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Unanswered ethical and scientific questions for trials of invasive interventions for coronary disease: The case of single vessel disease
© Jabbour et al; licensee BioMed Central Ltd. 2004
- Received: 21 December 2003
- Accepted: 29 March 2004
- Published: 29 March 2004
Trials in the 1990s demonstrated that medical therapy is as effective as invasive therapies for treating single-vessel coronary disease. Yet more recent studies enrolling patients with this condition have focused on evaluating only invasive approaches, namely, stenting versus coronary artery bypass surgery. Several ethical and scientific questions remain unanswered regarding the conduct of these later trials. Were they justified? Why wasn't a medical therapy arm included? Were subjects informed about the availability of medical therapy as an equivalent option? Was optimized medical therapy given prior to randomization? The absence of clear answers to these questions raises the possibility of serious bias in favor of invasive interventions. Considering that medical therapy is underutilized in patients with coronary disease, efforts should focus more on increasing utilization of medical therapy and proper selection of noninvasive interventions.
- Coronary heart disease
- coronary revascularization
- medical therapy
- invasive therapy
Two recent (2002) trials of surgical vs. percutaneous interventions for coronary disease [1, 2] raise serious questions about the conduct of research that focuses on management of coronary artery disease [CAD]. In both of these studies, symptomatic patients with proximal left anterior descending [LAD] stenosis – supposedly the stenosis site associated with the highest risk – experienced similar outcomes with stenting or with minimally invasive bypass surgery. These results leave the impression that physicians now have several properly validated invasive options from which to choose when treating patients with single-vessel CAD. This misleading perception ignores previous research on the efficacy of medical therapy in treating this condition, thereby casting doubt upon the ethical and scientific merits of these trials.
In the 1990s, two well-designed trials compared medical and invasive approaches for treating single-vessel CAD. In the ACME study, death and infarction rates were similar with either medical therapy or with angioplasty, although angioplasty was associated with greater relief of angina . The landmark MASS study focused on patients with high-grade proximal LAD stenosis . Again, rates of death or infarction as well as abolition of limiting angina were similar with medical therapy, angioplasty or bypass surgery.
In the 2002 trials, one of which received funding from industry, subjects were randomized to either stenting or to minimally invasive bypass surgery  (a medical therapy arm was not included). Several questions remain unanswered regarding the ethical justification for conducting these later trials. Were they really needed? Didn't the 1990 trials already demonstrate the equivalence of medical and invasive approaches for treating single-vessel CAD, including proximal LAD stenosis? The fact that we now have new invasive techniques is not per se sufficient reason for new trials to be conducted without concrete evidence that these techniques actually save more lives and prevent more infarctions. The populations studied were low risk by virtue of having chronic stable angina and normal left ventricular function. These cohorts would have done well on medical therapy. Why was medical therapy excluded from comparison? It seems that investigators had already decided that medical therapy was not as effective as the invasive strategies. Did these investigators ever tell their patients that medical therapy was equivalent to invasive interventions, based on previous research? Without this information, patients would not have been truly informed about all effective treatment options, when asked to consider joining either of the 2002 trials. Furthermore, rates of cardiac death or myocardial infarction were 3–6% with stenting and 6–10% with bypass in the recent studies. These rates are higher than those reported in the 1990 studies or in recent trials of aggressive lipid-lowering agents in similar populations . Therefore, the risks associated with the proposed invasive approaches cannot be assumed to be minimal.
There are also unanswered scientific questions regarding the more recent studies. Why wasn't intensive and tailored medical therapy tried before proceeding to randomization? Instead of committing valuable resources to conduct trials of newer and more costly interventions, efforts should focus on ensuring that everyone with CAD, especially those with limited access to health care, receives appropriate medical treatment. What was the medical therapy strategy after interventions? Aggressive medication use and risk factor modification could have reduced the relatively high event rates observed post-intervention in these trials, and may well have obviated the need for invasive interventions in the first place.
Another concern relates to the need for coronary angiography. Neither study describes the presence and severity of ischemia. Diegeler et al. do not even mention level of angina or use of anti-anginal medications prior to referral. Why were patients referred for angiography in the first place? It is probably too late to contemplate whether medications or revascularization is better once high-grade stenoses are detected. The interventionist almost always recommends "doing something". The treating physician, who commonly underestimates the efficacy of medications and overestimates the value of interventions,  is under pressure to follow the recommendation. The patient, who senses grave danger when hearing 90% or 95% stenosis (especially when coupled with the doctor's own anxiety), has no alternative but to "choose" an intervention. This is the path through which coronary angiography becomes a funnel for subsequent revascularization. Medical therapy has no chance here.
Investigator preference of invasive interventions over medical therapies for single-vessel CAD seems to extend to management of CAD in general. Several recent publications illustrate our case. The investigators of two recent studies favored invasive approaches to CAD in the elderly, despite outstanding results with medical therapy. In the TIME study, medically treated patients had slightly less overall risk of death and experienced no significant increase in risk of myocardial infarction after 6 months of therapy compared to those treated invasively, a remarkable finding considering that 31% of subjects had class IV angina . Reassuringly, participants in both treatment arms experienced reduced angina and improved quality of life to a similar extent, while clinical events remained comparable at 1 year . Similarly, Graham et al.  observed comparable outcomes with medical and invasive therapy among elderly patients. Why the authors of both studies chose to overstate the benefits of an invasive approach based on their own findings escapes us.  A balanced commentary justifiably questioned whether medical therapy was really optimal in these studies, but it failed to recommend optimizing medical therapy, which evidence already supports as the primary course of action in elderly patients with stable CAD .
Similarly, the debate over invasive vs. non-invasive therapy for acute coronary syndromes [ACS] exposes serious biases in favor of invasive therapy. Although a report of the RITA 3 trial found similar rates of death and myocardial infarction with both approaches, it overstated the benefits of invasive therapy in reducing refractory angina [12–14]. Certainly, patients with refractory symptoms need revascularization, but the exception should not become the rule. Given the equivalent effects of medical and invasive interventions on clinical events, the latter should be reserved for certain situations, e.g., for patients who are refractory to maximal medical therapy or for those with high risk indicators. An early invasive strategy for everyone with ACS makes no scientific, ethical, or economic sense.
It is the process leading to coronary angiography where we most need to focus in order to improve care and prevent unnecessary interventions. In the absence of high-risk indicators, maximal, intensive and tailored medical therapy, coupled with aggressive risk factor modification, should be the first choice of action. The provocation of mild-to-moderate ischemia or angina in patients taking submaximal doses of medications is not an adequate indication for coronary angiography. By the same token, when coronary angiography is performed, and single-vessel CAD stenosis is detected, the first question that should come to mind is not which invasive intervention is better but whether medical therapy has been given a fair chance. There is ample evidence in the medical literature that this more conservative approach is not being followed properly . The recent trials provide no new information that would lead us to disregard medical therapy as an effective and safe option for treating the patient with proximal LAD stenosis. On the contrary, the burden of proof is still on those advocating an invasive approach. If patients are told that an invasive approach is no more effective than medical therapy in preventing death or infarction or in abolishing limiting angina (and that medical intervention might even lead to more anginal relief), how many patients would still choose to undergo interventions that are costly and not free of complication? In addition, improvement in medical therapies since the two 1990 studies were published means potentially more benefits using a more conservative approach.
At a time when more studies are showing benefits of grossly underutilized medical therapies, we need to re-evaluate the current processes of peer review of studies of invasive management of CAD by research funding agencies and scientific journals. The purpose here is not to make adversaries but rather to detect subtleties that can uncover biases and correct them for the benefit of both patients and science. This is the only way for us to find balanced approaches for management of CAD. We encourage everyone to think together of more effective mechanisms than the occasional letter to the Editor.
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