Page 71 - BSAVA Guide to Pain Management in Small Animal Practice
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BSAVA Guide to Pain Management in Small Animal Practice



        VetBooks.ir  response to lidocaine. Despite this no longer   Currently the author [FC] is not aware of any
           being a possibility, a positive response to
                                                  prospective study or even case report
                                                  supporting the e cacy of lidocaine patches in
           lidocaine infusion is still an invaluable tool to
           diagnose neuropathic pain, in view of utilizing   providing analgesia in dogs and cats, despite
           other drugs inhibiting or blocking sodium   the products being available and having been
           channels. In a clinical setting, lidocaine infusion   used for many years (Meier et al.,     ; Burch et
           plays a big role, at least in dogs, in the control of   al.,    4;  eiland et al.,    6;  o et al.,    7;
           pain syndromes that are poorly responsive to    eil et al.,    7;  o et al.,    8; Saber et al.,
           opioids and NSAIDs. The commonly used      9;  ilhooly et al.,   11; Bai et al.,   1 ;
           protocol suggests a loading dose of 1   mg kg,   Joudrey et al.,   1  .
           followed by a continuous infusion of     mg
           kg h. Commonly observed side e ects are   Toxicity
           sedation and reduced appetite, but they are   Cardiovascular and neurological toxicity are
           generally mild and self-limiting, and rarely   ma or side e ects secondary to systemic
           require discontinuation of the therapy,   absorption or administration of local
           especially in the presence of neuropathic pain   anaesthetics. At high concentrations, local
             aler et al., 1996;  olli e et al.,    7;  utson et   anaesthetics also a ect potassium and calcium
           al.,   1 ; Papapetrou et al.,   1 ; Pr eklasa   channels, and this could further contribute to
            us y ska et al.,   16 .               systemic toxicity (Nakahira et al.,   16 .
                                                     The most common causes of severe
           Transdermal administration             systemic toxicity are accidental intravascular
           Lidocaine can also be delivered transdermally   administration and rapid systemic absorption
           using a patch, which is licensed to treat   after administration of large doses of
           postherpetic neuralgia (PHN) pain in humans.   anaesthetics. Neurological signs of toxicity are
           The drug transferred to the skin is believed to   depression and twitching, progressing to
           induce local analgesia by inhibiting   generalized seizures (Cox et al.,     ; Beecroft
           spontaneous discharge of injured small   and  avies,   16 .  oxic doses after intravenous
           nociceptive  bres  C and Aδ), without   administration have been well characterized in
           signi cantly a ecting the function of large   dogs, suggesting an acute neurological toxicity
           sensory  bres, therefore preserving sensation.   occurring for doses of bupivacaine and
            hile lidocaine patches are an e ective   ropivacaine greater than     mg kg, and
           treatment for PHN pain in human patients, they   greater than 1  mg kg for lidocaine   eldman et
           appear less e ective in treating neuropathic   al., 1989 .
           pain of di erent origin.  he role of lidocaine   Cardiovascular toxicity presents as
           patches in treating postoperative pain in   progressive cardiovascular depression, with
           humans is still controversial, with a few studies   arrhythmias, including tachycardia, ventricular
           and case reports reporting some e cacy, and   tachycardia and ventricular  brillation. In a
           meta-analyses suggesting that the overall   continuous intravenous infusion model, the
           e ect is negligible.                   cumulative dose that caused cardiovascular
              Systemic absorption is minimal, and not   collapse was  1 mg kg for bupivacaine,  7 mg
           su cient to support a systemic e ect of the   kg for levobupivacaine, 4  mg kg for
           drug. Studies in dogs and cats have    ropivacaine and 1 7 mg kg for lidocaine.  hile
           demonstrated minimal systemic absorption, as   all dogs in the lidocaine group could be
           in humans, and suggested that the patch may   resuscitated, mortality rates were     for
           deliver lidocaine for up to   days after   bupivacaine,     for levobupivacaine, and 1
           application on intact skin in dogs, and up to     for ropivacaine overdose. This study also neatly
           days in cats. A recent study suggests that   demonstrates that cardiotoxicity is a ected by
           absorption may be greater if the patch is   stereoselectivity, as levobupivacaine appears to
           applied directly over a skin incision in dogs.   be less toxic than bupivacaine   roban et al.,

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