CABG REVEAL: Atrial Fibrillation After Coronary Artery Bypass Graft

NCT ID: NCT02169622

Last Updated: 2020-11-06

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 51 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2013-06-18
• Study Completion Date: 2020-09-30

Brief Summary

Atrial Fibrillation is an abnormal heart rhythm that can occur after coronary heart bypass graft operations. How often this happens and what other problems occur for a person after these operations needs to be better understood. This study uses a device called the Reveal XT, a small device that records heart rhythms to track a patient's heart rhythms after the bypass surgery. The device is implanted at the time the bypass graft is made. The information that is gathered for this study will help physicians to provide better treatment and follow-up of the patients under their care.

Detailed Description

We will utilize the Reveal XT implantable loop recorder (ILR) in order to monitor the incidence of AF in our post-CABG patients. The Reveal XT has been shown to be superior in comparison to the more commonly used sporadic ECGs.6 Unfortunately, the occurrences of arrhythmias tend to be "unpredictable" and often paroxysmal. Observers are unlikely to have the opportunity to record ECGs at the time of event until it is too late. The ability of the Reveal XT to continuously record ECGs over long periods of time has made it a superior and powerful diagnostic tool in patients with arrhythmias and arrhythmia related complications.

This was evident in the large multicenter PICTURE study whereby a large number of diagnostic tests were undertaken in patients with unexplained syncope without providing conclusive data, but in the same study with the Reveal ILR, the mechanism of syncope in the vast majority of these patients were established often at first onset of an arrhythmia.7

"The equivalent efficacy", if not superiority, of Reveal ILRs above conventional ECGs and Holter-monitors in detecting AF was established in the "XPECT" trial.8 Its sensitivity in detecting events not seen with ECGs and Holter monitoring post COX MAZE procedure (surgical procedure for AF) and post ablations for paroxysmal AF and persistent AF is well established.

Conditions

Atrial Fibrillation

Study Design

• Observational Model Type: CASE_ONLY
• Study Time Perspective: PROSPECTIVE

Eligibility Criteria

Inclusion Criteria

• 60 years of age or older
• Presenting for elective Coronary Artery Bypass Graft at Saint Thomas West Hospital

Exclusion Criteria

• Patients <60 years of age
• Prior cardiac surgery
• Emergent surgery
• Need for concomitant cardiac surgery other than PFO closure
• Prior history of AF or Atrial flutter
• Prior atrial ablation
• Prior cardioversion
• Patients with prior permanent pacemaker
• Ejection fraction <35%
• Prior history of thyroid disease
• Prior history of a cardiomyopathy
• Patients without telephonic access

• Minimum Eligible Age: 60 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Saint Thomas Health

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Evelio Rodriquez, MD

Role: PRINCIPAL_INVESTIGATOR

Saint Thomas Heart at Saint Thomas

Locations

Saint Thomas West Hospital

Nashville, Tennessee, United States

Countries

United States

Other Identifiers

STH12-009

Identifier Type: OTHER

Identifier Source: secondary_id

STH12-009

Identifier Type: -

Identifier Source: org_study_id