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repeated after 30 minutes if the patient is still in shock,   was induced with ketamine (10mg/kg IM) and inhaled
          with no more than 1000mL of the fluid.  Hextend is a   isoflurane (4%) and oxygen (100% Fio ). Isoflurane was
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                                                                                              2
          plasma volume expander containing 6% hydroxyethyl   reduced to 1%–2% following airway instrumentation for
          starch (HES) in a physiologically balanced medium of   the remainder of the experiment. The animals were venti-
          electrolytes, glucose, and lactate (weight average, molec-  lated with a tidal volume of 8–10mL/kg and a respiratory
          ular weight 670kDa, molar substitution 0.75). The het-  rate of 12 breaths per minute using a Narkomed 3A anes-
          astarch component of Hextend creates oncotic pressure,   thesia machine (Drager Medical Systems, Telford, PA). The
          which would normally be provided by blood proteins,   left carotid artery was cannulated with a 20-gauge catheter
          and permits retention of intravascular fluid.  Several   used for monitoring. We used a GE Marquette Solar 800
                                                  15
          studies have demonstrated the benefits of Hextend. 16–21    monitor (GE Healthcare, Pittsburgh, PA) to continuously
          For example, Ogilvie  et al. demonstrated  a reduced   monitor HR, SBP, DBP, electrocardiogram, oxygen satura-
          number of early deaths and overall mortality when Hex-  tion, end-tidal carbon dioxide, and rectal temperature. In
          tend was administered. 22                          addition, the hemodynamics (SBP, DBP, HR, MAP, CO,
                                                             and SV) were continuously monitored using the Vigileo
          No study  has compared  IO  and IV routes  relative  to   Monitor (Edwards Lifesciences, Irvine, CA).
          time or hemodynamics relative Hextend administration
          in a hypovolemic model. The purposes of this study were   An 8.5 French × 10cm central venous catheter was in-
          to compare the time to administer 500mL of Hextend   serted in the right subclavian (Arrow International,
          and the hemodynamics of IV and IO routes in a Class II   Reading, PA) for the purpose of exsanguination. Fluid
          hemorrhage swine model. The hemodynamics included   deficit resulting from NPO time would potentially
          systolic blood pressure (SBP), diastolic blood pressure   change the volume of blood. Data were collected from
          (DBP), heart rate (HR), mean arterial pressure (MAP),   some subjects as early as 07:00 and some as late as
          cardiac output (CO), and stroke volume (SV). The re-  17:00. Hence, we administered a replacement of defi-
          search question that guided the study was as follows:  cit volume using normal saline so that the deficit would
                                                             not be confounding variable. The deficit was calculated
          Are there statistically significant differences between IO,   using the standard 4-2-1 method, Holiday-Segar for-
          IV, and control groups relative to time and hemodynam-  mula, before the experiment began. Normothermia was
          ics in the administration of Hextend?              maintained in each animal by the use of a Bair-Hugger
                                                             Model 505 forced air-warming blanket (Arizant Inc.,
                                                             Prairie, MN) to sustain body temperature greater than
          Procedures
                                                             36.0°C. Swine in the IV group had an 18-gauge IV cath-
          We used data from a pilot study and calculated a large   eter placed in the left ear, and swine in the IO group
          effect size (.6). Using an effect size of .6, an α of .05,   had a 2.5cm EZ-IO 15-gauge needle (Vidacare Inc., San
          and a power of .80, we calculated that we would need   Antonio, TX) placed in the humerus. The humerus was
          nine subjects per group. This study was a prospective,   used because it is one of the recommended sites for IO
          experimental mixed (within- and between-) subjects de-  administration of fluids and drugs. The IO placement
          sign. The research protocol was approved by the local   was verified via aspiration of blood and effortless infu-
          Institutional Animal Care and Use Committee (IACUC).   sion of a 20mL normal saline bolus. In all groups, we
          The animals received care in accordance with the Ani-  exsanguinated 30% of the swine’s blood volume, which
          mal Welfare Act and The Guide for the Care and Use of   was calculated based on the weight of each pig. Swine
          Laboratory Animals. Twenty-seven Sus scrofa Yorkshire-  have the same blood volume as humans (70mL/kg of
          cross swine weighing between 67 and 80 kg were equally   weight); therefore, a pig that weighs 70 kg has about
          assigned by the use of computer-generated random num-  4900mL of blood volume, and 30% exsanguination is
          bers to one of three groups: humerus IO (IO group) (n =   equal to 1470mL. Thirty percent blood loss represents a
          9), IV (IV group) (n = 9), and control group (n = 9). The   Class II hemorrhage. The blood was exsanguinated via
          rationale for using this weight range is that it represents   gravity from the subclavian over 15 to 20 minutes and
          the average weight of the U.S. Army Soldier.  To avoid   was weighed with an electronic scale (Thermal Indus-
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          any variability in subjects, we purchased the pigs from   tries of Florida, Owatonna, MN) for calculation of the
          the same vendor and used pigs approximately the same   30%. A container was placed on the scale and zeroed to
          size and the same gender (male). The swine were fed a   account for variations in container weights.
          standard diet and were observed for 3 days to ensure a
          good state of health. All of the swine were NPO after   Data (vital signs and hemodynamics) were collected im-
          midnight the day before the experiment.            mediately before and after the hemorrhage. After the
                                                             hemorrhage, we administered 500mL of Hextend ad-
          The swine were sedated with buprenorphine (0.01mg/kg   ministered via either the IO or IV route with a pneumatic
          IM) 30 minutes before anesthetic induction. Anesthesia   pressure bag. One investigator continuously monitored



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