[13] However, heparin alone has been shown to be limited in preventing thromboembolic events following aneurysm coiling.[13] Aspirin (acetylsalicylic acid) and clopidogrel (Plavix) are used in the management of elective endovascular treatment of cerebral aneurysms to prevent thromboembolic complications despite a lack of robust data to support this approach.[14,15] Although aspirin has shown efficacy in reducing the this website risk of intraoperative atherothrombotic complications, the antiplatelet agent is associated
with insufficient inhibition of platelet aggregation under shear stress, and an increased risk of gastrointestinal bleeding.[16,17] Clopidogrel may be a favorable alternative to aspirin as it has demonstrated greater efficacy in reducing thromboembolic events and less safety issues in patients with vascular disease.[18] The majority of thromboembolic complications associated with endovascular procedures occur perioperatively, which coincides with the period of maximal local prothrombotic activity, i.e. the initial 24 hours;
antiplatelet therapy MI-503 nmr initiated before Selleck CAL101 and/or during intervention may diminish thrombus formation.[9,13,19] Therefore, in this current historical control study, we sought to compare the efficacy of clopidogrel with that of aspirin for reduction in risk of periprocedural thromboembolic complications resulting from elective coil embolization for unruptured cerebral aneurysms by
evaluating abnormal Cediranib (AZD2171) high-intensity areas (HIA) diagnostic of ischemic lesions, i.e. restricted diffusion or silent ischemia, at 24 hours after the procedure. Methods Prospective data from the use of clopidogrel during coil embolization for unruptured cerebral aneurysms, collected from January 2007 through to December 2007 (clopidogrel was approved in Japan in 2006 and 2007 for use in stroke and acute coronary syndromes [ACS], respectively), were compared with retrospective data on the use of aspirin for the same procedure collected from February 2005 to December 2006. This study was conducted at Kohnan Hospital, Sendai, Japan, and the local ethics committee provided approval prior to study initiation. Eligible patients included those with signs and symptoms of suspected cerebral aneurysm who were evaluated and, following confirmation with imaging using either CT or MRI, were scheduled to undergo elective coil embolization for an unruptured cerebral aneurysm. Study inclusion was dependent on full clinical assessments including health status and life expectancy. Informed consent was required prior to the procedure. Data were collected on patient history of previous aneurysms (ruptured or unruptured).