Key result
Dual antiplatelet therapy in acute stroke patients was associated with prolonged mean time to initiate clotting (5.5 vs 4.6 minutes, P=0.04) compared to no antiplatelet therapy.
Why the study?
Does dual antiplatelet therapy alter coagulation measured by thrombelastography in patients with acute stroke?
Observational (n=202)
Does dual antiplatelet therapy alter coagulation measured by thrombelastography in patients with acute stroke?
Absolute Event Rate: 5.5% vs 4.6%
p-value: p=.04
Dual antiplatelet therapy is associated with a detectable coagulopathy on thrombelastography in acute stroke patients, whereas single antiplatelet therapy effects may not be demonstrated by TEG.
May warrant caution with dual antiplatelet therapy in acute stroke; leaves open effects on bleeding and outcomes.
Background: Thrombelastography (TEG) provides a global, dynamic measure of coagulation. We examined the effect of antiplatelet (AP) medications on coagulation in patients with acute stroke as measured by TEG. Methods: We reviewed prospectively collected data on patients presenting with acute ischemic stroke (AIS) and spontaneous intracerebral hemorrhage (ICH) between 2009 and 2014. Patient demographics and baseline TEG values were compared among 4 different drug use groups: aspirin only, clopidogrel only, both aspirin and clopidogrel, and no AP. Multivariable regression models were conducted to compare the differences in TEG components. Results: A total of 202 patients were included, 139 with AIS and 63 with ICH. Forty-eight (24%) patients were taking aspirin alone, 12 (6%) were taking clopidogrel, 16 (8%) dual AP, and 126 (62%) no AP. Dual AP use was associated with prolonged mean R (time to initiate clotting) of 5.5 minutes as compared to no AP use (4.6 minutes, P = .04). Additionally, mean maximal amplitude (MA; final clot strength) and angle (rate of clot formation) were decreased in the dual AP group (MA = 59.3 mm, angle = 57.8°) as compared to the no AP group (MA = 64.5 mm, angle = 64.5°; P = .04 and P = .01, respectively). Patients on single AP therapy (either aspirin or clopidogrel) did not differ from those on no AP therapy in any TEG parameters measured. Conclusion: Dual AP therapy is associated with a detectable coagulopathy which may have implications in the management of patients with AIS and hemorrhagic stroke. The effects of single AP therapy may not be demonstrated by TEG.
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McDonald et al. (2017) conducted an observational in Acute ischemic stroke and spontaneous intracerebral hemorrhage (n=202). Dual antiplatelet therapy vs. No antiplatelet therapy was evaluated on Mean R (time to initiate clotting) in minutes (p=.04). Dual antiplatelet therapy in acute stroke patients was associated with prolonged mean time to initiate clotting (5.5 vs 4.6 minutes, P=0.04) compared to no antiplatelet therapy.
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