Perioperative Depression and Postoperative Arrhythmia in Elective Coronary Bypass Graft Surgery

Official Title: “Perioperative Depression and Postoperative Arrhythmia in Elective Coronary Bypass Graft Surgery”

Postoperative arrhythmias (heart irregularities) are one of the most common complications after cardiac surgery and are associated with increased morbidity and mortality.

Preoperative depression may be an important co-factor in the generation of postoperative arrhythmias due to sympathetic hyperactivity evident in patients with depression.

Objectives: To determine the effect of preoperative depression on postoperative arrhythmia in patients undergoing elective coronary artery bypass graft (CABG) surgery.

Prospective observational study, 120 patients undergoing elective CABG surgery ECG will be preformed preoperatively on all patients. All patients will be assessed for signs of depression using the Prime MD Patient Health Questionnaire (Prime MD PHQ) one week before surgery and 6 weeks postoperatively.Based on the Prime MD PHQ results, patients will be divided into two groups: those with or without signs of depression. Heart rate and rhythm monitoring with Holter will be performed for 3 days postoperatively in order to compare the incidence of postoperative arrhythmias between groups.

The primary outcome is the number of patients with and without depression suffering from ventricular and/or supraventricular arrhythmias. Secondary outcomes include all cause mortality, non-fatal myocardial infarction, cardiac arrest, and congestive heart failure.

CABG surgery is the most common operative procedure in North America and arrhythmias are one of the most common postoperative complication. It is estimated that about a third of these cardiac patients suffer from preoperative depression and therefore may be exposed to a higher risk of perioperative morbidity and mortality. If an association between preoperative depression and postoperative arrhythmia is found, treatment modalities may be indicated to reduce the prevalence of perioperative arrhythmia in patients with preoperative depression undergoing cardiac surgery.

Inclusion Criteria:

• Patients between 18-75 years of age undergoing elective CABG surgery.
• Patients must provide informed consent

Exclusion Criteria:

• Patients with a history of arrhythmias (AF, supraventricular tachycardia, ventricular tachycardia, ventricular fibrillation, permanent pacemaker and/or defibrillator).
• Patients who are unable to read.
• Patients with significant psychiatric disorders other than depression.
• Patients with a history of pulmonary hypertension.
• Patients with a left ventricular ejection fraction < 40%.
• Patients with cognitive impairment as measured by the MMSE.
• Patients on antidepressants at the time of assessment

Gender Eligibility for this Clinical Trial: Both

Minimum Age for this Clinical Trial: 18 Years

Maximum Age for this Clinical Trial: 85 Years

Are Healthy Volunteers Accepted for this Clinical Trial?: No

Lead Investigator: University Health Network, Toronto Other

Overall Clinical Trial Officials and Contacts

Rita Katznelson, MD Principal Investigator Toronto General Hospital, UHN  

Information obtained from ClinicalTrials.gov on February 12, 2012

Link to the current ClinicalTrials.gov record. http://clinicaltrials.gov/show/NCT00622024

Study ID Number: REB#06-0116-AE

ClinicalTrials.gov Identifier: NCT00622024

Health Authority: Canada: Health Canada