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Ann Thorac Surg 2007;84:795-799
© 2007 The Society of Thoracic Surgeons
Department of Cardiac Surgery, Austin Hospital, Heidelberg, Melbourne, Australia
Accepted for publication April 5, 2007.
* Address correspondence to Dr Buxton, Austin Hospital, PO Box 5555, Heidelberg, Melbourne, Victoria, 3084, Australia (Email: brianbuxton{at}ozemail.com.au).
| Adult Cardiac Surgery:
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| Abstract |
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Methods: Protocol-directed percutaneous angiography has been performed at intervals weighted toward the end of the study period, or earlier when directed by symptoms. To date, 184 patients have been studied as per protocol, at time points up to 10 years (mean, 3.9), among whom there are 430 nontrial grafts in addition to the 184 trial grafts. Supplementary angiography (percutaneous or computed tomography) was offered at a fixed 5-year time point postoperatively: at this juncture, 193 trial grafts and 469 nontrial grafts have been imaged. Three masked investigators report grafts as angiographically successful if patent from proximal to distal anastomosis inclusive. Failed grafts include greater than 80% stenosis, string sign, or occlusion.
Results: In staggered protocol-directed angiography, overall patency of the in-situ internal thoracic artery grafts and free arterial grafts was 95.5% (210 of 220) and 91.4%% (150 of 164), respectively, which did not differ significantly (p = 0.13). Saphenous vein graft patency was 83.0% (191 of 230) with a trend to higher failure rate compared with free arterial grafts (p = 0.07), and was significantly lower than that of in-situ internal thoracic artery grafts (p = 0.01). At the optional 5-year time point, outcomes are similar to the protocol-directed findings, with patency of in-situ left and right internal thoracic artery grafts of 95.8% (204 of 213), which was significantly greater than that of the other two groups (p = 0.02 and p < 0.001). Patency of free arterial conduits and saphenous vein grafts was 89.1% (139 of 156) and 82.4% (201 of 244), respectively, which did not differ significantly (p = 0.09) at 5 years.
Conclusions: Although trending to superior patency compared with vein grafts, free arterial conduits have not matched the gold standard achieved by in-situ internal thoracic arteries at trial midpoint. Until the results from RAPCO are available, which will test types of free arterial graft against each other and will compare radial and vein grafts in the longer term, these observational data justify for now our current practice of maximal use of in-situ conduits supplemented by free radial grafts.
Sustained symptomatic and prognostic benefit from coronary artery revascularization is dependant on graft patency as well as progression of native disease. Numerous historical studies have demonstrated the superiority of internal thoracic artery (ITA) grafts over vein grafts with respect to patency and prognostic benefit [1–7], and the last decade has seen a considerable increase in the use of arterial conduits during coronary surgery. The Radial Artery Patency and Clinical Outcomes (RAPCO) study is one of several trials designed to determine whether the radial artery (RA) was superior or inferior to other conduits in its patency and clinical results [8–11]. Patients were randomly assigned to receive either a RA or a free right ITA if aged less than 70 years, and participants older than this were randomly assigned to receive either a RA or saphenous vein. Trial follow-up comprises a 10-year postoperative period with a program of clinical review and staggered angiography.
Our understanding of coronary graft patency is limited in two respects. The routine use after surgery of antiplatelet agents, statins, angiotensin-converting enzyme inhibitors, and beta blockers, added to greater operative awareness of careful conduit handling and anastomotic technique, may collectively influence the long0term patency of grafts, such that historical controls may not be applicable to coronary artery grafts performed in the modern era [12]. Furthermore, many of the data that we do have regarding graft patency are derived from symptom-directed angiography, which tends to overestimate graft failure [13].
In the RAPCO protocol [9], the trial graft was defined as the second graft: that is to say, the randomly selected conduit was applied to the best coronary target other than the left anterior descending artery. When the trial reports finally, it will describe only patency of the study graft. Yet patients received on average 3.3 grafts, and the angiograms performed in the RAPCO trial document the patency status of all grafts. Furthermore, the RAPCO angiograms are not biased by the presence of recurrent coronary symptoms, as the vast majority of patients in the trial remain well many years after their surgery.
Thus, we may utilize the angiographic findings in patients enrolled in this trial to derive a broad contemporary snapshot of the fate of coronary grafts in primarily well patients in the modern era, with a wider perspective than will ultimately be reflected by the trial results.
| Material and Methods |
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Postoperative selective coronary angiography was performed for each patient at a single time point during the 10-year follow-up period according to a randomly allocated, staggered program. That was weighted toward the second half of the study, as it was anticipated that the larger number of clinical events would occur in this time frame. By design, therefore, at the 5-year point, fewer than half of the patients had undergone a protocol-directed angiogram. Thus patients were offered, in addition, a voluntary 5-year "midtrial" angiogram for supplementary data. This could be performed by conventional percutaneous or computed tomography (CT) angiography technique.
All the postoperative angiograms were reported by three independent reviewers, including two cardiac surgeons and one cardiologist (or radiologist in the minority of cases in which CT angiography was performed). Simplified definitions of graft outcome were utilized, whereby grafts were defined as either "satisfactory" or "failed" if there was occlusion, string sign, or greater than 80% stenosis in the graft. All angiographic data are prospectively entered into a visual FoxPro 5.0 database (Microsoft Corporation, Seattle, Washington), which was used as the source of information for this study. Data were analyzed using SPSS software (SPSS, Chicago, Illinois).
| Results |
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The 14 breaches of protocol, whereby patients did not receive the intended conduit for the second graft, occurred either because the randomized conduit was not suitable for use or because the findings at surgery did not fit the protocol and the surgeon acted according to clinical need. These patients are included in the analysis, however, because the conduit, its target and its patency are all known and thus there is no necessity to analyze by intention to treat.
There were no significant differences in the age, sex distribution, urgency, or presence of hypertension, diabetes mellitus, or other comorbidity, among the three groups randomized to RA, right ITA, or SV, except that those patients who received a free right ITA as their second graft were younger by definition, as this was inherent in the design of the trial as described above.
The distributions of the targets for each conduit varies because the in-situ arterial grafts were placed to the LAD in all but 5 cases, whereas free arterial grafts were placed to the second targets in all but 6 cases. The saphenous vein grafts are spread throughout second to fourth targets.
Five-year optional angiography shows patency for the in-situ arterial conduits, free arterial conduits (RA or free right ITA), and reversed SV to be 96%, 89%, and 82%, respectively (see Fig 1). The patency of the in-situ arterial grafts is significantly better than that of the free arterial conduits (p = 0.02, Fishers exact test), and the free arterial conduits trended to superior patency over that of SV (p = 0.08, Fishers exact test). The patency rates for the three different conduit groups were similar irrespective of whether the patient was studied by percutaneous or CT angiography (
2, p > 0.4).
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| Comment |
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The patency of RA grafts in our series compares favorably with that described elsewhere [18–24], and is similar to that described by Possati and coworkers [24] who described patency of 88% in a series of 91 RA grafts, 92% of which were re-studied with follow-up of mean duration 8.8 years. Other series, although larger in patient numbers, have re-studied only a minority of RA grafts with mean follow-up varying from 1.2 to 5.6 years. The data presented in our series, although relating only to 98 RA grafts, benefit from the duration of follow-up at 3.9 and 5.0 years for the protocol-directed and elective angiography, respectively, from the absence of patient symptomatology acting as a confounding bias in estimations of graft failure [13], and from its unique 100% rate of graft reassessment.
Of concern, however, was the poor patency of RAs grafted to the third and fourth targets (Fig 4). We reiterate that this observation pertains to 6 cases only, and the numbers are too small for conclusions to be drawn, but clearly this merits further investigation. Because only 6 such grafts were performed, their performance does not alter the overall excellent patency of free arterial grafts, however.
The 82% patency of vein grafts at 5 years is gratifying, given that it includes poorer targets (such as fourth grafts) than does the free arterial cohort, and it is superior to that described in many historical series [3–7]. As with the radial artery data, our venous patency has the benefits of 100% angiographic follow-up, an acceptable midterm duration of review, and the absence of symptoms in most patients, thereby avoiding overestimation of graft failure and making this representative of outcomes in good clinical practice. It is noteworthy that the patency of vein grafts when placed to the third and fourth position is 80%, compared with 90% when a vein is used as the study graft to the second best target; and this insignificant difference contrasts with the wide discrepancy in patency noted with in the small proportion of RA conduits used for nonstudy targets. Data on more such RA grafts, placed to the lesser targets, are needed before it is clear whether venous conduits are preferable for third and fourth grafts.
Although there was a trend to higher patency for free arterial grafts than for vein grafts, the small difference did not achieve statistical significance. That may be because the sample size is too small, or because the follow-up duration is as yet inadequate, and the gap between vein grafts and free arterial grafts might widen beyond 5 years. Alternatively, the difference might be spurious, and may be merely a reflection of greater target heterogeneity with the venous grafts.
In conclusion, these unselected patency data compare favorably with other reports of more selective case series. In the modern era of careful conduit tissue handling and optimal use of antiplatelet agents, statins, angiotensin-converting enzyme inhibitors, and beta blockers in the postoperative period, patency results with vein grafts can be achieved that are close of those achieved with free arterial grafts. Nonetheless, there is a trend to superior patency with free arterial grafts particularly when placed to the second best target. Personal experience of use of free arterial grafts may have a role to play in their clinical and angiographic outcome, and the small benefit of free arterial grafts over vein grafts may be negated if the arterial conduit is at all diseased or if the surgical team has much greater experience with vein grafts.
| Acknowledgments |
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