The UK Society for Intravenous Anaesthesia
Based in the UK - as a resource for Anaesthesia Worldwide

Glasgow Meeting - May 2003

Total Intravenous Anaesthesia in Horses

R.E. Clutton, Division of Veterinary Clinical Studies, University of Edinburgh, Edinburgh EH25 9RG

While horses represent a high anaesthetic risk in comparison to smaller domestic species, they may still be anaesthetised by any member of the RCVS, whether or not the latter have specialised training in anaesthesia.  This partly explains why TIVA is the norm rather than the exception, as the veterinary surgeon/anaesthetist has an aversion to complex techniques, i.e., those involving anaesthetic machines and breathing systems.  Another reason is that the majority of routine operations performed on horses, e.g., dental extractions, castration, superficial wound management, are performed at the stable, i.e., under field conditions.  This favours techniques which are simple, have minimal equipment and personnel requirements and so are readily deployed in a range of environmental conditions.  In its simplest, and possibly most common form, field equine anaesthesia requires only a head collar, lead rope, a subject, an intravenous catheter (optional), needles, syringes, one or two bottles of drug, an anaesthetist/surgeon and an (optional) assistant.  Nevertheless, accurate risk assessment and case selection, and restriction to simple, frequently performed and short operations render these minimalist TIVA techniques rather safe.  In many situations, surgery may be performed on the standing animal using TIVA techniques referred to generically as standing surgical anaesthesia (SSA).

Problems in equine anaesthesia

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Size.  By necessity, drugs for large animals are either highly potent (dangerous) or concentrated (irritant) solutions.  Large (costly) doses are required.  An accurate subject mass is rarely available, and while it is difficult to overdose (large) horses, the consequences of under-dosage may be catastrophic for the subject and attendants.  Larger horses will need a larger casting area if general anaesthesia is planned and there is an increased risk of trauma on induction.

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Temperament.  Many practical problems associated with controlling undomesticated horses before anaesthesia are obvious, e.g. risk of injury, need for skilled assistance, risk of drug self-administration, denied venous access (time wastage, technique determination) poor quality recovery.  However, there are subtle interactions between a horse’s temperament and anaesthetics.

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P(A-a)O2  The combination of recumbency and general anaesthesia, combined with time and other subject - related factors produces large P(A-a)O2 values.  Hypoxaemia may predispose to myositis and if severe and, or prolonged, neurological injuries, cardiac arrhythmia and probably cardiac arrest.  Factors contributing to excessive P(A-a)O2 include recumbency, duration of anaesthesia, size, & conformation, body position, factors lowering FRC (pregnancy, hobbling, recent feeding, pregnancy), disease, drugs affecting PHV.

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Equine post-operative myopathy (EPAM), a sporadic serious complication associated with general anaesthesia in horses producing signs ranging from transient (24 - 72 h) lameness to severe generalised myositis necessitating euthanasia.  The pathogenesis is unclear but muscle hypoperfusion caused is probably involved.  Poor positioning, or excessive traction imposed by injudicious use of hobbles causes muscle ischaemia in susceptible muscle groups, e.g. triceps brachii.  Prolonged hypotension, particularly when produced by halothane, seems to exacerbate this condition.  Pre-disposing factors include: prolonged recumbency; prolonged hypotension; poor positioning; muscle tension; poor substrate?; animal size; mass; degree of muscling (breed, degree of training, energy level of diet).

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Maintaining unconsciousness. For several reasons it may be difficult to keep horses unconscious during anaesthesia.  These include: individual variation to anaesthetics and surgery, slow response to injected drugs; difficulty / variability in determining depth of anaesthesia; effect of surgical stimulation on consciousness.

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Haemodynamic instability and Level Of Training.  It is felt that anaesthetising horses fresh from training and on high levels of nutrition is associated with greater risk than in unconditioned animals. 

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Trauma on Recovery.  Injury is more likely during recovery than during induction, and is likely when very heavy animals, weakened by drugs and, or surgery attempt prematurely, (by pain?) to stand, e.g. the advanced pregnancy.  These may require physical assistance or else fractures may occur.  Myositis may result.  It seems that excitable animals are more likely to recover badly, especially after painful procedures. 

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Post-operative airway obstruction.  Airway obstruction does not occur when endotracheal tubes are in situ.  However, severe stertor may be apparent once the airway is extubated.  In the lightly anaesthetized animal this can cause severe panic and frenzied attempts to stand, which make the obstruction worse by increasing ventilatory efforts while increasing airflow resistance through increased turbulence.  Common causes include: turbinate mucosal swelling; epiglottic eversion; and post-anaesthesia Respiratory Obstruction (PARO).

Standing surgical anaesthesia

The objectives of standing surgical anaesthesia (SSA) are to produce conditions for surgery in the standing animal without ataxia.  Operations performed under SSA include dental extractions, ocular operations, wound debridement, castration, laparoscopy.  SSA is useful in high risk cases, when assistants are unavailable, or when overall conditions for general anaesthesia are unsatisfactory.  SSA is safer for the horse, but less safe for the surgeon.  Drugs involved in the production of SSA include acepromazine (or other phenothiazines) combined with a 2 agonists and opioids components.  The choice of a2 agonist and opioids are governed by factors indicated in table 1 and 2 respectively. 

Table 1.  a2 Components

 

Xylazine

Detomidine

Romifidine

 

 

 

 

Duration

~ 20 mins

~ 80 mins

> 80 mins

Cardiovascular status

! !

! ! ! !

! !

Sedation

+++

++

++

Muscle relaxation

++

+++

+

Ataxia

++

++++

+

Analgesia

++

++

++

Cost

£££

££

£

 

Table 2; Opioid Components

 

duration

analgesia

sedation

side effects

CDR

cost

 

 

 

 

 

 

 

Morphine

~ 2 - 4 h

+++

+++

++

2

p

Pethidine

~ 30 min

++

+/-

+++

2

pp

Methadone

~ 2 - 4 h

+++

+

+

2

ppp

Butorphanol

~ 2 - 4 h

++

+/-

+

3

£

Buprenorphine

~ 3 - 6 h

++

+/--

+

3 ~

££

Pentazocine

~ 30 min

?

+/--

?

3

£

True surgical anaesthesia is achieved when local anaesthetic techniques - infiltration, conduction block, or more complex neuraxial techniques - are superimposed upon SSA.  Pre-emptive analgesia is usually provided by the pre-surgical intravenous (IV) administration of NSAIDs, e.g. flunixin, phenylbutazone, carprofen.  Developments to this basic technique include the infusion of detomidine, butorphanol and, or lidocaine.

General anaesthesia: single doses with increments.

General anaesthesia is required for those operations, e.g. midline laparotomy, which cannot be performed in standing animals, when immobility is required, or when operator safety is of paramount importance.  When short procedures are anticipated, most practitioners would attempt to rely on a single injection technique. 

For many years, drug combinations based on chloral hydrate were commonly used, but were not particularly safe.  In the late 1960s, a proprietary etorphine / acepromazine mixture (Immobilon) proved very popular, principally because of the dramatic recovery observed when the opioid component was antagonised with diprenorphine.  Poor operating conditions and the lethality of this combination in veterinary surgeons, led to its replacement by single injection techniques based on acepromazine, succinylcholine and thiopental.  These in turn gave way to techniques in which a2 agonists were used for pre-anaesthetic medication and induction completed with either thiopental or ketamine.  The choice of pre-anaesthetic medication influences the “quality” of anaesthesia.  See table 3.

Table 3.  Field (General) Anaesthesia In Horses; Comparison of a2 - Ketamine Techniques.

 

Xylazine

Detomidine

Romifidine

 

 

 

 

Equi-potency

1.0 mg kg-1

20 mg kg -1

80 mg kg -1

Duration

 

 

longest*

Induction

+++++

+++ / --

++++ / -

Surgical anaesthesia

3 - 12 - 15 min

2 - 18 mins

8 - 15 mins

Surgery

A1

A1

A1

Recovery

++

+ / -

++++

Environment

sensitive

sensitive

robust

Pros

Induction

Mobility

Injection

volume

Recoveries

Mobility

Cons

Recovery signs

DOA

Recoveries

d rules

Inductions

Cost

£££

£

£

With embellishments, these techniques remain currently popular.  The author’s current favourite technique is detailed below:

 

PAM: romifidine 100 mg kg-1 IV

            Wait 5 minutes

I:     ketamine 2.5 mg kg-1 + diazepam 50 mg kg-1 IV

        Upon recumbency

Morphine 150 mg kg-1 IV

Flunixin 1.1 mg kg-1 IV

Top-ups (as required) ketamine (0.25 – 1.0 mg kg-1) + midazolam (12.5 – 50 mg kg-1

General anaesthesia: Infusions

The principal problem with contemporary techniques is the unpredictable duration of action, with the need for frequent (embarrassing) incremental dosing (clients are usually present at field operations).  For this reason, and the need to provide more stable conditions, glyceryl guaiacolate ether (GGE), or guaifenesin has become increasingly popular in TIVA techniques. 

GGE is regarded as a spinally-acting muscle relaxant and is used to provide maintenance conditions as part of several total intravenous anaesthetic techniques.  It acts as a muscle relaxant and a vehicle for other drugs.  Its mechanism of action is poorly understood; it acts on polysynaptic reflex arcs in the spinal cord, reticular formation and sub-cortical areas of the brain in a mephenesin-like manner. Its prominent feature is an ability to depress internuncial neurone transmission in the spinal cord without impairing breathing.  in North America, GGE is considered to have CNS depressant effects beyond muscle relaxation; elsewhere, it is not used as a sole anaesthetic but always given with other CNS depressant drugs.  

The fact that GGE solutions > 15% lead to haemolysis means that dilute solutions have to be infused.  The infusion of a2 agonist / ketamine / GGE solutions to produce conditions for more complex operations lasting up to 60 minutes is becoming increasingly common in veterinary practice, despite the drugs potential for accumulation.

General anaesthesia: advanced (non-field) TIVA techniques

Propofol has been assessed alone, and with other drugs for the provision of TIVA in horses.  Infusion rates of 0.18 – 0.33 mg kg-1 minute–1 have been used to maintain anaesthesia for an hour or so.  Haemodynamic variables are usually satisfactory although mean arterial pH tends to decrease, while modest hypercapnia and hypoxemia (PaO2 values of 42 to 57 mm Hg) are encountered.  Occasionally arterial hypotension is severe.  Recovery ranges from good in the majority of horses and acceptable in the rest.  Mean recovery times are usually rapid, being, after 1 hour about 60 +/- 30 minutes with 2 - 3 attempts to stand.

Propofol has been combined with ketamine for TIVA in horses.  After a loading dose propofol 0.5 mg kg–1 propofol was infused at 0.124 (0.009) mg kg-1 minute–1 along with ketamine at 40 mg kg–1 minute–1.  Respiratory and cardiovascular variables were better maintained compared with a sole propofol infusion in which arterial hypotension and marked respiratory depression were evident.

Propofol has also been infused with the a2 agonist medetomidine in horses.  After pre-anaesthetic medication with medetomidine (7 mg kg–1 ) anaesthesia was induced with propofol (2 mg kg-1 IV) and maintained for 4 hours, using an infusion of medetomidine (3.5 mg kg–1 hour –1 IV) and propofol at a rate ranging from 0.06 to 0.1 mg kg-1 minute–1. Mean arterial blood pressure was stable, mean PaO2 & PaCO2 did not change significantly but hypoxaemia was evident in some animals (minimal PaO2, 47 mm Hg).  Recovery was fast and uneventful.

It is unlikely that TCI or complex TIVA techniques based on ultra short-acting drugs will ever gain popularity in equine anaesthetic practice outside the institutions.   Their expense, complexity and the difficulty in managing side-effects put such techniques at a considerable disadvantage against contemporary options.

 

 

Page last revised: August 07, 2008.

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