P rimary percutaneous coronary intervention (PCI) is the preferred treatment for patients with ST-segment elevation myocardial infarction (STEMI) owing to improved vessel patency, decreased infarct size, lower rates of reinfarction, and improved survival compared with pharmacological reperfusion. However, stent thrombosis (ST) remains a major concern among STEMI patients with an excess 3-to 4-fold increased risk compared with PCI in an elective setting. In the present issue of Circulation, the Harmonizing Outcomes With Revascularization and Stents in Acute Myocardial Infarction (HORIZONS-AMI) trial investigators provide a detailed report of the incidence, timing, and predictors of ST, specifically addressing the impact of stent type and antithrombotic regimen through 2 years. 1 Definite or probable ST was common (4.4%), with little more than half of events falling into the early period (Ͻ30 days), and the remainder being observed in the late period (up to 2 years), without apparent differences in terms of stent type and antithrombotic regimen.
Primary Percutaneous Coronary Intervention and Stent TypeA recent systematic review comparing outcomes between drug-eluting stents (DES) and bare-metal stents (BMS) reported a 56% lower risk of repeat revascularization in favor of DES without differences in terms of death, MI, and ST. 2 A number of registry data extend the benefit of DES to more unselected patients undergoing primary PCI in routine clinical practice. Notwithstanding, there remains a nagging concern about the safety of DES in STEMI patients, particularly during long-term follow-up. What are the principal reasons underlying this clinical equipoise?
Article see p 1745First, very late ST has been recognized as a distinct entity complicating the use of DES, particularly in the off-label setting. Along this line, observational studies have reported an increased risk of very late ST with DES compared with BMS among STEMI patients. 3,4 Second, none of the individual STEMI trials have been powered adequately to address infrequent adverse events, such as very late ST. Third, histopathological analysis of autopsy specimens revealed more inflammation, fibrin deposition, and uncovered struts among lesions treated with DES in STEMI patients compared with those with stable lesions, suggesting a differential arterial response to DES depending on underlying plaque morphology. 5 Fourth, late acquired stent malapposition (LASM) was more common among DES (31%) than BMS (8%, Pϭ0.02) 13 months after PCI in the Intravascular Ultrasound (IVUS) substudy of HORIZONS-AMI. 6 Although it remains a matter of debate whether LASM is causally related to very late ST, LASM in the presence of vessel remodeling is presumably caused by extensive inflammation elicited by DES and highly prevalent among patients presenting with very late ST (75%). 7 Because LASM is a dynamic process and only appears over time, it may become clinically apparent only during very long-term follow-up. The notion of a differential healing response between DES and BMS...