Page 59 - 2022 Spring JSOM
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success rates or times to completion. Further, we hypothesized   each individual participant. Per the manufacturer’s recommen-
              that there would be no statistically significant differences be-  dations, participants were instructed first to ensure that the
              tween lighting conditions in perceived difficulty for IV and IO   NVGs were focused two-thirds of the way to infinity, then at-
              placement, user confidence, or user preference.    tach the Tarsier Eclipse to NVG tube, close the Tarsier Eclipse
                                                                 aperture to the smallest opening, and slowly open the Tarsier
                                                                 Eclipse to allow the appropriate amount of light needed, as
              Methods
                                                                 determined by the participant.
              Setting
              This study was conducted at the Naval Medical Center San Di-  Intravenous Access Mannequins
              ego (NMCSD). This study complied with the ethical guidelines   Multi-Venous IV Training Arms (Laerdal Medical) with over-
              of  the AMA  and  NMCSD, including Institutional  Research   lying modified IV Suture Sleeves (Strategic Operations) that
              Board approval. Written informed consent was acquired   employ dyed red water as simulated blood were used. IV ac-
              from each participant prior to data collection. All materials   cess also required nitrile gloves, elastic tourniquet, alcohol
              were provided by the participants, supplied by the NMCSD   pad, 18-gauge IV needle with catheter, MicroClave Clear neu-
              Bioskills Simulation Center, or purchased by the authors.  tral connector (ICU Medical), window transparent film dress-
                                                                 ing (6 × 7cm), 10mL syringe, and gauze sponge (5.1 × 5.1 cm).
              Participants
              The participants were 23 United States Navy medical personnel   Intraosseous Access Mannequins
              who met the inclusion criteria indicating previous Tactical Com-  SimMan 3G (Laerdal Medical) simulation legs were used for
              bat Casualty Care (TCCC)  training,  although  exact courses   tibial IO access. IO access also required the ChloraPrep Frepp
              were not collected, and being familiar with the use of NVGs.   (Becton, Dickinson) 1.5mL applicator (2% chlorhexidine glu-
              Tests of power using G*Power software indicated a minimum   conate/70% isopropyl alcohol), nitrile gloves, EZ-IO Power
              of 18 participants would be needed to achieve 80% power.  To   Driver, EZ-IO 25-mm 15-gauge needle set, and EZ-Connect
                                                          15
              ensure adequate power, we included 23 participants.  Extension Set (Teflex).

              Most (18/23; 78%) participants were US Special Operations   Procedures
              (SO) medics, with 17% (4/23) Special Amphibious Recon-
              naissance Corpsmen (SARCs), and 4% (1/23) Field Medical   Room Preparation
                                                                 A simulation laboratory was adapted for low-light conditions
              Service Technicians (FMSTs). Participants averaged 8.5 (±1.2)   by covering all possible light sources, so that ambient light was
              years of military service. None of the participants was color-  reduced to <0.3 lux, as confirmed by a lux meter. Two IV sim-
              blind, and 9% (2/23) reported wearing contact lenses. Partic-  ulation arm stations and two IO simulation leg stations were
              ipants ranged from familiar to expert with headlamps (mean   arranged in the room, separated by physical barriers.
              [M] = 4.7 ± 0.1 on 1-to-5 scale ranging from no familiarity to
              expert) and with NVGs (M = 4.4 ± 0.1). Most (18/23; 78%)
              had no familiarity with the focusing adaptors (M = 1.6 ± 0.3).   Informed Consent
                                                                 In a lighted room adjacent to the simulation lab, participants
              All participants reported using headlamps and NVGs in oper-  signed a consent form that provided an overview of the study
              ational environments, while 3 of 23 (13%) reported prior use   and detailed participant rights to privacy, confidentiality, and
              of NVG+A in operational environments.
                                                                 withdrawal from the study at any time or to refuse to answer
                                                                 any survey questions. Prior to signing the consent form, an
              Materials
                                                                 ombudsman was available to address all participant questions
              Tactical Headlamp                                  and concerns. Following informed consent, participants com-
              The Storm Headlamp (Black Diamond) is lightweight (110 g   pleted the pretest survey.

              with four AAA batteries), measures 2.54 × 5.08 × 2.54 cm,
              and has a maximum output of 350 lumens. White, red, green,   Training and Instructions
              and blue hues are available, but only green light was used in   After providing informed consent and completing the pre-
              our study, based on prior research demonstrating green as the   testing survey, participants entered the darkened simulation
              optimal hue for medical procedures of the hues available with   laboratory  room. Following  the 10-minute  dark-adaptation
              this headlamp, and to match the green phosphor color of the   period, participants familiarized themselves with the equip-
              NVGs described below. 16–18                        ment by green chem light illumination and were provided in-
                                                                 structions on the procedural steps listed here:
              Night Vision Goggles                               IV Procedure Steps
              AN/PVS-31 dual-tube green phosphor NVGs weigh 595 g and
              measure 11.55 × 7.62 × 6.6 cm. These NVGs were provided   1.  Identify venous access point.
              by the study participants and were attached to participants’   2.  Apply tourniquet.
              helmets by the participants themselves.            3.  Clean access site with alcohol wipe.
                                                                 4.  Insert IV catheter.
                                                                 5.  Connect MicroClave Clear neutral connector.
              Adaptors                                           6.  Apply window transparent film dressing.
              Tarsier Eclipse (Matbock) focusing adaptors weigh 453 g,
              measure 5 × 5 × 2.5 cm, and were provided by the study team.   7.  Attach 10mL syringe to the MicroClave Clear neutral
              The rubber housing slides onto the objective lens of the AN/  connector.
              PVS-31 NVGs and retains its position by friction. The adap-  IO Procedure Steps
              tors are focused by rotating the outside housing to increase   1.  Identify tibial IO insertion site.
              or decrease the aperture of the iris. The aperture was set by   2.  Clean insertion site with ChloraPrep.


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