Pituitary Flashcards

1
Q
  1. Why doesn’t hypopituitarism cause low blood pressure?
A

The adrenals are still able to produce aldosterone

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2
Q
  1. Which hypothalamic hormones affect prolactin release?
A

Dopamine – negative
TRH – positive
NOTE: hypothyroidism causes hyperprolactinaemia

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3
Q
  1. How might pituitary failure present in women?
A

Amenorrhoea and galactorrhoea

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4
Q
  1. What is the main problem with prolactinomas?
A

It might reduce/stop the production of other pituitary hormones (e.g. ACTH, TSH, GH)
High prolactin in itself is not much of an issue

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5
Q
  1. What is the CPFT?
A

Combined Rapid Anterior Pituitary Evaluation Panel

Test for pituitary function

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6
Q
  1. Which three stimuli of pituitary hormone secretion are used in the CPFT?
A

Hypoglycaemia – increases CRF/ACTH and increases GHRH/GH
TRH – increases TSH and prolactin
LHRH – increases LH and FSH

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7
Q
  1. What safety precautions must you take before subjecting a patient to hypoglycaemia?
A

No cardiac risk factors (needs a normal ECG)
No history of epilepsy
Ensure good IV access

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8
Q
  1. Describe the manifestations of increasing hypoglycaemia?
A

Initially, activation of the sympathetic nervous system will result in sweating, tachycardia etc.
When the blood glucose reaches < 1.5 mM, neuroglycopaenia may occur (loss of consciousness and confusion)

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9
Q
  1. What blood glucose concentration is normally required to stimulate the pituitary gland?
A

< 2.2 mM

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10
Q
  1. How should a patient be rescued if they experience severe hypoglycaemia during this test?
A

50 mL 20% dextrose

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11
Q
  1. Outline the dosing of various drugs in the CPFT.
A
5 mL syringe
Insulin (0.15 U/kg)
TRH 200 µg
LHRH 100 µg
NOTE: the patient may experience a warm flush and vomit when the drug is administered
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12
Q
  1. What should be measured in the blood and how often?
A

every 30 mins for 60 mins
Glucose
Cortisol
GH

every 30 mins for 120 mins
LH and FSH
TSH
Prolactin

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13
Q
  1. What level of cortisol and GH is considered a normal response?
A

Cortisol > 550 nM

GH > 10 IU/L

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14
Q
  1. List the order of hormone replacement in someone with panhypopituitarism.
A
HYDROCORTISONE 
Thyroxine 
Oestrogen 
GH 
NOTE: fludrocortisone is not necessary because the adrenals can still produce aldosterone
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15
Q
  1. How should a patient with a prolactinoma be treated?
A
Dopamine agonists (e.g. cabergoline) 
This reduces the size of the tumour and can avoid surgery
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16
Q
  1. What is disconnection hyperprolactinaemia?
A

Compression of the pituitary stalk by a tumour cuts off the negative effect of dopamine on pituitary prolactin secretion
This results in hyperprolactinaemia

17
Q
  1. Why do non-functioning adenomas need surgery?
A

They do NOT respond to dopamine agonists

18
Q
  1. Why might prednisolone replace hydrocortisone as the first-line steroid replacement agent?
A

It has a longer half-life meaning that once daily dosing is possible

19
Q
  1. How should you investigate a child with poor growth who is suspected of having a GH deficiency?
A

Take a random plasma GH measurement (GH is pulsatile but if you happen to measure it during a pulse and they have detectable GH then it shows that they are producing GH)
Exercise test
Insulin tolerance test (effective but dangerous so should NOT be done straight away)

20
Q
  1. Name two tests that may be used to investigate suspected acromegaly.
A

Oral glucose tolerance test

IGF-1 levels