonadotrophin deficiency is diagnosed the basal levels rather than the dynamic
response.
§ Males = low testosterone in the absence of raised basal gonadotrophins
§ Females = low oestradiol without elevated basal gonadotrophins and no
response to clomiphene.
§ Pre-pubertal children should have no response of LH or FSH to LHRH.
Difference in size of micro and macro adenoma
- Microadenoma < 10mm, usually benign
* Macroadenoma > 10mm, aggressive
Differentials of different prolactinaemia
Non-functioning pituitary adenoma– ↑↑ prolactin (1000-5000)
Prolactinoma– ↑↑↑ prolactin (>6000), no in ↑ in GH (>10) and cortisol (>550nM)
Acromegaly- ↑↑GH (even before baseline), ↑ Prolactin, no ↑ in cortisol
Treatment of prolactinoma
1st line Mx: Replacements (hydrocortisone, T4, oestrogen, GH), DA agonists (cabergoline, bromocriptine)- due to hypopituitarism
2nd line Mx: Transphenoidal excision (if visual/pressure Sx not responding to medical Tx)
Treatment of Non functioning Pit adenoma
Cabergoline/bromocriptine- dopamine agonists; watch and wait if asymptomaticCan do nothing if not causing patients any Sx
Treatment of Acromegaly
Mx:
1. Transsphenoidal surgery (best)
2. Pituitary radiotherapy (if surgery fails)
3. Cabergoline
4. Octreotide (expensive) - somatostatin analogue
(cannot stop once started)
5. GH antagonist - pegvisomant
Causes of excess ADH
Lung paraneoplastics- usually small cell
SSRI
SIADH
Causes of depleted ADH
Diabetes Insipidues
Neurogenis
Nephrogenic- lithium