Pascal Meier1,2, Alexandra J Lansky1, Andreas Baumbach3
Received 12 July 2013. Accepted 24 July 2013
1 Division of Cardiology, Yale Medical School, New Haven, Connecticut, USA
2 Yale—UCL Cardiovascular Research Programme, The Heart Hospital, University College London Hospitals UCLH, London, UK
3 Division of Cardiology, Bristol Heart Institute, Bristol, UK
* To cite: Meier P, Lansky AJ, Baumbach A. Heart Published Online First: doi:10.1136/heartjnl- 2013-304649
Pascal Meier, MD
Yale—UCL Cardiovascular Research Programme, The Heart Hospital, University College London Hospitals UCLH, UCLH16-18 Westmoreland Street, London W1G 8PH, UK; [email protected]
Abstract: Unstable coronary artery plaque is the most common underlying cause of acute coronary syndromes (ACS) and can manifest as unstable angina, non-ST segment elevation infarction (NSTE-ACS), and ST elevation myocardial infarction (STEMI), but can also manifest as sudden cardiac arrest due to ischaemia induced tachyarrhythmias. ACS mortality has decreased signiﬁcantly over the last few years, especially from the more extreme manifestations of ACS, STEMI, and cardiac arrest. This trend is likely to continue based on recent therapeutic progress which includes novel antiplatelet agents such as prasugrel, ticagrelor, and cangrelor.
In the USA every year nearly 1.2 million patients are hospitalized for acute coronary syndrome (ACS)1. However, the proportion of ACS with ST elevation myocardial infarction (STEMI) appears to be decli-ning2,3. We can only speculate upon the reasons: potential explanations include the reduction in smoking, the age structure of the population (STEMI is more common in middle age while non-ST segment elevation (NSTE-ACS) occurs more in the elderly), and broader use of statin therapy. Over the last few years there has been a signiﬁcant improvement in outcomes after STEMI in regard to mortality, cardiogenic shock, and heart failure1. Similar trends have been seen for other manifestations of ACS, such as sudden cardiac arrest (SCA)4,5. Astonishingly, the clinical outcomes for NSTE-ACS now appear to be worse than for STEMI. However, such ﬁgures are misleading, and short term (in-hospital) outcome is still better for NSTE-ACS than for STEMI, while the longer term mortality rate is higher for NSTE-ACS, but this is probably inﬂuenced by the different age and risk structure of the STEMI and NSTE-ACS populations: NSTE-ACS patients are generally older and often have multivessel (MV) coronary artery disease (CAD).
ST ELEVATION MYOCARDIAL INFARCTION
A major reason for the improved outcomes for STEMI over the last decades has been the increasing availability of primary percutaneous coronary intervention (PCI) services, which all try to continuously improve their performance (‘door-to-balloon time’). Initiatives include telemetric transmission of ECGs from the ambulance services, and training of ambulance staff in ECG interpretation. More important than door-to-balloon time is of course the overall ‘symptom onset to balloon time’. Patients have become much better informed about symptoms of ‘heart attacks’, and many ambulance services transfer patients with a suspected STEMI directly to a primary PCI service rather than going to the nearest hospital.
PRIMARY PERCUTANEOUS CORONARY INTERVENTION
Not only has the rate of primary PCI increased over the years, but progress in device technologies and adjunctive pharmacology has also improved the pro- cedural success rate – for example, the availability of stents and second generation drug eluting stents, thrombus aspiration devices, and safer and more effective periprocedural anticoagulation/antiplatelet treatments. Thrombus aspiration has been shown to improve outcomes in smaller randomized trials and is currently recommended by European and American PCI guidelines. However, its effect should probably not be overrated. A recent large scale randomized trial in 452 patients, INFUSE-AMI (Intracoronary Abciximab and Aspiration Thrombectomy in Patients with Large Anterior Myocardial Infarction) did not demonstrate an effect of manual thrombus aspiration on infarct size when used in conjunction with bivalirudin (and intracoronary abciximab)6,7. Intravenous glycoprotein (Gp) IIb/IIIa inhibitors have an immediate and potent platelet inhibitory effect and certainly improve thrombus resolution; they may reduce infarct size6 while their effect on clinical outcomes is somewhat more debatable. Bivalirudin, a direct thrombin inhibitor, which has anticoagulant and probably also antiplatelet effects (via suppression of thrombin dependent platelet activation8), can be used as an alternative to heparin and Gp IIb/IIIa inhibitors, and has shown reduced bleeding and even reduced mortality in the HORIZON-AMI trial (Heparin plus a glycoprotein IIb/IIIa Inhibitor versus Bivalirudin Monotherapy and Paclitaxel-Eluting Stents versus Bare-Metal Stents in Acute Myocardial Infarction)6. Bleeding reduction has become a key aim in primary PCI because of the well documented (but less well understood) association with increased mortality (Table 1).
Table 1. Bleeding avoidance strategies9
|Radial instead of femoral access||Reduces access site bleeding risk (and potentially also mortality in high risk groups)|
|Bivalirudin||Bivalirudin superior to heparin and glycoprotein IIb/IIIa inhibitors, reduces bleeding (and reduces mortality in STEMI patients)|
|Fluoroscopy guided puncture for femoral access||High (or low) puncture to be avoided. The femoral head has a consistent relationship with the common femoral artery, and localization using fluoroscopy is a useful landmark. However, randomized studies failed to show a clinical benefit but were underpowered
Fewer vascular complications with this approach in randomized trials
|Ultrasound guided puncture for femoral access||1347|
|Vascular closure devices||Controversial study results. Increasing evidence pointing towards a positive effect of vascular closure devices, especially if used with bivalirudin|
|Individualized bleeding risk assessment||Individualized risk assessment and adjustment of clinical practice using risk models, for example, NCDR CathPCI bleeding risk model (bivalirudin, radial access, etc)|
|NCDR, National Cardiovascular Database Registry; PCI, percutaneous coronary interventions; STEMI, ST elevation myocardial infarction.|
Transradial versus transfemoral access
Another rather elegant option used increasingly, which may reduce bleeding, involves the transradial approach instead of the traditional transfemoral access9. An increasing wealth of data indicate that this reduces bleeding in general; some data even suggest that it reduces mortality when used for primary PCI, but the latter effect is debatable10,11. A recent meta-analysis of nine studies involving 2977 patients with STEMI demonstrated an impressive nearly 50% reduction in mortality for the transradial approach (OR 0.53, 95% CI 0.33 to 0.84; p=0.008)10. While the authors concluded that the transradial approach should be preferred in STEMI patients, an accompanying editorial high- lighted some limitations of these data11. Some data indicate a negative impact of transradial PCI. Baklanov et al12 showed a longer median door-to-balloon time with transradial PCI. Another retrospective comparison by Cafri et al13, however, showed similar door-to-balloon time irrespective of the access route. Even in elderly people, where there is more advanced athero- sclerosis, the radial access does not seem to delay reperfusion as it does not lead to any increase in the door-to-balloon time14. There have also been concerns that transradial access may increase the risk of neurological complications compared to transfemoral access. However, in a retrospective analysis of the British Cardiovascular Intervention Society database conducted between January 2006 and December 2010, Ratib et al15 have shown that there is no signiﬁcant association between the use of radial access and the occurrence of neurological complications.
Overall, transradial PCI is certainly a promising technique when used by experienced operators. However, despite its bene- ﬁts, its use is highly variable across countries. In France and Japan it is the predominant access route11. In the UK, its use increased nearly fourfold from 17.2% in 2006 to 57% in 201116. The USA has the lowest rate of radial access adoption
for PCI worldwide (only one in six PCIs)17. Even here, there has been an increase in use of radial access. In the ﬁrst quarter of 2007, 1.2% of PCIs were by the transradial approach; this increased to 16.1% in the third quarter of 2012. There is little doubt that the increasing use of transradial PCI has led to a reduction in access site complications12,16,17,18.
While some data indicate that the transradial route may reduce mortality in STEMI patients, this has not been demon- strated in NSTE-ACS. In the RIVAL (Radial vs Femoral Access for Coronary Intervention) trial, currently the largest randomized trial on this topic, there was no difference in major clinical outcomes in NSTE-ACS patients19. In a cohort of high risk NSTE-ACS patients enrolled in the EARLY-ACS trial (Early Glycoprotein IIb/IIIa Inhibition in non-ST-Segment Elevation Acute Coronary Syndrome), there were no signiﬁcant differ- ences in either bleeding or ischaemic outcomes whether radial or femoral access was used20.
A recent consensus statement by the European Society of Cardiology (ESC) states that a default radial approach is feasible in routine practice in both stable and unstable patients21. The ESC recommends performing transradial PCI in STEMI patients only after the operator has become familiar with this approach in stable patients and in diagnostic procedures.
Culprit lesion PCI
Culprit lesion only treatment versus a ‘complete revascularization’ approach remains the subject of some debate. One could argue either way: a complete revascularization strategy may improve overall myocardial perfusion in the critical initial phase; but on the other hand, we know that major adverse complications are increased during acute PCI, and this also may have an impact on the outcome following treatment of non-acute, non- culprit lesions. A randomized study of 214 patients showed that angioplasty of the culprit vessel only was associated with higher rates of adverse events (50.0%) during a mean follow up of 2.5 years than MV PCI, regardless of simultaneous complete revascularization (23.1%) or a staged complete revascularization (20.0%)22. A recent report of the Ibaraki Cardiovascular Assessment Study registry of Japan showed signiﬁcantly higher mortality with PCI of a non-culprit lesion in the same setting as the culprit lesion than with PCI of only the culprit lesion23. In contrast, results based of the American College of Cardiology National Cardiovascular Database Registry (NCDR-CathPCI) showed similar morbidity and mortality rates with either single vessel or MV PCI24. While these data were conﬂicting, most studies were non-randomized and need to be interpreted with caution. A large meta-analysis of 18 randomized controlled trials (RCTs), including the above mentioned RCT, involved 40 280 patients and showed that staged PCI was associated with lower short and long term mortality compared to culprit vessel PCI and MV PCI25. Therefore, current guidelines discourage the performance of multivessel PCI for STEMI and suggest that non-culprit lesions should be staged26,27. However, if STEMI patients present in cardiogenic shock or after an SCA, they should be considered for complete revascularization in one sitting.
The time effect
The current ESC guidelines recommend that STEMI patients should be immediately transported within 2 h of onset of symptoms to a PCI-capable center without delay28. In clinical practice, it is extremely difﬁcult to achieve this goal of symptom onset-to-balloon time29. System delays have been shown to be associated with mortality at a median follow-up of 3.4 years in STEMI patients treated with primary PCI30. In a more recent study, shorter symptom onset-to-balloon time predicted lower mortality in the long term31. A longer treatment delay was seen in females, patients living in a rural area >22 km from hospital, and when patients were admitted to the emergency department of the hospital instead of direct emergency medical services (EMS) transportation. Researchers suggest that a more generalised use of ambulance/EMS would reduce treatment delays and associated mortality.
Optimal duration of monitoring/hospital stay
The duration of hospital stay has decreased dramatically over the years, which has a major impact on health care expenditure and on patient quality of life. Current practice is widely variable across countries and centres, but it is unclear whether early hos- pital discharges are safe32. It is very reassuring that, despite the continuous reduction in hospital stay, outcomes have signiﬁcantly improved (Figure 1).
Two new studies have demonstrated that discharging low risk STEMI patients within 2 days following primary PCI is safe and feasible34,35. Over 40% of the STEMI patients in one of the studies met early discharge criteria34. An early discharge could lower healthcare costs considerably.
Based on the literature, we propose the following criteria to deﬁne low risk patients for early discharge:
1. Age <70 years
2. Short pain to reperfusion interval (<4 h)
3. Uncomplicated primary PCI with good result (TIMI (Thrombolysis in Myocardial Infarction) 3 ﬂow and prompt complete ST elevation resolution)
4. Left ventricular ejection fraction >45% without symptoms of heart failure
5. No signiﬁcant arrhythmias during the ﬁrst 24 h
6. Socially supported, collaborative/compliant patient.
NON-ST ELEVATION ACS
There is a great need for proper risk prediction in ACS patients for clinical decision making, especially with regard to coronary angiography. There are several risk prediction models in use. The Global Registry of Acute Coronary Events (GRACE) is among the most commonly used scores. Recently, a mini-GRACE (MG) risk score has been developed which excludes creatinine and Killip class from the original eight-factor GRACE risk model. The adjusted mini-GRACE (AMG) risk score includes ‘prescription of a loop diuretic during admission’ in place of Killip class and creatinine concentration. Both risk scores showed good accuracy in the Myocardial Ischemia National Audit Project (MINAP), with the AMG risk score performing somewhat better than the MG risk score36.
Laboratory markers may further help with this risk stratiﬁcation. The maximal troponin value in patients presenting with NSTE-ACS has been shown to be an independent predictor of in-hospital morbidity and mortality37. Other predictive markers include interleukin 10, myeloperoxidase, and placental growth factor38.
Role and timing of PCI in NSTE-ACS
For intermediate to high risk patients, there is strong evidence supporting routine angiography rather than conservative management. However, the optimal time for coronary angiography is not clear. Though an early invasive approach seems favorable, studies testing the timing effect used varying time points for ‘early’ and ‘delayed’ angiography. In very high risk patients such as those with refractory angina, severe heart failure, life threatening ventricular arrhythmias or haemodynamic instability or an evolving myocardial infarction (MI), an urgent invasive approach is indicated. For patients not belonging to this high risk category, the optimal timing is not clear. There is no clear beneﬁt with regard to ‘hard’ clinical end points for an early invasive strategy within 24 h, but an increasing number of centers undertake an early invasive strategy within 24 h for intermediate to high risk patients. Such an approach is probably reasonable, as an earlier approach certainly helps to reduce hospital stay. Factors such as diabetes, renal function, left ventricular function, recurrent symptoms, and previous revascularization should be considered along with the TIMI or GRACE score.
Intravascular imaging guided PCI is a concept that evolved when devices such as intravascular ultrasound (IVUS) and more recently optical coherence tomography (OCT) became available. There are two different modes of use, either for the pre-PCI assessment in order to better understand the coronary plaque (stable or unstable plaque, diameter and length, thrombus burden, etc), or for post-PCI assessment of stent expansion and apposition. The advantages are obvious; in contrast to angiography as an eyeballing tool, which allows measurement of luminal diameters in a few orthogonal views, coronary IVUS provides a tomographic view. Furthermore, the resolution is much better than for angiography.
The ﬁrst concept, pre-PCI assessment of lesions has been tested in the multicenter PROSPECT (Providing Regional Observations to Study Predictors of Events in the Coronary Tree) study39. This study showed that IVUS can be used to deﬁne characteristics of vulnerable plaques. The highest risk phenotypes associated with non-culprit major adverse cardiac events (MACE) included thin-cap ﬁbroatheromas, plaque burden >70%, and minimal lumen area <4.0 mm. However, these data are not sufﬁcient to advocate using IVUS derived plaque characteristics to decide whether a lesion needs to be treated40.
While IVUS is based on ultrasound, OCT is based on light, which has a much shorter wavelength, and therefore achieves 10-fold better spatial resolution compared to IVUS41.This allows better deﬁnition of the thin ﬁbrous caps and the circumferential extent of the necrotic cores. It helps detect other microstructural features such as cholesterol crystals, thrombus, calcium deposits, ﬁbrous plaques, and lipid-rich plaques42. OCT can visualize features not seen by IVUS such as intimal ﬂaps and defects in the intima, disruptions in the media, and stent strut apposition.
A Japanese study that analyzed the culprit lesion in AMI patients found that the incidence of plaque rupture observed by OCT was signiﬁcantly higher than that observed by both angio- scopy and IVUS43. OCT was also superior in detecting ﬁbrous cap erosion and thin cap ﬁbroatheroma, and OCT could also estimate the ﬁbrous cap thickness.
However, the depth of imaging penetration is limited to only a few millimeters with this new technique44. So, it is unable to image the adventitia and assess the plaque burden. Therefore, Alfonso et al45 had the idea of a combined use of OCT and IVUS in patients with stent thrombosis. Since image length was shorter with OCT, they suggested overlapping OCT runs to cir- cumvent the problem. The challenge of OCT is that it requires a ﬁeld clear of blood for imaging.
Because OCT has superior resolution to IVUS, it clearly recognizes stent struts on heavily calciﬁed areas which are difﬁ- cult to identify with IVUS. Post-intervention OCT also produces a sharper image of the neointimal-thrombus boundary and provides a reliable diagnosis of in-stent restenosis or neoatherosclerosis. In current practice, OCT and IVUS seem to complement each other with their respective advantages and disadvantages. However, we have to be aware that data on cli- nical outcomes are limited and that these techniques add to procedural costs.
Aspirin is still the basis of every antiplatelet therapy. However, dual antiplatelet therapy of aspirin and a P2Y12 receptor blocker is clearly more effective and clopidogrel is the most commonly used agent for this purpose at the moment. However, the problems with this treatment are the rather long delay until maximal platelet inhibition is reached and the high rate of poor responders46. One approach that has been tested repeatedly is triple antiplatelet therapy using cilostazol. Even though results of this approach have indicated some beneﬁt, it is rarely used47,48. One reason for this is probably the development of newer generation P2Y12 receptor blockers such as prasugrel, ticagrelor, and cangrelor. They block the binding of ADP to the platelet receptor P2Y12, thereby inhibiting platelet aggregation.
Naturally, we would expect that stronger antiplatelet inhibition comes with an increased bleeding risk. Many patients therefore receive proton pump inhibitors (PPI). However, the data do not completely following this logic.
Prasugrel: The TRITON-TIMI 38 trial was a head-to-head comparison between aspirin and prasugrel versus aspirin plus clopidogrel in 13 608 moderate to high risk ACS patients under-going PCI. In most cases, the study drug was given after coronary angiography. At 15 months follow-up, MACE (cardiovascular death, non-fatal MI, or non-fatal stroke) was reduced with prasugrel (9.9% vs 12.1%; HR 0.81, 95% CI 0.73 to 0.90) This composite end point was mainly driven by a reduction in non-fatal MI. Major bleeding was somewhat increased with prasugrel (2.4% vs 1.8%; HR 1.32, 95% CI to 1.68). Bleeding was mainly increased in those with a history of stroke or transient ischemic attack, age ≥75 years or a bodyweight ≤60 kg. The TRILOGY ACS trial tested prasugrel versus clopidogrel with NSTE-ACS not undergoing PCI. There was no statistically signiﬁcant difference in MACE rate (13.9% vs 16.0%; HR 0.91, 95% CI 0.79 to 1.05).
Ticagrelor: In contrast to clopidogrel and prasugrel, ticagrelor binds reversibly to the P2Y12 platelet receptor. This agent was tested in the PLATO trial (18 624 patients) in patients with ACS, and also those who did not undergo PCI but had medical therapy. Treatment was started early, at a median of 5 h after hospital admission. This study showed a reduced risk for MACE (deﬁned as cardiovascular death, MI, or stroke) in the ticagrelor arm (9.8% vs 11.7%, HR 0.84, 95% CI 0.77 to 0.92), and there was also a reduced risk for cardiovascular mortality as a single end point. Overall, there was no signiﬁcant difference in the rates of major bleeding between the ticagrelor and clopidogrel groups (11.6% vs 11.2%, respectively). However, there was a higher risk of non-coronary artery bypass surgery related major bleeding (4.5% vs 3.8%).
Cangrelor: In contrast to these drugs, cangrelor is administered intravenously. It has been tested against placebo and against clopidogrel. The CHAMPION-
PLATFORM trial (placebo control) was stopped early because an interim analysis showed disappointing results. The CHAMPION-PCI trial (clopidogrel as a comparator) failed to show a signiﬁcant beneﬁt as well. The most recent and largest study, the CHAMPION-PHOENIX trial, compared cangrelor against pre-loading with 300-600 mg of clopidogrel. This study not only included ACS but also patients with stable CAD. It found a reduced risk for ischemic events (death, MI, ischemia-driven revascularization or stent thrombosis) over the ﬁrst 48 h without any increase in major bleeding risk49. Its role in clinical practice in the context of having ticagrelor and prasugrel available is not clear yet, and it has never been compared against these agents.
With additional and more potent antiplatelet therapies now available, the challenge is to decide which agent to use and when. Currently, the decision is usually based on clinical and risk factors; pharmacogenetics may also play a role in guiding therapies in the future50.
Gastrointestinal (GI) bleeding is one of the more common risks of strong antiplatelet therapy. Therefore, PPI are often prescribed as well. A recent study found, interestingly, that lower GI bleeding is more common than upper GI bleeding in patients on PPI51. Furthermore, the impact of PPI on the clopidogrel effect has been a matter of controversy for some time. Laboratory studies have suggested a reduced antiplatelet effect if PPI are used. However, studies looking at clinical end points have shown conﬂicting results. A recent systematic review provides a very good overview, including 33 studies, and concludes that clinical data are highly conﬂicting but that even newer, better designed studies do not show evidence of a relevant adverse effect of PPI in patients on clopidogrel regarding clinical outcomes52.
SUDDEN CARDIAC ARREST
SCA is a less common but often fatal presentation of ACS53. While there are other reasons for SCA, especially in younger patients, the most common cause for tachyarrhythmic cardiac arrests in patients over 40 is myocardial ischemia4,37. Most of these cardiac arrests occur out of hospital (out-of-hospital cardiac arrest (OHCA)). Survival for OHCA patients has been poor for several decades, averaging <10% to hospital discharge, and may be even lower, particularly in remote areas. However, in recent years survival has increased, especially in metropolitan areas. The London Ambulance Service observed an increase in survival rates from 12% to 32% between 2007 and 20125.
We can only speculate about the reasons for this improvement since few single interventions have really proven to be effective54. It is therefore more likely that it is the combination of multiple effective treatments that is responsible for the observed improvements in survival. Early chest compressions and early deﬁbrillation are the undisputed game changers55. It is likely that the availability of public automatic deﬁbrillators, deﬁbrilla- tors of the EMS and public awareness, and an increasing number of lay people trained in chest compression, played major roles56.
However, other factors such as therapeutic hypothermia and immediate angiography to deﬁne and potentially treat the underlying cause are important as well57,58. An observational study of 9971 patients with OHCA of suspected cardiac cause were assessed regarding the hospital they were referred to. Those treated at hospitals with 24 h cardiac interventional services had a better survival (OR 1.40, 95% CI 1.12 to 1.74; p=0.003).
Current guidelines recommend immediate angiography in patients after successful resuscitation for an OHCA (return of a spontaneous circulation) in case of ST elevations in the post-resuscitation ECG. However, the accuracy of post-resuscitation ECGs is unclear and there are grounds for recommending early angiography in all patients over 35-40 years, regardless of the ECG, if there is no obvious non-cardiac cause.
Cardiac rehabilitation after ACS
While it seems intuitive that cardiac rehabilitation programs are beneﬁcial by providing careful follow-up, supervised physical activity and guidance on lifestyle modiﬁcation, clinical data on its effect are controversial. Very recently, cardiac rehabilitation for ACS has been challenged again by the multicenter RCT of comprehensive cardiac rehabilitation in patients following acute MI (RAMIT: Rehabilitation After Myocardial Infarction Trial)59. In this study, cardiac rehabilitation in patients after an AMI had no effect on mortality or morbidity, cardiac medication, risk factors or lifestyle modiﬁcation. However, we have to be aware that the RAMIT trial was small and if we look at the evidence more comprehensively, by pooling all available RCTs as done by a Cochrane review (combining 47 studies), there is a signiﬁcant, albeit modest, effect on mortality60. This meta-analysis did not include the RAMIT ﬁndings which would have further reduced the estimated effect on all-cause mortality from 13% to 11%61. It is important to note that the Cochrane review focused on physical exercise based rehabilitation, the probability being that non-exercise based rehabilitation (patient education) has little effect on mortality after MI62.
The problem with combining results of multiple trials is, of course, that this does not account for the ‘evolution’ of such interventions63. The results of the recent OMEGA study, which was a non-randomized cohort study, have shown that a short term comprehensive cardiac rehabilitation program after acute MI signiﬁcantly improved the 1-year prognosis64. Those who attended rehabilitation programs had lower all-cause mortality than those who did not, but without randomized treatment assignment, interpretation of such data is difﬁcult. There was a signiﬁcant dose–response relationship; the more sessions attended the lower the all-cause mortality. However, low attenders were more likely to be smokers, and when adjustments were made for baseline differences in smoking status the dose–response association disappeared.
Though cardiac rehabilitation as currently provided in many countries may not be effective in reducing hard clinical end points, it still helps provide information, advice, and reassurance and helps in long term secondary prevention65.
The treatment options for ACS have improved signiﬁcantly over the past few years, contributing to notable improvements in outcomes. This is especially the case for STEMI, while long term mortality after an NSTE-ACS is still considerable. The very recent introduction of third generation antiplatelet therapies (prasugrel, ticagrelor) and the most recent intravenous form, cangrelor, are likely to continue to improve clinical outcomes after ACS. These more potent agents can increase bleeding risks, and considering the association between bleeding and outcomes, periprocedural bleeding avoidance strategies are important. They may include radial access angiography; ultrasound guided femoral access, and the use of bivalirudin.
Contributors: PM drafted the manuscript. AB, AJL and AB revised the manuscript critically for intellectual content. All three authors contributed signiﬁcantly to this paper and have approved the ﬁnal version.
Competing interests: None.
Provenance and peer review Commissioned; internally peer reviewed.
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