Page 26 - CASA Bulletin of Anesthesiologisy 2022 9(6)-1 (3)
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CASA Bulletin of Anesthesiology


                   Acetaminophen continues to be a crucial part of the perioperative multimodal analgesic
               regimen for its analgesic and opioid-sparing properties, which has been an important
               consideration in the setting of rising challenges with perioperative use of opioids (such as
               adverse events, misuse and abuse). However, the optimal dose and route of administration of
               acetaminophen for preemptive analgesia remains to unclear  .
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               Ketamine

                   Although primarily known as an anesthetic, ketamine has also been successfully used as an
               adjunct for perioperative pain management due to its safety profile & profound analgesic
               properties. Ketamine is a non-competitive NMDA antagonist derived from phencyclidine. At
               subanesthetic doses, ketamine can prevent central sensitization and subsequently reduce the risk
               of developing opioid induced hyperalgesia and opioid tolerance  . This can be particularly
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               helpful in spine surgery patients, many of whom are already opioid dependent and struggle with
               chronic pain which confer high risk for postoperative pain.

                   In the setting of acute postsurgical pain, ketamine infusions have recently been gaining favor
               as part of a multimodal opioid sparing analgesia regimen and is the standard of care in some
               institutions for the management of postoperative pain in opioid tolerant patients. In patients
               undergoing major lumbar spine surgery, intraoperative high-dose ketamine was shown to have
               morphine-sparing effects and decreased pain scores postoperatively  . Similarly in patients
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               undergoing scoliosis surgery, Hadi et al. reported that in combination with remifentanil, the use
               of ketamine resulted in lower pain scores, reduced morphine consumption, and prolonged time to
               first analgesic rescue  .
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                   In another study, perioperative ketamine with clonidine premedication has shown to
               potentiate the analgesic effects of opioids and reduce the consumption of morphine through
               patient controlled analgesia (PCA) following spine surgery  . In chronic pain patients, a study by
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               Nielson et al., demonstrated that postoperative morphine consumption and sedation 24 hours
               following spinal fusion surgery was significantly reduced in patients who received ketamine
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               infusions compared to placebo  .  Ketamine has been associated with nausea, headaches and
               disturbing psychomimetic effects (ie hallucinations, emergence phenomenon, sedation,
               disorientation). However, these are transient occurrences that last less than 60 minutes following
               administration. For these reasons, ketamine is considered to be a safe and relatively well
               tolerated medication  . The recommended dose of ketamine infusions for pain management
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               consists of a 0.1-1mg/kg bolus upon induction followed by an infusion ranging between 0.1-0.25
               mg/kg/hr. Ketamine also has promising prospects for chronic pain patients with concurrent
               depression. The closely intertwined relationship between chronic pain and depression is well
               known and commonly seen occurring together because they are mediated by the same
               modulatory neural system. Central nervous system nociceptive pathways (descending, ascending
               pain pathways in the midbrain, brainstem – periaqueductal gray matter, nucleus raphe, locus
               ceruleus) and brain regions involved in mood management are both mediated by
               neurotransmitters such as serotonin, glutamate and norepinephrine. There are a wide variety of
               antidepressants that are used to treat depression with associated pain such as SNRIs, SSRIs,
               TCAs and although they are effective in treating neuropathic pain, it has not always been
               effective in treating musculoskeletal pain. Chronic pain patients with clinical depression have
               worse physical, mental and social functioning compared to those without depression and





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