Page 86 - Journal of Special Operations Medicine - Fall 2017
P. 86

Figure 1  Locations for administration             Figure 2  Removing atropine autoinjector from clip.


































          Thigh injection site.




















          Buttocks injection site.
          Source:  http://www.globalsecurity.org/wmd/library/policy/army/fm/8-
          285/appe.pdf
          could effectively “rinse” out the drops, but this should not
          preclude clinical trial evaluation of ocular/conjunctival/nasal
          mucosal routes versus oral/sublingual. In the absence of IM   Removing atropine autoinjector from clip.
                                                             Source:  http://www.globalsecurity.org/wmd/library/policy/army/fm/8-
          injectors, such attempts to deliver systemic antidote may rep-  285/appe.pdf
          resent a true last chance at survival.
                                                             with host-nation personnel, be they conventional military or
          The ROA proposed here has few published data showing   sympathetic guerilla forces, are faced with a chemical threat and
          equivalent bioavailability to the IM route of the autoinjector.   lack enough autoinjectors to cover all friendly personnel. More
          Even if sublingual/oral mucosal administration ranged from   concerning would be exposure of a large civilian population,
          0.8mg to 1.2mg vs IM, it would be easy to keep ingesting   who undoubtedly would lack autoinjectors but could be treated
          drops in a manner that titrates to effect. One 5mL vial could   quickly at a casualty collection point by placing several drops
          be used to treat multiple victims, with little added weight to   of ophthalmic atropine into the mouth of symptomatic patients.
          the Operator’s load out.                           Projecting forward, conventional medical units could be asked
                                                             to assist with industrial mass casualty events (or chemical war-
          SOF Relevance                                      fare scenarios) where the numbers of injectors is limited. Similar
          Why should we  be concerned about alternative  atropine   scenarios can easily be envisioned in homeland defense.
          sources when U.S. military personnel operating in at-risk zones
          are provided with adequate atropine and 2-PAM autoinjectors?   Ideally, randomized and blinded studies would compare the
          It is easy to envision scenarios where U.S. Operators  working   bioavailability of sublingual/oral muscosal atropine to the

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