Page 34 - Journal of Special Operations Medicine - Fall 2015
        P. 34
     is a vascular clamp that was the third FDA-cleared JT.   sponsor approached the FDA in 2009. Preliminary
          The JETT was cleared for difficult inguinal bleeding; it   training experience with prototype JTs came from a mix
          is not restricted to the battlefield, as are the CRoC and   of corporate and military medical personnel, many of
          the AAJT. The JETT is not currently cleared for pelvic   whom were experienced in special operations. For exam-
          fracture stabilization, but the sponsoring company says   ple, Chris Murphy, of Combat Medical Systems, was a
          that such evidence is in review. The JETT has a belt and   prior US Army Special Operations Command ( USASOC)
          two pressure pads with threaded T handles, allowing   medical combat developer who worked with MSG John
          unilateral or bilateral groin application. Other evidence   Steinbaugh, then the USASOC medical combat devel-
          supportive of JETT use includes case reports in theater   oper, to develop prototypes; and one set of prototype
          and in Houston, Texas, where limited applications in   assessors included LTC Bob Mabry (US Army Medical
          the field have occurred; however, only one use has been   Department Center and School [AMEDDC&S]), LTC
          formally reported. 11,14,24                        (Ret) Don Parsons (AMEDDC&S), COL John Kragh
                                                             (USAISR), and Dr. Michael A. Dubick (USAISR). Pre-
          SAM Junctional Tourniquet                          liminary experience showed that a number of device
          The SAM  Junctional Tourniquet (SJT) (SAM Medical   strategies were plausible from anatomic, mechanical,
                   ®
          Products; www.sammedical.com) is a vascular clamp   fabrication,  and  production  standpoints,  but  early  in
          that was the fourth FDA-cleared JT. The SJT was cleared   this experience, a likely key to success appeared to be
          for both difficult inguinal bleeding and pelvic fracture   the quality of training of the user.
          immobilization; the SJT was based on the SAM Pelvic
          Sling II, a predicate device already cleared by the FDA for   In 2010, the only military organizations that were pre-
          pelvic fracture immobilization. The SJT has two target   pared for training with JTs were some units of Special
          compression devices, circular pneumatic discs that inflate   Operations  Forces  (SOF).  Stateside  SOF  training  was
          like sequential layers of a wedding cake. The SJT is not   focused and intense for users to improve skill levels and
          restricted to battlefield use, as are the CRoC and AAJT.   familiarity. However, details of their experience were
          The SJT was subsequently cleared for axilla bleeding. A   not made widely known; instead, they were either expe-
          recent case of groin use of an SJT had a distal pulse return   rienced firsthand or passed around by word of mouth.
          without loss of hemorrhage control; this case had only a   The quality of training seemed excellent—a hallmark
          single gunshot wound that was also packed.  Other evi-  trait of SOF medics. The ratio of trainers to trainees was
                                               25
          dence supportive of SJT use includes a manikin study, a   high, and the latter had trainers who were very famil-
          cadaver study, and a human volunteer study. 10,14,26  iar with their needs. Stepwise familiarization–practice–
                                                             rehearsal in a crawl–walk–run sequence was common.
                                                             The emphases were to master the basics and press the
          Experiences in the US Military Emergency           user to train to failure; that is, train to learn where the
          Tourniquet Program: 2008–2009
                                                             device, the user, or the system fails, to better understand
          The  Emergency  Tourniquet  Program  (the  Program),  a   best-care practices and limits. Such knowledge aided
          research and development program for out-of-hospital   spiral development of the JTs’ designs.
          hemorrhage control interventions in combat casualty
          care at the US Army Institute of Surgical Research   The first JT, the CRoC was cleared in 2010. Techni-
          ( USAISR), has gained broad experience in surveying   cally, JTs were a reworking of an old idea, but to today’s
          training of JT use over the years, beginning in 2008.    researchers and users, JTs are new. In 2010, with one
                                                         27
          The Program developed out of necessity to control hem-  JT cleared by the FDA, CRoCs were sent into theater
          orrhage after  11 September  2001 and was originally   and users were trained there. At this time in 2010, the
          focused on limb or regular tourniquets. Since 2009,   only military organizations that sought training with
          however, the emphasis within the Program has become   JTs were SOF. The initial use of the first JT was for a
          predominately on JTs. This small program with one full-  detainee and cannot be reported further. The training
          time person has been at or near the center of several re-  that prepared such use was said to be successful and
          search and development (R&D) activities either directly   uneventful. High-quality training tailored to user needs
          as a participant or indirectly as a consultant or reviewer.  was a key to success.
          In 2008, COL Lorne Blackbourne and other members of   Early, limited application of JTs in the battlefield came
          the Committee on Tactical Combat Casualty Care made   through a war mechanism. A few JTs were distributed
          junctional hemorrhage a research priority.  By 2009, the   to US Army Research and Development Command
                                              28
          main proponent of the R&D was the US Special Op-   personnel, but the details are sparse. One user, SFC
          erations Command, and medical developers within spe-  Robert  Tovmassian,  a  medic  assigned  to  a  helicopter
          cial operations conducted their own R&D program that   medical evacuation unit, noted the R&D enlisted person
          aided in development of the initial JT, whose commercial     brought the CRoC into theater and offered high-quality
          22                                        Journal of Special Operations Medicine  Volume 15, Edition 3/Fall 2015





