Accuracy and role of consumer facing wearable technology for continuous monitoring during endoscopic procedures.

ambulatory anesthesia endoscopy gastrointestinal monitoring remote sensing technology wearable electronic devices

Journal

Frontiers in digital health
ISSN: 2673-253X
Titre abrégé: Front Digit Health
Pays: Switzerland
ID NLM: 101771889

Informations de publication

Date de publication:
2024
Historique:
received: 24 04 2024
accepted: 22 08 2024
medline: 2 10 2024
pubmed: 2 10 2024
entrez: 2 10 2024
Statut: epublish

Résumé

Consumer facing wearable devices capture significant amounts of biometric data. The primary aim of this study is to determine the accuracy of consumer-facing wearable technology for continuous monitoring compared to standard anesthesia monitoring during endoscopic procedures. Secondary aims were to assess patient and provider perceptions of these devices in clinical settings. Patients undergoing endoscopy with anesthesia support from June 2021 to June 2022 were provided a smartwatch (Apple Watch Series 7, Apple Inc., Cupertino, CA) and accessories including continuous ECG monitor and pulse oximeter (Qardio Inc., San Francisco, CA) for the duration of their procedure. Vital sign data from the wearable devices was compared to in-room anesthesia monitors. Concordance with anesthesia monitoring was assessed with interclass correlation coefficients (ICC). Surveys were then distributed to patients and clinicians to assess patient and provider preferences regarding the use of the wearable devices during procedures. 292 unique procedures were enrolled with a median anesthesia duration of 34 min (IQR 25-47). High fidelity readings were successfully recorded with wearable devices for heart rate in 279 (95.5%) cases, oxygen in 203 (69.5%), and respiratory rate in 154 (52.7%). ICCs for watch and accessories were 0.54 (95% CI 0.46-0.62) for tachycardia, 0.03 (95% CI 0-0.14) for bradycardia, and 0.33 (0.22-0.43) for oxygen desaturation. Patients generally felt the devices were more accurate (56.3% vs. 20.0% agree, Smartwatches perform poorly for continuous data collection compared to gold standard anesthesia monitoring. Refinement in software development is required if these devices are to be used for continuous, intensive vital sign monitoring.

Sections du résumé

Background UNASSIGNED
Consumer facing wearable devices capture significant amounts of biometric data. The primary aim of this study is to determine the accuracy of consumer-facing wearable technology for continuous monitoring compared to standard anesthesia monitoring during endoscopic procedures. Secondary aims were to assess patient and provider perceptions of these devices in clinical settings.
Methods UNASSIGNED
Patients undergoing endoscopy with anesthesia support from June 2021 to June 2022 were provided a smartwatch (Apple Watch Series 7, Apple Inc., Cupertino, CA) and accessories including continuous ECG monitor and pulse oximeter (Qardio Inc., San Francisco, CA) for the duration of their procedure. Vital sign data from the wearable devices was compared to in-room anesthesia monitors. Concordance with anesthesia monitoring was assessed with interclass correlation coefficients (ICC). Surveys were then distributed to patients and clinicians to assess patient and provider preferences regarding the use of the wearable devices during procedures.
Results UNASSIGNED
292 unique procedures were enrolled with a median anesthesia duration of 34 min (IQR 25-47). High fidelity readings were successfully recorded with wearable devices for heart rate in 279 (95.5%) cases, oxygen in 203 (69.5%), and respiratory rate in 154 (52.7%). ICCs for watch and accessories were 0.54 (95% CI 0.46-0.62) for tachycardia, 0.03 (95% CI 0-0.14) for bradycardia, and 0.33 (0.22-0.43) for oxygen desaturation. Patients generally felt the devices were more accurate (56.3% vs. 20.0% agree,
Conclusion UNASSIGNED
Smartwatches perform poorly for continuous data collection compared to gold standard anesthesia monitoring. Refinement in software development is required if these devices are to be used for continuous, intensive vital sign monitoring.

Identifiants

pubmed: 39355612
doi: 10.3389/fdgth.2024.1422929
pmc: PMC11443421
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1422929

Informations de copyright

© 2024 AbiMansour, Kaur, Velaga, Vatsavayi, Vogt and Chandrasekhara.

Déclaration de conflit d'intérêts

VC is a consultant for Covidien LP and Boston Scientific, receives research funding from Micro-tech Endoscopy and is a shareholder at Nevakar Corporation. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Auteurs

Jad P AbiMansour (JP)

Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, United States.

Jyotroop Kaur (J)

Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, United States.

Saran Velaga (S)

Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, United States.

Priyanka Vatsavayi (P)

Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, United States.

Matthew Vogt (M)

Department of Anesthesia and Perioperative Medicine, Mayo Clinic, Rochester, MN, United States.

Vinay Chandrasekhara (V)

Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, United States.

Classifications MeSH