Intraoperative Echocardiography in Low-Risk CABG Surgery
Brief description of study
The goal of this pilot RCT is to assess the real-world feasibility of undertaking a trial that will randomize isolated CABG surgery patients to default (i.e. obligatory) as-needed (i.e. backup) intraoperative TEE. Trial outcomes will include subject recruitment, feasibility of intervention, incidence gastroesophageal dysfunction, and cardiac surgeon satisfaction with intraoperative management in each trial arm. Although this study is not powered to detect a difference in clinical outcomes between the default and as-needed intraoperative TEE groups, to plan for a future RCT, we will collect data on clinical outcomes (e.g. incidence of revascularization or death within 3 months of surgery, incidence of postoperative acute kidney injury (including serum creatinine levels), and incidence of dysphagia or odynophagia during hospitalization).
Eligibility of study
You may be eligible for this study if you meet the following criteria:
- Conditions: Medical Research
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Age: - 99 Years
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Gender: All
TBD
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