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during trauma care. Existing studies have primarily evalu-  Responses were recorded using a 5-point Likert scale, rang-
          ated these systems under laboratory conditions using crystal-  ing from “strongly disagree” to “strongly agree.” Additionally,
          loid or packed red blood cells, with performance varying by   medics were asked to identify which one device they would
                                                  ™
          heating mechanism and flow rate. The Buddy Lite  has not   prefer to deploy with, and to explain their choice using open-
          performed adequately at elevated flow rates, showing outlet   ended responses. The full survey instrument is provided in the
          temperatures  near  24–25°C  at  100mL/min  and  operational   Supplemental Information.
                                                         ™
          failures above 100–200mL/min. 9–11  The MEQU M Warmer
          has maintained outlet temperatures ≥35°C up to 200mL/min   Quantitative Likert-based data were transformed to integers
          without evidence of hemolysis in vitro. 11,12  The Thermal An-  in sequence (i.e., Likert ratings [LRs]), ranging from “strongly
            ®
          gel  performs effectively at lower flow rates (<100mL/min)   disagree” (–2) to “neutral” (0) and “strongly agree” (+2). LRs
          but demonstrates reduced warming capacity at higher flow   were summarized as median (interquartile range [IQR]) and
                           ™
          rates. 9,11  The QinFlow  devices have achieved outlet tempera-  compared using the Kruskal-Wallis test with Dunn’s multiple
          tures  of  approximately  34°C  when  warming  10°C  saline  at   comparisons test for post-hoc analysis. Multiplicity-adjusted
          200mL/min, while the NAR Quantum  has reported similar   P values were reported with statistical significance established
                                        ™
          specifications, though independent peer-reviewed validation is   at P<.05.
          not yet available. 9,13,14  Across all devices, increased flow rates
          reduce contact time with the heating element, leading to lower   Qualitative free-response data regarding blood warmer device
          outlet temperatures. 11,12,15                      preferences were qualitatively summarized. All available free-
                                                             text comments were compiled. Each respondent’s preference
          While the role of fluid warmers in trauma resuscitation has   comments were examined line-by-line to identify keywords
          been previously evaluated, little is known about the experi-  and phrases (e.g., “compact,” “easy to use,” “packability”)
          ences and preferences of medics who operate these devices   that reflected the respondents’ reasoning. Comments were
          in austere and unpredictable environments. Accordingly, the   then  compiled into  broader  categories  with conceptual  sim-
          present study aimed to evaluate the self-perceived ease of use,   ilarities. These categories were then selectively coded into a
          ruggedness, and efficacy of five commonly used blood warm-  final core theoretical construct that captured the overall ratio-
                              ™
                                                  ™
          ing devices—the QinFlow , M Warmer, Buddy Lite , Thermal   nale behind respondents’ preferences.
                                                       ™
          Angel , and the North American Rescue (NAR) Quantum —
              ®
          based on direct user feedback. This study aims to provide hu-  Results
          man factor–driven insights to guide optimal device selection
          for trauma resuscitation in austere deployed settings. Prod-  A total of 35 NSW HMs based in the state of Virginia were
          ucts were selected based on the biomedical market’s current   surveyed in this study. The surveyed HMs had a median of 5
          available prehospital fluid warmers. All devices were operated   (IQR 3–12) years of experience and 73% had reported de-
          according to manufacturer instructions. Devices used are sum-  ployment experience. Of those who had previously deployed
          marized in Table 1.                                and managed combat casualties (n=26), 27% (7/26) reported
                                                             managing a casualty using a blood warming device. Although
                                                             the data were normally distributed, the Brown-Forsythe test
          Methods
                                                             suggested a violation of the assumption of variance homoge-
          All experiments were approved by the Naval Medical Cen-  neity (P<.05). Therefore, the Kruskal-Wallis H-test was used
          ter Portsmouth Institutional Review Board, and the study was   to compare results due to its increased robustness against vari-
          conducted in accordance with ethical standards and applicable   ance inequality.
          Department of Defense regulations.
                                                             Quantitative analysis of the Likert-based questions demon-
          After initial hands-on equipment familiarization, a convenience   strated that there were statistically significant differences in all
          sample of active-duty Naval Special Warfare (NSW) Corpsmen   questions asked (Table 2). There were significantly different an-
          (HMs) was surveyed to evaluate the perceived usability of five   swers with regards to perceived warmers’ ease of use (P<.0001).
          different blood warming devices. The survey was developed   The M Warmer attained the highest perceived ease of use scores
          by a multidisciplinary panel of physicians and special warfare   (LR=2.00 [IQR 1.00–2.00]) compared to all other warmers,
          medics with extensive deployment and prehospital resuscita-  including the Buddy Lite (LR=1.00 [IQR 0.00–1.50], P=.0005),
          tion backgrounds. It was designed to capture medics’ perspec-  NAR Quantum (LR=1.00 [IQR –1.00 to 2.00], P=.0003), and
          tives on critical human factors that influence performance and   the QinFlow (LR=0.00 [IQR –1.00 to 1.00], P<.0001). There
          device preference in austere environments.         were no significant differences between the M Warmer and the
                                                             Thermal Angel (LR=1.00 [IQR 1.00–2.00], P=.134).
          Specifically, three domains were emphasized in the survey: ease
          of use, ruggedness, and perceived efficacy/confidence.  These   Perceptions of device efficacy also differed significantly be-
          domains were chosen based on their direct relevance to oper-  tween devices (P=.0006), with the M Warmer again ranking
          ational decision-making and the real-world constraints medics   the  highest (LR=2.00  [IQR  1.00–2.00]).  This was  signifi-
          face in forward-deployed, resource-limited settings. Ease of use   cantly higher than the Buddy Lite (LR=1.00 [IQR 0.00–1.00],
          reflected the need for intuitive interfaces and rapid device de-  P=.0002).  All other ratings were nonsignificant compared
          ployment during medical resuscitation. Ruggedness captured   to the QinFlow (LR=1.00 [IQR 0.00–2.00], P=.1300), NAR
          the medics’ perceptions of a device’s durability and ability to   Quantum (LR=1.00 [IQR 0.00–2.00], P=.1327), and Thermal
          withstand environmental extremes experienced in far forward   Angel (1.00 [IQR 1.00–2.00], P>.999).
          prehospital environments. Perceived efficacy and confidence
          were included to assess the psychological and clinical trust   Finally, there were also significant differences in perceived re-
          medics placed in their equipment.                  liability of device construction (P<.0001), with the M Warmer

          12  |  JSOM   Volume 26, Edition 1 / Spring 2026
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