Patient is unable to tolerate physical or emotional stress without additional exogenous
corticosteroids
o
long-term care revolves around recognizing the need for extra medication and
techniques for stress management
Teach patient importance of maintaining daily corticosteroid replacement therapy
Teach patient to appropriately increase dosing during stress
Teach patient signs and symptoms of corticosteroid deficiency and excess
Medic alert bracelet
Home BP monitoring
Emergency IM hydrocortisone kit
Pheochromocytoma

Rare condition caused by tumor of the adrenal medulla
Causes excess release of catecholamines (epinephrine, norepinephrine)-hormones that
control HR, BP, metabolism
o
The most dangerous immediate effect of the disease is severe hypertension
Occurs in both genders and at any age (most common in young to middle age adults)
Tumors usually benign, encapsulated, unilateral
BL tumors rarely occur
If untreated may lead to DM, cardiomyopathy and death
What does excess epi/norepi cause? HTN!
Pheochromocytoma
Severe episodic hypertension associated with:
o
Severe pounding headache
o
Tachycardia
o
Palpitations
o
Diaphoresis
o
Chest/abdominal pain
o
Anxiety
o
Triad – severe headache, tachycardia, profuse sweating
Often provoked by medications:
o
Antihypertensions
o
Opiods
o
Radiologic contrast dye
o
TCA’s – tricyclic antidepressant
Pheochromocytoma
Secondary cause of HTN (only 0.1% of all cases of HTN)
Often missed
Consider for patients who do not respond to traditional antihypertensives
Measurement of urinary fractionated metanephrines (Catecholamine metabolites) via
24 hour urine
Values are elevated in 95% of persons with pheochromocytoma
CT/MRI to diagnose tumors
DO NOT press on abd of pt with pheochromocytoma bc it could trigger release of
catecholamines and severe hypertension
Pheochromocytoma
Surgery
o
Open vs. Laparoscopic
o
Nursing care same as discussed for adrenalectomy
Pre-op

o
Manage BP via:
Alpha adrenergic blockers
Beta adrenergic blockers
The α-adrenergic receptor blocker phenoxybenzamine (Dibenzyline) is
given 7 to 10 days preoperatively to reduce BP and alleviate other
symptoms of catecholamine excess
Monitor blood glucose- long term exposure to epi and norepi can cause an increased risk
of DM
Avoid smoking, caffeine
Do not palpate abdomen
Pheochromocytoma
HTN usually resolves with tumor removal
HTN may persist after removal (10-30%)
o
Treat with routine antihypertensive meds
Metyrosine
o
Pharmacological treatment if nonsurgical candidate
o
Decreases catecholamine production by tumor
o
Can cause orthostatic hypotension
Stand slowly, hold onto secure object

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- Spring '10
- Cortisol, Adrenal cortex, ACTH stimulation test, Cushing Syndrome, Primary Adrenal Insufficiency, Urine cortisol levels