Nursing Management of Patients with Adrenal Disorders Flashcards
Adrenal Insufficiency
Primary: Addison’s Disease
May be hereditary; Lack of:
Glucocorticoids
Mineralocorticoids
Androgens
Secondary
Lack of pituitary ACTH
Lack of:
Glucocorticoids
Androgens
Clinical symptoms
Headache
Progressive weakness, Mild fatigue & Irritability
Weight loss
Anorexia, N / V
Orthostatic hypotension
Hyperkalemia
Hyponatremia
Abdominal pain, Diarrhea
Salt craving
Joint pain
Insidious onset; Often advanced before diagnosed
Usually 90% loss of adrenal cortices at time of diagnosis
Addison’s Disease Diagnostic Testing
Labs:
Hyperkalemia
Hyponatremia
Hypoglycemia
Anemia
Increased BUN
Imaging studies:
Localize tumor, identify adrenal calcification or enlargement
X-ray
CT scan
MRI
ACTH Stimulation Test
Baseline: Cortisol & ACTH
Synthetic ACTH given IVP
Levels rechecked after 30 & 60 minutes
Elevated Cortisol normal
Little or no increase in Cortisol (Addison’s disease)
High ACTH (Primary adrenal insufficiency)
CRH (Corticotrophin-releasing hormone) Stimulation Test Secreted by hypothalamus; central driver stress hormone system (hypothalamic–pituitary–adrenal axis)
Abnormal ACTH Test response
Synthetic CRH given IVP
Levels checked after 30 & 60 minutes
High ACTH levels with no Cortisol (Addison’s disease)
Absence of ACTH or delayed response (Secondary)
Treatment:Addison’s Disease
Glucocorticoid: Hydrocortisone (Gluco & Mineralo-corticoid properties)
2/3 total daily dose in AM
1/3 total daily dose in PM
Must be increased during times of stress to prevent Addisonian Crisis
Carry Emergency Kit at all times
100 mg Hydrocortisone IM syringes
Instructions for use
Mineralocorticoid: Fludrocortisone (Florinef)
Once daily in AM
Androgens (For women): Dehydro-epi-androsterone (DHEA)
Increase dietary salt intake
Acute Adrenal Insufficiency(Addisonian Crisis)
Sudden, penetrating pain in back, abdomen, legs
Severe vomiting
Diarrhea
Hypotension & Tachycardia
Hypo-natremia
Hyper-kalemia
Hypo-glycemia
Dehydration
Fever
Weakness
Confusion
Treatment
Management of shock; Volume expansion with
0.9% Saline
D5W
Correct electrolyte imbalance
Kayexalate
High-dose Hydrocortisone replacement:
100 mg IV bolus, then
100 mg IV every 8-hours x 24 hours
IV tapered to PO doses
Addison’s Disease:Nursing Interventions
Medication history
Frequent assessment:
Vital signs
Fluid & electrolyte status
Monitor mental status
Daily weight
Watch for signs of Cushing syndrome
Infection prevention
Assist with daily hygiene
Protect from stress & extremes
Light
Noise
Temperature
Addison’s Disease:Patient Teaching
Life-long Therapy; Medication dosing to reflect normal circadian rhythm & decrease side effects
Glucocorticoids in divided doses
Mineralocorticoids once in the morning
Take with food to decrease gastric distress
Need to increase corticosteroids during times of stress
Emergency Kit
Medical Alert Bracelet
Effects of Corticosteroid Therapy
Expected:
Anti-inflammatory action
Immunosuppression
Maintenance of normal BP
↓ Potassium & calcium
↑ Glucose & B/P
Delayed healing
Potential complications:
Peptic ulcer disease
Muscle atrophy / weakness
Mood & behavior changes
Moon Facies
Truncal obesity
Protein depletion
Decreased K+ & Ca+
Increased glucose & BP
Delayed healing
Susceptibility to infection
Suppressed immune response
Risk for acute Adrenal Crisis if therapy stopped abruptly
Syndrome of Inappropriate Antidiuretic Hormone (SIADH)
Release of ADH despite low / normal plasma osmolarity
Fluid retention
Low urine output
Weight gain without edema
Serum hypo-osmolarity
Dilutional hyponatremia
Concentrated urine with normal or increased intra-vascular volume
Interventions
Fluid restriction: 800 – 1000 mL / day
Frequent oral care
Distraction
Furosemide (Lasix) with Na+ > 125
Seizure / fall precautions
HOB flat or 10-degrees
IV Conivaptan (Vapriosol)
PO Tolvapan (Samsca)
Cushing’s Syndrome
Excess Corticosteroids
Adrenal Cortex Hormones(Corticosteroids)
Glucocorticoids
Regulate metabolism
Increase blood glucose
Critical in physiologic stress response
Mineralocorticoids
Regulate sodium & potassium balance
Androgens
Involved in growth & development
Sexual development in women
Cushing SyndromeEtiology & Pathophysiology
Chronic exposure to excess Glucocorticoids
Iatrogenic: Administration of exogenous corticosteroids (Prednisone)
ACTH-secreting pituitary adenoma
(85%; Cushing Disease)
Adrenal tumors
Ectopic production of ACTH by other tumors (Lung or Pancreas)
Cushing SyndromeManifestations: Excess Glucocorticoids
Weight gain
Truncal & general obesity
Moon face
Buffalo hump
Purplish, red striae
Loss of collagen
Thin skin
Easy bruising
Hyperglycemia
Glucose intolerance
Increased gluconeogenesis
Muscle wasting
Osteoporosis & back pain
Delayed wound healing
Cushing SyndromeManifestations: Excess Mineralocorticoids & Androgens
Excess Mineralocorticoids
Hypokalemia
Hypertension
Excess Androgens
Severe acne
Virilization in women
Increased body hair (Hirsutism)
Menstrual disorders
Feminization in men
Gynecomastia
Impotence
Cushing Syndrome Providing Emotional Support
Remain sensitive to patient feelings
Offer respect & unconditional acceptance
Offer reassurance that physical changes & emotional lability will resolve when hormone levels return to normal
Cushing SyndromeDiagnostic Studies
Late night, or midnight plasma or salivary cortisol
24-hour urine collection for free cortisol
Elevated (Above 100 mcg / 24-hours)
Low-dose Dexamethasone suppression test
CT or MRI to detect tumor
Plasma ACTH levels
High or normal with Cushing disease (pituitary etiology)
Low, normal, or high with Cushing syndrome
Hypokalemia & alkalosis; With ectopic ACTH syndrome & Adrenal cancer