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Conversion

               Simulated Method of Exchanging Tourniquet Use for Pressure Dressing Use



                       John F. Kragh Jr, MD *; James K. Aden 3rd, PhD ; Michael A. Dubick, PhD 3
                                                                      2
                                           1






          ABSTRACT
          Background: Given little data to assess guidelines, we sought   For example, SSG Matt Decker gave a combat medic presen-
          a way to exchange one type of intervention, field tourniquet   tation at a meeting of the Committee on Tactical Combat Ca-
                                                                                       7
          use, for another, use of a pressure dressing. The study purpose   sualty Care in 2016.  The minutes  note that he “is a [military]
                                                                             6
          was to test performance of controlling simulated bleeding with   reserve component flight medic and an emergency department
          a stepwise procedure of tourniquet conversion. Methods: An   nurse in his civilian job. He presented a case from Helmand
          experiment was designed to assess 15 tests of a caregiver mak-  Province in Afghanistan from early 2016 that involved Pro-
          ing tourniquet-dressing conversions. Tests were divided into   longed Field Care. His helicopter answered a 9-line [radioed]
          trials: tourniquet use and its conversion. In laboratory con-  request for evacuation of a casualty with a gunshot wound to
          ditions, the tourniquet trial was care under gunfire; then, the   his right thigh. He treated the casualty in place for 17 hours
          conversion trial was emergency healthcare. A HapMed Leg   because several problems prevented evacuation. Treatment[s]
          Tourniquet Trainer simulated a limb amputation. An investi-  included red blood cells, whole blood via Vampire [transfu-
          gator provided healthcare. Results: Mean (± standard devia-  sion] protocol, fentanyl, ketamine drip, multiple attempts
          tion [SD]) test time and blood loss were 9 ± 3.6 minutes and   (finally successful) to convert the limb tourniquet to other
          334 ± 353.9mL, respectively. The first test took 17 minutes. By   means of hemorrhage control, and more. SSG Decker’s lessons
          test number, times decreased; the last six took ≤7 minutes. All   learned included [among others]: Limb tourniquet conversion
          tourniquet trials controlled bleeding. Mean (±SD) tourniquet   can be difficult—be persistent.”
          pressure  and blood loss  were 222 ± 18.0mmHg  and 146 ±
          40.9mL, respectively. Bleeding remained uncontrolled in one   Given little data 8–11  and limited guidance reported 3–7,12–19  on
          conversion. Initial attempts to wrap a dressing were effec-  which to assess clinical guidelines, we preliminarily developed
          tive in 73% of tries (n = 11 of 15). Four of 15 wrap attempts   a way to simulate converting a tourniquet intervention to a
          (27%) were repeated to troubleshoot bleeding recurrence, and   wrap dressing intervention. For healthcare providers at work,
          the first three tests required a repetition. Mean (±SD) dress-  acquiring and using this conversion skill have practical im-
          ing pressures and blood losses were 141 ± 17.6mmHg and   portance for readiness. The purpose of this study was to test
          188 ± 327.4mL, respectively. Unsatisfactory conversion trials   performance of controlling simulated wound bleeding with a
          had a dressing pressure <137mmHg. Dressings and wraps hid   stepwise procedure of tourniquet conversion.
          the wound to impair assessment of bleeding. Conclusions: In
          testing a method of converting a limb tourniquet to a pres-  Methods
          sure dressing, the caregiver performed faster with experience
          accrual. The tourniquet results were uniformly good, but con-  This study was conducted in 2016 within the limits of proto-
          version results were worse and more varied. Simulating con-  col guidelines at the US Army Institute of Surgical Research.
          version was disappointing on a manikin and indicated that its   The design was a stepwise experiment of simulated caregiving
          redesign might be needed to suit this method. The procedural   in a laboratory. The study was to model a change or conver-
          method constituted a start for further development.  sion of one intervention, tourniquet use, into another, pressure
                                                             dressing. The steps of the conversion task were timed. One
          Keywords: bleeding control and prevention; bandage; dress-  tourniquet device was used, one model of hemostatic dressing
          ing, emergency; skill; tourniquets                 was used, and one pressure dressing design was used but in
                                                             two widths. The pressure dressing, an elastic bandage in the
                                                             form of a roll, also had a pneumatic bladder, and its func-
                                                             tion was assessed as either inflated or uninflated. We random-
          Introduction                                       ized order of width and inflation status. Originally, we were
          Since 2001, tourniquet use to stop bleeding from wounds has   to conduct 30 tests but other priorities from the operational
                            1,2
          become more common.  Irrespective of why someone applied   health community superseded completion, so here we report
          a tourniquet, it is often managed later by other caregivers who   the results of 15 tests. The community recently reprioritized
          may need to exchange the tourniquet for another intervention,   development of conversion guidelines, so we decided to report
          like a pressure dressing. 3–5                      results now.
          *Correspondence to: 3698 Chambers Pass, Joint Base San Antonio Fort Sam Houston, TX or john.f.kragh.civ@mail.mil
          1 Dr Kragh is a researcher of bleeding control at the Institute of Surgical Research (ISR), Fort Sam Houston, Texas, and an associate professor in
                                                                                  2
          the Department of Surgery, Uniformed Services University of the Health Sciences, Bethesda, Maryland.  Dr Aden is a statistician at the Brooke
                                            3
          Army Medical Center, Fort Sam Houston, Texas.  Dr Dubick is a researcher and chairperson of Hemorrhage Control and Resuscitation Research
          Department at the ISR.
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