{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,30]],"date-time":"2026-09-30T16:06:16Z","timestamp":1790784376061,"version":"4.1.0"},"reference-count":25,"publisher":"SAGE Publications","issue":"3","license":[{"start":{"date-parts":[[2021,10,11]],"date-time":"2021-10-11T00:00:00Z","timestamp":1633910400000},"content-version":"unspecified","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"content-domain":{"domain":["journals.sagepub.com"],"crossmark-restriction":true},"short-container-title":["J Endovasc Ther"],"published-print":{"date-parts":[[2022,6]]},"abstract":"<jats:sec>\n                    <jats:title>Objective:<\/jats:title>\n                    <jats:p>The aim of this study was to report 10-year real-world single-center experience with the GORE TAG conformable thoracic aortic graft (CTAG), focusing on rupture-free survival, aortic-related reintervention, and device-related complications during midterm and long-term follow-up (FU).<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods:<\/jats:title>\n                    <jats:p>This retrospective study analyzes results of thoracic endovascular aortic repair (TEVAR) performed between January 2009 and December 2018. Out of 419 TEVAR procedures within this period, 194 patients (male 57.2%, 111\/194), with a mean age of 65 \u00b1 13\u2009years, were treated with the CTAG device. Indication for TEVAR was a thoracic aortic aneurysm in 24.7% (48\/194), type B aortic dissection in 32.5% (63\/194), penetrating aortic ulcer 15.5% (30\/194), and miscellaneous 27.3% (53\/194). Emergently were operated 43.8% (85\/194) patients. Median follow-up (FU) including computed tomography imaging was 43.5\u2009months (Q1-Q3: 8.6\u201367.0) and was completed in 91.2% (177\/194) of patients.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results:<\/jats:title>\n                    <jats:p>Overall survival rates were 75.8% (95% confidence interval [CI] = [0.76\u20130.70]) and 56.6% (95% CI = [0.57\u20130.50]) at 12 and 60\u2009months, respectively. Cumulative incidence for aortic rupture was 11.9% (95% CI = [0.07\u20130.17]) at 60 and 90\u2009months, respectively. Cumulative incidence for aortic-related reintervention was 27.5% (95% CI = [0.21\u20130.34]) at 60 and 90\u2009months. Cumulative incidence for migration was 2.8% (95% CI = [0.004\u20130.05]) and 3.9% (95% CI = [0.007\u20130.07]) at 60 and 90\u2009months, respectively. New endograft infections or material fatigue were not observed.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions:<\/jats:title>\n                    <jats:p>The herein reported 10-year real-world single-center experience with the CTAG observed favorable long-term outcome. Thus, the device demonstrates appropriate persistent safety, efficacy, and clinical durability up to long-term FU in the treatment of diverse thoracic aortic pathologies.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1177\/15266028211049340","type":"journal-article","created":{"date-parts":[[2021,10,11]],"date-time":"2021-10-11T05:28:46Z","timestamp":1633930126000},"page":"370-380","update-policy":"https:\/\/doi.org\/10.1177\/sage-journals-update-policy","source":"Crossref","is-referenced-by-count":16,"title":["A 10-Year Single-Center Experience With the GORE TAG Conformable Thoracic Stent Graft in the Treatment of Thoracic Aortic Disease"],"prefix":"10.1177","volume":"29","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-5645-6347","authenticated-orcid":false,"given":"Denis","family":"Skrypnik","sequence":"first","affiliation":[{"name":"Department of Vascular and Endovascular Surgery, University Hospital Heidelberg, Heidelberg, Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Moritz S.","family":"Bischoff","sequence":"additional","affiliation":[{"name":"Department of Vascular and Endovascular Surgery, University Hospital Heidelberg, Heidelberg, Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-5463-324X","authenticated-orcid":false,"given":"Katrin","family":"Meisenbacher","sequence":"additional","affiliation":[{"name":"Department of Vascular and Endovascular Surgery, University Hospital Heidelberg, Heidelberg, Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Dorothea B.","family":"Kronsteiner","sequence":"additional","affiliation":[{"name":"Institute of Medical Biometry and Informatics, Heidelberg University, Heidelberg, Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Dittmar","family":"B\u00f6ckler","sequence":"additional","affiliation":[{"name":"Department of Vascular and 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