17 – Inhalation Anesthesia Application Flashcards

1
Q

Endotracheal intubation: advantages

A
  • Airway remains protected with seal
  • Good seal=more stable anesthesia
  • Can ventilate lungs
  • Minimal workspace pollution
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2
Q

Endotracheal intubation: disadvantages

A
  • Technical failures
  • Can become obstructed if not clean or very small diameter airways
  • Laryngeal trauma
  • Mucosal irritation or pressure necrosis
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3
Q

Principals of intubation

A
  • SURGICAL plane of anesthesia removes laryngeal reflexes
  • Risk of aspiration=high
  • Intubation at light depths of anesthesia promote regurgitation
  • Always secure tube in place
  • Use gentle technique
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4
Q

Always check placement of intubation tube: use at least 3 methods

A
  • Water vapor in tube (run under cold water first)
  • Air flow: test with hair
  • Palpate neck
  • Auscultate both sides of thorax with IPPV (can be tough with larger dogs)
  • Capnogram
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5
Q

IPPV

A
  • Intermittent positive pressure ventilation
  • Ex. pushing on chest and listening for sounds on both sides
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6
Q

Cuffed endotracheal tube (ETT)

A
  • Ensures you have a good seal
  • Bevel allows it to slip between vocal cords
  • *do NOT use in birds (have complete tracheal rings, unable to expand=get more tracheal necrosis)
  • Murphy eye: safety mechanism to allow air flow still if end gets twisted or squished
  • LUBE: help create the seal (not for ease of entry)
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7
Q

Cuffed ETT and lube

A
  • Don’t use too much as it will ‘plug’ the Murphy eye
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8
Q

Tube types and apparatus

A
  • Cuffed and non-cuffed
  • Red rubber and clear tubes
  • High volume/low pressure cuff or opposite
  • Select largest diameter and correct length
  • Always check tubes are serviceable BEFORE use
  • *using scopes can be helpful
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9
Q

ETT prior to anesthesia

A
  • Chose correct DIAMETER and LENGTH
    o Palpate trachea: select range of 3 diameters
    o Pre-measure: from thoracic inlet to the incisors
    o ET tube appropriate length (to thoracic inlet/point of shoulder)
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10
Q

ETT diameter

A
  • Want it to be as close to the tracheal diameter as possible
  • If go smaller=increased resistance!
  • *size indicated=inside diameter
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11
Q

Where do you tie the kling?

A
  • Connector: secure, but problem if connector ‘falls’ off
  • Directly to tube: increase apparatus dead space
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12
Q

Problems with ETT

A
  • Kinked tubes with neck flexion
  • Damaged tubes
  • Endobronchial intubation (go to far into one lung)
  • Tracheal damage (disconnect patient from circuit when moving them to prevent)
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13
Q

What is the correct cuff inflation technique?

A
  1. Ventilate lungs (10-15cmH2O) with O2
  2. Listen for leaks around the cuff
  3. Inflate cuff until you cannot hear a leak with IPPV
  4. Turn on anesthetic vaporizer
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14
Q

Inflate and deflate cuff timing

A
  • Inflate: ASAP
  • Deflate: just prior to extubation
    o Swallow in a dog
    o Ear flick/palpebral reflex in cat
    o Brachycephalic: want for muscle reflexes (not just the swallow)
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15
Q

V-gels: Supraglottic airway device (laryngeal mask)

A
  • Designed specifically for rabbits and cats
  • Sized correctly for each animal
  • Require special lobe
  • *problems with poor fitting and potential obstruction if moving the animal
    o Should be used with a CAPNOGRAM
  • NOT a complete seal
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16
Q

Pollution in workspace

A
  • Avoid chronic exposure to trace amounts of anesthetic gases
  • Use ‘low flow’ systems (never less than 0.5 L)
  • Use proper scavenging
  • Intubate patients when possible
  • Maintain equipment
  • Check for leaks before
  • If pregnant: reduce exposures as much as possible
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17
Q

Anesthetic agent uptake review

A
  • DEPTH of anesthesia is related to partial pressure of inhalant within the brain
    o Control PP with vaporizer
    o Changes alveolar and blood PP
  • RAPID induction/recovery
    o Less lipophilic=high MAC (less potent)
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18
Q

MAC levels (lowest to highest)

A
  • Isoflurane
  • Sevoflurane
  • Desflurane
  • N2O
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19
Q

Factors affecting MAC

A
  • Sedation and powerful opioid analgesics lower amount required (especially in dogs)
  • Body temperature (hypothermia causes CNS depression)
  • Species variation
  • Age (older require less anesthetic)
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20
Q

Factors affecting anesthetic uptake

A
  • Delivered concentration
  • Blood solubility of agent
  • Lipid solubility of agent
  • Lung ventilation
  • Cardiac output
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21
Q

Delivered concentration (factors affecting anesthetic uptake)

A
  • Set vaporizer high=faster uptake
  • Promotes movement of drugs from breathing system to lungs
22
Q

Blood solubility of agent (factors affecting anesthetic uptake)

A
  • Have a larger ‘blood’ compartment
  • Slower onset: takes longer to reach equilibrium
23
Q

Lipid solubility of agent (factors affecting anesthetic uptake)

A
  • Fat soluble agents have slower uptake
  • Go to fatty tissues
24
Q

Lung ventilation (factors affecting anesthetic uptake)

A
  • More alveolar ventilation enables more drug to enter (and leave)
25
Cardiac output (factors affecting anesthetic uptake)
- Higher the CO=slower the uptake o Hard to ‘mask down’ excited patients o Sick animals with hypovolemia requires less anesthetic
26
Where to set the vaporizer dial?
- Depends on if inducing or maintaining anesthesia - Assess depth of anesthesia (ALWAYS check your patient) - Rebreathing vs. non-rebreathing systems - Know MAC values and what other drugs are ‘anesthetic sparing’ - *using inhalants w/o a vaporizer is dangerous
27
Assess depth of anesthesia: 3 things
- Jaw tone - Palpebral - Eye position
28
Rebreathing systems
- Dilute fresh gas input because of LOW oxygen flows and recycled exhaled gases
29
Non-rebreathing systems
- ‘what you dial up, is what you get!’
30
Measuring anesthetic agents
- Rely on experience and vaporizer settings - Assess depth of anesthesia o Only give volatile agent that animal requires and NO more o Alveolar (exhaled %) most accurate measurement - Monitors can measure gas composition=expensive
31
Isoflurane colour code
- Purple
32
Isoflurane MAC dog
- 1.28
33
Isoflurane MAC cat
- 1.71
34
Isoflurane
- Rapid induction and recovery - Good muscle relaxation - Questionable analgesia - 0.2% metabolized in liver - *most commonly used inhalant
35
Isoflurane cardiopulmonary effects
- Dose dependent - MOST respiratory depressant of all IH drugs - Little effect on autonomic NS - Direct relaxation of smooth muscle of blood vessels - VASODILATION more pronounced compared to myocardial depression (HYPOTENSION likely to occur) - Little myocardial sensitization to catecholamines - Stable heart rate
36
Isoflurane with Acepromazine
- Tends to produce more HYPOTENSION
37
Isoflurane clinical use
- Induce with 2-4% - Maintain with 1-2% o Actually values depend on other anesthetic-sparing drugs (PIVA) - May need to ventilate lungs (respiratory depression) - Used in many species
38
Sevoflurane colour code
- Yellow
39
Sevoflurane MAC dogs
- 2.4%
40
Sevoflurane
- Rapid induction and recovery - Not as irritation to airways/mucous membranes as in isoflurane - Metabolism produces few Fl- ions (not problematic)
41
Sevoflurane and CO2 absorber form
- Compound A and carbon monoxide=TOXIC byproducts accumulate in rebreathing systems with low O2 flow
42
Sevoflurane cardiopulmonary effects
- Comparable to isoflurane - Dose dependant - Vasodilation > myocardial depression (HYPOTENSION likely) - Hepatic blood flow preserved - Minimal respiratory depression (animals breath well spontaneously)
43
Sevoflurane clinical use
- Induce: 3-7% (usually well tolerate, sweet smell compared to isoflurane) - Maintain: 2-4% (depends on other anesthetic-sparing drugs (PIVA)) - Used in many species (especially exotics) - Expensive (3x more than isoflurane) - Minimal advantages compared to isoflurane
44
Sevoflurane metabolism: % and safety margin
- 4-5% - High=rapid elimination from lungs reduce amount available for metabolism
45
Sevoflurane metabolism: Fluoride ions
- Can be NEPHROTOXIC in high amounts - Enzyme (P450) used for sevoflurane Fl- metabolism: not enough present in kidney to cause nephrotoxicity - NOT associated with clinical renal problems
46
CO2 absorber types
- CO2 absorbers contain hydroxide bases to remove CO2 - MONO-valent hydroxides (Na, K) cause more breakdown of inhalant compared to DI-valent hydroxides (Ca2+) - ‘soda-lime’ - ‘barium-hydroxide lime’
47
CO2 absorbers and sevoflurane degradation
- *special DI-valent CO2 absorber used with Sevoflurane
48
‘soda-lime’
- Has Na-OH and some K-OH - *monovalent
49
‘barium hydroxide lime’
- Has K-OH o Produces high operating temperatures and more sevoflurane breakdown
50
Sevoflurane: CO2 absorber and fires!
- Exothermic reaction - CO2 absorber canister temperatures normally operate 25-45 degree C) o High T can occur is use very low O2 flow and VERY DRY absorber - Sevoflurane creates the most HEAT and can cause canister FIRES! - Do NOT use DESSCIATED ABSORBER with sevoflurane
51
Partial IV technique (PIVA)
- IH drugs have little analgesia and can depress CV system (dose-dependent) - Other drugs can be used as an infusion or bolus to reduce IH concentration required - ‘anesthetic sparing’ effect - *useful for debilitated animals or animals undergoing invasive procedures