Balloon Guide Catheter Versus Non–Balloon Guide Catheter: A MR CLEAN Registry Analysis

Author:

Knapen Robrecht R.M.M.12,Goldhoorn Robert‐Jan B.3,Hofmeijer Jeannette45,Lycklamaà Nijeholt Geert J.6,van den Berg René7,van den Wijngaard Ido R.68,van Oostenbrugge Robert J.29ORCID,van Zwam Wim H.12,van der Leij Christiaan1,

Affiliation:

1. Department of Radiology and Nuclear Medicine Maastricht University Medical Center Maastricht the Netherlands

2. School for Cardiovascular Diseases Maastricht Maastricht University Maastricht the Netherlands

3. Department of Neurology Haaglanden Medical Center The Hague the Netherlands

4. Department of Neurology Rijnstate Hospital Arnhem the Netherlands

5. Department of Clinical Neurophysiology University of Twente Enschede the Netherlands

6. Department of Radiology Haaglanden Medical Center The Hague the Netherlands

7. Department of Radiology and Nuclear Medicine Amsterdam University Medical Center Amsterdam the Netherlands

8. Leiden University Medical Center Leiden the Netherlands

9. Department of Neurology Maastricht University Medical Center Maastricht the Netherlands

Abstract

Background Balloon guide catheters (BGCs) are used to prevent distal emboli during endovascular treatment for acute ischemic stroke. Although literature reports benefit of BGC, these are not universally used, and randomized head‐to‐head comparisons are lacking. This study compared functional, safety, and technical outcomes between patients treated with non‐BGC and with BGC during endovascular treatment in a nationwide prospective multicenter registry. Methods Patients from the MR CLEAN (Multicenter Randomized Clinical Trial of Endovascular Treatment for Acute Ischemic Stroke in the Netherlands) Registry, 2014 to 2018), who underwent endovascular treatment with a non‐BGC or BGC, were included. Primary outcome was the modified Rankin Scale score at 90 days, and secondary outcomes included procedure time and first‐attempt successful reperfusion (extended Thrombolysis in Cerebral Infarction ≥2C). Treatment‐effect modification and subgroups were analyzed according to first‐line thrombectomy technique and different sizes of non‐BGC. Results In total 2808 patients were included, and 1671 (60%) were treated with BGC. No differences in the modified Rankin Scale score at 90 days were seen between non‐BGC and BGC groups (adjusted common odds ratio [OR], 0.98 [95% CI, 0.82–1.10]). The non‐BGC was associated with faster procedure times compared with BGC (adjusted β: −2.99 [95% CI, −5.58 to −0.40]). A significant treatment effect was found between BGC use and thrombectomy technique. In subgroup analyses with stent retriever as first‐line technique, 90‐day modified Rankin Scale scores were significantly higher (more disability) in the non‐BGC group compared with the BGC group (adjusted common OR, 0.79 [95% CI, 0.65–0.96]). Direct aspiration combined with non‐BGC resulted in higher first‐attempt rates compared with BGC (adjusted OR, 1.55 [95% CI, 1.06–2.28]). Conclusions This large prospective multicenter registry showed no differences in clinical outcome between patients treated with non‐BGC and BGC. Subgroup analyses suggest that BGC outperforms the non‐BGC when stent retriever is used as first‐line technique, whereas non‐BGC outperforms the BGC when aspiration is used.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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