Page 72 - BSAVA Guide to Pain Management in Small Animal Practice
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5  |  Pharmacological treatment of pain



        VetBooks.ir     1 . It should be appreciated that the dose     einberg et al.,      . If lipid rescue is
                                                   not available, symptomatic treatment (anti-
             was a cumulative dose administered over a
                                                   convulsants, antimuscarinics, antiarrhythmics,
             signi cant amount of time and not as a rapid
             bolus. For comparison, another study reported a   inotropes, vasopressors and  uids  can
             single rapid intravenous bolus of 11 mg kg of   be attempted to control clinical signs while
             bupivacaine to cause severe cardiovascular   the toxic drug is cleared by the body (Aprea
             depression in dogs (Liu et al., 198  .  et al.,   11 .
               A study in cats demonstrated that, in a
             model of continuous intravenous infusion,   Alpha-2 agonists
             neurotoxicity occurred at 1  mg kg for lidocaine   Alpha   agonists such as medetomidine and
             and 4 mg kg for bupivacaine.  he cardiotoxic   dexmedetomidine (its active enantiomer) are
             dose was found to be 47 mg kg for lidocaine   widely used in small animal practice for
             and 18 mg kg for bupivacaine.  hile all cats in   sedation and pre-anaesthetic medication. They
             the lidocaine group could be resuscitated,   1    also have analgesic properties. They bind to
             cats in the bupivacaine group could not   alpha   adrenergic receptors in the cerebral
              Chadwick, 198  .                     cortex and locus coeruleus of the brain, causing
               It should be pointed out that these toxic   sedation, analgesia and a reduction in
             doses are all obtained administering the drug   sympathetic tone, and in the dorsal horn of the
             intravenously, thus they represent the clinical   spinal cord, causing analgesia. The mechanism
             scenario of accidental intravenous    of analgesia is complex and not well
             administration of a supra-clinical dose of local   understood. Agonism of alpha   receptors in
             anaesthetic, not the uncomplicated use in   peripheral and pulmonary blood vessels causes
             locoregional anaesthesia (Aprea et al.,   11 .  vasoconstriction, hypertension, re ex
               Published data about toxic intravenous   bradycardia and decreased cardiac output.
             doses should be taken with a pinch of salt, as    ther e ects include hypothermia, decreased
             the rate of absorption from tissues should be   gastrointestinal motility, diuresis and
             taken into account in a clinical setting, and   hyperglycaemia. All these e ects are dose
             therefore the current suggested maximum dose   dependent, and can be antagonized using
             is likely to be fairly conservative, as   atipamezole, although this also removes any
             demonstrated by clinical studies in humans. The   analgesic e ect.
             risk of toxicity probably is greater in smaller   Because of their sedative and
             animals, as a relatively small increase in the   cardiovascular e ects, alpha   agonists are
             administered volume results in a greater   unsuitable for use as the primary or sole
             increase of the amount of drug administered on   analgesic, but may provide additional analgesia
             the basis of body mass (Rosenberg et al.,    4 .  when used as part of an anaesthetic protocol.
               In the event of toxicity, intravenous infusion   They act synergistically with opioids. The
             of a lipid emulsion has been shown to dramati-  analgesic e ect is of a shorter duration than the
             cally improve haemodynamic side e ects of   sedative e ect, and re uires higher plasma
             bupivacaine overdose in experimental settings,   concentrations. They may be useful for treating
             and there are case reports describing its   neuropathic pain (Murrell and Hellebrekers,
             successful clinical use in veterinary medicine        .
             (Feldman et al., 1991;  einberg et al.,     ;
             O’Brien et al.,   1  . It is widely used in humans,   Clinical use
             although recently its e cacy and safety have   Inclusion of alpha   agonists as part of the
             been questioned (O’Brien et al.,   1 ; Picard   sedation or pre-anaesthetic protocol may
             and  eek,   16; Rosenberg,   16 . Lipid rescue   provide additional analgesia for the patient.
             protocols reported in veterinary medicine    owever, because of the cardiovascular e ects
             suggest infusing 1.  ml kg Intralipid     over   of these drugs, they are usually reserved for
             1     minutes, and repeating this if necessary   healthy patients without cardiac disease.

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