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Pilot Study of Emergency Department Patient Vital Signs Acquisition Using Experimental Video Photoplethysmography and Passive Infrared Thermography Devices

机译:急诊院患者生命符号采集使用实验型录像和无源红外热成像装置的试验研究

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Objective: Investigators conducted pilot sessions in live Emergency Department (ED) settings to prepare for formal comparative study of contact and experimental non-contact vital signs (VS) measurement devices. Methods: Contact-based cardiorespiratory monitors (CM) and video photoplethysmography (vPPG) measured heart rates (HR); contact thermometers and passive infrared thermography (pIR) obtained core and surface temperatures. Subject VS data comprised two 25-min CM and vPPG recordings (initial unprimed “Triage Check” window; four 1-min “Full Check” windows; 20min of “Resting” intervals) and temperature measurements. Results: Forty-eight of 102 approached patients participated: at least 5 subjects each in 0-12mo, 1-5y, 6-12y, 13-17y age-groups, and at least 2 subjects each in 18-29y, 30-39y, 40-49y, 50-59y, 60-69y, 70-79y, 80+y age-groups. Subjects were 40.4% female with median Fitzpatrick skin type of 3.0 (interquartile range 1-3: 2.0-5.0), ESI score of 3.0 (2.0-3.0), and core temperature of 98.6°F (97.9-99.1°F). Twelve subjects were excluded from vPPG analysis due to inadequate lighting, excessive motion, and/or datastream loss. From the remaining 36 subjects with median HRCM of 78.2bpm (69.8-94.8bpm), vPPG measured median HRvPPGof 75.0bpm (68.3-93.0bpm) from 170 (70.5%) of 241 possible Full Check windows; the median difference between HRCM and HRvPPG was 0.6bpm (-0.2-2.3bpm). All Emergency Severity Index (ESI) HR components for 34 subjects with Triage Check HRvPPGmeasurements matched CM-based ESI HR components. Median differences between contact and pIR temperatures ranged from ?5.4°F to ?4.4°F. Conclusion: vPPG and pIR devices experimentally measured select live VS with promising results. Significance: Pilot data and protocol testing set the groundwork for full-scale ED vPPG-pIR investigation.
机译:目的:调查人员在现场应急部门(ED)设置中进行了试验课程,为接触和实验性非接触生命标志(VS)测量装置的正式比较研究做好准备。方法:基于接触的心肺监测器(CM)和视频光学质溶血(VPPG)测量的心脏速率(HR);接触温度计和被动红外热成像(PIR)获得了核心和表面温度。主题VS数据包括两个25分钟的CM和VPPG录制(初始未提升的“分类检查”窗口;四个1分钟“完全检查”窗口; 20分钟的“休息”间隔)和温度测量。结果:102例接近患者参加了48名患者:至少5名受试者,每次,1-5Y,6-12y,13-17岁的年龄组,和至少2个受试者,每人18-29y,30-39y ,40-49Y,50-59Y,60-69Y,70-79Y,80 + y年龄组。受试者是40.4%的女性,中位菲茨帕特里克皮肤型3.0(四分位数范围1-3:2.0-5.0),ESI得分为3.0(2.0-3.0),核心温度为98.6°F(97.9-99.1°F)。由于照明,过度运动和/或数据流损失不足,由于光线,过度的运动和/或数据流损失不足,从VPPG分析中排除了12个受试者。从剩下的36个受试者与中位数 cm 78.2bpm(69.8-94.8bpm),VPPG测量中位数 vppg 75.0bpm(68.3-93.0bpm)从170(70.5%)241可能完整支票窗口;人力资源之间的中位数 cm 和小时 vppg 为0.6bpm(-0.2-2.3bpm)。所有紧急严重性指数(ESI)HR组件有34个具有分类检查HR的受试者 vppg 测量匹配基于CM的ESI HR组件。接触和PiR温度之间的中值差异范围为5.4°F至4.4°F。结论:VPPG和PIR设备通过有前途测量选择Live VS。意义:试验数据和协议测试设置全规模ED VPPG-PIR调查的基础。

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