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46 Cards in this Set
- Front
- Back
What are symptoms of addisons? |
1. hypotension,
2. fluid depletion, 3. hyperkalemia, 4. hyponatremia |
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Compare potency of steroids?
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cortisol = solucortef/hydrocortisone: 1
prednisone: 4; solumedrol/methylprednisolone): 5; dexamethasone: 25 |
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What are indications for an adrenalectomy?
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1. adrenal adenoma or carcinoma,
2. pheochromocytoma, 3. palliation for metastatic cancer |
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What is the dexamethasone suppression test?
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dexamethasone is given at bedtime, cortisol is checked in the AM with normal being <5mcg/100mL
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How much cortisol is secreted by the adrenals normally? under stress?
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normal-115-185mg/day
stress-200-500mg/day |
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Where are catecholamines produced? What stores catecholamines?
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catecholamines are produced and released by the adrenal medulla in response to stress
-chromaffin tissues located in the adrenal medulla |
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Where is the majority of the chromaffin granules that store norepi and epi located?
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70% adrenal medulla,
30% sympathetic chain - organ of Zuckerkandl |
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How do catecholamines affect glucose levels?
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catecholamines are hyperglycemic, glycogenolytic, lipolytic
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What are the cardinal signs of pheochromocytoma?
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1. paroxysmal htn,
2. orthostatic hypotension and 3. hypovolemia, 4. palpitations, 5. headache, 6. sweating, 7. N/V |
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How do you diagnose pheochromocytoma?
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1. 24 hour urine for catecholamines - VMA, metanephrines,
2. also serial serum catecholamines, 3. if 24 hours urine is positive do CT scan |
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What is the rozen criteria for surgical readiness for pheochromocytoma?
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blood pressure control:
1. no in hospital blood pressure >165/90, 2. no orthostatic BP<80/40, EKG criteria: 1. no ST changes for 2 weeks, 2, <1 PVCs in 5 min |
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What preop preparation should you do in patients with pheochromocytoma?
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correction of hypovolemia and HTN
-management includes fluids, phenoxybenzamine, and propranolol - admin alpha blocker before beta blocker |
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How long does stability of htn take after starting a patient with pheochromocytoma on both alpha and beta blockers?
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2 weeks
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What are the advantages of selective alpha 1 antagonists versus nonselective? What are examples of each?
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-selective alpha 1 blockers: doxazosin, terazosin, prazosin, limit the reflex tachycardia thus eliminating the need for preop beta blockers;
-nonselective: phentolamine, phenoxybenzaprine |
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What alpha blockers used for pheochromocytoma are short acting and which ones are long acting?
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short acting: terazosin, prazosin, phentolamine;
long acting: doxazosin, phenoxybenzaprine |
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What volatile anesthetic should you avoid in patients with pheochromocytoma?
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halothane, sensitizes the heart to catecholamines
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What are the typical intraop problems in patients with pheochromocytoma getting the adrenal gland removed?
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htn before vein is ligated,
hypotension afterwards |
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How long does it take for the blood pressure to normalize after an adrenalectomy in patients with pheochromocytoma?
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3 days (75% normotensive by this time)
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Why do you give patients with DKA potassium even if their serum K is normal?
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acidosis masks the presence of total body potassium depletion
-these pts can be profoundly depleted of K yet their serum levels are not often markedly low bc of the acidosis |
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What nerve is often involved in peripheral neuropathy in diabetics?
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lateral femoral cutaneous
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What are symptoms of hypoglycemia in the OR?
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htn, tachycardia, sweating, and cold-clammy skin
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How should you treat hypoglycemia in the OR?
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D5NS (50g/L)
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What should you consider in a patient with hypoglycemia?
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hepatoma
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What factors increase insulin requirement
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1. stress
2. steroids, 3. thyroid drugs, 4. oral contraceptives, 5. thiazides, 6. high carb diet, 7. infection, |
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What factors decrease insulin requirement?
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1. exercise,
2. aspirin, 3. alcohol |
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What are the main manifestations of ketoacidosis?
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1. acidosis,
2. hyperglycemia, 3. glucosuria, 4. dehydration |
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When should you start giving potassium when treating DKA?
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when Urine output is established (>1 cc/kg/hr)
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When should you give bicarb to DKA patients and why?
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pH<7.1;
- myocardial depression can be severe in diabetic patients if pH<7.1 |
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Why do type 1 DM patients tend to develop ketosis during the stress of surgery?
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catelcholamines, cortisol, ACTH, and glucagon all increase under the stress of anesthesia and all of these increase plasma glucose
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what are neonatal problems associated with maternal diabetes?
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1. respiratory distress syndrome - due to inhibitory effects of chronic hyperinsulinemia on surfactant production
2. cardiomegaly, 3. congenital abnormalities are more frequent; 4. hypoglycemia 5. macrosomia - due to chronic hyperinsulinemia and increased glycogen synthesis, lipogenesis, and protein synthesis |
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What are the components involved in the development of hyperosmolar hyperglycemic non-ketotic coma?
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1. insulin deficiency - liver insulin levels are high enough to permit the metabolism of free fatty acids so you don't see DKA
2. renal deficiency-insufficiency - impairs the ability to excrete glucose and leads to hyperosmolarity, 3. thirst deficiency |
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What are lab findings in hyperosmolar hyperglycemic non-ketotic coma?
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1. glucose >600,
2. osmolality>300-350, 3. pH>7.3, 4. ketones in serum or urine are minimal or absent |
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How do you treat patients with hyperosmolar hyperglycemic non-ketotic coma?
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1. hydrate - usually 6-8L dehydrated
2. insulin - don't treat too aggressively bc you don't want a quick shift of free water into the brain as hyperosmolarity decreases 3. when urine output is reestablished potassium should be given |
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What hormones increase with the stress of anesthesia and surgery?
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1. ACTH,
2. ADH, 3. aldosterone, 4. catecholamines, 5. cortisol, 6. glucagon, 7. thyroid hormone |
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Where in the hypothalamus is ADH and oxytocin produced?
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- oxytocin - paraventricular nuclei
- ADH - supraoptic nuclei |
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What type of change in serum osmolality causes a release of ADH?
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An increase in plasma osmolality of only 10 mosm (from normal of 285 to 295)
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What are factors associated with SIADH?
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1. postop period up to 96 hrs
2. PPV 3. endocrine disorders - pituitary injury, adrenal cortical insufficiency 4. carcinoma of the lung 5. infection, hemorrhage, trauma 6. drugs - chloropropamide, opioids, diuretics, antimetabolites |
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How does lithium effect ADH?
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it inhibits the action of ADH on the collecting duct of the renal tubule -> diabetes insipidus
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What is the function of PTH?
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maintains extracellular Ca concentration by causing bone reabsorption, renal ca reabsorption, and increasing intestinal absorption
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When does primary hyperparathyroidism occur most commonly?
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in women over age 60 and is most commonly secondary to an adenoma
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What is the nadir of Ca?
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3-7 days
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What are the mechanisms responsible for hypocalcemia?
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1. hypoparathyroidism
2. hungry bone syndrome - results in rapid remineralization |
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3 classes of hypothyroidism
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1. primary hypothyroidism - involves thyroid gland destruction from subtotal thyroidectomy, radioactive iodine therapy, neck irradiation, or chronic inflammation (Hashimotos thyroiditis)
2. Secondary hypothyroidism - hypothalmic or anterior pituitary dysfunction 3. thyroid gland hormone deficiency |
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What is hypothyroidism called in the neonate? What is the result?
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Cretinism - mental and physical retardation
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What are the effects of hypothyroidism on the circulatory system?
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1. decreased HR
2. decreased stroke volume 3. increased SVR 4. 40% reduction in cardiac output 5. peripheral vasoconstriction - accounts for the cold dry skin |
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What characterizes myxedema coma? |
It is hypothyroidism in severe form 1. CHF 2. hypoventilation - myxedematious infiltration of muscles of respiration 3. hypothermia - due to diminished response to the calorigenic effects of catecholamines 4. depressed consciousness |