A Study to Determine the Effect of Bi-Ventricular Pacing on Cardiac Hemodynamics After Coronary Artery Bypass Graft

Unity Health Toronto

Status and phase: Completed; Phase 1

Conditions: Coronary Disease

Treatments: Device: Ethicon TPW32 60 cm (pacing wires x 2)

Study type: Interventional

Funder types: Other

Identifiers

NCT00316368

05-318

Details and patient eligibility

About

The purpose of this study is to determine, using echocardiography, whether bi-ventricular pacing improves the contractile force by resynchronizing both ventricles, thereby improving and/or correcting the paradoxical septal movement.

Primary Hypothesis:

• Bi-ventricular pacing post cardiac surgery will result in at least a 10% increase in cardiac index (CI) as compared with standard atrio-right ventricular pacing.

Secondary Hypothesis:

• Bi-ventricular pacing post cardiac surgery will result in at least a 10% increase in cardiac index (CI) as compared with atrio-left ventricular pacing and right atrium pacing.

Full description

Clinical trials done to date have focused on the efficacy of biventricular pacing (BVP) in the treatment of patients with congestive heart failure, Intraventricular conduction delay, dilated cardiomyopathies, and post cardiac surgery. However, studies done in post cardiac surgery patients are limited by their small sample size (4-22 patients with overall of 51 patients), non-randomized pacing protocol and by their inability to determine a definitive mechanism for the improved hemodynamics observed with BVP. Therefore, we propose to complete a pilot study aimed at determining both the magnitude of the hemodynamic benefit associated with BVP, if any. In addition, we will investigate changes in intra-ventricular septal motion as a possible mechanism for the previously observed changes in cardiac hemodynamics.

Enrollment: 60 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• All elective/emergent patients requiring isolated coronary artery bypass graft (CABG) at St. Michael's Hospital.

Exclusion criteria

• Patient's age < 18 years.

• Known atrial fibrillation.

• Sinus tachycardia > 100 beats per minute (bpm).

• Post-operative CI < 2.

• High inotrope dosage post-operation:

  • Dopamine (Intropin) if > 10 µg/kg/min.
  • Dobutamine (Dobutrex) if > 10 µg/kg/min.
  • Norepinephrine (Levophed) if > 0.1 µg/kg/min.
  • Epinephrine if > 0.1 µg/kg/min.

• Need for intraaortic balloon pump (IABP).

• Unable or unwilling to give informed consent.

• Already participating in another clinical trial.