- Open Access
Debate: When should we intervene in unstable angina - Time for an old look?
© Current Controlled Trials Ltd 2000
Received: 3 April 2000
Accepted: 17 July 2000
Published: 4 August 2000
Current treatment modalities for patients with acute coronary syndromes center on early diagnosis, risk stratification and, increasingly, early treatment including invasive approaches. The appropriate timing of these invasive modalities in the context of the overall treatment program remains an area of controversy. Specifically, studies in the past recommended a period of medical 'stabilization' while current approaches are considerably more aggressive. The potential hazard of early intervention, in particular, has not properly been weighed against the benefit. This article hopes to provide a framework for examining the appropriate timing of intervention, specifically percutaneous coronary intervention, in acute coronary syndromes.
The natural history of acute coronary syndromes (ACS), formerly referred to as unstable angina, is characterized by an early, high-risk period followed by a longer period of diminishing risk, which ultimately is statistically indistinguishable from clinically stable coronary heart disease [1,2]. Classic studies have now demonstrated important effects of specific pharmacologic treatments for these patients [3,4]. However, a disturbingly persistent rate of death or myocardial infarction of 12.1% at 6months , and of 14.1%  and 12.2%  at 1 year, in conjunction with an increasingly aggressive approach to patient management, has led to the present controversy over the appropriate treatment of these patients. Specifically, the widespread availability of invasive services (at least in the USA) has accelerated the timing of invasive approaches to patient management. While some of this compressed care has been driven by third-party payors, a significant component of what to do and when is at the discretion of the physician. Therefore, a careful look at the time-honored approach defined as 'cooling off' and the current approach of 'do-it-now' is in order.
What is 'cooling off?'
Our earlier concept of clinical quiescence was based on eliminating the frequency of anginal episodes . In the early days of percutaneous transluminal coronary angio-plasty (PTCA), now referred to as percutaneous coronary intervention (PCI), 'hot' patients appeared to fare less well with our efforts . A period of 'cooling off' was therefore recommended by many prior to PCI . This period was in no way tantamount to benign neglect. The 'cooling off' period was defined, at that time, by state of the art antico-agulant, antiplatelet and anti-ischemic therapy. We have clearly learned much since these early studies. We now know that 'hot' patients truly have an underlying patho-physiology that has a strong inflammatory component . Moreover, the 'hot' plaque in these patients is characterized by increased fragility , enhanced thrombo-genicity [12,13], and cellular and molecular markers of inflammation . It is, in fact, the presence of these inflammatory markers in the sera of these patients that appears to correlate best with both short-term and long-term clinical outcome [15,16]. Treatment programs directed towards 'cooling off' these patients must thus take into account this pathophysiology. The lessons learned from prior studies of PCI in patients with ACS have clearly provided a strong rationale for the current use of potent antiplatelet and antithrombotic agents. It is notable, however, that while specific anti-inflammatory therapy (in contrast to anti-infection therapy) may not be available at present, treatment programs that include an aggressive approach to lipid lowering may confer significant benefit . The 'anti-inflammatory' sequelae of antioxidant and lipid lowering therapies are not, in fact, to be underestimated in their importance .
Early studies, as has already been noted, reported higher rates of adverse clinical events during PCI in patients with ACS. Although subject to considerable bias as a consequence of their retrospective nature, several studies did suggest that a period of 'stabilization' resulted in improved clinical outcomes . Given the presence of angiographically evident thrombus within the culprit vessel in such patients, algorithms were developed that included an extended period of anticoagulation prior to PCI. Our group reported improved procedural outcomes in patients with unstable angina who received an extended period of intravenous heparin . Importantly, a relatively well-defined 'cut point' was seen at 72h . It is also of note that this time dependence of procedural success was seen in both groups of patients (Fig. 1).
The advent of potent pharmacologic adjuncts, for example platelet glycoprotein IIb/IIIa receptor antagonists, and the enhanced procedural safety offered by stents have dramatically changed the current landscape. In lieu of any period of 'cooling down', patients are now referred for invasive coronary procedures with alacrity. The latter, coupled with an ever-increasing trend in the performance of combined diagnostic and interventional procedures, has resulted in PCI being performed at a very early stage in the natural history of ACS. It is during this early period that the hazard of intervention is greatest [5,20]. Specifically, the marked inflammatory response and liberation of cytokines , the generation of free radicals , the enhanced activity of both intrinsic and extrinsic pathways of coagulation , and the perturbations in endothelial function that characterize both the active lesion and the response to mechanical disruption  all contribute to this potential hazard.
Another issue, however, is now upon us: PCI itself is associated with myocardial damage as reflected in postprocedural increases in myocardial-specific enzymes [24,25]. These measures of myocardial necrosis following PCI are in fact found more frequently in the setting of ACS than in more clinically stable populations . While the etiology of the postprocedural enzyme release remains speculative, the possibility of distal thrombo-embolization consequent to plaque disruption is strongly supported by the mitigation of these events with the use of platelet glycoprotein IIb/IIIa receptor antagonists . In virtually every recent trial of PCI in the setting of ACS, the increase in postpro-cedural CPK-MB fraction is several-fold greater than the control (prePCI) rate . A second hazard is thus apparent, but whether this second hazard is disproportionately increased in patients undergoing 'early' PCI compared with a delayed procedure is unclear. An examination of the outcomes following PCI in clinical trials in which patients were randomized to either an 'aggressive' approach versus a 'conservative' approach (TIMI III , VANQWISH , FRISC-II ) or pharmacologic trials in which PCI was deferred as a consequence of the duration of infusion of the study drug (EPIC , CAPTURE , PURSUIT , PRISM-PLUS ) provides some interesting insights (Fig. 2).
Although these trials differed substantially in design, primary end-points and pharmacologic adjuncts, the theme of early versus deferred PCI is common to all. It can be seen that there is a statistically significant (inverse) relationship between short-term major adverse coronary events (MACE) rates as reported in the individual trials and the timing of intervention. Furthermore, it is of note that there is a 50% reduction of this MACE rate when intervention is deferred until at least 48h following randomization.
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