Cardiovascular Digital Health Journal (Aug 2021)

Physical activity, patient-reported symptoms, and clinical events: Insights into postprocedural recovery from personal digital devices

  • Victoria L. Bartlett, BA,
  • Joseph S. Ross, MD, MHS,
  • Nilay D. Shah, PhD,
  • Laura Ciaccio, MSc,
  • Joseph G. Akar, MD, PhD,
  • Peter A. Noseworthy, MD, FHRS,
  • Sanket S. Dhruva, MD, MHS

Journal volume & issue
Vol. 2, no. 4
pp. 212 – 221

Abstract

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Background: Personal digital devices may offer insights into patient recovery and an approach for remote monitoring after procedures. Objective: To examine associations between activity measured using personal digital devices, patient-reported outcome measures (PROMs), and clinical events among patients after catheter ablation for atrial fibrillation (AF) or bariatric surgery. Methods: We aggregated personal digital device, PROM, and electronic health record data in a study conducted at 2 health systems. We used Fitbit devices for step count assessments, KardiaMobile for cardiac rhythm assessments, and PROMs for pain and palpitations over 5 weeks. Results: Among 59 patients, 30 underwent AF ablation and 29 bariatric surgery. Thirty-six patients (63%) reported pain. There was no difference in median [interquartile range] daily steps between patients with and those without pain (4419 [3286–7041] vs 3498 [2609–5888]; P = .23). Among AF ablation patients, 21 (70%) reported palpitations. Median daily steps were lower among those with palpitations than among those without (4668 [3021–6116] vs 8040 [6853–10,394]; P = .03). When accounting for within-subject correlation, recordings of AF were associated with a significant mean decrease in median daily steps (–351; 95% confidence interval –524 to –177; P <.01). Patients who received a new antiarrhythmic drug prescription had AF recorded in a median of 5 [5–5] of 5 total weeks, whereas patients who did not receive a new antiarrhythmic recorded AF in a median of 1 [0–3] week (P = .02). Conclusion: Personal digital device and PROM data can provide insight into postprocedural recovery outside of usual clinical settings and may inform follow-up and clinical decision-making. (ClinicalTrials.gov Identifier: NCT03436082)

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