Page 51 - JSOM Spring 2020
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Characterizing a System for
                                       Measuring Limb Tourniquet Pressures




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                             Emma Hingtgen, BS ; Piper Wall, DVM, PhD *; Charisse Buising, PhD   3



              ABSTRACT
              Background: Pressure is an important variable in emergency   Most emergency use limb tourniquets do not provide tourni-
              use limb tourniquet science. This study characterizes one sys-  quet pressure measurements. The characteristics of any sys-
              tem for measuring tourniquet-applied pressure.  Methods: A   tem used to measure tourniquet pressures  are important to
              neonatal blood pressure cuff bladder was inflated to target   understanding how the system being used might influence the
              pressures  over atmospheric.  Unconstrained or constrained   measurements obtained and what the obtained measurements
              within 1-inch tubular polyester webbing, the neonatal cuff was   represent. The purpose of this study is to provide a characteri-
              placed in a 500mL Erlenmeyer flask. A 3-hole stopper provided   zation of one system for investigating the pressures under limb
              connections to flask interior (chamber) and bladder pressure   tourniquets.
              sensors and a 60mL syringe for altering chamber pressure: at-
              mospheric to >1500mmHg absolute to atmospheric.  Results:   Methods
              Within a finite range of chamber pressures, the neonatal cuff-
              based system accurately indicates applied pressure (minimum   As shown in Figure 1, a No. 1 neonatal blood pressure cuff
              and maximum 95% confidence interval linear regression   (2.2cm  ×  6.5cm bladder, single  tube)  was  placed inside  a
              slopes of 0.9871 to 0.9953 and  y-intercepts of –0.1144 to   500mL Erlenmeyer flask (Pyrex ). The neonatal cuff was ei-
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              2.157). The visually defined linear response ranges for blad-  ther unconstrained (Figure 1A–C) or constrained (Figure 1D)
              der inflation pressures were as follows for unconstrained/  by being fully enclosed in 1-inch tubular polyester webbing
              constrained: 100 to 400mmHg unconstrained/450mmHg   sewn closed at both ends. The Erlenmeyer flask had a size 7
              constrained for 10mmHg, 150 unconstrained/100 constrained   Twistit  3-hole rubber stopper (The Plasticoid Company, plas-
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              to 450mmHg for 12mmHg, 150 to 500mmHg for 15mmHg,   ticoid.com). Tight-fitting rigid tubing was forced through 1 of
              150 to 500mmHg unconstrained/550mmHg constrained for   the holes. Inside the flask, the rigid tubing was connected to the
              18mmHg, 150 to 550mmHg for 21mmHg. Below the linear   bladder of the neonatal cuff. Outside the flask, the rigid tubing
              response range, the inflated bladder system indicated higher   was connected by a 4-way stopcock to a gas pressure sensor
              pressures than chamber pressures. Above the linear response   system (Vernier Gas Pressure Sensor, Vernier LabPro interface,
              range, the system indicated progressively lower pressures than   and Logger Pro Softwar; Vernier Software and Technology,
              chamber pressures.  Conclusions: Within the linear response   www.vernier.com). The other 2 holes in the rubber stopper
              range,  the  bladder  pressure  accurately  indicates  surface-ap-  contained tapered valve connectors attached to 4-way stop-
              plied pressure.                                    cocks. One stopcock connected the flask interior to a second
                                                                 Vernier Gas Pressure Sensor for direct chamber pressure mea-
              Keywords: pressure; reference standards; tourniquet; hem-  surements. The other stopcock connected the flask interior to a
              orrhage; first aid; emergency treatment            60mL luer-lock syringe for adding air to or removing air from
                                                                 the chamber. To avoid air leak during chamber pressurization,
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                                                                 the stopper was held tightly in the flask via the rope, Parafilm
                                                                 (Bemis Company, www.bemis.com), and 2 hands.
              Introduction
              Pressure and time are the major determinants of tissue dam-  For each trial, the bladder of the neonatal cuff was inflated to
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              age with limb tourniquet use.  Pressure and surface area are   the following target pressures above atmospheric pressure: 10,
              the major determinants of tourniquet-applied force for arte-  12, 15, 18, and 21mmHg. For each target pressure, at least
              rial occlusion. Pressure, therefore, is an important variable   3 trials with starting bladder pressures within 0.5mmHg of
              in emergency use limb tourniquet science. This means tour-  the target pressure and of each other were completed. Because
              niquet producers, recommending or certifying organizations,   that stringency was not the initial strategy, some target pres-
              purchasing decision makers, and potential users should all   sures have more than 3 trials. In those instances, data from all
              have some interest in and access  to information concerning   the trials were analyzed and graphed, but only the 3 within
              the pressures associated with arterial occlusion and completed   0.5mmHg of the target pressure and of each other were used
              application of tourniquets they are considering.   as a triplicate for linear and nonlinear regressions.
              *Correspondence to piperwall@q.com
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              1 Ms Hingtgen is a researcher at Drake University.  Dr Wall is a researcher in the Surgery Education Department, UnityPoint Health Iowa Meth-
              odist Medical Center, Des Moines, IA.  Dr Buising is a professor of biology and the director of the Biochemistry, Cell and Molecular Biology
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              Program, Drake University, Des Moines, IA.
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