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Published on: November 19, 2019
Radial artery grafts vs saphenous vein grafts in coronary artery bypass surgery: a randomized trial
Steven Goldman1, Gulshan K Sethi, William Holman
1Cardiology Section (1-111C), Southern Arizona VA Health Care System, 3601 S Sixth Ave, Tucson, AZ 85723, USA. steven.goldman@va.gov
Insights
Radial artery grafts showed similar 1-year patency to saphenous vein grafts in coronary artery bypass grafting (CABG). This multicenter trial found no significant difference in graft patency for patients undergoing elective CABG.
Area of Science:
- Cardiovascular Surgery
- Vascular Grafting
- Clinical Trials
Background:
- Arterial grafts are often preferred over saphenous vein grafts for coronary artery bypass grafting (CABG), drawing from the success of the left internal mammary artery.
- However, the comparative effectiveness of radial artery grafts remains less understood.
Purpose of the Study:
- To compare the 1-year angiographic patency rates of radial artery grafts versus saphenous vein grafts in patients undergoing elective CABG.
- To evaluate secondary outcomes including early graft patency, myocardial infarction, stroke, repeat revascularization, and mortality.
Main Methods:
- A multicenter, randomized controlled trial involving 757 participants undergoing first-time elective CABG.
- The left internal mammary artery was used for the left anterior descending artery, with other vessels randomized to receive either a radial artery or saphenous vein graft.
- The primary endpoint was graft patency assessed via angiography at 1 year post-CABG.
Main Results:
- Analysis included 733 patients, with 366 in the radial artery group and 367 in the saphenous vein group.
- No significant difference in graft patency was observed at 1 year: 89% for radial artery grafts versus 89% for saphenous vein grafts (P = .98).
- Secondary endpoints, including graft patency at 1 week, myocardial infarction, stroke, repeat revascularization, and death, also showed no significant differences between the groups.
Conclusions:
- In Veterans Affairs patients undergoing first-time elective CABG, radial artery grafts did not demonstrate superior 1-year patency compared to saphenous vein grafts.
- The findings suggest comparable efficacy between radial artery and saphenous vein grafts for CABG in this patient population.
Context:
Arterial grafts are thought to be better conduits than saphenous vein grafts for coronary artery bypass grafting (CABG) based on experience with using the left internal mammary artery to bypass the left anterior descending coronary artery. The efficacy of the radial artery graft is less clear.
Objective:
To compare 1-year angiographic patency of radial artery grafts vs saphenous vein grafts in patients undergoing elective CABG.
Design, Setting, And Participants:
Multicenter, randomized controlled trial conducted from February 2003 to February 2009 at 11 Veterans Affairs medical centers among 757 participants (99% men) undergoing first-time elective CABG.
Interventions:
The left internal mammary artery was used to preferentially graft the left anterior descending coronary artery whenever possible; the best remaining recipient vessel was randomized to radial artery vs saphenous vein graft.
Main Outcome Measures:
The primary end point was angiographic graft patency at 1 year after CABG. Secondary end points included angiographic graft patency at 1 week after CABG, myocardial infarction, stroke, repeat revascularization, and death.
Results:
Analysis included 733 patients (366 in the radial artery group, 367 in the saphenous vein group). There was no significant difference in study graft patency at 1 year after CABG (radial artery, 238/266; 89%; 95% confidence interval [CI], 86%-93%; saphenous vein, 239/269; 89%; 95% CI, 85%-93%; adjusted OR, 0.99; 95% CI, 0.56-1.74; P = .98). There were no significant differences in the secondary end points.
Conclusion:
Among Veterans Affairs patients undergoing first-time elective CABG, the use of a radial artery graft compared with saphenous vein graft did not result in greater 1-year patency.
Trial Registration:
clinicaltrials.gov Identifier: NCT00054847.
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