CLINICAL RESEARCH
Seven-year outcome in the RITA-2 trial: coronary angioplasty versus medical therapy
Robert A. Henderson, FRCP, FESC*,*,
Stuart J. Pocock, PhD ,
Tim C. Clayton, MSc,
Rosemary Knight, RGN,
Keith A. A. Fox, FRCP, FESC ,
Desmond G. Julian, FRCP, FESC ,
Douglas A. Chamberlain, FRCP, FESC|| Second Randomized Intervention Treatment of Angina (RITA-2) Trial Participants
* Nottingham City Hospital, Nottingham, United Kingdom
London School of Hygiene and Tropical Medicine, London, United Kingdom
Royal Infirmary, Edinburgh, United Kingdom
London, United Kingdom
|| Pre-hospital Emergency Research Unit and Wales Heart Institute, University of Wales College of Medicine, Cardiff, United Kingdom
Manuscript received September 13, 2002;
revised manuscript received March 31, 2003,
accepted April 3, 2003.
* Reprint requests and correspondence: Dr. Robert A. Henderson, Department of Cardiology, Nottingham City Hospital, Hucknall Road, Nottingham NG5 1PB, United Kingdom.
rhender1{at}ncht.trent.nhs.uk
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Abstract
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OBJECTIVES: This study was designed to compare the long-term consequences of percutaneous transluminal coronary angioplasty (PTCA) and continued medical treatment.
BACKGROUND: The long-term effects of percutaneous coronary intervention need evaluating, especially in comparison with an alternative policy of continued medical treatment.
METHODS: The Second Randomized Intervention Treatment of Angina (RITA-2) is a randomized trial of PTCA versus conservative (medical) care in 1,018 patients considered suitable for either treatment option. Information on clinical events, interventions, and symptoms is available for a median seven years follow-up.
RESULTS: Death or myocardial infarction (MI) occurred in 73 (14.5%) PTCA patients and 63 (12.3%) medical patients (difference +2.2%, 95% confidence interval –2.0% to +6.4%, p = 0.21). There were 43 deaths in both groups, of which 41% were cardiac-related. Among patients assigned PTCA 12.7% subsequently had coronary artery bypass grafts, and 14.5% required additional non-randomized PTCA. Most of these re-interventions occurred within a year of randomization, and after two years the re-intervention rate was 2.3% per annum. In the medical group, 35.4% required myocardial revascularization: 15.0% in the first year and an annual rate of 3.6% after two years. An initial policy of PTCA was associated with improved anginal symptoms and exercise times. These treatment differences narrowed over time, mainly because of coronary interventions in medical patients with severe symptoms.
CONCLUSIONS: In RITA-2 an initial strategy of PTCA did not influence the risk of death or MI, but it improved angina and exercise tolerance. Patients considered suitable for PTCA or medical therapy can be safely managed with continued medical therapy, but percutaneous intervention is appropriate if symptoms are not controlled.
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Abbreviations and Acronyms
| | CABG | = coronary artery bypass graft | | CAD | = coronary artery disease | | LV | = left ventricular | | MI | = myocardial infarction | | PCI | = percutaneous coronary intervention | | PTCA | = percutaneous transluminal coronary angioplasty | | RITA | = Randomized Intervention Treatment of Angina |
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The optimal management of patients with angina pectoris remains controversial, but options include anti-anginal medication, percutaneous coronary intervention (PCI), or coronary artery bypass surgery. Several randomized clinical trials have compared percutaneous and surgical methods of myocardial revascularization, and some have reported long-term results (1–3). Overall, these trials suggest that percutaneous intervention is slightly less effective at relieving angina than is coronary artery bypass surgery, but there is no evidence that either revascularization strategy provides a prognostic advantage in the majority of patients.
For some patients with angina, revascularization is not considered essential for symptom relief or for prognostic reasons. Several small trials have compared percutaneous intervention with alternative medical treatment strategies in such patients, but most have reported only limited follow-up data (4–8). A meta-analysis of data available in 1998 concluded that percutaneous transluminal coronary angioplasty (PTCA) provides superior relief of angina at the cost of more coronary artery bypass surgery, but it could not reliably estimate the effects of the two treatment strategies on the risk of death or myocardial infarction (MI) (9).
The second Randomized Intervention Treatment of Angina (RITA-2) trial was designed to compare PTCA with continued medical treatment in patients in whom either strategy was considered a clinically acceptable treatment option. The primary trial end point was the five-year rate of death or non-fatal MI. The trial recruited 1,018 patients, and interim results have been published (10,11). In this article we report extended follow-up of the RITA-2 patients to a median seven years.
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Methods
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Trial design.
The design of RITA-2 has been reported previously (10). Patients were recruited at 20 centers in the U.K. and Ireland, and the ethics committee of each participating center approved the trial protocol. In brief, patients with arteriographically proven coronary artery disease (CAD) were considered for the trial if the supervising cardiologist thought that continued medical therapy and PTCA were both acceptable treatment options. Patients had to be over 18 years of age, but there was no upper age limit. Patients were not required to have current symptoms, but patients with multi-vessel disease, occluded coronary arteries, or impaired left ventricular (LV) function were potentially eligible for the trial. Patients with previous myocardial revascularization, significant left main stem disease, recent (within seven days) acute coronary syndrome, hemodynamically significant valve disease, or life-threatening non-cardiac disease likely to have a major influence on survival were excluded. Patients in whom revascularization was considered necessary for symptom relief or for prognostic reasons were also ineligible.
Before randomization, a participating interventional cardiologist reviewed the coronary arteriogram of a potentially eligible patient and identified at least one significant coronary stenosis in a major epicardial vessel that could be treated by coronary angioplasty. Patients who satisfied the eligibility criteria and consented to participate were subsequently randomized to initial treatment strategies of PTCA or continued medical management. Patients were stratified by center and by extent of disease (single or multi-vessel disease).
The trial protocol required that patients assigned to PTCA underwent dilation of the target stenosis (or stenoses) within three months of randomization. Stents and other coronary interventional techniques were used only if the initial balloon angioplasty result was unsatisfactory. The choice of medication after a randomized PTCA was not mandated, although clinicians were encouraged to discontinue anti-anginal drugs if a patient no longer had symptoms of angina. Patients in the PTCA group underwent additional coronary arteriography and revascularization procedures if considered appropriate by the supervising clinician, with the objective of detecting and treating restenosis.
Patients randomized to an initial strategy of medical management were prescribed appropriate anti-anginal medication for symptom relief. Coronary arteriography was repeated only for compelling clinical reasons, and myocardial revascularization procedures were reserved for patients whose symptoms were not controlled by optimal anti-anginal medication (usually a beta-adrenoceptor blocker, with a calcium antagonist, and/or with long-acting nitrate in maximally tolerated doses).
Data collection.
Patients were assessed at three months, six months, and yearly intervals after randomization. Research assistants at each participating center recorded trial data on specially prepared forms.
The pre-defined primary trial end point was the five-year rate of death and definite MI. An independent event validation committee, unaware of treatment assignment, reviewed all available information on deaths and MIs. The cause of death was classified as cardiac, other cardiovascular, or non-cardiovascular. Definite MI was diagnosed when new pathological Q-waves appeared on a follow-up electrocardiogram, or when a convincing clinical history was associated with electrocardiographic changes consistent with non–Q-wave infarction and cardiac enzyme activity above twice the upper limit of normal on at least two relevant serum samples.
As previously reported, angina was assessed with the Canadian Cardiovascular Society classification and breathlessness and physical activity were assessed by ordinal scales (10,12). Symptom-limited exercise tolerance tests were carried out using the Bruce protocol at three and six months and one and three years after randomization. Left ventricular function was assessed from LV angiograms using a wall motion score.
Statistical analysis.
A total of 1,018 patients were randomized at 20 participating centers. All data were analyzed by intention to treat, using standard methods. The percentages of patients with the primary end point of death or MI at five years in each treatment group were compared using Kaplan-Meier estimates. Times to death and death/MI are presented using Kaplan-Meier curves. The percentages of patients reporting other outcomes from follow-up interviews were compared using chi-squared tests. Analysis of co-variance was used to compare exercise time at three months and three years. Prognostic factors were determined by forward stepwise regression modeling: for the outcome of cardiac death or non-fatal MI, Cox regression was used, and for angina grade 2+ at five years, logistic regression was used.
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Results
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The 1,018 patients were randomized to coronary angioplasty (n = 504) or continued medical treatment (n = 514) from July 1992 to May 1996. Follow-up to September 30, 2001, is included in this report, the median follow-up period being seven years. Eighteen patients (1.8%) have been lost to follow-up. The five-year follow-up rate is 99.1%.
Baseline data and randomized PTCA.
Detailed information on baseline comparability and the randomized PTCA has been published earlier (10). In brief, 60% of patients had single-vessel disease, 53% had angina grade 2 or worse, 18% were female, and the median age was 58 years. At randomization 53% were receiving two or more anti-anginal drugs, 13% were taking lipid-lowering medication, 47% had had a previous MI, and 9% were treated for diabetes. The PTCA and medical treatment groups were similar with regard to all these baseline features.
The intended randomized PTCA was performed on 471 (93%) patients in the PTCA group, the median time from randomization to PTCA being five weeks. Angioplasty was attempted in a mean 1.4 vessel segments per patient (means 1.2, 1.6, and 1.9 segments for those with significant disease in 1, 2, and 3 epicardial vessels, respectively), of which 93% were successfully dilated. The randomized PTCA was complicated by emergency coronary artery bypass graft (CABG) in seven patients, non-fatal MI in seven patients (of whom 4 developed new electrocardiographic Q-waves), and one procedure-related death. Patient recruitment began before the widespread use of coronary stents, which were implanted during 44 (9%) randomized PTCAs. Of these, 32 occurred in the 160 patients randomized to PTCA during 1995 and 1996, the last 17 months of patient recruitment.
Death and MI.
To date, 43 patients have died in both treatment groups (Table 1). The survival plot (Fig. 1A) reveals comparable mortality between groups over eight years of follow-up. At five years follow-up, the mortality rate was 4.6% and 4.7% in the PTCA and medical groups, respectively (difference –0.1%, 95% confidence interval [CI] –2.7% to +2.5%).
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Figure 1 Cumulative risk of (A) death and (B) death or definite non-fatal myocardial infarction (MI). Bars show 95% confidence interval. Numbers show patients at risk of death or non-fatal MI. PTCA = percutaneous transluminal coronary angioplasty.
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Almost half the deaths were from non-cardiovascular causes. Although there were fewer cardiac deaths in the PTCA group—13 PTCA versus 22 medical—this difference is not statistically significant. Three of the seven cardiovascular deaths in the PTCA group were due to stroke.
To date, 32 and 23 patients in the PTCA and medical groups respectively have had a definite non-fatal MI (Table 1), five of whom (2 PTCA, 3 medical) have subsequently died. Thus, death or definite MI has occurred in 73 PTCA and 63 medical patients. The time-to-event plot (Fig. 1B) reveals an excess risk of this combined end point in the PTCA group in the first two months after randomization, which can be attributed to the eight procedure-related events mentioned earlier. Thereafter, the plots run parallel with a steady rate of end points up to eight years of follow-up. If the eight events related to the randomized PTCA are discounted, the subsequent rates of death or definite MI in the PTCA and medical groups are 2.0 and 1.8 per 100 patient-years of follow-up, respectively (difference +0.2, 95% CI from –0.5 to +0.8).
The pre-defined primary end point of death or definite MI at five years (including procedure-related events) occurred in 47 PTCA patients (9.4%) and 39 medical patients (7.6%) (difference +1.8%, 95% CI –1.7% to +5.2%, p = 0.31).
Subsequent interventions.
Since randomization, 64 patients randomized to PTCA (12.7%) and 63 (12.3%) patients randomized to medical treatment have had CABGs (Table 1). This includes the seven emergency CABGs after randomized PTCA and nine CABGs performed instead of the intended randomized PTCA.
In the PTCA group, additional non-randomized PTCA was required in 86 patients, 13 of whom also had CABG and 17 of whom required two or more such PTCAs. In the medical group, 139 patients subsequently had a first PTCA, of whom 20 also needed CABG during follow-up.
In total, the PTCA and medical groups had 106 and 174 non-randomized PTCAs during follow-up, and stents were implanted during 36% of these procedures in each group. Stent use increased over time: in 1992 to 1994, in 1995 to 1997, and in 1998 to 2001, the numbers of non-randomized PTCAs with stent insertion are 9 of 94 (9.6%), 42 of 113 (37.2%), and 50 of 73 (68.5%), respectively. There was no evidence of a difference in any outcome between patients with stents and those without stents.
In both treatment groups, the rate of non-randomized interventions (further PTCA and/or CABG) is much higher in the first year of follow-up (Fig. 2). In the PTCA group, 14.9% of patients required re-intervention in that first year (one-third of whom required CABG). This fell to a re-intervention rate of 3.8% in the next year and an average of 2.3% per annum over years 3 to 8 post randomization. In the medical group, 15% of the patients underwent a coronary intervention procedure in the first year (one-fifth of whom required CABG). In year 2, this fell to 6.4%, and in years 3 to 8 their coronary intervention rate averaged 3.6% per annum.
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Figure 2 Non-randomized intervention rates by year of follow-up. CABG = coronary artery bypass graft; PTCA = percutaneous transluminal coronary angioplasty.
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Over five years of follow-up, 10.5% of the PTCA group had a CABG, compared to 9.3% in the medical group. In the PTCA group, the five-year rate of re-intervention (PTCA and/or CABG) was 23.3% (16.2% and 28.9%, respectively, for patients with baseline angina grade <2 and  2). Information about coronary arteriography before these non-randomized revascularization procedures was available for 71 of 106 PTCA patients, and restenosis was demonstrated in 63%. By contrast, in the medical group 28.8% of patients had at least one coronary revascularization procedure by five years (20.2% and 37.5%, respectively, for patients with baseline angina grade <2 and 2), but 71.2% did not require any revascularization procedure.
Angina and breathlessness.
The prevalence of angina declined in both treatment groups during the first five years of follow-up (Fig. 3), but this symptomatic improvement was much more rapid in the PTCA group. At three months after randomization, 19.4% and 35.9% of the PTCA and medical groups, respectively, had angina grade 2 or worse (difference 16.5%, 95% CI 11.0% to 21.9%). By five years follow-up, the prevalence of angina grade 2 or worse in the PTCA group remained steady at 15.0%, whereas in the medical group the prevalence of angina was reduced to 21.4%. The five-year treatment difference is thus much smaller, 6.4% in favor of PTCA (95% CI 1.5% to 11.3%, p = 0.011). During the next three years, the prevalence of angina begins to increase slightly in both treatment groups.
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Figure 3 Prevalence of angina over time at baseline (base), three, and six months, and yearly intervals after randomization. P = coronary angioplasty group; M = medical group.
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The above results are based on analysis by intention to treat, but it is also relevant to consider the impact of non-randomized procedures on anginal symptoms. Figure 4 relates mean angina grade to time before and after the first non-randomized intervention; the vertical line at time 0 represents the moment of intervention. Patients without non-randomized interventions are not shown on these graphs. The angina grades are smoothed using a nearest-neighbor running-line smoother, with the data before and after the non-randomized intervention smoothed separately to allow a discontinuity. Pointwise 95% confidence intervals are also shown. The mean angina grade increases during the 6 to 12 months before the non-randomized intervention (especially in the medical group), whether the intervention is PTCA or CABG. The angina grade of patients immediately before their non-randomized intervention was recorded only for patients in the medical group; the mean is marked with a triangle (Fig. 4) and is consistent with the prior trend. After the non-randomized intervention, angina grade improves rapidly, especially where a CABG was done (Figs. 4B and 4D).
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Figure 4 Mean angina grades before and after non-randomized intervention. Panels A and B show data for the percutaneous transluminal coronary angioplasty (PTCA) group. Panels C and D show data for the medical group. Lines are smoothed averages and 95% confidence intervals. The circles show individual data points. Continued on next page. For the medical group (C and D), the triangle indicates angina grade immediately before non-randomized intervention. CABG = coronary artery bypass graft.
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Patients in the PTCA group had less use of anti-anginal drugs up to eight years follow-up compared with the medical group. For instance, at five years 70% and 83% of the PTCA and medical groups, respectively, were receiving at least one anti-anginal drug, 23% and 34% were receiving two drugs, and 8% and 11% were receiving triple-drug therapy. Anti-anginal treatment included a beta-blocker in 42% of the PTCA group and 53% of the medical group. In the PTCA group, 92% were taking aspirin, compared with 91% of the medical group. The use of HMG CoA reductase inhibitors increased over time, and at five years 51% of the PTCA group and 47% of the medical group were prescribed lipid-lowering medication. Angiotensin-converting enzyme inhibitors were prescribed for 20% of the PTCA group and 17% of the medical group.
The highly significant treatment difference in prevalence of breathlessness in early follow-up had largely disappeared after a few years: 42% versus 57% breathless at three months (p < 0.001) in the PTCA and medical groups, respectively, compared to 46% versus 50% at three years (p = 0.30).
Similarly the mean difference in Bruce exercise treadmill time at three months, +37 s in favor of PTCA based on 864 patients (95% CI 21 to 52 s), had reduced to +25 s mean benefit based on 749 patients (95% CI 6 to 44 s) by three years follow-up.
Prognostic factors.
In determining which patient baseline factors are linked to subsequent prognosis we considered two outcomes: - The combined incidence of cardiac death and definite non-fatal MI, excluding the eight such events related to randomized PTCA, since they are likely to have a different etiology. Thus 78 patients experienced this outcome.
- The presence of angina grade 2 or worse five years after randomization: this affected 173 of 948 patients seen at five years.
For each outcome the following baseline factors were considered: angina grade, unstable angina in the past three months, number of anti-anginal drugs, breathlessness grade, exercise treadmill time, age, gender, previous MI, treatment for diabetes mellitus (with diet, drugs, or insulin), treatment for hypertension, blood pressure, serum cholesterol, weight, height, body mass index, smoking history, electrocardiographic abnormality, LV function score, number of diseased vessels, and >50% stenosis in the proximal left anterior descending or other proximal vessel. By using forward stepwise regression modeling procedures the predictive models shown in Table 2 were derived.
For cardiac death and non-fatal MI, angina grade at randomization was the strongest predictor. Patients with both proximal left anterior descending and at least one other diseased proximal vessel (i.e., 50% stenosis) had an estimated three-fold increase in risk, but there were only 71 patients in this category. There was no treatment difference in risk after adjusting for these two factors.
For prevalence of angina grade 2+ after five years, the baseline exercise time and breathlessness at baseline were strongly predictive. Patients with more severe angina at baseline also had an increased risk; but angina grade was strongly associated with breathlessness and exercise time, and after taking these variables into account, baseline angina grade was less independently predictive of outcome. After adjusting for these three factors, there remained a 33% odds reduction in angina at five years for PTCA versus medical treatment (p = 0.031).
There was a trend for the 90 patients with diabetes mellitus to be at greater risk of death or MI (hazard ratio 1.17, 95% CI 0.56 to 2.43) or angina grade 2+ during follow-up (odds ratio 1.43, 95% CI 0.80 to 2.58), but there was no evidence of an interaction between diabetes and treatment for these two outcomes. Other subgroup analyses were explored for each of the baseline variables listed above, but for neither outcome were there any statistically significant interactions between treatment group and baseline factors.
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Discussion
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The RITA-2 trial provides the only currently available randomized evidence comparing the long-term consequences of PCI and medical treatment in patients with angina. Over a median seven years follow-up, we have demonstrated that initial policies of PTCA and medical therapy in patients considered suitable for either treatment are comparable with regard to risk of death and non-fatal MI, but an initial policy of PTCA was associated with a lower prevalence of angina and improved exercise tolerance.
The patients in our trial were selected from a large group of patients undergoing coronary arteriography and ranged from patients with no angina and single-vessel disease to those with severe symptoms and advanced coronary disease (10). Nevertheless our patients were at low cardiovascular risk, with a mortality of <1% per annum in both groups. The trial results therefore cannot be generalized to all patients undergoing PCI but are relevant to a substantial group of patients for whom optimal treatment has been uncertain and for whom percutaneous intervention or continued medical therapy both seem appropriate.
Other trials of coronary angioplasty versus medical therapy (4–8) provide important additional information but are too small to reliably estimate the effects of the two treatment strategies on mortality or risk of MI, and most have not reported long-term follow-up data. The TIME and ACIP trials are also relevant, but these trials compared a policy of early myocardial revascularization with continued medical therapy, and the long-term effects of percutaneous and surgical treatment cannot easily be separated (13,14).
The clinical significance of MI during PCI has recently been the subject of intense research interest. Some investigators report that the extent of myonecrosis, defined by the serum cardiac enzyme level, correlates closely with mortality during long-term follow-up (15,16). Other studies suggest that a small peri-procedural rise in cardiac enzyme level is not of prognostic importance (17–19). In RITA-2, the assigned coronary angioplasty procedures were associated with a small risk of MI, but as we did not routinely measure serum cardiac enzyme levels, the incidence of procedure-related myocardial injury may have been underestimated. Nevertheless, this procedural risk did not translate into increased mortality during follow-up, and although RITA-2 was not designed to compare the effects of the two treatments on long-term mortality, the data suggest that early coronary intervention is a safe strategy in low-risk patients with symptomatic CAD.
Many interventional cardiologists advocate dilation of severe coronary stenoses irrespective of symptoms, in the belief that this reduces the risk of progression to coronary occlusion, prevents MI, and improves prognosis. Our data do not support this belief, and in RITA-2, dilation of one or more coronary stenoses did not subsequently affect the incidence of MI or death over eight years of follow-up. Patients with more extensive CAD may gain prognostic benefit from coronary artery bypass surgery (20), but whether contemporary PCI influences prognosis in such patients can be elucidated only by additional randomized clinical trials.
Angina and exercise tolerance.
The RITA-2 data suggest that the main advantage of PTCA over medical management is an improved angina status and exercise tolerance over many years, but the long-term symptom data require careful interpretation. Shortly after randomization, there is a substantial reduction in anginal symptoms among patients treated by PTCA compared with patients assigned medical therapy. Thereafter this treatment difference attenuates because of symptomatic improvement in the medical management group, which can be largely explained by the effects of myocardial revascularization procedures in 35% of medical patients (Fig. 4). Thus, the intention-to-treat results for angina prevalence (grade 2 or worse) at five years show only 30% proportionately fewer cases in the PTCA group compared with the medical group. This narrowing of the observed treatment difference over time should not be interpreted as a decline in the effectiveness of an interventional strategy but as an inevitable consequence of the most severely affected medical group patients requiring coronary interventions. More complex statistical modeling of these issues has been undertaken and confirms this interpretation (21).
It is relevant to note that the most powerful predictors of symptomatic status at five years are breathlessness, exercise time, and angina grade at baseline. Furthermore, more severe angina grade at baseline is the strongest predictor of cardiac death or MI. By comparison, there was no evidence that other baseline variables, including the number of diseased vessels and LV function score, predict subsequent symptoms or cardiac events. This analysis has limited statistical power but implies that the management strategy for patients with coronary disease for which revascularization is not considered essential on prognostic grounds can be predominantly determined by symptoms. In RITA-2, patients with mild symptoms at baseline had a better prognosis, and among such patients the use of coronary angioplasty and the associated procedural risk can reasonably be delayed until worsening symptoms mandate intervention, particularly as the economic cost of the interventional strategy exceeds the cost of conservative care (22).
Study limitations.
The RITA-2 trial enrolled patients from 1992 to 1996, since when there have been considerable advances in both medical and interventional treatment. The use of coronary stents has increased markedly, and developments in stent design and deployment techniques, together with adjunctive use of clopidogrel and glycoprotein IIb/IIIa receptor antagonists, have all contributed to improvements in outcome after PCI (23,24). Randomized trials of multi-vessel stenting versus CABG, such as ARTS (25), ERACI-2 (26), and SOS (27) provide valuable information, but their follow-up period is still relatively short. The introduction of drug-coated stents has been heralded as a major advance, but there are no data concerning the long-term effects of this new technology (28). Other changes in practice include increasing use of hydroxymethyl glutaryl coenzyme A (HMG-CoA) reductase inhibitors (29,30), angiotensin-converting enzyme inhibitors (31), and thienopyridines (32) in patients with CAD.
The long-term prognostic and symptomatic implications of all these developments for patients considered eligible for PCI remain largely unexplored to date. The Clinical Outcome Utilizing Revascularization and Aggressive Drug Evaluation (COURAGE) trial is testing the hypothesis in more than 3,000 patients that optimal catheter-based coronary revascularization combined with intensive medical therapy is superior to intensive medical therapy alone (33). Further data will be available from the BARI-2D trial, a comparison of medical therapy and revascularization in patients with type 2 diabetes mellitus. These trials will be important contributions; but recruitment in both trials is ongoing, and hence, long-term results will not be known for several years. Meantime RITA-2 provides the best currently available insight into outcome many years after initial policies of percutaneous intervention or conservative management in patients with angina.
Conclusions.
In conclusion, we have demonstrated that PTCA reduces anginal symptoms and improves exercise tolerance in the long-term for patients who are considered suitable for treatment by percutaneous intervention or by continued medical therapy. However, among such patients PTCA does not appear to influence the disease natural history favorably with regard to risk of death and non-fatal MI. Treatment choice can therefore be determined principally by symptom status. Patients with mild to moderate angina can be safely managed with continued medical therapy, but percutaneous intervention is appropriate if symptoms are not controlled by medication. Other trial evidence is needed to update these long-term findings regarding percutaneous interventional treatment, in the light of increased use of coronary stents and recent developments in medical treatments.
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Appendix
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For a complete list of participants in the RITA-2 trial, please see the October 1, 2003, issue of JACC at http://www.cardiosource.com/jacc.html.
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Acknowledgments
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We thank the 1,018 patients who consented to participate in the trial. We greatly value the work of past RITA-2 trial coordinators (Bronwen Youard [1992 to 1996] and Claire Marley [1996 to 1998]) and RITA-2 trialists. We also thank Ian White for calculating the data analysis for Figure 4. The randomization service was provided by the Royal Free Hospital coronary care unit.
We particularly acknowledge the work and contribution of Rosemary Carey, who died on June 6, 2003.
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Footnotes
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The trial was supported by grants from the British Heart Foundation and Medical Research Council. Additional support was provided by Advanced Cardiovascular Systems Inc (U.S.), Intervention Ltd (U.K.), Cordis Ltd, Schneider (U.K.) and Nycomed Ltd.
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References
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1. Henderson RA, Pocock SJ, Sharp SJ, et al. Long-term results of RITA-1 trial: clinical and cost comparisons of coronary angioplasty and coronary-artery bypass grafting. Lancet. 1998;352:1419–1425[CrossRef][Medline]
2. BARI Investigators. Seven-year outcome in the Bypass Angioplasty Revascularization Investigation (BARI) by treatment and diabetic status. J Am Coll Cardiol. 2000;35:1122–1129[Abstract/Free Full Text]
3. King SB, Kosinski AS, Guyton RA, Lembo NJ, Weintraub WS. Eight-year mortality in the Emory Angioplasty versus Surgery Trial (EAST). J Am Coll Cardiol. 2000;35:1116–1121[Abstract/Free Full Text]
4. Folland ED, Hartigan PM, Parisi AF. Percutaneous transluminal coronary angioplasty versus medical therapy for stable angina pectoris: outcomes for patients with double-vessel versus single-vessel coronary artery disease in a Veterans Affairs Cooperative randomized trial. J Am Coll Cardiol. 1997;29:1505–1511[Abstract]
5. Hartigan PM, Giacomini JC, Folland ED, Parisi AF. Two- to three-year follow-up of patients with single-vessel coronary artery disease randomized to coronary angioplasty or medical therapy (results of a VA cooperative study). Am J Cardiol. 1998;82:1445–1450[CrossRef][Medline]
6. Hueb WA, Soares PR, Almeida DO, et al. Five-year follow-up of the Medicine, Angioplasty, or Surgery Study (MASS): a prospective, randomized trial of medical therapy, balloon angioplasty, or bypass surgery for single proximal left anterior descending coronary artery stenosis. Circulation. 1999;100(Suppl):II107–113
7. Pitt B, Waters D, Brown WV, et al. Aggressive lipid-lowering therapy compared with angioplasty in stable coronary artery disease. N Engl J Med. 1999;341:70–76[Abstract/Free Full Text]
8. Dakik HA, Kleiman NS, Farmer JA, et al. Intensive medical therapy versus coronary angioplasty for suppression of myocardial ischemia in survivors of acute myocardial infarction: a prospective, randomized pilot study. Circulation. 1998;98:2017–2023[Abstract/Free Full Text]
9. Bucher HC, Hengstler P, Schindler C, Guyatt GH. Percutaneous transluminal coronary angioplasty versus medical treatment for non-acute coronary heart disease: meta-analysis of randomised controlled trials. BMJ. 2000;321:73–77[Abstract/Free Full Text]
10. RITA-2 Trial Participants. Coronary angioplasty versus medical therapy for angina: the second Randomised Intervention Treatment of Angina (RITA-2) trial. Lancet. 1997;350:461–468[CrossRef][Medline]
11. Pocock SJ, Henderson RA, Clayton T, Lyman GH, Chamberlain DA. Quality of life after coronary angioplasty or continued medical treatment for angina: three-year follow-up in the RITA-2 trial. J Am Coll Cardiol. 2000;35:907–914[Abstract/Free Full Text]
12. Campeau L. Grading of angina pectoris. Circulation. 1976;54:522–523 (letter)[Medline]
13. TIME Investigators. Trial of invasive versus medical therapy in elderly patients with chronic symptomatic coronary-artery disease (TIME): a randomised trial. Lancet. 2001;358:951–957[CrossRef][Medline]
14. Davies RF, Goldberg AD, Forman S, et al. Asymptomatic cardiac ischaemia pilot (ACIP) study two-year follow-up. Outcomes of patients randomized to initial strategies of medical therapy versus revascularization. Circulation. 1997;95:2037–2043[Abstract/Free Full Text]
15. Califf RM, Abdelmeguid AE, Kuntz RE, et al. Myonecrosis after revascularization procedures. J Am Coll Cardiol. 1998;31:241–251[Abstract/Free Full Text]
16. Abdelmeguid AE, Topol EJ, Whitlow PL, Sapp SK, Ellis SG. Significance of mild transient release of creatine kinase-MB fraction after percutaneous coronary interventions. Circulation. 1996;94:1528–1536[Abstract/Free Full Text]
17. Stone GW, Mehran R, Dangas G, Lansky AJ, Kornowski R, Leon MB. Differential impact on survival of electrocardiographic Q-wave versus enzymatic myocardial infarction after percutaneous intervention: a device-specific analysis of 7147 patients. Circulation. 2001;104:642–647[Abstract/Free Full Text]
18. Saucedo JF, Mehran R, Dangas G, et al. Long-term clinical events following creatine kinase myocardial band isoenzyme elevation after successful coronary stenting. J Am Coll Cardiol. 2000;35:1134–1141[Abstract/Free Full Text]
19. Kini A, Marmur JD, Kini S, et al. Creatine kinase-MB elevation after coronary intervention correlates with diffuse atherosclerosis, and low-to-medium level elevation has a benign clinical course: implications for early discharge after coronary intervention. J Am Coll Cardiol. 1999;34:663–671[Abstract/Free Full Text]
20. Yusuf S, Zucker D, Peduzzi P, et al. Effect of coronary artery bypass graft surgery on survival: overview of 10-year results from randomised trials by the Coronary Artery Bypass Graft Surgery Trialists Collaboration. Lancet. 1994;344:563–570[CrossRef][Medline]
21. White IR, Carpenter J, Pocock SJ, Henderson RA. Adjusting treatment comparisons to account for non-randomised interventions: an example from an angina trial. Stat Med 2003;22:781–93
22. Sculpher MJ, Smith DH, Clayton T, et al. Coronary angioplasty versus medical therapy for angina. Health service costs based on the second Randomised Intervention Treatment of Angina (RITA-2) trial. Eur Heart J. 2002;23:1291–1300[Abstract/Free Full Text]
23. Bhatt DL, Bertrand ME, Berger PB, et al. Meta-analysis of randomized and registry comparisons of ticlopidine with clopidogrel after stenting. J Am Coll Cardiol. 2002;39:9–14[Abstract/Free Full Text]
24. Topol EJ, Mark DB, Lincoff AM, et al. Outcomes at 1 year and economic implications of platelet glycoprotein IIb/IIIa blockade in patients undergoing coronary stenting: results from a multicentre randomised trial. Lancet. 1999;354:2019–2024[CrossRef][Medline]
25. Serruys PW, Unger F, Sousa JE, et al. Comparison of coronary-artery bypass surgery and stenting for the treatment of multivessel disease. N Engl J Med. 2001;344:1117–1124[Abstract/Free Full Text]
26. Rodriguez A, Bernardi V, Navia J, et al. Coronary angioplasty with stenting versus coronary bypass surgery in patients with multiple-vessel disease (ERACI II): 30-day and one-year follow-up results. J Am Coll Cardiol. 2001;37:51–58[Abstract/Free Full Text]
27. The SOS Investigators. Coronary artery bypass surgery versus percutaneous coronary intervention with stent implantation in patients with multivessel coronary artery disease (the Stent or Surgery trial). Lancet. 2002;360:965–970[CrossRef][Medline]
28. Morice MC, Serruys PW, Sousa JE, et al. A randomized comparison of a sirolimus-eluting stent with a standard stent for coronary revascularization. N Engl J Med. 2002;346:1773–1780[Abstract/Free Full Text]
29. Scandinavian Simvastatin Survival Study Group. Randomised trial of cholesterol lowering in 4444 patients with coronary heart disease: the Scandinavian simvastatin survival study (4S). Lancet. 1994;344:1383–1389[CrossRef][Medline]
30. LIPID Study Group. Prevention of cardiovascular events and death with pravastatin in patients with coronary heart disease and a broad range of initial cholesterol levels. N Engl J Med. 1998;339:1349–1357[Abstract/Free Full Text]
31. Yusuf S, Sleight P, Pogue J, Bosch J, Davies R, Dugenais GThe HOPE Investigators. Effects of an angiotensin converting enzyme inhibitor, ramipril, on cardiovascular events in high-risk patients. N Engl J Med. 2000;342:145–153[Abstract/Free Full Text]
32. CURE Investigators. Effects of clopidogrel in addition to aspirin in patients with acute coronary syndromes without ST-segment elevation. N Engl J Med. 2001;345:494–502[Abstract/Free Full Text]
33. Boden W, O'Rourke R. Clinical outcome utilizing revascularization and aggressive drug evaluation. The COURAGE trial. Available at: http://www.cardiosource.com/trials/. Accessed September 6, 2002
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|
|
|
|
|
|
|
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|
|
|
|
|
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|
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|
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|
|
|
|
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|
|
|
|
|
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|
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|
|
|
|
|
|
|
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[Full Text]
[PDF]
|
|
|
|
|
|
|
H. B. Barner
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September 1, 2006;
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419 - 424.
[Abstract]
[Full Text]
[PDF]
|
|
|
|
|
|
|
Authors/Task Force Members, K. Fox, M. A. A. Garcia, D. Ardissino, P. Buszman, P. G. Camici, F. Crea, C. Daly, G. De Backer, P. Hjemdahl, et al.
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Eur. Heart J.,
June 1, 2006;
27(11):
1341 - 1381.
[Full Text]
[PDF]
|
|
|
|
|
|
|
I. Popescu, M. S. Vaughan-Sarrazin, and G. E. Rosenthal
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JAMA,
May 10, 2006;
295(18):
2141 - 2147.
[Abstract]
[Full Text]
[PDF]
|
|
|
|
|
|
|
C. A Daly, B. De Stavola, J. L L. Sendon, L. Tavazzi, E. Boersma, F. Clemens, N. Danchin, F. Delahaye, A. Gitt, D. Julian, et al.
Predicting prognosis in stable angina--results from the Euro heart survey of stable angina: prospective observational study
BMJ,
February 4, 2006;
332(7536):
262 - 267.
[Abstract]
[Full Text]
[PDF]
|
|
|
|
|
|
|
P Hjemdahl, S V Eriksson, C Held, L Forslund, P Nasman, and N Rehnqvist
Favourable long term prognosis in stable angina pectoris: an extended follow up of the angina prognosis study in Stockholm (APSIS)
Heart,
February 1, 2006;
92(2):
177 - 182.
[Abstract]
[Full Text]
[PDF]
|
|
|
|
|
|
|
P. F. Hoilund-Carlsen, A. Johansen, H. W. Christensen, W. Vach, M. Moldrup, P. Bartram, A. Veje, T. Haghfelt, and for the Myocardial Ischemia Logistics Evaluation S
Potential impact of myocardial perfusion scintigraphy as gatekeeper for invasive examination and treatment in patients with stable angina pectoris: observational study without post-test referral bias
Eur. Heart J.,
January 1, 2006;
27(1):
29 - 34.
[Abstract]
[Full Text]
[PDF]
|
|
|
|
|
|
|
D. T. Nash
The Case for Medical Treatment in Chronic Stable Coronary Artery Disease
Arch Intern Med,
December 12, 2005;
165(22):
2587 - 2589.
[Full Text]
[PDF]
|
|
|
|
|
|
|
P. Gabriel Steg and D. Himbert
Unmet medical needs and therapeutic opportunities in stable angina
Eur. Heart J. Suppl.,
September 1, 2005;
7(suppl_H):
H7 - H15.
[Abstract]
[Full Text]
[PDF]
|
|
|
|
|
|
|
J. A. Brinker, C. J. Davidson, and W. Laskey
Preventing in-hospital cardiac and renal complications in high-risk PCI patients
Eur. Heart J. Suppl.,
August 1, 2005;
7(suppl_G):
G13 - G24.
[Abstract]
[Full Text]
[PDF]
|
|
|
|
|
|
|
J. Abrams
Chronic Stable Angina
N. Engl. J. Med.,
June 16, 2005;
352(24):
2524 - 2533.
[Full Text]
[PDF]
|
|
|
|
|
|
|
D. G. Katritsis and J. P.A. Ioannidis
Percutaneous Coronary Intervention Versus Conservative Therapy in Nonacute Coronary Artery Disease: A Meta-Analysis
Circulation,
June 7, 2005;
111(22):
2906 - 2912.
[Abstract]
[Full Text]
[PDF]
|
|
|
|
|
|
|
T. A. Stukel, F. L. Lucas, and D. E. Wennberg
Long-term Outcomes of Regional Variations in Intensity of Invasive vs Medical Management of Medicare Patients With Acute Myocardial Infarction
JAMA,
March 16, 2005;
293(11):
1329 - 1337.
[Abstract]
[Full Text]
[PDF]
|
|
|
|
|
|
|
C.-N. Lee
Do Drug-Eluting Stents Mark The End of Coronary Artery Bypass Surgery?
Asian Cardiovasc Thorac Ann,
March 1, 2005;
13(1):
1 - 3.
[Full Text]
[PDF]
|
|
|
|
|
|
|
D. Rott
Advantage of percutaneous coronary intervention over medical therapy in angina relief and the placebo effect
J. Am. Coll. Cardiol.,
January 18, 2005;
45(2):
327 - 328.
[Full Text]
[PDF]
|
|
|
|
|
|
|
J. P. Curtis and H. M. Krumholz
Keeping the Patient in View: Defining the Appropriateness of Percutaneous Coronary Interventions
Circulation,
December 21, 2004;
110(25):
3746 - 3748.
[Full Text]
[PDF]
|
|
|
|
|
|
|
M. Pfisterer and for the TIME Investigators
Long-Term Outcome in Elderly Patients With Chronic Angina Managed Invasively Versus by Optimized Medical Therapy: Four-Year Follow-Up of the Randomized Trial of Invasive Versus Medical Therapy in Elderly Patients (TIME)
Circulation,
September 7, 2004;
110(10):
1213 - 1218.
[Abstract]
[Full Text]
[PDF]
|
|
|
|
|
|
|
ADDITIONAL ARTICLES ABSTRACTED IN ACP JOURNAL CLUB
Evid. Based Med.,
September 1, 2004;
9(5):
131 - 131.
[Full Text]
[PDF]
|
|
|
|
|
|
|
W. E. Boden
Surgery, angioplasty, or medical therapy for symptomatic multivessel coronary artery disease: Is there an indisputable "winning strategy" from evidence-based clinical trials?
J. Am. Coll. Cardiol.,
May 19, 2004;
43(10):
1752 - 1754.
[Full Text]
[PDF]
|
|
|
|
|
|
|
B. R. Chaitman, S. L. Skettino, J. O. Parker, P. Hanley, J. Meluzin, J. Kuch, C. J. Pepine, W. Wang, J. J. Nelson, D. A. Hebert, et al.
Anti-ischemic effects and long-term survival during ranolazine monotherapy in patients with chronic severe angina
J. Am. Coll. Cardiol.,
April 21, 2004;
43(8):
1375 - 1382.
[Abstract]
[Full Text]
[PDF]
|
|
|
|
|
|
|
Angioplasty vs. Medical Therapy: Long-Term Data
Journal Watch Cardiology,
October 31, 2003;
2003(1031):
1 - 1.
[Full Text]
|
|
|
|
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