Biodegradable polymer drug-eluting stents (DES) are innovative concepts in the era of percutaneous coronary intervention. We systematically reviewed the latest randomized evidence on the efficacy and safety of biodegradable polymer DES as compared to durable polymer DES. MEDLINE, Embase, and the Cochrane database were searched in August 2013 for eligible randomized controlled trials (RCTs) comparing biodegradable polymer DES with durable polymer DES. Clinical outcomes of interest were mortality, myocardial infarction (MI), target lesion revascularization (TLR), target vessel revascularization (TVR), and stent thrombosis. A total of 20 RCTs randomizing 20 021 participants were included, of whom 11 045 were allocated to biodegradable polymer DES and 8976 to durable polymer DES. Treatment of biodegradable polymer DES was not associated with a significant reduction of any of the clinical outcomes (all-cause mortality, odds ratio
IntroductionThe ongoing quest for innovative stent design for percutaneous coronary intervention (PCI) led us to the era of drug-eluting stents (DES) with biodegradable polymer coatings, which offer the antirestenotic benefits of traditional DES in the immediate vessel healing stage without any durable polymer-related complications such as polymer delamination, arterial inflammation, and delayed vascular dealing, thereby providing the long-term safety benefits of a bare-metal stent (BMS) after the polymer coatings degrade. 1 -4 Existing meta-analyses of randomized trials investigating the efficacy and safety of biodegradable polymer DES vs durable polymer DES are available. 5,6 However, due to different study inclusion criteria they came to conflicting conclusions. With the recent availability of