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Anaesthesia Flashcards

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1
Q

What occurs in the pre-op phase of anaesthesia?

A 
Owner consent and admission to practice
Full exam/history, ASA classification and planning stage
Set up machine/equipment
Prepare meds/drugs/fluids
Premed patient
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2
Q

What happens in the induction phase of anaesthesia?

A

IV catheter placement
Pre-oxygenation
Admin of induction agent
Security of airway

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3
Q

What happens in the maintenance phase of anaesthesia?

A

Maintain anaesthesia - gas/TIVA/injectable
Placement of local/regional blocks
Continue to surgery/diagnostics

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4
Q

What happens in the recovery phase of anaesthesia?

A

Cessation of gaseous maintenance/CRIs
Antagonism of injectable drugs
Removal of airways device
Move to recovery area

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5
Q

What is the anaesthesia triad?

A

Analgesia
Narcosis
Muscle relaxation

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6
Q

What did the CEPSAF enquiry discover?

A

50% of deaths occurred within 3 hours of recovery
Sick animals had higher risk than healthy ones
Risk significantly higher with GA than sedation
Cats had twofold increase in risk

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7
Q

What are the species-specific problems seen?

A 
Extremes of size
Hyper-/hypothermia
Aggression/risk of injury
Drug sensitivities in breeds
Obesity
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8
Q

List some breed-specific problems with anaesthetic drug use.

A

Brachycephalic
Boxers = ACP / cardiomyopathy
Collies/sheepdogs/shepherds = MDR1 gene
Greyhounds = lack of cytochrome P450 / body fat
Dobermann = Von Willebrand factor / dilated cardiomyopathy
Miniature schnauzer = females sick sinus syndrome

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9
Q

What can VNs do/not do in terms of inducing/maintaining anaesthesia?

A

Can administer a specific amount of meds directed by VS / act as VS hands to maintain

Cannot admin meds incrementally or to effect

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10
Q

What information needs to be gathered from an owner during the pre-op assessment?

A 
Full history
Owner questioning - any concerns?
Previous reactions to drugs?
Breed/species
Confirm pre-op fasting times
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11
Q

What is assessed in the pre-op clinical examination?

A 
MMs/CRT
Thoracic auscultation
Heart murmur?
Pulse quality and effort
Ventilatory effort
Temperature
Swellings/distension
Temperament
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12
Q

What is the goal of pre-op fasting?

A

To reduce the volume of the stomach contents

To prevent GOR/regurgitation and aspiration

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13
Q

What are the recommended guidelines for pre-op fasting?

A

Cats = 6-8 hours
Dogs = 8-10 hours
Rabbits/small furries = no starvation but may withhold food ~30 mins pre-op

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14
Q

What diagnostic tests may be run prior to anaesthesia induction?

A 
Bloods
Urine
Radiography
ECG
Echocardiology
Ultrasound
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15
Q

What are the injectable anaesthetic agents and what animals are they licensed for?

A

Propofol - dogs, cats
Alfaxalone - dogs, cats, rabbits
Ketamine - horses, dogs, cats
Tiletamine / zolazepam - dogs, cats

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16
Q

What are the injectable drugs for euthanasia?

A 
Pentobarbital
Secobarbital sodium (quinalbarbital sodium) plus cincocaine hydrochloride = Somulose
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17
Q

What factors affect the effect of anaesthetic injectables?

A 
Blood flow to brain
Amount of non-ionised drug
Lipid solubility
Molecular size
Conc. gradient
Protein binding
Distribution
Metabolism
Excretion
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18
Q

What makes the ideal injectable anaesthetic agent?

A 
Rapid onset
Non-irritant
Minimal cardiopulmonary effects
Rapid metabolism and elimination
Non-cumulative
Good analgesia
Good muscle relaxation
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19
Q

What are the key points regarding propofol as an injectable anaesthetic?

A 
Rapid onset of action
Highly plasma protein bound (96-98%) and lipid soluble
Rapidly metabolised and eliminated
Non-cumulative in DOGS
No analgesia
Fair muscle relaxant
Non-irritant
Post-induction apnoea, hypotension, Heinz body anaemia in cats
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20
Q

What are the key points regarding alfaxalone as an injectable anaesthetic?

A 
Non-irritant (?IM)
20% plasma protein bound
Rapid onset
Rapid metabolism and elimination
Non-cumulative
Preserves baroreceptor tone
Some respiratory depression
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21
Q

What are some key points regarding ketamine as an injectable anaesthetic?

A 
Poor muscle relaxation (not used as sole agent)
Reflexes maintained
Maintains CVS/respiraotyr function
Analgesia/antihyperalgesia
Slow onset
Non-cumulative
50% plasma protein bound
Increase intraocular-/intracranial pressure
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22
Q

What factors affect recovery from injectable anaesthetics?

A

Drug factors, e.g. dose
Species, breed and age
Co-morbidities, e.g. CVS/hepatic/renal function

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23
Q

When is TIVA useful and what are its ideal properties?

A

Used to reduce exposure to inhalants, or “in the field” when machines are not available
Ideal properties = rapid metabolism and elimination, fast onset, high therapeutic index, pharmacokinetics available

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24
Q

In which three ways can anaesthesia be induced by injection and what are the advantages/disadvantages of each?

A

IV = quickest onset (2-10mins), reliable, less stress BUT relies on IV catheter - IV only for Propofol/Alfaxalone

IM = fairly quick (10-20mins), reliable if actually IM BUT can be painful, slower onset

SC = easy to administer, less painful than IM BUT can cause pain, longer onset (30-45mins), lower efficacy

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25
Q

Which two ways can anaesthesia be induced through inhalation and what are the advantages/disadvantages?

A

Chamber inductions = easy to set up/use, cheap, no technical skill BUT very stressful, difficult to observe patient, risk of exposure

Face masks = cheap, easy to set up/use, can give oxygen/VAs quickly BUT does not protect airway, increases dead space, risk of exposure

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26
Q

Describe the laryngeal mask airway (LMA).

A

Easy to use - sits over airway
Reduced complications compared to ETT
Reduced airway pollutants compared to face mask
Not really designed for veterinary species

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27
Q

Describe the supraglottic airway device (V-GEL).

A

Species specific / weight specific design

Training needed before use

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28
Q

Describe ET tubes.

A

Allows airway protection
Prevents atmospheric exposure
Allows accurate provision of anaesthetic agents
Some have a cuff system

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29
Q

What is the point of a cuff on an ET tube?

A 
Allows a tight seal in the trachea
Prevents gas leaking around tube
Prevents contents going into patient lung
Allows accurate delivery of VAs/oxygen
Allows direct route to lungs
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30
Q

What equipment should you prepare for ET intubation?

A 
Laryngoscope
Tubes - range of sizes (length = incisors to shoulder tip)
Local anaesthetics (cats)
Tie
Cuff syringe
Swab/suction/mask for preoxygenation
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31
Q

What are the common complications during induction?

A 
Injury - us or them
Lack of airway patency
Aspiration/regurgitation
Hypothermia
CVS/respiratory system dysfunction
Post-induction apnoea
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32
Q

List the patient safety features on anaesthetic machines.

A 
Pin-index system and NIST for pipelines
Colour-coded pressure gauges and flowmeters
Oxygen flowmeter "touch coded"
Ratio regulators
Nitrous oxide cut-out
Alarm whistle
Air intake valve
Reserve oxygen cylinders
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33
Q

What is the difference between active and passive scavenging?

A

Active = waste gases/anaesthetic agents drawn outside of building by a fan and vent system, requires an air break to prevent negative pressure being applied to patient breathing system

Passive = gas is pushed by patient expiratory effort into tubing either into tubing leading outside of building or into a canister containing activated charcoal

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34
Q

What makes the ideal inhalational agent?

A 
Non-irritant
Minimal effects on CVS and respiratory function
Rapid uptake and elimination
Non-toxic
Non-flammable and chemically stable
Easily vaporised
Good analgesia and muscle relaxation
35
Q

Define MAC and what factors can affect it.

A

MAC = Minimum Alveolar Concentration
Reduced by: other drugs (e.g. premed), hypothermia, pregnancy, geriatric/neonatal animals, hypothyroidism
Increased by: hyperthermia, young animals, hyperthyroidism, admin of catecholamines/sympathomimetics

36
Q

How can we reduce exposure to inhalant anaesthetic agents?

A

Well-ventilated theatres/recovery areas (15-20 air changes)
Use IV induction agents where possible
Use cuffed ET tubes
Connect animal to breathing system before turning on gases
Use low flows
Check for leaks
Flush breathing system with oxygen before disconnecting animal
Use key fill vaporisers

37
Q

Define vapour.

A

Vapour = gaseous state of a substance that at ambient temp. and pressure is a liquid.

38
Q

Define partial pressure.

A

Partial pressure = pressure that individual gas exerts in a mixture of gases.

39
Q

Define partition coefficient.

A

Partition coefficient = ratio of the concentration of a compound in two solvents at equilibrium.

40
Q

What are the disadvantages of using IM injectable anaesthetics?

A

Difficult to control depth - slow onset and unpredictable
Limited access
Limited range of drugs

41
Q

What are the disadvantages of IV injectable anaesthetics?

A

Can result in unstable plane of anaesthesia - bolus techniques
Can get cumulative effects of some drugs

42
Q

What are the advantages/disadvantages of inhalational anaesthetics?

A 
A = easy to administer/calculate, suitable for most patients, easy to adjust depth
D = requires specialist equipment, has impact on BP through vasodilation, personnel risks
43
Q

What are the advantages/disadvantages of injectable anaesthetics?

A 
A = available in all settings, can be administered by a nurse, provides good level of sedation
D = careful dosing needed, limited choice of drugs, not so easy to change depth quickly if at all
44
Q

What factors help us decide which maintenance technique to use?

A 
Species
Behaviour
Procedure
Facilities
Expertise
Budget
45
Q

What must we consider when positioning patients for anaesthesia?

A 
Prevent muscle/nerve damage
Prevent post-op pain
Optimise ventilation
Nasal congestions
Protect eyes, apply ocular lubricant-opioids
46
Q

What are the four ways in which heat can be lost during anaesthesia?

A

Convection - loss of body heat to cool air surrounding body
Conduction - loss of body heat to surfaces that in contact with body
Radiation - loss of body heat to structures not in contact with body
Evaporation - loss of boy heat from moisture evaporation

47
Q

What effects can hypothermia have?

A 
CNS depression
Hypotension
Bradycardia
Hypoventilation
Decreased basal metabolic rate
Decreased urine output
48
Q

How can we reduce the risk of hypothermia?

A 
Keep anaesthetic time minimal
Minimise wetting of patient/fur
Maintain a high ambient temp.
Use heat and moisture exchangers
Use appropriate breathing systems
Use warmed fluids for IVFT
Keep patient warm from point of premed
Use insulating materials
49
Q

Describe Stage 1 of anaesthesia.

A

Begins at time of induction and lasts until unconsciousness.
Pulse and resp. rates elevated
Breath-holding can occur
Pupils may dilate

50
Q

Describe Stage 2 of anaesthesia.

A

Lasts from onset of unconsciousness until rhythmic breathing is present
All cranial nerve reflexes present and may be hyperactive
The eye may appear wide and open and pupil dilated - soon rotate to ventromedial position

51
Q

Describe Plane 1 of Stage 3 of anaesthesia and what it is suitable for.

A

Respiration becomes regular and deep
Spontaneous limb movement is absent, but pinch reflex may be brisk
Nystagmus, if present, will start to slow and disappear
Eyeball is ventromedial, opening the eye will show the sclera
This plane is suitable for minor procedures e.g. abscess lancing, skin suturing

52
Q

Describe Plane II of Stage 3 of anaesthesia and what it is suitable for.

A

Eye position ventromedial and eyelids may be partially separated
Palpebral reflex is sluggish or absent, although corneal reflexes persist
Muscles appear relaxed, pedal reflex begins to go
Tidal volume may decrease as resp. rate settles/HR and BP may be slightly reduced
This plane is suitable for most surgical procedures

53
Q

Describe Plane III of Stage 3 of anaesthesia and what it is suitable for.

A

Eyeball becomes central and eyelids begin to open
Pupillary diameter increases
Pedal reflex is lost and abdominal muscles are relaxed
HR and BP may be low
This plane is suitable for all procedures

54
Q

Describe Stage 4 of anaesthesia.

A

Overdose!
Characterised by progressive respiratory failure
Pulse may be rapid or very slow and become impalpable
Eye may become central with no palpebral reflex
CRT prolonged
Sometimes accessory respiratory muscle activity, indicated by twitching in throat - this may mimic inadequate anaesthesia

55
Q

What are the pros and cons of both indirect/non-invasive methods of measuring arterial BP?

A

Doppler = inexpensive, efficient, detects pulse flow in low flow states, good in cats, quick results BUT systolic only

Oscillometric = systolic, diastolic and MAP BUT less reliable, interference/movement, not so useful in small animals, more expensive

56
Q

Define systolic, diastolic and mean arterial pressure.

A 
Systolic = a measure of the force the heart exerts on the walls of the arteries
Diastolic = the pressure in the arteries when the heart is between contractions
Mean = the intravascular pressure in the vessel during one complete cardiac cycle
57
Q

How does a Doppler machine work?

A

Emit an ultrasound signal
Produce auditory signal generated by frequency shift of underlying RBCs
An inflatable cuff is placed around limb
The cuff is inflated
At some point, the noise will stop (as flow stops)
The BP is the measured point when flow returns

58
Q

Which vessel is most commonly used for direct/invasive BP measurements and why?

A

Metatarsal/dorsal pedal artery
Easy to secure in place
Easy to maintain for post-op monitoring
Less risk of a large haematoma

59
Q

How does a haemodynamic monitoring system work?

A

Electronic system with fluid-filled tubing
Catheter detects pressure waves in arterial system
Fluid column in tubing system carries pressure wave to diaphragm of electronic transducer
Converts to an electrical signal
Monitor indicates arterial BP

60
Q

What should we do if faced with a low BP?

A 
Identify underlying cause!
Try reducing volatile agent
Consider concurrent use of local blocks/topping up analgesia
Manage bradycardia
Consider fluids/drug therapy
61
Q

What information do we gain from capnography?

A

Inspired carbon dioxide (numerical value)
Expired carbon dioxide (numerical value)
Respiratory rate (numerical value)
Capnograph (waveform)

62
Q

What are the pros and cons of side stream capnography?

A 
Pros = cheaper, less likely to break, easy to replace if it does break
Cons = not quite real time, takes some FGF requirement, sample line can get easily damaged and needs changing regularly
63
Q

What are the pros and cons of mainstream capnography?

A 
Pros = real time results, no need for sample line = no requirement for FGF
Cons = very expensive to buy, can be damaged easily = £££, can add drag to system
64
Q

Describe a capnograph waveform.

A 
Baseline (should always return to this)
Expiration
(Alpha angle = ventilation perfusion of lungs)
Alveolar plateau (where gas is sampled)
(Beta angle = rebreathing)
Inspiration
65
Q

What are the ideal values from a capnograph?

A 
End tidal CO2 (ETCO2) = dogs 35-45mmHg, cats 28-35mmHg
Inspiratory CO2 (INCO2) = all species 0
66
Q

What can cause a high ETCO2?

A

Hypoventilation
Reduced resp. rate
Reduced tidal volume

67
Q

What can cause a low ETCO2?

A 
Hyperventilation
Low cardiac output
Decreased metabolic rate
Hypothermia
Pulmonary embolism
Leak in sampling line
Poor sampling technique (dilution)
Leak in breathing system
68
Q

What can cause a high INCO2?

A

Non-rebreathing system = too low FGF, too much dead space

Rebreathing system = exhausted absorbent, faulty/sticky valves

69
Q

On what lead do we run anaesthesia ECG?

A

Lead II.

70
Q

How do we attach ECG leads to small animals?

A 
Red = right fore
Yellow = left fore
Green/black = left hind
71
Q

What do each part of an ECG trace show us?

A

P wave = atrial depolarisation
QRS complex = ventricular depolarisation
T wave = ventricular repolarisation

72
Q

What information will a pulse oximeter give you?

A

Haemoglobin oxygen saturation levels (%)
Heart/pulse rate (numerical value)
Some machines give a waveform

73
Q

How does a pulse oximeter work?

A

Light absorption, differentiation of wavelengths
Probe = light emission from one side (red light/infrared), light detector on other side
Oxyhaemoglobin - absorbs greater amounts of infrared and lower red light
Deoxyhaemoglobin - absorbs more red light than oxyhaemoglobin

74
Q

Where can we position a pulse ox probe?

A

Hairless and unpigmented - tongue, inter-digital, ear, prepuce, vulva, skin webbing

75
Q

What are the benefits of pulse oximetry?

A 
Non-invasive
Available in almost all settings
Non-painful
Quick and easy to set up and use
Gives a clear reading
Can be used on conscious and unconscious patients
76
Q

What are the limitations of pulse oximetry?

A

False readings
Susceptible to damage
Doesn’t work well in anaemia
Can cause tissue compression in small animals
Patient movement
Poor perfusion (hypothermia, shock, vasoconstriction)
Too thin tissue (e.g. cat ear)
Interference
No differentiation between oxyhaemoglobin and carboxyhaemoglobin

77
Q

When do we extubate dogs/rabbits?

A

Watch for signs that laryngeal reflexes are returning

Watch to see if other reflexes returning and/or spontaneous movement

78
Q

When do we extubate cats?

A

Have very sensitive larynxes so danger of laryngospasm if you wait for swallowing
Need to extubate before this point - earlier reflexes e.g. ear flick / blink

79
Q

When is late extubation appropriate?

A

May be necessary in patients at high risk of airway obstruction, e.g. brachycephalic dogs
NOT suitable in cats due to risk of laryngospasm
Will need to monitor patients carefully

80
Q

What are the patient’s stages of anaesthetic recovery?

A 
Extubation
Lift head
Assume sternal recumbency
Stand
Full recovery with no signs of sedation/ataxia
81
Q

What can be the physiological signs of pain in recovery?

A

Heart rate
Respiration rate
Temperature
Blood pressure

82
Q

What behaviour changes should we watch for in recovering patients?

A 
Inappetence
Reluctance to stand/move / difficulty in mobility
Vocalisation
Panting
Lip-smacking
Aggression
Sleeping more
Reacting badly to being touched
83
Q

What other considerations for patient comfort should we have in recovery?

A 
Full bladder
Cold / hot
Wet bedding
Tight stitches
Clipper rash
Need to defecate
Fear/anxiety
84
Q

How do we conduct post-op feeding in recovery?

A

Feed when awake/able to stand and swallow, unless GI surgery/sedation/CRIs/follow-up imaging
Bland, soft food
Little and often
Assisted feeding in smalls e.g. rabbits

Veterinary Nursing (65 decks)

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