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57 Cards in this Set

  • Front
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Adrenal Disorders

Hypofunction: Production of adrenocortical steroids may decrease as a result
of inadequate secretion of adrenocorticotropin hormone (ACTH).
Adrenal Disorders

Hypofunction
Insufficiency of adrenocortical steroids causes problems through the loss of _______ & ________ action.
aldosterone and cortisol
Adrenal Disorders
-Hypofunction:

Impaired secretion of cortisol results in???
hypoglycemia.
Adrenal Disorders
-Hypofunction

Reduced aldosterone secretion causes (3)
hyperkalemia,
hyponatremia,
hypovolemia
Adrenal Disorders
-Hypofunction


K+ retention also promotes reabsorption of hydrogen ions, which can lead to .
acidosis
4 Adrenal Disorders
Pheochromocytoma

Addison’s disease

Cushings Syndrome


Hyperaldosteronism
Adrenal Disorders

Pheochromocytoma – is what?





hypofuncton or hyperfunction of the adrenal gland?
secreting tumor that grows off adrenal gland




(adrenal gland hyperfunction)
Adrenal Disorders


-Addison’s disease –you have to “add” back what you don’t have



hypofuncton or hyperfunction of the adrenal gland?
(adrenal gland Hypofunction)
Adrenal Disorders


Cushings Syndrome
hypofuncton or hyperfunction of the adrenal gland?
hyperfunction of the adrenal gland

you have more than enough couchin - too much
Adrenal Disorders

Hyperaldosteronism:
-secretion of what?




hypofuncton or hyperfunction of the adrenal gland?
excessive mineralocorticoid production or excessive androgen production





(adrenal gland hyperfunction)
Addison’s Disease

deficiency of what 3 hormone?
-A deficiency of adrenocorticotropic hormone.



-Hyposecretion of glucocorticoids (Cortisol) and mineralocorticoids (aldosterone)
Addison’s Disease


-most often occurs in response to?
-often occurs in response to a stressful event (surgery, trauma, severe infection)
Addison’s Disease

Condition is FATAL if not treated
-what happens?
(sodium levels fall and potassium levels rise rapidly..severe hypotension results from the blood volume depletion that occurs with the loss of aldosterone)
Addison’s Disease

Caused by:
autoimmune,
adrenal hemorrhage,
adrenalectomy,
tumor,
fungal infection,
TB
Addison’s Disease - Assessment
*Lethargy, fatigue & muscle weakness
*GI disturbances (diarrhea, n/v, abdominal pain, anorexia)
*Weight Loss
-Menstrual Changes, Impotence in men
Addison’s Disease - Assessment


glucose level
potassium levels
sodium levels
calcium levels

hypertensive or hypotensive?
-Hypoglycemia
-Hyperkalemia
-Dehydration
-Emotional disturbances after awhile
-Hyponatremia
-hypercalcemia
-hypotension
Interventions for Addison’s Disease

-Monitor VS, weight, I & O, electrolyte balance


-Monitor levels of what (2)
blood glucose & potassium levels
Interventions for Addison’s Disease

Glucocorticoid deficiencies are treated with _________
hydrocortisone
Interventions for Addison’s Disease

Mineralocorticoid deficiencies can be treated with __________if needed
Florinef

(maintains electrolyte balance –Na and K)
Interventions for Addison’s Disease


aim to promote what?

monitor for fluid ____




prevent what?
-aim to promote fluid balance,

monitor for fluid deficit,

prevent hypoglycemia
“Addisonian Crisis”


A life-threatening event caused by ACUTE adrenal insufficiency secondary to a stressful event (surgery, trauma, infection)

so what hormones are there a need for?
–the need for cortisol and aldosterone is greater than the available supply.
“Addisonian Crisis”

sodium level
potassium level

hypertension or hypotension



hypoglycemia or hyperglycemic
Can cause hyponatremia which can cause seizure,

hyperkalemia,

severe hypotension from the blood volume depletion that occurs with the loss of aldosterone,


hypoglycemia, and shock,



need to wear medical bracelet
Pathophysiology of Acute Adrenal Crisis / Adrenal Insufficiency

usually related to what?
Usually related to bilateral adrenal hemorrhage!
Pathophysiology of Acute Adrenal Crisis / Adrenal Insufficiency


sodium levels


potassium levels
Unless treatment is initiated promptly, sodium levels fall and potassium levels rise rapidly.
Assessment in “Addisonian Crisis”


4
-Severe headache
-Severe abdominal, leg and low back pain
-Generalized weakness
-Irritability
Assessment in “Addisonian Crisis”


3
-Severe headache
-Severe abdominal, leg and low back pain
-Generalized weakness
-Irritability
“Addisonian Crisis” – Interventions


-Administer IV Glucocorticoids as ordered
-Following resolution of crisis, administer (3)
oral gluccorticoids & mineralocorticoids


-insulin product (usually sq or ivp)
“Addisonian Crisis” – Interventions

-Monitor VS, neuro status, noting irritability and confusion
-Monitor I and O, blood glucose, Na & K+
-Administer fluids prn (NS)
-Protect patient from infection
yes!
Cushing’s Syndrome

Condition resulting from
the hypersecretion of glucocorticoids (cortisol) from the adrenal cortex
Cushing’s Syndrome(Hypercortisolism)



3 causes
Increased pituitary secretion of adrenocorticotropic hormone (ACTH) which causes hyperplasia of the adrenal cortex in both adrenal glands and an excess of most hormones secreted by the adrenal cortex


Pituitary Adenoma





Adrenal Adenoma
Cushing’s Syndrome(Hypercortisolism)


The excess glucoroticoids affect metabolism and all body systems.
Nitrogen, carbohydrate, and mineral metabolism are altered. An increase in total body fat results. The fat is redistributed to produce the typical body pattern of truncal obesity “buffalo hump” and “moon face”
Cushing’s Syndrome - Assessment


-Truncal Obesity with thin extremities
-Moon face
-Buffalo hump
-Generalized muscle wasting & weakness
-Fragile skin that bruises easily
-immunosuppression and increased risk for infection result from excess cortisol
-Reddish/purplish striae on abdomen & upper thighs
yes
Cushing’s Syndrome - Assessment

-Hirsutism-caused by an increase in __________production (also causes acne) hirsutism is increased hair growth.


_______ hormone alteration.

Doesn’t affect men but it affects woman and the woman become mascularized. Hair distribution will increase (mustache, side burns) ---thick and coarse.. Hair up abdomen.



Alteration in ovulation (fertility problems and getting pregnant)
-Hypertension
androgen



sex hormone
Cushing’s Syndrome - Assessment

-both sodium and water are reabsorbed and retained, leading to hypovolemia and edema formation

-increased androgen production decreases what?

-sodium?
-glucose?
-potassium?
-WBC?

-
-the production of estrogens and progesterone and oligomenorrhea occurs as a result (scant or infrequent menses)


-increased sodium level
-increased blood glucose
-decreased potassium

-high levels of corticosteriods kill lymphocytes and shrink organs containing lymphocytes such as the liver, spleen, and lymph nodes. Protection from the inflammatory and immune responses is reduced
Cushing’s Syndrome - Interventions

monitor what?

what is the best indicator for fluid retention and overload?
-Monitor VS, I & O, electrolytes (we monitor these for anything with the anterior pituitary)




weight (best indicator for fluid retention and overload)
Cushing’s Syndrome - Interventions


tell me about skin care
-Good skin care b/c because the pt with fluid overload and dependent edema is at risk for skin breakdown.
Cushing’s Syndrome - Interventions

-restriction of ??????






-Allow patients to express feelings related to body image
both fluid and sodium intake to control fluid volume
Cushing’s Syndrome - Interventions

-Drug therapy involves the use of drugs that interfere with
adrenocorticotropic hormone (ACTH) production or adrenal hormone synthesis for temporary relief.

Administer adrenal enzyme inhibitors, i.e., Lysodren, Cytadren, Modrastane to decrease cortisol production “adrenal inhibitors” look at back of word
Cushing’s Syndrome - Interventions

Diagnosis


normal level
salivary cortisol levels are used to detect hypercortisolism in a patient’s saliva.





(normal salivary cortisol is lower than 2.0 ng/mL. higher levels indicate hypercortisolism.
Cushings Syndrome

Additional laboratory findings that accompany hypercortisolism include:



glucose?
WBC?
sodium?
calcium?
potassium?
-increased blood glucose
-decreased lymphocyte found
-increased sodium level
-decreased serum calcium level
-decreased serum potassium level
Cushing’s Syndrome – Interventions


-Prepare patient for possible radiation treatment if caused by
pituitary adenomas)
Cushing’s Syndrome – Interventions

-Prepare for possible hypophysectomy if condition is caused by
increased pituitary secretion of ACTH is causing adrenal hyperfunction
Cushing’s Syndrome – Interventions

-Prepare for adrenalectomy if condition is from what?
from adrenal adenoma (tumors) causing hypercorticolism
Pheochromcytoma

-what is it?
a catecholamine-producing tumor that arises from the adrenal gland which produces excess adrenaline.
Pheochromcytoma

-what do the tumors store, produce, and release?
excessive epinephrine and norepinephrine, which stimulates adrenergic receptors which mimic the action of the sympathetic nervous system
Pheochromcytoma


-tumors that arise from where?
Arise from the central portion of the adrenal gland which is called the adrenal medulla.




The adrenal medulla is responsible for the normal production of adrenaline which our body requires to help maintain blood pressure and to help cope with stressful situations.
A tumor which arises from the adrenal medulla and overproduces adrenaline can be a deadly tumor because of the severe elevation in blood pressure it causes
Pheochromcytoma

S/S
S/S
Headaches (severe)
Excess sweating (generalized)
Racing heart (tachycardia and palpitations)
Anxiety / nervousness (feelings of impending death)
Pheochromcytoma

S/S
Nervous shaking (tremors)
Pain in the lower chest or upper abdomen
Nausea (with or without nausea)
Weight loss
Heat intolerance -very hot
Pheochromcytoma


what is the main treatment?
Surgery is the main treatment for a pheochromocytoma. One or both adrenal glands are removed.
Who Should be Examined for a Pheochromocytoma
-Patients with very difficult to control hypertension
-Patients requiring more than 4 blood pressure medications
-Patients with onset of hypertension before the age of 35
-Patients with onset of hypertension after the age of 60
-Patients with signs or symptoms of pheochromocytoma
-foods or beverages high in tyramine (aged cheese, red wine) also induce hypertension
Diagnosing Pheochromocytomas

24 hour urine collection that shows elevated levels of (2)
catacholamines and metanephrines (metabolite of epinephrine)
Diagnosing Pheochromocytomas


24 hour urine collection that shows elevated levels of catacholamines and metanephrines


This study is designed to measure production of the different types of what?
adrenaline compounds that the adrenal makes.




-This test measures different types of adrenaline (epinephrine, norepinephrine, dopamine) as well as the break-down products of these compounds which the liver and kidney have degraded.
Surgical Treatment of Pheochromocytomas


All pheochromocytomas should be removed how?
by surgery, one ore more of the adrenal glands are removed.
Surgical Treatment of Pheochromocytomas

-tumors may be inoperable because of the patient’s other medical conditions. Treatment then is medical with
alpha adrenergic and beta adrenergic blocking agents, because the tumors do not respond well to chemotherapy or radiation therapy (Calcium channel blockers, sodium channel blockers, beta, we have to block)
Surgical Treatment of Pheochromocytomas


what is the hallmark of this disease and the most common complication after surgery?
hypertension


Monitor BP closely.
Surgical Treatment of Pheochromocytomas


-palpation when doing a head to toe asessment
Do not palpate the abdomen because this action could cause a sudden release of Catecholamines and severe hypertension.
Surgical Treatment of Pheochromocytomas

what is now the preferred method for removing pheochromocytomas and is available in most hospitals in the U.S.
-The vast majority of patients can be treated with the new technique of minimally invasive Laparoscopic Adrenalectomy.