Endocrinology Flashcards

1
Q

Ix & Mx Acromegaly

A
Ix: 1st Serum IGF-1 levels + serial GH levels...
if IGF is + --> OGTT to confirm
Mx: 1st line--> Trans-sphenoidal sx
somatostatin analogue: octeride
dopamine agonist: bromocriptine
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2
Q

Ix & Mx addisons
Ix & Mx cushings
Ix & Mx conn’s

A

ADDISON
Ix: synacthen test
Mx: hydrocortisone, fludracortisone

CUSHINGS
Ix: dexamethasone suppression test, 24 hr free urinary cortisol
Mx: transphenoidal resection

CONNS
Ix: 1st line: aldosterone/renin ratio ( high aldosterone + low renin (negative feedback due to sodium retention from aldosterone)
2nd: high-resolution CT abdomen
if normal…
Adrenal venous sampling (AVS) : to distinguish btw unilateral adenoma & bilateral hyperplasia
Mx: Spironolactone

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3
Q

SE of steroids

A
Cataracts
Osteoporosis
Retarded growth
Thinning skin
Immunosupression
Cushings features
Oedema
Suppresion oh HPA axis
Teratogenic
Emotional disturbance: depression, anx
Raised BP
Obesitry
Increased body hair growth
Diabetes
STRIAE
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4
Q

steroid rules

A

Don’t STOP

-Dont stop abruptly—> addisonian crisis

Sick day rules (double the dose)
Treatment card steroid
Osteoporosis prevention bisphos +Ca, vit D
PPI

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5
Q

Carbimazole SE

A

Agranulocytosis

crosses the placenta, but may be used in low doses during pregnancy

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6
Q

Levothyroxine SE (4)

A

Levi maskeen he was underground so no sun (osteoporosis) and his friends all died so he heart hurts :(

Hyperthyroidism: due to over tx
OSTEOPOROSIS
worsening of angina
AF

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7
Q
CAH
Cx
presenting?
Ix
Mx
A

21-hydroxylase deficiency
responsible for converting progesterone into aldosterone & cortisol-> so instead the progesterone is converted to TESTOSTERONE
they get: low aldosterone, low cortisol and abnormally high testosterone.

features: AMBIGUOUS genitalia” and an LARGE clitoris due to the high testosterone levels.

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8
Q

most common cause of ambiguous genitalia?

A

CAH

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9
Q

DKA diagnosis

causes

A

PH <7.3 or HCO3 <15
glucose more than 11 mmol
ketones more than 3

Cx:
infection, missed insulin doses, myocardial infarction, pump failure

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10
Q

initial AIMS of DKA

A

–> Commence IV 0.9% sodium chloride
–> Give 10U soluble insulin (e.g. Actrapid®) stat either i/m or s/c if likely to be
delay of longer than 15 mins from diagnosis, in starting iv insulin
–> Commence IV fixed rate insulin
–> Establish appropriate monitoring (hrly capillary blood glucose and blood ketones plus 2 hrly K+ by VBG
–> Clinical and biochemical assessment of patient
–> Review IV fluid regimen based on patient’s clinical and biochemical assessment and blood glucose levels

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11
Q

Mx?

when do u give dextrose and how much?

A

Give 10 U (e.g. Actrapid®) stat either i/m or s/c
0.1/kg/hr

1) FLUIDS--> 6L 
1L--> over 1 hr
1L--> over 2 hrs
1L--> over 2hrs
1L--> over 4hrs
1L--> over 4hrs
1L--> over 6hrs

2) if K+ 3.5-5.5
ADD K to the second bag
20 mmol per 500ml fluid

once blood G is < 14 mmol/l an infusion of 5% dextrose should be started

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12
Q

DKA resolution is defined a

A

pH >7.3
blood ketones < 0.6 mmol/L
bicarbonate > 15.0mmol/L

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13
Q

DKA complic

A
DEATH
cerebral edema--> bc of fluids
VTE--> dehydration
Hypoglycemia
Aryhtmmia--> K
Sepsis
AKI-> dehydration
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14
Q

HHS pathophysiology

A

SO DEHYDRATEDDDDDDD

Hyperglycaemia results in osmotic diuresis with associated loss of Na and K

Severe volume depletion results in a significant raised serum osmolarity (typically > than 320 mosmol/kg), resulting in hyperviscosity of blood.

Despite these severe electrolyte losses and total body volume depletion, the typical patient with HHS, may not look as dehydrated as they are, because hypertonicity leads to preservation of intravascular volume.

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15
Q

Hypogylcemia Mx

A

Oral glucose tablets 10-20g
awake can’t swallow–> glucogel, IM glucagon 1mg
unconscious–> 75ml of 20% Glucose or 150ml of 10%

be careful in giving glucagon in malnourished, bc they have no glycogen stores.

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16
Q

Hypogylcemia Cx

A

EXPLAIN

EXogenous drugs--> insulin, gliclazide
Pituitary insufficiency 
Liver disease
Adrenal insufficiency/Addisonion crisis/Alcohol
Insulinoma
Nutritional deficiency
17
Q

lactic acidosis causes

A

decreased oxygen leads to increased pyruvate–> lactic acidosis