Antithrombotic treatment and major adverse cardiac events after bleeding in patients with myocardial infarction: a retrospective analysis of nationwide registry data

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Standard

Antithrombotic treatment and major adverse cardiac events after bleeding in patients with myocardial infarction : a retrospective analysis of nationwide registry data. / Nabi, Hafsah; Rørth, Rasmus; Tajchman, Daniel H; Holmvang, Lene; Torp-Pedersen, Christian; Gislason, Gunnar; Fosbøl, Emil L.; Køber, Lars; Sørensen, Rikke.

I: European Heart Journal - Cardiovascular Pharmacotherapy, Bind 6, Nr. 1, 2020, s. 14-21.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Nabi, H, Rørth, R, Tajchman, DH, Holmvang, L, Torp-Pedersen, C, Gislason, G, Fosbøl, EL, Køber, L & Sørensen, R 2020, 'Antithrombotic treatment and major adverse cardiac events after bleeding in patients with myocardial infarction: a retrospective analysis of nationwide registry data', European Heart Journal - Cardiovascular Pharmacotherapy, bind 6, nr. 1, s. 14-21. https://doi.org/10.1093/ehjcvp/pvz025

APA

Nabi, H., Rørth, R., Tajchman, D. H., Holmvang, L., Torp-Pedersen, C., Gislason, G., Fosbøl, E. L., Køber, L., & Sørensen, R. (2020). Antithrombotic treatment and major adverse cardiac events after bleeding in patients with myocardial infarction: a retrospective analysis of nationwide registry data. European Heart Journal - Cardiovascular Pharmacotherapy, 6(1), 14-21. https://doi.org/10.1093/ehjcvp/pvz025

Vancouver

Nabi H, Rørth R, Tajchman DH, Holmvang L, Torp-Pedersen C, Gislason G o.a. Antithrombotic treatment and major adverse cardiac events after bleeding in patients with myocardial infarction: a retrospective analysis of nationwide registry data. European Heart Journal - Cardiovascular Pharmacotherapy. 2020;6(1):14-21. https://doi.org/10.1093/ehjcvp/pvz025

Author

Nabi, Hafsah ; Rørth, Rasmus ; Tajchman, Daniel H ; Holmvang, Lene ; Torp-Pedersen, Christian ; Gislason, Gunnar ; Fosbøl, Emil L. ; Køber, Lars ; Sørensen, Rikke. / Antithrombotic treatment and major adverse cardiac events after bleeding in patients with myocardial infarction : a retrospective analysis of nationwide registry data. I: European Heart Journal - Cardiovascular Pharmacotherapy. 2020 ; Bind 6, Nr. 1. s. 14-21.

Bibtex

@article{c8aadbe327e8415597a4260f6c1974a6,
title = "Antithrombotic treatment and major adverse cardiac events after bleeding in patients with myocardial infarction: a retrospective analysis of nationwide registry data",
abstract = "AIMS: The aim of this study was to describe the use of antithrombotic therapy following a bleeding event among patients with myocardial infarction (MI), and the associated risk of major adverse cardiac events (MACE).METHODS AND RESULTS: Using Danish nationwide registries, patients hospitalized with a bleeding event within 1 year after MI were identified. Antithrombotic treatment with aspirin, clopidogrel, and/or vitamin K antagonists (VKA) was determined at the bleeding and at Day 90 and 180 post-bleed. Based on guidelines, patients were stratified into four groups: expected, reduced, discontinued, or intensified treatment. Risk of MACE (ischaemic stroke, MI, or death) within the first year was assessed by Cox proportional hazard models. A total of 3324 patients with a bleeding after MI were included. At Day 90 post-bleed, 1052 (31.7%) received expected antithrombotic treatment, 1301 (39.2%) reduced, 164 (4.9%) intensified, and 807 (24.3%) no treatment. Major adverse cardiac events occurred in 637 (19.2%) patients. With dual antiplatelet therapy as reference, adjusted hazard ratios for MACE were: aspirin 1.81 (1.06-3.09), clopidogrel 1.08 (0.64-1.82), VKA 1.08 (0.47-2.48), VKA + aspirin 1.97 (0.95-4.07), VKA + clopidogrel 0.26 (0.03-1.91), triple 1.73 (0.50-5.95), and no treatment 1.93 (1.11-3.36).CONCLUSION: The majority of MI patients reduced or discontinued their antithrombotic therapy post-bleed. Patients in monotherapy with aspirin or no treatment post-bleed had a higher risk of MACE Further studies of optimal antithrombotic treatments after a bleed are needed.",
author = "Hafsah Nabi and Rasmus R{\o}rth and Tajchman, {Daniel H} and Lene Holmvang and Christian Torp-Pedersen and Gunnar Gislason and Fosb{\o}l, {Emil L.} and Lars K{\o}ber and Rikke S{\o}rensen",
year = "2020",
doi = "10.1093/ehjcvp/pvz025",
language = "English",
volume = "6",
pages = "14--21",
journal = "European Heart Journal - Cardiovascular Pharmacotherapy",
issn = "2055-6837",
publisher = "Oxford University Press",
number = "1",

}

RIS

TY - JOUR

T1 - Antithrombotic treatment and major adverse cardiac events after bleeding in patients with myocardial infarction

T2 - a retrospective analysis of nationwide registry data

AU - Nabi, Hafsah

AU - Rørth, Rasmus

AU - Tajchman, Daniel H

AU - Holmvang, Lene

AU - Torp-Pedersen, Christian

AU - Gislason, Gunnar

AU - Fosbøl, Emil L.

AU - Køber, Lars

AU - Sørensen, Rikke

PY - 2020

Y1 - 2020

N2 - AIMS: The aim of this study was to describe the use of antithrombotic therapy following a bleeding event among patients with myocardial infarction (MI), and the associated risk of major adverse cardiac events (MACE).METHODS AND RESULTS: Using Danish nationwide registries, patients hospitalized with a bleeding event within 1 year after MI were identified. Antithrombotic treatment with aspirin, clopidogrel, and/or vitamin K antagonists (VKA) was determined at the bleeding and at Day 90 and 180 post-bleed. Based on guidelines, patients were stratified into four groups: expected, reduced, discontinued, or intensified treatment. Risk of MACE (ischaemic stroke, MI, or death) within the first year was assessed by Cox proportional hazard models. A total of 3324 patients with a bleeding after MI were included. At Day 90 post-bleed, 1052 (31.7%) received expected antithrombotic treatment, 1301 (39.2%) reduced, 164 (4.9%) intensified, and 807 (24.3%) no treatment. Major adverse cardiac events occurred in 637 (19.2%) patients. With dual antiplatelet therapy as reference, adjusted hazard ratios for MACE were: aspirin 1.81 (1.06-3.09), clopidogrel 1.08 (0.64-1.82), VKA 1.08 (0.47-2.48), VKA + aspirin 1.97 (0.95-4.07), VKA + clopidogrel 0.26 (0.03-1.91), triple 1.73 (0.50-5.95), and no treatment 1.93 (1.11-3.36).CONCLUSION: The majority of MI patients reduced or discontinued their antithrombotic therapy post-bleed. Patients in monotherapy with aspirin or no treatment post-bleed had a higher risk of MACE Further studies of optimal antithrombotic treatments after a bleed are needed.

AB - AIMS: The aim of this study was to describe the use of antithrombotic therapy following a bleeding event among patients with myocardial infarction (MI), and the associated risk of major adverse cardiac events (MACE).METHODS AND RESULTS: Using Danish nationwide registries, patients hospitalized with a bleeding event within 1 year after MI were identified. Antithrombotic treatment with aspirin, clopidogrel, and/or vitamin K antagonists (VKA) was determined at the bleeding and at Day 90 and 180 post-bleed. Based on guidelines, patients were stratified into four groups: expected, reduced, discontinued, or intensified treatment. Risk of MACE (ischaemic stroke, MI, or death) within the first year was assessed by Cox proportional hazard models. A total of 3324 patients with a bleeding after MI were included. At Day 90 post-bleed, 1052 (31.7%) received expected antithrombotic treatment, 1301 (39.2%) reduced, 164 (4.9%) intensified, and 807 (24.3%) no treatment. Major adverse cardiac events occurred in 637 (19.2%) patients. With dual antiplatelet therapy as reference, adjusted hazard ratios for MACE were: aspirin 1.81 (1.06-3.09), clopidogrel 1.08 (0.64-1.82), VKA 1.08 (0.47-2.48), VKA + aspirin 1.97 (0.95-4.07), VKA + clopidogrel 0.26 (0.03-1.91), triple 1.73 (0.50-5.95), and no treatment 1.93 (1.11-3.36).CONCLUSION: The majority of MI patients reduced or discontinued their antithrombotic therapy post-bleed. Patients in monotherapy with aspirin or no treatment post-bleed had a higher risk of MACE Further studies of optimal antithrombotic treatments after a bleed are needed.

U2 - 10.1093/ehjcvp/pvz025

DO - 10.1093/ehjcvp/pvz025

M3 - Journal article

C2 - 31274145

VL - 6

SP - 14

EP - 21

JO - European Heart Journal - Cardiovascular Pharmacotherapy

JF - European Heart Journal - Cardiovascular Pharmacotherapy

SN - 2055-6837

IS - 1

ER -

ID: 237702819