Article Text

Download PDFPDF
Aspiration catheter failure leading to carotid-cavernous fistula during stroke thrombectomy
  1. Mario Agrait1,
  2. Joanna Kee-Sampson1,
  3. Grzegorz Brzezicki2,
  4. Saeed Bashir1,
  5. Jerry Matteo1,
  6. Travis Meyer1 and
  7. Daniel Siragusa1
  1. 1Interventional Radiology, University of Florida College of Medicine, Jacksonville, Florida, USA
  2. 2Department of Neurosurgery, University of Florida College of Medicine, Jacksonville, Florida, USA
  1. Correspondence to Dr Joanna Kee-Sampson; joannakee{at}gmail.com

Abstract

Endovascular thrombectomy in acute ischaemic stroke commonly uses aspiration catheters, either alone or in combination with stent retrievers. The Penumbra Aspiration System (Penumbra, Alameda, California, USA) was first approved by the US Food and Drug Administration in 2007, with low reported device-related complications. We present a case of a previously unreported complication related to malfunction of a Penumbra aspiration catheter during stroke thrombectomy resulting in a carotid-cavernous fistula.

  • stroke
  • thrombectomy
  • fistula
  • device

Statistics from Altmetric.com

Request Permissions

If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.

Footnotes

  • Twitter @JKeeSampson

  • Contributors DS and GB performed and managed this case and identified it for the case report. MA and JK-S did the literature search, wrote the article and selected the images. All authors contributed to the editing process.

  • Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.

  • Competing interests None declared.

  • Patient consent for publication Next of kin consent obtained.

  • Provenance and peer review Not commissioned; internally peer reviewed.

  • Supplemental material This content has been supplied by the author(s). It has not been vetted by BMJ Publishing Group Limited (BMJ) and may not have been peer-reviewed. Any opinions or recommendations discussed are solely those of the author(s) and are not endorsed by BMJ. BMJ disclaims all liability and responsibility arising from any reliance placed on the content. Where the content includes any translated material, BMJ does not warrant the accuracy and reliability of the translations (including but not limited to local regulations, clinical guidelines, terminology, drug names and drug dosages), and is not responsible for any error and/or omissions arising from translation and adaptation or otherwise.