Background It is still uncertain whether coronary bifurcations with lesions involving a large side branch (SB) should be treated by stenting the main vessel and provisional stenting of the SB (simple) or by routine two-stent techniques (complex). We aimed to compare clinical outcome after treatment of lesions in large bifurcations by simple or complex stent implantation.
Methods The study was a randomised, superiority trial. Enrolment required a SB≥2.75 mm, ≥50% diameter stenosis in both vessels, and allowed SB lesion length up to 15 mm. The primary endpoint was a composite of cardiac death, non-procedural myocardial infarction and target lesion revascularisation at 6 months. Two-year clinical follow-up was included in this primary reporting due to lower than expected event rates.
Results A total of 450 patients were assigned to simple stenting (n=221) or complex stenting (n=229) in 14 Nordic and Baltic centres. Two-year follow-up was available in 218 (98.6%) and 228 (99.5%) patients, respectively. The primary endpoint of major adverse cardiac events (MACE) at 6 months was 5.5% vs 2.2% (risk differences 3.2%, 95% CI −0.2 to 6.8, p=0.07) and at 2 years 12.9% vs 8.4% (HR 0.63, 95% CI 0.35 to 1.13, p=0.12) after simple versus complex treatment. In the subgroup treated by newer generation drug-eluting stents, MACE was 12.0% vs 5.6% (HR 0.45, 95% CI 0.17 to 1.17, p=0.10) after simple versus complex treatment.
Conclusion In the treatment of bifurcation lesions involving a large SB with ostial stenosis, routine two-stent techniques did not improve outcome significantly compared with treatment by the simpler main vessel stenting technique after 2 years.
Trial registration number NCT01496638.
- coronary bifurcations
- complex coronary lesions
- drug eluting stents
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What is already known about this subject?
Previous comparisons of one-stent and two-stent techniques for coronary bifurcation stenting have shown conflicting results but indicated that most bifurcations with large side branches (SBs) are effectively treated by the simple provisional SB stenting technique. Two-stent techniques have important procedural advantages in allowing for securing the SB first in cases with difficult SB access or high risk of occlusion.
What does this study add?
Patients with a coronary bifurcation lesion involving a large side branch (SB) may be treated safely using a two-stent technique, in particular when using newer generation drug-eluting stents. As many patients had no need for a second stent in the simple provisional stenting group, future research should focus on evaluation of tools for identification of lesions requiring SB treatment.
How might this impact on clinical practice?
Using newer generation drug-eluting stents, there is at least no penalty in treating coronary bifurcation lesions with two-stent techniques.
Coronary bifurcations are predilection site for atherosclerosis due to regions of low endothelial shear stress resulting in pathological intimal thickening and plaque formation.1 Treatment of bifurcation lesions constitute about 15% of coronary interventions and are consequently of major clinical interest. Currently, the simple, provisional side branch (SB) stenting technique is the recommended strategy for bifurcation lesion treatment.2–8 With one exception,9 previous studies have shown no benefit of preplanned two-stent techniques in comparison to the simple strategy. In simple provisional SB stenting, a stent is deployed in the main vessel (MV) across the SB, and if needed, the SB is subsequently treated by balloon dilatation or stent implantation.10 Planned stenting of both MV and SB may be accomplished using a number of different techniques, such as T-stenting, T and protrude (TAP), culotte and crush techniques. In earlier studies on simple versus complex bifurcation stenting, inclusion of patients with small and possibly physiological insignificant SBs was a major limitation for extending results to clinically important bifurcation lesions involving a large SB.2 4–6 10 Therefore, we designed the present study to address the unsolved question of simple provisional SB stenting versus complex two-stent treatment in patients with bifurcation lesions involving a large SB.
Study design and patient selection
The Nordic Baltic Bifurcation Study IV (Nordic Baltic IV) was a prospective, randomised, multicentre trial comparing the simple provisional SB stenting technique versus complex stenting of both the MV and the SB in the treatment of coronary bifurcation lesions. A total of 450 patients were included from December 2008 to December 2012 in centres in Norway, Sweden, Finland, Lithuania, Latvia and Denmark. Inclusion criteria were stable angina pectoris, unstable angina pectoris or silent ischaemia, a ‘true’ bifurcation lesion (Medina 1.1.1 or 1.0.1 or 0.1.1), lesion11 in the left anterior descending artery (LAD)/diagonal, circumflex artery (Cx)/obtuse marginal branch, right coronary artery/posterior descending artery/posterolateral branch, or left main coronary artery (LMCA)/LAD/Cx with an MV diameter ≥3.0 mm and SB diameter ≥2.75 mm by visual estimate. Exclusion criteria were ST-elevation myocardial infarction within 24 hours, SB lesion length >15 mm, expected survival <1 year, s-creatinine >200 µmol/L, allergy to aspirin, clopidogrel, ticlopidine, sirolimus or everolimus. All patients provided written informed consent.
When guide wires were inserted in both the MV and the SB, eligible patients were randomised 1:1 to the simple or the complex group by an independent web-based trial management system (TrialPartner, Public Health and Quality Improvement, Central Denmark Region, Aarhus, Denmark). Randomisation was performed in permutated blocks by centre with stratification according to gender, age>70 years, diabetes mellitus and participation in the angiographic substudy. Neither the operator nor the patients were blinded to the treatment allocation.
Radial or femoral approach was allowed using 6–8F guiding catheters. Unfractionated heparin, low-molecular weight heparin or bivalirudin and GPIIbIIIa inhibitors were used according to local hospital routine. The recommended implantation steps in the simple group were (1) predilatation of stenosed areas of the MV to be covered by stent, (2) therapeutic dilatation of the SB using a balloon with a diameter equal to or greater than the SB reference size and (3) stenting of the MV, jailing the SB wire. If normal flow (Thrombolysis In Myocardial Infarction (TIMI) flow=III) was achieved in both the MB and the SB, and there was less than 75% residual diameter stenosis of the SB ostium, the procedure was terminated. Kissing balloon inflation (KBI) was indicated if TIMI flow <III, or if the SB ostium had more than 75% diameter stenosis after MV stenting. In case of TIMI flow <III after KBI, stenting the SB was indicated using a T-stenting12 or the culotte technique.13 Final KBI was mandatory if the SB was stented.
The culotte implantation technique was recommended for planned complex stenting. Other two-stent techniques were allowed at the operator’s discretion except classic crush14 and simultaneous kissing stent (SKS) techniques.15 Final KBI was mandatory in any two-stent procedure.
Lifelong aspirin was prescribed to all patients and clopidogrel was indicated for 12 months. Ticlopidine was indicated if patients did not tolerate clopidogrel. The sirolimus eluting stent ‘Cypher Select+’ (Cordis, USA) was the study stent in the first 225 patients and the Xience V or Xience Prime, everolimus eluting stents (Abbott, USA) were the study stent in the remaining 225 patients. The change in study stent during enrolment was a post hoc adjustment, as the Cypher stent supply was unexpectedly discontinued during the enrolment period. If the study stents could not be implanted, another drug-eluting stent (DES) or bare metal stent was allowed at the discretion of the operator. Different types of DES were not allowed in the same vessel.
The primary endpoint was the composite of major adverse cardiac events (MACE); cardiac death, non-procedural myocardial infarction, clinically indicated target lesion revascularisation and definite stent thrombosis within 6 months after the index procedure. Secondary endpoints were the composite MACE endpoint at 2 years, all-cause mortality, cardiac death, non-procedural myocardial infarction, clinically indicated target lesion revascularisation or target vessel revascularisation, and definite, probable or possible stent thrombosis.
Cardiac death was defined as death from coronary artery disease including myocardial infarction, sudden death with a possible or definite cardia cause, death from heart failure including cardiogenic shock, and death related to a cardiac procedure within 28 days from the procedure. Cardiac death did not include death due to pulmonary embolism, cerebrovascular attacks or other vascular but non-cardiac events. Non-procedural myocardial infarction required evidence of myocardial necrosis by at least one of the following criteria: (1) detection of a rise and/or fall of cardiac biomarkers with at least one value above the 99th percentile of the upper reference limit (URL) and evidence of ischaemia in the myocardium documented by either symptoms of ischaemia, ECG changes indicative of acute ischaemia (new ST-T changes, new left bundle branch block (LBBB), new pathological Q waves in the ECG), evidence of new loss of viable myocardium or new cardiac wall motion abnormality. (2) Sudden and unexpected cardiac death with at least one of the following: cardiac arrest, symptoms suggestive of myocardial ischaemia, presumably new ST-segment elevation, or new LBBB, and/or evidence of fresh thrombus by coronary angiography and/or at autopsy. (3) Pathological findings suggestive of acute myocardial infarction.16 Assessment of procedural cardiac biomarkers was recommended. In patients with normal baseline biomarker values, elevations of cardiac biomarkers (CK-MB) greater than 3×99th percentile URL defined index procedure-related myocardial infarction. Patients with stable angina pectoris or silent ischaemia were considered to have normal baseline markers if values were not assessed. If cardiac biomarkers were elevated before the procedure and not stable in two samples 6 hours apart, the diagnosis of periprocedural myocardial biomarker increase could not be made. If biomarker values were stable or falling, a 20% or more increase of the value in the second sample after the procedure was required. Elevations of CK-MB greater than 3×99th percentile URL and greater than 5×99th percentile URL were assessed independently. Stent thrombosis was classified as definite, probable or possible, and definite stent thrombosis was categorised as acute, subacute, late and very late according to the Academic Research Consortium(ARC) criteria.17 Target lesion revascularisation was defined as repeat revascularisation by percutaneous coronary intervention (PCI) or coronary artery bypass surgery of the target lesion defined as the stented or balloon-treated segments and their 5 mm margins in all three coronary branches.
Quantitative coronary analysis
Coronary angiograms of pre-PCI, post-PCI and 8-month follow-up were analysed by the Core laboratory for interventional coronary imaging, Aarhus University Hospital, Denmark and by Pauls Stradins Clinical University Hospital, Riga, Latvia, using validated software dedicated to segmental bifurcation analysis (QAngioXA 7.3, Medis Medical Imaging, Leiden, The Netherlands). All included patients had assessment of pre-PCI and post-PCI angiograms and follow-up angiograms were analysed in patients completing the 8-month angiographic follow-up. Analysis principles of the dedicated bifurcation quantitative coronary analysis (QCA) for the Nordic-Baltic bifurcation studies were previously reported.18 The analysed segments were the proximal MV, distal MV and SB. The bifurcation core segment was analysed in combination with the proximal MV. The three edge segments comprised the 5 mm margins to the stented, or balloon treated segments. If the SB was not treated by stent or balloon, the first 5 mm of the SB was defined as both the lesion and the edge segment. Binary (re)stenosis was defined as ≥50% diameter stenosis. All analyses were cross-evaluated by the same second observer to ensure consistency in methods between the two core laboratories. The QCA was not blinded due to the evident appearance of simple or complex stenting techniques in the analysed angiograms.
The sample size estimate for the primary superiority outcome measure of 6-month MACE was based on the limited available evidence at conceptualisation of the study. With expected MACE rates of 10% in the simple group and 3% in the complex group, α=0.05 and power=0.80, a sample of 194 patients were required in each group (two-sided χ2 test). Sample size was initially set to 400 patients in total but was increased during enrolment to 450 patients to accommodate for potential lower than expected event rates and patients lost to follow-up.
Categorical variables are reported as number and percentages and were analysed using the χ2 test or Fisher exact test if 2×2 cell values were below five. Continuous variables following a Gaussian distribution were analysed by the independent sample t-test and presented as mean±SD. Non-Gaussian variables were analysed by Mann-Whitney U-test and presented as median and IQR. Rates of the primary endpoint of 6-month MACE and its individual components are presented as risk differences. Two-year outcomes are resented as Kaplan-Meier estimates, HRs and 95% CIs, and were compared by unadjusted Cox regression analysis. The analysis was performed according to the intention-to-treat principle. Patients lost to follow-up were censored at day of withdrawal or last contact. Post hoc subgroup analysis was performed by Cox regression analysis with test for interaction of the subgroup variable and treatment allocation. Results are given as HR and 95% CI and presented by forest plot. Per protocol analysis for 2-year MACE excluded any patient that did not receive an MV stent and patients in the two-stent group without SB stenting. Two-sided p values below 0.05 indicated significance. All analyses were performed using STATA V.12 (STATA Corp, Texas, USA).
Patient and lesion characteristics
A total of 450 patients were assigned to simple stenting (n=221) or complex stenting (n=229) (figure 1). Two-year follow-up was available in 446 patients. Age was 64±12 vs 63±11 years, 16.3% and 15.3% had diabetes and 39.1% vs 35.3% had prior coronary artery bypass grafting or PCI in simple and complex groups, respectively (table 1). The predominant lesion location was LAD and diagonal (74.1% vs 76.7%). Reference diameter by visual estimate of the MV was 3.5±0.4 mm and 3.4±0.3 mm (p=0.02), and the SB reference diameter was 2.9±0.2 mm and 2.9±0.2 mm by visual estimate and 2.4±0.5 mm and 2.5±0.5 mm by QCA in simple and complex groups, respectively (table 2). Mean SB stenosis before treatment by visual estimate was 74.4%±14.4% and 77.1%±12.1%, p=0.04, and by QCA was 44.3%±18.5% and 47.3%±17.6%, p=0.95 for simple and complex groups, respectively (table 3: QCA for angiographic follow-up group results).
In the simple group, any SB balloon treatment was performed in 78.4% of cases and the SB was stented in 3.7% of cases. In the complex group, the techniques were culotte (65.6%), mini crush (21.5%), T-stenting (7.1%) or other (5.8%). The SB was stented in 96% and 91% had KBI. Reported causes for not stenting the SB in attempted two-stent techniques included (1) not able to pass balloon into the SB, and (2) not able to pass stents into the SB. Residual binary SB stenosis after treatment was 28.0% in the simple group and 2.7% (p<0.0001) in the complex group. Periprocedural biomarker release was assessable in 182 (83%) and 187 (82%) patients in the simple and complex stenting groups. The biomarkers were increased in 7.7% vs 9.6% (p=0.51) for CK-MB greater than 3×99th percentile URL and 5.0% vs 3.7% (p=0.57) for CK-MB greater than 5×99th percentile URL in the groups of simple and complex stenting, respectively.
The primary endpoint of MACE at 6 months was 5.5% vs 2.2% (RD 3.2%, 95% CI −0.2 to 6.8, p=0.07) and at 2 years 12.9% vs 8.4% (HR 0.63, 95% CI 0.35 to 1.15, p=0.12) after simple versus complex treatment (figure 2). Individual endpoints at 6 months and 2 years are shown in figure 3 and table 4. Per protocol analysis for 2-year MACE was 12.9% in 218 vs 8.7% in 219 patients (p=0.16). Angina pectoris by Canadian Cardiovascular Society score ≥II at 2-year follow-up was 3.9% in the simple group and 4.1% in the complex group (RD −0.2%, 95% CI −4.0 to 3.4, p=0.89). In the subgroup treated by first generation DES, the rate of 2-year MACE rate was 12.9% vs 10.3% (HR 0.77, 95% CI 0.36 to 1.67, p=0.51) and after treatment by newer generation DES MACE was 12.0% vs 5.6% (HR 0.45, 95% CI 0.17 to 1.17, p=0.10) after simple versus complex treatment (figure 2). Other subgroup results are presented in figure 4. Eight-month angiographic follow-up was completed in 307 patients assigned to simple (n=153) or complex stenting (n=154). After the index procedure, SB binary residual stenosis was 28.0% vs 2.7% (p<0.001). After 8 months, the binary (re)stenosis rate was 1.3% vs 0.7% (p=0.56) in the proximal MV, 1.3% vs 1.3% (p=0.99) in the distal MV and 20.3% vs 5.2% (p<0.001) in the SB after simple versus complex stenting, respectively.
In the randomised Nordic-Baltic Bifurcation Study IV, treatment of bifurcation lesions involving a large SB resulted in 6-month MACE of 5.5% vs 2.2% and 2-year MACE of 13.2% vs 8.3%, both statistically non-significant, after treatment by the simple provisional SB stenting technique or planned two-stent techniques, respectively. Two-stent procedures were associated with less angiographic SB stenosis at 8-month follow-up but procedure time, fluoroscopy time, use of contrast and use of stents were all increased in the two-stent group.
One or two stents for bifurcations
The study addresses one of the main questions in coronary bifurcation treatment; routine stenting of both MV and SB or stenting of the MV only with optional SB treatment if reduced flow or a severe stenosis is detected after MV stent implantation. Earlier randomised clinical trials on simple versus complex bifurcation stenting, with the exception of the DKCRUSH-II study,9 were in favour of the simple one-stent strategy.4–7 19 In the BBC ONE study, there were more myocardial infarctions at 9 months in the two-stent group (3.6% vs 11.2%; p=0.001) driven by periprocedural biomarker elevation.2 In the 5-year follow-up in the Nordic-Baltic Bifurcation Study I, there was no statistically significant difference in MACE after simple versus complex strategies (15.8% vs 21.8%; p=0.12) but an indication of more favourable long-term results after simple stenting using first generation DES.3 In the DKCRUSH-II study, the double kissing crush two-stent technique reduced new revascularisations as compared with optional SB stenting at 5 years.20 However, in that study, the difference between the study groups was possibly influenced by a study-related angiographic follow-up, and the 1-year event rates in the two-stent group were numerically higher than in the one-stent group of Nordic-Baltic I and IV.
Compared with earlier studies, Nordic-Baltic IV was the first randomised study comparing one-stent versus two-stent strategies in bifurcations involving large SB (≥2.75 mm) with angiographic significant disease. Although our MACE rate was higher in the simple group (12.8%) compared with the complex group (8.3%), mostly driven by a statistically insignificant difference in target lesion revascularisation (9.2% vs 6.1%, p=0.23), we failed to document a significant advantage in the use of complex two-stent techniques. However, the numerically lower MACE rates do suggest that two-stent procedures were at least safe in the treatment of patients with significant SB disease.
Our good results using two-stent techniques are in line with the DK-CRUSH II results.20 Still, the double kissing crush technique applied in the DK-CRUSH study series was later found to be superior to culotte stenting in patients with unprotected LMCA disease by the same group of investigators21 leading to the recent ESC recommendation of the double kissing crush technique for the treatment of Medina Class 1.1.1 distal LMCA bifurcation lesions.22 In Nordic-Baltic IV, applying predominantly the culotte and mini-crush techniques, the success rate of KBI was 92%, whereas the success rate of KBI using the double kissing crush technique was 96%–100% in the DK-CRUSH study series.8 17–19 KBI in culotte was successful in 96 of 97 cases in the 200 pts EBC TWO trial but still yielded similar outcome compared with provisional T stenting for large bifurcations.20 We do not know if the relatively favourable results in the two-stent group of Nordic-Baltic IV might have been further improved using the double kissing crush technique.
In the provisional SB stenting group, the strict cross-over criteria resulted in SB stenting in only 3.7% of cases. The numerically increased rate of target lesion revascularisation suggests that some SBs might have been undertreated by relying solely on visual assessed diameter stenosis and reduction in TIMI flow for SB stenting. Large SBs may supply a larger territory and the increased rate of angiographic SB restenosis after simple stenting may indicate a clinical relevant difference between the two strategies. We were not able to demonstrate a significant difference for longer SB lesions >5 mm likely due to the small subsample. Still, the numerical difference (16.5% vs 9.6%) could indicate that longer lesions more often require SB stenting which would be in line with other reports.23 24 Previous studies on simple versus complex stenting documented a large variation, from 2% to 31%, in SB stenting using the simple optional SB stenting technique.2 6 9 10 25 Currently, the generally accepted criteria for SB intervention in coronary bifurcations are based on angiographic indication of reduced flow, stenosis severity >75% DS, and SB stenosis length >5 mm,26 but physiological measurements such as fractional flow reserve assessment27 or use of intravascular ultrasound28 and optical coherence tomography29 imaging techniques might improve our angiography-based decisions on indication for SB revascularisation.
In Nordic-Baltic IV, it was recommended to perform a ‘therapeutic predilation’ of the SB with a balloon sized according to the SB reference diameter. Pan et al demonstrated that a similar strategy reduced both the rate of SB TIMI flow <III and the need for subsequent KBI and the SB predilation did not impair SB rewiring.30 The SB predilation rate in Nordic-Baltic IV was 64%, and the total rate of SB balloon dilatation was 78%, leaving 22% in the simple one-stent group without any SB treatment. This lack of SB intervention might indicate a suboptimal treatment, although it is unknown if the SB in these patients was left with a functionally significant stenosis.
In Nordic-Baltic IV, the mean lesion length in the SB was 5.5 mm compared with 10 mm in the BBK study4 and 15 mm in the DKCRUSH II study.20 The longer SB lesions likely contributed to the higher rate of cross over to SB stenting in the simple groups in these studies of 19% and 28%, respectively. The authors of the present study believe that it makes little sense to randomise patients with long significant lesions in a large SB, in one-stent versus two-stent technique studies as such SB lesions may require stenting in any case.
The study was initiated before introduction and recommendation of the proximal optimisation technique (POT)31 to improve proximal stent apposition and facilitate wiring of a SB jailed by a stent.26 Despite the potential advantages of this additional procedural step,32–34 the clinical importance has yet to be fully determined35 and optimal execution clarified.36 It is therefore uncertain to which extent the lack of systematic postdilatation of the proximal segment negatively impacted our results, and if POT has different effects in simple and complex techniques.
The provisional stenting approach was performed using less contrast and less radiation in shorter procedures, as in previous studies.6 10 25 These procedural characteristics of the simple one-stent technique may be of considerable importance in selecting strategy, especially in high-risk and frail elderly patients. At the same time, the presented 2-year results by the two strategies do not contradict the choice of a two-stent strategy in selected cases with functional significant SB stenosis or in case of high risk of SB compromise, difficult SB access or anticipated difficult access after MV stent implantation.
Duration of dual antiplatelet therapy
The recommended duration of dual antiplatelet therapy (DAPT) was 12 months in Nordic-Baltic IV independent of treatment indication and complexity of treatment. The present ESC recommendation is 6 months DAPT after PCI indicated by stable angina pectoris with the provision that prolonged DAPT may be considered after complex PCI including two-stent bifurcation treatment.37 We cannot rule out a minor positive effect on outcomes for the two-stent group compared with patients treated with one-stent techniques at the expense of increased bleeding risk in both groups.38 Our results, however, indicate that such potential positive effect for two-stent techniques may be countered by using first generation DES in half of the patients in this trial. An individualised assessment of treatment complexity, treatment result and the patients perceived bleeding risk is recommended when determining the optimal duration of DAPT.37
First and newer generation DES
During the first half of enrolled patients, the first generation Cypher Select+ was used as stent, while the newer generation Xience stent was used as stent in the latter part. The equal results of Cypher and Xience in the simple group but more than 50% reduction in MACE in the complex group after treatment by newer generation stent compared with first-generation stents may indicate an improved safety of two-stent techniques using newer generation stents. This could indicate an important advancement in the safety of two-stent techniques that may be associated with increased mortality when performed with first-generation DES.19 The hypersensitive reaction induced in some patients by the polymer of first-generation stents39 may have been aggravated by higher strut density in overlapping40 and crushed stent segments, and the closed cell design might have limited the expansion of stents implanted through stent cells as in the culotte technique.41 The newer generation Xience stent features a more biocompatible polymer and open cell design and thus might provide a larger safety gain in two-stent techniques than in single stent techniques.42 43 It is possible that due to the favourable results in the complex group by second generation DES and the consistent documentation of double kissing crush as a superior two-stent technique, we might have underestimated the positive effect of the combination of best stent and best technique for two-stent treatment. On the other hand, less conservative SB intervention criteria might have reduced the rate of early target lesion revascularisation, although such more liberal SB treatment strategy during provisional stenting is not backed by published results. Recent guidelines recommend PCI for treatment of LMCA stenosis in patients with low (≤22) SYNTAX score.22 This has increased the focus on optimal bifurcation stenting as 80%–85% of LMCA treatments involve the distal LMCA bifurcation.44 45 In Nordic-Baltic IV, only a small portion of cases were treated for distal LMCA bifurcation stenosis. Thus, extrapolation of our results to this lesion subset should be done with caution given the specific technical challenges in distal LMCA bifurcation PCI.46
Enrolled patients had rather short SB lesions, thus limiting conclusions to this relevant subset of bifurcation lesions. The use of angiographic SB inclusion criteria might have led to inclusion of some patients with physiologically insignificant SB disease favouring the simple one-stent technique, and despite randomisation, the SB diameter stenosis before treatment was less severe in the simple group indicating a potentially lower overall risk in this group. The sample size estimate for Nordic-Baltic IV was based on the limited available evidence at time of conceptualisation and we cannot exclude that the study was underpowered to detect a true difference between the two treatment strategies. It was strongly recommended to perform only clinically driven and fractional flow reserve (FFR)-guided revascularisation in the follow-up period but the planned 8-month angiographic follow-up might still have led to more revascularisation. The plateau of the MACE curves before the increase in revascularisation seen around the 8-month time point could also reflect that patients truly requiring revascularisation awaited the planned follow-up and some cases were treated before the patient would normally seek a doctor. As the safety of the techniques studied might change over time, the reported 2-year results added clinically relevant information to this report but very long-term follow-up is needed to make a final assessment of one versus two stents for coronary bifurcation treatment.
In the treatment of coronary bifurcation lesions involving a large SB with ostial stenosis, routine stenting of both the MV and the SB did not improve outcome significantly compared with treatment by the simpler MV stenting technique after 2 years.
We thank Jakob Hjort (Aarhus University Hospital, Denmark) for data-management assistance and Helle Bargsteen and Lars Peter Jørgensen (Aarhus University Hospital, Denmark) for data retrieval and verification. We highly appreciated the invaluable support from involved operators and staff at all participating institutions.
IK and NRH contributed equally.
Funding Cordis Corp and Abbott Vascular supported the study equally by funding the pr. patient fee to participating centers.
Competing interests IK received institutional research grants from Cordis, Abbott and speaker fee from Astra Zeneca. NRH has received institutional research grants from Cordis, Abbott, Terumo, Biosensors, Biotronik, Medis medical imaging, Reva Medical, Boston Scientific, St. Jude Medical and Medtronic and has received speaker fees and personal honorarium from St. Jude Medical, Terumo, Reva Medical and Biotronik. LOJ has received institutional research grants from Terumo, Biosensors and Biotronik. JFL has received institutional research grants from Cordis, Abbott, Terumo, Biosensors, Biotronik, Medis medical imaging, Reva Medical, Boston Scientific, Heartflow, St. Jude Medical and Medtronic and has received speaker fees from Biotronik, Biosensors, Tryton, Boston Scientific, St. Jude Medical, Terumo, Reva medical, Cordis, Astra Zeneca and Abbott. GL has received speaker fees from Astra Zeneca.
Patient consent for publication Obtained.
Ethics approval The study was approved by the national or local medical ethics committees and was approved by the Danish Data Protection Agency. ClinicalTrials.gov identifier: NCT01496638.
Provenance and peer review Not commissioned; externally peer reviewed.
Data availability statement Data will not be made available.
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