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    <subfield code="a">10.3390/jcm9051526</subfield>
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    <subfield code="2">sideral</subfield>
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    <subfield code="a">eng</subfield>
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  <datafield tag="100" ind1=" " ind2=" ">
    <subfield code="a">Laredo, Viviana</subfield>
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  <datafield tag="245" ind1=" " ind2=" ">
    <subfield code="a">No differences in gastrointestinal bleeding risk among clopidogrel-, ticagrelor-, or prasugrel-based dual antiplatelet therapy</subfield>
  </datafield>
  <datafield tag="260" ind1=" " ind2=" ">
    <subfield code="c">2020</subfield>
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    <subfield code="a">Access copy available to the general public</subfield>
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    <subfield code="a">The risk for gastrointestinal bleeding from dual antiplatelet therapy (DAPT) with new antiplatelets (prasugrel/ticagrelor) compared to clopidogrel is unclear. Aim: To determine the risk and type of major (gastrointestinal bleeding requiring hospitalization) and minor (anemia and iron deficiency) gastrointestinal events with different types of DAPT. Methods: Retrospective observational cohort study of patients who started DAPT after percutaneous coronary intervention. Follow-up was censored after 12 months of DAPT, when a major gastrointestinal event occurred, or when DAPT was discontinued. Results: Among 1, 327 patients (54.03% were treated with clopidogrel-based DAPT, 38.13% with ticagrelor-based DAPT, and 7.84% with prasugrel-based DAPT), 29.5% had at least one gastrointestinal event. Patients taking clopidogrel-DAPT were older, with more comorbidities, and higher gastrointestinal risk compared to those taking other DAPT regimens. Adjusted hazard ratios (HRs) showed no between-group differences in the risk for major (clopidogrel vs. new antiplatelets: HR 0.996; 95% confidence interval 0.497-1.996) and minor (HR 0.920; 0.712-1.189) gastrointestinal events. Most patients received proton pump inhibitors while on DAPT (93.3%) and after withdrawal (83.2%). Conclusion: Prasugrel- or ticagrelor-based DAPT was not associated with increased gastrointestinal bleeding risk when compared to clopidogrel-DAPT. New antiplatelets do not necessarily need to be restricted to patients with low gastrointestinal risk.</subfield>
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    <subfield code="u">http://creativecommons.org/licenses/by/3.0/es/</subfield>
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    <subfield code="a">4.241</subfield>
    <subfield code="b">2020</subfield>
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    <subfield code="a">MEDICINE, GENERAL &amp; INTERNAL</subfield>
    <subfield code="b">39 / 169 = 0.231</subfield>
    <subfield code="c">2020</subfield>
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    <subfield code="e">T1</subfield>
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    <subfield code="a">info:eu-repo/semantics/article</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Sostres, Carlos</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0001-7466-3876</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Garcia, Sandra</subfield>
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    <subfield code="a">Carrera-Lasfuentes, Patricia</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Revilla-Marti, Pablo</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Lanas, Ángel</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0001-5932-2889</subfield>
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  <datafield tag="710" ind1="2" ind2=" ">
    <subfield code="1">1007</subfield>
    <subfield code="2">610</subfield>
    <subfield code="a">Universidad de Zaragoza</subfield>
    <subfield code="b">Dpto. Medicina, Psiqu. y Derm.</subfield>
    <subfield code="c">Area Medicina</subfield>
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  <datafield tag="773" ind1=" " ind2=" ">
    <subfield code="g">9, 5 (2020), 1526  [10 pp.]</subfield>
    <subfield code="p">J. clin.med.</subfield>
    <subfield code="t">JOURNAL OF CLINICAL MEDICINE</subfield>
    <subfield code="x">2077-0383</subfield>
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    <subfield code="a">2021-09-02-09:47:05</subfield>
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