Lecture 5 - Volatile Anesthetics Flashcards

1
Q

what are the inhaled anesthetics?

which is a gas at room temp? which are liquids?

What can they reliably be used for?

what desired effect is not achieved ?

A

liquids at room temperature – Sevoflurane, Desflurane, Isoflurane

Gas at room temperature – N2O

Reliable for: Unconsciousness, Amnesia, Immobility

Disadvantage:
They are not analgesics
Patients body will still respond to the pain (eg tachycardia and HTN)

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2
Q

what is monitored when the patient is under anesthesia ?

which levels allow for monitoring concentrations in the brain?

A
Vital Signs: ECG, HR, BP, O2 Sats, 
	Spontaneous Respiration -- if the patient is breathing on their own 
		(tachypnic would indicate  pain) 
	Movement in response to surgery
	Levels of Exhaled gases -- 
		O2, CO2, N2O, volatile anesthetics
		Correlate with levels in the brain
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3
Q

what are the mechanisms behind:

  • Immobility
  • Amnesia
  • CNS depression -
A

Poorly understood overall
Immobility – acting on the spinal cord
Amnesia - hippocampus, amygdala, cerebral cortex
CNS Depression:
Enhance inhibitory NTs – GABA and Glycine
Block Excitatory – NMDA

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4
Q

what is Minimum Alveolar Concentration (MAC)

what is the goal MAC for surgical anesthesia ?

which of the inhaled anesthetic agents cannot achieve this goal on its own?

A

Definition: Concentration of anesthetic required to suppress movement to surgical stimulus in 50% of patients

Goal MAC = 1 - surgical anesthesia

N2O Max MAC = .7; must be used in combination with other drugs

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5
Q

what are 5 important characteristics to know about inhaled anesthetics

A

The dose needed to achieve MAC = 1
(lowest to highest – Isoflurane < Sevoflurane < Desflurane < N2O)

Blood Gas Partition Coefficient (solubility of the gas in the blood) (most soluble to least – Iso > Sevo > N20 > Des)

Blood brain coefficienct (measure of brain solubility)
(Sevo, Iso, Des, N2O

Oil Gas partition coefficient – lipid solubility
(Iso> Sevo> Des> N20)

Vapor pressure

% Metabolized – clinically insignificant

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6
Q

Isoflurane – charactersitic profile

whats the significance of its solubility?

A

the most lipid and blood soluble — Longer emergence;
second most brain soluble —
Least dose needed for MAC = 1 — most potent
○ Not very expensive — used a lot

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7
Q

Sevoflurane characteristic profile

A
  • Medium solubility- good for longer cases and obese patients
    * Medium potency
    * Not very expensive

Used for inhaled induction in pediatrics - (for kids woh hate needles; can knock them out first)

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8
Q

Desflurane characteristic profile

A
  • Desflurane:
    * Least soluble- good for longer cases and obese patients
    * Least potent- highest dose needed to achieve 1 MAC, so have to use a lot of it

Most expensive compound — therefore not used that often

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9
Q

N2O Characteristic profile

A

• N2O: Not used much
○ Increases n/v
○ Not good for surgeries on spaces/organs that contain air (bowel, lungs ear) → will cause distension because diffuses faster into air filled space than nitrogen can leave
○ Cannot achieve 1 MAC alone, so have to use in combination with another agent
○ In pediatrics, can use for inhalation induction along with sevoflurane

Not very expensive

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10
Q

Pharmacokinetics –

equilibriation between what three partial pressures?

how long does it take P(brain) to equilibriate wiht PA

how is Pbr measured?

A
  • PA ↔ Pa ↔ Pbr
    * Alveolar arterial brain partial pressure
    * Uptake from alveoli into systemic circulation
    * Uptake from circulation into brain- site of action of anesthetics
    * Redistribution of anesthetic throughout body

6-12 minutes for Pbr to equilibriate with PA

	• P alveolar mirrors Pbr --  can't measure the Pbr directly 
		§ P-alveolar -- also measure of rate of induction and recovery from anesthesia; also a measure of potency
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11
Q

Factors Determining PA:

A

Solubility – want to be less solubule in blood than it is in lipid and brain (N2O<iso)

Inspired anesthetic partial pressure (PI)
Alveolar Ventilation – Increased ventilation accerlates induction by more rapidly increasing PA

Cardiac Output – Low CO = faster induction; high CO = harder to load up quickly

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12
Q

Emergence From Anesthesia —
what happens when the gas is turned off?
at what MAC does a patient awake?

A

PA=zero
Partial pressure gradient is reversed
• Stored anesthetic in tissues diffuses down its concentration gradient into the blood and is exhaled

wake up; MAC = .2-.3

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13
Q

Factors for Emergence –

A
  • Solubility of agent
    * Less soluble agents will allow faster emergence
    * Depends on alveolar ventilation
    * More ventilation allows faster emergence
    * Depends on cardiac output
    * Lower CO (slower moving train) allows faster emergence; can offload all of the gas into the Alveoli, which then gets exhaled and the patient emerges faster; but this plays a very small role

Tissue Concentration:

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14
Q

Inhaled anesthetics –
effects on the Circulatory system (MAP, HR, other)
which can prolong QT interval?

A

MAP –
VA – the volatile anesthetics cause vasodilation and decrease MAP and SVR
N20 = no change

HR – Small increase (Iso>des); Small Decreased (N2O and sevo)

VAs are cardioprotective (ischemic preconditioning)

VA(esp Sevo) may prolong QT

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15
Q

Inhaled anesthetics –
Respiratory Effects:

which drugs are best for inhalation induction? why?

why must patients be intubated on these drugs?

A

Increase respiratory rate and decrease TV
Decrease in FRC –
Increase in dead space
Bronchodilation

Inhalation induction using sevo and N2O because are nonpungent

Depression of pharyngeal and laryngeal reflexes —- and must intubate

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16
Q

Inhaled anesthetics: CNS effects

which has some mild analgesic properties?

A

All cause cerebral vasodilation
Increased cerebral blood flow (CBF)
Increased intracranial pressure (ICP)

Uncoupling effect – paradoxically increased CBF but decrased Cerebral metabolic rate
therefore neuroprotective

analgesic: N2O has some mild analgesic properties

17
Q

Inhaled anesthetics

effects on Neuromuscular system; Renal system; hepatic system

A

Neuromuscular effects:
• VA cause dose-related skeletal muscle relaxation – decreased tone
• VA enhance activity of all paralytics –

Decreased renal blood flow:
• Decreased GFR, decreased urine output; usually clinically insignificant mild transient decreases

Decreased hepatic blood flow — most are metabolized in the liver, but still insignificant