Issue: April 2015
February 23, 2015
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CADISS: No difference in treatment with antiplatelets, anticoagulants after cervical artery dissection

Issue: April 2015
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NASHVILLE, Tenn. — For prevention of stroke, major bleeding or death, it did not matter whether patients with cervical artery dissection were treated with antiplatelet drugs or anticoagulants, according to findings from the CADISS study.

Perspective from Natalia Rost, MD, MPH

Hugh S. Markus, BA, BM Bch, DM, FRCP, and colleagues enrolled 250 patients diagnosed with cervical artery dissection (118, carotid dissection; 132, vertebral dissection) at local hospitals in the United Kingdom and Australia.

Carotid and vertebral dissection accounts for 10% to 25% of stroke in young and middle-aged patients and is associated with risk for recurrent stroke, Markus, from the Stroke Research Group of the department of neurology at the University of Cambridge, said during a presentation. “This has led people to widely use anticoagulants and antiplatelet agents in an attempt to reduce risk of embolization. But there is really no evidence for either approach, and physicians use different approaches, often believing one approach is particularly good for little reason at all. There are also no [randomized controlled trial] data to govern this choice.”

Furthermore, he said, previous research has estimated that the rate of early recurrent stroke in this population is as low as 1% and as high as 15%, “so we are a bit uncertain as to how high this recurrent stroke risk is, and how intensively we need to treat these patients.”

Patients were randomly assigned antiplatelet agents — aspirin, dipyridamole or clopidogrel alone or in dual combination, as determined by the treating physician — or anticoagulation in the form of low–molecular-weight heparin followed by warfarin. The primary endpoint was ipsilateral stroke and death at 3 months.

Four cases of ipsilateral stroke occurred: three in the antiplatelet group, one in the anticoagulant group. There was one case of major bleeding, a subarachnoid hemorrhage in the anticoagulant group. No deaths were reported during the study period.

The groups did not differ in the incidence of the primary endpoint in the intention-to-treat population (OR = 0.335; 95% CI, 0.006-4.233). The low rate of events is “very reassuring,” Markus said.

A central review of imaging failed to confirm dissection in 52 patients, Markus said. Therefore, the researchers conducted a per-protocol analysis of patients whose dissection was confirmed and also found no difference between the groups in the primary endpoint (OR = 0.346; 95% CI, 0.006-4.39), he said.

Failure to confirm dissection was generally due to poor image quality or to other pathologies such as atherosclerosis being found, according to Markus. “This means that some patients may not be getting the appropriate diagnosis, and dissection has a rather different long-term prognosis than other forms of stroke,” he said.

The researchers determined that, based on the per-protocol endpoint of stroke, death or major bleeding with a power of 0.8 and a significance level of 0.05, it would take a sample size of 9,752 patients to show a difference between the two treatments, Markus said. – by Erik Swain

References:

CADISS trial investigators. Lancet Neurol. 2015;doi:10.1016/S1474-4422(15)70018-9.

Markus HS, et al. Plenary Session II: LB3. Presented at: International Stroke Conference; Feb. 11-13, 2015; Nashville, Tenn.

Disclosure: Markus reports receiving a grant from the Stroke Association for this study.