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editorial
. 2021 Feb 27;7:138–139. doi: 10.1016/j.xjtc.2021.02.038

Commentary: Intraoperative graft patency assessment: Just do it!

Derrick Y Tam 1, Stephen E Fremes 1,
PMCID: PMC8311918  PMID: 34318226

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Stephen E. Fremes, MD, MSc, FRCSC, and Derrick Y. Tam, MD, PhD

Central Message.

Systematic transit time flowmetry of grafts is recommended to complement thorough clinical evaluation, although surgical judgment is essential before graft revision, as false positives can occur.

See Article page 131.

Drs Akhrass and Bakaeen1 provided an informative summary and expert surgeon's overview of the benefits and potential risks of intraoperative graft assessment for coronary bypass graft surgery. The early and late outcomes of coronary bypass surgery are contingent on the reproducible construction of fully patent anastomoses with quality conduits to important coronary targets. The authors have reviewed the key tools used to assess graft patency intraoperatively. We agree with the authors that transit time flowmetry (TTFM), particularly when combined with epicardial ultrasound (ECUS), provides the surgeon with reassurance of graft functionality. TTFM is a Class IIa recommendation in the 2018 European Revascularization Guidelines.2 The use of flowmetry is not a substitute for comprehensive clinical assessment and technical precision but is meant to supplement clinical assessment and uncompromising execution. However, a common observation is that intraoperative graft failure, while infrequent, may be unheralded and without other clinical cues.

Given the controversy surrounding the EXCEL trial, the prognostic importance of perioperative myocardial infarction has been questioned.3 Yet, it is well accepted that clinically defined perioperative myocardial infarction is not a benign event and is commonly associated with graft occlusion. Biancari and colleagues,4 in a meta-analysis of 9 studies of 1104 patients with perioperative myocardial infarction, reported early mortality was 12.6%. Graft failure was present in 62% of patients taken to the catheterization laboratory and in 79.8% of patients taken directly back to the operating room without angiography.

The evidence supporting the practice is largely observational. In the only randomized trial comparing TTFM with indocyanine green fluorescent angiography (ICG), the sensitivity to detect 50% graft stenosis or occlusion was far greater with ICG (83% vs 25%) according to early postoperative angiography—as nonocclusive stenoses may not result in flow disturbances.5 Also, when ICG and TTFM were compared with usual care in a later randomized controlled trial that was likely underpowered, intraoperative graft assessment was not associated with improved graft patency at 1 year; however, graft stenosis alone was numerically lower (3/160, 5.5% vs 8/152, 15.4%, P = .09).6 In a meta-analysis of 35 TTFM studies (almost entirely observational) including 8943 patients and 15,673 grafts, graft revision on a per-patient basis was 4.3% and 2.0% on a per-graft basis.7 However, graft revision was performed in only 25.1% of abnormal grafts, indicating the importance of combining TTFM with clinical judgment. Abnormal TTFM results were associated with graft occlusion and worse short-term clinical outcomes.7

The authors caution that falsely positive findings can be seen in certain patient scenarios leading to unnecessary graft revision, which, in turn, may then lead to patient harm. We concur with the authors that ECUS is complementary to TTFM, mainly in the identification of TTFM false positives. Di Giammarco and associates8 reported in a consecutive patient series including 717 grafts analyzed with both TTFM and ECUS that ECUS identified only 3 of 678 (0.4%) TTFM false negatives but determined that 35 of 39 TTFM positive grafts were false positives. Durable graft patency is necessary for favorable long-term outcomes following coronary surgery. There is considerable evidence that conduit is the key driver.9, 10, 11 That said, quality assurance is imperative. One of the potential limitations of the methodology is the number of false positives from TTFM alone. It is essential that TTFM findings are not used in isolation but are combined with careful clinical assessment. However, poor decision-making may result from a lack of familiarity with the technology and the reporting. That speaks to the importance to routinely check graft patency intraoperatively, ie, just do it!

Footnotes

Disclosures: The authors reported no conflicts of interest.

The Journal policy requires editors and reviewers to disclose conflicts of interest and to decline handling or reviewing manuscripts for which they may have a conflict of interest. The editors and reviewers of this article have no conflicts of interest.

References

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