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The Carrier Delivery-Assist Catheter in Stroke Thrombectomy

Dolia, J.; Yelam, T.; Grossberg, J. A.; Batista dos Reis, S.; Pabaney, A. H.; Siddu, M.; Vela-Duarte, D.; Jankowitz, B. T.; Tanweer, O.; Xu, J.; Cuellar-Saenz, H. H.; Shah, R.; Abecassis, I. J.; Ding, D.; Mehta, T.; Sheth, S. A.; Samaha, J. N.; Al Kasab, S.; Shah, K. A.; Froehler, M. T.; Ali, A.; Hassan, A. E.; Miller, S.; Miller, J.; Kass-Hout, T.; Morsi, R. Z.; Limaye, K.; Martins, P. N.; Haussen, D. C.

2026-04-28 neurology
10.64898/2026.04.27.26351898 medRxiv
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IntroductionDelivering large-bore aspiration catheters through tortuous anatomy remains challenging during mechanical thrombectomy (MT). The Carrier delivery-assist catheter (DAC) was designed to facilitate aspiration catheter navigation, but multicenter data remain limited. We evaluated the efficiency and safety of the Carrier DAC. MethodsWe performed a multicenter retrospective study of prospectively collected data from patients undergoing MT at 15 U.S. Comprehensive Stroke Centers (September 2024-September 2025). Co-primary endpoints were puncture-to-clot engagement time and first-pass effect (FPE; eTICI 2c-3). A pre-specified single-center analysis compared upfront contact aspiration using the Carrier DAC versus standard 0.021'' microcatheter techniques with identical aspiration catheter sizes. ResultsThe multicenter cohort included 211 Carrier-assisted MTs. Median aspiration catheter inner diameter was 0.071'', with super-bore catheters used in 5.7%. Median puncture-to-clot time was 12 minutes, and FPE was achieved in 50.7%. Median puncture-to-reperfusion time was 20 minutes, and mFPE occurred in 74.4%. Parenchymal hematoma and subarachnoid hemorrhage occurred in 11.8% and 6.6%, respectively. Cavernous tortuosity did not affect primary endpoints. The single-center analysis included 242 patients. Carrier use was associated with shorter puncture-to-clot times and numerically higher FPE rates without increased hemorrhagic complications. ConclusionsThe Carrier DAC enables efficient navigation of large-bore aspiration catheters and may reduce procedural time while maintaining procedural safety. Prospective studies are warranted.

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