After OPCAB, patients have been reported to have less myocardial injury as determined by biochemical analyses. Koh and colleagues measured serial troponin T release and reported less damage during OPCAB than ONCAB [1]. Dijk and colleagues reported that creatine kinase-MB release after OPCAB was reduced compared with ONCAB [2]. Although it is difficult to distinguish myocardial stunning from irreversible injury even with biochemical markers, electrocardiography, or functional assessment [3], several studies confirmed that off-pump surgery improved left ventricular contractility early after surgery [4, 5]. In the late follow-up period, there was no significant difference between ONCAB versus OPCAB in the incidence or extent of irreversible myocardial injury [4], or in left ventricular function at 6 months [5].
Cardiac magnetic resonance imaging is reported to be reliable for detecting perioperative small myocardial necrosis [8]. Rahimi and colleagues reported that revascularization-related hyper-enhancement was found in 32% of patients and predicted an adverse cardiac event after percutaneous coronary intervention or coronary artery bypass grafting [9]. Pegg and colleagues reported that the incidence of new irreversible myocardial injury was significantly higher in OBCAB than ONCAB under cardiac arrest [6].
It is generally accepted that IABP has a beneficial effect in reducing cardiac work or myocardial afterload. However, it is unclear whether there is an increase in blood flow through stenotic coronary vessels or increased collateral flow. Williams and colleagues reported that, after IABP in patients who had unstable angina with left anterior descending coronary artery stenosis, O2 consumption was reduced, but great cardiac vein flow was also reduced [10]. Yoshitani and colleagues reported that use of IABP decreased diastolic intraluminal pressure distal to the stenosis, especially when the stenosis was severe [11]. In contrast, Takeuchi and colleagues reported a significant increase in coronary flow distal to the stenosis [12].
Several studies have reported that blood flow in bypass grafts was markedly increased by IABP. In an animal model, IABP increased diastolic flow by 75% in aortocoronary bypass grafts and by 38% in ITA grafts [13]. In that experimental study, graft flow was measured after on-pump surgery and cardiac arrest. In a clinical study, Onorati and colleagues found highly significant increases of 50–90% in blood flow in all kinds of grafts [14]. In their report, 78% of patients underwent ONCAB. Rubino and colleagues reported an increase in graft flow of 55–95% with IABP in patients after ONCAB [15]. Takami and colleagues examined graft flow in 84 patients, 45% of who had ONCAB, and reported that mean flow was significantly increased by 23% [16]. In general in these previous studies, the mean increase in graft flow was greater as the proportion of ONCAB increased. Consequently, Onorati and colleagues concluded that a combination of IABP and TTFM were useful for detecting graft failure [14], such that no increase in flow with IABP indicated a failed graft.
However, these results may be contradictory to the concept of “autoregulation”, which is characterised by the adaptability of vascular resistance to changes in blood pressure over a wide range, and is essential for maintaining appropriate flow distribution in different regions and layers with variable vascular resistance, such as the endocardial or epicardial myocardium [17]. In addition, in patients with multivessel disease, vascular resistance in the area of the collateral receiving vessel must be significantly lower than that in the area of the collateral delivering vessel. According to a few papers investigating the effects of IABP in normal coronary arteries, there was an increase in coronary flow of only 1.1% [18] or 11% [19].
Balacumaraswami and colleagues investigated arterial pressure and blood flow in bypass grafts and compared ONCAB with OPCAB [20]. After ONCAB, graft flow was significantly higher for all grafts than after OPCAB, and the flow/pressure ratio was greater for all grafts after ONCAB [20]. The study mentioned that reactive hyperaemia resulting from cardiopulmonary bypass and myocardial ischemia was the mechanism for increased graft flow, in spite of lower arterial pressure. Cardiopulmonary bypass causes not only a systemic inflammatory response and multiorgan dysfunction [21], but also a cardiac hyperaemic state, resulting in impairment of autoregulation. In addition, Ono and colleagues reported that impaired autoregulation of cerebral blood flow by cardiopulmonary bypass was detected in 20% of their patients, and associated with perioperative stroke [22].
In the present study, there was no significant difference in graft flow between on IABP and off IABP after OPCAB, suggesting that OPCAB has specific physiological characteristics. We suggest that autoregulation may be preserved or minimally damaged by OPCAB as there is only localized rather than global cardiac ischemia. In addition, the increase in flow with IABP in proportion to the increase in diastolic pressure in previous studies may be attributable to a “hyperaemic state” induced by cardiopulmonary bypass and cardiac arrest. In the current study, graft flow on IABP was markedly lower than flow without IABP in 26% of bypass grafts. One reason for this is that reduced cardiac work and oxygen demand with IABP could decrease coronary flow, irrespective of higher diastolic pressure. Another possibility is that there is decreased resistance through the stenotic portion of the native coronary artery when diastolic blood pressure increases [23]. Thus, IABP may increase blood flow through the native coronary artery with severe stenosis or the collateral circulation, rather than the bypass graft without stenosis. This would be consistent with the absence of an increase in pressure in the vessel distal to the severe stenosis, as reported by Yoshitani and colleagues [11].
There are implications arising from this study. As mentioned in previous papers, one explanation for subendocardial damage in OBCAB may be inadequate coronary perfusion to distal territories [6]. We suggest, first, that another possible explanation may be preserved autoregulation after OPCAB, which would function to protect from malperfusion even in coronary circulation with variable vascular resistance. Second, TTFM during OPCAB may reflect a more physiological and natural coronary circulation compared with ONCAB. Therefore, TTFM during OPCAB is considered reliable for detecting not only technical failure, but also future graft occlusion associated with poor graft flow resulting from moderate native coronary stenosis or poor flow demand [24]. Third, even in our limited experience, the patency of a graft is not correlated with an increase or decrease in graft flow with IABP, in contrast to the effect of IABP after ONCAB. Consequently, preserved autoregulation would play a definitive role in the perioperative safety of OPCAB. We suggest that autoregulation may be associated with a lower risk of hypoperfusion syndrome as a result of in situ ITA grafting, even after division of the old saphenous vein graft in redo off-pump surgery. Conversely, there may be a concern over increased risk of coronary spasm during OPCAB because of the absence of vasodilatation by induced hyperaemia.
This study has a few limitations. First, the number of patients was limited. If a larger number of bypass grafts were analysed, differences in graft flow between on IABP and off IABP may have reached statistical significance. However, we consider that any difference would never be as great as those reported in previous ONCAB studies. Second, selection bias might have been present, as most of our patients had unstable angina and urgent or emergency surgery was required. In such situations, coronary flow could be impaired by the underlying myocardial stunning. In addition, preoperative angiography showed coronary flow of TIMI grade II in 5 patients, which might be associated with ischemic damage on microvascular circulation. We presume that, however, increased graft flow during IABP cessation, which was seen in 26% of bypass grafts, could not be explained by microvacular damage or myocardial stunning. These were inevitable limitations of a retrospective observational study in the clinical field. Taking these into account, however, we believe that this study indicates that there is regulation of coronary flow after OPCAB, in contrast to the state after ONCAB.
