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Meta-analysis finds no outcome differences between free versus in situ right internal mammary artery in CABG

Meta-analysis finds no outcome differences between free versus in situ right internal mammary artery…
Photo by Nellie Adamyan / Unsplash
Key Takeaway
Consider clinical context over outcome differences when choosing between free or in situ RIMA as second conduit in CABG.

This meta-analysis pooled data from 13 studies involving 9899 patients undergoing coronary artery bypass grafting (CABG). It compared using the free right internal mammary artery (fRIMA) versus the in situ right internal mammary artery (isRIMA) as a second conduit, with median follow-up durations ranging widely from 1 to 20 years across the included studies.

The analysis found no statistically significant differences between the two techniques across multiple clinical endpoints. For overall mortality, the hazard ratio was 1.16 (95% CI: 0.79-1.69). Graft occlusion showed a hazard ratio of 1.04 (95% CI: 0.90-1.21). Major adverse cardiac events had a hazard ratio of 0.87 (95% CI: 0.62-1.21), and repeat revascularization showed a hazard ratio of 1.34 (95% CI: 0.68-2.66).

Safety and tolerability data were not reported in the meta-analysis. Key limitations include the inherent constraints of the available evidence, the wide variation in follow-up duration (1-20 years), and the absence of absolute event rates. The analysis notes that the choice between fRIMA and isRIMA may be guided by clinical context, surgeon preference, patient anatomy, and target vessel characteristics rather than expected differences in major clinical outcomes.

Study Details

Study typeMeta analysis
Sample sizen = 9,899
EvidenceLevel 1
Follow-up240.0 mo
PublishedMar 2026
View Original Abstract ↓
OBJECTIVES: There is debate regarding the optimal choice for a second conduit in coronary artery bypass grafting. The right internal mammary artery (RIMA) is commonly employed as a second conduit; however, it is unclear whether the free (fRIMA) or in situ (isRIMA) configuration yields superior outcomes. We performed a systematic review and meta-analysis to compare clinical outcomes between fRIMA and isRIMA as the second conduit. METHODS: A comprehensive search of PubMed (MEDLINE), EMBASE, and CENTRAL was performed through May 2025 to identify studies comparing outcomes in patients undergoing coronary artery bypass grafting with either fRIMA or isRIMA as a second conduit. The outcomes of interest were overall mortality, graft occlusion, major adverse cardiac events (MACE), and repeat revascularization. Data with 95% confidence intervals (CIs) were extracted. Pooled analysis was performed using a random-effects model. RESULTS: A total of 13 studies with 9899 patients were included (fRIMA, n = 3095; isRIMA, n = 6804). The median study follow-up duration ranged from 1 to 20 years across the studies. No statistically significant differences were observed in overall mortality (hazard ratio [95% CI] = 1.16 [0.79-1.69]), graft occlusion (1.04 [0.90-1.21]), MACE (0.87 [0.62-1.21]), and repeat revascularization (1.34 [0.68-2.66]). CONCLUSIONS: In this meta-analysis, no statistically significant differences were observed between fRIMA and isRIMA configurations across the evaluated clinical outcomes. These findings suggest that, within the limitations of available evidence, the choice between fRIMA and isRIMA may be guided by clinical context, surgeon preference, patient anatomy, and target vessel characteristics rather than expected differences in major clinical outcomes.
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