Remote monitoring of atrial fibrillation recurrence using mHealth technology (REMOTE-AF)

Gamith Adasuriya, Andrey Barsky, Ines Kralj-Hans, Siddhartha Mohan, Simrat Gill, Zhong Chen, Julian Jarman, David Jones, Haseeb Valli, Georgios V Gkoutos, Vias Markides, Wajid Hussain, Tom Wong, Dipak Kotecha, Shouvik Haldar*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

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Abstract

Aims: This proof-of-concept study sought to evaluate changes in heart rate (HR) obtained from a consumer wearable device and compare against implantable loop recorder (ILR)-detected recurrence of atrial fibrillation (AF) and atrial tachycardia (AT) after AF ablation.

Methods and results: REMOTE-AF (NCT05037136) was a prospectively designed sub-study of the CASA-AF randomized controlled trial (NCT04280042). Participants without a permanent pacemaker had an ILR implanted at their index ablation procedure for longstanding persistent AF. Heart rate and step count were continuously monitored using photoplethysmography (PPG) from a commercially available wrist-worn wearable. Photoplethysmography-recorded HR data were pre-processed with noise filtration and episodes at 1-min interval over 30 min of HR elevations (Z-score = 2) were compared with corresponding ILR data. Thirty-five patients were enrolled, with mean age 70.3 ± 6.8 years and median follow-up 10 months (interquartile range 8–12 months). Implantable loop recorder analysis revealed 17 out of 35 patients (49%) had recurrence of AF/AT. Compared with ILR recurrence, wearable-derived elevations in HR ≥ 110 beats per minute had a sensitivity of 95.3%, specificity 54.1%, positive predictive value (PPV) 15.8%, negative predictive value (NPV) 99.2%, and overall accuracy 57.4%. With PPG-recorded HR elevation spikes (non-exercise related), the sensitivity was 87.5%, specificity 62.2%, PPV 39.2%, NPV 92.3%, and overall accuracy 64.0% in the entire patient cohort. In the AF/AT recurrence only group, sensitivity was 87.6%, specificity 68.3%, PPV 53.6%, NPV 93.0%, and overall accuracy 75.0%.

Conclusion: Consumer wearable devices have the potential to contribute to arrhythmia detection after AF ablation.

Study Registration: ClinicalTrials.gov Identifier: NCT05037136 https://clinicaltrials.gov/ct2/show/NCT05037136
Original languageEnglish
Pages (from-to)344-355
Number of pages12
JournalEuropean Heart Journal - Digital Health
Volume5
Issue number3
Early online date12 Feb 2024
DOIs
Publication statusPublished - May 2024

Keywords

  • Wearables
  • Ablation
  • Atrial fibrillation
  • Remote monitoring
  • Digital health

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