AI Article Synopsis

  • This study examines the link between using the AngioSeal vascular closure device and the risk of deep vein thrombosis (DVT) in patients with aneurysmal subarachnoid hemorrhage (aSAH) after undergoing angiography.
  • Researchers reviewed data from 2005-2018 involving 459 aSAH patients, finding that those who used AngioSeal had a higher incidence of ipsilateral DVT (7.6%) compared to those who underwent manual compression (3.4%).
  • The study concludes that the AngioSeal device significantly increases the risk of DVT in aSAH patients receiving femoral artery access for cerebral angiography within 14 days post-pro

Article Abstract

Background: Deep vein thrombosis (DVT) is a known complication in patients with aneurysmal subarachnoid hemorrhage (aSAH). This study investigated the association between use of the AngioSeal (St. Jude Medical, Minnetonka, MN) vascular closure device and the risk of ipsilateral and any DVT event after angiography in patients with aSAH.

Methods: We conducted a review of our institutional cerebral angiography database for the years 2005-2018 to identify all adult patients who underwent angiography for aSAH. We compared the incidence of DVT (occurring within 14 days) between aSAH patients who underwent manual compression versus the AngioSeal closure device.

Results: A total of 459 aSAH patients underwent angiography; 262 underwent manual compression (57.1%) and 197 received AngioSeal (42.9%). There was a 3.4% rate of ipsilateral DVT in the manual compression group and 7.6% in the AngioSeal closure device group (χ2 test, P = 0.04). Similarly, the rate of any DVT was 8.8% for manual compression and 16.8% for patients who received AngioSeal (χ2 test, P = 0.01). On multivariate analysis, AngioSeal remained a significant independent predictor of ipsilateral DVT (odds ratio 2.4, P = 0.04) and any DVT (odds ratio 2.3, P = 0.01).

Conclusions: In aSAH patients undergoing cerebral angiographic procedures with access through the femoral artery, the use of AngioSeal closure device was found to be associated with a significantly increased risk of ipsilateral DVT within 14 days.

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Source
http://dx.doi.org/10.1016/j.wneu.2019.09.170DOI Listing

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