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persons participated one at a time to apply tourniquets: a cli-  Wilcoxon method or Tukey least significant difference (LSD)
          nician-scientist, an associate researcher, a military cadet, and   method was used, whichever was most appropriate. The num-
          a research scientist, numbered users 1 through 4, respectively.  ber of pairwise comparisons for the nine glove groups was
                                                             36 ([{9 – 1} × 9]/2); the number of pairwise comparisons for
          The limb tourniquet model was the generation 6 Combat Ap-  the four individual users and six individual tourniquet devices
          plication Tourniquet (C-A-T; C•A•T Resources, www.combat   was six and 15, respectively. LSD and Dunnett corrections
          tourniquet.com).  Tourniquets  were  already  unwrapped and   were  used  for  pairwise  comparisons.  Pairwise  comparisons
          reconfigured for one-handed use. The user donned the gloves   of group means were then put into levels based on statistical
          by glove group in a randomized order. After starting, the user   significance.
          unrouted the tourniquet band by removing it from its course
          through a slit in the buckle, and then the user applied the tour-  A mixed-model ANOVA was also used, which included the
          niquet to the manikin. If wear or tear of a tourniquet device   user as a random effect in the model. User effects were pre-
          occurred, it was replaced upon completion of the test. Each   sented as a percentage of the overall variance component
          user started with an unused tourniquet. Two devices sustained   based on the restricted maximal likelihood variance method.
          wear or tear and were replaced, making a total of six devices   R  was reported as the percentage  of the response variable
                                                              2
          used in the study.                                 variation that is explained by a linear model. Significance for
                                                             results was established when p < .05. All statistical analyses
          Because the intervention required the glove group, the tour-  were  conducted  with  SAS  software  (JMP  version  12.0;  SAS
          niquet, and the user altogether, there was no capacity to sta-  Institute, http://www.sas.com) and MS Excel 2003 (Microsoft;
          tistically differentiate between them for an individual test.    www.microsoft.com).
                                                         20
          However, looking at all tests allowed analysis of effects of us-
          ers, gloves, and devices. The number of tests was 180. The   Results
          four users performed five tests of the nine glove groups each,
          for a total of 45 tests each.                      Effectiveness in Bleeding Control
                                                             For users, 179 of the 180 tests (99%) ended with effectiveness,
          The manikin on which we tested the performance of tourniquet   and interuser differences were not statistically significant (p =
          use was reported previously.  Briefly, a HapMed  Leg Tour-  .4252). User 2 had the ineffective test.
                                22
                                                 ™
          niquet Trainer (CHI Systems, http://www.chisystems.com)
          simulated a right thigh with an amputation injury. Run-time   For gloves, 99% of the tests resulted with effectiveness, and
          feedback was off. Metrics included effectiveness in bleeding   intergroup differences were not significant (p = .8154). The
          control as a yes or no result, time in seconds to determination   ineffective test was with cold gloves layered under mittens.
          of bleeding control, trial time (sum of time to determination
          of bleeding control and time to remove the tourniquet from   For devices, six individual tourniquets were used. Users 1 and
          its wrapper), distal pulse stoppage (yes or no), patient status   3 had one each; users 2 and 4 had two each. Of 180 tests, 179
          (stable, bleeding, or dead), tourniquet placement (none [no   resulted in effectiveness, and the ineffective test was with de-
          tourniquet detected], good [location], or incorrect [location]),   vice U2-2 (user 2’s second device). Interdevice differences were
          tourniquet pressure (amplitude in mmHg and categorized as   not significant (p = .2965).
          loose, good, or tight), blood loss in milliliters, and test status.
          Test status was a composite binary result (i.e., satisfactory or   Pulse Stoppage
          unsatisfactory result) indicating whether the test was, in ag-  For users, gloves, and devices, 99% of tests resulted in pulse
          gregate, satisfactory for all the following metrics: patient sta-  stoppage, and interuser, interglove, and interdevice differ-
          tus was stable, tourniquet placement was good, and pressure   ences were not significant (p = .4252, .8154, and .2965, re-
          was good. The manikin reported satisfactory test status as a   spectively). User 2 had the test without stoppage, which was
          ‘go’. Pulse stoppage was determined by the user; the manikin   performed with cold gloves layered under mittens and device
          determined the rest.                               U2-2.

          All data were generated during the present study except for   Patient Status
          time to unwrap, which came from the prior study.  Unwrap-  For users, 99% of tests resulted with the patient as stable, and
                                                 11
          ping times were specific to the user, glove group, and model of   interuser differences were not significant (p = .4252). User 2’s
          C-A-T tourniquet, but there was only one set of nine times for   final test ended with bleeding.
          each user because there were nine glove groups. To simulate a
          realistic time it takes to use a tourniquet, an additional metric   For gloves, results were similar: 99% of tests ended with the
          was generated by summing the time to unwrap and the trial   patient stable; one test, in which cold gloves were layered un-
          time; this was used as an overall time. No bleeding occurred   der mittens, ended with bleeding (p = .8154).
          while unwrapping.
                                                             For devices, 99% of tests resulted with the patient as stable.
          Descriptive statistics were used to portray results. Categorical   The test with bleeding was with device U2-2. Interdevice dif-
          data were analyzed by contingency tables, and likelihood ra-  ferences were not significant (p = .2965).
          tios were calculated. Continuous data (e.g., time to determina-
          tion of bleeding control) were summarized by median (range)   Tourniquet Placement: Incorrect Placement or
          or mean (standard deviation), which were analyzed using   Good Placement at the Correct Site
          analysis of variance (ANOVA) to see differences. Fixed-effect   For users, gloves, and devices, 99% of tests resulted with good
          tests were made by glove group and by tourniquet device.   tourniquet placement,  and interuser, interglove, and inter-
          For pairwise comparisons of group means, a nonparametric   device differences were not significant (p = .4252, .8154, and

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