Clinical validation of automated QTc measurements from single lead ECG using a novel smartwatch

Abstract Funding Acknowledgements Type of funding sources: None. Introduction A possible side-effect of various medical drugs is prolongation of the electric repolarization of the heart, measured as the corrected QT-interval (QTc). Patients treated with these drugs should be monitored frequently via...

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Bibliographic Details
Published inEuropace (London, England) Vol. 24; no. Supplement_1
Main Authors Mannhart, D, Hennings, EH, Lischer, ML, Vernier, CV, Du Fay De Lavallaz, JDF, Knecht, SK, Schaer, BS, Osswald, SO, Kuehne, MK, Sticherling, CS, Badertscher, PB
Format Journal Article
LanguageEnglish
Published Oxford University Press 19.05.2022
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Summary:Abstract Funding Acknowledgements Type of funding sources: None. Introduction A possible side-effect of various medical drugs is prolongation of the electric repolarization of the heart, measured as the corrected QT-interval (QTc). Patients treated with these drugs should be monitored frequently via an ECG to screen for early changes indicating possible life-threating arrythmias. Especially during the Covid-19 pandemic, remote patient monitoring gained importance. The Withings Scanwatch offers automated analysis of the QTc remotely, thereby obviating the need for in-person visits. We aimed to compare automated QTc-measurements using a single lead ECG (SL-ECG) of a novel smartwatch (Withings Scanwatch, SW-ECG) with manual-measured QTc from a nearly simultaneously recorded standard 12-lead ECG. Methods We enrolled consecutive patients referred to a tertiary hospital for cardiac workup in a prospective, observational study. To obtain a SW-ECG, patients were instructed to keep their index finger on the stainless steel ring on the top case of the smartwatch continuously for 30 seconds The QT-interval was manually interpreted by two blinded, independent cardiologists through the tangent-method, using lead II or V5/V6. Bazett’s formula was used to calculate QTc. Results We prospectively enrolled 317 patients (48% female, mean age 63.3 ± 17.2 years). The smartwatch was able to automatically measure QTc-intervals in 177 patients (56%). The diagnostic accuracy of SW-ECG for detection of a QTc-interval ≥ 460ms as quantified by the area under the curve (AUC) was 0.91 (95%CI 86.4-95.9). The Bland-Altman analysis resulted in a bias of 6.6ms (95% limit of agreement (LoA) –58.6ms to 71.9ms) comparing automated QTc measurements via SW-ECG with manual QTc-measurement via 12-lead ECG (Figure 1). In 12 patients (6.9%) the difference between the two measurements was greater than the LoA. Premature ventricular complexes, noise or differences in heart rate were responsible in 8.3%, 83.0% and 8.3%, respectively, for observed outliers. Conclusion In this clinical validation of a direct-to-consumer smartwatch we found fair to good agreement between automated-SW-ECG QTc-measurements and manual 12-lead-QTc measurements. The SW-ECG, however, was only able to automatically calculate QTc-intervals in one half of all assessed patients. Our work shows, that the automated algorithm of the SW-ECG needs to be improved to be useful in a clinical setting.
ISSN:1099-5129
1532-2092
DOI:10.1093/europace/euac053.573