STEMI indicates ST-segment elevation myocardial infarction; PCI, percutaneous coronary intervention.aA total of 2575 patients underwent primary PCI for treatment of STEMI at 11 international sites during the inclusion period. No reliable data for patients assessed for eligibility are available.bOne patient treated with bare-metal stent did not undergo PCI and was assumed to have 1 lesion.
Major adverse cardiac events included a composite of cardiac death, target vessel–related reinfarction, and ischemia-driven target-lesion revascularization. P values are 2-sided from Cox proportional hazards regression models χ2 test. HR indicates hazard ratio.
BMI indicates body mass index (calculated as weight in kilograms divided by height in meters squared); LVEF, left ventricular ejection fraction; TIMI, thrombolysis in myocardial infarction. Two patients randomized to receive the biolimus-eluting stent and 1 patient randomized to receive the bare-metal stent could not be included in the stratified analyses for lesion characteristics (reference vessel diameter and lesion length) due to missing angiography.
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Räber L, Kelbæk H, Ostojic M, et al. Effect of Biolimus-Eluting Stents With Biodegradable Polymer vs Bare-Metal Stents on Cardiovascular Events Among Patients With Acute Myocardial Infarction: The COMFORTABLE AMI Randomized Trial. JAMA. 2012;308(8):777–787. doi:10.1001/jama.2012.10065
Context The efficacy and safety of drug-eluting stents compared with bare-metal stents remains controversial in patients with ST-segment elevation myocardial infarction (STEMI) undergoing primary percutaneous coronary intervention (PCI).
Objective To compare stents eluting biolimus from a biodegradable polymer with bare-metal stents in primary PCI.
Design, Setting, and Patients A prospective, randomized, single-blinded, controlled trial of 1161 patients presenting with STEMI at 11 sites in Europe and Israel between September 19, 2009, and January 25, 2011. Clinical follow-up was performed at 1 and 12 months.
Intervention Patients were randomized 1:1 to receive the biolimus-eluting stent (n = 575) or the bare-metal stent (n = 582).
Main Outcome Measures Primary end point was the rate of major adverse cardiac events, a composite of cardiac death, target vessel–related reinfarction, and ischemia-driven target-lesion revascularization at 1 year.
Results Major adverse cardiac events at 1 year occurred in 24 patients (4.3%) receiving biolimus-eluting stents with biodegradable polymer and 49 patients (8.7%) receiving bare-metal stents (hazard ratio [HR], 0.49; 95% CI, 0.30-0.80; P = .004). The difference was driven by a lower risk of target vessel–related reinfarction (3 [0.5%] vs 15 [2.7%]; HR, 0.20; 95% CI, 0.06-0.69; P = .01) and ischemia-driven target-lesion revascularization (9 [1.6%] vs 32 [5.7%]; HR, 0.28; 95% CI, 0.13-0.59; P < .001) in patients receiving biolimus-eluting stents compared with those receiving bare-metal stents. Rates of cardiac death were not significantly different (16 [2.9%] vs 20 [3.5%], P = .53). Definite stent thrombosis occurred in 5 patients (0.9%) treated with biolimus-eluting stents and 12 patients (2.1%; HR, 0.42; 95% CI, 0.15-1.19; P = .10) treated with bare-metal stents.
Conclusion Compared with a bare-metal stent, the use of biolimus-eluting stents with a biodegradable polymer resulted in a lower rate of the composite of major adverse cardiac events at 1 year among patients with STEMI undergoing primary PCI.
Trial Registration clinicaltrials.gov Identifier: NCT00962416
Primary percutaneous coronary intervention (PCI) is the reperfusion therapy of choice among patients with ST-segment elevation myocardial infarction (STEMI) owing to a lower risk of reinfarction and improved survival compared with fibrinolysis.1,2 Bare-metal stents minimize the risk of infarct vessel reocclusion and reinfarction compared with balloon angioplasty, but are associated with restenosis due to neointimal hyperplasia.3,4 Early generation drug-eluting stents releasing sirolimus or paclitaxel from durable polymers reduce the need for repeat revascularization compared with bare-metal stents.5-7 However, vessel healing is delayed with evidence of chronic inflammation related at least in part to the persistence of durable polymer components in patients with acute STEMI.8
In addition, acute myocardial infarction (MI) is a predictor of thrombotic stent complications occurring late after drug-eluting stent implantation, particularly in the presence of a high thrombus burden, raising concerns regarding the balance of risks and benefits of these devices in this clinical setting.9,10 Two meta-analyses in patients with acute MI confirmed a lower risk of repeat revascularization with early generation drug-eluting stents compared with bare-metal stents, however, at the expense of a 2-fold increased risk of very late stent thrombosis.11,12
Newer-generation drug-eluting stents with biodegradable polymers provide controlled drug release with subsequent degradation of the polymer rendering the stent surface more closely to a bare-metal stent after the period of biodegradation. The unrestricted use of stents eluting biolimus, an equipotent sirolimus analogue, from biodegradable polylactic acid was noninferior and potentially better than sirolimus-eluting stents in terms of major adverse clinical events in a large clinical trial with follow-up of 4 years, with a substantially reduced risk (80%) of stent thrombosis occurring beyond 1 year.13,14 A stratified analysis suggested a particularly pronounced benefit among patients with acute STEMI. We therefore performed a multicenter, randomized trial to compare the efficacy and safety of stents eluting biolimus from a biodegradable polymer with bare-metal stents of otherwise identical design.
The COMFORTABLE AMI trial (Comparison of Biolimus Eluted From an Erodible Stent Coating With Bare Metal Stents in Acute ST-Elevation Myocardial Infarction) was a multicenter, randomized, assessor-blinded, superiority trial in patients presenting with STEMI undergoing primary PCI. The full study design was reported elsewhere.15 The study complied with the Declaration of Helsinki and was approved by all institutional ethics committees. All patients provided written informed consent.
Patients aged 18 years or older with symptom onset within 24 hours and ST-segment elevation of at least 1 mm in 2 or more contiguous leads, true posterior MI, or new left bundle branch block were eligible for randomization in the presence of at least 1 culprit lesion within the infarct vessel. There was no limit regarding the number of treated lesions, vessels, or complexity. Exclusion criteria were presence of mechanical complications of acute MI, known allergy to any study medication, use of vitamin K antagonists, planned surgery unless dual antiplatelet therapy could be maintained throughout the perisurgical period, history of bleeding diathesis or known coagulopathy, pregnancy, participation in another trial before reaching the primary end point, inability to provide informed consent, and noncardiac comorbid conditions with life expectancy of less than 1 year. Patients were recruited between September 19, 2009, and January 25, 2011, in 11 centers throughout Europe and Israel (Denmark [n = 1], Israel [n = 1], the Netherlands [n = 1], Serbia [n = 1], Switzerland [n = 6], and the United Kingdom [n = 1]).
Randomization was performed via a web-based system after diagnostic angiography. The allocation sequence was computer generated in randomly varying blocks of 2, 4, and 6, and stratified by center. Patients were randomly allocated on a 1:1 basis to treatment with stents eluting biolimus from a biodegradable polylactic acid polymer (BioMatrix, Biosensors Europe SA) or bare-metal stents of otherwise identical design (Gazelle, Biosensors Europe SA).
Both stent types were available in diameters of 2.25, 2.50, 2.75, 3.00, 3.50, and 4.00 mm and in lengths of 8, 11, 14, 18, 24, and 28 mm. Before stent implantation, thrombus aspiration was recommended in all patients whenever aspiration was deemed technically feasible. Predilation of the culprit lesion was left to the discretion of the operator. Complete revascularization of all lesions within the infarct vessel had to be performed with the randomly allocated study stent. Nonculprit vessels were treated by default with biolimus-eluting stents at baseline and during follow-up and did not contribute to the primary end point. Staged procedures for the treatment of nonculprit vessels were permitted within 3 months with the uniform use of biolimus-eluting stent in all lesions.
Acetylsalicylic acid (≥250 mg) was administered before the procedure. In centers where prasugrel was available, an initial dose of 60 mg (including patients preloaded with clopidogrel) was administered followed up with a daily dose of 10 mg. If prasugrel was not available or contraindicated, clopidogrel was administered at a loading dose of 600 mg, followed up with a dose of 75 mg twice daily for 7 days, followed up with a maintenance dose of 75 mg once daily. Dual antiplatelet therapy was prescribed for the duration of at least 1 year in all patients. Unfractionated heparin was routinely administered with a minimal dose of 5000 IE or a dose of 70 to 100 IU/kg to maintain an activated clotting time of 250 seconds. Bivalirudin was administered at a dose of 0.75 mg/kg intravenously followed up with an infusion of 1.75 mg/kg per hour during the duration of the procedure. The use of glycoprotein IIb/IIIa inhibitors was left to the discretion of the operator.
We assessed creatinine kinase, creatinin kinase-MB, and troponin at admission and thereafter every 8 hours until the peak creatinine kinase had been reached. A 12-lead electrocardiogram was performed before the procedure, within 24 hours after the procedure, before discharge, and in case of recurrent signs of ischemia.
Independent study monitors verified source data according to a prespecified monitoring plan.15 Data were stored in a central database (Cardiobase, Clinical Trials Unit, and Department of Cardiology, Bern University Hospital, Switzerland, and 2mT, Ulm, Germany). Follow-up appointments were scheduled at 30 days and 1 year, and patients were questioned about the occurrence of angina, any adverse events, hospitalization, and cardiovascular medication intake. All serious adverse events were submitted to Clinical Trials Unit, University of Bern, Bern, Switzerland, in a blinded fashion. Any death, reinfarction, revascularization, stent thrombosis, cerebrovascular accident, and bleeding event was independently adjudicated by a blinded clinical event committee. An independent data and safety monitoring board blinded to treatment groups periodically reviewed all event information and compared safety outcomes between groups.
Angiograms were centrally assessed by the core laboratory at Bern University Hospital by blinded personnel. The bare-metal stent and biodegradable polymer-based drug-eluting stent were indistinguishable on angiography. The core laboratory assessment encompassed quantitative coronary angiography using dedicated software (XAangio XA 7.1, Medis) and the assessment of the SYNTAX MI score,16 and thrombolysis in MI (TIMI) flow grade.
The prespecified primary end point was the device-oriented composite of cardiac death, target vessel–related reinfarction, and ischemia-driven target-lesion revascularization at 1 year. Secondary end points included the patient-oriented composite of death, any reinfarction, and any revascularization, as well as target vessel–related reinfarction and any revascularization (percutaneous and surgical procedures), cardiac death, all-cause mortality, Q-wave and non–Q-wave reinfarction, stroke, stent thrombosis according to the definitions of the Academic Research Consortium, and device and lesion success. Detailed definitions of all primary and secondary end points were reported elsewhere.15
Target-lesion revascularization was defined as a repeated revascularization due to a stenosis within the stent or within the 5-mm borders proximal or distal to the stent. Target-vessel revascularization was defined as any repeat PCI or surgical bypass of any segment within the entire major coronary vessel proximal and distal to a target lesion, including upstream and downstream branches and the target lesion itself. A revascularization was considered ischemia-driven if the diameter stenosis of the treated lesion was at least 50% on the basis of quantitative coronary angiography in the presence of ischemic signs or symptoms, or if there was a diameter stenosis of at least 70% irrespective of the presence of ischemic signs or symptoms.
Our trial was powered for superiority on the primary clinical end point at 1 year. On the basis of the HORIZON-AMI6 and LEADERS trials,13 we assumed an incidence of major adverse cardiac events of 14% within 1 year in the bare-metal stent group and a 40% relative risk reduction associated with the biolimus-eluting stent, corresponding to a rate of major adverse cardiac events of 8.4%. Enrollment of 1064 patients would therefore provide 80% power to detect a relative risk of 0.60 with 2-sided α = .05.
All analyses were performed according to the intention-to-treat principle, with inclusion of all randomized patients in the analysis according to the group they were originally allocated. Cox proportional hazards regression models were used to compare clinical outcomes between the groups, with patients censored at the time of their last known contact. Correspondingly, we constructed time-to-event curves using Kaplan-Meier estimates and the proportional hazards assumption was tested and met in each case.
Categorical variables are reported as numbers and percentages, and groups are compared using χ2 or Fisher exact tests (low counts). Continuous variables are reported as means ±standard deviations, and groups are compared using unpaired t tests. Times are reported as medians (interquartile ranges [IQRs]), and groups are compared using Wilcoxon Mann-Whitney rank sum test.
We prespecified stratified analyses of the primary end point at 1 year according to age, sex, diabetes, renal failure, lesion length, and vessel size. In addition, we performed post hoc analyses stratified according to left ventricular ejection fraction, left anterior descending artery lesion localization, preprocedural TIMI flow, time from pain onset to balloon time, thrombus aspiration, and multivessel treatment. All stratified analyses were accompanied by tests for interaction between stent type and subgroup. There were positive treatment × patient characteristics interactions for age and sex. In view of a correlation between age and sex (P < .001), we explored treatment × age interactions separately in men and women. All analyses were performed with STATA version 12.1 (StataCorp) and 2-sided P < .05 was considered statistically significant.
A total of 1161 patients were randomly assigned to receive biolimus-eluting stents with biodegradable polymer (578 patients) or bare-metal stents (583 patients). Three patients allocated to the biolimus-eluting stent and 1 patient allocated to the bare-metal stent did not confirm their initial written consent and had to be excluded, resulting in 575 patients with 629 infarct-vessel lesions randomly assigned to biolimus-eluting stents and 582 patients with 648 infarct-vessel lesions randomly assigned to bare-metal stents for final analyses (Figure 1). A total of 31 patients refused or were lost to follow-up at a median of 31 days in the biolimus-eluting stent group and 32 days in the bare-metal stent group.
Baseline medications and clinical, angiographic, and procedural characteristics were similar in both groups (Table 1, Table 2, and Table 3). The mean (SD) age of patients was 60.6 (11.8) years and 79% were men. The median (IQR) time from symptom onset to balloon inflation was 234 (164-386) minutes and from hospital admission to balloon inflation was 44 (32-72) minutes. Thrombus aspiration was performed in 62% of patients and 47% received a glycoprotein IIb/IIIa antagonist during the procedure. No differences were observed in lesion complexity between both groups including the SYNTAX MI score (mean, 15; SD, 8). At discharge, 43% of patients received prasugrel and 57% of patients received clopidogrel. The use of dual antiplatelet therapy was high and balanced in both treatment groups throughout the entire follow-up period up to 1 year (Table 2).
Clinical outcomes during follow-up are shown in Table 4. At 1 year, the primary end point of major adverse cardiac events (cardiac death, target vessel–related reinfarction, and ischemia-driven target-lesion revascularization) occurred in 4.3% of patients receiving biolimus-eluting stents and 8.7% of patients receiving bare-metal stents (hazard ratio [HR], 0.49; 95% CI, 0.30-0.80; P = .004) (Figure 2A). For cardiac death alone, the percentages were smaller (2.9% of patients received biolimus-eluting stents and 3.5% of patients received bare-metal stents; HR, 0.81; 95% CI, 0.42-1.56; P = .53) (Figure 2B). The treatment effect in favor of patients receiving biolimus-eluting stents was attributable to both a lower risk of target vessel–related reinfarction (0.5% vs 2.7%; HR, 0.20; 95% CI, 0.06-0.69; P = .01) (Figure 2C) and ischemia-driven target-lesion revascularization (1.6% vs 5.7%; HR, 0.28; 95% CI, 0.13-0.59; P < .001) (Figure 2D). Differences between stent types with respect to the primary outcome emerged early and continued throughout the study period.
Among patients treated with biolimus-eluting stents, 3 target vessel–related reinfarctions resulted from definite stent thrombosis in 2 patients and restenosis in 1 patient. Among patients treated with bare-metal stents, 15 target vessel–related reinfarctions resulted from definite stent thrombosis in 10 patients, restenosis in 4 patients, and spontaneous MI in 1 patient. The risk of target vessel–related reinfarction associated with stent thrombosis or restenosis was lower among patients treated with biolimus-eluting stents vs bare-metal stents (HR, 0.22; 95% CI, 0.06-0.75; P = .02).
The findings for the primary end point were consistent across stratified analyses for diabetes, renal failure, left ventricular ejection fraction, left anterior descending artery, thrombus aspiration, time from pain onset to balloon inflation, multivessel treatment, small vessel disease, and lesion length (Figure 3). A significant interaction with stent type was observed for age and sex. Men were on average 6.5 years younger than women. In exploratory analyses, we found HRs below the point estimate of the primary end point in the overall cohort (HR = 0.49) in women younger than 65 years (HR, 0.40; 95% CI, 0.80-1.95), in men younger than 65 years (HR, 0.25; 95% CI, 0.10-0.61), and in men 65 years or older (HR, 0.43; 95% CI, 0.16-1.11), but not in women 65 years or older (HR, 1.89; 95% CI, 0.65-5.54).
At 1 year, rates of definite stent thrombosis amounted to 0.9% among patients receiving biolimus-eluting stents and 2.1% among patients receiving bare-metal stents (HR, 0.42; 95% CI, 0.15-1.19; P = .10). Five patients treated with biolimus-eluting stents experienced definite stent thrombosis while receiving dual antiplatelet therapy, whereas 12 patients treated with bare-metal stents experienced definite stent thrombosis with 11 patients receiving dual antiplatelet therapy and 1 patient not taking acetylsalicylic acid and clopidogrel. We observed no differences in all-cause and cardiac mortality between the groups at 1 year. In addition to the device-oriented primary outcome measure, we recorded a lower risk of the comprehensive patient-oriented composite of death, any reinfarction, and any revascularization in favor of biolimus-eluting stents (8.4% vs 12.2%; HR, 0.68; 95% CI, 0.47-0.98; P = .04).
Staged procedures were performed after a median duration of 12.0 days (IQR, 4.0-41.5 days) among patients treated with biolimus-eluting stents and after a median duration of 6 days (IQR, 3-33 days; P = .25). A total of 1 ischemia-driven target-lesion revascularization was associated with a staged procedure in the biolimus-eluting stent group compared with 2 ischemia-driven target-lesion revascularization events in the bare-metal stent group.
In this randomized, multicenter, assessor-blinded trial in patients with STEMI, compared with the use of bare-metal stents, the use of biolimus-eluting stents with a biodegradable polymer was associated with a significant 4.4% absolute reduction and 51% relative reduction in the risk of major adverse cardiac events at 1 year, which prevents 42 events per 1000 patients treated with biolimus-eluting stents compared with bare-metal stents at 1 year. Findings were also robust for the more comprehensive patient-oriented composite of any death, reinfarction, or revascularization. Accordingly, our results suggest better clinical outcomes in terms of major adverse cardiac events of a stent releasing biolimus from a biodegradable polymer compared with a bare-metal stent for the treatment of patients with STEMI.
In the single largest trial enrolling patients with STEMI,6 paclitaxel-eluting stents resulted in a 41% lower risk of target-lesion revascularization compared with bare-metal stents. In our trial, biolimus-eluting stents were associated with a 4.1% absolute reduction and a 72% relative reduction in the risk of ischemia-driven target-lesion revascularization compared with bare-metal stents. This risk reduction is notable as repeat revascularizations were due to recurrent ischemia in the absence of protocol-mandated angiographic follow-up before assessment of the primary end point at 1 year. Rates of revascularization with the biolimus-eluting stent in our study were lower than in the LEADERS trial,13 which enrolled patients with a broad spectrum of indications and lesions. Explanations for this finding include the larger reference vessel diameter in vessels causing acute MI (3.0 vs 2.6 mm) and the lack of routine angiographic follow-up, as well as less ischemia in vessels subtending previously infarcted myocardium.13
Despite a similar risk profile and mortality in our study compared with patients with STEMI enrolled into previous large-scale randomized trials,5,6 we observed a lower absolute rate of repeat revascularization in both treatment groups. This observation is consistent with a recent trial comparing newer-generation everolimus-eluting stents with bare-metal stents among patients with STEMI18 and is potentially related to improved lesion preparation due to thrombus aspiration19 and more potent antithrombotic medications, such as prasugrel,20 reducing the risk of stent thrombosis–related revascularization. Notwithstanding, the absolute risk reduction of 4.1% in our trial means that 24 patients need to be treated with biolimus-eluting stents to prevent 1 major adverse cardiac event.
Differences in favor of biolimus-eluting stents over bare-metal stents in our study with respect to the primary end point were not limited to efficacy but also driven by an 80% lower risk of target vessel–related reinfarction. This difference in safety has not been observed in previous randomized trials comparing drug-eluting and bare-metal stents among patients with STEMI,5,6,21-26 but is consistent with the findings of a recent meta-analysis12 reporting a lower risk of reinfarction during the first year with a number needed to treat of 79 compared with 45 in our study.
In exploring the mechanism for the lower risk of target vessel–related reinfarction, we observed that the device-related adverse events definite stent thrombosis or target-lesion revascularization due to restenosis were responsible for target vessel–related reinfarction in 17 of 18 cases and were less common among patients receiving biolimus-eluting stents than patients receiving bare-metal stents (3 vs 14, respectively; P = .01). In contrast with most previous trials among patients with STEMI, dual antiplatelet therapy was balanced between patients receiving biolimus-eluting stents and those receiving bare-metal stents throughout the entire study period rendering differences in antiplatelet therapy unlikely as an explanation for the differential in target vessel–related reinfarction.
We found positive interactions between stent type and age and sex. Because age and sex were correlated, we further explored these interactions and found estimated HRs below the point estimate of the primary end point for the overall cohort (HR = 0.49) in younger women and men irrespective of age, but not in women aged 65 years or older. It is unclear whether our results reflect a lack of benefit in women or in those aged 65 years or older, or in the subgroup of elderly women only. We are unaware of biological mechanisms that might explain interactions with age or sex, and in view of the lack of mechanisms and the large number of stratified analyzes, chance should also be considered as an explanation of our findings.
A numerically lower rate of definite stent thrombosis was observed (0.9% vs 2.1%, P = .10) with the use of biolimus-eluting stents vs bare-metal stents at 1 year, with most events occurring during the peri-interventional period. Although this finding has to be interpreted cautiously, a similar statistically nonsignificant reduction at up to 1 year among patients with STEMI has been observed in a recent meta-analysis12 comparing early generation drug-eluting stents with bare-metal stents. Moreover, a significant reduction in the risk of stent thrombosis has been reported in the EXAMINATION trial18 comparing newer-generation everolimus-eluting stents with bare-metal stents (0.5% vs 1.9%, P = .01). Experimental data indicate lower thrombogenicity of drug-eluting stents compared with bare-metal stents suggesting a possible thromboresistant effect of polymer coatings during the immediate peri-interventional period.27 The latter may be particularly important among patients with STEMI who carry a higher baseline risk of stent thrombosis due to a large thrombus burden9 and increased platelet activation.28
In addition, biolimus is the limus analogue with the highest lipophilicity used for drug elution on currently available stent platforms.29 Among patients with STEMI, the acute coronary lesions predominantly consist of lipid-rich, ruptured plaques with large necrotic cores.30 Theoretically, the increased lipophilicity of the drug biolimus may provide a more rapid and homogeneous drug distribution, potentially leading to a more potent anti-inflammatory and antithrombotic local effect. However, this hypothesis requires validation in dedicated studies assessing the properties of various drugs used for elution on drug-eluting stents in the presence of lipid-rich plaques.
Our results have to be interpreted in view of the following limitations. First, the trial indicated superiority on the primary composite outcome but was not powered to address individual components of efficacy or safety. Moreover, observed event rates were lower than anticipated. In view of the size of the observed treatment effect and results of previous trials, we consider it unlikely that estimates of efficacy would substantially differ in a larger patient cohort. The inclusion of safety outcomes in the primary composite outcome is meaningful as cardiac death or target vessel–related reinfarction may be device related. Event rates of cardiac death or target vessel–related reinfarction were of similar magnitude as ischemia-driven target-lesion revascularization in our trial providing a similar weight of efficacy and safety parameters within the composite end point.
Second, the biolimus-eluting stent used in our study is currently not approved by the US Federal Drug Administration and not considered as standard of care in the United States. The biolimus-eluting stent has been shown to be noninferior compared with the sirolimus-eluting CYPHER stent in a randomized trial of 1707 all-comer patients for the composite clinical end point of major adverse events at 9 months and 4 years.13,14 On the basis of these data, the biolimus-eluting stent is recommended as one of a few drug-eluting stents for clinical use in the European guidelines on myocardial revascularization.31 It remains to be determined how this stent platform performs compared with newer-generation durable polymer-based drug-eluting stents. Similarly, the optimal duration of dual antiplatelet therapy after implantation of biolimus-eluting stents with a biodegradable polymer has not been established.
Third, although our trial had very few exclusion criteria, the results apply only to patients with characteristics similar to those enrolled. Patients who were unable to provide written informed consent before the procedure had to be excluded from participation in this trial introducing an element of selection bias. Because no reliable data for reasons leading to patient exclusion were collected, we cannot determine the proportion of patients excluded due to poor clinical condition and those refusing participation in the trial.
Fourth, the P2Y12 inhibitor prasugrel was administered instead of clopidogrel in 40% of patients and may have contributed to the low overall event rates in our study. Although the use of prasugrel was higher than in previous trials comparing drug-eluting stents with bare-metal stents among patients with STEMI, it conforms to the recommendations of the American College of Cardiology/American Heart Association guidelines for the management of STEMI and reflects contemporary practice.
Fifth, our study does not address late events beyond 1 year. However, in a previous study,14 biolimus-eluting stents were shown to reduce the risk of stent thrombosis beyond 1 year by 80% compared with early generation sirolimus-eluting stents providing support for the improved long-term biocompatibility of drug-eluting stents with biodegradable polymer coatings.
In conclusion, compared with a bare-metal stent, the use of a biolimus-eluting stent with a biodegradable polymer resulted in a lower rate of the composite of major adverse cardiac events at 1 year among patients with STEMI undergoing primary PCI.
Corresponding Author: Stephan Windecker, MD, Department of Cardiology, Bern University Hospital, 3010 Bern, Switzerland (email@example.com).
Author Contributions: Drs Räber and Windecker had full access to all of the data in the study and take responsibility for the integrity of the data and the accuracy of the data analysis.
Study concept and design: Räber, Kelbæk, Trelle, Lüscher, Meier, Jüni, Windecker.
Acquisition of data: Räber, Kelbæk, Ostojic, Baumbach, Tüller, von Birgelen, Roffi, Moschovitis, Khattab, Wenaweser, Bonvini, Pedrazzini, Kornowski, Weber, Lüscher, Taniwaki, Meier, Windecker.
Analysis and interpretation of data: Räber, Kelbæk, Ostojic, Baumbach, Heg, Tüller, von Birgelen, Roffi, Moschovitis, Khattab, Wenaweser, Bonvini, Pedrazzini, Kornowski, Weber, Trelle, Lüscher, Taniwaki, Matter, Meier, Jüni, Windecker.
Drafting of the manuscript: Räber, Windecker.
Critical revision of the manuscript for important intellectual content: Räber, Kelbæk, Ostojic, Baumbach, Heg, Tüller, von Birgelen, Roffi, Moschovitis, Khattab, Wenaweser, Bonvini, Pedrazzini, Kornowski, Weber, Trelle, Lüscher, Taniwaki, Matter, Meier, Jüni, Windecker.
Statistical analysis: Heg, Jüni, Windecker.
Obtained funding: Ostojic, Matter, Jüni, Windecker.
Administrative, technical, or material support: Räber, Kelbæk, Ostojic, Baumbach, Heg, Tüller, von Birgelen, Roffi, Moschovitis, Khattab, Wenaweser, Bonvini, Pedrazzini, Kornowski, Weber, Trelle, Lüscher, Taniwaki, Matter, Meier, Jüni, Windecker.
Study supervision: Räber, Jüni, Windecker.
Conflict of Interest Disclosures: All authors have completed and submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest. Clinical Trials Unit (CTU Bern), which is part of the University of Bern, Bern, Switzerland, has a staff policy of not accepting honoraria or consultancy fees. However, CTU Bern is involved in design, conduct, or analysis of clinical studies funded by Abbott Vascular, Ablynx, Amgen, AstraZeneca, Biosensors, Biotronic, Boehringer Ingelheim, Eisai, Ei Lilly, Exelixis, Geron, Gilead Sciences, Nestlé, Novo nordisc, Padma, Roche, Schering-Plough, St. Jude Medical, and Swiss Cardio Technologies. Dr Baumbach reported being on advisory boards and receiving consultancy fees from Boston Scientific, Medicines Company, and Abbott Vascular; and receiving payment for lectures from Medicines Company and Japan Stent Inc. Dr Tüller reported receiving travel expenses from Biotronik, Biosensors, Terumo, and Medtronic. Dr von Birgelen reported board memberships and receiving lecture fees from Abbott Vascular, Medtronic, and Boston Scientific; receiving consultancy fees from Medtronic; unpaid consultancies from Abbott Vascular, Boston Scientific, Biosensors, Biotronik, and Cordis; receiving grants from Abbott Vascular, Boston Scientific, Biosensors, Biotronik, Cordis, Medtronic, and St Jude Medical; payment for lectures from Abbott Vascular, Boston Scientific, Medtronic, and MSD; and receiving payment for development of educational presentations from Cordis. Dr Roffi reported receiving grants from Boston Scientific, Abbott Vascular, Medtronic, and Biosensors; and payment for lectures from Lilly-Daiichy Sankyo. Dr Khattab reported receiving payment for lectures from Biosensors. Dr Wenaweser reported receiving consultancy fees from NVT, grants from Medtronic, and payment for lectures from Medtronic, Edwards Lifesciences, and Cordis, and payment for development of educational presentations from Medtronic. Dr Lüscher reported receiving research grants to the institution from Abbott, Biosensors, Biotronik, Boston Scientific, and Medtronic, and consultant payments from AstraZeneca, Boehringer Ingelheim, Bayer, Merck, and Pfizer. Dr Matter reported receiving grants from MSD, Eli Lilly, AstraZeneca, and Bayer; expert testimony from MSD; payment for lectures from MSD, AstraZeneca, and Roche; and having patents from Mabimmune, CH. Dr Meier reported receiving research contracts to the institution from Abbott, Boston Scientific, Biosensors, and Cordis. Dr Jüni is an unpaid steering committee or statistical executive committee member of trials funded by Abbott Vascular, Biosensors, Medtronic, and St. Jude Medical. Dr Windecker reported receiving research contracts to the institution from Abbott, Boston Scientific, Biosensors, Biotronik, Cordis, Medtronic, and St. Jude Medical. All other authors reported no conflicts of interest.
Funding/Support: The COMFORTABLE AMI trial was investigator-initiated, managed by the Clinical Trials Unit, University of Bern, Bern, Switzerland, and supported by the Swiss National Science Foundation (grant 33CM30-124112), and an unrestricted research grant from Biosensors Europe SA, Morges, Switzerland (Drs Jüni and Windecker). Dr Räber is the recipient of a research fellowship (SPUM) funded by the Swiss National Science Foundation.
Role of the Sponsor: The sponsors had no role in the design and conduct of the study; in the collection, analysis, and interpretation of the data; or in the preparation, review, or approval of the manuscript.
Statistical Analysis: The primary statistical analysis was performed by statisticians Dik Heg, PhD, and Peter Jüni, MD, of the Clinical Trials Unit, Bern University Hospital, Bern, Switzerland.
The COMFORTABLE AMI Trial Investigators:Steering Committee: Lorenz Räber, Peter Jüni, Stephan Windecker; Data and Safety Monitoring Board: Jonathan Sterne, Bristol, United Kingdom (chair), Michel Bertrand, Lille, France; Philip Urban, Geneva, Switzerland; Clinical Events Committee: Pascal Vranckx, Hasselt, Belgium (chair), Gerrit Hellige, Aarau, Switzerland, Igal Moarof, Aarau, Switzerland; Data Management and Monitoring: Clinical Trials Unit, University of Bern, Switzerland-Brigitte Wanner, Anna Plym, Lucia Kacina, Sandro Baumgartner, Timon Spörri; Electronic Data Capture: 2mT GmbH, Ulm, Germany–Jürgen Nagler-Ihlein, Thorsten Ihlmann; Core Angiographic Laboratory: Bern University Hospital, Bern, Switzerland.
Study Sites, Collaborators:Catheterization Laboratory, Rigshospitalet, Copenhagen, Denmark: Thomas Engstrøm, Lene Holmvang, Erik Jørgensen, Maria D. Radu, Kari Saunamäki; Department of Cardiology, Clinical Center of Serbia, Belgrade, Serbia: Branko Beleslin, Dejan Orlic, Jelena Kostic, Vladan Vukcevic; Bristol Heart Institute, Bristol, United Kingdom: Sujatha Kesavan, Julian Strange, Tom W. Johnson; Cardiology Department, Triemlispital, Zurich, Switzerland: Franz Eberli, David Kurz, Rainer Zbinden; Thoraxcentrum Twente, Twente University, Enschede, the Netherlands: K. Gert van Houwelingen, Martin G. Stoel, J. Hans W. Louwerenberg; Cardiocentro, Lugano, Switzerland: Tiziano Mocetti, Maria Grazia Rossi; Division of Cardiology, University Hospital, Geneva, Switzerland: David Carballo, Francois Mach, Pierre-Frédéric Keller; Cardiology Department, University Hospital Zurich, Zurich, Switzerland: Roberto Corti, Roland Klingenberg, Ulf Landmesser; Rabin Medical Center, Petach Tikva, Israel, and Tel Aviv University, Tel Aviv, Israel: Abid Assali, Hana Vaknin-Assa; Herzzentrum Bodensee, Kreuzlingen, Switzerland: Michael Pieper; Cardialysis B.V., Rotterdam, the Netherlands: Hector M. Garcia Garcia; Institute of Social and Preventive Medicine, University of Bern, Bern, Switzerland: Bindu Kalesan.
Online-Only Material: The Author Video Interview is available here.
This article was corrected for errors on September 24, 2012.
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