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TL Adrenal Gland
Cushing's, Addison's, Pheochromocytoma
Question | Answer |
---|---|
Define Cushing’s syndrome. | hyperfunction of the adrenal gland cortex resulting in elevated serum cortisol or ACTH levels |
What effect does excessive cortisol have on the body? | causes life-threatening changes in physiologic and metabolic functioning |
Who is most at risk for Cushing’s Syndrome? | Women 30-40 years old |
What is the cause of primary Cushing’s syndrome? | tumor of the adrenal cortex |
What is the cause of secondary Cushing’s syndrome? | disorder of the pituitary or hypothalamus = too much ACTH or ectopic tissue like ACTH-producing cancer of the lung, bronchus, or pancreas; in either case the result would be hyperplasia/secretion of the Adrenal cortex, or just too much steroid use |
What are the clinical manifestations of Cushing’s syndrome? | weakness, muscle wasting, thin skin, bruising, emotional lability, skin infections, poor wound healing, striae, hirutism, HTN, fluid overload, weight gain, osteoporosis, truncal obesity, moon facies, fat pad-neck, amenorrhea, impotence, decreased libido |
What lab findings are typical of Cushing’s syndrome? | INCREASED: cortisol, sodium, glucose, calcium, and potassium; elevated urine 17 Ketosteroids; ACTH up or down; Positive ACTH suppression test; normal BUN |
Briefly explain how the ACTH suppression test works. | Dexamethasone is given. Dexamethasone is a synthetic cortisol. If the hypothalamus/pituitary gland works it should respond by decreasing ACTH levels. |
Give 5 nursing diagnoses applicable to the client with Cushing’s syndrome. | Fluid volume excess; risk for injury; risk for infection; disturbed body image; deficient knowledge |
What are the postoperative interventions for client who has had adrenalectomy? | encourage deep breathing (no coughing for transphenoidal surgery), mouth breathing -nasal packing, turning q2 hr, ankle dorsiflexion q hr, minimize stress on incision by log roll from lying to seated and vice versa, watch for CSF leaks, HOB 30% |
What post-adrenalectomy interventions are purposed toward preventing Addisonian crisis? | Give IV NS infusion bolus and cortisol as prescribed |
What symptoms alert the nurse to possible Addisonian crisis post adrenalectomy? | dry, tenting skin; decreased BP; increased pulse; decreased level of consciousness; anorexia; weakness |
What medications would the nurse expect for the patient with Cushing ’s syndrome? | Meturapone, Octreotide (Sandostatin), mitotane (Lsodren) |
What does meturapone do? | directly inhibits cortisol production and secretion by the adrenal cortex |
What does octreotide (Sandostatin) do? | Sandostatin is a somatostatin analog that suppresses ACTH secretion |
What does mitotane (Lysodren) do? | Suppresses the function of the adrenal cortex and decreases the metabolism of corticosteroids, thus decreasing serum cortisol |
What symptoms should the client with Cushing’s disease report to their provider? | signs of hyperglycemia, hypoglycemia, and signs of infection |
What does the client with Cushing’s syndrome need to know about self- care? | about the disorder, wear medica alert bracelet, how to take medication, diet should be high protein, vitamin B and C to support immune system, supplemental potassium and calcium, how to care for postoperative wound and postoperative cortisol replacement |
What kind of diet is appropriate for the client with Cushing’s syndrome? | High protein, high in vitamin B and C to support immune system, Supplemental potassium and calcium |
Define Addison’s disease. | insufficient level of cortisol |
What are some potential causes of Addison’s? | destruction of the adrenal cortex, caused by autoimmune disorder, tuberculosis, septicemia, AIDS, bilateral adrenalectomy, or sudden cessation of long term steroid medication |
Who is most at risk for Addison’s disease? | Women <60years of age |
What is the function of cortisol? | to increase rate of glucose sysnthesis, glycogen formation, release of fatty acids, and breakdown of fatty acids, and to exert anti-inflammatory effects to suppress the immune system |
What happens when aldosterone and cortisol are decreased? | leads to hyponatremia, hyperkalemia, decreased extracellular fluid, decreased intravascular volume, decreased glucneogenesis, hypoglycemia, and stress intolerance |
What causes the “eternal tan” of Addison’s disease? | High ACTH levels lead to hyperpigmentation from increased stimulation of malanocytes |
What are the clinical manifestations of Addison’s disease? | hyperpigmentation, delayed wound healing, tachycardia, dysrhythmias, hypotension; dehydration, hypovolemia; weight loss; anorexia, nausea, vomiting; diarrhea; depression; lethargy; emotional lability; confusion; muscle weakness; tremors; muscle/joint pain |
Define Addison’s crisis. | life threatening response to sudden withdrawal of steroids or increased stress manifested by severe hypotension, circulatory collapse, shock, and coma |
What labs are common to the patient with Addison’s disease? | decreased serum cortisol, glucose, sodium; increased potassium, BUN, and ACTH levels; decreased urine 17 ketosteroids; no increase in cortisol with ACTH stimulation test; CT scan positive |
What is the treatment for Addison’s disease? | replace corticosteroids and mineralosteroids |
What are some applicable nursing diagnoses for Addison’s disease? | Deficient fluid volume; Risk for ineffective therapeutic regimen management; deficient knowledge; risk for electrolyte imbalance |
What do we need to do for the client admitted with Addison’s? | maintain fluid/lyte balance – lab values, I&O, daily weight; encourage 3000mL fluid/day & increased sodium in diet; protect from falls; administer hydrocortisone (Cortef) replaces cortisol; Fludrocortisone (Florinef) for mineralcorticosteroids replacement |
What does the client with Addison’s need to know about self care? | about Addison’s, symptoms to report; need for life long medication and disease management, no OTC w/o HCP okay; how to administer medication; how to adjust dose to stress; medic alert bracelet; IM cortisol; diet- immune system, up sodium, potassium down |
Define pheochromcytoma (malignant HTN). | increased level of catecholamine secretion from chromaffin tissue in the adrenal medulla leading to increase sympathetic stimulation; rapid acute HTN; life-threatening requires treatment within first hour |
Explain the pathophysiology of pheochromocytoma. | tumors in the adrenal medulla cause mega secretion of epinephrine and norepinephrine leading to rapid increased vasoconstriction causing acute HTN |
What are the clinical manifestations of Pheochromocytoma? | Rapid rise in BP- systolic 200-300 and diastolic 150-175, visual changes, HA, LOC changes/confusion |
What will lab and diagnostic tests show for the patient with pheochromocytoma? | increase urine and serum catecholamines, Renal CAT scan shows tumor of adrenal glands |
How is pheochromocytoma treated? | adrenalectomy (usually just one), medication therapy, management of stress |
What are some applicable nursing diagnoses for the client with pheochromocytoma? | risk for injury; frisk for interrupted thought processes, deficient knowledge |
What do we do for the client admitted with pheochromocytoma? | pre/post-adrenalectomy care, monitor BP; monitor for changes in LOC or confusion, Administer Alpha and beta blockers as prescribed, administer drugs to suppress catecholamine secretion like metyrosine (Demser) |
What does the client with pheochromocytoma need to know about self care? | Report changes in vision or LOC, facial edema, headaches, take antihypertensives on time, avoid physical and emotional stress |