Adrenal Dysfunction Flashcards

1
Q

What is Cushing’s disease?

A

Hypersecretion of the adrenal cortex of one or all hormones (cortisol and androgens)

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2
Q

What causes Cushing’s disease?

A

Cortisol secreting tumor (most are benign)
Or adrenal hyperplasia r/t oversecretion of SCTH (caused by pituitary tumor or ectopic secretion caused. By bronchial carcinoid tumor)

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3
Q

What causes Cushing’s Syndrome?

A

Exogenous administration of glucocorticoids

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4
Q

*General appearance of pt with Cushing’s

A

Moon face
Buffalo hump
Truncal obesity
Weight gain
Pathologic fractures (makes bones porous b/c pulls out Ca)
Paper-like skin
Striae
Bruising

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5
Q

*Diagnostics of Cushing’s

A

Serum test looking for:
*Increased serum cortisol, Na, blood sugar
*Decreased serum calcium, potassium, lymphocytes

CT, MRI looking for tumor

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6
Q

*Client problems for pts with Cushing’s

A

Fluid volume overload
Fatigue (nutrition not good)
Body image disturbance
Risk for injury (fractures)
Risk for infection
Risk for impaired skin integrity

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7
Q

Treatment options for pts with Cushing’s disease

A

Medications
Radiation
*Surgery = best therapy

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8
Q

*Nursing actions for pt’s post-op after adrenal tumor removal

A

Lifelong hormone replacement if bilateral adrenalextomy
Hormone replacement for 1-2 yrs if unilateral adrenalectomy
Medic-alert bracelet
Additional hormones may be needed in times of stress

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9
Q

What is a pheochromocytoma?

A

Catecholamine-secreting (epi and norepi) tumor of the chromaffin cells usually found in the adrenal medulla

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10
Q

Patho of a pheychromocytoma

A

Excess secretion of epinephrine and norepinephrine causing severe symptoms (extremely high BP) and even death

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11
Q

S/S of a pt with pheochromocytoma

A

Hyperglycemia
N/V
Palpitations
*Hypertension
Apprehension
HA
Sweating
Psychoneurosis

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12
Q

Diagnostics for pheochromocytoma

A

Increased urinary catecholamines (epi/norepi)
Elevated serum catecholamines
CT scan
MRI

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13
Q

Interventions to treat pheochromocytoma

A

*Adrenalectomy is treatment of choice (removal of adrenal gland)

*Pt will likely be given alpha-adrenergic blockers first for stabilization of BP for 2-3 weeks

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14
Q

Nursing actions for caring for a pt with pheochromocytoma

A
  • Altered tissue perfusion: peripheral (vascular checks, monitor VS)
  • Altered comfort (HA): *quiet dark room away from nurse’s station, analgesics, avoid interruptions, limit visitors
  • Potential for injury r/t sustained HTN: *Limit activity, avoid caffeine, smoking, sudden position changes, VS, neuro assess, BS checks
    *Do not palpate abdomen (causes sudden release of epi/norepi causing HTN crisis)
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