Exam 2: Inhalational Agents Flashcards

1
Q

Characteristics of ether:

A

Easy to make and administer
Potent
Not organotoxic
Highly flammable

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2
Q

Characteristics of chloroform:

A
Pleasant odor and nonflammable
Hepatotoxin 
Severe CV depressant
High incidence of death
Difficult to administer
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3
Q

First halogenated hydrocarbon anesthetic:

A

Fluroxene; withdrawn due to organ toxicity

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4
Q

Characteristics of methoxyflurane:

A

Nonexplosive, nonflammable halogenated methyl ethyl ether
Most potent of volatile agents: MAC 0.16
B/G coeff 12
Metabolites nephrotoxic

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5
Q

Areas affected to produce hypnosis/sedation and immobility with GA:

A

Hypnosis/sedation: cortex, hippocampus

Immobility: spinal cord

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6
Q

Meyer-Overton theory:

A

Absorption of anesthetic molecules expands hydrophobic region of lipid bilayer, distorts membrane, alters membrane function

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7
Q

Fluidization theory:

A

Binding of anesthetic molecules to lipid bilayer modifies membrane structures, alters conductance or induces conformational change in channels

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8
Q

Lipid theory:

A

Demonstrates a correlation between anesthetic potency and lipid solubility

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9
Q

Protein/lipid interface theory:

A

Anesthetics displace lipids necessary for protein function

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10
Q

Protein receptor theory:

A

Anesthetics occupy protein receptor sites and block ionic conductance during membrane excitation

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11
Q

Guedel’s four stages of anesthesia:

A
  1. Amnesia/analgesia
  2. Delirium/excitement
  3. Surgical anesthesia (4 planes)
  4. Overdose
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12
Q

Pupils/resp pattern/pulse/BP in stage I:

A

Pupils normal and reactive
Respirations regular, small?
Pulse irregular
BP normal

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13
Q

Pupils/resp pattern/pulse/BP in stage II:

A

Pupils dilated, overreactive to light
Respirations irregular
Pulse irregular and fast
BP high

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14
Q

Pupils/resp pattern/pulse/BP in stage III:

A

Pupils normal, unresponsive
Respirations fast, small
Pulse steady and slow
BP normal

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15
Q

Pupils/resp pattern/pulse/BP in stage IV:

A

Pupils dilated and unresponsive
Respirations minimal and irregular
Pulse weak and thready
BP low

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16
Q

Only inorganic anesthetic gas:

A

Nitrous oxide

17
Q

N2O most commonly used in combination with:

A

Induction agent, NMB, opioids, and/or VA

18
Q

C2HClBrF3 is:

A

Halothane

19
Q

C2HOClF5 is:

A

Isoflurane

20
Q

C3H2OF6 is:

A

Desflurane

21
Q

C4H2OF7 is:

A

Sevoflurane (with SEVen F’s)

22
Q

Lower weight halogens add:

A

Less potency than higher weight ones

23
Q

Chloride substitution effects on VA:

A

More stability, but myocardial depression

24
Q

Fluoride substitution effects on VA:

A

Reduction in flammability, but also potential for renal damage

25
Q

Factors that do not affect MAC:

A
Species
Sex
Gender
Duration of anesthesia
Acid-base disturbances
PaO2
26
Q

Factors that decrease MAC:

A
↑ age
Hypothermia
Hyponatremia
Hypotension
Hypoxemia
Anemia
Pregnancy
Drugs (benzos, opioids, ketamine, α2 agonists, LAs)
ETOH (acutely)
27
Q

Factors that increase MAC:

A

Hyperthermia
CNS stimulants
Less than 1 y/o

28
Q

% of MAC that will make 95% of patients immobile to stimulus:

A

1.3 * MAC

29
Q

MAC awake is:

A

The concentration that permits voluntary response

30
Q

MAC awake of des/sevo/iso:

A

1/3 MAC

31
Q

MAC awake of halothane:

A

1/2 MAC

32
Q

MAC awake of N2O:

A

60% of MAC

33
Q

Mechanism by which halothane potentiates arrythmias:

A

↓ SA node depolarization; prone to junctional rhythms

↓ AV node, purkinje conduction

34
Q

Epi max doses when using halothane:

A

10ml 1:100k or 20ml 1:200k within 10 min

30ml 1:100k or 60ml 1:200k within an hour

35
Q

Presentation of VA-associated hepatitis:

A

Fever, anorexia, nausea, chills, myalgias, rash, fever, arthralgia, and eosinophilia –> jaundice 3-6 days later

36
Q

Risk factors for VA-associated hepatitis:

A
Prior exposure #1
Age > 40
Obesity
Female gender
Mexican ethnicity
Genetic susceptibility
Multiple brief procedures in short amt of time
Enzyme induction
37
Q

Enzyme that metabolizes VAs:

A

CYP 450 2E1

38
Q

Pathogenesis of VA-associated hepatitis:

A

2E1 oxidizes VAs to yield reactive intermediates that bind covalently to hepatocellular macromolecules, triggering immunologic response –> massive hepatic necrosis