Introduction
In the clinical trial settings, heterogenous definitions of complex PCI have been applied across numerous studies in tailoring the duration of DAPT [
1‐
5], resulting in a variety of outcome assessments reported in previous studies that limits the interpretation and generalizability of study results [
6]. Since its initial introduction, although PCI complexity has been recognized as a contributor to future stent-driven ischemic events, several studies have examined the relationship of complex PCI with future bleeding events, reporting inconsistent results, in which some have confirmed its predictive value [
4,
5] and some have not [
1‐
3]. Against this background, the 2017 ESC dual antiplatelet therapy (DAPT) guidelines has been proposed to standardize the definition of high thrombotic risk (HTR) criteria of stent-driven recurrent ischemic events, including a composite of clinical (chronic kidney disease [CKD] and prior stent thrombosis on adequate antiplatelet therapy) and procedural characteristics (diffuse multivessel disease in diabetic patients, at least three stents implanted, at least three lesions treated, bifurcation with two stents implanted, total stent length > 60 mm, treatment of chronic total occlusion (CTO), or stenting of the last remaining coronary artery) [
7]. Given these high-risk characteristics were mainly derived from previously published reports, data on the applicability of DAPT guideline-endorsed HTR criteria in the real-world practice is scare, especially in East Asian patients.
In this context, patients with HTR features may benefit from a longer duration of DAPT regimen to reduce risk of recurrent ischemic events [
1]. However, concomitant high bleeding risk (HBR) may be present, making its benefits offset at least in part in these patients. It is known that patients at HBR remain at increased risk of both ischemic and hemorrhagic events after PCI. To date, HBR patients had not been well defined and the eligibility criteria of HBR patients were different among contemporary clinical trials [
8‐
10]. Although several bleeding prediction scores are currently available to estimate the bleeding risks of the individual patient [
11‐
14], they have moderate accuracy for predicting bleeding, with an average C statistics about 0.7. With this in mind, the Academic Research Consortium for HBR (ARC-HBR) developed a consensus definition of patients at HBR based on review of the available evidence in clinical trials [
15]. Considering the mutual role and possibly competing role of HTR and ARC-HBR features on outcomes, whether DAPT guideline-endorsed HTR features exert similar or differential impact on the long-term occurrence of adverse events among patients with and without ARC-HBR after PCI in the real-world setting has not been well studied. Therefore, the purpose of this study was to (1) assess the ability of ESC guideline-endorsed HTR criteria to stratify ischemic and bleeding risk, and (2) examine whether ARC-HBR affects the association between HTR features and clinical outcomes differently using prospective data from an all-comers population receiving PCI with drug-eluting stents (DES).
Methods
Patient population
A total of 10,724 consecutive patients undergoing PCI at Fuwai Hospital (National Center for Cardiovascular Diseases, Beijing, China) were prospectively entered into the Fuwai PCI Registry (January 2013 to December 2013). For the present study, exclusion criteria were treatment by balloon angioplasty alone without stent placement, implantation of bioresorbable scaffolds or bare-metal stents, and unavailability of guideline-endorsed high-risk features for ischemic events at index PCI. Finally, 10,167 patients were selected for this analysis. The study was conducted based on the principles of the Declaration of Helsinki, and its protocol was approved by the hospital’s ethical review board (Fuwai Hospital & National Center for Cardiovascular Diseases, Beijing, China). All patients provided written informed consent for prospective follow-up before the intervention. Demographic and clinical characteristics, angiographic and procedural information, and follow-up data were systematically and prospectively collected in our dedicated PCI registry by independent research personnel. Details of the measurements and biochemical analysis are contained in the supplementary material method.
Procedures and patient follow-up
The PCI procedure and best available medical therapy were performed in accordance with the current procedural guidelines [
16,
17]. Detailed information on procedures is shown in the supplementary material method. After index PCI, patients were followed up at 1, 6, and 12 months and annually thereafter. Follow-up data were collected through medical records, telephone communications, or face-to-face interviews after hospital discharge by well-trained cardiologists who were blind to the purpose of the present study, until death occurred or up to the last day of the follow-up period. Patients were advised to return for coronary angiography if indications of ischemic events occurred. For patients treated for adverse events at other medical institutions, external medical records, discharge letters, and coronary angiography documentation were systematically collected and reviewed. The median follow-up duration was 29 months (interquartile range [IQR]: 26.5 to 31.1 months).
Definitions and clinical outcomes
HTR criteria endorsed by 2017 ESC DAPT guidelines in the present study were defined with at least 1 of the following characteristics: diffuse (lesion length ≥ 20 mm) multivessel disease in diabetic patients, CKD (estimated glomerular filtration rate [eGFR] < 60 mL/min), at least three stents implanted, at least three lesions treated, bifurcation with two stents implanted, total stent length > 60 mm, or treatment of CTO. Patients are considered to be at HBR if at least 1 major or 2 minor criteria are met. In the present analysis, we modified the ARC-HBR definitions because several major and minor ARC-HBR criteria were not exactly captured in our registry. Therefore, those patients with at least one major criterion such as oral anticoagulation at discharge, severe CKD (eGFR< 30 ml/min), severe anemia (hemoglobin< 11 g/dL), thrombocytopenia (platelet count< 100 × 10
9/L), previous stroke (≤12 months), and those with ≥2 minor criteria such as age ≥ 75 years, moderate CKD (eGFR 30–59 mL/min), or mild anemia (hemoglobin 11–12.9 g/dL for men and 11–11.9 g/dL for women) were classified as the HBR group. The primary ischemic outcome was major adverse cardiac event (MACE), defined as a composite of cardiac death, myocardial infarction (MI), target vessel revascularization (TVR), or definite/probable stent thrombosis (ST). The primary bleeding outcome was clinically relevant bleeding, defined as the Bleeding Academic Research Consortium (BARC) type 2, 3 or 5 bleeding [
18]. Device oriented composite endpoints (DOCE) was defined as a composite of cardiac death, target-vessel (TV) MI, and target lesion revascularization (TLR). Detailed information on secondary outcomes and endpoint definitions are presented in the supplementary material method.
Statistical analysis
Continuous variables are expressed as mean ± SD or median (interquartile range) and compared with the Student’s t-test or the Mann-Whiney U test, respectively. Categorical data are reported as numbers and percentages, and were compared using chi-square or Fisher’s exact test as appropriate. Cumulative event rates for ischemic and bleeding events were constructed using Kaplan-Meier method among those with and without HTR features and after substratifying all subjects by both HTR and HBR. Event rates were compared across groups using the log-rank test. Furthermore, the cumulative incidences of primary ischemic and bleeding outcomes were assessed according to the number of ESC-HTR criteria (0, 1 to 2, and ≥ 3 high-risk characteristics). The adjusted effect of “HTR features” on adverse events was estimated with multivariable Cox proportional hazard regression model, including “HTR features” as either a categorical or a continuous (per increase in number of HTR features) covariate in the Cox model, The covariates included in the model were age, sex, current smoking, hyperlipidemia, hypertension, acute coronary syndrome (ACS), left ventricular ejection fraction, peripheral artery disease, previous MI, previous revascularization (PCI and/or coronary artery bypass graft [CABG]), hemoglobin, white blood cell count, platelet count, type of DES, and duration of DAPT. Additionally, to evaluate the effect of the individual HTR features components on primary ischemic and bleeding outcomes, each was included as a separate predictor in the multivariable Cox model. Forming interaction testing was performed between HTR features and ARC-HBR on both ischemic and bleeding outcomes. All tests were two-sided and a P-value of < 0.05 was considered to be statistically significant. All analyses were performed with SPSS version 22.0 (SPSS Inc., Chicago, Illinois, USA).
Discussion
This study was the first study to validate the DAPT guideline-endorsed HTR criteria and characterized the interplay between these HTR criteria, ARC-HBR status, and clinical outcomes in an all-comer patient population with unselected use of DES from a prospective real-world registry. The salient findings of the present analysis were as follows: (1) HTR criteria recommended by 2017 ESC DAPT guidelines successfully identified those patients with very HTR after PCI, who represented 44% of patients in this all-comers registry; (2) ECS-endorsed HTR criteria showed a significantly greater risk of MACE while maintaining a similar risk of clinically relevant bleeding. In addition, HTR was associated with lower risks of DOCE, as well as cardiac death, MI, any revascularization, ST, and stroke; (3) The independent impact of HTR features on thrombotic events was substantial and uniform irrespective of HBR status, and there was no an interaction between HTR features and HBR on clinically relevant bleeding, suggesting that intensified DAPT may be beneficial to patients at HTR features; (4) Individual HTR features, such as ≥3 stents implanted and ≥ 3 lesions treated, which were the angiographic subset most consistently and strongly associated with increased ischemic risk but not for bleeding, may be helpful to guide potent P2Y12 inhibitors or prolongation of DAPT.
The extent and complexity of CAD significantly affect the optimum invasive method for revascularization and strongly influence outcomes after PCI [
19,
20]. In case of PCI as the preferred strategy, patients with coronary anatomic complexity and challenging subsets of lesions result in complex PCI procedures and at higher risk for adverse clinical events [
21,
22]. Although patients who underwent complex PCI have consistently been reported to be associated with a higher incidence of subsequent ischemic events, the relative risks of complex PCI in terms of clinically relevant bleeding are a matter of debate [
1‐
5]. Given that there have been no universal criteria of complex PCI with regard to angiographic and lesion-related features, leading to different outcome assessments reported in previous studies [
6], the 2017 ESC DAPT guidelines proposed the concept of HTR features of stent-driven ischemic events, defined according to 9 clinical and procedural criteria, to identify patients who may receive more benefit from a longer period of DAPT [
7]. In routine clinical practice, clinical decision-making on upfront DAPT duration and intensity after complex PCI warrants a simultaneous appraisal of both ischemic and bleeding complications. It is known that patients at HBR need careful evaluation owing to their high risk of thrombotic and bleeding complications when determining potency or duration of antithrombotic management [
9,
23]; however, whether ESC-endorsed HTR features confer a similar or differential risk for ischemic and bleeding events among those with and without HBR has, to our knowledge, not yet been elucidated in all-comer patients cohort because HBR patients are mostly excluded from randomized controlled trials (RCT) of PCI [
24,
25]. We, therefore, performed the present analysis that, with approximately 10,000 patients, represents one of the largest real-world population assessing the impact of ESC-HTR features on clinical outcomes after coronary DES implantation and whether this effect is influenced by HBR status.
This large single-center PCI cohort reflecting a real-world setting were coherent with those of prior findings using randomized trial data in that ESC-HTR features not only exerted an adverse impact on MACE and DOCE proportional to the number of HTR criteria present, but also on all individual endpoints including cardiac death, MI, definite/probable ST, and TVR [
1,
2,
5]. On the other hand, the HTR criteria group did not experience a parallel increase in the risk of clinically relevant bleeding, as compared with those at non-HTR criteria. This was in line with two large analyses showing comparable bleeding risks between complex and non-complex PCI groups [
1,
2]. In contrast to our findings, an all-comer sample of Bern PCI registry described that patients having at least 1 of high-risk features of stent-related recurrent ischemic events had a higher risk of bleeding (BARC 3–5) and ischemic (DOCE) events [
26], making optimal duration and intensity of DAPT challenging for these patients. Several reasons might explain for the lack of a significant association noted in our study between HTR features and clinically relevant bleeding. First, the conflicting results may be attributable to differences in the proportions of each HTR component. Owing to the fact that CKD has emerged as a common contributor to both type of ischemic and bleeding complications [
13,
27], the proportion of CKD that was markedly lower (4.0%) in our study than in Bern PCI registry (24.7%) might account for the similar risk of clinically relevant bleeding in HTR versus non-HTR features group in the present study. Second, considering that patients with diabetes or multivessel CAD represent an advanced state of atherosclerosis, with higher rates of in-hospital events, as well as recurrent atherothrombotic coronary events and death [
28‐
31], diffuse multivessel disease in diabetic patients (18.5%) constituted the majority of our DAPT guideline-endorsed HTR features, thereby being positioned to clinical tendencies to ischemic events. Given the low number of patients with diffuse multivessel disease and diabetes (2.7%) in Bern PCI registry [
26], it would be possible to detect a difference in the effect of HTR features on bleeding events. It should also be mentioned that high as many as 20% of our patients had undergone a PCI with total stent length > 60 mm (of note, the proportion of patients with long stent stenting in Bern PCI registry was 6.5%). Third, there is evidence demonstrating an increased risk of bleeding events in patients with baseline higher categories of bleeding risk prediction scores [
32,
33]. Lower bleeding risk of our study patients, compared with Bern PCI registry (PRECISE-DAPT score: 10.6 ± 8.5 vs. 20.6 ± 13.3), may have partly explain difference in the risk of clinically relevant bleeding. In addition, differences in the intensity of DAPT (clopidogrel vs. more potent P2Y
12 inhibitors) may, in part, relate to the discordant results. Indeed, Ueki et al. [
26] showed that nearly 40% of patients involved used of more potent P2Y
12 inhibitor such as ticagrelor and prasugrel, yet only clopidogrel was used as a P2Y
12 inhibitor for DAPT in our study because potent P2Y12 receptor blockers such as ticagrelor or prasugrel were not available in China during the study period.
While individual patient risks of ischemia and bleeding are related to many common risk factors, little is known regarding the impact of HTR features and the risk of adverse events according to the underlying bleeding risk [
34]. In the current analysis from the Fuwai PCI registry, we found no convincing evidence of an interaction between HTR features and ARC-HBR in regard to the risk of ischemic and bleeding outcomes. In other words, ARC-HBR further increases the risk of long-term adverse events after PCI of both ESC-HTR and non-ESC-HTR criteria to a comparable degree. Bleeding risk may not be increased to the same extent as ischemic risk in HTR patients, which sets the rationale for supporting that ESC-HTR features may be a useful parameter for risk stratification of patients with HBR after PCI. Given the higher risk of ischemic complications in patients with ESC-HTR characteristics, effective antiplatelet therapy may be particularly important for these patients. Consistent with this hypothesis, longer-term DAPT has recently been shown to be more effective in patients who underwent complex PCI [
1].
Study limitations
First, the study has an innate limitation regarding its observational nature with registry data. PCI procedures was determined at the discretion of the attending physician and might have been influenced by several factors such as underlying demographics, clinical presentation at admission, and physician’s preference. Despite the implementation of multivariable Cox regression analysis to adjust for potential confounding factors and minimize the bias from different baseline characteristics, residual confounding cannot be excluded. Second, although majority of ESC-endorsed HTR features were taken into account in this analysis, information on prior ST on adequate antiplatelet therapy and stenting of the last remaining coronary artery were not captured in Fuwai PCI dataset, thus limiting their applicability in our population and representing an important restriction. Furthermore, because Fuwai PCI registry was not designed to investigate the performance of ARC-HBR criteria, some ARC-HBR criteria were not applicable. Thus, the prevalence of HBR patients would have been underestimated in our study. Third, despite the sample size of this cohort, the analyses assessing the effect of HTR features on clinical outcomes in the HBR subgroup and the interaction testing for the effect of HTR features on clinical outcomes, stratified by presence or absence of HBR, are likely underpowered. Finally, all patients were treated with clopidogrel, although approximately 60% of patients enrolled presented with acute coronary syndromes, and ticagrelor had not yet been approved during the time of enrollment. Our findings warrant confirmation in larger samples treated with potent P2Y12 inhibitors.
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