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Risk and timing of clinical events according to diabetic status of patients treated with everolimus-eluting bioresorbable vascular scaffolds versus everolimus-eluting stent: 2-year results from a propensity score matched comparison of ABSORB EXTEND and SPIRIT trials.

Identifieur interne : 000C89 ( PubMed/Curation ); précédent : 000C88; suivant : 000C90

Risk and timing of clinical events according to diabetic status of patients treated with everolimus-eluting bioresorbable vascular scaffolds versus everolimus-eluting stent: 2-year results from a propensity score matched comparison of ABSORB EXTEND and SPIRIT trials.

Auteurs : Carlos M. Campos [Brésil] ; Adriano Caixeta [Brésil] ; Marcelo Franken [Brésil] ; Antonio L. Bartorelli [Italie] ; Robert J. Whitbourn [Australie] ; Chiung-Jen Wu [Taïwan] ; Hsien Li Paul Kao [Taïwan] ; Mohd Ali Rosli [Malaisie] ; Didier Carrie [France] ; Bernard De Bruyne [Belgique] ; Gregg W. Stone [États-Unis] ; Patrick W. Serruys [Royaume-Uni] ; Alexandre Abizaid [Brésil]

Source :

RBID : pubmed:28471086

Abstract

to compare the occurrence of clinical events in diabetics treated with the Absorb bioresorbable vascular scaffold (Absorb BVS; Abbott Vascular, Santa Clara, CA) versus everolimus-eluting metal stents (EES; XIENCE V; Abbott Vascular, Santa Clara, CA) BACKGROUND: There are limited data dedicated to clinical outcomes of diabetic patients treated with bioresorbable scaffolds (BRS) at 2-year horizon.

DOI: 10.1002/ccd.27109
PubMed: 28471086

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Le document en format XML

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<nlm:affiliation>Department of Cardiology, St Vincent's Hospital, Fitzroy, Victoria, Australia.</nlm:affiliation>
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<name sortKey="Wu, Chiung Jen" sort="Wu, Chiung Jen" uniqKey="Wu C" first="Chiung-Jen" last="Wu">Chiung-Jen Wu</name>
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<name sortKey="Li Paul Kao, Hsien" sort="Li Paul Kao, Hsien" uniqKey="Li Paul Kao H" first="Hsien" last="Li Paul Kao">Hsien Li Paul Kao</name>
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<nlm:affiliation>Department of Cardiology, National Taiwan University Hospital, Taipei, Taiwan.</nlm:affiliation>
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<nlm:affiliation>Department of Cardiology, Institute Jantung Negara, Kuala Lumpur, Malaysia.</nlm:affiliation>
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<name sortKey="Carrie, Didier" sort="Carrie, Didier" uniqKey="Carrie D" first="Didier" last="Carrie">Didier Carrie</name>
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<nlm:affiliation>Department of Cardiology, Hôpital de Rangueil CHU, Toulouse, France.</nlm:affiliation>
<country xml:lang="fr">France</country>
<wicri:regionArea>Department of Cardiology, Hôpital de Rangueil CHU, Toulouse</wicri:regionArea>
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<name sortKey="De Bruyne, Bernard" sort="De Bruyne, Bernard" uniqKey="De Bruyne B" first="Bernard" last="De Bruyne">Bernard De Bruyne</name>
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<name sortKey="Stone, Gregg W" sort="Stone, Gregg W" uniqKey="Stone G" first="Gregg W" last="Stone">Gregg W. Stone</name>
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<nlm:affiliation>Department of Interventional Cardiology, Columbia University Medical Center, New York.</nlm:affiliation>
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<name sortKey="Serruys, Patrick W" sort="Serruys, Patrick W" uniqKey="Serruys P" first="Patrick W" last="Serruys">Patrick W. Serruys</name>
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<nlm:affiliation>International Centre for Circulatory Health, NHLI, Imperial College London, United Kingdom.</nlm:affiliation>
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<name sortKey="Abizaid, Alexandre" sort="Abizaid, Alexandre" uniqKey="Abizaid A" first="Alexandre" last="Abizaid">Alexandre Abizaid</name>
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<nlm:affiliation>Department of Interventional Cardiology, Instituto Dante Pazzanese de Cardiologia, São Paulo, Brazil.</nlm:affiliation>
<country xml:lang="fr">Brésil</country>
<wicri:regionArea>Department of Interventional Cardiology, Instituto Dante Pazzanese de Cardiologia, São Paulo</wicri:regionArea>
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<title level="j">Catheterization and cardiovascular interventions : official journal of the Society for Cardiac Angiography & Interventions</title>
<idno type="eISSN">1522-726X</idno>
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<date when="2017" type="published">2017</date>
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<div type="abstract" xml:lang="en">to compare the occurrence of clinical events in diabetics treated with the Absorb bioresorbable vascular scaffold (Absorb BVS; Abbott Vascular, Santa Clara, CA) versus everolimus-eluting metal stents (EES; XIENCE V; Abbott Vascular, Santa Clara, CA) BACKGROUND: There are limited data dedicated to clinical outcomes of diabetic patients treated with bioresorbable scaffolds (BRS) at 2-year horizon.</div>
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<DateCreated>
<Year>2017</Year>
<Month>05</Month>
<Day>04</Day>
</DateCreated>
<DateRevised>
<Year>2017</Year>
<Month>05</Month>
<Day>04</Day>
</DateRevised>
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<ISSN IssnType="Electronic">1522-726X</ISSN>
<JournalIssue CitedMedium="Internet">
<PubDate>
<Year>2017</Year>
<Month>May</Month>
<Day>04</Day>
</PubDate>
</JournalIssue>
<Title>Catheterization and cardiovascular interventions : official journal of the Society for Cardiac Angiography & Interventions</Title>
<ISOAbbreviation>Catheter Cardiovasc Interv</ISOAbbreviation>
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<ArticleTitle>Risk and timing of clinical events according to diabetic status of patients treated with everolimus-eluting bioresorbable vascular scaffolds versus everolimus-eluting stent: 2-year results from a propensity score matched comparison of ABSORB EXTEND and SPIRIT trials.</ArticleTitle>
<ELocationID EIdType="doi" ValidYN="Y">10.1002/ccd.27109</ELocationID>
<Abstract>
<AbstractText Label="OBJECTIVES" NlmCategory="OBJECTIVE">to compare the occurrence of clinical events in diabetics treated with the Absorb bioresorbable vascular scaffold (Absorb BVS; Abbott Vascular, Santa Clara, CA) versus everolimus-eluting metal stents (EES; XIENCE V; Abbott Vascular, Santa Clara, CA) BACKGROUND: There are limited data dedicated to clinical outcomes of diabetic patients treated with bioresorbable scaffolds (BRS) at 2-year horizon.</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">The present study included 812 patients in the ABSORB EXTEND study in which a total of 215 diabetic patients were treated with Absorb BVS. In addition, 882 diabetic patients treated with EES in pooled data from the SPIRIT clinical program (SPIRIT II, SPIRIT III and SPIRIT IV trials) were used for comparison by applying propensity score matching using 29 different variables. The primary endpoint was ischemia driven major adverse cardiac events (ID-MACE), including cardiac death, myocardial infarction (MI), and ischemia driven target lesion revascularization (ID-TLR).</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">After 2 years, the ID-MACE rate was 6.5% in the Absorb BVS vs. 8.9% in the Xience group (P = 0.40). There was no difference for MACE components or definite/probable device thrombosis (HR: 1.43 [0.24,8.58]; P = 0.69). The occurrence of MACE was not different for both diabetic status (insulin- and non-insulin-requiring diabetes) in all time points up to the 2-year follow-up for the Absorb and Xience groups.</AbstractText>
<AbstractText Label="CONCLUSION" NlmCategory="CONCLUSIONS">In this largest ever patient-level pooled comparison on the treatment of diabetic patients with BRS out to two years, individuals with diabetes treated with the Absorb BVS had a similar rate of MACE as compared with diabetics treated with the Xience EES. © 2017 Wiley Periodicals, Inc.</AbstractText>
<CopyrightInformation>© 2017 Wiley Periodicals, Inc.</CopyrightInformation>
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<LastName>Campos</LastName>
<ForeName>Carlos M</ForeName>
<Initials>CM</Initials>
<Identifier Source="ORCID">http://orcid.org/0000-0003-1734-6924</Identifier>
<AffiliationInfo>
<Affiliation>Department of Cardiology, Hospital Israelita Albert Einstein, São Paulo, Brazil.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Caixeta</LastName>
<ForeName>Adriano</ForeName>
<Initials>A</Initials>
<AffiliationInfo>
<Affiliation>Department of Cardiology, Hospital Israelita Albert Einstein, São Paulo, Brazil.</Affiliation>
</AffiliationInfo>
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<LastName>Franken</LastName>
<ForeName>Marcelo</ForeName>
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<Affiliation>Department of Cardiology, Hospital Israelita Albert Einstein, São Paulo, Brazil.</Affiliation>
</AffiliationInfo>
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<LastName>Bartorelli</LastName>
<ForeName>Antonio L</ForeName>
<Initials>AL</Initials>
<AffiliationInfo>
<Affiliation>Centro Cardiologico Monzino, IRCCS, Milan, Italy.</Affiliation>
</AffiliationInfo>
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<LastName>Whitbourn</LastName>
<ForeName>Robert J</ForeName>
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<AffiliationInfo>
<Affiliation>Department of Cardiology, St Vincent's Hospital, Fitzroy, Victoria, Australia.</Affiliation>
</AffiliationInfo>
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<LastName>Wu</LastName>
<ForeName>Chiung-Jen</ForeName>
<Initials>CJ</Initials>
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<Affiliation>Department of Cardiology, Chang Gung Memorial Hospital, Niao-Sung Hsiang, Taiwan.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Li Paul Kao</LastName>
<ForeName>Hsien</ForeName>
<Initials>H</Initials>
<AffiliationInfo>
<Affiliation>Department of Cardiology, National Taiwan University Hospital, Taipei, Taiwan.</Affiliation>
</AffiliationInfo>
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<LastName>Rosli</LastName>
<ForeName>Mohd Ali</ForeName>
<Initials>MA</Initials>
<AffiliationInfo>
<Affiliation>Department of Cardiology, Institute Jantung Negara, Kuala Lumpur, Malaysia.</Affiliation>
</AffiliationInfo>
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<LastName>Carrie</LastName>
<ForeName>Didier</ForeName>
<Initials>D</Initials>
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<Affiliation>Department of Cardiology, Hôpital de Rangueil CHU, Toulouse, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>De Bruyne</LastName>
<ForeName>Bernard</ForeName>
<Initials>B</Initials>
<AffiliationInfo>
<Affiliation>Department of Cardiology, Cardiovascular Center Aalst, Belgium.</Affiliation>
</AffiliationInfo>
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<LastName>Stone</LastName>
<ForeName>Gregg W</ForeName>
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<AffiliationInfo>
<Affiliation>Department of Interventional Cardiology, Columbia University Medical Center, New York.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Cardiovascular Research Foundation, New York.</Affiliation>
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<LastName>Serruys</LastName>
<ForeName>Patrick W</ForeName>
<Initials>PW</Initials>
<AffiliationInfo>
<Affiliation>International Centre for Circulatory Health, NHLI, Imperial College London, United Kingdom.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Abizaid</LastName>
<ForeName>Alexandre</ForeName>
<Initials>A</Initials>
<AffiliationInfo>
<Affiliation>Department of Interventional Cardiology, Instituto Dante Pazzanese de Cardiologia, São Paulo, Brazil.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<CollectiveName>ABSORB Cohort B and the SPIRIT II, III, and IV Investigators.</CollectiveName>
</Author>
</AuthorList>
<Language>eng</Language>
<PublicationTypeList>
<PublicationType UI="D016428">Journal Article</PublicationType>
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<ArticleDate DateType="Electronic">
<Year>2017</Year>
<Month>05</Month>
<Day>04</Day>
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<MedlineJournalInfo>
<Country>United States</Country>
<MedlineTA>Catheter Cardiovasc Interv</MedlineTA>
<NlmUniqueID>100884139</NlmUniqueID>
<ISSNLinking>1522-1946</ISSNLinking>
</MedlineJournalInfo>
<KeywordList Owner="NOTNLM">
<Keyword MajorTopicYN="N">DES-stent</Keyword>
<Keyword MajorTopicYN="N">bioabsorbable devices/polymers</Keyword>
<Keyword MajorTopicYN="N">coronary artery disease</Keyword>
<Keyword MajorTopicYN="N">diabetes mellitus</Keyword>
<Keyword MajorTopicYN="N">drug eluting</Keyword>
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<Month>11</Month>
<Day>20</Day>
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<Year>2017</Year>
<Month>03</Month>
<Day>01</Day>
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<Year>2017</Year>
<Month>03</Month>
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   |texte=   Risk and timing of clinical events according to diabetic status of patients treated with everolimus-eluting bioresorbable vascular scaffolds versus everolimus-eluting stent: 2-year results from a propensity score matched comparison of ABSORB EXTEND and SPIRIT trials.
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