Page 77 - JSOM Winter 2019
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hemorrhage with 19.2% of hemorrhages due to junctional in-  the abdomen, thorax, and brain) and more effective compres-
              juries. Kragh et al. later reviewed all coalition deaths between   sions due to counterpressure on the diaphragm secondary to
              2001 and 2010 and concluded that 20% of all potentially sur-  the AAJT; in addition, because the AAJT blocks both venous
              vivable deaths were secondary to junctional hemorrhage —a   and arterial flow, it may increase pressure, resulting in greater
                                                          5
              consistent figure.                                 coronary and carotid blood flow. 20
              A study of the UK Joint Theatre Trauma Registry identified all   Placed at the Axilla or Groin
              UK combat-related pelvic junctional vascular injuries between   In human studies looking at the outcome of arterial occlusion,
              2008 and 2011. This study identified 37 casualties who died   there are two studies looking at groin application and one
              due to pelvic/lower limb junctional injury.  An injury at this   looking at axillary use. In total, this equated to 31 groin ap-
                                               6
              level would be amenable to AAJT use. Morrison et al. per-  plications and 13 axillary applications with a 100% occlusion
              formed a retrospective 10-year review of our UK casualties in   rate; no other axillary or groin devices on the market currently
              Afghanistan and Iraq highlighting 165 casualties who survived   demonstrate a 100% occlusion rate.  This high level of effec-
                                                                                             9
              beyond point of wounding with injuries amenable to zone 1   tiveness is suggestive that the device is easy to use; however,
              or zone 3 aortic occlusion.  When these 165 are split into died   further work is needed to collect real-use data on time to effect
                                  7
              en route, died in hospital, and survivors, those with potential   and how easy it is to use. Effectiveness outside of studies on
              benefit from zone 3 occlusion amounted to 40.9%, 43.3%,   animal models and healthy human volunteers are limited, but
              and 41.4%, respectively. A UK civilian retrospective popula-  there are case reports of successful axillary and groin use of
              tion-based analysis of the 2012–2013 Trauma Audit and Re-  the AAJT. 21,22  Both of these case reports were for penetrating
              search Network (TARN) data also looked at those who might   gunshot wounds in junctional regions.
              benefit from aortic occlusion in trauma. The authors found
              that  4.9%  had an  indication  for  aortic  occlusion,  of which   Usability
              40.6% (n = 161) would have required zone 3 occlusion. 8
                                                                 Practicalities
                                                                 The AAJT is an external device, so it can be both used in the
              Effectiveness
                                                                 sterile  in-hospital  environment or  deployed  in an unsterile,
              Placed at the Aortic Bifurcation                   chaotic environment such as the modern asymmetric battle-
              There are four healthy volunteer human studies looking at the   field. It can sit in a medical rucksack or webbing, and small
              effectiveness of the AAJT placed at the aortic bifurcation. Re-  tears in packaging, which will often occur in the deployed aus-
              sults were dichotomous with a pooled average of 52%.  The   tere environment, do not indicate that the product becomes
                                                         9
              four studies had flow cessation percentages of 94%, 78% (re-  unserviceable. The AAJTs stored dimension is 7.5 inches (W) ×
              duced flow in 100%), 27%, and 11%. 10–13  This low marker   6.5 inches (D) × 2 inches (H) with a weight of 17 oz (1.06 lb).
                                                                                                               23
              of effectiveness should be taken with caution; it appears the   These  qualities  mean  the  device  could  be  easily  stored  in  a
              reason for failure was not device failure but pain resulting in   Role 1 (prehospital) environment and carried during high-risk
              the healthy volunteer being unable to tolerate the device. For   missions. An even smaller pack has been developed.
              example, in the study by Kragh et al. with 11% effectiveness,
              89% could not tolerate the AAJT and therefore their appli-  Time to Effect
              cation was deemed ineffective.  This is similar to a separate   In human studies, time to effectiveness for abdominal use has
                                      13
              study by Kragh et al. with an effectiveness of 27%.  Yet, in   been quoted as 92 and 171 seconds.  The author agrees that
                                                                                             9
                                                       10
              another study, only one British airborne soldier appeared to be   this is a quick device to apply. In contrast, REBOA use by a
              unable to tolerate the device with an effectiveness of 94%. 11  Special Operations Surgical Team has been shown to take be-
                                                                 tween 5 and 9 minutes to achieve aortic occlusion. 24
              Overall numbers reported in the literature are small, but when
              looking at why the device has failed, it is suggested that the   Robustness
              underlying reason is pain. It is highly likely that the acutely   There are individual reports in human studies of the AAJT
              unwell trauma patient, who is hypotensive with significant or   breaking during use. One such case had no effect on its effec-
              catastrophic bleeding and possibly in a periarrest state, would   tiveness, with a side prong breaking off from the male end of
              be able to tolerate an abdominal application of the AAJT.  the snap-together buckle. In another case, breakage occurred
                                                                 of the pressure gauge on removal of the device after its use. 25,26
              There is only one case report of AAJT use at the aortic bifurca-  Real-life case reports of use reveal no evidence of breakage or
              tion in real life trauma, and this was in a military patient in Af-  malfunction. 14,21,22  Further data are likely to become apparent
              ghanistan with bilateral lower limb amputations.  There was   only once more reports of its use are available.
                                                    14
              almost immediate effect following application and no evidence
              of any complications 48 hours after use. The patient survived.   Suitability During Patient Transfer
              Much of the current literature for AAJT use comes from an-  In the three case reports of real-life use, the AAJT has been
              imal models. These models have repeatedly demonstrated an   effective in transport. 14,21,22  Patients trying to remove painful
              excellent ability for the AAJT to effectively control bleeding   stimulus such as the C-A-T is not an uncommon phenomenon,
              distal to the aortic bifurcation. 15–19            but in the case of the AAJT, one patient thought it was more
                                                                 comfortable than a C-A-T when applied at the groin.  There
                                                                                                          21
              One such recent animal study explored AAJT use during trau-  has been one report of the AAJT dislodging when placed at the
              matic cardiac arrest. The authors found that survival, alongside   axilla when the patient sat up but it was reapplied and then
              other markers of CPR efficacy, were significantly improved in   continued to be effective.  Nevertheless, the patient must be
                                                                                     22
              the AAJT group. Speculated explanations for this included   observed and the AAJT rechecked regularly, especially after
              sequestration of resuscitation  fluid above the AAJT (i.e., to   any movement.

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