Biochemistry Flashcards

1
Q

What are the clinical features of adrenocortical insufficiency?

A
Lethargy 
Anorexia 
Pigmentation of hands and mouth 
Abdominal pain 
Weight loss
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2
Q

How does a lack of mineralocorticoid affect the kidneys?

A

Na+ cannot be retained and is then lost from ECF

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3
Q

What does a reduced ECF volume result in?

A

Hypotension, dehydration, dizziness and lethargy

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4
Q

Excess pigmentation reflects an excess of which hormone?

A

ACTH

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5
Q

Degradation of ACTH releases which hormone?

A

Melanocyte stimulating hormone

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6
Q

Hypovolaemia and hypotension stimulate release of what?

A

Arginine vasopressin

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7
Q

Which test is definitively used to diagnose adrenal insufficiency?

A

Synacthen test

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8
Q

Describe the short synacthen test

A

ACTH analogue given IV at 250micrograms and cortisol should normally increase

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9
Q

What does a long synacthen test determine?

A

If adrenal insufficiency is primary or secondary

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10
Q

What is Addison’s disease?

A

Primary adrenal insufficiency

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11
Q

What is psuedohyponatraemia?

A

When lipoproteins and proteins have a larger volume in the blood than they should
This then gives a lower absolute amount of Na+ but overall conc is fine

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12
Q

What commonly causes secondary psuedohyponatraemia?

A

Administration of corticosteroids

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13
Q

Describe the circulating blood volume in oedema?

A

Reduced

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14
Q

What is relative adrenal insufficiency?

A

Inability to respond adequately to cortisol

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15
Q

Which test allows you to determine between central and nephrogenic diabetes insipidus?

A

Water depravation

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16
Q

Describe the water depravation test in nephrogenic diabetes insipidus?

A

ADH analogue is given but there is not response

17
Q

What does hyperkalaemia look like on an ECG?

A

Tall tented T waves

18
Q

What may result in decreased excretion of potassium?

A

Renal failure

Hypoaldosteronism

19
Q

What is the most common cause of hypoaldosteronism?

A

ACE inhibs

Sprionolactone

20
Q

What may result in the redistribution of potassium out of cells?

A

Metabolic acidosis
Release from damaged cells (rhabdomyolysis)
Insulin deficiency

21
Q

How is hyperkalaemic periodic paralysis inherited?

22
Q

What is hyperkalaemic periodic paralysis?

A

Rare condition were paralysis occurs after exercise

23
Q

How is the risk of hyperkalaemia reduced when giving blood products?

A

Using fresh blood

“Washing” units prior to transfusion

24
Q

What is given to treat hyperkalaemia?

A

Calcium carbonate
Insulin
Dextrose

25
Mineralocorticoid activity is to do with...
Exchange of potassium and hydrogen
26
What are the 3 main causes of psuedohyperkalaemia?
Delay in centrifugation of the sample, or if chilled In-vitra haemolysis Increase in plt or WCC
27
What are the symptoms of hypercalcaemia?
Moans, bones, groans and stones and arrhythmia Psychiatric features Bone pain GI problems Renal calculi (and thirst and polyuria)
28
What most commonly causes primary hyperparathyroidism?
Parathyroid adenoma (which secretes PTH)
29
How do some tumours cause hypercalcaemia?
Parathyroid hormone related peptide (acts like PTH)
30
What is tertiary hyperparathyroidism?
When PTH secretion becomes independent to calcium feedback after long standing cause of hyperparathyroidism is removed
31
What is the management of hypercalcaemia?
Saline (to restore GFR and promote diuresis) Bisphosphonates Desonumab
32
How is familial benign hypercalcaemia investigated?
Urine calcium excretion is too low to match the serum calcium
33
Where is ADH released from?
Posterior pituitary