DISORDERS OF ADRENAL GLANDS

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Questions and Answers

Epinephrine and norepinephrine are released by which part of the adrenal gland in response to stimulation from the sympathetic nervous system?

  • Adrenal medulla (correct)
  • Pituitary gland
  • Hypothalamus
  • Adrenal cortex

Which of the following is a primary function of glucocorticoids?

  • Maintaining blood glucose levels through gluconeogenesis and decreasing glucose use. (correct)
  • Promoting sodium and water excretion to lower blood pressure.
  • Lowering blood glucose levels by promoting glycogenesis.
  • Stimulating muscle growth and increasing strength.

What is the primary effect of mineralocorticoids, such as aldosterone, on electrolyte balance?

  • Promoting potassium retention and sodium excretion.
  • Maintaining equal balance of sodium, potassium, and water.
  • Promoting sodium and water retention in exchange for potassium excretion. (correct)
  • Decreasing sodium and water retention, leading to increased potassium retention.

Which hormone stimulates the secretion of mineralocorticoids?

<p>Angiotensin II (C)</p> Signup and view all the answers

What causes Ectopic Cushing's syndrome?

<p>A non-pituitary site tumor. (A)</p> Signup and view all the answers

Which of the following clinical manifestations is commonly observed in Cushing's syndrome due to the effects of hypercortisolism?

<p>Moon face and buffalo hump. (D)</p> Signup and view all the answers

What dietary modifications are typically recommended for a patient undergoing treatment for Cushing's syndrome?

<p>Low-calorie, low-sodium, high-potassium diet with fluid restriction. (D)</p> Signup and view all the answers

Which electrolyte imbalances are most likely to be observed in a patient with hyperaldosteronism (Conn's syndrome)?

<p>Hypernatremia and hypokalemia. (C)</p> Signup and view all the answers

A patient with Conn's syndrome (hyperaldosteronism) is at risk for several complications related to electrolyte imbalances. Which of the following is the most life-threatening complication that requires immediate intervention?

<p>Cardiac arrhythmias secondary to hypokalemia. (B)</p> Signup and view all the answers

A researcher is investigating the effects of a novel drug on adrenal function. They hypothesize that the drug will selectively inhibit the synthesis of androgens in the adrenal cortex without affecting glucocorticoid or mineralocorticoid production. To test this hypothesis, which enzyme would be the most appropriate target for the drug?

<p>$17\alpha$-hydroxylase/17,20-lyase (CYP17A1) (A)</p> Signup and view all the answers

What is the primary intervention following an adrenalectomy to address temporary suppression of renin-induced aldosterone?

<p>Fluid volume replacement (A)</p> Signup and view all the answers

A female patient exhibits hirsutism and virilism. Which hormonal imbalance is MOST likely the cause?

<p>Androgen excess (A)</p> Signup and view all the answers

Which of the following is NOT a typical manifestation of catecholamine excess due to pheochromocytoma?

<p>Hypotension (A)</p> Signup and view all the answers

What nursing intervention is MOST important in the pre-operative management of a patient with pheochromocytoma?

<p>Preventing hypertensive crisis (D)</p> Signup and view all the answers

A patient post-unilateral adrenalectomy requires corticosteroid therapy. What is the typical duration of this treatment?

<p>First few days or weeks post-op (C)</p> Signup and view all the answers

The Clonidine Suppression Test is used to assess for pheochromocytoma. A positive result for pheochromocytoma would reveal:

<p>Elevated catecholamine levels (C)</p> Signup and view all the answers

Which of the following electrolyte imbalances is associated with mineralocorticoid deficiency in Addison's disease?

<p>Hyponatremia and hyperkalemia (D)</p> Signup and view all the answers

What is a common cause of primary Addison's disease?

<p>Autoimmune destruction of the adrenal cortex (D)</p> Signup and view all the answers

A patient with Addison’s disease is at risk for Addisonian crisis. Which intervention is MOST critical to prevent this life-threatening complication?

<p>Educating the patient on stress management and the importance of lifelong steroid replacement therapy (C)</p> Signup and view all the answers

A patient with known Addison's disease presents with severe hypotension, confusion, and profound weakness following a minor surgical procedure. Initial laboratory results reveal severe hyponatremia and hyperkalemia. Beyond immediate stabilization with IV fluids and electrolyte correction, what is the MOST critical immediate intervention?

<p>Intravenous administration of high-dose hydrocortisone (A)</p> Signup and view all the answers

Flashcards

Adrenalectomy

Surgical removal of adrenal tumor.

Post-Adrenalectomy Fluid Imbalance

Occurs after adrenalectomy due to temporary renin suppression, leading to fluid volume deficit.

Androgen Excess

Excess androgen secretion, often due to adrenal adenoma, carcinoma or hyperplasia.

Signs of Androgen Excess in Females

Virilization and hirsutism.

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Pheochromocytoma

A tumor of the adrenal medulla that produces excessive catecholamines.

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Pheochromocytoma - 5 Hs

Hypertension, headache, hyperhidrosis, hypermetabolism, and hyperglycemia.

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VMA Test

24-hour urine test to measure catecholamine metabolites.

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Clonidine Suppression Test

Used to confirm pheochromocytoma; catecholamine levels remain elevated after administration.

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Mineralocorticoid Deficiency

Deficiency in mineralocorticoids leading to hyponatremia, hyperkalemia, hypotension, hemoconcentration and mild acidosis.

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Addison's Disease

Occurs when the adrenal cortex doesn't produce enough cortical hormones.

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Adrenal Medulla Function

Releases epinephrine and norepinephrine in response to the sympathetic nervous system.

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Glucocorticoids Function

Maintain blood glucose levels through gluconeogenesis, reduce inflammation, and affect protein and fat metabolism.

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Mineralocorticoids Function

Maintain normovolemia by increasing sodium and water retention, while excreting potassium.

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Cushing's Syndrome Causes

Excess cortisol, can be primary (adrenal), secondary (pituitary), ectopic (non-pituitary), or iatrogenic (medication-induced).

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Cushing's Syndrome Manifestations

Moon face, buffalo hump, muscle wasting, thin skin, easy bruising, emotional instability, high BP, and osteoporosis.

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Cushing's Syndrome Management

Adrenalectomy or pituitary tumor excision, irradiation of the pituitary gland, or adrenal enzyme inhibitors (Mitotane, Metyrapone).

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Cushing's Syndrome Nursing Care

High-calorie, low-sodium, high-potassium diet, diuretics, insulin replacement, ROM exercises, and assistance with ambulation.

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Conn's Syndrome Signs

Hypertension, hypernatremia, and hypokalemia.

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Hypokalemia Effects

Muscular weakness, paresthesia, cardiac arrhythmias, metabolic alkalosis, and impaired urine concentration.

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Cushing's Syndrome Nursing Actions

Monitoring daily weights and I&O, ensuring adequate rest, and avoiding stress and infection.

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Study Notes

  • Adrenal glands sit atop the kidneys
  • Adrenal glands consist of the adrenal gland, capsule, cortex, medulla and blood vessels

Adrenal Medulla

  • It reacts to the Autonomic Nervous System (SNS)
  • It releases epinephrine and norepinephrine

Adrenal Cortex

  • Produces Glucocorticoids
  • Produces Mineralocorticoids
  • Produces Androgens

Glucocorticoids

  • Maintains blood glucose level and gluconeogenesis; decreases use of glucose
  • Glucocorticoids are anti-inflammatory and immunosuppressive
  • Causes CHON catabolism
  • Encourages lipolysis (fat breakdown)
  • Encourages Na & H20 retention and K+ excretion
  • Increases gastric acid and pepsin production
  • Decreases scar tissue formation, and increases platelet
  • Stimulates appetite and emotional stability
  • Increases serum levels & neutrophils

Mineralocorticoids

  • Maintains normovolemic state to increase Na & H20 retention in exchange of potassium excretion
  • Secreted in the presence of Angiotensin II

Androgens

  • Gonadal sex hormones regulate reproductive and sexual functions

Hypersecretion and Cortisol Excess

  • Can lead to Cushing's Syndrome

Cushing's Syndrome

  • With primary cause it is Cushing's Syndrome
  • With secondary cause it is Cushing's Disease
  • With ectopic cause it is Cushing's Syndrome coming from a non pituitary site
  • Due to latrogenic causes it is latrogenic cushing's

Cushing's Syndrome Symptoms

  • Moon face & buffalo hump are caused by adipose deposition to trunks and face
  • Muscle wasting, fatigue, and apathy is due to hypo K and Na & H20 favoring
  • Pale, purplish striae is shown as thinning of skin & weakening of collagenous fibers
  • Bruises easily due to ecchymosis formation (easily traumatized)
  • Causes insomnia, nightmares, mood swings and emotional stability
  • Can lead to decreased libido, breast atrophy, clitoromegaly, amenorrhea and voice deepening in women
  • Causes osteoporosis due to bone matrix wasting
  • Leads to low resistance to infection/poor wound healing
  • Affects Blood glucose
  • Affects WBC, Na, K and Ca

Cushing's Syndrome Complications

  • Can involve neuropsychiatric disorders
  • Leads to arterial atherosclerosis and vascular disease
  • Leads to liver steatosis
  • Can weaken bones and cause osteoporosis especially of the femoral neck
  • Leads to cardiac disease, may result spinal and vertebral fractures
  • Leads to infertility and sexual dysfunction
  • May lead to visceral obesity
  • Infections may occur
  • Can lead to myopathy

Cushing's Syndrome Management

  • Involves Adrenalectomy; excision of adrenal (primary) or pituitary tumor (secondary)
  • Can involve Irradiation of the PG if due to pituitary adenoma
  • Can involve drug therapy with adrenal enzyme inhibitors, with Mitotane, Metyrapone, and Aminoglutethimide

Nursing Management

  • DIET: decreased CALORIE, decreased Na, increased K, increased fluids
  • Administer diuretics
  • Insulin replacement may be needed
  • Encourage ROM
  • Assist with ambulation

Nursing Diagnosis

  • Risk for injury/falls
  • Risk for infection
  • Risk for impaired tissue integrity
  • Monitor Daily weights, and I & O
  • Promote Adequate rest
  • Avoid stress & infection

Aldosterone Excess

  • Also known as Hyperaldosteronism can lead to Conn's Syndrome
  • 3 Major Signs may occur: Hypertension, Hypernatremia, and Hypokalemia

Hypokalemia

  • Affects muscular contraction causing weakness, paresthesia, hypoactive bowel movements and hypoactive DTR
  • Can cause Cardiac arrhythmias
  • Can lead to loss of kidney's ability to concentrate & acidify the urine
  • Can cause Metabolic alkalosis

Management of Hyperaldosteronism

  • Adrenalectomy/ excision of tumor
  • Na+ & fluid restriction, Potassium replacement
  • After surgery there is typically a temporary suppression of Renin-induced Aldosterone and fluid volume deficit
  • If there is an ALDOSTERONE DEFICIT:
    • Treat MILD cases of acidosis, Hyperkalemia with Na bicarbonate, sodium polystyrene sulfonate (Kayexalate) after surgery
    • Treat severe cases with Fludrocortisone

Androgen Excess

  • Results from Adrenal adenoma/carcinoma, or Adrenal hyperplasia
  • Causes no obvious signs in males
  • Causes Hirsutism, and virilism in females

Adrenal Medulla Catecholamine Excess

  • Causes Pheochromocytoma which is a tumor producing catecholamine

Pheochromocytoma Manifestations are known as "The 5 H's"

  • Hypertension
  • Headache
  • Hyperhidrosis
  • Hypermetabolism
  • Hyperglycemia
  • Death may occur with shock, CVA, renal failure, dysrhythmia or aneurysm

Pheochromocytoma Diagnostic Tests

  • Utilize the Vanillylmandelic Acid (VMA) Test with a 24 hour urine specimen; the norm is up to 9 mg/24h
  • Check for a Total Plasma Catecholamine Concentration, using a butterfly needle inserted 30 mins before the blood specimen when drawn
    • Normal EPI=100 pg/ml
    • Normal NorEpi = 100 – 550 pg/ml
  • Use a Clonidine Suppression Test with Catapres (Clonidine)
    • NORMAL: If 2 -3 hrs catecholamine decreases @least 40% from the baseline
    • (+) PHEOCHROMOCYTOMA indicates catecholamines remain elevated

Pheochromocytoma Treatment

  • CT Scan, MRI, UTZ
  • Includes Adrenalectomy
    • UNILATERAL requires corticosteroids for the 1st few days or weeks post op
    • BILATERAL requires lifetime steroid Tx
  • Pre-Op Priority – HPN to prevent hypertensive crisis
  • Bed rest, non-stimulating environment, elevate head of bed
  • Phentolamine (Regitine)
  • Sodium nitroprusside (Nipride)
  • Diuretics (Lasix)
  • Corticosteroid therapy and BP measurement is necessary
  • Avoid stimulants, and smoking

Hyposecretion

  • Can lead to Addison's Disease
  • Occurs when adrenal cortex is inadequate to meet the patient's need for cortical hormones
  • Can be caused by:
    • Primary, secondary, and iatrogenic factors
    • Autoimmune, idiopathic and sx - adrenalectomy
    • TB or Histoplasmosis

Mineralocorticoids Deficiency

  • Causes Hyponatremia
  • Causes Hyperkalemia
  • Causes Hypotension
  • Causes Hemoconcentration (DHN)
  • Causes Mild acidosis
  • Causes DHN and decreased cardiac output

Glucocorticoid Deficiency

  • Decreased blood glucose
  • Causes Hypotension
  • Causes Stress intolerance
  • Causes Nausea and Vomiting
  • Causes Weight loss
  • Causes Sodium depletion
  • Causes Apathy, lethargy
  • Causes Confusion, psychosis
  • Causes Hyperpigmentation

Androgen Deficiency

  • Causes Loss of body hair, and loss of libido
  • May cause impotence
  • Disrupts Menstrual/ fertility disorders

Addison's Disease Management

  • Glucocorticoids (Cortisone & Hydrocortisone) in Steroid therapy -Give 2/3 dose in AM and 1/3 dose @ night with meals, milk, & antacid
  • Encourage small frequent feedings
  • Encourage: Increased CHO & CHON
  • Avoid stress and trauma
  • Avoid strenuous exercise especially during hot weather
  • Consume salt tablets or salty foods if excessively sweating

Addisonian Crisis

  • Occurs with an Absolute or complete absence of adrenocortical hormones
  • Precipitated by stress, infection, trauma or surgery
  • Precipitated by abruptly withdrawing glucocorticoid replacement therapy

Addison'S Disease Manifestations

  • Hypotension -Shock (vascular collapse)
  • Hypovolemia
  • Hypoglycemia
  • Leads to muscle weakness and Coma

Addisonian Crisis Treatment

  • Treat with IVF
  • Administer IV glucocorticoids and vasopressor
  • Increase dosage of steroids to treat shock
  • Treat with antibiotics
  • Strictly enforce CBR and eliminate all stressful stimuli
  • Protect from infection

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