{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,19]],"date-time":"2026-05-19T12:51:55Z","timestamp":1779195115465,"version":"3.51.4"},"reference-count":18,"publisher":"Wiley","issue":"5","license":[{"start":{"date-parts":[[2018,12,10]],"date-time":"2018-12-10T00:00:00Z","timestamp":1544400000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Cathet Cardio Intervent"],"published-print":{"date-parts":[[2019,4]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:sec><jats:title>Objectives<\/jats:title><jats:p>The Magmaris\u2010ACS Registry is the first assessment of the Magmaris implantation in the acute coronary syndrome (ACS) population.<\/jats:p><\/jats:sec><jats:sec><jats:title>Background<\/jats:title><jats:p>Bioresorbable vascular scaffolds (BRS), the newest coronary stent technology, was developed to overcome the limitations of the metallic drug\u2010eluting stents (DES). Current promising data of the Magmaris in patients with stable angina have encouraged to validate the second generation BRS in ACS indications.<\/jats:p><\/jats:sec><jats:sec><jats:title>Methods<\/jats:title><jats:p>The study population consisted of the consecutive patients who underwent PCI with the Magmaris BRS in the settings of ACS. Patients with ST\u2010segment elevation myocardial infarction were excluded from enrolment. Baseline demographic and angiographic characteristics, as well as 30\u2010day and 6\u2010month clinical, follow up were prospectively analyzed.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>Fifty patients were enrolled at mean age 62.9\u2009\u00b1\u20098.4 years (unstable angina\u201452% and non\u2010ST\u2010segment myocardial infarction [NSTEMI]\u201448%). Treated fifty\u2010one de novo lesions were located in LAD (37%), LCx (14%), and RCA (49%), respectively. Angiographic success in the target lesion was 100%. One case of recurrent ischemia was observed a day after the index procedure, due to the significant distal edge dissection a regular metallic DES overlapping Magmaris was implanted. No other in\u2010hospital events occurred (procedural success 98%). Six\u2010Month follow up showed none device\u2010oriented endpoints such as cardiac mortality, target vessel myocardial infarction or target vessel revascularization. None early scaffold thrombosis was reported.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusion<\/jats:title><jats:p>The use of the Magmaris BRS in non\u2010ST elevation ACS patient is associated with a procedural safety and promising early angiographic and clinical outcomes. Long\u2010term follow\u2010up and further evaluation in large prospective randomized controlled trials are needed.<\/jats:p><\/jats:sec>","DOI":"10.1002\/ccd.28036","type":"journal-article","created":{"date-parts":[[2018,12,10]],"date-time":"2018-12-10T13:44:50Z","timestamp":1544449490000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":18,"title":["Early outcome of magnesium bioresorbable scaffold implantation in acute coronary syndrome\u2014the initial report from the Magmaris\u2010ACS registry"],"prefix":"10.1002","volume":"93","author":[{"given":"Adrian","family":"Wlodarczak","sequence":"first","affiliation":[{"name":"Department of Cardiology Copper Health Center  Lubin Poland"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-5849-4849","authenticated-orcid":false,"given":"Magdalena","family":"Lanocha","sequence":"additional","affiliation":[{"name":"Department of Cardiology 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