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Discussion and Conclusion: Understanding the impact of ex-  Conclusion:  Preliminary data from this arctic immersion
              treme  cold environments  on the performance  of  life-saving   CBRN simulation suggests that current CBRN protocols re-
              techniques is critical to the success of potential arctic opera-  quire increased time to completion and that material dysfunc-
              tions. Preliminary data from this study demonstrate the signif-  tion is common in arctic temperatures. Final data from these
              icant impact the cold environment has on the performance of   trials should inform the revision of current CPGs.
              LSIs. Future analysis will include linear regression and further
              analysis into the failure of medical equipment in extreme cold.   Detection of Progressive Venom-Induced Consumption
              This trial has demonstrated the feasibility and utility of future   Coagulopathy (VICC) by Thromboelastography (TEG) in a
              work at the National Science Foundation laboratory focused   Severe Rabbit Model of Crotalid Envenomation
              on human performance in extreme cold.
                                                                 Phylicia Irons, LT, MC USN , Chris  Treager, LCDR, MC
                                                                                        1,2
                                                                 USN 1,2,3 , David Spivey, LT, MC USN , Fernando Gonzalez,
                                                                                              1,2
              Assessing Performance of Chemical Exposure Management   LT, MC USN , Sean Stuart, CDR, MC USN , Tyler Lopachin,
                                                                           1,2
                                                                                                  2,4
              in the Arctic Environment using the Cryosphere Austere   LT, MC USN , Lorie Gower , Diana Sheldon , Dr. Emily
                                                                                        2,6
                                                                           2,5
                                                                                                      2,6
              Medicine Platform (CAMP)
                                                                 Friedrich , Brittany Lassiter 2,6
                                                                        2
              Anderson AL , Bebarta VS , Giesbrecht G , Keenan S , Ritter,   1   Department of Emergency Medicine, NMRTC-Portsmouth,
                        1
                                              2
                                                       1
                                  1
              AC , Getz T , Eisenhauer IF , Eazor J , Comart C , Vallin T ,   Portsmouth, VA
                                    1
                                           1
                1
                                                     1
                       1
                                                             1
              Lemery J 1                                         2   Combat  Trauma  Research  Group,  NMRTC-Portsmouth,
              1   Department of Emergency Medicine, University of Colo-  Portsmouth, VA
               rado School of Medicine, Aurora, CO, USA          3   Bravo Surgical Company, 2d Medical Battalion, 2d MLG,
              2   University of Manitoba, Winnipeg, MB, Canada    Portsmouth, VA
                                                                 4   Joint Task Force-Civil Support, Fort Eustis, VA
              Introduction: The Department of Defense has identified read-  5   3d Medical Battalion, 3d MLG, Okinawa, Japan
              iness for future warfare in the circumpolar north as strategic   6   General Dynamics Information Technology, Falls Church,
              initiative. Operations in extreme cold temperatures require spe-  VA
              cific modifications to accommodate and optimize human per-
              formance and to ensure medical device functionality in the event   Introduction: About 8,000 venomous snake bites occur in the
              of chemical, biologic, radiologic, and nuclear (CBRN) threats.   United States yearly, 95% from pit vipers. Mortality occurs
              Rendering medical care requires cognitive and manual dexter-  from venom-induced consumption coagulopathy (VICC).
              ity, yet a paucity of literature exists on human performance,   Crotalidae polyvalent immune Fab (CroFab) treats envenom-
              material performance, and the effectiveness of current military   ation, but supply is limited and costly. Evaluation of VICC by
              clinical practice guidelines. In this study we assess performance   thromboelastography  (TEG)  has  been  successfully  tested  by
              of Tactical Combat Casualty Care (TCCC) CBRN initial man-  our group during in vitro simulated pit viper envenomation.
              agement guidelines in an extreme cold (–24ºC) environment to   This study compares TEG and conventional testing in the de-
              identify human and material performance limitations of current   tection and reversal of VICC after CroFab administration.
              approaches to CBRN care under these conditions.
                                                                 Methods:  An IACUC-approved protocol  using  Oryctolagus
              Methods:  Thirty  emergency  medical  services  (EMS)  med-  cuniculus was used in this two-phase study. Phase 1 determined
              ics performed TCCC CBRN clinical practice guideline (CPG   the lethal dose (LD50) of intravenous (IV) Crotalus  atrox
              ID:69) tasks in the National Ice Core Facility in room tem-  venom required  for VICC using 3 groups, obtaining  blood,
              perature (20ºC) and extreme cold (–24ºC) environments. Thir-  and performing the analysis with TEG and conventional coag-
              ty-minute acclimatization preceded simulated performance of   ulation markers. Phase 2 utilized 3 arms: untreated, medium,
              11 life-saving interventions (LSIs) while maintaining chemical   and max dose CroFab. Each arm received the calculated LD50
              exposure precautions. LSIs were timed and observed for ef-  IV venom followed by CroFab. After CroFab, blood was col-
              ficacy  and equipment  malfunction. Neuropsychological  and   lected to monitor coagulopathy. For comparison, values were
              cognitive testing was performed before and after each period   converted to a unitless value based on reference ranges.
              of simulation.
                                                                 Results: In Phase 1, PT showed a difference between dose
              Results:  Preliminary results from 6 participants who com-  groups at T+10min after envenomation. In contrast, R time
              pleted both simulation periods demonstrated longer time   showed differences at T+1min with more prolonged R time
              to completion of CBRN tasks at extreme cold versus room   in higher doses.  Thrombocytopenia was demonstrated at
              temperature (35.8 vs. 26.9min, P<.05, 95% CI for difference   T+1min, while MA did not show a difference until T+10min.
              5.3–12.5min). Individual tasks most affected by the cold envi-  In Phase 2, when comparing PT and R time between the dose
              ronment included donning of mission oriented protective pos-  groups, TEG showed higher sensitivity in the early detection
              ture (MOPP) gear, cricothyroidotomy, peripheral intravenous   of the reversal  of VICC. Thrombocytopenia was more  pro-
              access, and CYANOKIT deployment.                   nounced in the untreated arm with a significant difference at
                                                                 T+10min, whereas the MA did not show sensitivity toward the
              Discussion:  Preliminarily, this study demonstrated delayed
              time to deployment of current CBRN CPGs in an arctic envi-  detection of reversal. With CroFab, the α-angle did not show
              ronment and identified lessons learned from MOPP gear us-  differences between groups until T+180min and did not reach
              age in the extreme cold. We identified equipment malfunction   a significant difference, while fibrinogen showed no difference
              and medic performance limitations of arctic temperatures. We   overall and there was no difference between the two.
              promise future data on the remaining participants and on hu-  Discussion: In our model, certain TEG markers detected en-
              man and neurocognitive performance, which should inform   venomation faster than standard methods. We found that TEG
              CPG revision and future research to improve approaches to   markers can detect correction of VICC after CroFab sooner
              prehospital field care.                            than traditional markers. Overall, these findings suggest TEG
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