Article Text

Download PDFPDF
Original research
Multi-centric European post-market follow-up study of the Neuroform Atlas Stent System: primary results
  1. Pierre-Henri Lefevre1,
  2. Peter Schramm2,
  3. André Kemmling3,
  4. Xavier Barreau4,
  5. Gaultier Marnat4,
  6. Michel Piotin5,
  7. Ansgar Berlis6,
  8. Isabel Wanke7,
  9. Alain Bonafe1,
  10. Emmanuel Houdart8
  11. ATLAS EU PMCF Investigators
  1. 1Neuroradiology department, Gui de Chauliac Hospital Montpellier University Hospital, Montpellier, France
  2. 2Department of Neuroradiology, University Medical Center Schleswig-Holstein, Luebeck, Germany
  3. 3Institute of Neuroradiology, University Medical Center Schleswig-Holstein, Luebeck, Germany
  4. 4Interventional and Diagnostic Neuroradiology, Bordeaux University Hospital, Bordeaux, France
  5. 5Department of Interventional Neuroradiology, Fondation Rothschild Hospital, Paris, France
  6. 6Department of Diagnostic and Interventional Neuroradiology, Klinikum Augsburg, Augsburg, Bayern, Germany
  7. 7Neuroradiology Department, Hirslanden Clinic, Zurich, Switzerland
  8. 8Neuroradiology Department, Lariboisière Hospital, Paris, France
  1. Correspondence to Dr Pierre-Henri Lefevre, Neuroradiology department, Hôpital Gui de Chauliac Service de Neuroradiologie, 34295 Montpellier, France; ph.lefevre30{at}gmail.com

Abstract

Background Few prospective series have described the safety and effectiveness of the Neuroform Atlas Stent System. We aimed to investigate the efficacy and safety of the device in patients treated for unruptured aneurysm.

Methods ATLAS EU PMCF is a consecutive, prospective, multicentric study that included patients with unruptured saccular aneurysm of all sizes. Follow-up visits were scheduled at 3–6 months and 12–16 months with digital subtraction angiography (DSA) or MRI imaging follow-up as per the site standard of care. The primary efficacy endpoint was adequate aneurysm occlusion (Raymond Roy occlusion grade I and II) on 12 month angiography. The primary safety endpoint was any major stroke or ipsilateral stroke or neurological death within 12 months.

Results Of the 106 patients consented, 105 were treated with at least one Neuroform Atlas stent. There was a failed implantation attempt in 1 patient, 85 patients received lateral stenting, and 19 patients received Y-stenting. Mean aneurysm neck size was 4.2 mm (range 1.9–33 mm). Adequate occlusion was observed in 95.1% immediately after the procedure and in 98.9% of cases at 1 year DSA follow-up. Overall, 1.0% (1/102; 95% CI 0.0% to 5.3%) of patients experienced a primary safety endpoint of major stroke. Three minor strokes resulted in a modified Rankin Scale score of 2.

Conclusions In this multicentric, prospective study, stent-assisted coiling of medium size unruptured aneurysms with the Neuroform Atlas stent resulted in a favorable rate of satisfactory occlusion. In our findings, the use of the Y-stenting technique was associated with increased rates of procedural complications.

  • aneurysm
  • coil
  • stent

Data availability statement

Data may be obtained from a third party and are not publicly available.

Statistics from Altmetric.com

Data availability statement

Data may be obtained from a third party and are not publicly available.

View Full Text

Footnotes

  • Collaborators ATLAS EU PMCF Investigators and coordinators: Ansgar Berlis, Christoph Maurer, Martin Seidler, Ilse Kummer, Sabine Hanisch, Gabriele Jochum-Pfeilsticker, Marius Hartmann, Steffen Reissberg, Sascha Schiffler, Nadja Rieckehr, Werner Weber, Annika Kowoll, Anushe Weber, Sebastian Fischer, Mara Postert, Peter Schramm, Thomas Eckey, André Kemmling, Alexander Neumann, Ramona Schramm, Alain Bonafé, Vincent Costalat, Carlos Riquelme, Pierre-Henri Lefevre, Grégory Gascou, Marinette Moynier, Emmanuel Houdart, Vittorio Civelli, Alexis Guédon, Jean-Pierre Saint-Maurice, Marc-Antoine Labeyrie, Alexandre Parpaleix, Baptiste Bonnet, Kamil Zelenak, Jana Zelenakova, Branislav Kolarovszki, Michel Piotin, Raphael Blanc, Stanislas Smajda, Jean-Philippe Desilles, Gabriele Ciccio, Robert Fahed, Hocine Redjem, Mylène Hamdani, Malek Ben Maacha, Lucia Lopes, Xavier Barreau, Gaultier Marnat, Florent Maire, Marine Premont, Laura Albizu, Jean-Christophe Gentric, Julien Ognard, Géraldine Viard, Ana Paula Narata, Vladimir Charron, Nicolas Charron

  • Contributors The last two authors contributed equally to the manuscript. All authors made substantial contributions to the conception and design, analysis, and interpretation of data; drafted or critically revised the article; and gave final approval of the version to be published.

  • Funding The ATLAS EU PMCF study (Evaluation of Safety and Performance of the Neuroform Atlas™ Stent System for Intracranial Aneurysm Treatment – Post Market Clinical Follow-up) was funded by Stryker Neurovascular (Fremont, California, United States).

  • Competing interests P-HL reports paid lectures with Stryker, Medtronic and Phenox outside the present study. PS reports speaker honoraria and travel support from Penumbra, Phenox and Stryker outside the present study. AK reports consulting and proctoring activities with Phenox, Penumbra, Stryker, Acandis outside the present study. XB reports service and related fees with Stryker outside this study and within past 3 years. Proctored or received service-related fees from MicroVention (Proctor). GM reports paid lectures with Microvention and Medtronic. MP reports shares in Basecamp Vascular. ABe reports a proctoring activity for Stryker outside this study and within past 3 years, proctored or received service-related fees from MicroVention (Proctor), Sequent Medical (Proctor), Phenox (lecture honorary, CEC), and Penumbra (lecture honorary). IW is speaker for Bayer, not related to the product. ABo is consultant for Stryker, Balt and Phenox. EH is the principal investigator of the present ATLAS EU study.

  • Provenance and peer review Not commissioned; externally 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.

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.