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occur  by  hybrid  maneuvers  such  as  manual  compres­  adjuncts should be considered. Study of human factors
              sion during the tourniquet placement and application   in out­of­hospital healthcare, such as learning curves by
              before the tourniquet is made fully effective.  It is un­  lifesaving intervention (eg, tourniquet use or airway in­
                                                     10
              clear if this process occurred in the present study. Blood   terventions), may help refine best care practices.
              loss was continuous data, but hemorrhage control was
              binary (ie, yes or no); in actuality, hemorrhage control   In summary, whether emergency tourniquet had ex­
              can be partial in that it can exist as incomplete stoppage   posure  to  heat  or  not,  damage  rates  were  similar;  all
              of flow. In the way we used hemorrhage control in the   measures of performance except one, blood loss, were
              present study, partial hemorrhage control was reduced   similar irrespective of exposure, but they were not wors­
              to no hemorrhage control, meaning that control was not   ened by heat.
              attained completely. Hemorrhage control as a rate in
              mL/s is calculable with the methods available and may   Funding
              offer opportunities for further study; for example, one
              user, the physician assistant, in the present study had   This project was funded with internal US Army Medical
              rates ranging from 3mL/s to 19mL/s, a 6­fold difference,   Research and Materiel Command funds and the Defense
              while the other had rates ranging from 4mL/s to 9mL/s,   Health Program (Proposal 201105: Operational system
              a 2­fold difference.                               management and postmarket surveillance of hemor­
                                                                 rhage control devices used in medical care of US Service­
              The strength of the present testing is that it was a focused,   persons in the current war). The study was performed
              controlled experiment that provided a definitive answer   at USAISR.
              to the specific exposure addressed. By using a laboratory
              study, investigators (both had formal tourniquet training   Disclaimer
              and  also  had  field  experiences  in  out­of­hospital  care)
              were able, with the aid of an experienced research team   The opinions or assertions contained herein are the pri­
              (including a biostatistician), to implement an experiment   vate views of the authors and are not to be construed
              that answered a question from the field. Operational   as official or reflecting the views of the Department of
              medicine  is  often  based on  hospital  medicine, but the   Defense or US Government. The authors are employees
              context of operational medicine in the field often is sub­  of the US Government. This work was prepared as part
              stantially different; environmental exposure of medical   of their official duties and, as such, there is no copyright
              devices is more of an issue in the field than in the hospital.  to be transferred.

              Limitations of the study include the order of testing, as   Disclosures
              learning of users with increasing test numbers (a mea­
              sure of experience) was observed; this learning was   The authors declare no conflicts of interest.
              confounding in the assessment of other variables, but
              the effect of learning was small enough not to affect the   References
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              Testing of Tourniquets Exposed to Prolonged Heat                                                37
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