Page 25 - BSAVA Guide to Pain Management in Small Animal Practice
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BSAVA Guide to Pain Management in Small Animal Practice



        VetBooks.ir  administration of lidocaine systemically to small   suggesting that doses higher than 1  g kg h
           animals. Studies have investigated the
                                                  might be needed to provide signi cant
                                                  analgesia in the absence of other analgesic
           antinociceptive e ects of a lidocaine CRI in
           dogs undergoing surgery and found con icting   drugs  van  ostrom et al.,   11 .  his study also
           results, with one study showing that lidocaine   clearly showed that it is not possible to obtain
           blunted autonomic responses to surgery   analgesia from alpha   agonists without
             rtega and Cru ,   11 , and another showing   concurrent sedation. Consideration must be
           no e ect of lidocaine on autonomic responses   given to the cardiovascular e ects of alpha
            Columbano et al.,   1  . Anecdotally, lidocaine   agonists when deciding whether to use even a
           is reported to be e cacious in the management   low dose CRI in individual patients because the
           of visceral pain although there is limited   cardiovascular e ects are still apparent.
           evidence to support this view.  oses of    Infusions of alpha   agonists will also increase
               g kg min preceded by a loading dose of    urine production; therefore, bladder
             mg kg administered over 1  minutes are   management  taking dogs outside fre uently to
           recommended in dogs; be aware that lidocaine   toilet or expressing the bladder  is important in
           will reduce the  AC of the inhalant agent so   dogs that receive an alpha   agonist CRI.
           depth of anaesthesia should be monitored
           carefully when lidocaine is administered during   Ketamine
           surgery. Lidocaine infusions are not    etamine is widely used as part of in ectable
           recommended for analgesia in cats due to   anaesthesia protocols and will contribute to
           negative e ects on the cardiovascular system   perioperative analgesia through antagonism of
            Pypendop and Ilkiw,      .            the N methyl   aspartate receptor.  ore
                                                  recently, the analgesic e ects of
           Alpha-2 agonists                       subanaesthetic doses of ketamine have been
           Alpha   agonists such as medetomidine and   recogni ed  Laskowski et al.,   11;  ang et al.,
           dexmedetomidine are widely used for      14 , whereby ketamine is administered as a
           premedication and as such contribute to   CRI during surgery and postoperatively at
           perioperative analgesia.  owever, the analgesia   doses ranging from   1   g kg min. A few
           from clinical doses of alpha   agonists is   studies have been conducted in dogs
           relatively short  1   g kg dexmedetomidine   investigating the analgesic e ects of low dose
           provides analgesia for approximately 4    ketamine administered by CRI and found
           minutes ; therefore, dexmedetomidine or   variable results about the e cacy of this
           medetomidine must be given by a CRI to   intervention.  agner et al.        investigated
           provide sustained analgesia.  ne study has   the analgesic e ects of 1   g kg min
           investigated the postoperative analgesic e ects   ketamine administered intraoperatively
           of dexmedetomidine given by CRI in dogs after   followed by    g kg min ketamine
           invasive surgery and showed similar analgesia   postoperatively in dogs undergoing forelimb
           was provided by a dexmedetomidine CRI at    amputation and found that pain scores were
           1  g kg h or morphine  .1 mg kg h  Valtolina   signi cantly lower in dogs that received
           et al.,    9 .  owever, a signi cant number of   ketamine compared with a group that did not
           dogs in both groups re uired rescue analgesia   receive a ketamine CRI.  owever, the
           with morphine highlighting the importance of   di erence in pain scores was numerically small
           pain scoring with any analgesic regimen. An   and the biological relevance of this di erence
           experimental study in dogs compared the   can be  uestioned. In contrast, Sarrau et al.
           sedative and analgesic e ects of           7  found no e ect on postoperative
           dexmedetomidine alone using a          analgesic re uirements between dogs
           neurophysiological model and found that doses   undergoing mastectomy receiving either a
           of      g kg h dexmedetomidine were    high dose or low dose ketamine CRI and a
           re uired to provide analgesia in this model,   control group that did not receive ketamine. In

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