Endocrinology Flashcards

1
Q

What is the role of ADH?

A

Produced by the posterior pituitary in response to HYPERTONICITY/ ↑salt in the blood

so if ↑salts then ADH causes fluid reabsorbed to dilute = less urine/more concentrated urine is produced and vice versa

also causes arteriolar vasoconstriction therefore increasing peripheral vascular resistance to increase BP

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2
Q

Define diabetes insipidus

What are the two main pathophysiologies?

A

Excessive urination without glycosuria

1) Nephrogenic - kidneys fail to respond to ADH
2) Cranial - posterior pituitary doesn’t produce enough ADH

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3
Q

Give 3 causes of nephrogenic diabetes insipidus

A

Chronic kidney disease

Iatrogenic e.g. Lithium use

Inherited causes

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4
Q

Give 3 causes of cranial diabetes insipidus

A

Infection e.g. meningitis, encephalitis, TB

Trauma

Hypoperfusion/haemorrhage e.g. Sheehan’s syndrome

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5
Q

How does diabetes insipidus normally present?

A

Polydipsia
Polyuria (>3l per day)
Dehydration

+ hypernatraemia

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6
Q

Which blood tests should be ordered to investigate diabetes insipidus and why?

A

U&E - assess fluid status, check Na+ levels

Urine and serum osmolality - low urine but high serum osmolality

Calcium - hypercalcaemia can cause nephrogenic too

BM - diabetes mellitus presents similarly so need to rule out

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7
Q

What bedside/more conservative test can be done to confirm a diagnosis of diabetes insipidus?

A

Water deprivation test!

Cranial = high urine osmolality after the synthetic ADH as kidneys are still able to respond = water is reabsorbed

Nephrogenic = low osmolality throughout as kidneys don’t respond to ADH

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8
Q

What is the difference between primary and secondary adrenal insufficiency?

A

Primary = Destruction of the zona glomerulosa and zona fasciulata = ↓ mineralocorticoid production (aldosterone) and ↓ glucocorticoid (cortisol)

Secondary = seen upon withdrawal of long term steroids as body becomes reliant on exogenous steroids

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9
Q

What are 4 causes of Addison’s/primary adrenal insufficiency?

A

ADDISONS
TB
Mets
Congenital adrenal hyperplasia

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10
Q

What are 4 symptoms of Addison’s?

A
very non specific
weight loss
N&V
Low mood
unexplained abdo pain
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11
Q

What are 3 signs of Addison’s?

A

Postural hypotension/syncope

Hypogylcaemia

Hyperpigmentation

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12
Q

What are the signs of an addisonian crisis?

A

Signs of shock (↑HR, ↓BP, ↓urine output, altered mental state)

+ known Addisons / known long term steroid user and a precipitating factor e.g. withdrawal, surgery, trauma, infection

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13
Q

What is the managment of an addisonian crisis?

A

Hydrocortisone 100mg IV 6hrly, treat underlying cause, IV fluids


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14
Q

What test is diagnostic for Addison’s disease?

A

Short synacthen test

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15
Q

What is the management of Addison’s disease?

A

Steroid replacement - Hydro or Fludrocortisone = long term

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16
Q

Define primary hyperaldosteronism

A

Excess aldosterone production that is independent of the RAAS

SO ↑ aldosterone/mineralocorticoid

17
Q

What are the two most likely causes of primary hyperaldosteronism and what is the management?

A

Conn’s Syndrome = adrenocortical adenoma. Mx = surgery

Bilateral adrenal hyperplasia. Mx = spironolactone

18
Q

What are the 3 main features of primary hyperaldosteronism?

A

Na+ and water retention = Hypertension, fluid overload

Hypokalaemia

Alkalosis

19
Q

What is the function of aldosterone?

A

Activates and up regulates Na/K pump

Upregulates ENac

Stimulates K+ secretion

↑ Na and water BUT. ↓ K

20
Q

Define secondary hyperaldosteronism

A

Reduced renal perfusion leads to an increase in Renin production = upregulation of RAAS

21
Q

What are 4 causes of secondary hyperaldosteronism?

A

renal artery stenosis

CCF

diuretics

liver failure