Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/202643
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dc.contributor.authorTesta, Luca-
dc.contributor.authorSquillace, Mattia-
dc.contributor.authorVentrella, Nicoletta-
dc.contributor.authorMoreno, Raul-
dc.contributor.authorJiménez Valero, Santiago-
dc.contributor.authorSerra, Antoni-
dc.contributor.authorGomez Hospital, Joan Antoni-
dc.contributor.authorBellamoli, Michele-
dc.contributor.authorPopolo Rubbio, Antonio-
dc.contributor.authorBedogni, Francesco-
dc.date.accessioned2023-10-09T10:09:22Z-
dc.date.available2023-10-09T10:09:22Z-
dc.date.issued2023-09-06-
dc.identifier.issn2297-055X-
dc.identifier.urihttp://hdl.handle.net/2445/202643-
dc.description.abstractBackgroundThird generation drug-eluting stents (DES) potentially offer better technical performance and reduced neointimal proliferation than previous generation DES. The XLIMIT non-inferiority trial evaluated the performance of the Xlimus (a novel sirolimus-eluting coronary stent system) in terms of endothelialization and tissue healing compared to the bioresorbable polymer Synergy DES.MethodsA total of 177 patients undergoing percutaneous coronary intervention (PCI) were randomized in a 2:1 ratio (2 Xlimus: 1 Synergy). The primary endpoints, defined as the in-stent neointimal volume weighted by the sum of the lengths of the implanted stent (ISNV) and the in-stent neointimal percent volume obstruction (%VO) were evaluated at 6-9 months by means of optical coherence tomography (OCT). Additional OCT parameters as well as clinical endpoints were also collected.ResultsMost of the patients were males (77.4%), and the mean age was 64 years. One third of the population had stable angina/silent ischemia. A total of 300 stents (237 lesions) were analyzed: 198 (152 lesions) were in the Xlimus group, and 102 (85 lesions) in the Synergy group. The ISNV in the Xlimus group was 30.7 & PLUSMN; 24.5 mm3 while in the Synergy group it was 26.5 & PLUSMN; 26.7 mm3: the difference between the two means was 0.08 (-0, 04-0, 45), p = 0.018, thus meeting the non-inferiority hypothesis. The %VO was 16.3% & PLUSMN; 10.4% and 13.3% & PLUSMN; 10.8% in the Xlimus and Synergy groups, respectively: the difference between the two means was 3.0 (-0, 06-4, 2), (p = 0.01), thus meeting the non-inferiority hypothesis. No difference was found with respect to the secondary OCT endpoints as well as for clinical endpoints.ConclusionsThe study results confirm that the biological interaction of the Xlimus and Synergy DES with the coronary artery is comparable, and that translates in very reassuring OCT parameters at follow-up: as such, the Xlimus is non-inferior to the Synergy.-
dc.format.extent8 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherFrontiers Media SA-
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.3389/fcvm.2023.1199475-
dc.relation.ispartofFrontiers in Cardiovascular Medicine, 2023, vol. 10, p. 1199475-
dc.relation.urihttps://doi.org/10.3389/fcvm.2023.1199475-
dc.rightscc by (c) Testa, Luca et al., 2023-
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.sourceArticles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))-
dc.subject.classificationAssaigs clínics-
dc.subject.classificationPròtesis vasculars-
dc.subject.classificationCirurgia vascular-
dc.subject.otherClinical trials-
dc.subject.otherBlood vessel prosthesis-
dc.subject.otherVascular surgery-
dc.titleA randomized control trial to assess optical coherence tomography parameters of the Xlimus drug-eluting stent: the XLIMIT trial-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/publishedVersion-
dc.date.updated2023-10-05T11:21:51Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
dc.identifier.pmid37745092-
Appears in Collections:Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))

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