Key result
Magnesium-based bioresorbable scaffold implantation in ACS patients resulted in a 13.3% rate of device-oriented composite events at 2 years, mainly driven by target lesion revascularization (11.1%).
Why the study?
The study sought to evaluate 24-month clinical outcomes and investigate 18-month angiographic performance, healing, and bioresorption by OCT in ACS patients treated with magnesium-based bioresorbable scaffolds.
What are the long-term clinical, angiographic, and optical coherence tomography outcomes of magnesium-based bioresorbable scaffolds in patients with acute coronary syndrome?
Cohort (n=90)
Yes
What are the long-term clinical, angiographic, and optical coherence tomography outcomes of magnesium-based bioresorbable scaffolds in patients with acute coronary syndrome?
Magnesium-based bioresorbable scaffolds in ACS patients are associated with a high rate of device-oriented composite events at 2 years, primarily driven by target lesion revascularization due to scaffold collapse.
Early event clustering warrants close monitoring after MgBRS in ACS; leaves open long-term advantage over DES post-resorption.
BACKGROUND: This study sought to evaluate the clinical outcomes of patients treated with magnesium-based bioresorbable scaffolds (MgBRS) in the context of acute coronary syndromes (ACS) at long-term follow-up (24 months). The study also aims to investigate the MgBRS performance by angiography and the healing and bioresorption pattern by optical coherence tomography (OCT) at 18 months. METHODS: Between December 2016 and December 2018, a total of 90 patients admitted for ACS and treated with MgBRS (Magmaris, Biotronik AG, Bülach, Switzerland) were enrolled in a multicenter prospective study. Clinical follow-up was performed in all patients at 24 months and angiographic and OCT follow-up in 51.5% of patients at 18 months. Serial OCT was available in 33 patients (36.7%). RESULTS: At a 2-year follow-up, 88.8% were free of symptoms, no cardiac death was reported, and the device-oriented composite event (DOCE): consisting of cardiac death, target vessel myocardial infarction, and target lesion revascularization (TLR) was 13.3%. Stent thrombosis and TLR were observed in 2.2 and 11.1%, respectively. Binary restenosis was observed in 21.7% of cases and in-stent late lumen loss was 0.61 ± 0.75 mm. By serial OCT imaging, the minimal lumen area was significantly reduced greater than 40% (from 6.12 ± 1.59 to 3.5 ± 1.55 mm2, p < .001). At follow-up, area stenosis was 44.33 ± 23.07% and half of the patients presented indiscernible struts. The principal observed mechanism of restenosis was scaffold collapse. CONCLUSIONS: At long-term follow-up, MgBRS implantation in ACS patients showed a high rate of DOCE, mainly caused by clinically driven TLR. MgBRS restenosis was caused by scaffold collapse in most of the cases.
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Gutiérrez et al. (2021) conducted a cohort in Acute coronary syndromes (ACS) (n=90). Magnesium-based bioresorbable scaffolds (MgBRS) was evaluated on Device-oriented composite event (DOCE) consisting of cardiac death, target vessel myocardial infarction, and target lesion revascularization. Magnesium-based bioresorbable scaffold implantation in ACS patients resulted in a 13.3% rate of device-oriented composite events at 2 years, mainly driven by target lesion revascularization (11.1%).
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