Lecture 10: Maintenance of Anesthesia (Exam 2) Flashcards

1
Q

What are some currently used inhalants

A
  • Isoflurane
  • Sevoflurane
  • Desflurane
  • N2O
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2
Q

What are the characteristics of a desirable inhalant

A
  • Less reactive
  • more potent
  • nonflammable (halogenated by adding Fl, Cl, or Br)
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3
Q

What properties determine the method of admin

A
  • Boiling point
  • Liquid density (specific gravity)
  • Vapor pressure
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4
Q

What properties help to determine kinetics in the px

A
  • Blood/gas partition coefficient
  • Oil/gas partition coefficient
    Both are used to determine the solubility of the gas
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5
Q

Define a gas

A

Agent that exists in gaseous form @ room temp & sea level pressure

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6
Q

What is an example of a gas

A

N2O

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7
Q

Define a vapor

A

Gaseous state of a substance that @ ambient temp & pressure is a liquid

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8
Q

What are some examples of a vapor

A
  • Isoflurane
  • Sevoflurane
  • Halothane
  • Desflurane
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9
Q

What gases laws are used to predict the behavior of a gas

A
  • Boyle’s law
  • Charle’s law
  • Gay-Lussac’s law
  • Dalton’s law of partial pressure
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10
Q

Define Boyle’s law

A

For a fixed amount of gas @ a constant temperature, the pressure exerted by the gas inversely proportional to its volume

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11
Q

Define Charle’s law

A

The volume of a fixed amount of gas is directly proportional to its absolute temperature when the pressure remains constant

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12
Q

Define Gay-Lussac’s law

A

The pressure of a gas increases as the temperature increases if the volume of the gas remains constnat

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13
Q

define Dalton’s law of partial pressure

A

The total pressure exerted by a mixture of non-reacting gases is equal to the sum of the partial pressures of each individual gas in the mixture

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14
Q

What is vaporization

A

Change in state from a liquid to a gas

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15
Q

At what point is the gas saturated

A

When the equilibrium is reached & no further loss of molecules to the gas phase occurs

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16
Q

Define the vapor pressure of an anesthetic

A

The measure of the ability to evaporate (enter the gas phase)

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17
Q

Saturated vapor pressure = what

A

Max concentration of molecules in vapor state

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18
Q

What is the saturated vapor pressure (SVP) dependent on

A

The temperature which is unique for each anesthetic agent

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19
Q

What happens when the temp of a liquid increases

A
  • More molecules escape liquid phase & enter the gas phase
  • Higher vapor pressure
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20
Q

What happens if the temp of a liquid decreases

A

Lower vapor pressure/concentration

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21
Q

T/F: The SVP of most anesthetics is safe for clinical use

A

False; it is not safe

22
Q

What are the two streams that gases are diverted into

A
  • By pass
  • Vaporizing chamber
23
Q

Describe modern vaporizers

A
  • Variable-bypass
  • Concentration-calibrated
  • Agent-specific
  • Temperature compensated
24
Q

What affects the speed of induction & recovery

A

The rate of uptake & distribution in the body that is effected by the gas in tissues and “in the blood” (AKA the blood/gas coefficient)

25
Q

Is a lower or higher blood/gas partition coefficient more desirable

A

Lower number

26
Q

What is the oil/gas partition coefficient

A

The solubility of the gas in a lipid (oil) correlates w/ the anesthetic potency

27
Q

(more/less) gas dissolves in solvent as temperature increases

28
Q

What increases alveolar delivery (Pa)

A
  • Increased inspired anesthetic concentration
  • Increased alveolar ventilation
29
Q

What increases inspired anesthetic concentration

A
  • Increased vaporization of agent
  • Increased vaporizer dial setting
  • Increased fresh gas flow
  • Decreased gas volume of patient breathing circuit
30
Q

What increases alveolar ventilation

A
  • Increased minute ventilation
  • Decreased dead space ventilation
31
Q

What factors decrease removal from alveoli

A
  • Decreased blood solubility of anesthetic
  • Decreased cardiac output
  • Decreased alveolar-venous anethetic gradient
32
Q

Define minimum alveolar concentration (MAC)

A
  • The min alveolar concentration of inhaled anesthetic @ 1 atmosphere that produces immobility in 50% of subjects exposed to a supramaximal noxious stimulus
  • Corresponds to ED50
33
Q

What is the relationship between potency & MAC

A

Inverse relationship (the higher the potency the lower the MAC)

34
Q

At what MAC is ED95 achieved (95% of px are anesthetized)

A

1.2 to 1.4

35
Q

What MAC is surgical anesthesia

36
Q

Fill out the MAC Values for these species:

37
Q

What factors can increase MAC

A
  • Hyperthermia
  • Drugs that cause CNS stimulation
  • Increased metabolic rate &/or stress (like hyperthyroidism)
38
Q

What Factors decrease MAC

A
  • Blood pressure < 50 mmHg
  • Hypothermia
  • Drugs that cause CNS depression
  • Smaller body weight/size
  • Age of animal
  • Hyponatremia
  • PaO2 < 40 mmHg or PaCO2 > 95 mmHg
  • Pregnancy
  • Disease state
39
Q

What factors do not effect MAC

A
  • Blood pressure > 50 mmHg
  • Anticholinergics
  • Duration of anesthesia
  • Gender
  • Abnorm potassium
  • Metabolic alkalosis or acidosis (paO2 > 40 mmHg or PaCO2 of 10-95 mmHg)
40
Q

Describe Isoflurane

A
  • Stable in storage (no preservative needed)
  • Low blood-gas solubility
  • More potent than sevoflurane
  • Fairly rapid induction & recovery (good muscle relaxation)
  • < 1% metabolized in body (mostly in the lungs)
  • Reasonable cost
  • Mask induction (noxious odor may lead to breath holding & bronchoconstriction)
  • Produces carbon monoxide when exposed to desiccated CO2 absorbent
  • Hypoventilation is common
41
Q

What causes hypotension when using Isoflurane

A

Due to vasodilation & decreased myocardial contractility

42
Q

Describe sevoflurane

A
  • Lower-blood gas partition coefficient than isoflurane (more rapid induction & recovery)
  • Lower potency than isoflurane
  • Similar cardio-respiratory depression to isoflurane
  • Good muscle relaxation (could trigger malignant hyperthermia
  • Mask induction has less odor & smoother induction
  • ~ 3% metabolized in the body (rest is eliminated via lungs)
  • Can be degraded by CO2 absorbents to produce compound A
43
Q

What are the pharmacodynamics of inhalant anesthetics

A
  • MOA: multiple cell receptors & ion channels; spinal cord & brain involved
  • Reversible immobilization results in all species even plants & protozoa
44
Q

What are the effect of inhalant anesthetics on the CNS, Resp, & CV system

A
  • CNS - decrease cerebral metabolic rate (oxygen consumption); either no change or an increase in cerebral blood flow; decrease in cerebral BF; decrease in cerebral perfusion pressure; increase in ICP
  • Resp - drug & species specific depression of ventilation causes increased CO2; bronchodilation; desflurane irritates the airway
  • CV - can decrease cardiac output & BP; arrhythmias associated w/ certain drugs may be exaggerated
45
Q

What is TIVA & PIVA

A

Anesthetic techniques utilizing IV infusion of one or more drugs to produce a suitable anesthetic state

46
Q

Why should TIVA be limited to 1 hour

A

B/c of prolonged recovery times associated w/ longer TIVA time

47
Q

T/F: Supplemental O2 is still provided during TIVA & PIVA

48
Q

What is an example of TIVA

A

“Triple drip” infusion of ketamine, xylazine, & guaifenesin to produce general anesthesia in a horse having a castration

49
Q

Give an example of PIVA

A

“MILK” + reduced isoflurane concentration for a dog having a TPLO

50
Q

Describe Guaifenesin (GG)

A
  • Centrally acting muscle relaxant w/ sedative props
  • Co-admin w/ other anesthetic agents for the IV induction &/or maintenance of anesthesia
  • Used in horses & ruminants
  • MOA is unclear but likely effects sites in the brain & spinal cord
  • No analgesic props
  • Wide therapeutic margin but OD can result in cardio-resp depression
  • Hepatic metabolism & renal excretion (more rapidly eliminated in female ponies)
  • Precipitates out of solution when stored below room temp & should be rewarmed before us
  • Prepared as a 5 to 15% solution in .9% NaCl or 5% dextrose