endocrinology Flashcards

(34 cards)

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
best agents for BP control in phaeochromocytoma
phenoxybenzamine, (alpha blocade) then propranolol to treat tachycardia
26
how to calculate anion gap
sodium-chloride-bicarb
27
treatment of thyroid storm
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
3 main features of myxoedema coma
altered mental state hypothermia (or abscence of fever despite severe infection presence of a precipitating event
29
managmetn of myxoedema coma
thyroid replacment treat preciptant 100mg hydrocrotsone 8 hourly supportive therapy
30
managment of pituitary apoplexy
hydrocortisone 100mg 6 hourly supportive measures neurosurgeons
31
features of diabetes insipidus
polyuria poydipsia dilute urine dehydration
32
biochemical markers of DI
high plasma osmolality low urine osmolality high serum sodium (deranged pituitary function tests and remember CT head)
33
treatment of cranial DI
desmopressin/DDAVP
34
ECG changes in hypocalcamiatreatment of hypocalcaemia
calcium gluconate, low thershold for magnesium sulphate