Endocrine - Adrenal Flashcards

1
Q

Adrenal Gland

A

Cortex 80-90%

Medulla 10-20%

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2
Q

Adrenal Gland Function

A
  • Blood glucose regulation
  • Protein turnover
  • Fat metabolism
  • Na+/K+/Ca2+ balance
  • CV tone maintenance
  • Modulates tissue response to injury or infection
  • Stress response*
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3
Q

Adrenal Cortex

A

Zona glomerulosa - aldosterone (mineralocorticoid)
Zone fasciculata - cortisol (glucocorticoid)
Zona reticularis - androgenic

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4
Q

Adrenal Medulla

A

Epinephrine 80%

Norepinephrine 20%

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5
Q

Cushing’s Syndrome

A

Any excessive cortisol secretion
Exogenous steroids
ACTH dependent or independent

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6
Q

Cushing’s Disease

A

Inappropriate ACTH from anterior pituitary secretion
1° pituitary tumor
2° adrenal tumor

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7
Q

ACTH Dependent

A

Pituitary corticotrophy tumors (microadenomas)
Non-endocrine tumors - lung, kidney, or pancreas
Ectopic corticotrophin syndrome

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8
Q

ACTH Independent

A

Benign or malignant adrenocortical tumors

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9
Q

Cushing’s S/S

A
Sudden weight gain (central)
Facial fat "moon face"
Electrolyte abnormalities
Systemic HTN
Glucose intolerance
Menstrual irregularities
Decreased libido
Skeletal muscle wasting
Depression & insomnia
Osteoporosis
Hypercoagulable
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10
Q

Cushing’s Diagnosis

A

Plasma & urine cortisol levels
CRH stimulation test
Dexamethasone suppression test
Inferior petrosal sinus sampling

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11
Q

Cushing’s Treatment

A

Surgical
- Transsphenoidal microadenectomy
- Adrenalectomy
Irradiation

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12
Q

Cushing’s

Anesthetic Management

A

Preop evaluation - HTN, intravascular volume, electrolytes, hypokalemia metabolic alkalosis, CHF, glucose control
Positioning - osteoporosis/osteomalacia vertebral compression fractures
Skeletal muscle weakness - ↓muscle relaxants requirements (maintain 1 twitch)
Cortisol - 100mg IV glucocorticoid intraop
Blood loss - type & screen, CVP, A-line
Anesthetic agents - depress adrenal response to stress & ACTH

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13
Q

Cushing’s

Anesthetic Complications

A
Transsphenoidal microadenomectomy
- VAE
- Transient DI
- Meningitis
Adrenalectomy
- Laparoscopic vs. open
- Pulmonary complications
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14
Q

Conn’s Syndrome

A

Excessive aldosterone

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15
Q

Primary Hyperaldosteronism

A

Excessive aldosterone secretion from functional tumor

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16
Q

Secondary Hyperaldosteronism

A

↑circulating serum renin stimulates aldosterone release (renovascular HTN)

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17
Q

Conn’s S/S

A

Non-specific
Asymptomatic
Systemic HTN (headache, diastolic BP 100-125mmHg) reflects aldosterone induced Na+ retention ↑fluid retention
Hypokalemia - skeletal muscle cramps, weakness, metabolic acidosis

18
Q

Hyperaldosteronism

Anesthetic Considerations

A
Correct ↓K+
Avoid hyperventilation → hypokalemia
HTN (A-line)
Assess cardiac/renal status
Fluids w/ vasodilators & diuresis
Monitor acid-base balance
Replace exogenous cortisol 100mg/day
19
Q

Addison’s Disease

A

1° adrenal insufficiency
- Most common cause idiopathic/autoimmune
- Asymptomatic until 90% adrenal cortex destroyed
Deficiency all adrenal cortex secretions - mineralocorticoids, glucocorticoids, & androgens

20
Q

Addison’s S/S

A
Chronic fatigue
Muscle weakness
Hypotension
Weight loss
Anorexia
Nausea/vomiting
Diarrhea
↑BUN
Hyponatremia
Hyperkalemia
Hypoglycemia
Abdominal or back pain
Hyperpigmentation
21
Q

Addison’s Diagnosis

A

Baseline plasma cortisol level <20mcg/dL
Cortisol level <20mcg/dL after ACTH stim test
- Normal response >25mcg/dL
- Positive test indicates adrenal cortex impairment

22
Q

Addisonian Crisis

A
Steroid-dependent who do not receive ↑dose during stress
Stress → circulatory collapse
- Hypoglycemia
- Electrolyte imbalance
- Depressed mentation
100mg IV cortisol Q4-6H
Inotropic support
23
Q

Addison’s

Anesthetic Considerations

A
Administer exogenous corticosteroids
Continue steroid dose DOS
Intraop hypotension
- Measure CVP
- Vasopressor
- Fluids
- Cortisol 100mg IV
Measure blood glucose
Monitor electrolytes (avoid LR)
Avoid Etomidate
Inhalational agents sensitive to drug-induced myocardial depression
Titrate muscle relaxants d/t skeletal muscle weakness
24
Q

Minor Surgery Cortisol

A

25mg hydrocortisone

25
Major Surgery Cortisol
100mg bolus followed by infusion at 10mg/hr OR 100mg Q6H
26
Hypoaldosteronism
Congenital aldosterone deficiency Hyporeninemia loss angiotensin stim Non-steroidal inhibit prostaglandin synthesis - inhibit renin release & exacerbate condition in renal insufficiency
27
Hypoaldosteronism S/S
Hyperkalemic acidosis Severe hyperkalemia Hyponatremia Myocardial conduction defects
28
Hypoaldosteronism Treatment
Mineralocorticoid-fludrocortisone | Liberal Na+ intake
29
Pheochromocytoma
Catecholamine-secreting tumor Originates in adrenal medulla & related tissues Most common young to mid-adult life
30
Pheochromocytoma S/S
``` 1° - HTN continuous or paroxysmal - Headache - Diaphoresis/pallor - Palpitations or tachycardia Associated S/S - Orthostatic hypotension d/t volume depletion - Anxiety - Tremors - Chest pain - Epigastric pain - Flushing - Painless hematuria ```
31
Pheochromocytoma | Duration & Frequency
1hr or less | Daily to once every few months
32
Pheochromocytoma Diagnosis
``` Urine tests Plasma levels* NE/Epi breakdown products - Normetanephrine >400 - Metanephrine >220 CT/MRI ```
33
Pheochromocytoma Treatment
``` Surgical excision α blockade - Phenoxybenzamine α 1&2 - Prazosin selective α1 Restore intravascular volume ↓Hct Insulin release Persistent tachycardia β blockade (Esmolol) DO NOT ADMINISTER NON-SELECTIVE β BLOCKADE W/O α BLOCKADE (unable to maintain CO) ```
34
Pheochromocytoma | Preop Considerations
Optimize the patient ↑SVR → myocardial ischemia, ventricular hypertrophy, CHF, cardiomyopathy Cerebral hemorrhage history Hyperglycemia ↓circulating insulin w/ ↑glycogenolysis Blood pressure <165/90 48hours prior to surgery Standing BP >80/45 EKG w/o ST or T wave changes <1 PVC Q5min
35
Pheochromocytoma | Anesthetic Considerations
``` Communication w/ surgeon Continue adrenergic blockade Fluid management: - Pre-hydrate hypovolemia - Falsely ↑Hct - Type & cross - Renal function - Fluid replacement plan Benzodiazepine & opioid pre-medication A-line ```
36
Pheochromocytoma | Induction & Laryngoscopy
``` Lidocaine 1-2mg/kg Opioid (no Morphine d/t histamine & catecholamine release) to blunt SNS response - Sufentanil 0.5-1mcg/kg - Fentanyl 3-5mcg/kg Propofol 3mg/kg Nitroprusside 1-2mcg/kg Phentolamine α blocker Esmolol β blocker Avoid drugs that release histamine ```
37
Pheochromocytoma | Intraop Considerations
MAC 1.5-2 Combined general anesthetic w/ continuous lumbar epidural Muscle relaxant - Vecuronium or Rocuronium Surgical ligation tumor venous drainage ↓catechols → prepare for hypotension - DC antihypertensives - ↓volatile inhalational agent - Volume 1st - Administer pressors (phenylephrine or norepinephrine) NE infusion until vasculature adapts to ↓α stim
38
Pheochromocytoma | Cardiovascular Control
``` Nitroprusside preferred Phentolamine - tachyphylaxis, tachycardia, & longer duration Magnesium sulfate Ca2+ channel blockers Esmolol preferred Labetalol Metoprolol ```
39
Pheochromocytoma | AVOID
Histamine releasers (Morphine or Atracurium) Halothane - sensitizes myocardium → epinephrine Succinylcholine fasciculations → catechol release from tumor Avoid ↑HR (Pancuronium or Atropine) Metoclopramide → catechol release
40
Pheochromocytoma | Postop Considerations
Adequate analgesia - PCA & opioids 50% patients remain HTN - Elevated catecholamine levels 10 days postop - Continue antihypertensive therapy Early extubation (young, no lung involvement) Hypoglycemia d/t excess insulin release & ineffective lipolysis & glycogenolysis Steroid supplementation d/t adrenal manipulation Postop HTN > 10 days - Occult tumors (repeat surgery) - Volume overload - Continue monitoring