Page 58 - BSAVA Guide to Pain Management in Small Animal Practice
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5  |  Pharmacological treatment of pain



        VetBooks.ir  cleaned with water. The skin should be allowed   animals or children in the household who could
                                                   be at risk, and will the client ensure safe and
             to dry, the patch applied  rmly and covered
             with an adhesive dressing. An Elizabethan collar
                                                   signed, informed consent from the client. After
             may be required to prevent the animal licking or   appropriate use of the patch? It is wise to obtain
             removing the patch. In the time since most of   use, the patch should be removed and folded
             the veterinary studies have been published, the   inwards while wearing gloves, and returned to
             type of patch has been changed from a liquid   the practice for appropriate disposal, or the
             gel patch to one with the drug contained in an   animal should return to the clinic for proper
             adhesive matrix. Therefore, it is unknown   removal and disposal of the patch.
             whether the matrix type patches confer similar
             pharmacokinetics in animals. The rate of   Remifentanil: Remifentanil is an unlicensed,
             absorption from the patch to the skin depends   ultra-short-acting full MOP agonist. Its onset
             on the surface area of the patch; several si es   and duration of action are less than 6  seconds,
             are available, and patches may be partially   meaning that it is only suitable for intravenous
             covered to reduce the surface area in contact   infusion, no bolus is required, and the dose rate
             with the skin if required. Absorption also   is rapidly titratable. The very short duration of
             depends on skin perfusion, which is in uenced   action is due to its metabolism in plasma by
             by factors such as skin thickness, skin and   esterase enzymes. The main indication is for
             ambient temperature, volaemic status and   intraoperative analgesia in patients with liver
             degree of vasoconstriction. Care must be taken   dysfunction. Since its e ects resolve almost as
             if a patient is being actively warmed that the   soon as it is discontinued, it is imperative that
             patch is not over-warmed as this has been   analgesia is provided with another opioid for the
             shown to result in high plasma fentanyl   postoperative period.
             concentrations, with the possibility of over-
             sedation and/or severe respiratory depression.   Pethidine: Pethidine (meperidine) is a full MOP
              he uptake of fentanyl is slow; onset of   agonist that has been licensed in dogs and cats
             analgesia is about  4 hours in dogs or 1  hours   for many years. Because it was originally
             in cats and therefore the patch should be   developed as an anticholinergic agent, it causes
             applied the day before elective surgery, or   less bradycardia than other opioids and may be
             another means of analgesia provided for the   useful in patients whose cardiac output is rate
              rst 1  to  4 hours. Variable uptake means that,   dependent, for example, paediatric patients or
             in some patients, adequate analgesia is not   those with cardiac disease. Pethidine causes
             achieved with a patch alone, emphasizing the   histamine release and should not be
             importance of regular pain assessment.   administered intravenously. Since it is less
             Analgesia can be supplemented with another   potent than other opioids, a large volume is
             opioid (e.g. methadone) if required and   required for intramuscular injection.
             multimodal analgesia is recommended. The   Intramuscular injection of pethidine is painful.
             duration of use of a single patch application is   These factors, and its short duration of action
             about 7  hours from the time of application,       to 1   minutes  make it unsuitable for
             bearing in mind that adequate analgesic levels   providing sustained analgesia, but is it useful as
             will not be reached for the  rst 1  to  4 hours.   a sedative or pre-anaesthetic medication in
             Although absorption from the patch declines   selected cases. Its metabolite, norpethidine
             rapidly after   days of use, a used fentanyl   (which is renally excreted), can cause central
             patch still retains a signi cant amount of   nervous system stimulation and seizures. This is
             fentanyl, which could be harmful to a human if   unlikely to occur except in overdose or in
             ingested (Reed et al.,   11 . If planning to   animals with severe renal dysfunction. Pethidine
             discharge a patient with a fentanyl patch   can be a contributor to serotonin toxicity (see
             attached, careful consideration of the risks   textbox later), and should not be used with other
             should be made; for example, are there other   drugs that increase serotonin concentrations.

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