Background: Meta-analysis of clinical trials supports the use of early antithrombotic medication in ischemic stroke and transient ischemic attack. It is not known whether this therapy is delivered within the 85% threshold that is acceptable in North America's Get With The Guidelines stroke program.
Aim: to investigate the pooled proportion of patients receiving antiplatelet therapy within 48 hours of ischemic stroke.
Methods: PubMed to November 2022 was searched for studies reporting "stroke", "audit", "antithrombotic", "national" and "registry". Multilevel random effects meta-analysis was used to cluster studies by country.
Results: There were 45 studies describing 1,178,595 patients. The pooled proportion of patients receiving antithrombotic therapy within 48 hours was 81.1%, (95% CI 74.5, 87.8, p<0.0001, I=99.99%). The high heterogeneity was due to within-country (I=55.4%) and between-country heterogeneity (I=44.6%). There was no statistical significance (p=0.35) between low- to middle- income countries (LMIC) - 81.8%, (95% CI 76.1, 87.4, p<0.01, I=100%) and high-income countries (HIC) - 86.8%, (95% CI 81.2, 92.3, p<0.01, I=99.7%) nor any difference between contemporary studies (2008 and later) - 86.5%, (95% CI 82.3, 90.8, p<0.01, I=100%) - and studies published before 2008 - 69.9%, (95% CI 57.4, 82.4, p<0.01, I=99.7%). Sensitivity analysis showed no difference when excluding single centre studies, observations with n<500, or both. Meta-regression showed proportion of antiplatelet administration at 48 hours to increase significantly with subsequent year of publication (β=0.01, 95% CI 0.00, 0.02, p<0.05).
Conclusion: Our key finding is that the majority of countries do not yet provide early antiplatelet therapy at a level acceptable by Get With The Guidelines hospitals.
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http://dx.doi.org/10.1016/j.jstrokecerebrovasdis.2024.108213 | DOI Listing |
Ann Vasc Dis
December 2024
Division of Cardiology, Central Japan International Medical Center, Minokamo, Gifu, Japan.
Evidence for antithrombotic therapy after endovascular therapy (EVT) is limited. This retrospective, multicenter, observational study enrolled 732 consecutive patients with lower extremity artery disease who underwent EVT between January 2018 and December 2019. Overall, 570 patients who received single antiplatelet therapy (SAPT) and dual antiplatelet therapy (DAPT) were selected and divided into the SAPT (n = 189) and DAPT (n = 381) groups.
View Article and Find Full Text PDFJ Hand Surg Asian Pac Vol
December 2024
Department of Human Enhancement and Hand Surgery, Nagoya University Graduate School of Medicine, Nagoya, Japan.
To investigate the impact of antithrombotic drug continuation or interruption on postoperative outcomes in patients with carpal tunnel syndrome (CTS) who undergo endoscopic carpal tunnel release (ECTR). This prospective, randomised, open-label, parallel group trial was conducted between December 2016 and October 2022 of CTS patients on antithrombotic medications who underwent ECTR. The 65 participants were randomly assigned to either maintain antithrombotic therapy (, 34 patients) or suspend it (, 31 patients).
View Article and Find Full Text PDFJ Stroke Cerebrovasc Dis
December 2024
Stroke and Aging Research Group, Department of Medicine, Monash University, Melbourne, Australia. Electronic address:
Int J Stroke
December 2024
Division of Neurology, McMaster University, Hamilton, ON, Canada.
Background: Secondary stroke prevention in patients with atrial fibrillation (AF) is one of the fastest growing areas in the field of cerebrovascular diseases. This Scientific statement from the World Stroke Organization Brain & Heart Task Force provides a critical analysis of the strength of current evidence this topic, highlights areas of current controversy, identifies knowledge gaps, and proposes priorities for future research.
Methods: We select topics with the highest clinical relevance and perform a systematic search to answer specific practical questions.
J Am Heart Assoc
December 2024
Arbor Research Collaborative for Health Ann Arbor MI USA.
Background: People with kidney failure have a high risk of cardiovascular morbidity/death, including thromboembolic events. Factor XIa inhibitors are a new class of anticoagulants in development that may offer antithrombotic benefits with a lower risk of incremental bleeding events than traditional therapies. We investigated major adverse vascular events (MAVEs), a relevant composite outcome for testing novel antithrombotic agents, in a large cohort of patients on hemodialysis, to better understand the key requirements to adequately design a phase 3 trial.
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