Page 41 - CASA Bulletin of Anesthesiology 2019 Issue 6
P. 41

Vol.6,  No.6, 2019


                                                                                           DOI: 10.31480/2330-4871/104
          ly leads to a plasma concentration of about 2 mcg/ml   cular block and delayed emergence from anesthesia.
          [37]. So there is an inbuilt margin of safety when ad-  Mg potentiates neuromuscular blocking drugs and
          ministering this dose. Cardiac arrest is possible with   CNS depressants and these effects need to be tak-
          extreme toxicity and given its low therapeutic index it   en into  consideration. The depth of  neuromuscular
          is wise to administer lidocaine by continuous infusion   block should be carefully monitored and adequacy of
          rather than by large intravenous bolus doses. If local   neuromuscular reversal should be confirmed prior to
          anesthetic systemic toxicity is suspected a bolus dose   extubation.
          of 1.5 ml/kg intralipid followed by an infusion of 0.25
          ml/kg/min should be administered [35].               Regional blocks and centroneuraxial blocks
          Gabapentin/Pregabalin                                  Many procedures can be performed under  region-
                                                               al or centroneuraxial anesthesia. The use of catheters
             Gabapentinoids are derivatives of the inhibitory   for  ongoing  post-operative  infusion  can  greatly  limit
          neurotransmitter gamma aminobutyric acid (GABA).     or entirely eliminate the use of perioperative opioids.
          Both gabapentin 300 mg PO and pregabalin 150         Many perineural regional techniques like paravertebral
          mg PO are effective analgesics that are also useful   and pectoral nerve blocks have been used successfully
          in neuropathic pain. Their use leads to lower pain   [41]. Local wound infiltration with local anesthetic has
          scores, reduced opioid consumption and opioid relat-  become common in lower limb joint replacement sur-
          ed side effects [38,39]. They can be continued into   gery because of great efficacy and the absence of motor
          the post-operative period. Excessive sedation, dizzi-  block [42]. Transversus abdominis  plane  (TAP) blocks
          ness and visual disturbances can be a problem with   and the erector spinae plane (ESP) block for abdominal
          high doses after prolonged periods.                  and thoracic surgeries lead to better analgesia and re-
          Magnesium                                            duced opioid use [43,44].
             Magnesium (Mg) has analgesic action by regulating   Mixed agonist/antagonist drugs acting on opioid
          calcium flux into the cell and acting as an NMDA recep-  receptors
          tor antagonist.  It also  suppresses neuropathic  pain.  It   Mixed agonist/antagonist drugs acting on opioid re-
          has been shown to reduce the need for post-operative   ceptors like dezocine and buprenorphine are generally
          opioids  and  improve  post-operative  pain  scores  [40].   regarded  as  less  addictive  and  respiratory  depressant
          The loading dose is 30-50 mg/kg and it may be followed   than the full agonists but they may also have a lower
          up by an intravenous infusion of 10 mg/kg/hr.        analgesic ceiling than the full agonists. These drugs do,
             Side effects are hypotension and bradycardia that   however, offer significant advantages in the treatment
          respond readily to standard therapy but are more     of opioid addicted patients. Dezocine has been shown
          common when higher doses are administered. When      to alleviate morphine-induced  dependence and im-
          using Mg intra-operatively it is important to reduce   prove patient experience in both preclinical and clinical
          the amount of muscle relaxants and anesthetic drugs   studies [45,46].
          that are administered to prevent residual neuromus-    In summary, the perioperative use of opioids has

                                    Table 2: Risk and benefits of opioid and non-opioid analgesics.
                         Opioid Analgesia               Opioid free/ Opioid Sparing Analgesia
           Risks         Respiratory depression         Bradycardia with dexmedetomidine
                         Need for post-op ventilation with   Hepatic damage with acetaminophen
                         ventilator associated pneumonia  Bleeding, renal impairment and bronchospasm with ketorolac
                         Addiction                      Hallucinations, tachycardia and addiction with ketamine
                         Nausea & Vomiting              Tinnitus, seizures and cardiac arrest with lidocaine
                         Gastrointestinal dysfunction, ileus  Sedation with gabapentin
                         Pruritus                       Hypotension with magnesium
                         Urinary retention
           Benefits      Analgesia                      No respiratory depression
                         Ready acceptance of poor patient   No addiction except for ketamine
                         outcomes by peers, due to the   Less need for post op ventilation
                         conventional nature of the analgesic   No nausea and vomiting
                         therapy
                                                        No gastrointestinal dysfunction and ileus
                                                        No pruritus
                                                        No urinary retention

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