Page 12 - JSOM Fall 2024
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FIGURE 1  Study outline (n=20).

                                                Recruitment from medical school
                                                          (n=20)
                                                                                Excluded
                                                                                  (n=0)
                                                     Random allocation


                                 Group 1                                         Group 2
                                  (n=10)                                         (n=10)

                             Initial questionnaire                           Initial questionnaire
                             Hand measurements                              Hand measurements


                        Ventilate manikin without BENGI                  Ventilate manikin with BENGI
                      Scenario 1 (500mL at 10min  for 5min)           Scenario 1 (500mL at 10min  for 5min)
                                                                                          –1
                                          –1
                      Scenario 2 (750mL at 10min  for 5min)  ≥2 weeks   Scenario 2 (750mL at 10min  for 5min)
                                          –1
                                                                                          –1
                      Scenario 3 (300mL at 10min  for 5min)  later    Scenario 3 (300mL at 10min  for 5min)
                                          –1
                                                                                          –1
                       Scenario 4 (20mL at 6min  for 5min)             Scenario 4 (20mL at 6min  for 5min)
                                                                                         –1
                                         –1
                            Post-visit questionnaire                        Post-visit questionnaire
              Exclusion of scenario 4                                                    Exclusion of scenario 4
                  participants                                                               participants
                    (n=3)                                                                       (n=1)

                                                       Data analysis


          The solid line shows the participants’ path in group 1 (n=10) and the dotted lines for group 2 (n=10). The test lung was not switched out for the
          neonatal lungs for four participants (1 participant from group 1, 3 participants from group 2), and these scenario 4 data were excluded from the
          final analysis (n=16 for scenario 4); however, their scenarios 1 through 3 were included (n=20).
          BENGI = bag-valve-mask emergency narration guided instrument.

          provided by an onboard speaker, instructs the user to initiate   the target tidal volume calculated as |ΔV | = |V Ttarget  − V |. Sec-
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          inspiration. Other automatically triggered cues include “Bag   ondary outcomes included an absolute deviation from target
          faster,” “Bag slower,” or “Leak detected.” In this study, audio   RR, |ΔRR|, and changes in inter- and intra-participant varia-
          cues were muted, and indication for proper RR was provided   tion in V  and RR delivery.
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          by a metronome, as onboard audio cues may exceed timing
          between breaths when played.                       Participants were randomly assigned via computer-generated
                                                                             25
                                                             block randomization  (2 blocks of 10) to ventilate either with
          Study Design and Participants                      (n=10) or without (n=10) the BENGI during the first session.
          The Institutional Review Board of Louisiana State University   The participants and researchers were unblinded to the order
          Health Sciences Center Shreveport approved this study pro-  of sessions by the nature of the intervention. The participant’s
          tocol (study no. 00001766). In this randomized, prospective,   healthcare role  and basic life support (BLS) and advanced
          crossover, manikin simulation pilot study (Figure 1), partici-  cardiovascular life support (ACLS) certifications were docu-
          pants (n=20) were locally recruited from the associated medi-  mented, and their hand size and grip strength were measured.
          cal school. Based on previous studies with similar devices, 20–22    Participants were briefed on the primary study outcome and
          we determined a sample size of 20 to be adequate for our pilot   instructed how bag squeezing and releasing influences V  and
                                                                                                         T
          study. Inclusion criteria were age >18 years and in or preparing   RR. Participants were told the target V  and RR for each sce-
                                                                                           T
          for a healthcare profession; having had prior training was not   nario. The participants were given a description of how the au-
          mandatory. Participants manually ventilated a manikin for 5   dio “Go” cue (scenarios 1–3) and metronome cue (scenario 4)
          minutes under four different scenarios, at different target V s   would instruct the participant when to initiate a rescue breath
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          (500, 750,  300, and  20mL for  scenarios  1, 2, 3,  and 4, re-  using the BENGI. They were instructed on how the LED sig-
          spectively; see supplementary material for further explanation)   nals relate to the target V . No explanation on the other audio
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          and RRs (10min for scenarios 1–3 and 60min  for scenario   cues was given, and no help on interpretation of audiovisual
                       −1
                                               −1
          4). Manual ventilation either with or without guidance from   cues was provided during bagging sessions, unless the partic-
          the BENGI was performed during two separate bagging ses-  ipant failed to initiate a rescue breath after three subsequent
          sions with a period of at least 2 weeks between sessions. The   “Go” audio cues. The participants were blinded to their per-
          primary outcome was absolute deviation of V  or |ΔV |, from   formance throughout the study.
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          10  |  JSOM   Volume 24, Edition 3 / Fall 2024
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