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Wearability Testing of Ambulatory Vital Sign Monitoring Devices: Prospective Observational Cohort Study

机译:动态生命标志监测设备的耐磨性测试:前瞻性观察队列研究

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Background Timely recognition of patient deterioration remains challenging. Ambulatory monitoring systems (AMSs) may provide support to current monitoring practices; however, they need to be thoroughly tested before implementation in the clinical environment for early detection of deterioration. Objective The objective of this study was to assess the wearability of a selection of commercially available AMSs to inform a future prospective study of ambulatory vital sign monitors in an acute hospital ward. Methods Five pulse oximeters (4 with finger probes and 1 wrist-worn only, collecting pulse rates and oxygen saturation) and 2 chest patches (collecting heart rates and respiratory rates) were selected to be part of this study: The 2 chest-worn patches were VitalPatch (VitalConnect) and Peerbridge Cor (Peerbridge); the 4 wrist-worn devices with finger probe were Nonin WristOx2 3150 (Nonin), Checkme O2 (Viatom Technology), PC-68B, and AP-20 (both from Creative Medical); and the 1 solely wrist-worn device was Wavelet (Wavelet Health). Adult participants wore each device for up to 72 hours while performing usual “activities of daily living” and were asked to score the perceived exertion and perception of pain or discomfort by using the Borg CR-10 scale; thoughts and feelings caused by the AMS using the Comfort Rating Scale (CRS); and to provide general free text feedback. Median and IQRs were reported and nonparametric tests were used to assess differences between the devices’ CRS scores. Results Quantitative scores and feedback were collected in 70 completed questionnaires from 20 healthy volunteers, with each device tested approximately 10 times. The Wavelet seemed to be the most wearable device (P.001) with an overall median (IQR) CRS score of 1.00 (0.88). There were no statistically significant differences in wearability between the chest patches in the CRS total score; however, the VitalPatch was superior in the Attachment section (P=.04) with a median (IQR) score of 3.00 (1.00). General pain and discomfort scores and total percentage of time worn are also reflective of this. Conclusions Our results suggest that adult participants prefer to wear wrist-worn pulse oximeters without a probe compressing the fingertip and they prefer to wear a smaller chest patch. A compromise between wearability, reliability, and accuracy should be made for successful and practical integration of AMSs within the hospital environment.
机译:背景技术及时识别患者恶化仍然具有挑战性。守护监测系统(AMSS)可以为当前监测实践提供支持;然而,他们需要在实施前进行彻底测试,在临床环境中进行早期发现恶化。目的本研究的目的是评估各种市售AMS的耐磨性,以通知对急性医院病房的外国生命体征监视器的未来预期研究。方法选择五个脉冲血管计(4个用手指探针和1个腕部磨损,收集脉冲率和氧饱和度)和2个胸部贴片(收集心率和呼吸率)是本研究的一部分:2个胸部磨损的斑块是vitalpatch(vitalconnect)和peerbridge cor(peerbridge);带有手指探针的4个腕带的装置是非肾上腺素毒品毒素2 3150(非本文),Checkme O2(ViAtom技术),PC-68B和AP-20(来自Creative Medical);并且1个单独的手腕磨损的装置是小波(小波健康)。成人参与者在执行通常的“日常生活活动”的同时戴上每台设备长达72小时,并被要求通过使用Borg CR-10规模来评分对疼痛或不适的感知劳动和感知;使用舒适评级规模(CRS)由AMS引起的思想和感受;并提供一般的免费文本反馈。报告中位数和IQRS和IQRS,非参数测试用于评估设备CRS分数之间的差异。结果在70名已完成的20个健康志愿者中收集了定量分数和反馈,每个设备测试了大约10次。小波似乎是最可穿戴的设备(P <.001),总中位数(IQR)CRS评分为1.00(0.88)。 CRS总分中胸部斑块之间的耐磨性没有统计学上显着的差异;然而,VitalPatch在附件部分(P = .04)中的中位数(IQR)得分为3.00(1.00)。一般疼痛和不适分数和穿着的时间的总百分比也反映了这一点。结论我们的结果表明,成人参与者更喜欢佩戴手腕脉冲血管计,而无需压缩指尖,他们更喜欢佩戴较小的胸部贴片。应在医院环境内的成功和实际集成AMSS之间的耐磨性,可靠性和准确性之间的折衷。

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