Long-Term Outcomes With Drug-Eluting Balloon for the Treatment of In-Stent Restenosis and De Novo Lesions: The Novara-Biella-Trento (NOBITRE) Registry
Drug-coated balloons (DCBs) have emerged for percutaneous coronary interventions (PCI) of in-stent restenosis or particular anatomical subsets. We provide a real-world analysis of the prognostic determinants and long-term outcomes of patients treated with DCB for any lesion in a comprehensive multic...
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Veröffentlicht in: | Angiology 2023-05, Vol.74 (5), p.488-495 |
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description | Drug-coated balloons (DCBs) have emerged for percutaneous coronary interventions (PCI) of in-stent restenosis or particular anatomical subsets. We provide a real-world analysis of the prognostic determinants and long-term outcomes of patients treated with DCB for any lesion in a comprehensive multicenter registry. The primary study endpoint was the occurrence of major cardiovascular events (MACE: composite of all-cause death, myocardial infarction, and target vessel revascularization) at the longest available follow-up. We included 267 patients (196 treated for in-stent restenosis and 71 for de novo lesions), with a median follow-up of 616 [368–1025] days. MACE occurred in 70 (26.2%) of the patients and related with higher rates of in-stent restenosis (P = .04), longer and more type C lesions (P = .05 and P = .04). At multivariate Cox-regression, type C lesions emerged as the only independent predictor of MACE (adjusted OR [95% CI] = 1.83[1.13–2.97], P = .014), mainly driven by target vessel revascularization (adjusted OR[95% CI] = 1.78[1.05–2.95], P = .03) not conditioning survival. In-stent restenosis emerged as major determinant of TLF (adjusted OR[95% CI] = 2.59[1.17–5.75], P = .02). DCBs represent a treatment option for any lesion; however, type C and restenotic lesions are associated with an increased risk of MACE and target lesion failure, where the optimal strategies for patients’ selection and lesion preparation are still undefined. |
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We provide a real-world analysis of the prognostic determinants and long-term outcomes of patients treated with DCB for any lesion in a comprehensive multicenter registry. The primary study endpoint was the occurrence of major cardiovascular events (MACE: composite of all-cause death, myocardial infarction, and target vessel revascularization) at the longest available follow-up. We included 267 patients (196 treated for in-stent restenosis and 71 for de novo lesions), with a median follow-up of 616 [368–1025] days. MACE occurred in 70 (26.2%) of the patients and related with higher rates of in-stent restenosis (P = .04), longer and more type C lesions (P = .05 and P = .04). At multivariate Cox-regression, type C lesions emerged as the only independent predictor of MACE (adjusted OR [95% CI] = 1.83[1.13–2.97], P = .014), mainly driven by target vessel revascularization (adjusted OR[95% CI] = 1.78[1.05–2.95], P = .03) not conditioning survival. In-stent restenosis emerged as major determinant of TLF (adjusted OR[95% CI] = 2.59[1.17–5.75], P = .02). DCBs represent a treatment option for any lesion; however, type C and restenotic lesions are associated with an increased risk of MACE and target lesion failure, where the optimal strategies for patients’ selection and lesion preparation are still undefined.</description><identifier>ISSN: 0003-3197</identifier><identifier>EISSN: 1940-1574</identifier><identifier>DOI: 10.1177/00033197221110961</identifier><identifier>PMID: 37005331</identifier><language>eng</language><publisher>Los Angeles, CA: SAGE Publications</publisher><subject>Cardiovascular Agents - adverse effects ; Coronary Artery Disease ; Coronary Restenosis - etiology ; Coronary Restenosis - therapy ; Drug-Eluting Stents - adverse effects ; Humans ; Percutaneous Coronary Intervention - adverse effects ; Registries ; Risk Factors ; Treatment Outcome</subject><ispartof>Angiology, 2023-05, Vol.74 (5), p.488-495</ispartof><rights>The Author(s) 2022</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c340t-44882a55d21bdb76cd6d63365f81766fc83b66693289231f76c304f4a768cca23</citedby><cites>FETCH-LOGICAL-c340t-44882a55d21bdb76cd6d63365f81766fc83b66693289231f76c304f4a768cca23</cites><orcidid>0000-0001-6506-8397</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1177/00033197221110961$$EPDF$$P50$$Gsage$$H</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.1177/00033197221110961$$EHTML$$P50$$Gsage$$H</linktohtml><link.rule.ids>314,776,780,21799,27903,27904,43600,43601</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37005331$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Verdoia, Monica</creatorcontrib><creatorcontrib>Zilio, Filippo</creatorcontrib><creatorcontrib>Viola, Orazio</creatorcontrib><creatorcontrib>Brancati, Marta Francesca</creatorcontrib><creatorcontrib>Fanti, Diego</creatorcontrib><creatorcontrib>Soldà, Pier Luigi</creatorcontrib><creatorcontrib>Rognoni, Andrea</creatorcontrib><creatorcontrib>Bonmassari, Roberto</creatorcontrib><creatorcontrib>De Luca, Giuseppe</creatorcontrib><title>Long-Term Outcomes With Drug-Eluting Balloon for the Treatment of In-Stent Restenosis and De Novo Lesions: The Novara-Biella-Trento (NOBITRE) Registry</title><title>Angiology</title><addtitle>Angiology</addtitle><description>Drug-coated balloons (DCBs) have emerged for percutaneous coronary interventions (PCI) of in-stent restenosis or particular anatomical subsets. We provide a real-world analysis of the prognostic determinants and long-term outcomes of patients treated with DCB for any lesion in a comprehensive multicenter registry. The primary study endpoint was the occurrence of major cardiovascular events (MACE: composite of all-cause death, myocardial infarction, and target vessel revascularization) at the longest available follow-up. We included 267 patients (196 treated for in-stent restenosis and 71 for de novo lesions), with a median follow-up of 616 [368–1025] days. MACE occurred in 70 (26.2%) of the patients and related with higher rates of in-stent restenosis (P = .04), longer and more type C lesions (P = .05 and P = .04). At multivariate Cox-regression, type C lesions emerged as the only independent predictor of MACE (adjusted OR [95% CI] = 1.83[1.13–2.97], P = .014), mainly driven by target vessel revascularization (adjusted OR[95% CI] = 1.78[1.05–2.95], P = .03) not conditioning survival. In-stent restenosis emerged as major determinant of TLF (adjusted OR[95% CI] = 2.59[1.17–5.75], P = .02). DCBs represent a treatment option for any lesion; however, type C and restenotic lesions are associated with an increased risk of MACE and target lesion failure, where the optimal strategies for patients’ selection and lesion preparation are still undefined.</description><subject>Cardiovascular Agents - adverse effects</subject><subject>Coronary Artery Disease</subject><subject>Coronary Restenosis - etiology</subject><subject>Coronary Restenosis - therapy</subject><subject>Drug-Eluting Stents - adverse effects</subject><subject>Humans</subject><subject>Percutaneous Coronary Intervention - adverse effects</subject><subject>Registries</subject><subject>Risk Factors</subject><subject>Treatment Outcome</subject><issn>0003-3197</issn><issn>1940-1574</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU9PwyAYxonR6Jx-AC-G4zygUFpovTmdumTZklnjsWEt7WpamEBN_CJ-XqmbXkw8vf9-z5MXXgDOCL4khPMrjDGlJOFBQAjBCSN7YECSECMS8XAfDPo56oEjcGztqy8jgtkhOKLcp146AJ8zrSqUStPCRedy3UoLX2q3hnemq9Ck6VytKjgWTaO1gqU20K0lTI0UrpXKQV3CqUJPrs-X0vqobW2hUAW8k3Cu3zWcSVtrZa9huv7uCCPQuJZNI5D3UU7D0XwxnqbLyYW3qGrrzMcJOChFY-XpLg7B8_0kvX1Es8XD9PZmhnIaYofCMI4DEUVFQFbFirO8YAWjlEVlTDhjZR7TFWMsoUGcBJSUnqA4LEPBWZznIqBDMNr6box-6_z-WVvbvN9NSd3ZLOBJyGKGo8ijZIvmRltrZJltTN0K85ERnPXnyP6cw2vOd_bdqpXFr-Ln_z1wuQWsqGT2qjuj_HP_cfwCwDCQsw</recordid><startdate>202305</startdate><enddate>202305</enddate><creator>Verdoia, Monica</creator><creator>Zilio, Filippo</creator><creator>Viola, Orazio</creator><creator>Brancati, Marta Francesca</creator><creator>Fanti, Diego</creator><creator>Soldà, Pier Luigi</creator><creator>Rognoni, Andrea</creator><creator>Bonmassari, Roberto</creator><creator>De Luca, Giuseppe</creator><general>SAGE Publications</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-6506-8397</orcidid></search><sort><creationdate>202305</creationdate><title>Long-Term Outcomes With Drug-Eluting Balloon for the Treatment of In-Stent Restenosis and De Novo Lesions: The Novara-Biella-Trento (NOBITRE) Registry</title><author>Verdoia, Monica ; Zilio, Filippo ; Viola, Orazio ; Brancati, Marta Francesca ; Fanti, Diego ; Soldà, Pier Luigi ; Rognoni, Andrea ; Bonmassari, Roberto ; De Luca, Giuseppe</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c340t-44882a55d21bdb76cd6d63365f81766fc83b66693289231f76c304f4a768cca23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Cardiovascular Agents - adverse effects</topic><topic>Coronary Artery Disease</topic><topic>Coronary Restenosis - etiology</topic><topic>Coronary Restenosis - therapy</topic><topic>Drug-Eluting Stents - adverse effects</topic><topic>Humans</topic><topic>Percutaneous Coronary Intervention - adverse effects</topic><topic>Registries</topic><topic>Risk Factors</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Verdoia, Monica</creatorcontrib><creatorcontrib>Zilio, Filippo</creatorcontrib><creatorcontrib>Viola, Orazio</creatorcontrib><creatorcontrib>Brancati, Marta Francesca</creatorcontrib><creatorcontrib>Fanti, Diego</creatorcontrib><creatorcontrib>Soldà, Pier Luigi</creatorcontrib><creatorcontrib>Rognoni, Andrea</creatorcontrib><creatorcontrib>Bonmassari, Roberto</creatorcontrib><creatorcontrib>De Luca, Giuseppe</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Angiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Verdoia, Monica</au><au>Zilio, Filippo</au><au>Viola, Orazio</au><au>Brancati, Marta Francesca</au><au>Fanti, Diego</au><au>Soldà, Pier Luigi</au><au>Rognoni, Andrea</au><au>Bonmassari, Roberto</au><au>De Luca, Giuseppe</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Long-Term Outcomes With Drug-Eluting Balloon for the Treatment of In-Stent Restenosis and De Novo Lesions: The Novara-Biella-Trento (NOBITRE) Registry</atitle><jtitle>Angiology</jtitle><addtitle>Angiology</addtitle><date>2023-05</date><risdate>2023</risdate><volume>74</volume><issue>5</issue><spage>488</spage><epage>495</epage><pages>488-495</pages><issn>0003-3197</issn><eissn>1940-1574</eissn><abstract>Drug-coated balloons (DCBs) have emerged for percutaneous coronary interventions (PCI) of in-stent restenosis or particular anatomical subsets. We provide a real-world analysis of the prognostic determinants and long-term outcomes of patients treated with DCB for any lesion in a comprehensive multicenter registry. The primary study endpoint was the occurrence of major cardiovascular events (MACE: composite of all-cause death, myocardial infarction, and target vessel revascularization) at the longest available follow-up. We included 267 patients (196 treated for in-stent restenosis and 71 for de novo lesions), with a median follow-up of 616 [368–1025] days. MACE occurred in 70 (26.2%) of the patients and related with higher rates of in-stent restenosis (P = .04), longer and more type C lesions (P = .05 and P = .04). At multivariate Cox-regression, type C lesions emerged as the only independent predictor of MACE (adjusted OR [95% CI] = 1.83[1.13–2.97], P = .014), mainly driven by target vessel revascularization (adjusted OR[95% CI] = 1.78[1.05–2.95], P = .03) not conditioning survival. In-stent restenosis emerged as major determinant of TLF (adjusted OR[95% CI] = 2.59[1.17–5.75], P = .02). DCBs represent a treatment option for any lesion; however, type C and restenotic lesions are associated with an increased risk of MACE and target lesion failure, where the optimal strategies for patients’ selection and lesion preparation are still undefined.</abstract><cop>Los Angeles, CA</cop><pub>SAGE Publications</pub><pmid>37005331</pmid><doi>10.1177/00033197221110961</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0001-6506-8397</orcidid></addata></record> |
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subjects | Cardiovascular Agents - adverse effects Coronary Artery Disease Coronary Restenosis - etiology Coronary Restenosis - therapy Drug-Eluting Stents - adverse effects Humans Percutaneous Coronary Intervention - adverse effects Registries Risk Factors Treatment Outcome |
title | Long-Term Outcomes With Drug-Eluting Balloon for the Treatment of In-Stent Restenosis and De Novo Lesions: The Novara-Biella-Trento (NOBITRE) Registry |
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