TY - JOUR
T1 - Feasibility of commercially marketed health devices for potential clinical application
AU - Uchimura, Kevin D.
AU - Adamson, Teagan L.
AU - Karaniuk, Kara M.
AU - Spano, Mark L.
AU - La Belle, Jeffrey T.
N1 - Funding Information:
Special thanks to Dr. Heather Ross for her invalu-able assistance in developing this paper. In addition, the authors thank all members of the OnBody Sensing team at Arizona State University for their efforts in collecting data as well as all those who partici-pated in the study. The authors also thank ASU SIF funding for supporting our research.
Publisher Copyright:
© 2019 by Begell House, Inc.
Copyright:
Copyright 2019 Elsevier B.V., All rights reserved.
PY - 2019
Y1 - 2019
N2 - Concerns have been raised regarding the lack of validation on consumer-marketed health-monitoring de-vices. An investigation to characterize current health monitoring devices was carried out in the laboratory using widely accepted clinical and industry criteria. In total, 16 unique devices were examined. These devices were assessed according to their sensing modalities: step count, blood pressure, body temperature, electrocardiogram, blood oxygen saturation, and respiratory rate. Devices were tested at rest and immediately following exercise. Our results revealed that only four devices meet target requirements for accuracy. The AliveCor, a portable ECG monitor, accurately detected the heart rate for 87% of all recordings. To meet the target criterion for accuracy, the heart rate must be within ± 5 beats/minute or 10% of the standard measurement, whichever is lower. The Withings Pulse Ox, the Tinké, and the Santamedical SM-110 measured blood oxygen saturation with 2.1, 2.6, and 1.4 root-mean-square (rms) error, respectively. For blood oxygen saturation, the device should demonstrate rms error of < 3%. However, the Withings Pulse Ox and the Tinké failed to meet the accuracy criteria for their alternative biosensing capabilities: step count and respiratory rate, respectively. We conclude that the use of consumer-marketed health-monitoring devices for clinical or medical purposes should be under-taken with caution, especially in the absence of FDA or comparable clearance.
AB - Concerns have been raised regarding the lack of validation on consumer-marketed health-monitoring de-vices. An investigation to characterize current health monitoring devices was carried out in the laboratory using widely accepted clinical and industry criteria. In total, 16 unique devices were examined. These devices were assessed according to their sensing modalities: step count, blood pressure, body temperature, electrocardiogram, blood oxygen saturation, and respiratory rate. Devices were tested at rest and immediately following exercise. Our results revealed that only four devices meet target requirements for accuracy. The AliveCor, a portable ECG monitor, accurately detected the heart rate for 87% of all recordings. To meet the target criterion for accuracy, the heart rate must be within ± 5 beats/minute or 10% of the standard measurement, whichever is lower. The Withings Pulse Ox, the Tinké, and the Santamedical SM-110 measured blood oxygen saturation with 2.1, 2.6, and 1.4 root-mean-square (rms) error, respectively. For blood oxygen saturation, the device should demonstrate rms error of < 3%. However, the Withings Pulse Ox and the Tinké failed to meet the accuracy criteria for their alternative biosensing capabilities: step count and respiratory rate, respectively. We conclude that the use of consumer-marketed health-monitoring devices for clinical or medical purposes should be under-taken with caution, especially in the absence of FDA or comparable clearance.
KW - Fitness devices
KW - MHealth
KW - Quantified self
KW - Readmission
KW - Wearable sensors
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U2 - 10.1615/CritRevBiomedEng.2019026110
DO - 10.1615/CritRevBiomedEng.2019026110
M3 - Article
AN - SCOPUS:85067971121
SN - 0278-940X
VL - 47
SP - 159
EP - 167
JO - Critical Reviews in Biomedical Engineering
JF - Critical Reviews in Biomedical Engineering
IS - 2
ER -