Busy. Please wait.
or

show password
Forgot Password?

Don't have an account?  Sign up 
or

Username is available taken
show password

why


Make sure to remember your password. If you forget it there is no way for StudyStack to send you a reset link. You would need to create a new account.
We do not share your email address with others. It is only used to allow you to reset your password. For details read our Privacy Policy and Terms of Service.


Already a StudyStack user? Log In

Reset Password
Enter the associated with your account, and we'll email you a link to reset your password.

Remove ads
Don't know
Know
remaining cards
Save
0:01
To flip the current card, click it or press the Spacebar key.  To move the current card to one of the three colored boxes, click on the box.  You may also press the UP ARROW key to move the card to the "Know" box, the DOWN ARROW key to move the card to the "Don't know" box, or the RIGHT ARROW key to move the card to the Remaining box.  You may also click on the card displayed in any of the three boxes to bring that card back to the center.

Pass complete!

"Know" box contains:
Time elapsed:
Retries:
restart all cards




share
Embed Code - If you would like this activity on your web page, copy the script below and paste it into your web page.

  Normal Size     Small Size show me how

chapter 44

pituitary and adrenal disorders exam 5

QuestionAnswer
negative feedback ↑levels inhibit ↓levels stimulate
positive feedback ↑levels stimulate ↓levels inhibit
pituitary gland is located in stella turcica and is connected to hypothalamus via infundibular stalk
anterior pituitary hormones GH ACTH TSH FSH LH PROLACTIN MELANOCYTE STIM HORM (MSH)
posterior pituitary hormones ADH OXYTOCIN
glucose tolerance test for GH suppression give standard amount of glucose IV and measure levels for 120 minutes; glucose supresses GH in neg-feedback process; if large decrease in GH occurs then it is a positive sign of hyperpituitarism
hyperpituitarism excessive production of one or more anterior pituitary hormones
hyperpituitarism leads to prolactinemia gigantism acromegaly
S&S of hyperpituitarism visual deficits and HA; enlargement of hands, feet, paranasal and frontal sinuses, soft tissues; initially have increased strength progressing rapidly to weakness and fatigue
elevation of any hormone requires further evaluation and follow-up
most reliable test for acromegaly glucose tolerance test; normal results is for the level to fall during testing but it will remain unchanged in acromegaly
tx for acromegaly somatostatin analog - SE: suppresses insulin secretion removal of adenoma -
skeletal changes seen in acromegaly cannot be reversed with tx
soft tissue hypertrophy can improve with tx
postop nursing care of pt with hyperpituitarism monitor neurological status closely, strict doc of I&O and specific gravity due to risk of DI or SIADH, note any clear, colorless drainage and notify provider might be CSF leak, nuchal rigidity a sign of meningitis, pt might have a stereotactic frame for radiation therapy, pin care will be needed, emergency removal of frame may be required if pt has seizures, watch for ICP, avoid valsalva maneuvers - coughing, straining, vomiting, sneezing might disrupt surgical site and cause CSF leak, no heavy lifting
postop nursing care of pt with hyperpituitarism continued or bending from the waist for 2-3 months after surgery, notify surgeon of fluid retention or diuresis, electrolyte imbalances
hypopituitarism inadequate secretion of GH
dwarfism definition height that is 40% below normal children
panhypopituitarism inadequate secretion of GH in adults Sheehan syndrome, tumors, chronic recurrent infections, removal of pituitary gland, suppression of pituitary hormones from drug therapy
s&s of hypopituitarism depends on stage of life; early onset: short stature but proportional, delayed or absent sexual maturation, mental retardation, accelerated aging
s&s of panhypopituitarism Simmonds chachexia - muscle and organ wasting, disruption of digestion and metabolism, hypoglycemia, hypothyroidism, decreased pigmentation of skin, gonads may atrophy
tx of panhypopituitarism deficient hormones are replaced, men get testosterone women get estrogen unless they have hx of breast cancer or prostate cancer
tx of hypopituitarism GH is admin to children until the person reaches a height of 5 feet
nursing care of hypopituitarism be aware of mental acuity, emotional stability and affect
disorders of posterior pituitary disorders DI SIADH
another name for ADH vasopressin
ADH maintains fluid balance by promoting reabsorption of water in the renal tubules when body water is decreased or very concentrated
ADH release causes increased water retention; distal tubules and collecting ducts do not reabsorb sufficient water resulting in an increased plasma osmolarity, massive dehydration ensues; cardiac arrest and death if left untreated
diabetes insipidus DI; excessive output of dilute urine
neprogenic DI is an inherited defect
neurogenic DI is a defect in either the production or secretion of ADH
dipsogenic DI is a disorder of thirst stimulation
S&S, DX and tx of DI massive diuresis, dehydration, and thirst, irregular heart beat, can excrete up to 30 L of urine per day; dx: 24 hr urine test, specific gravity will be extremely low, osmolarity is also decreased; tx: IV fluid replacement, vasopressors,
nursing care of DI measure I&O q 15-30 minutes, fluid replacement is prescribed based on output, daily weight, if self-care is in doubt refer to home nursing care
SIAHD water imbalance related to increase in ADH synthesis, secretion or both; it is usually a temp condition
S&S, DX and tx of SIAHD dilutional hyponatremia and water retention, water retention, weight gain without edema; dx: serum and urine electrolytes and osmolality, urine that has higher osmolality than serum is positive; tx: typertonic saline given slowly over 4-6 hrs, fluid restriction of 800-1000 mL/day, diuretic can be used only if the serum sodium is at least 125 mEq/L; vasopressor receptor antagonist - vaptains
nursing care of SIAHD describe mental status q4h in the alert pt and hourly if there is evidence of impairment, for cerebral edema elevate HOB 30-45 degrees, report declining neurological status or weight gain of more than 2 lb/day
adrenal glands triangle shaped, located on the kidneys, medulla or cortex
adrenal medulla contains sympathetic ganglia, stimulation of SNS causes medulla to secrete epi and norepi (catecholamines, neurotransmitters), these bind to adrenergic receptors
norepi binds to alpha-adrenergic receptors
epi binds to beta-adrenergic receptors
adrenal cortex outer portion of gland; endocrine system, outer: zona glomerulosa middle: zona fasciculata inner: zona reticularis secretes the steroids mineralocroticoids, glucocorticoids, androgens and estrogens
zona glomerulosa produces mineralcorticoids, most abundant is aldosterone; maintains adequate extracellular fluid volume (ECF),
aldosterone is regulated by serum levels of K, renin-angiotensin mechanism and ACTH
renin is produced by juxtaglomerular cells of renal afferent arterioles, release is stimulated by decreased ECF
renin acts of plasma proteins to release angiotensin I which is catalyzed in the lungs to angiotensin II,
angiotensin II stimulates the secretion of aldosterone which results in sodium and water retention; compensatory mechanism that plays a very important role in shock states
glucorticoids are produced by zona reticularis and zona fasciculata, most abundant is cortisol; glucocorticoid must be present for other processes to occur
glucocorticoid functions control of carbs, lipid, fat metabolism, regulation of antiinflam and immune responses, control of emotional states
adrenal androgens are produced in the zona fasciculata and zona reticularis of adrenal cortex these are also produced there estrogens, progesterone; primary source of endogenous estrogen in postmenopausal women
androgens primary function is masculinization in men
s&s of adrenal dysfunction HA, lightheadedness with position changes, muscle weakness, N/V, abd pain, mentrual dysfunction, erectile dysfunction, fat pads under clavicles, buffalo hump, obesity of trunk
vitiligo loss of pigmentation
age related changes adrenal function remains adequate, cortisol secretion declines affecting ability to conserve sodium and adapt to position changes
addison's disease adrenal hypofunction; most common cause= idopathic atrophy, other causes: TB, hemorrhage, fungal infection, AIDS, gram-neg sepsis, abrupt withdrawal of exogenous steroids
s&s of adrenal insufficiency hypoglycemia, decreased production of gastric acid, glomerular filtration rate slows, hyperkalemia, hyponatremia, skin hyperpigmentation, unexplained abd pain
hyperkalemia promotes hydrogen ion retention causing metabolic acidosis
skin hyperpigmentation is the result of increased secretion of beta-lipoprotein or MSH, direct result of hypercortisolism and lack of negative feedback
acute adrenal crisis (addisonian crisis) any factor that causes stress can initiate a crisis; severe addison's disease symptoms (see other card, I'm not typing it again)
s&s and dx of acute adrenal crisis (addisonian crisis) low serum and urinary cortisol level, decreased fasting glucose, hyponatremia, hyperkalemia, increased BUN, abnormal ECG, salt craving, weight loss,
most accurate measure of steroid secretion 24 hr urine test
tx of acute adrenal crisis (addisonian crisis) replace deficient steroids; in divided doses, morning dose is 2/3 of daily dose; mimics normal human hormonal variations
goal for tx of acute adrenal crisis (addisonian crisis) restore the blood levels to normal
nursing care for acute adrenal crisis (addisonian crisis) monitor fluid and electrolyte balance, daily weights, monitor for inadequate tissue perfusion, IV NS, watch for postural hypotension, hypovolemia, exercise legs before standing to promote venous return, high protein, low carb diet, encourage rest to avoid depletion of glycogen supplies,
adrenal hypersecretion Cushing's syndrome excess amts of corticosteroids, particularly glucocorticoid; excess cortisol
excess production of ACTH due to pituitary tumor Cushing disease
single exogenous cause of cushing syndrome prolonged admin of high doses of corticosteroids
s&s of hyperadrenalism obesity, facial redness, hirsutism, menstrual disorders, hypertension, muscle wasting, moon face, striae on abd, breasts, buttocks or thighs, hypokalemia of uncertain cause
small cell cancer of the lungs can secrete ACTH which stimulates excess cortisol secretion
promptly d/c drugs that supress adrenal function if trauma or shock occurs b/c the pts ability to adapt is diminished
nursing care of pts with Cushing Syndrome avoid exposure to people with infections, skin is extremely fragile - inspect daily, fractures occur easily, low calorie diet that is sufficient in protein and calcium
nursing care for adrenalectomy pt monitor and correct any electrolyte imbalance, strict hand washing, high doses of cortisol are given IV for several days,
s&s of acute adrenal insufficiency vomiting, weakness, hypotension, joint pain, pruritus, emotional disturbances
pheochromocytoma is a benign tumor of the adrenal medulla that causes excessive secretion of catecholamines; s&s: hypertension, hypermetabolism, hyperglycemia; DBP 115 or greater, severe HA, diaphoresis; tx: removal of the tumor
overall mission of the endocrine system to maintain homeostasis
main symptom of SIADH water retention
Created by: nursingTSJC2013