Key result
Bridging therapy with low-molecular-weight heparin after acute stroke was associated with a higher risk of the composite endpoint compared to no bridging (11.3% vs 5.0%; OR 2.3; 95% CI 1.4-3.7).
Why the study?
Bridging therapy with low-molecular-weight heparin reportedly leads to worse outcomes in acute cardioembolic stroke due to intracerebral bleeding, but remains common in clinical practice.
Does bridging therapy with low-molecular-weight heparin increase adverse clinical outcomes in patients with atrial fibrillation after acute stroke?
Observational (n=1,810)
Does bridging therapy with low-molecular-weight heparin increase adverse clinical outcomes in patients with atrial fibrillation after acute stroke?
Odds Ratio: 2.3 (95% CI 1.4–3.7)
Absolute Event Rate: 11.3% vs 5%
p-value: p=<0.0001
In patients with atrial fibrillation and acute cardioembolic stroke, bridging therapy with full-dose low-molecular-weight heparin is associated with increased risks of both early ischemic recurrence and hemorrhagic transformation.
Should not yet change LMWH bridging practice after AF stroke; leaves open randomized confirmation of this observational harm signal.
Background and Purpose- Bridging therapy with low-molecular-weight heparin reportedly leads to a worse outcome for acute cardioembolic stroke patients because of a higher incidence of intracerebral bleeding. However, this practice is common in clinical settings. This observational study aimed to compare (1) the clinical profiles of patients receiving and not receiving bridging therapy, (2) overall group outcomes, and (3) outcomes according to the type of anticoagulant prescribed. Methods- We analyzed data of patients from the prospective RAF and RAF-NOACs studies. The primary outcome was defined as the composite of ischemic stroke, transient ischemic attack, systemic embolism, symptomatic cerebral bleeding, and major extracerebral bleeding observed at 90 days after the acute stroke. Results- Of 1810 patients who initiated oral anticoagulant therapy, 371 (20%) underwent bridging therapy with full-dose low-molecular-weight heparin. Older age and the presence of leukoaraiosis were inversely correlated with the use of bridging therapy. Forty-two bridged patients (11.3%) reached the combined outcome versus 72 (5.0%) of the nonbridged patients (P=0.0001). At multivariable analysis, bridging therapy was associated with the composite end point (odds ratio, 2.3; 95% CI, 1.4-3.7; P<0.0001), as well as ischemic (odds ratio, 2.2; 95% CI, 1.3-3.9; P=0.005) and hemorrhagic (odds ratio, 2.4; 95% CI, 1.2-4.9; P=0.01) end points separately. Conclusions- Our findings suggest that patients receiving low-molecular-weight heparin have a higher risk of early ischemic recurrence and hemorrhagic transformation compared with nonbridged patients.
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Altavilla et al. (2019) conducted an observational in Acute cardioembolic stroke with atrial fibrillation (n=1,810). Bridging therapy with low-molecular-weight heparin vs. No bridging therapy was evaluated on composite of ischemic stroke, transient ischemic attack, systemic embolism, symptomatic cerebral bleeding, and major extracerebral bleeding observed at 90 days after the acute stroke (OR 2.3, 95% CI 1.4-3.7, p=<0.0001). Bridging therapy with low-molecular-weight heparin after acute stroke was associated with a higher risk of the composite endpoint compared to no bridging (11.3% vs 5.0%; OR 2.3; 95% CI 1.4-3.7).
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