• Shuffle
    Toggle On
    Toggle Off
  • Alphabetize
    Toggle On
    Toggle Off
  • Front First
    Toggle On
    Toggle Off
  • Both Sides
    Toggle On
    Toggle Off
  • Read
    Toggle On
    Toggle Off
Reading...
Front

Card Range To Study

through

image

Play button

image

Play button

image

Progress

1/85

Click to flip

Use LEFT and RIGHT arrow keys to navigate between flashcards;

Use UP and DOWN arrow keys to flip the card;

H to show hint;

A reads text to speech;

85 Cards in this Set

  • Front
  • Back
in DKA one will see what symptoms
diaphoretics,
NV but no D - b/c there is NO ENTERITIS.

seen usually w/ type1 and unusually w/ type2
viral causes for autoimmune DM (type1)
coxsackie
mumps
rubella
habitus of a DM1 pt

habitus and usual outlook of a DMtype2 pt?
skinny, autoimmunity,
fat, develops insulin Resistance over time, B-islet cells produce too much insulin and this over time causes the b-iselt cells to atrophy
Dx criteria for DM
random plasma glucose >200 w/ sx
random plasma after 2 hr OGT >200 on 2 visits
fasting plasma glucose >126
examples of different types of insulin:

rapid acting
regular
long acting
lispro, aspart
pump
nph glargine and detemir - onset w.in 2 hrs and last till maxx - 24+ hrs.
management for type2DM
start w/ metformin and then put on sulfonylurea or thiazolidonenoe if hba1c >7 after 2-3 mo
if hba1c after 2nd drug added is still >8.5 then start on insulin additionally or?
third agent, acrarbose, etc?
#1 complication for dm2
hhnk

then retinopthy, nepropathy, neuroapthy, atherosclerosis
dka patho and sx?
extremely low insulin levels leads to too much glucose 300-800 and sx: dry membranes, kussmal = slow deep breaths, and mental status change, polyuria, polydip, and hypervent, and hypovolemic
tx
aggressive IVF and insulin, kcl and tx the cause
causes of dka
mi or high stress, infections, mucromycosis, burns, etoh high use
hhnk >800 seen in
type 2 dm pts w/ same reasons as above card and NO ACIDOSIS seen w/ this versus in DKA
dm drug that causes gi issues most comonly and acidosis most rarely usually first line, what is its moa?
decreases hepatic gluconeogenesis, increases insulin activity - metformin
dm drug that causes a 24hr hypoglycemia and are contraindicated in pts w/ RF and hepatic issues most common problem is weight gain, moa?
stimulate insulin release from the b-islet cells - sulfonyl - glyburide
dm drug that causes a 24hr hypoglycemia and $$$, like a sulfonyls and even have same moa, moa?
stimulate insulin release - meglitinide
causes flatulence and decreases gi carb absportion
acarbose
moa for glitazones and issues w/ them?
cause hpeatic gluconegenesis reduction and wt gain and increase serum ldl and rare liver tox also a/w chf!!
2 types of diabetic retinonopathy?
background retinopathy (no neo vascularazation) -cotton wooling and edema.
proliferative retinopathy ( w/ neovasc) - hemmoraghic type - use laser photocoag to correct
kimmelstein gn - findings?
see nodules, mesangial expansion, basement membrane degeneration and, see labs w. hypoalbuminurura
diabteic neuropathy sx
begins in feet, and ascend w/ stocking glove pattern
decreased pain and vibratory sense
can also get gastroparesis and impotence commonly and tx w/ gabapentin and carbamzapeine, PHEYNTOIN
complications w/ dm neuropathy
charcot joints = repetitive foot trauma can cause foot deformity and joint destruction.
htnsive pt/ dm never give?
bb they mask hypoglycemia
hypoglycemia common causes:
reactive - decrease in serum gluc after eating so eat smaller meals more frequently

iatrogenic = too much insulin, excess administration due to sulfonylurea (glipizde) problem, cpep will be elevated, will see a high insulin lvl and low glucose.

insulinoma - b-iselt tumor, cpep elevated and will see on ct or mri get surgery done or use octreotide

fasting

etoh induced -

pit/adrenal insuff -lo cortisol, so tx is replace cortisol. do acth stim test, if still high then - d/t a non renal/adrenal cause (small cell) if low levels of acth - adrenal tumor
in pregnancy tbg is high and total t3,4 is high but?
free t3,4 is normal
______________ can occur from increase basal metabolic rate, from hyperthyroid
osteoporosis
a factituous hyperthyroidism will show a ___________ scan
normal thy uptake scan
a increased thy scan seen w._________________
graves and adenomas (tox multinodular goiter)
main indications for calcitonin
paget's bone disease ( disease of too much osteoblasts and osteoclasts and you get tibial bowing, deafness, kyphosis and increased cranial diameter

and post menopausal osteoprosis
graves sx -
exopthalmos, pretibial myxedema, painless goiter, and tsi ab's found on serum
tx for graves
subtotal thyroidectomy and radioablation

prorpthyouracil and methimazole

atenolol
plummer's disease or toxic multinodular goiter sx or labs?
single or multiple hyperactive nodules

increased scan at site of nodule, and hot nodule seen on labs
subacute thyroiditis - de quervain's thyroidits sx and labs?
enlarged goiter and hyper then hypo condition due to viral stimulus

PAINFUL GOITER AND FEVER AND INCREASED ESR AND DECREASED UPTAKE ON THYROID SCAN.

NSAIDs and b-b
decreased uptake on thyroid scan seen w. (2) disease?
silent thyroiditis - post partum and bx shows inflammation ( not really hypo, hyper)

de quervain's- painful, fever, decreased uptake on thyroid scan.
ab's seen w/ hashimoto thryoidsitis
increased tsh, antimicrosmal abs, antithyrolgobulin abs, decreased uptake on thyroid scan - cold scan!! - HYPO CONDItion
THYROID CA - nodules should be worked up by?
tsh levels, thyroid function tests and us, fna w/ biopsy
most common form of thyroid cancer
papilary- of columnar gland cells
most aggressive cancer form for thyroid
anaplastic - poorly diff, can cause hoarseness and dysphagia and can hit the recurrent laryngeal nerve and prognosis is poor
produces calcitonin, thyroid cancer?
produces calcitonin - medullary thyroid ca a/w men type 2a,2b cancer of the parafolicular c cells see spiral things.
malignant nodule workup?
scan - cold usually,

observe - small and cystic nodules
solid and benign - do sx and radioablation
levothyroxine

malignant tumor - resect - <1cm lobectomy if larger do total thyroidectomy w/ ablation

synthroid post surgery for replacement
labs:

primary hyperPTH
HIGH PTH

HIGH CA

LO PO4
MAIN CAUSES OF HYPERPTH
ADENOMA (PIT) OR/AND HYPERPLASIA OF THE GLAND
sx of hyperpth
bones, groans, stones, and psych overtones
tx for hyperPTH
single adenoma- remove nodule

hyperplasia - remove all 4 and implant a portion of one in the forearm muscle so there is some endogenous pth

tx hypercalcemia w/ ivf and alendronate
hyperpth - secondary causes
malnurtition, malabsp, and renal disease, or ca-wasting drugs
secondary hyperpth (NON RENAL) labs
HIGH PTH
LO PO4
LO CA AND VIT D
SECONDARY HYPERPTH ( RF) LABS
HIGH PTH
HIGH PO4
LO CA, VITD
HYPOPTH MOST COMMON CAUSE
D/T SURGICAL REMOVAL - OF PARATHYOID OR AUTOIMMUNE GLAND DESTRUCTION - LEADS TO HYPO CA
HYPO PTH LABS
lo ca, high phos, lo pth
signs and symptoms seen w/ hypopth
trosseou sign - carpal spasm w/ bp cuff inflation

chvostek sign - tap facial nerve
tx for hypopth
ca and vitD suuplementaion
psuedohypoparathyroidism
hypocalcemia resulting from tissue non responsiveness to pth

high pth
lo calcium
high po4

--- looks like secondary hyperpth w/rf
tx of psueohypopth?
ca supplementation. vitD
TRH stimulates? (2)
tsh and PTL
drugs that cause hyperPTL
phenothiazines

risperidone

haldol

m-dopa

verapamil
sx for hyperPTL

tx?
amenorrhea, galatorrhea, lo libido, ED, bilateral hemianopsia, gynecomastia
cabergoline, bromocriptine, pergolide, transphenoidal surgery
to test for excess GH like in acromegaly?
give 1 hr 100g glucose test look for increased GH
sx for acromegaly?
organomegaly,LVH, diastolic dysfunction, dm, cord compression,vision loss, insulin resistance

childhood form - gigantism
tx for acromegaly?
surgical resection for adenoma ( adenoma is mcc)
ORDER OF HORMONE DEFICIENCIES SEEN IN PANHYPOPIT
GOOD LUCK FINDING TX FOR PITUITARY ACCIDENTS

GH - GROWTH FAILURE

LH
- AMENORHEA, IMPOTENCE
FSH

TSH - HYPOTHY

PTL - NO LACTTAION

ACTH - DECREASED SKIN PIGMENT, FATIGUE, WT LOSS, LO APPETITE.
TEST FOR LO LH?

LO GH?

LO TSH?

LO PTL?

LO ACTH?
GIVE MEDROXYPORGESTERONE - STILL LOW

GIVE 2 HR INSULIN OGT - STILL LOW

LO TSH, T4 T3

CORTISOL DOES NOT INCREASE FOLLOWING ADMINISTRATION OF INSULIN
CUSHINGS DISEASE
EXCESS ACTH BY PIT ADENOMA
CUSHINGS SYNDROME
EXCESS CORTISOL INTAKE - MCC FOR CUSHINGS
DETERMINE CAUSE OF CORTISOL EXCESS
LO DEXAME TEST SUPP TEST - 1-2 MG GIVEN PM AND LO CORTISOL NORMALLY FOUND


HIGH SUPP TEST - 8MG/DAY FOR 2 DAYS AND USED TO DETERMINE CAUSE OF CORTISOL EXCESS.
WHAT WILL LOW DOSE DEXAMTHASONE SUPPRESSION TEST SHOW FOR A CUSHING'S SYNDROME PT?
NO DECREASE
cushing's syndrome sx
mr. cushings

menstural iregularities

rounded facies

central obestiy

cervical fat pad

urinary cortisol increase

glucose increased = insensitivity

purple striae on abdomen

suppression of immune system

htn, hyper cortisolism, hirsutism

iatrogenic

neoplasm

glucose intolerance

growth retardation
cushings labs
hyperglycemia, glycosuria, hypokalemia
if after low dose dexameth test the next am the cortisol level is still found low that means
cushing's not due to intrisnsic cause, due to exogenous steroid administration - remove the pills
if after low dose dexameth test there is no change in cortisol following the morning then we will say:
dx of cuhsing's do 24 hr urinary cortisol
if after no change is seen on dexameth test and ater 24hr urinary cortisol is done, we see high urinary cortisol, what does that tell us?

normal urinary cortisol?
high- do high dose dexamth test to determine exact cause, if suppressed this time - think pit adenoma

if not suppressed - get acth level - think adrenal tumor if level is low, if high, no adrenal acth secreting tumor like paraneoplastic small cell


normal not cushings
most common complication for cushin's adrenal tumor sugrery
avn of hip
excess aldosterone secretion caused by a unliateral adenoma
hyperaldosteronism
labs seen w/ hyperaldosteroneism
lo k
hi na
met alkalosis
lo renin - in conns
always whether its primary or secondary hyperaldos will see - increased 24hr urinary aldosterone
adrenal insufficiency types:
primary - addison's - autoimmune destruction due to hemorrhage (waterhous F syndrome - meningococcal sepsis and hemorrhage into adrenals bilaterally) - see increased msh, and skin pigment (only seen w/ primary!!)

secondary - due to decreased acth production to chronic steroid use (adrenal atrophy) or insufficient acth production by pit. -
Tertiary - hypothalamic failure - CRH not produced.
labs in hyperaldosteroneism
decreased na and increased k ( like on k sparer) secondary to low aldosterone, decreased cortisol (adrenal insuff) and eosiniophillia

addisons/primary adrenal insuff - see increased acth, increase msh.

secondary insfuff/tertiary - see decreased acth

the low cortison goes UPPP w/ acth analog administration (cosyntropin stim test- dx test for addisons)

in primary insuff/addisons - NO CHANGE

in secondary/tert insuff - see increase!!
tx for adrenal insuff
mineralocorticoid and glucocorticoid replacment
complications of adrenal insuff
Addisonian crisis- weakness, fever, ams, vascular collapse, in times of stress, need for cortisol.
causes of eosinophilia -
drugs, neoplasm, allergies, addisons, ain, collagen vasc disease, parasitic pneumonitis, ascaris lumbracoides
cah - types:

recall: 1 first number - then we see htn
1 2nd number - then we see virilization
17a - amenorrhea, ambiguous genatalia, htn lo k, hi na, decreased androgens
21a- excess testoserone, ambiguous genitalia, virilization, precocious puberty, hotn, hi k lo na.
11b- virilization, precpuberty in males, ambig genitalia in women and htn, and increased secondary dexoycorticosterone, + androgens. WE SEE BOTH HTN AND VIRILIZATION!!!!

**21 is the most common form of cah
what is the pheocromocytoma rule of 10s?
10% malignant

10% multiple
10% bilateral
10% extradrenal
10%kids
10%familial
10%calcify
diaphorectic w/ intermittent tachycardia and htn, headache

tx?
pheo

get 24hr urinary metanphrines, catecholamines and vma


surgery a, before beta
men 1 a/w
PITY - acromegaly (GH secreting adenoma), cushings (excess cortisol- syndrome), galactorrhea

PARA- hyperPTH, hypercalcemia

Pancreas - zollinger ellison -gastrin producing tumor in duoenum or panc - increased fasting gastrin levels.
men2a a/w
medullary thyroid carcinoma (recall- psammoma bodies a/w papillary) - increased calcitonin lvls

parathroid - increased PTH - hypercalcemia

pheo- increased urine and serum catcholamines
men2b a/w
medullary thyroid ca

pheo

mucosal neuroma - NF? marfanoid habitus
baby born w/ poor feeding, lethargy, bulgining fontanelles, thick tongue, constipation, umbilical hernia, poor growth, hypotonic, skin dry, jaundice prolonged
severely hypothryoid infant - cretinism.

which sx is seen fist?? - prolonged jaundice!
bx shows thyroid w/ germinal centers
hypothyroidism