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Postoperative Atrial Fibrillation in Cardiac Surgery

Recruiting
Conditions
Post-operative Atrial Fibrillation
Registration Number
NCT06958029
Lead Sponsor
Khon Kaen University
Brief Summary

This multicenter observational study aims to investigate the incidence and identify risk factors associated with postoperative atrial fibrillation (POAF) in patients undergoing cardiac surgery at three medical centers in Thailand. The study will examine patient characteristics, surgical factors, and anesthetic management practices that may contribute to the development of this common postoperative complication.

Detailed Description

Postoperative atrial fibrillation (POAF) is a common complication following cardiac surgery, with incidence rates reported between 15-30% after valve surgery and 18-74% after coronary artery bypass grafting. POAF typically occurs within 72 hours after surgery and is associated with increased morbidity, mortality, length of hospital stay, and healthcare costs.

The Society of Thoracic Surgeons has identified five major postoperative complications associated with cardiac surgery, including POAF, which can significantly affect patient outcomes. This multicenter observational study will examine the incidence and risk factors of POAF in cardiac surgery patients across three medical centers in Thailand: Srinagarind Hospital at Khon Kaen University, Northeastern Thailand Cardiac Center, and Surat Thani Hospital.

The study will collect data on patient demographics, comorbidities, preoperative laboratory values, perioperative characteristics, surgical procedures (valve surgery, CABG, combined procedures), and postoperative complications. By identifying risk factors associated with POAF, this study aims to develop preventive strategies and improve management protocols for patients at high risk for this complication.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
275
Inclusion Criteria
  • Age ≥ 18 years
  • Patients undergoing cardiac valve surgery or coronary artery bypass grafting (CABG) procedures
Exclusion Criteria
  • Patients undergoing aortic surgery
  • Patients undergoing MAZE procedure
  • Incomplete medical records
  • Patients who required mechanical circulatory support before surgery
  • Patients who died during surgery or within 3 days after surgery

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Incidence72 hours postoperatively

The incidence of POAF

Secondary Outcome Measures
NameTimeMethod
Risk factors72 hours postoperatively

Risk factors associated with POAF

Trial Locations

Locations (1)

Faculty of Medicine, Khon Kaen University

🇹🇭

Khon Kaen, Thailand

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