1. Introduction
The cornerstone of treatment for patients presenting with acute coronary syndromes (ACS) is timely mechanical revascularisation with percutaneous coronary intervention (PCI) and potent antiplatelet pharmacotherapy. Bleeding is a recognised and important complication of PCI, and there is a significant body of evidence that associates peri-procedural (i.e., peri-PCI) bleeding with poor clinical outcomes, including an increased risk of both short- and long-term mortality [1,2,3]. Major bleeding complications occur at either the arterial access site, commonly the femoral and radial artery, or from non-access site sources (predominantly gastrointestinal, intracranial, and retroperitoneal) [3]. Numerous studies have demonstrated that the femoral approach is independently associated with worse major bleeding outcomes [1,4,5,6,7,8]. Other major published predictors of bleeding include, but are not limited to, older age, female sex, low body mass index (BMI), renal impairment, and the use of potent antiplatelet agents and fibrinolytic therapy [9,10].
However, there is paucity of data in contemporary Australian practice pertinent to the clinical impact of PCI-related bleeding. Therefore, the primary objective of this study was to investigate the association between bleeding severity in PCI and short-term clinical outcomes in a large Australian multicentre registry of an all-comers population. This study used a standardised and robust model for defining bleeding, developed by the Bleeding Academic Research Consortium (BARC) [11]. Furthermore, this study secondarily investigated the effect of baseline and procedural characteristics on the severity of BARC-defined bleeding.
2. Methods
2.1. Study Population
We retrospectively analysed patient data from the Victorian Cardiac Outcomes Registry (VCOR) between January 2014 and December 2017. The VCOR is a state-wide population-based clinical quality registry that collects data related to PCI procedures and outcomes from all 30 public and private hospitals around Victoria. It is coordinated by Monash University in conjunction with the Department of Health and Human Services, and the Victorian Cardiac Clinical Network. The registry records on standardised case reports form PCI-related data, including patient demographics, procedural characteristics, and clinical outcomes and complications, with a 30-day follow-up period. Data are entered by trained hospital staff in real time as the patient progresses through a hospital admission, and data entry personnel are registered with VCOR. Participant data are prospectively entered into the VCOR unless they choose to ‘opt-out’. Regular auditing activities by the central registry ensures data integrity.
2.2. Definitions
The primary outcome was 30-day major adverse cardiac and cerebrovascular events (MACCE), a composite of clinical events occurring in-hospital and up to 30-days post discharge. MACCE was defined as all-cause mortality, new or recurrent myocardial infarction (MI) or stent thrombosis, target vessel revascularisation, or nonfatal stroke. Patients with missing 30-day MACCE data were excluded from the analysis.
ACS was defined as a composite of ST-elevation myocardial infarction (STEMI), non-STEMI (NSTEMI), and unstable angina (chest pain at rest with unchanged cardiac biomarkers and ECG). Stable angina as an indication for PCI was defined as chest pain syndrome associated with exertion due to inducible myocardial ischaemia. Coronary lesion type was defined according to the American College of Cardiology (ACC) and the American Heart Association (AHA) classification as type A, type B1, type B2, and type C in order of increasing complexity [12].
New renal impairment was defined as an increase of ≥25% or ≥44.2 mmol/L in serum creatinine up to 5 days after the index PCI, when compared to baseline. Cardiogenic shock was defined as a sustained (>30 min) episode of hypotension (systolic blood pressure (SBP) < 90 mmHg), or the use of vasopressors to maintain the SBP > 90 mmHg, together with evidence of end-organ hypoperfusion (e.g., altered mentation, reduced urine output) and increased left ventricular filling pressures, such as pulmonary congestion. MI was defined as new elevation of cardiac biomarkers ≥ 20% compared to baseline levels, as well as one of the following: (1) ST-segment elevation distinct from the initial ischaemic event, (2) symptoms of myocardial ischaemia lasting ≥ 20 min, (3) development of new Q-waves in 2 or more contiguous leads, (4) angiographic evidence of flow limitation, and (5) evidence of new abnormalities in regional wall motion on imaging [13]. Stroke was defined as an ischaemic or haemorrhagic event of the brain during the initial PCI or the course of the admission, manifesting as a persistent neurological deficit. Anti-thrombotic therapy includes unfractionated heparin and low molecular weight (LMW) heparin.
In-hospital and outcomes up to 30 days were recorded, including rehospitalisation, readmission, MI, stent thrombosis, bleeding event, stroke, MACCE, and major adverse cardiac events (MACE), which was defined as MACCE minus stroke. These were verified from medical records, patients, and/or their primary care physician.
The BARC bleeding criteria were divided into three categories: type 0 (no bleed), type 1&2 (‘minor’ bleed), and type 3&5 (clinically significant or ‘major’ bleed) [11]. A bleeding event as defined in VCOR refers to a new bleeding event either during the cardiac catheter lab visit, after the lab visit, or any subsequent lab visits but prior to discharge. The timing of bleeding events is, therefore, between PCI and the date of discharge, i.e., ‘in-hospital bleeding’. In case of BARC 5 fatal bleeding, this refers to a bleeding event that directly causes death with no other explainable cause. BARC type 4 bleeds refer to PCI patients who underwent coronary artery bypass graft (CABG) surgery and had a subsequent bleed. These bleeds are not directly associated with the PCI procedure and were, therefore, excluded from our analysis. However, patients requiring CABG surgery (as a potentially emergent complication of PCI) without BARC 4 bleeds were not excluded. These patients may have experienced PCI-related bleeding complications, affecting MACCE outcomes independent of their CABG surgery. The individual definition and criteria comprising the BARC types are detailed in the Appendix A.
2.3. Statistics
Continuous variables are presented as mean ± standard deviation (SD) or median with interquartile range (IQR), and categorical variables are presented as frequencies and percentages. Differences between the 3 BARC groups were evaluated using one-way analysis of variance (ANOVA) or Kruskal–Wallis test for continuous variables, and a chi-square test for categorical variables. p-values were calculated to demonstrate statistical significance between any two of the BARC groups. If significant (p < 0.05), post-hoc pairwise comparisons were conducted to evaluate which two BARC groups were different (i.e., BARC 0 versus BARC 1&2, BARC 1&2 versus BARC 3&5, and/or BARC 0 versus BARC 3&5).
The independent effect of BARC-defined bleeding and other clinically relevant characteristics on cumulative in-hospital and 30-day MACCE (the primary outcome) was evaluated using a logistic regression model. Variables included in the multivariable analysis were the 3 BARC categories, characteristics that were clinically significant in the univariate analysis, as well as pre-defined variables that represented well-described predictors of bleeding, which included age, female sex, BMI, procedural creatinine, diabetes, peripheral vascular disease (PVD), out-of-hospital cardiogenic shock (OHCA), cardiogenic shock, fibrinolytic therapy, administration of glycoprotein IIb/IIIa inhibitors (GPI), and mode of vascular access [14,15,16,17]. The effect of baseline patient and procedural characteristics on the severity of BARC-defined bleeding were also assessed using logistic regression. All tests were 2-tailed and assessed at the 5% significance level. No adjustments for multiple comparisons were made.
Yearly rates for mode of vascular access, BARC-defined bleeding, in-hospital MACCE, and cumulative in-hospital and 30-day MACCE from 2014 to 2017, among STEMI patients and ACS patients other than STEMI, were also shown for descriptive purposes.
3. Results
Of 37,913 patients enrolled in the VCOR from January 2014 to December 2017, we analysed the data of 37,866 patients (n = 47 excluded for BARC 4 bleeding and missing 30-day MACCE data). The mean age was 66 years and 76.5% were male. Of 37,886 patients, 91.2% (n = 34,555) experienced no bleeding (BARC 0), 7.9% (n = 3007) experienced a minor bleed (BARC 1&2), and 0.9% (n = 324) experienced a clinically significant major bleed (BARC 3&5). Notable baseline characteristics in this all-comers population included diabetes mellitus requiring medication prevalence of 22%, history of prior PCI (32.6%), history of prior CABG (7.7%), and moderate to severe heart failure (13.2%), defined by the New York Heart Association (NYHA) as left ventricular ejection fraction (LVEF) < 45%.
Baseline patient characteristics of the three BARC groups are presented in Table 1. Compared to the BARC 0 group, more patients with BARC 1&2 bleeds and BARC 3&5 bleeds were female, older, and had a lower BMI (all p < 0.001). There were stepwise increases in BARC-defined bleeding among patients with worsening renal impairment (estimated glomerular filtration rate (eGFR) < 60%) with or without dialysis, those with moderate to severe LV systolic dysfunction, OHCA, cardiogenic shock, in-hospital pre-procedural cardiac arrest, or were administered GPI, or fibrinolytic therapy (all p < 0.001). In contrast, there were no significant differences between BARC groups in rates of patients with diabetes, patients on chronic oral anticoagulant therapy, and patients administered fibrinolytic therapy ≤ 24 h prior to PCI (p = not significant).
Procedural characteristics of patients in the 3 BARC groups are presented in Table 2. There were stepwise increases in bleeding severity among patients who had PCI with femoral vascular access, and an inverse relationship in bleeding severity was observed among patients with radial access (both p < 0.001). The BARC 3&5 group had higher rates of STEMI presentations, left main coronary artery (LMCA) involvement, coronary lesion type B2 and C, and the use of bare metal stents, and thrombus aspiration devices, procedural intubation, and extracorporeal mechanical support (all p < 0.001).
In-hospital outcomes and outcomes up to 30 days (events recorded from day of discharge to day 30 post discharge) within the three BARC groups are presented in Table 3. There was an increase in adverse in-hospital outcomes with increasing severity of BARC-defined bleeding, including but not limited to increased length of hospital stay, new renal impairment, cardiogenic shock, recurrent MI, stroke, MACE, MACCE, and mortality (all p < 0.001). For example, in-hospital MACCE occurred in 30.9% of patients who had BARC 3&5 bleeding, compared to 5.6% of patients who had BARC 1&2 bleeding and 2.7% of patients who had no bleeds (all p < 0.001). At 30-day follow-up, there was a graded increase in incidence of new heart failure, and 30-day MACE, MACCE, and mortality, with increasing severity of bleeding (all p < 0.05). There were also more rehospitalisations among patients with BARC 3&5 bleeding compared to patients who had BARC 1&2 bleeding or BARC 0 bleeding (p < 0.001).
Medications prescribed at discharge are presented in Table 4. Patients who experienced BARC 3&5 bleeding were prescribed fewer antiplatelet agents including aspirin, thienopyridine, and ticagrelor, as well as beta-blockers, angiotensin converting enzyme (ACE) inhibitors or angiotensin receptor blockades (ARBs), and statins, compared to patients who experienced no bleeding (all p < 0.001). However, there were more patients in the BARC 3&5 cohort prescribed oral anticoagulants (p < 0.001).
Using multivariable analysis, we identified predictors of cumulative in-hospital and 30-day MACCE. Cardiogenic shock was the strongest predictor (OR 13.99, 95% Confidence Interval (CI): 11.61–16.86), followed by BARC 3&5 bleeding (OR 4.37, 95% CI: 3.20–5.98) (Figure 1). Other predictors of cumulative in-hospital and 30-day MACCE included BARC 1&2 bleeding (OR 1.57, 95% CI: 1.33–1.85), OHCA (OR 2.92, 95% CI: 2.31–3.68), age (OR 1.02, 95% CI: 1.02–1.03), female sex (OR: 1.20, 95% CI: 1.06–1.37), pre-procedural creatinine (OR: 1.002, 95% CI: 1.002–1.003), diabetes (OR 1.22, 95% CI: 1.07–1.39), PVD (OR 1.50, 95% CI: 1.19–1.90), GPI use (OR 1.82, 95% CI: 1.56–2.12), and fibrinolytic therapy (OR 1.37, 95% CI: 1.03–1.82) (all p < 0.05).
Baseline characteristics that independently predicted BARC-defined bleeding were older age (OR 1.02, 95% CI: 1.01–1.02), female sex (OR 1.34, 95% CI: 1.22–1.47), fibrinolytic therapy (OR 1.77, 95% CI: 1.46–2.15), antiplatelet agents including GPI (OR 1.53, 95% CI: 1.35–1.72) and ticagrelor (OR 1.42, 95% CI: 1.30–1.54), severe NYHA heart failure (defined as LVEF < 30%) (OR 1.26, 95% CI: 1.06–1.49), cardiogenic shock (OR 1.42, 95% CI: 1.10–1.84), mechanical ventricular support (OR 1.85, 95% CI: 1.32–2.57), and procedural intubation (OR 1.50, 95% CI: 1.12–2.00) (all p < 0.05) (Figure 2). Radial access (OR: 0.66, 95% CI: 0.61–0.72) was protective against BARC bleeding.
Figure 3 illustrates yearly rates for mode of vascular access, BARC-defined bleeding, in-hospital MACCE, and cumulative in-hospital and 30-day MACCE from 2014 to 2017 among STEMI patients and patients with ACS other than STEMI. Across these four years of VCOR data, there was an observable upward trend in uptake of radial access and a decrease in the rate of femoral access. No discernible trends, however, could be observed in the rates of bleeding and MACCE.
4. Discussion
In this large, contemporary Australian multicentre registry of an all-comers population undergoing PCI, the major finding was a stepwise increase in in-hospital MACCE correlating with greater severity of bleeding: BARC 0 (2.7%), BARC 1&2 (5.6%), and BARC 3&5 (30.9%), as well as 30-day MACCE: BARC 0 (1.4%), BARC 1&2 (1.8%), and BARC 3&5 (3.1%). Additionally, there were increases in the length of hospital stay, and risk of rehospitalisation with BARC 3&5 bleeding. Following adjustment of clinically important variables, clinically significant BARC 3&5 bleeds remained predictive of cumulative in-hospital and 30-day MACCE (OR 4.37, 95% CI: 3.20–5.98, p < 0.001). Independent predictors of bleeding included female sex, age, fibrinolytic therapy, and ticagrelor use, while radial access was associated with a lower risk of bleeding (all p < 0.001).
Rates of major bleeding have been variably defined and variably reported among large, multicentre PCI studies [18,19,20,21]. Kwok et al. conducted a meta-analysis of 42 studies (n = 533,333) that evaluated the clinical impact of peri-procedural bleeding complications, incorporating various definitions of bleeding, including TIMI, GUSTO, STEEPLE, HORIZON-AMI, CRUSADE, BARC, and REPLACE-2 [18]. In this meta-analysis, 1.3% of PCI patients across these studies experienced major bleeding, corroborating our findings. We investigated VCOR data which utilises the BARC model to define PCI-related bleeding. The BARC definition was developed in 2010 to enable a standardised and clinically relevant approach to grading bleeding severity [22]. It is reported to capture a larger number of bleeding events [23] and informs 1-year prognosis and mortality with greater sensitivity to commonly used bleeding definitions, including TIMI and REPLACE-2 [22]. The multinational Global Registry of Acute Coronary Events (GRACE) between 1999 and 2002 reported major bleeding rates of 5.5%, however, only ACS patients were included [19]. Our study patients, however, reflected a more contemporary, ‘all-comers’ population, and thus, lower risk patients who were undergoing PCI for stable angina and non-ACS indications were also included. Studies which have analysed similar all-comers populations, including the CathPCI registry between 2004 and 2011 (n = 3,386,688) and the prospective ADAPT-DES trial (n = 8582), reported that 1.7% and 1% of patients experienced major bleeding respectively, which are congruent with our findings [20,21].
Rates of adverse in-hospital and 30-day outcomes in our study, especially mortality and MACCE, were similarly observed in analyses of other large registries including CathPCI [20,24], the British Cardiovascular Intervention Society (BCIS) [18,25], and the Swedish Coronary Angiography and Angioplasty Registry (SCAAR) [18,25]. The rate of in-hospital mortality in patients enrolled in CathPCI between 2004 and 2011 was 2.5%, and 30-day MACE in patients ≥ 65 years old between 2004 and 2008 was 5.7%, similar to our findings as well as those from studies analysing the SCAAR and BCIS registries [18,20,24,25]. However, we evaluated a more contemporary population as evident with changes to ACS management over time, including PCI techniques such as radial access. Uptake of radial access was 51.5% in our study, compared to 41–45% and 46% among the BCIS and SCAAR datasets, respectively. The rates of both in-hospital and 30-day mortality and MACCE were significantly higher among patients who experienced greater severity of bleeding in our study. In the meta-analysis by Kwok et al., 17.3% of patients who had major bleeding experienced MACE, compared to 5.4% of patients who experienced no bleeding complications [18]. Our study findings add to the existing body of evidence which collectively underscore the correlation between increasing severity of PCI-related bleeding and poor clinical outcomes, including MACCE but also increased length of hospital stay and risk of rehospitalisation.
In our study, major bleeding was an independent predictor of cumulative in-hospital and 30-day MACCE (OR = 4.4) after adjusting for clinically important variables including age, sex, BMI, diabetes, PVD, pre-procedural creatinine, OHCA, cardiogenic shock, mode of vascular access, GPI, and fibrinolytic therapy. The independent adverse impact of PCI-related bleeding on clinical outcomes has been consistently reported in numerous studies [1,2,3,18,19,20,26]. Kwok et al. showed that major bleeding after PCI was independently associated with a 3-fold increase in mortality and MACE, and this was maintained at one year [3,18]. This is similar to the findings of US-based all-comers registries, including CathPCI [20,24] and the cardiac catheterization database [27], as well as the prospective ADAPT-DES trial which found that patients, across 11 sites in the US and Germany, were 3.4-fold more likely to experience MACE outcomes if they experienced bleeding with an associated decrease in haemoglobin (∆Hgb) ≥ 4 g/Dl [21]. Our study substantiates the current state of literature that underscore the impact of bleeding on adverse outcomes with relevance to contemporary, local Australian practice. Collectively, this highlights the need for strategies to address bleeding and mitigate bleeding consequences.
Fibrinolytic therapy and GPI use were also predictive of cumulative in-hospital and 30-day MACCE, independent of clinically important variables, including bleeding. In contemporary Australian practice, these agents are predominantly used in high-risk patients, which could explain the additive effect of GPI and fibrinolysis use on MACCE. Intravenous GPI is often administered in patients with high-risk clinical or angiographic characteristics (e.g., with those with large thrombus burden), and fibrinolytic therapy is commonly used when there is delay in primary PCI, or if the patient is not at a PCI-capable centre [28]. However, both fibrinolysis and GPI increase bleeding risk in patients undergoing PCI due to their mechanism of action and might well contribute to the MACCE rates through potentiating bleeding.
Currently, aspirin and P2Y12 inhibitors (clopidogrel, ticagrelor, and prasugrel) are the recommended antiplatelet treatment for patients during and after PCI, with studies showing significant reduction to 30-day MACE compared to aspirin alone (p = 0.0001) [29]. Patients who have mechanical heart valves or atrial fibrillation will also require additional oral anticoagulation, which increases bleeding risk further [30]. Indeed, ticagrelor use in our study independently predicted major bleeding (OR 1.42). A downtrend in the use of clopidogrel has been reported in patients enrolled in the Melbourne Interventional Group (MIG) registry (2009–2013), with the uptake of ticagrelor at 45% as the dominant P2Y12 inhibitor of choice by the latter half of 2013 [31]. All these studies collectively highlight the link between the efficacy of antiplatelet agents in preventing recurrent thrombosis and ischaemic sequelae, with balancing bleeding risk related to the efficacy of the antiplatelet therapy. A contemporary initiative by the Academic Research Consortium for High Bleeding Risk (ARC-HBR), in 2019, provided a framework to stratify PCI patients with high bleeding risk [32]. A tailored approach for high-bleeding risk patients with judicious efforts to minimise the use of potent antiplatelet agents among older age patients, female sex, and low BMI may mitigate bleeding consequences.
The potential mechanisms by which major bleeding might increase mortality and MACCE are likely multifactorial. Some studies suggest that the frequent cessation of anti-thrombotic or antiplatelet therapy among patients who experience major bleeding, could subsequently increase their risk of ischaemic events [18,26,33]. In our study, patients who experienced major bleeding were prescribed fewer antiplatelet agents at discharge, including aspirin, thienopyridine, and ticagrelor (all p < 0.001). Anaemia is known to independently predict adverse outcomes in patients undergoing PCI [26,34,35]. This could be through the deleterious effect of blood transfusions [34], or the endogenous production of erythropoietin in response to anaemia, manifesting clinically as increased risk of stroke, MI, and mortality among STEMI patients [35,36]. There may also be short-term haemodynamic consequences of anaemia through tachycardia, hypotension, and congestive cardiac failure, all of which can increase myocardial oxygen demand [26].
In our analysis, femoral vascular access predicted major bleeding (OR 1.52, 95% CI: 1.39–1.64), substantiating the results of numerous prior studies [1,4,5,6,7,8]. In particular, the meta-analysis by Ferrante et al. analysed 24 studies, including MATRIX and RIVAL, and underscored that PCI with femoral access was associated with increased risk of major bleeding compared to radial access, particularly among ACS patients [6]. In the 2018 European Guidelines, radial access was a class I recommendation among patients with ACS undergoing PCI [37]. This is unless there are overriding procedural considerations, including the operator’s expertise with radial access. In our study, while femoral access did not independently predict cumulative in-hospital and 30-day MACCE, this could be explained in part by the effect of other stronger variables on MACCE, including BARC 3&5 bleeding, cardiogenic shock, and OHCA.
Interestingly, while the uptake of femoral access has significantly decreased since 2014, the rate of major bleeding, as well as in-hospital and 30-day outcomes, have not changed appreciably. Similar trends were noted in the MIG registry between 2005 and 2016 [38]. A potential reason for the lack of improvement in 30-day mortality and adverse outcomes, highlighted by Biswas et al., is that 30 days may be too short a time frame to observe a mortality benefit as a result of procedural changes to PCI techniques [38]. Additionally, as noted above, other stronger predictors than vascular access would likely have had a major effect on 30-day outcomes.
However, our study findings add to the body of literature emphasising the importance and adverse impact of bleeding on clinical outcomes. Any bleeding portends an adverse effect on outcome. These findings underscore the need for strategies to minimise bleeding, including adoption of radial access for PCI procedures and also meticulous care with prescription of antiplatelet and anticoagulant combination therapy among high-risk patients, such as those of older age, females, low BMI, and patients with severe heart failure.
Our study results should be interpreted in the context of several limitations, including its retrospective design and observational nature. Firstly, due to the large number of variables being compared between the different BARC categories of bleeding, the results and p-values presented in the univariate analysis should be interpreted with caution and regarded as hypothesis-generating because of the confounding effect of multiple testing. However, the data provide trends in patient and procedural characteristics across increasing severity of BARC bleeding. Secondly, there were likely additional confounding variables that were not measured or could not be measured which could impact clinical outcomes. Thirdly, BARC 0 and BARC 1&2 complications might have been underreported as these frequently did not require hospital-based intervention. Fourthly, patients who had CABG surgery without BARC 4 bleeds were not excluded, which might have affected 30-day MACCE outcomes. Fifthly, the timing of occurrence of any bleeding event in relation to development of in-hospital or 30-day MACCE was not individually verified or adjudicated given that VCOR is a state-wide database and the large number of clinical and bleeding events. Sixthly, VCOR also does not capture non-access site bleeding and severity of non-access site bleeds, which could have adversely impacted on outcomes. Finally, the follow-up duration of 30 days in our study was short, and longer-term follow-up may be necessary in order to ascertain significant differences in rates of adverse outcomes with contemporary procedural changes, including radial access and dynamic changes to antiplatelet and anticoagulant regimens.
5. Conclusions
Bleeding, especially major bleeding, is uncommon (~1%) in contemporary PCI practice. However, major bleeding is independently predictive of in-hospital and 30-day MACCE. With increasing severity of bleeding, there were also stepwise increases in in-hospital and 30-day mortality, length of hospital stay, and rehospitalisation. Efforts to mitigate bleeding and its consequences may improve patient morbidity and mortality.
S.M., W.C. Conceptualisation, S.M., S.V., W.C. Methodology, S.V. Formal statistical analysis, S.M., S.V., S.N., W.C. Investigation, S.M. Writing—original draft preparation, S.M., S.V., S.M., D.T.D., A.L.B., J.L., C.M.R., N.C., W.C. Writing—review and editing, W.C., S.N. Supervision, D.T.D., A.L.B. Data acquisition. All authors have read and agreed to the published version of the manuscript.
This research received no external funding.
Samer Noaman is supported by a scholarship from the NHMRC CRE-COI and National Heart Foundation Fellowship. Christopher Reid is supported by a NHMRC Principal Research Fellowship (1136372) and William Chan is supported by the Alfred Hospital Research Trust and the Harold Cora Brennan Benevolent Trust.
The authors declare no conflict of interest.
Enlarge this image.Figure 1. Independent predictors of cumulative in-hospital and 30-day MACCE. BARC = bleeding academic research consortium, CI = confidence interval, MACCE = major adverse cardiac and cerebrovascular events, OHCA = out-of-hospital cardiac arrest, OR = odds ratio.
Enlarge this image.Figure 2. Independent predictors of BARC bleeding. BARC = bleeding academic research consortium, CI = confidence interval, NYHA = New York health association, OHCA = out-of-hospital cardiac arrest, OR = odds ratio.
Enlarge this image.Figure 3. Trends in mode of vascular access, bleeding, and MACCE between 2014 and 2017 among STEMI patients, and ACS patients excluding STEMI. (a) STEMI patients, (b) ACS patients (excluding STEMI).
Baseline clinical characteristics.
| BARC 0 (n = 34,555) | BARC 1&2 (n = 3007) | BARC 3&5 (n = 324) | p-Value | |
|---|---|---|---|---|
| CLINICAL CHARACTERISTICS | ||||
| Age—years, mean ± SD | 65.7 (11.9) | 67.6 (12.2) | 68.4 (12.7) | <0.001 *† |
| Male, n (% of BARC) | 26,637 (77.1%) | 2117 (70.4%) | 214 (66.0%) | <0.001 *† |
| Female, n (% of BARC) | 7918 (22.9%) | 890 (29.6%) | 110 (34.0%) | <0.001 *† |
| BMI (kg/m2), mean ± SD | 28.9 (5.4) | 28.3 (5.5) | 27.7 (5.4) | <0.001 *† |
| Diabetes mellitus on medication, n (%) | 7599 (22.0%) | 658 (21.9%) | 72 (22.2%) | 0.98 |
| Diabetes on insulin, n (%) | 2602 (7.5%) | 208 (6.9%) | 31 (9.6%) | 0.11 |
| Diabetes on oral medications, n (%) | 4997 (14.5%) | 450 (15.0%) | 41 (12.7%) | 0.11 |
| Peripheral vascular disease, n (%) | 1230 (3.6%) | 101 (3.4%) | 22 (6.8%) | 0.01 †‡ |
| Cerebrovascular disease, n (%) | 1281 (3.7%) | 119 (4.0%) | 20 (6.2%) | 0.051 |
| Previous CABG, n (%) | 2645 (7.7%) | 252 (8.4%) | 14 (4.3%) | 0.03 †‡ |
| Previous PCI, n (%) | 11,366 (32.9%) | 913 (30.4%) | 81 (23.1%) | <0.001 *†‡ |
| Chronic oral anticoagulant therapy, n (%) | 2029 (5.9%) | 183 (6.1%) | 21 (6.5%) | 0.80 |
| eGFR <30, n (%) | 838 (2.4%) | 108 (3.6%) | 28 (8.6%) | <0.001 *†‡ |
| eGFR 30–59, n (%) | 5629 (16.3%) | 652 (21.7%) | 93 (28.7%) | <0.001 *†‡ |
| eGFR >60, n (%) | 25,287 (73.2%) | 2088 (69.4%) | 185 (57.1%) | <0.001 *†‡ |
| Dialysis, n (%) | 377 (1.1%) | 54 (1.8%) | 10 (3.1%) | <0.001 *† |
| LVEF, n (%) | - | - | - | - |
| 1 = Normal function (>50%) | 20,112 (58.2%) | 1606 (53.4%) | 126 (38.9%) | <0.001 *†‡ |
| 2 = Mild dysfunction/impairment (45–50%) | 5664 (16.4%) | 557 (18.5%) | 59 (18.2%) | <0.001 *†‡ |
| 3 = Moderate dysfunction/impairment (35–44%) | 3055 (8.8%) | 290 (9.6%) | 56 (17.3%) | <0.001 *†‡ |
| 4 = Severe dysfunction/impairment (<35%) | 1352 (3.9%) | 182 (6.1%) | 50 (15.4%) | <0.001 *†‡ |
| Out of Hospital Cardiac Arrest, n (%) | 723 (2.1%) | 116 (3.9%) | 56 (17.3%) | <0.001 *†‡ |
| Cardiogenic shock, n (%) | 734 (2.1%) | 123 (4.1%) | 83 (25.6%) | <0.001 *†‡ |
| In-hospital pre-procedure cardiac arrest, n (%) | 500 (1.4%) | 77 (2.6%) | 32 (9.9%) | <0.001 *†‡ |
| Pre-procedure intubation, n (%) | 536 (1.6%) | 106 (3.5%) | 61 (18.8%) | <0.001 *†‡ |
| Glycoprotein IIb/IIIa inhibitors, n (%) | 3377 (9.8%) | 452 (15.0%) | 98 (30.2%) | <0.001 *†‡ |
| Anti-thrombotic therapy, n (%) | 30,588 (88.5%) | 2757 (91.7%) | 292 (90.1%) | <0.001 * |
| Aspirin pre-loading, n (%) | 31,102 (90.0%) | 2822 (93.8%) | 288 (88.9%) | <0.001 *‡ |
| Thienopyridine pre-loading, n (%) | 14,891 (43.1%) | 1176 (39.1%) | 92 (28.4%) | <0.001 *†‡ |
| Ticagrelor pre-loading, n (%) | 13,237 (38.3%) | 1402 (46.6%) | 140 (43.2%) | <0.001 *† |
| Fibrinolytic therapy, n (%) | 1000 (2.9%) | 135 (4.5%) | 27 (8.3%) | <0.001 *†‡ |
| Fibrinolytic therapy ≤24 h prior to PCI, n (%) | 754 (2.2%) | 110 (3.7%) | 24 (7.4%) | 0.09 |
Values are n (%) or mean ± standard deviation (SD), or median (interquartile range). p-values in bold are statistically significant. ACS = acute coronary syndrome, BARC = Bleeding Academic Research Consortium, BMI = body mass index, CABG = coronary artery bypass graft, eGFR = estimated glomerular filtration rate, LVEF = left ventricular ejection fraction, PCI = percutaneous coronary intervention. * BARC 0 versus BARC 1&2. † BARC 0 versus BARC 3&5. ‡ BARC 1&2 versus BARC 3&5.
Baseline procedural characteristics.
| BARC 0 (n = 34,555) | BARC 1&2 (n = 3007) | BARC 3&5 (n = 324) | p-Value | |
|---|---|---|---|---|
| PROCEDURAL CHARACTERISTICS | ||||
| Door-to-balloon time (minutes), median (IQR) | 73.0 (46.0, 125.0) | 74.0 (47.0, 125.0) | 71.0 (47.0, 126.0) | 0.76 |
| Symptom-to-balloon time (minutes), median (IQR) | 234.0 (152.0, 507.0) | 246.5 (156.0, 541.0) | 217.0 (146.0, 488.0) | 0.28 |
| PCI indication, n (%) | - | - | - | - |
| 1 = Early Primary PCI for STEMI < 12 hours | 5336 (15.4%) | 574 (19.1%) | 127 (39.2%) | <0.001 *†‡ |
| 2 = Late Primary PCI for STEMI | 776 (2.2%) | 105 (3.5%) | 18 (5.6%) | <0.001 *†‡ |
| 3 = Thrombolytics for STEMI | 971 (2.8%) | 135 (4.5%) | 27 (8.3%) | <0.001 *†‡ |
| 4 = PCI post cardiac arrest or cardiogenic shock (non-MI) | 99 (0.3%) | 14 (0.5%) | 9 (2.8%) | <0.001 *†‡ |
| 5 = PCI for ACS other than STEMI | 11,897 (34.4%) | 1083 (36.0%) | 89 (27.5%) | <0.001 *†‡ |
| 6 = Stable angina | 12,916 (37.4%) | 925 (30.8%) | 41 (12.7%) | <0.001 *†‡ |
| 7 = Other | 2560 (7.4%) | 171 (5.7%) | 13 (4.0%) | <0.001 *†‡ |
| Femoral percutaneous entry, n (%) | 16,710 (48.4%) | 1772 (58.9%) | 218 (67.3%) | <0.001 *†‡ |
| Radial percutaneous entry, n (%) | 17,789 (51.5%) | 1232 (41.0%) | 101 (31.2%) | <0.001 *†‡ |
| Intra-vascular ultrasound, n (%) | 334 (1.0%) | 88 (2.9%) | 7 (2.2%) | <0.001 *† |
| Thrombus aspiration device, n (%) | 1327 (3.8%) | 165 (5.5%) | 42 (13.0%) | <0.001 *†‡ |
| Fractional flow reserve, n (%) | 934 (2.7%) | 72 (2.4%) | 7 (2.2%) | 0.51 |
| Procedural intubation required, n (%) | 262 (0.8%) | 43 (1.4%) | 34 (10.5%) | <0.001 *†‡ |
| Intra-aortic balloon pump (IABP), n (%) | 116 (0.3%) | 22 (0.7%) | 18 (5.6%) | <0.001 *†‡ |
| Extracorporeal mechanical support, n (%) | 12 (0.0%) | 3 (0.1%) | 14 (4.3%) | <0.001 †‡ |
| Location of PCI, n (%) | - | - | - | - |
| LAD artery | 13,962 (40.4%) | 1237 (41.1%) | 148 (45.7%) | 0.12 |
| RCA | 10,701 (31.0%) | 997 (33.2%) | 118 (36.4%) | 0.006 *† |
| LCx artery | 5383 (15.6%) | 441 (14.7%) | 38 (11.7%) | 0.07 |
| LMCA | 600 (1.7%) | 75 (2.5%) | 17 (5.2%) | <0.001 *†‡ |
| Graft vessel | 668 (1.9%) | 75 (2.5%) | 3 (0.9%) | 0.042 * |
| Other: PCI on any other vessel | 7349 (21.3%) | 564 (18.8%) | 58 (17.9%) | 0.002 * |
| Coronary lesion type, n (%) total | - | - | - | - |
| Type A | 3788 (11.0%) | 378 (12.6%) | 29 (9.0%) | 0.013 * |
| Type B1 | 12,977 (37.6%) | 1211 (40.3%) | 93 (28.7%) | <0.001 *†‡ |
| Type B2/C | 20,031 (58.0%) | 1650 (54.9%) | 225 (69.4%) | <0.001 *†‡ |
| Stent thrombosis, n (%) | 361 (1.0%) | 36 (1.2%) | 16 (4.9%) | <0.001 †‡ |
| Type of stent(s), n (%) total | - | - | - | - |
| None | 2143 (6.2%) | 218 (7.2%) | 47 (14.5%) | <0.001 †‡ |
| Bare metal stent | 3696 (10.7%) | 310 (10.3%) | 64 (19.8%) | <0.001 †‡ |
| Drug eluting stent | 28,230 (81.7%) | 2441 (81.2%) | 209 (64.5%) | <0.001 †‡ |
| Type of balloon(s) used, n (%) total | - | - | - | - |
| No balloon | 32,400 (93.8%) | 2794 (92.9%) | 279 (86.1%) | <0.001 †‡ |
| Plain balloon | 1954 (5.7%) | 194 (6.5%) | 44 (13.6%) | <0.001 †‡ |
| Drug eluting balloon | 206 (0.6%) | 21 (0.7%) | 1 (0.3%) | 0.62 |
| Multivessel PCI, n (%) | 2037 (5.9%) | 181 (6.0%) | 30 (9.3%) | 0.038 †‡ |
Values are n (%) or mean ± SD, or median (interquartile range). P-values in bold are statistically significant. ACS = acute coronary syndrome, BARC = Bleeding Academic Research Consortium, LAD = left anterior descending, LCx = left circumflex, LMCA = left main coronary artery, MI = myocardial infarction, PCI = percutaneous coronary intervention, RCA = right coronary artery, STEMI = ST-elevation myocardial infarction. * BARC 0 versus BARC 1&2. † BARC 0 versus BARC 3&5. ‡ BARC 1&2 versus BARC 3&5.
In-hospital outcomes and outcomes up to 30 days.
| BARC 0 | BARC 1&2 | BARC 3&5 | p-Value | |
|---|---|---|---|---|
| IN-HOSPITAL OUTCOMES | ||||
| Length of stay (days), mean ± SD | 2.0 (1.0, 4.0) | 3.0 (1.0, 5.0) | 8.5 (5.0, 16.5) | <0.001 *†‡ |
| New renal impairment, n (%) | 668 (1.9%) | 169 (5.6%) | 82 (25.3%) | <0.001 *†‡ |
| New requirement for dialysis, n (%) | 91 (0.3%) | 24 (0.8%) | 38 (11.7%) | <0.001 *†‡ |
| Cardiogenic shock, n (%) | 500 (1.4%) | 86 (2.9%) | 78 (24.1%) | <0.001 *†‡ |
| Recurrent myocardial infarction, n (%) | 236 (0.7%) | 38 (1.3%) | 17 (5.2%) | <0.001 *†‡ |
| PCI, n (%) | 986 (2.9%) | 139 (4.6%) | 9 (2.8%) | <0.001 * |
| Planned PCI, n (%) | 847 (2.5%) | 112 (3.7%) | 5 (1.5%) | 0.015 †‡ |
| TVR (PCI), n (%) | 198 (0.6%) | 38 (1.3%) | 2 (0.6%) | 0.14 |
| TLR, n (%) | 160 (0.5%) | 28 (0.9%) | 1 (0.3%) | 0.36 |
| CABG, n (%) | 188 (0.5%) | 43 (1.4%) | 41 (12.7%) | <0.001 *†‡ |
| Planned CABG, n (%) | 94 (0.3%) | 24 (0.8%) | 10 (3.1%) | 0.005 †‡ |
| TVR (CABG), n (%) | 129 (0.4%) | 25 (0.8%) | 26 (8.0%) | 0.39 |
| Definite stent thrombosis n (%) | 62 (0.2%) | 17 (0.6%) | 3 (0.9%) | <0.001 *†‡ |
| Probable stent thrombosis n (%) | 24 (0.1%) | 5 (0.2%) | 2 (0.6%) | <0.001 *†‡ |
| Possible stent thrombosis n (%) | 9 (0.0%) | 3 (0.1%) | 3 (0.9%) | <0.001 *†‡ |
| No stent thrombosis n (%) | 34,460 (99.7%) | 2982 (99.2%) | 316 (97.5%) | <0.001 *†‡ |
| Stroke, n (%) | - | - | - | - |
| Haemorrhagic | 11 (0.0%) | 7 (0.2%) | 17 (5.2%) | <0.001 †‡ |
| Ischaemic | 56 (0.2%) | 12 (0.4%) | 5 (1.5%) | <0.001 †‡ |
| Mortality, n (%) | 555 (1.6%) | 89 (3.0%) | 73 (22.5%) | <0.001 *†‡ |
| MACE, n (%) | 882 (2.6%) | 156 (5.2%) | 88 (27.2%) | <0.001 *†‡ |
| MACCE, n (%) | 932 (2.7%) | 168 (5.6%) | 100 (30.9%) | <0.001 *†‡ |
| OUTCOMES UP TO 30 DAYS (EXCLUDING IN-HOSPITAL OUTCOMES) | ||||
| New heart failure, n (%) | 261 (0.8%) | 54 (1.8%) | 12 (3.7%) | <0.001 *†‡ |
| 30-day myocardial infarction, n (%) | 150 (0.4%) | 17 (0.6%) | 1 (0.3%) | <0.001 *†‡ |
| 30-day definite stent thrombosis, n (%) | 82 (0.2%) | 7 (0.2%) | 1 (0.3%) | <0.001 *†‡ |
| 30-day probable stent thrombosis, n (%) | 9 (0.0%) | - | 2 (0.6%) | <0.001 *†‡ |
| 30-day possible stent thrombosis, n (%) | 12 (0.0%) | 4 (0.1%) | - | <0.001 *†‡ |
| 30-day stroke, n (%) | - | - | - | - |
| 1 = Haemorrhagic | 9 (0.0%) | 3 (0.1%) | - | 0.36 |
| 2 = Ischaemic | 30 (0.1%) | 2 (0.1%) | - | 0.36 |
| Rehospitalisation, n (%) | 4339 (12.6%) | 368 (12.2%) | 51 (15.7%) | <0.001 *†‡ |
| Cardiac readmission, n (%) | 2941 (8.5%) | 230 (7.6%) | 19 (5.9%) | <0.001 *†‡ |
| 30-day Mortality, n (%) | 169 (0.5%) | 22 (0.7%) | 7 (2.2%) | <0.001 *†‡ |
| Cardiac Mortality, n (%) | 72 (0.2%) | 10 (0.3%) | 3 (0.9%) | 0.54 |
| 30-day MACE, n (%) | 438 (1.3%) | 47 (1.6%) | 8 (3.4%) | 0.007 *†‡ |
| 30-day MACCE, n (%) | 472 (1.4%) | 51 (1.8%) | 7 (3.1%) | 0.03 *†‡ |
Values are n (%) or mean ± SD, or median (interquartile range). p-values in bold are statistically significant. CABG = coronary artery bypass graft, MACE = major adverse cardiac events, MACCE = major adverse cardiac or cerebrovascular events, PCI = percutaneous coronary intervention, TVR = target vessel revascularization, TLR = target lesion revascularization. * BARC 0 versus BARC 1&2. † BARC 0 versus BARC 3&5. ‡ BARC 1&2 versus BARC 3&5.
Medications at discharge from hospital.
| BARC 0 | BARC 1&2 | BARC 3&5 | p-Value | |
|---|---|---|---|---|
| Aspirin, n (%) | 33,014 (95.5%) | 2841 (94.5%) | 232 (71.6%) | <0.001 †‡ |
| Thienopyridine, n (%) | 17,868 (51.7%) | 1370 (45.6%) | 119 (36.7%) | <0.001 *†‡ |
| Ticagrelor, n (%) | 15,470 (44.8%) | 1468 (48.8%) | 95 (29.3%) | <0.001 *†‡ |
| Beta blockers, n (%) | 23,390 (67.7%) | 2213 (73.6%) | 198 (61.1%) | <0.001 *† |
| ACE-I/ARB*, n (%) | 24,211 (70.1%) | 2193 (72.9%) | 159 (49.1%) | <0.001 *†‡ |
| Statin, n (%) | 24,211 (70.1%) | 2193 (72.9%) | 159 (49.1%) | <0.001 *†‡ |
| Other dyslipidaemia medications, n (%) | 2745 (7.9%) | 212 (7.1%) | 18 (5.6%) | 0.12 |
| Oral anticoagulation, n (%) | 2425 (7.0%) | 226 (7.5%) | 33 (10.2%) | <0.001 *†‡ |
Values are n (%) or mean +/− SD, or median (interquartile range). p-values in bold are statistically significant. ACE-I = angiotensin converting enzyme inhibitors, ARB = angiotensin receptor blockades. * BARC 0 versus BARC 1&2. † BARC 0 versus BARC 3&5. ‡ BARC 1&2 versus BARC 3&5.
Appendix A
Bleeding Academic Research Consortium (BARC) definition of PCI-related bleeding [
| Type | Definition |
|---|---|
| 0 | No bleeding |
| 1 | Bleeding that is not actionable and does not cause the patient to seek unscheduled performance of studies, hospitalisation, or treatment by a healthcare professional. May include episodes leading to self-discontinuation of medical therapy by the patient without consulting a healthcare professional |
| 2 | Any overt, actionable sign of haemorrhage (e.g., more bleeding than would be expected for a clinical circumstance, including bleeding found by imaging alone) that does not fit the criteria for type 3, 4, or 5, but does meet at least one of the following criteria: (1) requiring nonsurgical, medical intervention by a healthcare professional, (2) leading to hospitalisation or increased level of care, or (3) prompting evaluation |
| 3 a |
|
| 3 b |
|
| 3 c |
|
| 4 |
|
| 5 a | Probable fatal bleeding: no autopsy or imaging confirmation but clinically suspicious |
| 5 b | Definite fatal bleeding: overt bleeding or autopsy or imaging confirmation |
References
1. Vranckx, P.; Frigoli, E.; Rothenbuhler, M.; Tomassini, F.; Garducci, S.; Ando, G.; Picchi, A.; Sganzerla, P.; Paggi, A.; Ugo, F. et al. Radial versus femoral access in patients with acute coronary syndromes with or without ST-segment elevation. Eur. Heart J.; 2017; 38, pp. 1069-1080. [DOI: https://dx.doi.org/10.1093/eurheartj/ehx048]
2. Ndrepepa, G.; Neumann, F.J.; Richardt, G.; Schulz, S.; Tolg, R.; Stoyanov, K.M.; Gick, M.; Ibrahim, T.; Fiedler, K.A.; Berger, P.B. et al. Prognostic value of access and non-access sites bleeding after percutaneous coronary intervention. Circ. Cardiovasc. Interv.; 2013; 6, pp. 354-361. [DOI: https://dx.doi.org/10.1161/CIRCINTERVENTIONS.113.000433]
3. Kwok, C.S.; Khan, M.A.; Rao, S.V.; Kinnaird, T.; Sperrin, M.; Buchan, I.; de Belder, M.A.; Ludman, P.F.; Nolan, J.; Loke, Y.K. et al. Access and non-access site bleeding after percutaneous coronary intervention and risk of subsequent mortality and major adverse cardiovascular events: Systematic review and meta-analysis. Circ. Cardiovasc. Interv.; 2015; 8, e001645. [DOI: https://dx.doi.org/10.1161/CIRCINTERVENTIONS.114.001645] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/25825007]
4. Kinnaird, T.; Anderson, R.; Ossei-Gerning, N.; Gallagher, S.; Large, A.; Strange, J.; Ludman, P.; de Belder, M.; Nolan, J.; Hildick-Smith, D. et al. Vascular Access Site and Outcomes among 26,807 Chronic Total Coronary Occlusion Angioplasty Cases from the British Cardiovascular Interventions Society National Database. JACC Cardiovasc. Interv.; 2017; 10, pp. 635-644. [DOI: https://dx.doi.org/10.1016/j.jcin.2016.11.055] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/28385401]
5. Komocsi, A.; Aradi, D.; Kehl, D.; Ungi, I.; Thury, A.; Pinter, T.; Di Nicolantonio, J.J.; Tornyos, A.; Vorobcsuk, A. Meta-analysis of randomized trials on access site selection for percutaneous coronary intervention in ST-segment elevation myocardial infarction. Arch. Med. Sci.; 2014; 10, pp. 203-212. [DOI: https://dx.doi.org/10.5114/aoms.2014.42570]
6. Ferrante, G.; Rao, S.V.; Juni, P.; Da Costa, B.R.; Reimers, B.; Condorelli, G.; Anzuini, A.; Jolly, S.S.; Bertrand, O.F.; Krucoff, M.W. et al. Radial Versus Femoral Access for Coronary Interventions Across the Entire Spectrum of Patients With Coronary Artery Disease: A Meta-Analysis of Randomized Trials. JACC Cardiovasc. Interv.; 2016; 9, pp. 1419-1434. [DOI: https://dx.doi.org/10.1016/j.jcin.2016.04.014] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/27372195]
7. Karrowni, W.; Vyas, A.; Giacomino, B.; Schweizer, M.; Blevins, A.; Girotra, S.; Horwitz, P.A. Radial versus femoral access for primary percutaneous interventions in ST-segment elevation myocardial infarction patients: A meta-analysis of randomized controlled trials. JACC Cardiovasc. Interv.; 2013; 6, pp. 814-823. [DOI: https://dx.doi.org/10.1016/j.jcin.2013.04.010]
8. Valgimigli, M.; Gagnor, A.; Calabro, P.; Frigoli, E.; Leonardi, S.; Zaro, T.; Rubartelli, P.; Briguori, C.; Ando, G.; Repetto, A. et al. Radial versus femoral access in patients with acute coronary syndromes undergoing invasive management: A randomised multicentre trial. Lancet; 2015; 385, pp. 2465-2476. [DOI: https://dx.doi.org/10.1016/S0140-6736(15)60292-6]
9. Wlodarczyk, J.; Ajani, A.E.; Kemp, D.; Andrianopoulos, N.; Brennan, A.L.; Duffy, S.J.; Clark, D.J.; Reid, C.M. Incidence, Predictors and Outcomes of Major Bleeding in Patients Following Percutaneous Coronary Interventions in Australia. Heart Lung Circ.; 2016; 25, pp. 107-117. [DOI: https://dx.doi.org/10.1016/j.hlc.2015.06.826]
10. Pilgrim, T.; Windecker, S. Antiplatelet therapy for secondary prevention of coronary artery disease. Heart; 2014; 100, pp. 1750-1756. [DOI: https://dx.doi.org/10.1136/heartjnl-2013-305399]
11. Mehran, R.; Rao, S.V.; Bhatt, D.L.; Gibson, C.M.; Caixeta, A.; Eikelboom, J.; Kaul, S.; Wiviott, S.D.; Menon, V.; Nikolsky, E. et al. Standardized bleeding definitions for cardiovascular clinical trials: A consensus report from the Bleeding Academic Research Consortium. Circulation; 2011; 123, pp. 2736-2747. [DOI: https://dx.doi.org/10.1161/CIRCULATIONAHA.110.009449] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/21670242]
12. Ryan, T.J.; Faxon, D.P.; Gunnar, R.M.; Kennedy, J.W.; King, S.B., 3rd; Loop, F.D.; Peterson, K.L.; Reeves, T.J.; Williams, D.O.; Winters, W.L., Jr. et al. Guidelines for percutaneous transluminal coronary angioplasty. A report of the American College of Cardiology/American Heart Association Task Force on Assessment of Diagnostic and Therapeutic Cardiovascular Procedures (Subcommittee on Percutaneous Transluminal Coronary Angioplasty). Circulation; 1988; 78, pp. 486-502. [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/2969312]
13. Noaman, S.; Goh, C.Y.; Vogrin, S.; Brennan, A.L.; Andrianopoulos, N.; Dinh, D.T.; Lefkovits, J.; Reid, C.M.; Walton, A.; Al-Mukhtar, O. et al. Comparison of short-term clinical outcomes of proximal versus nonproximal lesion location in patients treated with primary percutaneous coronary intervention for ST-elevation myocardial infarction: The PROXIMITI study. Catheter. Cardiovasc. Interv.; 2019; 93, pp. 32-40. [DOI: https://dx.doi.org/10.1002/ccd.27665] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/30019827]
14. Rao, S.V.; Eikelboom, J.A.; Granger, C.B.; Harrington, R.A.; Califf, R.M.; Bassand, J.P. Bleeding and blood transfusion issues in patients with non-ST-segment elevation acute coronary syndromes. Eur. Heart J.; 2007; 28, pp. 1193-1204. [DOI: https://dx.doi.org/10.1093/eurheartj/ehm019] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/17456480]
15. Numasawa, Y.; Kohsaka, S.; Ueda, I.; Miyata, H.; Sawano, M.; Kawamura, A.; Noma, S.; Suzuki, M.; Nakagawa, S.; Momiyama, Y. et al. Incidence and predictors of bleeding complications after percutaneous coronary intervention. J. Cardiol.; 2017; 69, pp. 272-279. [DOI: https://dx.doi.org/10.1016/j.jjcc.2016.05.003]
16. Idris, H.; French, J.K.; Shugman, I.M.; Hopkins, A.P.; Juergens, C.P.; Thomas, L. Influence of Age and Gender on Clinical Outcomes Following Percutaneous Coronary Intervention for Acute Coronary Syndromes. Heart Lung Circ.; 2017; 26, pp. 554-565. [DOI: https://dx.doi.org/10.1016/j.hlc.2016.10.021]
17. D’Ascenzo, F.; Grosso, A.; Abu-Assi, E.; Kinnaird, T.; Ariza-Sole, A.; Manzano-Fernandez, S.; Templin, C.; Velicki, L.; Xanthopoulou, I.; Cerrato, E. et al. Incidence and predictors of bleeding in ACS patients treated with PCI and prasugrel or ticagrelor: An analysis from the RENAMI registry. Int. J. Cardiol.; 2018; 273, pp. 29-33. [DOI: https://dx.doi.org/10.1016/j.ijcard.2018.09.020]
18. Kwok, C.S.; Rao, S.V.; Myint, P.K.; Keavney, B.; Nolan, J.; Ludman, P.F.; de Belder, M.A.; Loke, Y.K.; Mamas, M.A. Major bleeding after percutaneous coronary intervention and risk of subsequent mortality: A systematic review and meta-analysis. Open Heart; 2014; 1, e000021. [DOI: https://dx.doi.org/10.1136/openhrt-2013-000021]
19. Moscucci, M.; Fox, K.A.; Cannon, C.P.; Klein, W.; Lopez-Sendon, J.; Montalescot, G.; White, K.; Goldberg, R.J. Predictors of major bleeding in acute coronary syndromes: The Global Registry of Acute Coronary Events (GRACE). Eur. Heart J.; 2003; 24, pp. 1815-1823. [DOI: https://dx.doi.org/10.1016/S0195-668X(03)00485-8]
20. Chhatriwalla, A.K.; Amin, A.P.; Kennedy, K.F.; House, J.A.; Cohen, D.J.; Rao, S.V.; Messenger, J.C.; Marso, S.P. National Cardiovascular Data Registry. Association between bleeding events and in-hospital mortality after percutaneous coronary intervention. JAMA; 2013; 309, pp. 1022-1029. [DOI: https://dx.doi.org/10.1001/jama.2013.1556]
21. Redfors, B.; Genereux, P.; Witzenbichler, B.; Kirtane, A.J.; McAndrew, T.; Weisz, G.; Stuckey, T.D.; Henry, T.D.; Maehara, A.; Mehran, R. et al. Bleeding Severity after Percutaneous Coronary Intervention. Circ. Cardiovasc. Interv.; 2018; 11, e005542. [DOI: https://dx.doi.org/10.1161/CIRCINTERVENTIONS.117.005542] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/29870382]
22. Ndrepepa, G.; Schuster, T.; Hadamitzky, M.; Byrne, R.A.; Mehilli, J.; Neumann, F.J.; Richardt, G.; Schulz, S.; Laugwitz, K.L.; Massberg, S. et al. Validation of the Bleeding Academic Research Consortium definition of bleeding in patients with coronary artery disease undergoing percutaneous coronary intervention. Circulation; 2012; 125, pp. 1424-1431. [DOI: https://dx.doi.org/10.1161/CIRCULATIONAHA.111.060871] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/22344040]
23. Vranckx, P.; White, H.D.; Huang, Z.; Mahaffey, K.W.; Armstrong, P.W.; Van de Werf, F.; Moliterno, D.J.; Wallentin, L.; Held, C.; Aylward, P.E. et al. Validation of BARC Bleeding Criteria in Patients with Acute Coronary Syndromes: The TRACER Trial. J. Am. Coll. Cardiol.; 2016; 67, pp. 2135-2144. [DOI: https://dx.doi.org/10.1016/j.jacc.2016.02.056] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/27151345]
24. Rao, S.V.; Dai, D.; Subherwal, S.; Weintraub, W.S.; Brindis, R.S.; Messenger, J.C.; Lopes, R.D.; Peterson, E.D. Association between periprocedural bleeding and long-term outcomes following percutaneous coronary intervention in older patients. JACC Cardiovasc. Interv.; 2012; 5, pp. 958-965. [DOI: https://dx.doi.org/10.1016/j.jcin.2012.05.010] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/22995883]
25. Kunadian, V.; Qiu, W.; Lagerqvist, B.; Johnston, N.; Sinclair, H.; Tan, Y.; Ludman, P.; James, S.; Sarno, G. National Institute for Cardiovascular Outcomes Researchet al. Gender Differences in Outcomes and Predictors of All-Cause Mortality after Percutaneous Coronary Intervention (Data from United Kingdom and Sweden). Am. J. Cardiol.; 2017; 119, pp. 210-216. [DOI: https://dx.doi.org/10.1016/j.amjcard.2016.09.052] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/27816119]
26. Manoukian, S.V.; Feit, F.; Mehran, R.; Voeltz, M.D.; Ebrahimi, R.; Hamon, M.; Dangas, G.D.; Lincoff, A.M.; White, H.D.; Moses, J.W. et al. Impact of major bleeding on 30-day mortality and clinical outcomes in patients with acute coronary syndromes: An analysis from the ACUITY Trial. J. Am. Coll. Cardiol.; 2007; 49, pp. 1362-1368. [DOI: https://dx.doi.org/10.1016/j.jacc.2007.02.027]
27. Kinnaird, T.D.; Stabile, E.; Mintz, G.S.; Lee, C.W.; Canos, D.A.; Gevorkian, N.; Pinnow, E.E.; Kent, K.M.; Pichard, A.D.; Satler, L.F. et al. Incidence, predictors, and prognostic implications of bleeding and blood transfusion following percutaneous coronary interventions. Am. J. Cardiol.; 2003; 92, pp. 930-935. [DOI: https://dx.doi.org/10.1016/S0002-9149(03)00972-X]
28. Chew, D.P.; Scott, I.A.; Cullen, L.; French, J.K.; Briffa, T.G.; Tideman, P.A.; Woodruffe, S.; Kerr, A.; Branagan, M.; Aylward, P.E. et al. National Heart Foundation of Australia & Cardiac Society of Australia and New Zealand: Australian Clinical Guidelines for the Management of Acute Coronary Syndromes 2016. Heart Lung Circ.; 2016; 25, pp. 895-951.
29. Bellemain-Appaix, A.; Brieger, D.; Beygui, F.; Silvain, J.; Pena, A.; Cayla, G.; Barthelemy, O.; Collet, J.P.; Montalescot, G. New P2 Y12 inhibitors versus clopidogrel in percutaneous coronary intervention: A meta-analysis. J. Am. Coll. Cardiol.; 2010; 56, pp. 1542-1551. [DOI: https://dx.doi.org/10.1016/j.jacc.2010.07.012]
30. Chan, W.; Ajani, A.E.; Clark, D.J.; Stub, D.; Andrianopoulos, N.; Brennan, A.L.; New, G.; Sebastian, M.; Johnston, R.; Walton, A. et al. Impact of periprocedural atrial fibrillation on short-term clinical outcomes following percutaneous coronary intervention. Am. J. Cardiol.; 2012; 109, pp. 471-477. [DOI: https://dx.doi.org/10.1016/j.amjcard.2011.10.004]
31. Yudi, M.B.; Clark, D.J.; Farouque, O.; Eccleston, D.; Andrianopoulos, N.; Duffy, S.J.; Brennan, A.; Lefkovits, J.; Ramchand, J.; Yip, T. et al. Clopidogrel, prasugrel or ticagrelor in patients with acute coronary syndromes undergoing percutaneous coronary intervention. Intern. Med. J.; 2016; 46, pp. 559-565. [DOI: https://dx.doi.org/10.1111/imj.13041]
32. Urban, P.; Mehran, R.; Colleran, R.; Angiolillo, D.J.; Byrne, R.A.; Capodanno, D.; Cuisset, T.; Cutlip, D.; Eerdmans, P.; Eikelboom, J. et al. Defining High Bleeding Risk in Patients Undergoing Percutaneous Coronary Intervention. Circulation; 2019; 140, pp. 240-261. [DOI: https://dx.doi.org/10.1161/CIRCULATIONAHA.119.040167]
33. Spencer, F.A.; Moscucci, M.; Granger, C.B.; Gore, J.M.; Goldberg, R.J.; Steg, P.G.; Goodman, S.G.; Budaj, A.; FitzGerald, G.; Fox, K.A. et al. Does comorbidity account for the excess mortality in patients with major bleeding in acute myocardial infarction?. Circulation; 2007; 116, pp. 2793-2801. [DOI: https://dx.doi.org/10.1161/CIRCULATIONAHA.107.694273] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/18025530]
34. Doyle, B.J.; Rihal, C.S.; Gastineau, D.A.; Holmes, D.R., Jr. Bleeding, blood transfusion, and increased mortality after percutaneous coronary intervention: Implications for contemporary practice. J. Am. Coll. Cardiol.; 2009; 53, pp. 2019-2027. [DOI: https://dx.doi.org/10.1016/j.jacc.2008.12.073] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/19477350]
35. Holroyd, E.W.; Mustafa, A.H.; Khoo, C.W.; Butler, R.; Fraser, D.G.; Nolan, J.; Mamas, M.A. Major Bleeding and Adverse Outcome following Percutaneous Coronary Intervention. Interv. Cardiol.; 2015; 10, pp. 22-25. [DOI: https://dx.doi.org/10.15420/icr.2015.10.1.22] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/29588669]
36. Najjar, S.S.; Rao, S.V.; Melloni, C.; Raman, S.V.; Povsic, T.J.; Melton, L.; Barsness, G.W.; Prather, K.; Heitner, J.F.; Kilaru, R. et al. Intravenous erythropoietin in patients with ST-segment elevation myocardial infarction: REVEAL: A randomized controlled trial. JAMA; 2011; 305, pp. 1863-1872. [DOI: https://dx.doi.org/10.1001/jama.2011.592] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/21558517]
37. Neumann, F.J.; Sousa-Uva, M.; Ahlsson, A.; Alfonso, F.; Banning, A.P.; Benedetto, U.; Byrne, R.A.; Collet, J.P.; Falk, V.; Head, S.J. et al. 2018 ESC/EACTS Guidelines on myocardial revascularization. Kardiol. Pol.; 2018; 76, pp. 1585-1664. [DOI: https://dx.doi.org/10.5603/KP.2018.0228]
38. Biswas, S.; Duffy, S.J.; Lefkovits, J.; Andrianopoulos, N.; Brennan, A.; Walton, A.; Chan, W.; Noaman, S.; Shaw, J.A.; Dawson, L. et al. Australian Trends in Procedural Characteristics and Outcomes in Patients Undergoing Percutaneous Coronary Intervention for ST-Elevation Myocardial Infarction. Am. J. Cardiol.; 2018; 121, pp. 279-288. [DOI: https://dx.doi.org/10.1016/j.amjcard.2017.10.025]
© 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
Details
; Noaman, Samer 3 ; Dinh, Diem T 4 ; Brennan, Angela L 4 ; Lefkovits, Jeffrey 4 ; Reid, Christopher M 5 ; Cox, Nicholas 6 ; Chan, William 3 1 Department of Medicine, University of Melbourne, Melbourne 3010, Victoria, Australia;
2 Department of Medicine-Western Health, Melbourne Medical School, University of Melbourne, Melbourne 3010, Victoria, Australia;
3 Department of Medicine, University of Melbourne, Melbourne 3010, Victoria, Australia;
4 School of Public Health & Preventive Medicine, Monash University, Melbourne 3004, Victoria, Australia;
5 School of Public Health & Preventive Medicine, Monash University, Melbourne 3004, Victoria, Australia;
6 Department of Cardiology, Western Health, St Albans 3021, Victoria, Australia;