Abstract

Antiplatelet drugs are often discontinued early after ischaemic stroke, either because of poor compliance, complications or withdrawal of care. It is unclear whether this places patients at increased risk of recurrence. We explored the association between cardiovascular event rate and persistence with prescribed antiplatelet drugs. We used a matched case-control design using the Virtual International Stroke Trials Archive (VISTA). Cases were patients who had an acute coronary syndrome, recurrent stroke or transient ischaemic attack within 90days post-stroke and were matched for age±10years and sex with up to four controls. Antiplatelet use was categorized as persistent (used for >3days and continued up to day 90), early cessation (used antiplatelet <3days) or stopped/interrupted users (used for >3days but stopped prior to day 90). These categories were compared in cases and controls using a conditional logistic regression model that adjusted for potential confounders. A total of 970 patients were included, of whom 194 were cases and 776 were matched controls. At 90days, 10 cases (5.2%) and 58 controls (7.5%) stopped/interrupted their antiplatelet. The risk of cardiovascular event was not different in stopped/interrupted users (adjusted odds ratio 0.70, 95% confidence interval 0.33, 1.48; P=0.352) and early cessations (adjusted odds ratio 1.04, 95% confidence interval 0.62, 1.74; P=0.876) when compared to persistent users. We found no increased risk in patients who stopped and interrupted antiplatelets early after stroke but the study was limited by a small sample size and further research is needed.

Highlights

  • There is a risk of recurrence following acute ischaemic stroke [1]

  • Antiplatelet therapy is recommended for secondary prevention after ischaemic stroke

  • Interrupting or stopping antiplatelet therapy increases the risk of cardiovascular events

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Summary

Introduction

There is a risk of recurrence following acute ischaemic stroke [1]. Antiplatelet therapy is given to reduce this risk and the risk of other vascular outcomes [2, 3]. National Institute for Health and Clinical Excellence (NICE) and Scottish Intercollegiate Guidelines Network (SIGN) guidelines recommend that antiplatelet therapy must be started early and continued indefinitely for long term secondary stroke prevention [3, 4]. In the UK guidelines favour aspirin therapy for 2-weeks followed by clopidogrel or the combination of low-dose aspirin and dipyridamole. Persistence with antiplatelet regimens is variable after stroke. Rates of aspirin discontinuation of less than 10% to almost 50% reported [5, 6].

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