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Related Experiment Video

Updated: Nov 27, 2025

Optimized Management of Endovascular Treatment for Acute Ischemic Stroke
09:21

Optimized Management of Endovascular Treatment for Acute Ischemic Stroke

Published on: January 18, 2018

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Initial experience with the CatchView thrombectomy device for acute ischemic stroke.

Murat Velioglu1, Yilmaz Onal2, Abdulbaki Agackiran3

  • 1Radiology, Fatih Sultan Mehmet Training and Research Hospital, Istanbul, Turkey.

Journal of Neurointerventional Surgery
|December 4, 2020
PubMed
Summary

The CatchView (CV) device shows promise for acute ischemic stroke (AIS) treatment. Initial results indicate high recanalization rates and encouraging clinical outcomes, warranting further investigation in endovascular therapy.

Keywords:
stentstrokethrombectomy

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Area of Science:

  • Neurology
  • Interventional Cardiology
  • Vascular Surgery

Background:

  • Acute ischemic stroke (AIS) poses a significant health challenge.
  • Mechanical thrombectomy is a key endovascular treatment for AIS.
  • The CatchView (CV) device is a novel thrombectomy tool.

Purpose of the Study:

  • To evaluate the initial clinical experience with the CatchView (CV) thrombectomy device in AIS patients.
  • To assess the safety and efficacy of the CV device for clot removal.

Main Methods:

  • Retrospective analysis of 53 AIS patients treated with the CV device (Jan 2019-Feb 2020).
  • Recorded baseline characteristics including NIHSS and IV-tPA administration.
  • Defined successful recanalization as modified TICI 2b-3 and good outcome as mRS ≤2 at 90 days.

Main Results:

  • Successful recanalization achieved in 84.9% of patients.
  • Good clinical outcomes at 90 days observed in 43.39% of patients.
  • Low rates of symptomatic hemorrhage (3.77%) and distal emboli (5.66%) were noted.

Conclusions:

  • The CatchView (CV) device demonstrated encouraging results for successful recanalization in AIS.
  • Initial experience suggests the CV device is a viable option for endovascular stroke treatment.
  • Further studies are needed to confirm long-term efficacy and safety.