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Diagnosis of Atrial Fibrillation in Postoperative Thoracic Surgery Using a Smartwatch

Diagnosis of Atrial Fibrillation in Postoperative Thoracic Surgery Using a Smartwatch

Recruiting
18 years and older
All
Phase N/A

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Overview

Postoperative atrial fibrillation (POAF) occurs in approximately 20% of patients following thoracic surgery. Early diagnosis is essential to prevent complications such as heart failure, stroke, myocardial infarction, and increased mortality. Smartwatches equipped with single-lead ECG capabilities and algorithms to detect asymptomatic atrial fibrillation (AF) offer a potential solution. This study aims to evaluate the effectiveness of smartwatches in detecting POAF compared to standard care.

Eligibility

Inclusion Criteria:

  • Adults (>18 years old).
  • Patients undergoing major thoracic surgery with one-lung ventilation within the past 48 hours.
  • Scheduled pneumonectomy or lobectomy.
  • Admission to a conventional surgical unit postoperatively.
  • Ability to perform single-lead ECG using a smartwatch.
  • Coverage under a social security system.
  • Signed informed consent

Exclusion Criteria:

  • History of atrial fibrillation.
  • Requirement for telemetry for AV block or tachyarrhythmias (>140 bpm).
  • Dependency on a pacemaker.
  • Participation in another interventional clinical trial affecting POAF incidence.
  • Mediastinal, pleural, or chest wall surgery.
  • Reoperations or surgeries performed more than 48 hours prior.
  • Pregnant women.
  • Patients under guardians or similar legal protection.

Study details
    Postoperative Atrial Fibrillation
    Thoracic Surgery
    Smartwatches
    Rhythm Monitoring
    Cardiovascular Prognosis
    Asymptomatic Atrial Fibrillation
    Randomized Trial

NCT06724718

Centre Hospitalier Universitaire, Amiens

15 October 2025

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