Exam 5 (drugs only) Flashcards

1
Q

4 IV anesthetics used for induction

  • name
  • which one has rapid induction/emergence?
  • good to use with hypotensive patients?
  • hallucinations?
  • inhibits cortisol?
  • alpha-2 adrenergic agonist?
  • analgesic effects
  • does NOT cause respiratory depression
A
  1. Propofol
    - rapid induction/emergence
  2. Ketamine
    - sympathomimetic and vagolytic
    - good for hypotensive patients
    - hallucinations
  3. Etomidate
    - inhibits cortisol
    - increased risk of death
  4. Dexmedetomidine
    - alpha-2 adrenergic agonist
    - analgesia
    - no respiratory depression so good for people with critical breathing
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2
Q

When is etomidate and good choice for IV anesthesia induction?

A

Severe cardiomyopathy - does not alter hemodynamics

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3
Q

Divide the 4 inhalation anesthetics in volatile vs gaseous

A

Volatile

  • isoflurane
  • desflurane
  • sevoflurane

Gaseous
-nitrous oxide

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4
Q

Desflurane vs sevoflurane

  • which one has lower solubility?
  • Faster increase in [alveolar]?
A

-desflurane has lower solubility and faster uptake

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5
Q

Side effects of nitrous oxide?

A
  • Bone marrow depression
  • Peripheral neuropathies w/ long term exposure
  • Diffusion into and expansion of closed gaseous spaces
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6
Q

Side effect of halothane?

A

• Hepatic metabolites could cause immune reaction
-Immune-mediated hepatitis
• No longer used

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7
Q

Isoflurane vs. desflurane vs. sevoflurane

  • which one is the least pungent volatile anesthetic?
  • bronchodilator?
  • weak coronary vasodilator?
  • low solubility -> rapid induction/emergence
  • tachycardia and HTN risk
A

• Isoflurane
– Weak coronary vasodilator

• Desflurane
– Low solubility – rapid induction and emergence
– Rapid increases in concentration can produce tachycardia and hypertension

• Sevoflurane
– Least pungent volatile anesthetic
– Bronchodilator

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8
Q

Name 3 drugs better than warfarin for txing anticoagulation in afib patients

A

Dabigatran
Apixaban
Rivaroxaban

-less intracranial bleeding and more effective

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9
Q

Carbamazepine (Tegretol)

  • indications
  • pharmacokinetics
  • adverse effects
A

 Indication: partial onset seizures only

 Pharmacokinetics: liver metabolized, moderate protein binding, many interactions

 Adverse effects: drowsiness, nausea, dizziness, visual disturbance. Rash 5%. Rare: aplastic anemia, severe rash, liver failure ~1/200,000

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10
Q

Phenytoin (Dilantin)

A

  Indications: partial and generalized onset

 Pharmacokinetics: non-linear with
clinically important saturation, highly
protein bound, many interactions

 Adverse effects: drowsiness, dizziness, unsteady gait, gum hypertrophy. Rash ~5%. Rare liver failure, aplastic anemia, severe rash

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11
Q

Lamotrigine (Lamictal)

A

 Indications: partial or generalized onset seizures

 Pharmacokinetics: liver metabolized, low protein binding, few interactions

 Adverse effects: sedation is uncommon, dizziness. Rash ~5%. Rare severe rash

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12
Q

Levetiracetam (Keppra)

A

 Indications: partial or generalized onset seizures

 Pharmacokinetics: not liver metabolized, no protein binding, no important interactions

 Adverse effects: drowsiness, irritability. Rash, liver failure, aplastic anemia not seen

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13
Q

Valproate (Depakote)

A

 Indications: partial or generalized onset seizures (drug of choice for most generalized onset seizures; be wary of teratogenesis)

 Pharmacokinetics: liver metabolized, highly protein bound, many interactions

 Adverse effects: drowsiness, weight gain, tremor, hair loss. Rash rare. Liver failure rare but more common in children.

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14
Q

What is the least sedating anticonvulsant?

A

Lamotrigine

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15
Q

Anticonvulsant with least drug ix and protein binding?

A

levetiracetam

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16
Q

Drugs of choice for partial seizure

A

carbamazepine, levetiracetam, lamotrigine

17
Q

Generalized onset seizure drug of choice

A

Valproate

18
Q

Drugs that induce metabolism of other drugs

A

Carbamazepine and phenytoin

19
Q

Drugs that inhibit metabolism of other drug

A

Valproate

20
Q

Drugs that are highly protein bound

A

Valproate and phenytoin

21
Q
  1. Therapeutic range for phenytoin
  2. Guidelines for dose increase
    If level < 7
    If level 7 - 11
    If level > 11
A
  1. 10 - 20 mcg/ml
  2. Guidelines
     if level < 7, increase daily dose 100 mg
     if level 7-11, increase daily dose 50-60 mg
     if level > 11, increase daily dose 25-30 mg
22
Q

Midazolam.

  • anesthesia stage
  • class
  • half life
  • elimination
A
  • premedication
  • benzodiazepine
  • 6 hours (short)
Elimination
-redistribution is most important
•  Conjugated to glucuronides
•  Eliminated by the kidney
•  Elimination slowed in the elderly, critically ill (especially in sepsis)
23
Q

2 opioids used for anesthesia premedication.

  • elimination
  • which has longer half life
A

Morphine

  • has active metabolite M6G
  • eliminated through urine
  • acidemia prolongs half life

Fentanyl
• Short duration of action after a single dose due to high lipid solubility & redistribution

• Elimination half-life is longer than that of morphine (2-16 h v. 1.5-6 h)