Page 17 - JSOM Winter 2022
P. 17

Improvised Management of Polycythemia Vera
                                        Using Whole Blood Transfusion Kits



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                                                               1
                                  Brandon M. Carius, DSc, PA-C *; Peter M. Dodge, BS, NRP ;
                                                           3
                                     Joshua A. Bates, 68W ; Philip Castaneda, DSc, PA-C 4





              ABSTRACT
              Polycythemia vera (PV) is a frequent myeloproliferative dis-  complaint of a persistent pruritic neck rash. He reported these
              ease resulting in excessive red blood cells, white blood cells,   symptoms to his primary care provider approximately 2
              and platelets rarely identified in military populations. Increased   months after arrival overseas without planned management for
              blood viscosity and platelets can lead to fatal myocardial in-  his PV. He had previously been referred to a physical evaluation
              farction and stroke. Historically, regimented phlebotomy man-  board (PEB) for PV and retained by the Army. He reported tak-
              aged this condition, but modern medicinal advances now are   ing aspirin 81mg daily and lisinopril 20mg daily as part of his
              utilized. These immunosuppressive medications are generally   treatment for PV and hypertension, respectively. Additionally,
              incompatible with active-duty service and can lead to medical   prior to transfer overseas, he received near-weekly phlebotomy
              discharge. Phlebotomy therefore is critical for readiness and   treatments at a civilian institution for PV management, which
              health; however, this can be challenging in resource-limited en-  was last performed approximately 3 months prior to his pre-
              vironments, necessitating effective improvisation. We describe   sentation. Upon arrival to the ED, his blood pressure (BP) was
              an active-duty Soldier with PV symptoms consisting of subster-  135/83mmHg with a heart rate (HR) of 72 beats per minute;
              nal chest pressure, bilateral lower extremity paresthesias, and   his remaining vital signs were also within normal limits. Phys-
              persistent pruritic neck rash. He had an elevated hematocrit   ical exam revealed a mildly erythematous maculopapular rash
              (Hct) of 47%, necessitating phlebotomy and posing a challenge   along the neck. An electrocardiogram showed no acute findings
              to his primary care team. The local emergency medicine team   of cardiac strain or ischemia, and troponin levels were not el-
              employed blood collection bags from whole blood (WB) trans-  evated. A complete blood count (CBC) found significantly ele-
              fusion kits, including proven volume estimation methods, to   vated levels of white blood cells (WBC), red blood cells (RBC),
              routinely draw one unit of blood and effectively manage this   hemoglobin (Hgb), and Hct (Table 1).
              condition. This is the first reported case in military literature of
              PV managed with improvised field resources and techniques.  Consultation with internal medicine determined a need for im-
                                                                 mediate phlebotomy given the patient’s elevated Hct of 47%.
              Keywords: phlebotomy; hematology; blood disorder; case report  AN Hct level above 45% can lead to complications such as
                                                                 stroke and myocardial infarction. However, the laboratory
                                                                 personnel determined that they could not facilitate such a large
                                                                 volume in a measured way without numerous venipunctures.
              Introduction
                                                                 Through coordination with local military medical personnel,
              PV is a well-established medical disease of excessive production   ED staff secured a WB transfusion kit and collected one unit of
              of blood cells with fatal outcomes if not managed correctly.   blood from the patient using proven field-expedient measuring
              Medication therapy is effective but generally not compatible   techniques of paracord at 6.5 inches around the waistline of
              with active-duty military service. Routine phlebotomy is there-  the collection bag (Figures 2 and 3).  ED staff proceeded to
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              fore the best management option; however, this can be seem   repeat this procedure over the next 9 months after telecon-
              difficult with limited access to dedicated laboratory resources.   sultation with hematology and in coordination with internal
              The availability of WB transfusion kits in operational settings   medicine during the patient’s tour of duty to maintain a largely
              may enable frontline providers to supplement specialty care   stable CBC profile, which relieved much of the patient’s symp-
              and decrease the risk of PV complications. We report a case of   toms. The patient maintained his daily medications during this
              an active-duty Soldier with PV whose condition was success-  time and had no significant adverse events from the procedure
              fully managed by phlebotomy utilizing WB transfusion kits,   or his polycythemia vera condition. Despite the authors pre-
              with a subsequent relevant review of the literature.  viously utilizing this process in a deployed setting, this is the
                                                                 first reported case of such management in military literature.
              Case Presentation
              A 44-year-old active-duty man diagnosed with PV was trans-  Discussion
              ferred to the local emergency department (ED) for acute man-
              agement after complaining of ongoing substernal chest pressure   PV  is  a  myeloproliferative  neoplastic  disorder  characterized
              and bilateral lower extremity paresthesias, with a secondary   by excessive stem cell production resulting in abnormally high

              *Correspondence to brandon.m.carius.mil@mail.mil
              1 Brandon M. Carius is affiliated with the Department of Emergency Medicine, Madigan Army Community Hospital, Joint Base Lewis-McChord,
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              WA.  Peter M. Dodge is affiliated with the University of New Hampshire, Durham, NH.  Joshua A. Bates is affiliated with the 5th Medical Re-
                 2
              cruiting Battalion, Dallas, TX.  Philip Castañeda is affiliated with the Department of Emergency Medicine, Madigan Army Community Hospital,
                                   4
              Joint Base Lewis-McChord, WA
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