Endo Flashcards

1
Q

GH deficiency in adults

A

Central obesity, increased LDL and cholesterol, reduced lean muscle mass

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2
Q

Insulin’s affect on GH

A

When insulin decreases the glucose level, GH should rise, failure to do so indicates pituitary insufficiency

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3
Q

Hormones to replace in panhypopituitarism

A

First: Cortisone, then thyroxine, testosterone, estrogen, recombinant human growth hormone

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4
Q

2 hormones of the posterior pituitary

A

Oxytocin and ADH

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5
Q

What are low in panhypopituitarism

A

TSH, thyroxine, ACTH, Cortizone, LH/FSH, testosterone, estrogen?
GH – pulsatile however, prolactin

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6
Q

Cosyntropin stim test in panhypopituitarism

A

Should be normal – Cortizone will rise as the adrenal gland is normal – in response to cosyntropin, however if chronic will be decreased as the adrenal gland has atrophied

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7
Q

Causes of nephrogenic DI

A

Chronic pyelonephritis, amyloidosis, myeloma, SCD
Also, hypercalcemia and hypokalemia may inhibit ADH affect on kidney
Lithium

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8
Q

Treatments for nephrogenic DI

A

Hydrochlorthiazide, amiloride, indomethacin

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9
Q

Unusual presentations of acromegaly

A

Carpal tunnel syndrome, body odor, deep voice, big tongue, colon polyps, skin tags, arthralgias, hypertension, cardiomegaly, CHF, erectile dysfunction – increase prolactin
GH abuse may result in similar presentation

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10
Q

Diagnosis and treatment for acromegaly

A

Initial: I GF – 1
Best: glucose suppression test – glucose will not suppress GH
Will see glucose intolerance and hyperlipidemia
MRI after acromegaly is identified
Treatment: transphenoidal resection of the pituitary
Cabergoline – dopamine will inhibit GH release
Octreotide, pegvisomant- GH antagonist
Radio therapy if unresponsive

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11
Q

GH and insulin

A

GH is anti-insulin, but it makes insulin like growth factor; and has insulin like effects on proteins and amino acids

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12
Q

What may raise prolactin levels

A

GH release, hypothyroidism, pregnancy, exercise, renal insufficiency, chest wall stimulation, antipsychotics, methyldopa, metoclopramide, opioids, try cyclic antidepressants, verapamil– The only CCB
Dopamine and Hibbetts prolactin a lease so, meds that inhibit dopamine raise prolactin

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13
Q

Test to get first if high prolactin, and when can you get an MRI

A

Thyroid function test, pregnancy test, BUN/creatinine, LFTs– Both kidney and liver failure increase prolactin
Can get an MRI after high prolactin is confirmed, secondary causes like meds are excluded, patient is not pregnant

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14
Q

Treatment for hyperprolactinemia

A

Dopamine agonist: cabergoline is better than bromocriptine

If no response, transphenoidal surgery, radiation is rarely needed

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15
Q

Hypothyroidism is characterized by almost all body processes being slow down except?

A

Menstrual flow, which is increased

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16
Q

How to treat hypothyroidism based on TSH

A

If TSH is more than double the upper limit of normal with normal T4, replace hormone
If less than double, get anti– TPO/anti-thyroglobulin antibodies, if positive replace thyroid hormone

17
Q
What is the cause of the hyperthyroidism?
Eye and skin findings?
Tender thyroid?
Nontender, normal exam?
Involuted gland is not palpable? 
High TSH?
A

Eye and skin findings: Graves– Only one to have TSH receptor antibodies
Tender thyroid: subacute thyroiditis
Nontender, normal exam: painless – silent – thyroiditis
Involuted gland is not palpable: exogenous is thyroid hormone use
High TSH: pituitary adenoma

18
Q

Hyperthyroidism treatments

A

Methimazole > PTU: Block hormone production, PTU inhibits conversion to active form
Iodinated contrast material: block peripheral conversion to active form, also block release of existing hormone

19
Q

Treatment for eye problems in graves

A

Steroids, radiation if not responding, severe cases may need decompressive surgery

20
Q

First step if small mass found on thyroid gland without symptoms or tenderness

A

Get T4/TSH levels, if + patient has a hyperfunctioning gland, does not need immediate biopsy as malignancy is not hyperfunctioning
If normal T4/TSH and greater than 1 cm: FNA, no need for US or RAIU– These cannot exclude cancer

21
Q

Presentation of hypercalcemia

A

Acute: confusion, stupor, lethargy, constipation

Short QT interval, hypertension, osteoporosis, nephrolithiasis, DI, renal insufficiency

22
Q

When hypercalcemia does not resolve after fluids and bisphosphonates

A

Calcitonin, works rapidly whereas bisphosphonate take several days to work
Cinacalcet: may work in hyper PTH but not useful for malignancy, as PTH is already maximally suppressed
Prednisones: controls hypercalcemia from sarcoidosis or other granulomatous disease

23
Q

Treatment for hyperparathyroidism

A

Surgical removal, if not possible give cinacalcet

24
Q

Magnesium and calcium

A

Will magnesium needs to bow calcium because Magnesium is necessary for PTH to be released from the gland, low levels also lead to increased urinary loss of calcium

25
Q

Albumin and calcium

A

For every point decrease in albumin, the calcium level decreases by 0.8
However free calcium is normal

26
Q

EKG in hypocalcemia

Another unique finding?

A

Prolonged QT

slit lamp exam shows early cataracts

27
Q

Best initial tests for hypercortisolism

A

Best: 24 hour urine cortisol
Next: 1 mg overnight dexamethasone suppression test, should normally suppress morning Cortizone levels, if suppressed hypercortisolism can be excluded, Does have false positives: Depression, alcoholism, obesity
Another: midnight salivary cortisol

28
Q

Determining the cause of hypercortisolism

A

Best initial: ACTH
if low source is adrenal
If elevated, pituitary – suppresses with high dose dexamethasone
Or ectopic – lung cancer, carcinoid – not suppressed: get MRI, then sample the inferior petrosal sinus after stimulating patient with CRH, as some pituitary lesions are too small to be seen on MRI
If no pituitary lesion scan the chest for an ectopic source

29
Q

Affects of cortisol

A

Hyperglycemia, hyperlipidemia, hypokalemia, metabolic alkalosis– Excretes potassium and hydrogen ions at distal tubule
leukocytosis from demargination of wbc’s

30
Q

Presentation of chronic adrenal failure and acute adrenal crisis

A

Both: weakness, fatigue, AMS, N/V, anorexia, hypotension, hyponatremia, hyperkalemia, metabolic acidosis, hypoglycemia, high BUN, eosinophilia
Chronic: hyperpigmentation
Acute crisis: profound hypotension, fever, confusion, coma

31
Q

Adrenal failure diagnosis and treatment

A

Cosyntropin stimulation test fails to increased cortisol – cosyntropin is synthetic ACTH
Treatment: replace steroids with Hydro Cortizone, fludrocortisonehas mineral corticoid affects

32
Q

Treatment of hyperaldosteronism

A

If unilateral: resect by laparoscopy

If bilateral: spironolactone

33
Q

Diabetes diagnosis

A

-2 fasting blood glucose levels over 125 mg/dL
-Dash single glucose level above 200 mg/dl with symptoms of diabetes
-Increased glucose level and oral glucose tolerance test
Hemoglobin A-1 C greater than 6.5%

34
Q

Metformin

A

Works by blocking gluconeogenesis

Contra indicated in those with renal dysfunction because it can cause metabolic acidosis

35
Q

Most accurate measure of DKA severity

A

Serum bicarbonate level, as it is a measure of the anion gap, if bicarb is low the anion gap is increased

36
Q

How to prevent nephropathy in diabetics

A

Screen for microalbuminuria annually:between 30–300 mg per 24 hours is positive, Start on ace or ARB which decrease intraglomerular hypertension decreasing damage to the kidneys
Dipstick for urine becomes trace positive at 300 mg per 24 hours– Not as sensitive

37
Q

Diabetic gastroparesis

A

Diabetes decreases the ability of the got to stretch, leads to decreased mobility
Treat with metoclopramide and erythromycin