Page 46 - Journal of Special Operations Medicine - Summer 2014
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throughout the experiment, and the body temperature   Table 1  Time to Onset and Recovery Benchmarks in Minutes
          of the swine was maintained at greater than 36.0°C.   (Mean ± SD)
          EMG data were obtained following a modified method                                     Mean    p
          previously described by Shi et al.  Subdermal needle elec-           IV        IO      Ratio  Value
                                      8
          trodes (Medtronic USA, Jacksonville, FL) were placed in   Onset   0.55 (0.26) 0.97 (0.40)  0.59  .048
          the sternomastoid muscle for direct EMG recording on    90
          a Nerve Integrity Monitor (NIM) Response 3.0 monitor   Onset max  2.90 (1.39) 4.20 (1.33)  0.58  .162
          (Medtronic USA). Once baseline EMG amplitudes were   25% Recovery  6.0 (2.3)  6.6 (2.3)  0.90  .760
          established, 3mg/kg succinylcholine was administered in   50% Recovery  8.9 (2.9)  8.6 (3.1)  1.03  .900
          a single bolus via either a 20g IV catheter placed in an   75% Recovery  11.2 (3.4)  10.3 (3.7)  1.09  .740
          auricular vein or a 15g IO needle (Vidacare Corpora-
          tion, San Antonio, TX) inserted in the proximal medial   95% Recovery  12.9 (3.8)  11.4 (4.2)  1.13  0.650
          aspect of the tibia, followed by a 10mL normal saline
          flush. A dose of 3mg/kg was used after a standard hu-  Figure 1  Comparison of individual times to 90% reduction
          man dose of 1.5mg/kg failed to produce maximal EMG   of EMG by route of administration.
          suppression during model development.

          EMG amplitudes  were measured  at baseline and at
          10-second intervals for 2 minutes, at 30-second inter-
          vals for the next 8 minutes, and then every minute for
          the next 10 minutes. The animal was allowed to recover
          for 60 minutes, and the experiment was conducted again
          via the alternate route of administration.

          The initial data were transformed to percent of baseline
          and graphed as percent baseline versus time. Individual
          onset and recovery data were plotted using Excel (Micro-
          soft, Redmond, WA). The time from the end of injection   was no statistical difference in the recovery of neuro-
          to 90% reduction of baseline EMG activity (Onset )   muscular function between IO and IV administration.
                                                        90
          and the time to maximum reduction (Onset peak) were   The results are similar to a study in which sheep were
          used to characterize the onset of neuromuscular block-  administered  succinylcholine via the IO route  and re-
          ade.  Recovery from neuromuscular blockade was char-  spiratory arrest was used as a measure of onset.  The
              9
                                                                                                        11
          acterized by the time from injection to return of 25%,   investigators found the mean time to respiratory arrest
          50%, 75%, and 95% of baseline EMG activity. The    was 30 seconds after IV administration compared with
                                                     10
          results were compared using a multivariate analysis of   57 seconds after IO administration but concluded that
          variance. All analyses were performed with SPSS version   it made little clinical difference. However, in emergent
          18 (SPSS Inc., Chicago, IL). Significance in this study   medical conditions requiring immediate endotracheal
          was indicated by p < .05.                          intubation for airway protection, time is critical. Any
                                                             time delay in the placement of a definitive airway may
                                                             lead to unacceptable patient outcomes. Therefore, de-
          Results
                                                             velopment of administration techniques that would pro-
          Times used to characterize onset and duration of paraly-  duce equivalent onset to IV administration when using
          sis after succinylcholine administration are summarized   the IO route would be useful to the emergency care pro-
          in Table 1. The mean time to a 90% reduction in EMG   vider. Increasing the dose of succinylcholine or adminis-
          activity was statistically longer after IO administration   tering a larger flush volume following administration of
          compared with IV administration (p = .048). Individual   succinylcholine may accelerate onset when using the IO
          subject comparison of time to a 90% reduction in EMG   route and should be investigated.
          activity is presented in Figure 1. There was no statistical
          difference in mean time to recovery of all benchmarks.  Further, data on the onset and duration of succinylcho-
                                                             line administered via the sternal IO route should also be
                                                             investigated. There is a possibility that any delay in on-
          Discussion
                                                             set of drug action may be minimized by administration
          This study has two major findings. First, the time from   via the sternal IO route, which is anatomically closer
          administration to 90% reduction in EMG activity was   to the effect site than the tibial IO route. This concept
          statistically longer after tibial IO administration com-  was demonstrated in a study comparing peak arterial
          pared with peripheral IV administration. Second, there   blood concentrations of Evans blue– and indocyanine



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