Endocrine Flashcards

1
Q

what do ketones represent

A

increased lipolysis in the context of absent glucose

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2
Q

causes of hypoglycemia

A

-meds: insulin, oral hypoglycemics
-decreased oral intake in DM with insulin
-critical illness: sepsis, liver failure
-EtOH
-malnourishment,
-cortisol deficiency
- pancreatic tumours (insulin secreting)

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3
Q

threshold value for adult hypoglycemia

A

3.9 aka 4

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4
Q

Tx of hypoglycemia

A

25 g of glucose carbs or 25 g or IV dextrose 50mL of D50 is 1 amp, then run infusion usually

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5
Q

when is glucagon not effective, what is the dose

A

in elderly or alcoholics, dose= 1 mg IM

dextrose is always better choice

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6
Q

4 I’s that cause DKA

A

-insulin (lack of)
-infection
-ischemia
-illicit drugs (cocaine)

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7
Q

3 criteria for dx fo DKA

A

hyperglycemia, ketosis, WAGMA

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8
Q

why can bicarb sometimes be normal in DKA

A

concurrent metabolic alkalosis from vomiting

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9
Q

walk through DKA mgmt

A

-rehydrate with 1-2 L NS
-once initial bolus done, consider switching to 1/2 NS once hyponatremia is corrected
- replace K if needed, if less than 3.5 add 40 meq/L, if 3.5-5 add 20 meq/L
-start insulin and after K > 3.5 at 0.1U/kg/hr
-continue insulin until gap closed, once glucose < 14 switch to D5 1/2NS.

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10
Q

when to give bicarb in DKA?

A

consider if pH < 6.9, evidence of impending CV collapse, or life-threatening hyperK

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11
Q

how to spot cerebral edema?

A

HA, AMS, vomitting. usually occurs 6-10 hrs after tx started.
tx= reducing IVF rate and giving mannitol.

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12
Q

difference of HHS vs DKA

A

slower process than DKA, higher glucose, higher osmolality, more volume depletion, normal pH

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13
Q

criteria for HHS dx

A

glc >33
osmolality >315
bicarb >15
pH > 7.3
may or may not have ketones

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14
Q

Tx of HHS

A
  • basically same as DKA except they they need ++ fluid (often 8-12 L light)

give 2L over first 1 hr, continue intil hemodynamically stable then insulin/potassium is same as DKA

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15
Q

typical HHS pt

A

elderly, weak, T2DM, with limited oral intake
33% have no previous dx of DM

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16
Q

anterior and posterior pituitary hormones are:

A

post: oxytocin, ADH

ant: GLFTAP

17
Q

causes of hypopituitarism

A

pituitary tumour (most common, can be benign or malignant)
pituitary apoplexy (hemm)
sheehan syndrome (post partum hypoperfusion of pituitary)
other: infection, trauma, radiation, surgery, infiltrative dz

18
Q

treatment of hypopit

A

supportive, give steroids and thyroid hormone (if deficient), NEED to give steroids before Synthroid as it will cause adrenal crisis if dont

19
Q

3 ways parathyroid hormone increases Ca

A

increased kidney resorption
increase osteoclasts
increase GI resorption

20
Q

signs of myxedema coma?

A

hypothermia, AMS is characteristic

other findgins:
bradycardia, hypotension, resp failure,
edema, low ECG voltage, hypoglycemia, hyponatremia

often precipitated by major illness, cardiac or neuro event

21
Q

treatment of myxedema coma?

A

-supportive care
-empiric replacement of steroid (hydro cort 100 mg IV)
-then levothyroxine 500 ug IV

22
Q

precipitants of thyroid storm

A

infection, DKA, iodine load, stroke, ACS, PE, trauma, surgery

23
Q

clinical features of thyroid storm

A

tachycardia
hyperthermia
HF
CNS effects
GI/hepatic dysfunction

24
Q

scoring system for thyroid storm

A

Burch-Wartofsky
looks at temp, CNS, GI, HR, ?afib, CHF and precipitating event

25
Q

mgmt of thyroid storm

A

supportive care
propranolol
methimazole or PTU
steroid (dex or HC), will decrease t4 to t3 conversion
can also give inorganic iodine, 1 hr after PTU

26
Q

1 common drug for inducing hypo and hyper thyroidism

A

hypo: Lithium
hyper: amiodarone

27
Q

3 hormones released by adrenals

A

cortisol, aldosterone, catecholamine

28
Q

pheochromocytoma, what is it, what are symtpoms

A

adrenal tumor that causes release of catecholamine. classic triad: HA, sweating, tachycardia.. + other symptoms of epi/norepi excess

29
Q

adrenal insufficiency, what is it

A

decreased cortisol or aldosterone or both

if primary it will be both as issue is wiht gland, if secondary will just be cortisol as ACTH decreaed from pituitary

30
Q

how to know if adrenal insufficiency involves aldo deficiency too?

A

they will be hyperK

31
Q

adrenal crisis s/s? causes?

A

life threatning, refractory hypotension, hypoglyecmia, (hypoNa and hyperK if primary insufficiency)

32
Q

tx of acute adrenal crisis

A

hydrocortisone 100 mg IV if primary as it will replace both cortisol and aldo

if no hypoNa or hyper K and no known dx of adrenal insufficiency give dexamethasone 6 mg IV as it wont interfere with ACTH stim test

33
Q

waterhouse-Friedrichson syndrome

A

bilat adrenal hemm due to infection, often meningococcal.

34
Q

causes of adrenal insufficiency

A

primary: autoimmune, infectios, infiltrative, drugs, waterhouse-Friedrichson syndrome

secondary: prolonged steroid use, pituitary tumour, basal skull #, ICA stroke or aneurysm

35
Q

adrenal crisis (aka addison’s crisis) trigger?

A

acute physiologic stress, pituitary apoplexy, withdrawl of chronic steroids