Page 45 - Journal of Special Operations Medicine - Spring 2015
P. 45

Descriptive statistics were used to analyze results, with   were ineffective in the study group was 0% (zero of 300;
              continuous  data  represented  by  means  and  standard   p = .32; Table 2).
              deviations, and categorical data represented by propor­
              tions. Statistical testing included mixed­models analysis   Table 2  Hemorrhage Control Results by Exposure
              of variance to see if any tourniquet device or model was    Exposure Group by Hemorrhage Control
              different from the rest (SAS Institute, Cary, NC; www.
              sas.com).  Users were considered a random effect in the               Hemorrhage Control*  Comparison of
                      12
                                                                                                      Percentages
              model. Pairwise comparisons were adjusted using the   Group           No    Yes  Total   (p Value)
              Tukey method. Comparison of proportions such as ef­  Heat exposure
              fectiveness percentages was made with the χ  test, while     Tests, No.   0   300   300 †
                                                    2
              continuous data were compared with use of the Student      Frequency    0   50    50
              t test. All statistical analyses were conducted using SAS      (percentage of total)  0  100
              and MS Excel 2003 (Microsoft, www.microsoft.com).     Row percentage
              Significance for results was established when p values   No heat exposure
              were < .05.                                          Tests, No.        1   299    300
                                                                    Frequency       0.2   49.8   50      .32
                                                                     (percentage of total)  0.33  99.66
              Results                                              Row percentage
                                                                 Total
              Damage varied by tourniquet model. Only one model,     Tests, No.      1   599    600
              the SOFTT­W, had damage, and the damage was of only      Frequency    0.2  99.8   100
              one component: The time label fell off the strap of six de­  (percentage of total)
              vices. The label is simply a place for the user to write the     Row percentage
              time of tourniquet application, and label loss led to no   Notes: *Hemorrhage control refers to data (yes or no) on whether
              ineffectiveness. Inability to record the time of tourniquet   bleeding was stopped.
                                                                 Data refer to the product of the tourniquet number per exposure
                                                                 †
              placement did not alter outcomes. The six SOFTT­W de­  group (15), number of users (2), and the number of tests/tourniquet/
              vices had this label come off during their first test. Dam­  user/exposure group (10).
              age was distributed equally with three tourniquets each
              in the groups with heat exposure and those with no heat   The pulse results were the same as the hemorrhage con­
              exposure (20% [three of 15] per group; p = 1; Table 1).  trol (yes or no) results. The proportion of tests that did
                                                                 not stop the pulse in the control group was 0.33% (one
              Effectiveness did not vary by heat exposure. The pro­  of 300), while the proportion of tests that did not stop
              portion of ineffective tests in the control group was   the pulse in the study group was 0% (zero of 300; p =
              0.33% (one of 300), while the proportion of tests that   .32). Since the one test that was ineffective was the same
                                                                 test that did not have the pulse stopped, hemorrhage
                                                                 control (yes) and pulse stoppage were separate but asso­
              Table 1  Tourniquet Damage Results by Exposure
                                                                 ciated measures of the phenomenon of limb hemorrhage
                         Exposure Group by Device Damage         control.
                                 Hemorrhage Control*  Comparison of
                                                   Percentages   All tourniquet devices except one were fully effective;
              Group              No    Yes  Total   (p Value)    the exception was a single SOFTT­W device that failed
              Heat exposure                                      only in one test. This SOFTT­W failed in its fifth test
                Tourniquets, No.             30*                 after four prior successes; it was also successful in all its
                 Frequency       27    3     50                  15 following tests. This SOFTT­W failed by its inabil­
                  (percentage of total)  45   5
                Row percentage   90    10                        ity to adequately tighten the strap: The strap material
                                                       1         bunched within the buckle, the strap was unable to slide
              No heat exposure
                Tourniquets, No.             30*                 through the buckle, and slack could not be removed
                 Frequency       27    3     50                  from the strap.
                  (percentage of total)  45   5
                Row percentage   90    10                        The mean time to effectiveness was 4 seconds less in the
              Total                                              heat­exposure group (p < .0001; Table 3). The mean
                Tourniquets, No.             60*                 time to effectiveness was 2 seconds less for the more ex­
                 Frequency                   100                 perienced user (p < .02).
                  (percentage of total)  54   6
                Row percentage   90    10
              Note: *The data refer to the number of tourniquets of any type used   The difference in mean pressures between the no­heat­
              in the experiment and that were examined for visible damage. Damage   exposure group and the heat­exposure group was
              reported refers to a label that came off the device.   2mmHg; this difference was not statistically significant



              Testing of Tourniquets Exposed to Prolonged Heat                                                35
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