endocrinology Flashcards

1
Q

What are the diagnostic criteria for DKA

A

ketonaemia>3mmol/l (or significant ketonuria)
Bloog glucose >11 (or known DM)
serum bicarbonate<15 or venous pH<7.3

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2
Q

when should 10% dextrose be added to rescutaition/replacemetn fluid in DKA?

A

when BM<14

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3
Q

what is the initial rate of fixed rate insulin in DKA?

A

0.1units per KG per hour

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4
Q

WHat are the diagnostic criteria for HHS?

A

clinical hypovolaemia
BM>30mmol/l without significant keonaemia or acidosis
serum osmolarity>320mmol/l

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5
Q

how is serum osmolality calculated?

A

2xNa +glucose +urea

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6
Q

what is the normal osmolar gap

A

10msom/kg

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7
Q

when should insulin infusion be started in HHS?

A

once BM is no longer falling with IV fluids alone

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8
Q

dose of glucagon in hypoglycaemia

A

1mg IM

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9
Q

which patients have reduced glycogen stores

A

alcoholics, sulphynourea, liver failure, malnourished

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10
Q

what is produced by the zona glomerulosa?

A

mineralocorticoids e.g aldosterone

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11
Q

what is produced by the zona fasciculata?

A

glucocorticoids e.g cortisol

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12
Q

what is produced by the zona reticularis?

A

androgens

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13
Q

what is produced by the adrenal medulla

A

catecholamines e.g. adrenaline/noradrenaline

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14
Q

biocehmical markers of adrenocortical insufficiency

A
hyponatraemia
hyperkalaemia
high urea/creatinine
hypoglycaemia
metabolic acidosis
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15
Q

low cortisol and low acth indicates?

A

secondary adrenal insufficinecy

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16
Q

low corstiol and high ACTH

A

primary adrenal insufficincy (addison’s disease)

17
Q

principal cause of addision’s disease?

A

idiopathic/likely automimmune destuction

18
Q

management of acute adrenocortical insufficiency

A

a to E resucitation, fluids as guided by cardiovascular status
hydrocorisone 100mg IV
fludrocorisone only in primary insufficneccy
monitor for hypoglycamia and treat if needed
treat any underlying infection

19
Q

biochemical markes of cushing’s syndrpome

A

hypergy;ycaemia
hypokalaemia
hypernatraemia

20
Q

most common cause of cushing’s syndorme

A

chronic glucocorticoid administration

21
Q

cause of cushing’s disease

A

ACTH secreting pituitary tumour

22
Q

treatement of cushing’s disease

A

removal of pituitary adenoma, if can’t be located, bilateral adrenalectomy

23
Q

phaechromocytomas arise in?

A

adrenal medulla

24
Q

diagnosis of phaeochoromocytoma?

A

24 hour urinary free catecholamine level

diagnostic imaging to localise tumour

25
Q

best agents for BP control in phaeochromocytoma

A

phenoxybenzamine, (alpha blocade) then propranolol to treat tachycardia

26
Q

how to calculate anion gap

A

sodium-chloride-bicarb

27
Q

treatment of thyroid storm

A

high dose carbimazole/PTU then potassium iodide - inhibit synthesis and release
betablockers (80mg propanolol po) - stop peripheral conversion t4 to t3
sedation wwith benzos
glucocorticoid - stop peropherial conversion and prevent adc insufficinecy
-treat underlying cause, eg antibtics
supportive managemnt , e.g fluids or NGT

28
Q

3 main features of myxoedema coma

A

altered mental state
hypothermia (or abscence of fever despite severe infection
presence of a precipitating event

29
Q

managmetn of myxoedema coma

A

thyroid replacment
treat preciptant
100mg hydrocrotsone 8 hourly
supportive therapy

30
Q

managment of pituitary apoplexy

A

hydrocortisone 100mg 6 hourly
supportive measures
neurosurgeons

31
Q

features of diabetes insipidus

A

polyuria
poydipsia
dilute urine
dehydration

32
Q

biochemical markers of DI

A

high plasma osmolality
low urine osmolality
high serum sodium
(deranged pituitary function tests and remember CT head)

33
Q

treatment of cranial DI

A

desmopressin/DDAVP

34
Q

ECG changes in hypocalcamiatreatment of hypocalcaemia

A

calcium gluconate, low thershold for magnesium sulphate