adrenals Flashcards

hypoadrenalism: explain the basis of the management of syndromes of adrenal insufficiency (including Addisons disease, pituitary-dependent (secondary) adrenal insufficiency, acute adrenal insufficiency and congenital adrenal hyperplasia); explain what protective measures should be undertaken for patients with adrenocortical insufficiency

1
Q

what is Addison’s disease

A

primary hypoadrenalism due to issue with adrenal gland meaning it cannot produce sufficient steroid hormones

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2
Q

expected blood test results for Addison’s including time

A

low Na+ and high K+; 9am cortisol levels low (should be high), ACTH levels high

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3
Q

Addison’s test to measure cortisol response to stess and confirm diagnosis

A

short synATCHen test by giving 250ug synACTHen IM and measuring cortisol response

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4
Q

typical 9am Addison’s patient cortisol levels, and levels at 9:30am after giving 250ug synACTHen IM

A

9am: 100 (270-900); 9:30am: 150 (>600), showing in presence of high ACTH they cannot produce cortisol

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5
Q

what else stimulates aldosterone release besides CRH and ACTH in hypothalamo-pituitary-adrenal axis

A

RAAS: angiotensinogen converted to angiotensin I in liver by renin -> angiotensin I converted to angiotensin II in lungs by ACE -> increase in aldosterone production and release

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6
Q

what 4 things stimulate RAAS

A

hyperkalaemia, hyponatraemia, reduced renal blood flow, B1-adrenoceptor stimulation

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