Summary
Stroke prevention guidelines recommend oral anticoagulants (OAC) for atrial fibrillation
(AF) patients at moderate/high risk of stroke, and antiplatelet or no therapy for
those at low/moderate risk. Outcomes for AF patients receiving antiplatelet/no therapy
in ‘real-life’ clinical practice were explored. This study compared clinical event
rates (stroke/bleeding) for AF patients treated with OAC therapy, antiplatelets or
no therapy in usual clinical practice to event rates in OAC-treated AF patients from
optimally-monitored ‘real-life’ settings (anticoagulation clinics). We searched biomedical
literature (1994–2010) using PubMed to identify ‘real-world’ studies of clinical event
rates for AF patients receiving OAC therapy, antiplatelets, or no therapy; event rates
were extracted for each treatment and setting. We identified 136 studies of thromboembolic
events and 86 of bleeding events. Ischaemic stroke rates (30 studies) were higher
for AF patients receiving no therapy (median: 4.45/100 person-years; range: 0.25–5.9)
or antiplatelet-therapy (median: 4.45/100 person-years; range: 2.0–10) compared to
OACtreated patients monitored in anticoagulation clinics (median: 1.72/100 person-years;
range: 0.97–2.00), or from a non-specialized setting (median 1.66/100 person-years;
range: 0–4.9). Major bleeding rates (32 studies) for patients receiving antiplatelet/no
therapy were similar to OAC-treated patients from both clinical settings. As in randomised
clinical trials, AF patients in ‘real-world’ clinical practice receiving antiplatelet/no
therapy have higher rates of ischaemic stroke than OAC-treated patients. Antiplatelet/no
therapy was associated with similar bleeding rates to OAC therapy. Increasing utilisation
of anticoagulants in clinical practice could improve patient outcomes.
Keywords
Atrial fibrillation - oral anticoagulation - antiplatelets - stroke - bleeding