Abstract:
The black-footed cat (Felis nigripes) is the rarest, smallest wild felid species of southern Africa
and is categorized as vulnerable on the IUCN Red List 2012 (Sliwa 2008). These cats are
solitary, nocturnally active predators with a high metabolic rate. In order to fuel this metabolism
they hunt all night, catching and consuming approximately one fifth of their body weight. In
order to facilitate research studies and sample collection a reliable, safe, fully reversible
anaesthetic drug combination for use in the field is imperative to enable the cats to resume
their hunting as quickly as possible post anaesthesia. Both the captive and the free-ranging
populations face many survival challenges, including renal amyloidosis, and the use of an
anaesthetic drug combination that does not compromise renal function would be of major
benefit. To date, there is no published data on the physiological effects of any anaesthetic
protocol in this species. The butorphanol-medetomidine-midazolam combination has been
safely and successfully used in a variety of domestic and other wild animal species, and
recently it has been used in black-footed cats in the field and zoo setting.
We used the butorphanol-medetomidine-midazolam drug combination to anaesthetise blackfooted
cats, both in captivity and in the wild. As the drug doses currently used in wild freeranging
animals are approximately twice as high as those required in captive animals,
concerns have been raised regarding the physiological safety of using a higher dose of this
anaesthetic combination in these animals. My aim was to document, evaluate and compare the
anaesthetic and physiological effects induced by the use of two different doses of the
butorphanol-medetomidine-midazolam combination to effectively and safely anaesthetise
captive and free-ranging black-footed cats.
Due to the differing physiological stressors associated with the capture methods in the freeranging
black-footed cats these animals were divided into two groups, namely those that were
dug out of burrows, and those that had been caught after a short intense chase. Once
captured, all the cats were hand injected into a hind limb muscle group with the anaesthetic
drug combination. Injections for different mass categories had been prepared prior to capture
and the doses that were given were based on quick visual estimates of an animal s mass. In
total, 23 black-footed cats, nine captive and 14 free-ranging, were anaesthetised. Times to
induction, quality of anaesthesia and times to recovery after reversal of the effects of the
anaesthetic drugs were recorded. Physiological variables recorded every 10 minutes during
anaesthesia were heart rate, respiratory rate, SpO2, ETCO2, rectal temperature, systolic, mean
and diastolic non-invasive blood pressures. Three central venous blood samples, taken at 20-
minute intervals during anaesthesia, were analyzed for pH, lactate and glucose concentrations
and cTCO2 and base excess were determined. Anaesthetic induction and recoveries were quick, smooth and uneventful with mean times of
5.9 minutes and 4.5 minutes respectively. We determined that even higher doses than our
original target doses were required for induction and maintenance of a 45 minute anaesthesia.
The quality and depth of anaesthesia were optimal for the minor sampling procedures
performed, with the majority of cats maintaining a deep level of anaesthesia (Score 5) for 45
minutes before the antagonist combination was administered. Cardiac variables remained
within normal physiological limits throughout the anaesthesia. Mild hyperventilation, moderate
hypoxaemia and a mild to moderate lactic acidosis were initially recorded in the chased freeranging
animals. The respiratory and acid-base variables in the other two groups of cats were
within clinically acceptable limits. A gradual decrease in body temperature, despite the animals
being placed on hot water bottles, was recorded in all the cats and thus a better means to
mitigate this heat loss is recommended. Hyperglycaemia was recorded in all black-footed cats,
and the fear, anxiety and exertion of the chase would have contributed to the hyperglycaemia
induced by the use of the ?2 adrenoreceptor-agonist medetomidine in the anaesthetic drug
combination.
Intramuscular injection of butorphanol, medetomidine and midazolam in black-footed cats
induces rapid and smooth induction and is a safe and effective anaesthesia in both captive and
free-ranging animals, despite higher doses used in free-ranging animals. The method used to
capture free-ranging animals had a greater influence on the physiological stability of the
anaesthetised animals than did the dose of drugs used. If black-footed cats exert themselves
during a chase, before they receive this anaesthetic drug combination, they develop mild to
moderate hypoxaemia, tissue hypoxia and metabolic lactic acidosis during the anaesthesia.
Therefore, oxygen supplementation during anaesthesia is recommended in black-footed cats if
they are chased directly before induction.