Endocrine and Metabolic Emergencies Flashcards

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1
Q

Most common cause of hospitalization, mortality, and morbidity in children with established type 1 DM

A

DKA

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2
Q

Whyis there hypotension with DKA if fluid is being pulled into the vascular with the osmotic load?

A

Initially there’s increase in volume of vasculature but as glucose spills into urine it carries H20 with it

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3
Q

What is your first step in the management of a patient with DKA even prior to receiving lab results?

A

aggressive fluid therapy (NS)

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4
Q

After initial resuscitation of patient with DKA, what should you alternate NS administration with?

A

0.45% NS

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5
Q

What is the ideal way to administer insulin therapy when treating DKA?

A

continuous intravenous infusion of small doses of regular insulin through an infusion pump (0.1 units/kg per hour)

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6
Q

What electrolyte needs replacement therapy with DKA due to combination of acidosis, osmotic diuresis, and vomiting?

A

potassium

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7
Q

potentially the most life-threatening electrolyte derangement during treatment of DKA if treatment causes changes to occur too rapidly

A

severe hypokalemia

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8
Q

When should you consider phosphate replacement during the management of DKA?

A

Should be withheld unless concentration less than 1 mg/dL

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9
Q

Occurs in patients with poorly controlled or undiagnosed type II DM. Includes Severe hyperglycemia, hyperosmolality, RELATIVE LACK of ketonemia

A

hyperosmolar hyperglycemic state (also referred to as nonketotic hyperosmolar state)

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10
Q

A patient’s lab results come back as follows: serum glucose > 600mg/dL, plasma osmolality > 315 mOsm/kg, bicarb > 15, and pH > 7.3. Serum ketones are negative to mildly positive. What is your suspected diagnosis?

A

hyperosmolar hyperglycemic state (also referred to as nonketotic hyperosmolar state)

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11
Q

Why are mortality rates higher with hypersomolar hyperglycemic state than DKA?

A

usually occurs in older diabetic patients who are unable to compensate for fluid losses

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12
Q

Often precipitates hyperosmolar hyperglycemic state

A

acute illness such as pneumonia or UTI

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13
Q

Symptoms include: HA, drowsiness, mental dullness, amnesia, seizures, coma when due to hypoglycemia

A

neuroglyopenic

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14
Q

At what glucose levels do symptoms of hypoglycemia become noticeable?

A

54 mg/dL

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15
Q

Difficulty with recognizing symptoms during the stage where hypoglycemia can easily be managed

A

hypoglycemia unawareness

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16
Q

What is the preferred treatment fo hypoglycemia on an outpatient basis?

A

15-20g of glucose

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17
Q

When should you re-check glucose levels in hypoglycemic patient after they’ve ingested 15-20g of glucose?

A

after 15 minutes

18
Q

should be prescribed for all patients at significant risk for severe hypoglycemia

A

glucagon

19
Q

What is the initial management of hypoglycemia in the ED?

A

D50W in adults followed by infusion of D10W at a rate to maintain serum glucose above 100 mg/dL

20
Q

How often should you check glucose levels in ED hypoglycemic patient?

A

q 30 minutes for 2 hours

21
Q

can be given after initial glocuse therapy has been initiated in the patient with sulfonylurea ingestion

A

Octreotide (somatostatin analogue)

22
Q

What are other underlying etiologies of hypoglycemia if patient is not a diabetic?

A

ETOH use and sepsis

23
Q

Failure of adrenal glands to produce essential BASAL secretion of steroids. Insidious wasting disease

A

adrenal insufficiency

24
Q

Failure to RESPOND to the increased demands caused by stress or SUDDEN INABILITY to secrete essential steroids. Life-threatening condition

A

adrenal crisis

25
Q

Adrenal insufficiency that results from destruction or dysfunction of the adrenal cortex

A

Addison’s

26
Q

Results from inadequate stimulation of adrenal cortex by ACTH (***By far the most common cause is chronic administration of exogenous steroids!)

A

Secondary adrenal insufficiency

27
Q

what are the effects of decreased cortisol from adrenal insufficiency?

A

decreased blood glucose

28
Q

what are the effects of decreased aldosterone from adrenal insufficiency?

A

hyperkalemia, hyponaturemia

29
Q

How can you tell if severe hypotension is due to adrenal crisis?

A

resistant to catecholamine and IV fluid administration. Need to replace cortisol

30
Q

Why might an adrenal crisis be confused with an AAA?

A

both present with marked hypotension and abdominal flank pain

31
Q

What is the primary treament of an adrenal crisis?

A

IV glucocorticoids

32
Q

Surgically correctable form of HTN. Usually located in adrenal medulla. Presents with palpitations, sweating, headaches, fainting spells, and hypertensive emergencies

A

pheochromocytoma

33
Q

What is the rule of 90s that goes with a pheo?

A

90% of the time they arise in adrenal medulla, is unilateral, not malignant, occurs in adults

34
Q

How is the diagnosis of a pheo made?

A

Demonstrating elevated urinary excretion of catecholamines or their metabolites DURING a period of hypertension

35
Q

What should be initiated in a patient with a pheo who is going to undergo surgery?

A

initiate an alpha blockage first followed by beta blocker 3-4 days after

36
Q

Occurs in individuals with long-standing preexisting hypothyroidism presents with life-threatening decompensation

A

Myxedema Coma

37
Q

Major difference in vital signs with myxedema coma compared to other life-threatening endocrine disorders

A

bradycardia

38
Q

What is pharmacological treatment for a myxedema coma?

A

IV levothyroxine followed by reduced daily dose until orals tolerated. administration of glucocorticoid

39
Q

What is the most common cardiographic finding of hyperthryroidism?

A

a. fib

40
Q

What are the two primary symptoms that differentiate thyriod storm from hyperthyroidism?

A

fever and CNS dysfunction

41
Q

What is the pharmacological treatment of a thyroid storm?

A

beta blockers, PTU/Methimazole, iodine