Adrenal disease Flashcards

1
Q

What are the adrenal glands?

size, location

What are the two parts?

How are they regulated?

A
  • The adrenal glands are multifunctional and secrete a variety of hormones
  • Located just above each kidney, no larger than a walnut and wighing < a grape
  • Two parts of the adrenal glands:
    • Cortex (makes up 80-90% of gland)
      • zona glomerulosa
      • zona fasciculata
      • zona reticularis
    • Medulla (makes up 10-20% of gland)
  • Regulation- by hypothalamus, anterior pituitary, and adrenal cortex (HPA axis)
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2
Q

What does the adrenal cortex release?

A
  • Glucocorticoids (cortisol)
  • Mineralcorticoids (aldosterone)
  • Androgens
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3
Q

What does the adrenal medulla release?

A
  • Epinephrine (80%)
  • Norepinephrine (20%)
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4
Q

What are the physiologic functions of the adrenal gland?

A
  • Blood glucose regulation
  • protein turnover
  • fat metabolism
  • Na, K, and Ca balance
  • maintenance of cardiovascular tone
  • modulation of tissue response to injury or infection
  • Survival as a result of stress- most important
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5
Q

What is cushing’s syndrome?

What are the two causes?

A
  • Hypercorticism- excessive cortisol secretion
  • ACTH dependent
    • Pituitary corticotroph tumors (microadenomas)
    • Non-endocrine tumors of lung, kidney, or pancrease that cause extopic corticotropin syndrome
  • ACTH independent
    • benign or malignant adrenocortical tumors
    • (the adrenal gland releasing cortisol without being told to do so by the release of ACTH)
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6
Q

What are the signs and symptoms of Cushing’s?

A
  • Sudden weight gain (usually central)
  • thickening of the facial fat (moon face)
  • Electrolyte abnormalities
  • systemic hypertension
  • glucose intolerance
  • menstrual irregularities
  • decreased libido
  • skeletal muscle wasting
  • depression and insomnia
  • osteoporosis
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7
Q

How is cushings disease diagnosed?

A
  • Plasma and urine cortisol levles
    • 24 hr urine- 17-hydroxycorticosteroids
    • plasma cortisol levels
    • if both are elevated, pt has cushing’s syndrome
  • CRH stimulation test- used to determine cause of cushings
    • inject pt with CRH and if they have increase in ACTH then it is a pituitary adenoma. (isnt that supposed to happen???)
  • Dexamethasone suppression test- Dexamethasone should suppress cortisol levels. W/pituitary adenoma, it will do that d/t negative feedback
    • if you have a lung ACTH releasing tumor or something on the adrenal, it will not have negative feedback
  • Inferior petrosal sinus sampling- injecting with ACTH and measuring ACTH levels in sinuses and compare to a more peripheral site. Not often used.
  • CT & MRI once diagnosis is confirmed
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8
Q

How is cushings treated?

A
  • Surgical
    • transphenoidal microadenectomy- via the sphenoid sinus to remove the adenoma from the pituitary gland
    • Adrenalectomy- remove the adrenal gland; may have to be removed bilaterally
  • Irradiation
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9
Q

What are your preoperative considerations for a pt with cushings syndrome?

A
  • HTN- may be on medications, may have cardiac compromise d/t htn
  • Intravascular volume- are they on diuretics? Often Spironolactone
  • Electrolytes- hypokalemia, hypernatremia
  • Acid/bas status- hypokalemic metabolic alkalosis
  • Cardiac compromise- CHF
    • EKG, do they have angina?
  • Diabetes- check BS
    • control with small amounts of insulin, 1-5 units q hour
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10
Q

What are your positioning considerations for a pt with cushing’s syndrome?

A
  • High risk of fractures- Osteoporosis and osteomalacia
  • Obesity- but oddly distributed fat (cone shaped arm, difficut to fit with appropriate BP cuff)
  • Use appropriate padding
    • may need to ramp d/t fat pad on back of neck
  • Check position throughout case
  • Be careful when moving to and from stretcher, very fragile
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11
Q

Patients with Cushing’s syndrome have muscle weakness. How can we address this?

A
  • Hypokalemia is a contributing factor- treat pre-op with 80-100 mEq/day oral K
  • Decrease doses of muscle relaxants
  • Use a peripheral nerve stimulator
    • maintain 1 or 1/2 twitch at all times if possible so you know you can reverse
  • May need post-op ventilatory support
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12
Q

What medication do you need to give a pt who has had a unilateral or bilateral adrenalectomy?

A
  • 100 mg glucocorticoid/24 hours- usually started intraoperatively
  • Dose is reduced over 3-6 days to a maintenance dose
  • may also need mineralcorticoid supplementation
  • continued therapy may not be needed if only one glad was removed–depends on the function of the remaining gland
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13
Q

How much blood loss do you expect to see with an adrenal removal surgery?

A
  • May be significant blood loss
  • Type and screen before case (laproscopic)
    • type and cross for major surgery (open)
  • CVP/swan
  • A-line
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14
Q

What do you need to consider regarding anesthetic agents for a pt with cushing’s syndrom or an adrenal surgery?

What about epidural?

A
  • Drugs or techniques are not likely to influence attempts to decrease cortisol levels
    • all inhaled agents depress adrenal response to stress and ACTH
    • Etomidate- inhibits enzymes involved in cortisol and aldosterone synthesis- long term infusion can cause adrenocortical suppression
  • Changes caused by anesthetic agents or drugs are insignificant when compared to the increase in cortisol secretion with surgical stress
  • Can do an epidural but it might be difficult to get d/t osteoporosis
    • other option for post-op pain is a PCA pump
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15
Q

What are some complications you might expect in a transphenoidal microadenomectomy surgery?

A
  • VAE
    • pt will be in high sitting position, will need central line and doppler to monitor
  • transient diabetes insipidus
  • meningitis
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16
Q

What are some complications you might expect for an adrenalectomy surgery?

A
  • Laparoscopic
    • always be prepared for a laproscopic procedure to become an open procedure
    • insufflation and all the problems that go along with that
  • Open
    • pulmonary complications post op
17
Q

What is Conn’s syndrome?

A
  • Primary hyperaldosteronism
  • Excess secretion of aldosterone from a functional tumor
    • occurs more in women than men; rarely in children
18
Q

What causes secondary hyperaldosteronism?

A
  • increased circulating renin stimulates the release of aldosterone
19
Q

What are the signs and symptoms of Conn’s disease?

A
  • Systemic HTN- d/t aldosterone induced Na retention and increased fluid retention
    • HA
    • DBP 100-125 mmHg
    • may be resistant to treatment
  • Hypokalemia
    • skeletal muscle cramps or weakness
    • metabolic alkalosis
20
Q

What are your anesthesia considerations for hyperaldosteronism?

A
  • Correct decreased K level and HTN (Spironolactone)
  • Assess cardiac/renal status
  • Avoid hyperventilation which may further decrease K
  • Monitors: A-line, swan
  • Adequate fluids w vasodilators or diuresis
  • Check acid/base and electrolytes frequently
  • exogenous cortisol 100 mg every 24 hours- for removal or manipulation of adrenal gland
21
Q

What is Addison’s disease?

A
  • Primary adrenal insufficiency
    • most commonly idiopathic or autoimmune
    • no symptoms until 90% of adrenal cortex has been destroyed
  • Deficiency of all adrenal cortex secretions:
    • mineralcorticoids
    • glucocorticoids
    • androgens
  • Other causes:
    • cancer
    • HIV
    • bacterial and fungal infections
22
Q

What are the signs and symptoms of Addison’s disease?

A
  • Chronic fatigue
  • muscle weakness
  • hypotension
  • wt loss
  • anorexia, N/V/D
  • increased BUN and hemoconcentration due to hypovolemia
  • hyponatremia
  • hyperkalemia
  • hypoglycemia
  • abdominal or back pain
  • hyperpigmentation in sun-exposed areas and the distal extremeties
    • b/c these hormones stimulate melanocyte production
23
Q

How is Addison’s disease diagnosed?

A
  • Baseline plasma cortisol level <20 mcg/dL ???
    • nml am cortisol = 10-20
    • nml 3-4 pm cortisol = 3-10
  • Cortisol level <20 mcg/dL after ACTH stimulation test
    • Cortisol levels are measured 30 to 60 minutes following administration of ACTH
    • Normal response is a plasma cortisol level >25 mcg/dL
  • Positive test yields a poor response to ACTH and is indicative of adrenal cortex impairment
24
Q

What is an addisonian crisis?

A
  • Addisonian crisis is triggered in a pt who is dependent on exogenous steroids and do not receive enough during stress
  • Stress leads to circulatory collapse
    • hypoglycemia
    • electrolyte imbalance
    • depressed mentation
  • Rx: IV cortisol 100 mg q 4-6 hour for 24 hours
    • D5 0.9 NS
    • hypovolemic- replace with colloid or whole blood
    • Inotropic support
25
Q

What are the steroid management recommendations for a pt with addison’s disease have a surgery?

A
  • Administer exogenous corticosteroids
    • If on a daily dose, have them take it day of surgery
  • 25 mg hydrocortisone for minor surgery
  • 100 mg bolus hydrocortisone followed with infusion at 10 mg/hr OR 100 mg q 6 hours
26
Q

How should you handle intraoperative hypotension for a patient with Addison’s disease?

A
  • Rule out usual causes of shock
  • measure CVP- administer fluids
  • Vasopressor- even if it doesnt have much effect before cortisol
  • administer Cortisol 100 mg IV
  • fluids
  • invasive monitoring
27
Q

What labs are you conserned about for a pt with Addison’s disease before and during the case?

A
  • Glucose- check pre-op and every hour
    • treat hypoglycemia with dextrose
  • check electrolytes frequently
    • concern for K levels- consider avoiding LR
28
Q

What anesthetic medications do you need to be careful with in a patient with Addison’s disease?

A
  • Avoid Etomidate!
  • Inhalation Agents can suppress adrenal function AND cause myocardial depression
    • might want to do balanced technique with opioids and propofol
  • Titrate muscle relaxants b/c pt already has muscle weakness
    • Use PNS!
29
Q

What causes hypoaldosteronism?

A
  • Congenital deficiency
  • Hyporeninemia- d/t long standing diabetes and renal failure and/or treatment with ACE inhibitors causing loss of angiotensin stimulation
  • Nonsteroidal inhibitors of prostaglandin synthesis
    • may inhibit renin release and exacerbate condition in presence of renal insufficiency
30
Q

What are the signs and symptoms of hypoaldosteronism?

A
  • Hyperkalemic acidosis
  • Severe hyperkalemia
  • hyponatremia
  • myocardial conduction defects
31
Q

How is hypoaldosteronism treated?

A
  • Mineralocorticoids- fludrocortisone
  • Liberal sodium intake