Endocrine Part 1 Flashcards

1
Q

Chronic Adrenocortical Insufficiency is a disorder in which

A

the adrenal gland does not produce enough hormones

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2
Q

Secondary adrenocortical insufficiency is when the

A

pituitary fails to secrete ACTH

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3
Q

Causes of secondary adrenocortical insufficiency

A
  • Exogenous glucocorticoid use (MCC)

- Hypopituitarism

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4
Q

On the other hand, primary adrenal insufficiency is

A

Adrenal gland destruction, so a lack of cortisol AND aldosterone

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5
Q

True or False: In secondary adrenal insufficiency, there is a lack of cortisol only. The aldosterone is intact because of the renin angiotensin aldosterone system?

A

True!

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6
Q

Causes of primary adrenal insufficiency

A
  • Autoimmune (MC)
  • Infection (TB, HIV)
  • Vascular
  • Medications (Ketoconazole, Rifampin, Phenytoin)
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7
Q

Symptoms of adrenocortical insufficiency (lack of cortisol)

A
  • Weakness, myalgias, fatigue
  • Nonspecific GI symptoms
  • Abnormal menstruation
  • Mild hyponatremia, salt craving
  • Hypotension
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8
Q

Symptoms in Primary (Addison’s Disease) due to lack of sex hormones and aldosterone

A
  • Hyperpigmentation (increased ACTH stimulates melanocytes)
  • Orthostatic Hypotension
  • Loss of libido, amenorrhea, and loss of pubic hair in women
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9
Q

What do the labs show in Primary Adrenocortical insufficiency?

A
  • Elevated ACTH

- Hyperkalemia, Metabolic Acidosis

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10
Q

What do the labs show for secondary adrenocortical insufficiency

A
  • Decreased ACTH

- Hypoglycemia

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11
Q

What is the screening test for adrenal insufficiency?

A
  • High dose ACTH stimulation test

- -This test is positive if insufficient or absent rise in serum cortisol ( < 18) after ACTH administration

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12
Q

Treatment for adrenal insufficiency

A
  • Glucocorticoid replacement (Hydrocortisone)

- Mineralocorticoid replacement (Fludricortisone) ONLY in Addison’s

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13
Q

What are some patient education tips if they have adrenal insufficiency?

A
  • Patients must be treated with IV glucocorticoids and IV isotonic fluids before and after surgery
  • During illness/stress/surgery, oral dosing needs to be adjusted to triple the dose
  • Everyone should carry a medical alert tag and injectable form of cortisol
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14
Q

Explain the pathophysiology of Adrenal (Addisonian) Crisis

A

-Triggered by a stressful event (trauma, illness, surgery) and usually the response is to increase cortisol by three-fold. Patients with this are unable to do so to meet the demand.

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15
Q

Etiologies of Addisonian Crisis

A
  • Abrupt withdrawal of glucocorticoids (without tapering)

- Bilateral adrenal infarction

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16
Q

Symptoms of Addisonian Crisis

A
  • Shock is the primary manifestation
  • Hypotension
  • Hypovolemia
17
Q

What do labs show for Addisonian Crisis

A
  • Hyponatremia
  • Hyperkalemia
  • Hypoglycemia
18
Q

Treatment for Addisonian Crisis

A

-Isotonic fluids (normal saline or D5N5) + IV hydrocortisone or Dexamethasone

19
Q

Cushing’s Syndrome is signs and symptoms related to

A

Cortisol excess

20
Q

What are the four main causes of Cushing’s Disease

A
  • Long-term high-dose glucocorticoid therapy (MC exogenous cause)
  • Pituitary gland ACTH overproduction (MC endogenous cause)
  • Adrenal tumor (Adenoma)
  • Ectopic ACTH producing tumor (Small cell lung cancer)
21
Q

Symptoms of Cushing’s Disease

A
  • Weight gain, proximal muscle weakness
  • Central obesity
  • Moon facies
  • buffalo hump
  • Supraclavicular fat pads
  • Thin extremities
  • Striae
  • Acanthosis Nigricans
  • Hypertension
22
Q

What are the screening test options for Cushing’s?

A
  • 24 hour urinary free cortisol (most specific)
  • Nightime salivary cortisol
  • Low dose overnight Dexamethasone suppression test
23
Q

To differentiate Cushing’s from other causes, what is the diagnostic that is done?

A

Baseline ACTH + High-dose dexamethasone suppression test

suppression of cortisol with high dose

24
Q

Treatment for Cushing’s

A
  • Corticosteroid use: gradual taper

- Cushing Disease: Transsphenoidal Resection