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Device deployment failed in 1\u00a0case (1%). Procedure-related symptomatic procedural complications consisted of 2\u00a0(2%) major events (1\u00a0major stroke and 1\u00a0vessel perforation with intracranial hemorrhage and infarction) and 6\u00a0minor events (6\u00a0minor strokes). Procedural morbidity was 5%. There were no late ischemic or hemorrhagic events during follow-up. Complete and favorable aneurysm occlusion was achieved in 54% (40\/74) and 62% (46\/74) at a\u00a0mean of 5\u00a0months, 71% (27\/38) and 87% (33\/38) at a\u00a0mean of 12\u00a0months, and 76% (25\/33) and 97% (32\/33) at a\u00a0mean of 35\u00a0months, respectively.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusion<\/jats:title>\n                    <jats:p>The results demonstrate progressive aneurysm occlusion beyond 12\u00a0months after DED implantation with an almost 100% favorable occlusion rate. Procedural morbidity was low and there were no late complications.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1007\/s00062-024-01423-1","type":"journal-article","created":{"date-parts":[[2024,5,30]],"date-time":"2024-05-30T11:02:23Z","timestamp":1717066943000},"page":"789-798","update-policy":"https:\/\/doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":3,"title":["Long-term Safety and Efficacy of the Derivo Embolization Device in a\u00a0Single-center Series"],"prefix":"10.1007","volume":"34","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-2620-7611","authenticated-orcid":false,"given":"Lukas","family":"Goertz","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"David","family":"Zopfs","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jonathan","family":"Kottlors","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jan","family":"Borggrefe","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Lenhard","family":"Pennig","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Marc","family":"Schlamann","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Christoph","family":"Kabbasch","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"297","published-online":{"date-parts":[[2024,5,30]]},"reference":[{"key":"1423_CR1","doi-asserted-by":"crossref","unstructured":"Shankar JJS, Tampieri D, Iancu D, et\u00a0al. 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FD serves as consultant\/ proctor for MicroVention Inc.\/Sequent Medical, Balt (Irvine, CA, USA), Cerenovus\/Johnson&Johnson (Irvine, CA, USA); received speakers honoraria from Cerenovus\/ Johnson&Johnson, Acandis (Pforzheim, Germany), Asahi (Tokyo, Japan), Q`Apel (Fremont, CA, USA), Penumbra (Alameda, CA, USA), Medtronic, Stryker; received scientific grants from Cerenovus\/ Johnson&Johnson.  CK serves as consultant for Acandis GmbH and as proctor for MicroVention Inc.\/Sequent Medical. DZ is on the speaker\u2019s bureau of Philips (Amsterdam, the Netherlands) and lecturer for Amboss GmbH (Cologne, Germany). The other authors declare that they have no competing interests.","order":2,"name":"Ethics","group":{"name":"EthicsHeading","label":"Conflict of interest"}},{"value":"For this article no studies with human participants or animals were performed by any of the authors. All studies mentioned were in accordance with the ethical standards indicated in each case.","order":3,"name":"Ethics","group":{"name":"EthicsHeading","label":"Ethical standards"}}]}}