acromegaly, hypopit. & hyperaldo. Flashcards

1
Q

The following flashcards are going to be from the endocrine disorders/problems blackboard recording video

A
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2
Q

What is acromegaly?

A

an overproduction of growth hormone

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3
Q

what is the usual cause of by patients develop acromegaly?

A

caused by a benign pituitary tumor

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4
Q

how does acromegaly present itself in a patient?

A

overgrowth in hands, feet, face

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5
Q

what are the major complications for patients who have acromegaly ?

A

thick tongue, hypertrophy of vocal cords, sleep apnea

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6
Q

what are some complications, listing them through systems, that patients with acromegaly can experience?

skin
eyes
pancreas
endocrine
life span ?

A

skin thickens = leathery
vision changes from pressure
GH causes hyperglycemia
hyperlipidemia
life expectancy is decreased by 5-10 years

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7
Q

what is the diagnosis for acromegaly ? (3)

A

testing of insulin-like growth factor 1

GH response to oral glucose tolerance test
(GH levels would fall normally, with acromegaly, levels are stable or increase)

MRI

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8
Q

what is the treatment of acromegaly ?

A

transsphenoidal removal of pituitary gland with replacement of target hormone replacement
( steroids, thyroid hormone, sex hormones )

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9
Q

how does a transsphenoidal work? surgery wise

A

up through the upper lip and goes up even further

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10
Q

what are post-op care we are going to need to perform on a patient who is post-op from acromegaly removal? (3)

A

oral care Q4 hours
observe for transient DI
neurologic evaluation

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11
Q

what are 3 things we are going to tell patients post-op care from acromegaly ?

A

no tooth brushing for 10 days

avoid valsalva ( straining )

surgery may result in infertility loss of FSH and LH

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12
Q

now are going to talk about hypopituitary disorders

A
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13
Q

what is the anterior pituitary hormones?

A

ACTH, TSH, FSH,LH, GH

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14
Q

what is the posterior pituitary hormones?

A

ADH
oxytocin

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15
Q

what is selective hypopituitarism ?

A

deficiency of one hormone

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16
Q

what is panhypopituitarism?

A

deficiency of all pituitary hormones

17
Q

what is the most common reasons why patients end up developing hypopituitary disorders?

A

pituitary tumor
( most common ^ )

autoimmune disorder
infection
gland damage

18
Q

its important to note that when patients end up developing hypopituitary disorders, the symptoms are going to be what?

A

related to the hormone that is affected.

( meaning if you have two hormones, a & b, and a is being affected, you are only going to see symptoms that are related to A. nothing of B symptoms will show )

19
Q

If there is a tumor growing up in the pituitary, which more than often is the main cause for these disorders, what are we worrying about?

think about how the tumor is taking up space and where the pituitary is located

A

vision changes
loss of smells
n/v
seizures
headache

20
Q

what is the treatment for hypopituitarism ?

A

surgery ( transphenoidal or radiation )

21
Q

for post op management for patients with hypopitutairy, what do we want to monitor ?

A

vision changes
neuro function
mental status
hematoma affecting optic nerve
CSK leakage

22
Q

what do we want to educate patients on after post op care for hypopitu ?

A

no
noseblowing
coughing
sneezing
straining with bowel
for 48 hours

23
Q

additional information
what type of dressing do patients have after surgery for hypo pit?

A

mustache dressing
- we look for csf leakage
- halo sign

24
Q

most of the time
if we are removing the entire pituitary, we are more than likely replacing what?

A

all the hormones
- gh
- corticosteroids
- thyroid hormone
- sex hormones

25
Q

now we are going to talk about is hyperaldosteroinism

A
26
Q

hyperaldosteronism is another name for what?

A

conn’s syndrome

27
Q

excess aldosterone does what to our electrolytes? (2)

A

sodium and fluid retention
potassium & hydrogen excretion

28
Q

are 2 major complications from hyperaldosteronism?

A

hypertension
hypokalemic alkalosis

29
Q

what is primary hyperaldosteronism?

A

solitary adrenocortical adenoma
( tumor )

30
Q

what is secondary hyperaldosteronisms?

A

nonadreal cause
- renal artery stenosis
- renin secreting tumors
- chronic kidney disease

31
Q

since patients with hyperaldosteronism, they end up having hypernatremia, what does that put them at risk for ?

A

seizures, coma, death
( remember think of neuro when you see sodium )

32
Q

what are the symptoms associated with hypokalemia?

A

muscle weakness
faitgue
dysrhtymias
glucose intolernace
metabolic alkalosis - tetanty

33
Q

how do you diagnosis hyperaldosteronisms ?

A

lab tests

34
Q

how do we treat hyperaldosteronism?

A

adrenalectomy to remove adenoma

35
Q

before we go into surgery for patients with hyperaldosteronism, what do we have to do ?

A

potassium-sparing diuretics
antihypertensive
oral potassium supplements
sodium restrictions

36
Q

what medication will we use prior to starting surgery for patients with hyperaldosteronism and what does it do?

A

helps decrease/shrink the adrenal gland

dexamethasone

37
Q

nursing management of hyperaldosteronism

careful assessment
- fluid and electorally balance
- cardiovascular status

patient teaching
- medication and side effects
- signs and symptoms of hypokalemia and hyperklamiea
- blood pressure management

A