Anaesthesia (Small and equine) Flashcards

1
Q

ASA statuses?

A

ASA 1: normal healthy animal
ASA 2: mild systemic disease
ASA 3: moderate systemic disease
ASA 4: severe systemic disease, constant life threat
ASA 5: moribund, not expected to survive following 24h

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2
Q

Aims of anaesthesia?

A

Unconsciousness
Analgesia
Muscle relaxation

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3
Q

Which anaesthetic drugs do/do not achieve analgesia, unconsciousness and muscle relaxation? (ACP, benzo, a2, opioids, barb, ket, propofol, inhalation, N2O, local)

A
Analgesics: 
- A2 agonists
- Opioids
- Ketamine
- N20
- local 
Sedatives:
- ACP
- A2 agonists
- Opioids
Loss of consciousness:
- Barbiturates
- Ketamine
- Propofol
- Inhalationals
Muscle relaxation:
- ACP
- Benzodiazepines
- A2 agonists
- Barbiturates
- Propofol
- Inhalationals
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4
Q

What is balanced anaesthesia?

A

Using safe doses of 2+ agents or methods to:

  • Reduce dose of each
  • Reduce side effects
  • Optimise analgesia
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5
Q

Advantages and disadvantages of injectable induction of anaesthesia?

A

Advs:

  • Not much equipment needed
  • Generally rapid and smooth
  • No enviro pollution

Disadvs:

  • Once delivered, retrieval impossible
  • Must have accurate weight (good estimate in LA)
  • CV and resp depression
  • Accidental self administration
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6
Q

Ideal induction agent?

A
Easy to put into solution and stable with a long shelf life
Cheap
Not painful on injection
Rapid onset
Smooth induction and recovery
Rapid redistribution, metabolism and clearance
No active metabolites
Safe
No side effects
Analgesia
Muscle relaxation
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7
Q

Propofol - Side effects? Benefits over alfaxolone?

A

Vasodilation with no compensatory increase in HR (-> hypotension -> reduced blood flow to vital organs)
Post-induction apnoea (so should pre-oxygenate for 5 mins)
Cats:
- Repeated doses are cumulative (takes couple of days to remove from body)
- Potential for Heinz body anaemia (due to oxidative damage to RBCs)

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8
Q

Alfaxalone - Side effects? Benefits over propofol?

A

Vasodilation with compensatory increase in heart rate (so CO maintained better than propofol)
Post-induction apnoea (but less than propofol)
Not cumulative in cats (can use multiple times in short period)
Can give IM and IV
More twitching than propofol (avoid in seizure patients as can’t tell if seizing or twitching)

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9
Q

Ketamine - Features? Side effects?

A

Excellent analgesia
Induction agent
Increase in sympathetic tone - vasoconstriction
Direct negative inotrope
(So CO maintained due to opposite effects of vasoconstriction and negative inotropy)
Often get post-induction apnoea
Can give IM and IV
Causes muscle rigidity - ideally use with a drug that gives muscle relaxation
Propofol/alfaxolone and ketamine often used for co-induction - uses analgesia of ketamine and reduce doses to reduce side effects
Dogs and cats will often salivate excessively
Often will keep cranial nerve reflexes so hard to tell how asleep
Good in horses as small volume needed, takes about 2 mins to work, often go down nicely

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10
Q

Etomidine - What is it? When used?

A
Induction agent
Only one with virtually no CV effects
Good for animals with CV compromise
Stops adrenal glands working
Not really used in practice
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11
Q

Thiopental - What is it? When used?

A
Induction agent
Stopped using in UK
Used in equine
Only drug able to use at sensible volume when horse is too light on table
CV effects - arrhythmias etc
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12
Q

Advantages and disadvantages of inhalation agents for induction of anaesthesia?

A
Advs:
- Doesn't require IV access
Disadvs:
- Prolonged induction time
- Likely to cause distress
- Airway irritation
- Enviro pollution
- Requires tight fitting mask or chamber
- Increased risk of death compared to injectable

Don’t use unless have to
Sevoflurane if have to - smells nicer, quicker induction, reduced chance of dying

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13
Q

Why monitor anaesthesia?

A
Maintain physiology
Maintain adequate anaesthetic depth 
Prevent pain
Safety
Legal implications
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14
Q

What reflexes/other visual things can be monitored during anaesthesia? How do they change with depth?

A

Palpebral reflex: brisk/spontaneous -> sluggish -> absent (check both as becomes refractory)
Anal: brisk -> sluggish -> absent tone
(Corneal)
Eye position: central -> ventral -> central
Pupil: dilated -> constricted -> dilated
Lacrimation: decreases as deepens
Changes in autonomic tone: sweating
Muscle tone: tension in tendon of sternocephalicus, jaw tone
Movement = either very light or about to die

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15
Q

CV monitoring under anaesthesia?

A

HR/pulse:
- Dogs: 50-120
- Cats: 60-140
- Horses: 24-40
Central vs peripheral artery palpation gives indication of perfusion
Mucous membrane colour indicates oxygenation and perfusion
CRT depends on blood volume and capillary tone:
- <1 second = poor perfusion or hypovolaemia
- >2 seconds = maldistributive shock

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16
Q

Respiratory monitoring under anaesthesia?

A
Normal rate:
- Dog and cats: 10-30
- Horses: 8-10
Bradypnoea:
- Too deep
- Hypocapnia
- Isoflurane, propofol, fentanyl
- Alkalosis
Tachypnoea:
- Too light
- Hypoxia, hypercapnia
- Methadone
- Poor analgesia
- Acidosis
Watch reservoir bag movement - % inhaled
Mucous membrane colour - cyanosis = severe hyperaemia
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17
Q

Normal blood pressure under anaesthesia?

A

Systolic: 80-130mmHg
Diastolic: 40-60mmHg
Mean: >60mmHg

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18
Q

Types of blood pressure monitoring under anaesthesia? Advs and disadvantages?

A

Non invasive BP:
- Oscillometric or Doppler
- Intermittent readings or SBP or MAP
- No risk of infection
- Need correctly fitting cuffs (easy to get inaccurate values)
Invasive BP
- Continuous readings of SBP, DBP and MAP
- Invasive/risk of infection
- Allows arterial blood sampling (blood gases)
- More expensive equipment

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19
Q

What is pulse oximetry? What does it tell you? Normal values? Limitations?

A
Measures % saturation of oxygen of Haemoglobin (SpO2)
Normal: 97-99%
Measures pulse
Indirect indication of perfusion (plesthysmograph)
Limitations:
- Hypotension/vasoconstriction
- Affected by bright light
- Non pigmented mucosa
- Movement sensitive
- Probe may blanch capillary bed
- 'Beeps' may be over-interpreted
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20
Q

What is capnography? What are normal values? What does it tell you? Parts of curve?

A
Measures end tidal CO2 (EtCO2)
Normal: 35-45mmHg
>60mmHg = hypoventilation
<35mmHg = hyperventilation
Other uses:
- correct placement of ETT
- Confirms pulmonary circulation (CCPR)
- Indicates problems e.g. with breathing system
Curve:
- Respiratory baseline (should be 0)
- Expiratory upstroke
- Alveolar plateau
- EtCO2
- Inspiratory downstroke
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21
Q

What is sedation?

A

Mental calming
Sleepiness and disinterest in environment
Decreases responsiveness to a stimuli
Animals can still be aroused

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22
Q

Why use a premedication?

A
Relieves anxiety
Smooths induction, maintenance and recovery phases
Anaesthetic sparing effects
Pre-emptive analgesia
Reduces muscle tone
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23
Q

Reasons to use sedation?

A

Premedication
Chemical restraint
May provide analgesia
Reduce muscle tone

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24
Q

Ideal premedication?

A
Reduce fear and anxiety
Easy to administer
Quick onset
Reasonable duration of action
Antagonisable
Predictable and reliable
Safe
Effective in many species
Minimal resp, CV and other side effects
Analgesia
Muscle relaxation
Amnesia
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25
Q

Ideal sedative?

A
High therapeutic index
Reliable and predictable
Rapid onset of action
Well absorbed by all routes
Non irritant to tissues
Non painful on injection
No side effects
Practical volume to administer
Analgesia and some muscle relaxation
Antagonisable
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26
Q

Acepromazine - Type of drug? Effects? Side effects? Onset? Duration?

A

Phenothiazine
Mental calming die to dopamine antagonism
Commonly used as a premedication, often with opioids
Unpredictable sedative
No analgesia
Many other sites of action leads to side effects
Potentiates CNS depressant effects of other sedative and anaesthetic agents
Vasodilation, hypotension, bradycardia (-> CV collapse -> syncope, especially in brachycephalic dogs) - care in CV compromised patients
Will cause pharyngeal muscle relaxation (problem in brachycephalic dogs)
Anti-emetic
Anti-histaminic
Avoid in very excited animals
Can cause excitation at high doses/overdoses
Beware in paediatric patients
Avoid in breeding stallions
Hypothermia
Not reversible
Onset: 30-40 mins
Duration: 4-6 hours

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27
Q

Azaperone - Type of drug? How does it work? When used? Side effects?

A

Butyrophenones
Used in pigs
Antidopaminergic and anti-adrenergic effects in reticular activating system of CNS
Avoid large doses in boars - penile prolapse
Care in brachycephalic pigs
Hypothermia

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28
Q

A2 agonists - Examples? How it works? Advs? Side effects? Care?

A

Examples:
- Xylazine
- Detomidine
- Medetomidine
- Dexmedetomidine
- Romifidine
How it works:
- Suppression of activity in reticular activating system
- A2 agonism in the locus coeruleus in brainstem
Advs:
- Analgesia (of shorter duration than the sedation)
- Muscle relaxation
- Reversible: atipamezole
- All can be given IV, IM or SC
- Some can be given transmucosally/oromucosally
- Predictable, dose dependent sedation
- Sedation may be profound
- Anaesthetic sparing effect
Side effects:
- Hormonal effects - diuresis, hyperglycaemia
- GI effects
- Sweating
- Initial hypertension and peripheral vasoconstriction -> reflex bradycardia -> relaxation of peripheral vascular tone -> eventual state of peripheral vasculature and BP stays fairly close to normal
- Significantly reduces CO
- Sinus arrhythmia, SA block and AV blocks possible
- High doses can lead to hyperaemia
- Can be absorbed across mucous membranes
- Suppression of thermoregulation

Care in CV compromised patients!
Care in sick/debilitated patients!
Care if diabetes mellitus!
Care if laryngeal dysfunction!

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29
Q

Benzodiazepines - What do they do? How do they work? Effects? Side effects? Examples?

A

Unreliable sedation in healthy animals
Useful in ‘at risk’ patients
GABA-specific benzodiazepine binding sites - brain and spinal cord
Central muscle relaxation
No analgesia
Anticonvulsant
Side effects:
- Minimal CVS depression
- Midazolam will cause greater CV depression than diazepam at higher doses
- Minimal respiratory depression
- Enhances the depression caused by other drugs
- Binds to some plastics (giving sets etc)
- Postural muscle weakness
- Care if hepatic disease
Can be reversed by flumazenil or surmazenil
Examples:
- Midazolam
- Diazepam
(None licensed)

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30
Q

Opioids - What do they do? Effects? Side effects? Examples?

A
Potent, efficacious analgesics
Bind to opioid receptors
Also effects on resp, GIT and CV systems
Can cause sedation alone in severely compromised animals where low level sedation is required
But often sedation is poor
Used with other sedatives to improve the quality of sedation
Can be antagonised
Examples:
- Pethidine
- Methadone
- Morphine
- Fentanyl
- Buprenorphine
- Butorphanol
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31
Q

Advantages and disadvantages of inhalation agents for maintenance of anaesthesia?

A
Also delivers oxygen
Can ventilate fairly easily if required
Easy to alter anaesthetic level
Easy to remove from the animal
Low running costs

Expensive equipment
Cannot deliver without specialist equipment
Must have an airway

32
Q

What can be used for muscle relaxation on induction?

A

A2 agonist
GGE
Benzodiazepine

33
Q

Advantages and disadvantages of intravenous agents for maintenance of anaesthesia?

A

No need for specialist equipment
Bolus or TIVA

Cumulative effect - prolonged recovery, slower changes in depth
Doesn’t deliver oxygen unless supplemented
Once given, can’t be easily removed
Drugs can be expensive

34
Q

Ideal maintenance agent?

A
No side effects or negative interactions with other drugs
Safe in every species
Rapid control of depth
Cheap
Not an environmental contaminant
Antagonisable
Easy to use
Minimal/no metabolism
Muscle relaxation
Analgesia
Safe to use
Pleasant smell for inhalation/non painful on injection
Can administer by variety of routes
35
Q

What is MAC? What is it affected by?

A

Minimal alveolar concentration
= alveolar concentration at which 50% of patients will respond to a standard noxious stimulus
Expressed as a %
Allows comparison of potency (ie how much we need for desired effect)
Majority of animals should be adequately anaesthetised at 1.2-1.5 x MAC
If need more than this then think why? - not enough analgesia, leak (more drugs = more side effects)
Affected by:
- Species
- Age
- Hypoxia
- Profound hypotension
- Temperature
- Circulating catecholamines
- Pregnancy
- Other drugs

36
Q

How are inhalation agents delivered during anaesthesia?

A
Starts as liquid
Put into vaporiser
Get liquid and vapour above this liquid
Oxygen flows over and picks up the vapour
Delivered via breathing system to animal
37
Q

Bolus v constant infusions of intravenous anaesthetic agents?

A

Bolus:
- Not ideal as have more at risk and too awake periods (depth not constant, going up and down)
Constant infusion:
- At desired depth more consistently

38
Q

Species differences with inhalation agents for anaesthesia maintenance?

A

Horses more susceptible to the respiratory depressant effects
Nitrous oxide will move into gas filled spaces - can make colic/pneumothorax etc worse, care in ruminants
Costs of TIVS with propofol and alfaxolone makes them less likely to be used in larger animals
Propofol and cats!

39
Q

Factors influencing choice of maintenance agent?

A
Licensing
Food producing
Species
Equipment level
Duration of anaesthesia
Need for secure airway
Need for oxygen
Need for analgesia
Cost
Availability
Familiarity
Health status
In clinic or field
40
Q

Body compartments?

A

60% BW is water in adult
40% ICF: 20% ECF
15% ISF: 5% plasma

41
Q

What is the circulating volume in different species?

A

Circulating volume = intravascular volume + volume of cells
Dogs and horses: 8-9% BW = 80-90ml/kg
Cats, rabbits, sheep and cows: 6-7% BW = 60-70ml/kg

(If PCV is 0.4L/L, then circulating volume is 5% + 4% = 9%)

42
Q

Where are Na+, Cl-, K+ and protein found: ECF, plasma, ICF?

A

ECF: Na+ and Cl-
Plasma: Na+, Cl-, colloidal proteins
ICF: K+ and proteins

43
Q

Maintenance fluid requirement?

A

2-3ml/kg/hr

50-75ml/kg/day

44
Q

Types of fluid loss? What happens to PCV and TP?

A

Whole blood loss (haemorrhage):
- Lose water, colloidal particles, red cells and electrolytes
- Lost exclusively from the intravascular compartment
- PCV/TP not altered in short term
- Replace with blood, or colloids and crystalloids
ECF loss (D+, V+, diuresis):
- Lose Na+, Cl- and water
- Lost from ISF and intravascular compartments
- Osmotic potential of the remaining ECF doesn’t change and ICF not affected
- Replace with Hartmann’s or normal saline
Protein rich ECF loss (exudates, effusions, PLE, PLN):
- Lose Na+, Cl-, water and proteins
- Lost from ISF and intravascular comparments
- Replace with colloids
Pure water loss (dehydration):
- Lose water
- Lost from all 3 compartments
- Osmotic potentials all increase equally but stay at normal ratios between compartments
- Replace with Aquapharm 18/6

45
Q

ECF volume replacers? What do they do? Examples?

A

For each litre administered, only 250ml remains in the intravascular space
Hartmann’s:
- 131mmol Na+, 5mmol K+, 111mmol Cl-, 29mmol lactate
- Contains ‘bicarbonate sparing’ lactate ion
Normal saline (0.9%)
- 150mmol Na+, 150mmol Cl-

46
Q

Types of fluids for fluid therapy?

A

ECF volume replacers - Hartmann’s, normal saline
Maintenance solutions/water replacers - Aquapharm 18, Aquapharm 6
Plasma volume expanders - colloids, hypertonic saline

47
Q

Maintenance solutions/water replacers? What do they do? Examples?

A

Normal fluid losses = hypotonic to ECF and contains more K+
But can’t put a solution into the vascular space that is too hypotonic as would cause haemolysis
Low Na+
Aquapharm 18:
- 4% glucose, 0.18% NaCl (with K added)
Aquapharm 6:
- 5% dextrose (with K added for maintenance)
Glucose/dextrose metabolised by RBCs and prevent haemolysis

48
Q

Plasma volume expanders? What do they do? Examples?

A

Must always be followed by ECF replacers to pay back fluid taken from ISF
Only transient effect

Colloids:
- Large molecules that can’t pass through (healthy) vascular endothelium
- So increase the colloidal osmotic pressure of the plasma and ‘pull’ water in from ISF
Hypertonic saline (7.2% NaCl):
- Draws water in from ISF
- Causes a pulmonary-vagal reflex which leads to haemodynamic effects such as venoconstriction and a bypass of pulmonary circulation

49
Q

Blood/blood products? What do they do? Examples?

A

Provide circulating volume but not expansion (ie 1L of blood gives 1L of circulating volume increase)

50
Q

Benefits of enteral fluids? Advs over parenteral?

A

‘Feeds the gut’
Natural
No need for sterility
Owner/farmer can do

Parenteral needs sterility, risk of air/thrombus embolism, expensive, veterinary procedure

51
Q

How to monitor fluid therapy?

A

Urine production/specific gravity
Pulse quality
Skin tent
PCV/TP etc

52
Q

How to decide on an alagesic drug?

A
Type of pain expected
Degree of pain expected
What is available
Ease of administration
Licensing
Safe to use
53
Q

What parts of the pain pathway do different analgesics work on?

A

NSAIDs and opiates: nerve terminal, dorsal horn of spinal cord, brainstem/cerebrum
NMDA antagonists, Calcium channel blockers and tramadol: dorsal horn and brainstem/cerebrum
Local anaesthetics: nerve terminal only

54
Q

NOLANP?

A
NSAIDs
Opioids
Local anaesthetics
A2 agonists
NMDA antagonists
Paracetamol
55
Q

NSAIDs: How do they work? Contraindications? Side effects?

A

Work on COX enzymes
Inhibit prostaglandin release
Don’t use if think animal is hypotensive as reduces renal perfusion (less of problem in horses, still use in colic cases)
Long term use - GI upset

56
Q

What affects the onset of action, duration of action and potency of local anaesthetic drug?

A
Onset of action:
- Less alkaline pH = faster onset
Duration of action:
- Increased protein binding = longer duration
- Vasodilation = shorter duration
Potency:
- Increased lipophilicity = increased potency
- Small size = increased potency
57
Q

What toxicities do local anaesthetic drugs have?

A
Lidocaine:
- Respiratory depression
- Seizures
Bupivacaine:
- Cardiotoxicity
58
Q

Paracetamol: Licensing?

A

Licensed in dogs in combination with codeine
Can use with NSAIDs or steroids (despite datasheet)
Not cats

59
Q

Which drugs are used for chronic pain?

A

As for acute, plus:

  • Gabapentin
  • Amantadine
  • Antidepressants
  • Green lipped mussel
  • Elk velvet antler
  • Capsacin
60
Q

What are the main peri-anaesthetic complications?

A

Hypotension
Hypoventilation/hypoxaemia
Hypothermia
Pain

61
Q

Risk factors for perianaesthetic mortality? Mortality rate in different species?

A

Pre-existing patholgies
Overweight/underweight
Procedure urgency and duration
Emergency procedures

Dogs: 1 in 600 overall, 1 in 75 ASA 3-5
Cats: 1 in 400 overall, 1 in 70 ASA 3-5
Horses: 1 in 100 non colic, 1 in 20 colic

62
Q

What should blood pressure kept at under anaesthetic? Why?

A

MAP >60mmHg for perfusion of vital organs (brain, heart, kidneys)
- >70mmHg often wanted in large horses to reduce risk of myopathy
SAP >80mmHg
Hypotension if MAP <60 or SAP <80 -> hypo perfusion of vital organs and extremities -> inadequate delivery of oxygen and removal of waste products

63
Q

Causes of hypotension under anaesthesia?

A
Hypovolaemia:
- Haemorrhage
- Pre-existing fluid deficits
- Fluid loss due to evaporation
- "Third" spacing
- Inadequate intra-op fluids
Vasodilation:
- Anaesthetic drugs
- Severe metabolic or respiratory acidosis
- Endotoxaemia
- Septicaemia
- Anaphylactic reaction
Decreased CO due to arrhythmias:
- Bradycardia
- AV block, AF, VT
Obstruction of venous return:
- Secondary to IPPV
- Pericardial effusion, mediastinal tumours, tension pneumothorax, surgical retraction of organs
64
Q

What to do if hypotension under GA?

A

Check BP device - cuff/transducer position and repeat measurement
Anaesthetic level - lighten?
Fluids - bolus
Positive inotropes - B1 agonist (Dobutamine in horses)
Vasopressors - a1 agonist
Positive chronotropes

65
Q

Consequences of intra-op hypotension?

A

Poor recovery
Myopathy
Organ injury

66
Q

Causes of bradycardia under GA? Treatment?

A
Drugs - high doses of mu opioids, a2 agonists
High vagal tone
Hypothermia
CNS disease (increased ICP)
Hyperkalaemia

Treatment:

  • Check if necessary, what’s the BP?
  • Atipamezole if a2 agonists were used
  • Anticholinergics: atropine vs glycopyrrolate
  • Treat underlying cause
67
Q

Causes of sinus tachycardia under GA? Consequences? Treatment?

A

Caused by SNS stimulation:

  • Pain
  • Inadequate anaesthesia
  • Hyperthermia
  • Hypotension
  • Hypovolaemia
  • Hypoxaemia
  • Hypercapnia
  • Hypoglycaemia

Consequences:

  • Decreased diastolic filling and decreased ejection and coronary perfusion time -> myocardial ischaemia
  • Greatly reduced CO

Treat underlying cause of SNS stimulation

68
Q

What is hypoxaemia? Measurements?

A

= Abnormally low O2 content in the systemic arterial blood (PaO2)
Mild: 80-90mmHg
Moderate: 60-80mmHg
Severe: <60mmHg

69
Q

What are the general effects of anaesthesia on respiratory system?

A

Respiratory centres and chemoreceptors are depressed by GA agents and mu opioid agonists -> reduced ventilatory drive
Depressant effects of anaesthetic drugs on intercostal muscles and diaphragm -> hypoventilation and hypercapnia
Lung volume at end of expiration (FRC) is reduced, esp in dorsal recumbency
When FRC is close or less than closing capacity -> atelectasis develops:
- Gas trapped in alveoli absorbed into circulation
- Big problem in obese patients
Atelectasis also develops as a result of lung compression and surfactant dysfunction
Blood flowing to atelectatic areas is not taking part in gas exchange -> shunt

70
Q

How to recognise hypoxaemia?

A

Gold standard is arterial blood gas to measure PaO2
Pulse oximetry: SpO2
Visual inspection of MM colour:
- Cyanosis when >5g/dl of deoxyHb in the blood
- Normal Hb is around 15g/dl
- If animal is anaemic with Hb<5g/dl, can never become cyanotic
- Cyanosis is late indicator of hypoxaemia

71
Q

Pulse oximetry:

A
Non invasive method to measure peripheral oxygen saturation (SpO2) of Hb
Affected by:
- vasoconstriction
- movement
- light
Add from rotation notes
72
Q

Causes of hypoxaemia under GA?

A
Inadequate O2 supply: 
- Empty cyclinder
- Blocked hosing
Airway obstruction:
- Blocked/kinked ETT or respiratory tract (e.g. with blood/mucus)
Profound hypoventilation -> hypercapnia:
- Opioids
- Dorsal recumbency
V/Q mismatch and shunt
Circulatory failure
Poor gas exchange (increased diffusion barrier)
Increased O2 requirements
73
Q

What to do if hypoxaemia under GA (e.g. SpO2<90%, PaO2 low on blood gas analysis)?

A

Check O2 supply and patency of ETT
Give O2/increase inspired O2 if possivle
IPPV to reduce effects of hypoventilation/hypercapnia on promoting hypoxaemia
B2 agonist (salbutamol inhaler in horses, 2 puffs/100kg)

74
Q

Consequences of hypothermia under GA?

A

CV changes:
- Bradycardia
- Hypotension
- Increased blood loss/coagulopathy
- PCV increases -> blood more viscous which increases myocardial work
Respiratory changes:
- Hypoventilation with CO2 retention (respiratory acidosis)
- Slight left shift of Hb/O2 dissociation curve -> impedes tissue oxygen delivery
- Decreased mucociliary activity -> increased risk of airway obstruction/infection
- Immunosuppression - increased risk of infections
CNS depression:
- MAC reduction so beware of deepening anaesthesia
Post-op:
- Slow recovery (slow metabolism/elimination of drugs)
- Shivering once >34C -> increase metabolic rate, increases oxygen demand, increases cardiopulmonary work
- Delayed wound healing, increased wound infection

75
Q

Signs of anaphylaxis?

A
Hypotension
Tachycardia
Tachypnoea
Arrhythmias
Bronchoconstriction
Sweating, hives (horses)
Facial/periorbital/sublingual/laryngeal oedema
Death
76
Q

Difference between anaphylactic and anaphylactoid reactions?

A

Anaphylactic reaction = IgE mediated, requires previous exposure to the agent
Anaphylactoid reaction = IgE independent, no immune trigger necessary
Both cause rapid degranulation of mast cells -> histamine release, PG, LT

77
Q

Treatment of anaphylaxis?

A

Antihistamines - chlorphenamine
Corticosteroids
CV support - Iv fluids, epinephrine CRI, O2, CPR