Geographic variation and risk factors for systemic and limb ischemic events in patients with symptomatic peripheral artery disease: Insights from the REACH Registry.
Identifieur interne : 000650 ( PubMed/Curation ); précédent : 000649; suivant : 000651Geographic variation and risk factors for systemic and limb ischemic events in patients with symptomatic peripheral artery disease: Insights from the REACH Registry.
Auteurs : Jérémie Abtan [France] ; Deepak L. Bhatt [États-Unis] ; Yedid Elbez [France] ; Emmanuel Sorbets [France] ; Kim Eagle [États-Unis] ; Christopher M. Reid [Australie] ; Iris Baumgartner [Suisse] ; David Wu [États-Unis] ; Mary E. Hanson [États-Unis] ; Hakima Hannachi [États-Unis] ; Puneet K. Singhal [États-Unis] ; Philippe Gabriel Steg [France] ; Gregory Ducrocq [France]Source :
- Clinical cardiology [ 1932-8737 ] ; 2017.
Abstract
Patients with symptomatic peripheral artery disease (PAD) are at high risk of ischemic events. However, data about predictors of this risk are limited.
DOI: 10.1002/clc.22721
PubMed: 28520087
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<author><name sortKey="Hannachi, Hakima" sort="Hannachi, Hakima" uniqKey="Hannachi H" first="Hakima" last="Hannachi">Hakima Hannachi</name>
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<author><name sortKey="Singhal, Puneet K" sort="Singhal, Puneet K" uniqKey="Singhal P" first="Puneet K" last="Singhal">Puneet K. Singhal</name>
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<country xml:lang="fr">France</country>
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</affiliation>
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<author><name sortKey="Ducrocq, Gregory" sort="Ducrocq, Gregory" uniqKey="Ducrocq G" first="Gregory" last="Ducrocq">Gregory Ducrocq</name>
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<series><title level="j">Clinical cardiology</title>
<idno type="eISSN">1932-8737</idno>
<imprint><date when="2017" type="published">2017</date>
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<front><div type="abstract" xml:lang="en">Patients with symptomatic peripheral artery disease (PAD) are at high risk of ischemic events. However, data about predictors of this risk are limited.</div>
</front>
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<pubmed><MedlineCitation Status="In-Process" Owner="NLM"><PMID Version="1">28520087</PMID>
<DateCreated><Year>2017</Year>
<Month>05</Month>
<Day>18</Day>
</DateCreated>
<DateRevised><Year>2017</Year>
<Month>09</Month>
<Day>23</Day>
</DateRevised>
<Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1932-8737</ISSN>
<JournalIssue CitedMedium="Internet"><Volume>40</Volume>
<Issue>9</Issue>
<PubDate><Year>2017</Year>
<Month>Sep</Month>
</PubDate>
</JournalIssue>
<Title>Clinical cardiology</Title>
<ISOAbbreviation>Clin Cardiol</ISOAbbreviation>
</Journal>
<ArticleTitle>Geographic variation and risk factors for systemic and limb ischemic events in patients with symptomatic peripheral artery disease: Insights from the REACH Registry.</ArticleTitle>
<Pagination><MedlinePgn>710-718</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1002/clc.22721</ELocationID>
<Abstract><AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">Patients with symptomatic peripheral artery disease (PAD) are at high risk of ischemic events. However, data about predictors of this risk are limited.</AbstractText>
<AbstractText Label="HYPOTHESIS" NlmCategory="OBJECTIVE">We analyzed baseline characteristics and 4-year follow-up of patients enrolled in the international REduction of Atherothrombosis for Continued Health (REACH) Registry with symptomatic PAD and no history of stroke/transient ischemic attack to describe annual rates of recurrent ischemic events globally and geographically.</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">The primary outcome was systemic ischemic events (composite of cardiovascular death, myocardial infarction, or stroke) at 4 years. The secondary outcome was limb ischemic events (composite of lower limb amputation, peripheral bypass graft, and percutaneous intervention for PAD) at 2 years. Multivariate analysis identified risk factors associated with recurrent ischemic events.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">The primary endpoint rate reached 4.7% during the first year and increased continuously (by 4%-5% each year) to 17.6% by year 4, driven mainly by cardiovascular mortality (11.1% at year 4). Japan experienced lower adjusted ischemic rates (P < 0.01) vs North America. Renal impairment (P < 0.01), congestive heart failure (P < 0.01), history of diabetes (P < 0.01), history of myocardial infarction (P = 0.01), vascular disease (single or poly, P < 0.01), and older age (P < 0.01) were associated with increased risk of systemic ischemic events, whereas statin use was associated with lower risk (P = 0.03). The limb ischemic event rate was 5.7% at 2 years.</AbstractText>
<AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">Four-year systemic ischemic risk in patients with PAD and no history of stroke or transient ischemic attack remains high, and was mainly driven by cardiovascular mortality.</AbstractText>
<CopyrightInformation>© 2017 Wiley Periodicals, Inc.</CopyrightInformation>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Abtan</LastName>
<ForeName>Jérémie</ForeName>
<Initials>J</Initials>
<AffiliationInfo><Affiliation>FACT (French Alliance for Cardiovascular Trials), French Clinical Research Infrastructure Network, University Hospital Departments-FIRE, Hôpital Bichat, Public Assistance Hospitals of Paris, Paris Diderot University, Sorbonne University Paris Cité, and National Institute of Health and Medical Research, U-1148 Paris, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Bhatt</LastName>
<ForeName>Deepak L</ForeName>
<Initials>DL</Initials>
<Identifier Source="ORCID">http://orcid.org/0000-0002-1278-6245</Identifier>
<AffiliationInfo><Affiliation>Heart and Vascular Center, Brigham and Women's Hospital, and Harvard Medical School, Boston, Massachusetts.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Elbez</LastName>
<ForeName>Yedid</ForeName>
<Initials>Y</Initials>
<AffiliationInfo><Affiliation>FACT (French Alliance for Cardiovascular Trials), French Clinical Research Infrastructure Network, University Hospital Departments-FIRE, Hôpital Bichat, Public Assistance Hospitals of Paris, Paris Diderot University, Sorbonne University Paris Cité, and National Institute of Health and Medical Research, U-1148 Paris, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Sorbets</LastName>
<ForeName>Emmanuel</ForeName>
<Initials>E</Initials>
<Identifier Source="ORCID">http://orcid.org/0000-0003-0559-6301</Identifier>
<AffiliationInfo><Affiliation>FACT (French Alliance for Cardiovascular Trials), French Clinical Research Infrastructure Network, University Hospital Departments-FIRE, Hôpital Bichat, Public Assistance Hospitals of Paris, Paris Diderot University, Sorbonne University Paris Cité, and National Institute of Health and Medical Research, U-1148 Paris, France.</Affiliation>
</AffiliationInfo>
<AffiliationInfo><Affiliation>Avicenne Hospital Hôpital, Public Assistance Hospitals of Paris, Paris, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Eagle</LastName>
<ForeName>Kim</ForeName>
<Initials>K</Initials>
<AffiliationInfo><Affiliation>Cardiovascular Center, University of Michigan, Ann Arbor, Michigan.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Reid</LastName>
<ForeName>Christopher M</ForeName>
<Initials>CM</Initials>
<AffiliationInfo><Affiliation>Monash University, Clayton, Victoria, Australia and Curtin University, Bentley, Perth, Western Australia.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Baumgartner</LastName>
<ForeName>Iris</ForeName>
<Initials>I</Initials>
<AffiliationInfo><Affiliation>University Hospital of Bern, Bern, Switzerland.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Wu</LastName>
<ForeName>David</ForeName>
<Initials>D</Initials>
<AffiliationInfo><Affiliation>Merck & Co., Inc., Kenilworth, New Jersey.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Hanson</LastName>
<ForeName>Mary E</ForeName>
<Initials>ME</Initials>
<Identifier Source="ORCID">http://orcid.org/0000-0003-4785-7207</Identifier>
<AffiliationInfo><Affiliation>Merck & Co., Inc., Kenilworth, New Jersey.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Hannachi</LastName>
<ForeName>Hakima</ForeName>
<Initials>H</Initials>
<AffiliationInfo><Affiliation>Merck & Co., Inc., Kenilworth, New Jersey.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Singhal</LastName>
<ForeName>Puneet K</ForeName>
<Initials>PK</Initials>
<AffiliationInfo><Affiliation>Merck & Co., Inc., Kenilworth, New Jersey.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Steg</LastName>
<ForeName>Philippe Gabriel</ForeName>
<Initials>PG</Initials>
<AffiliationInfo><Affiliation>FACT (French Alliance for Cardiovascular Trials), French Clinical Research Infrastructure Network, University Hospital Departments-FIRE, Hôpital Bichat, Public Assistance Hospitals of Paris, Paris Diderot University, Sorbonne University Paris Cité, and National Institute of Health and Medical Research, U-1148 Paris, France.</Affiliation>
</AffiliationInfo>
<AffiliationInfo><Affiliation>National Heart and Lung Institute, Imperial College School of Medicine, Royal Brompton Hospital, Imperial College, London, United Kingdom.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Ducrocq</LastName>
<ForeName>Gregory</ForeName>
<Initials>G</Initials>
<AffiliationInfo><Affiliation>FACT (French Alliance for Cardiovascular Trials), French Clinical Research Infrastructure Network, University Hospital Departments-FIRE, Hôpital Bichat, Public Assistance Hospitals of Paris, Paris Diderot University, Sorbonne University Paris Cité, and National Institute of Health and Medical Research, U-1148 Paris, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><CollectiveName>REACH Registry Investigators</CollectiveName>
</Author>
</AuthorList>
<Language>eng</Language>
<PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType>
</PublicationTypeList>
<ArticleDate DateType="Electronic"><Year>2017</Year>
<Month>05</Month>
<Day>18</Day>
</ArticleDate>
</Article>
<MedlineJournalInfo><Country>United States</Country>
<MedlineTA>Clin Cardiol</MedlineTA>
<NlmUniqueID>7903272</NlmUniqueID>
<ISSNLinking>0160-9289</ISSNLinking>
</MedlineJournalInfo>
<KeywordList Owner="NOTNLM"><Keyword MajorTopicYN="N">Ischemic Risk</Keyword>
<Keyword MajorTopicYN="N">Peripheral Artery Disease</Keyword>
<Keyword MajorTopicYN="N">Vorapaxar</Keyword>
</KeywordList>
</MedlineCitation>
<PubmedData><History><PubMedPubDate PubStatus="received"><Year>2017</Year>
<Month>01</Month>
<Day>12</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="revised"><Year>2017</Year>
<Month>03</Month>
<Day>24</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="accepted"><Year>2017</Year>
<Month>03</Month>
<Day>30</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="pubmed"><Year>2017</Year>
<Month>5</Month>
<Day>19</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="medline"><Year>2017</Year>
<Month>5</Month>
<Day>19</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="entrez"><Year>2017</Year>
<Month>5</Month>
<Day>19</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
</History>
<PublicationStatus>ppublish</PublicationStatus>
<ArticleIdList><ArticleId IdType="pubmed">28520087</ArticleId>
<ArticleId IdType="doi">10.1002/clc.22721</ArticleId>
</ArticleIdList>
</PubmedData>
</pubmed>
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