Page 86 - JSOM Fall 2020
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TABLE 5  Initial Ketamine Route and Dose (mg) for Training Casualties
                  Number of   % of
           Route  Casualties  Casualties  Mean (SD)  95% CI*  Range (mg) Minimum Dose (mg) Maximum Dose (mg)  IQR
            IM       10       29.4    37.00 (18.135)  25.76–48.24  55         20              75         25
            IN       8        23.5    58.13 (27.247)  39.25–77.01  95         25             120         10
            IO       0         0          —            —         —            —               —          —
            IV       16       47.1    48.44 (28.967)  34.25–62.63  85         15             100         33
          *Due to sample sizes <30, variations may be noted with 95% CI calculations and SD should be considered

          TABLE 6  Pain Scores Pre- and Post-Ketamine Administration    As demonstrated in Schauer’s 2015  Battlefield Analgesia:
          (N = 30*)                                          TCCC Guidelines Are Not Being Followed. These changes
                          Median          Minimum  Maximum   were not fully implemented for in theater training until March
                          (IQR)    Range   Pain     Pain     of 2014, demonstrating a 5-month lag from the announce-
           Pre-ketamine   8.0 (3)    5       5       10      ment.  During the time period of this study, from July 2013 to
                                                                 3
           Post-ketamine  0.0 (3)    8       0       8       March 2014, less than half of all patients received analgesia at
          *Four casualties excluded related to incomplete pain documentation.  the point of injury, with the highest rates of adherence occur-
                                                             ring within the SOF community. The delay in adoption, and
          in the tactical setting is important for patient comfort, tactical   lower rates of use of ketamine and pain treatment may have
          efficiency, and consensus that pain associated with traumatic   been attributed in part to a paucity of civilian clinical training
          events can potentiate posttraumatic stress disorder (PTSD)   opportunities, minimal use of ketamine during training events,
          and chronic pain syndromes.  Previous studies have found   and the lack of experience of supervising physicians with ket-
                                  1
          that by treating pain, it can help prevent the development of   amine. While the trend for better adherence would improve
          PTSD.  This study demonstrated pain scores were greatly re-  over time, the overall compliance with the TCCC analgesic
               5–7
          duced after the administration of ketamine. The dissociative   guidelines remains suboptimal. 2,4
          effects of ketamine may also play a role in long term benefit to
          the psychological health of the combat casualty, and therefore   There are surgeons and emergency medicine physicians who
          amnesia may not be a deleterious effect. 5         are not comfortable receiving a minimally responsive or unre-
                                                             sponsive trauma patient who has been given ketamine in the
          Ketamine is thought to act as an NMDA receptor antago-  prehospital setting (personal communication). When given in
          nist at the GABA receptor complex causing anesthesia.  It is   larger doses, ketamine can cause significant sedation and on
                                                      8
          further postulated that ketamine excites delta and mu opioid   initial presentation to a trauma center, an obtunded trauma
          receptors  within  the basal  ganglia  and thalamus  producing   patient may cause the attending physician concern regard-
          analgesia, as well as stimulating catecholamine receptors and   ing the possible presence of TBI despite no physical findings.
          decreasing production of nitric oxide leading to a decrease of   This  concern  may  result  in  additional  testing  and  possibly
          hemodynamic instability frequently seen with opiates.  Thus,   unnecessary procedures such as endotracheal intubation. A
                                                    9
          ketamine has prevalent mechanistic uses for sedation, analge-  well-documented GCS by the medic prior to the administra-
          sia, and anxiolysis.                               tion of ketamine would help assuage this concern. Ideally, a
                                                             prehospital system should gain the buy in from their receiv-
          Ketamine was formally endorsed by the Defense Health Board   ing hospitals prior to using ketamine in the field. This method
          in 2012 along with endorsement from the TCCC.  In recent   could increase awareness with the use of ketamine and ad-
                                                  1
          years, low dose ketamine has been utilized in far forward en-  dress points of concern in different practice patterns. It may
          vironments and is currently the first line pain medication for   be worth noting that the documentation of the mental status
          patients in shock or at risk of bleeding according to TCCC   and Glasgow Coma Score prior to ketamine administration
          guidelines.  Discordant with the TCCC and DHB approving   may reduce the concern for altered mental status related to
                  10
          the use of ketamine as a front analgesic, only 39% of patients   ketamine in trauma patients.
          in Afghanistan from October 2012 to March 2013 received
          pain control at the point of injury despite receiving good pain   US military medical officers should have a pain management
          control at Role 1 health care facilities in deployed locations. 11  protocol for their organization and this protocol should be in


          TABLE 7  Other Drugs Administered With Ketamine (mg*)
                                   Number of   % of     Range   Minimum   Maximum
               Drug        Route   Casualties  Casualties  (mg)  Dose (mg)  Dose (mg)  Mean (SD)   95% CI**
           Midazolam        IM        3         8.82      1        4         5       4.667 (0.577)  4.01–5.32
           Midazolam        IN        3         8.82    0.70      1.80      2.50     2.10 (0.361)  1.69–2.51
           Midazolam        IV        9        26.47      2        1         3       2.11 (0.546)  1.75–2.47
           Hydromorphone    IV        3         8.82     —         2         2       2.00 (0.000)     —
           Ondansetron      IM        1         2.94     —         4         4       0.00 (0.000)     —
           Ondansetron   Unknown      2         5.88      4        4         8       6.00 (2.828)  2.08–9.92
           OTFC (µg)        PO        8        23.53     800      800       1600    900 (282.843)  704.00–1095.99
          *Oral transmucosal fentanyl citrate (OTFC) doses are in µg, not mg.
          **Due to sample sizes <30, variations may be noted with 95% CI calculations and SD should be considered.


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