• Anesthesia and analgesia · Oct 2020

    Antistasis Retrograde Flow Vascular Catheter: A Novel Solution to Thrombogenicity: A Computational Fluid Dynamics Study.

    • Ahmed Abdelaal Ahmed Mahmoud M Alkhatip, Hany M Yassin, Ehab Farag, Mohamed K Hamza, Mahmoud H Bahr, AhmedAhmed GodaAGFrom the Department of Anesthesia, Beni Suef University Hospital and Faculty of Medicine, Beni Suef University, Beni-Suef, Egypt., Mohamed Farid El Emady, Amr M Sallam, Mohamed Elayashy, Mohamed Abdelhaq, Ahmed M Kamal, and Mohamed A Elramely.
    • From the Department of Anesthesia, Beni Suef University Hospital and Faculty of Medicine, Beni Suef University, Beni-Suef, Egypt.
    • Anesth. Analg. 2020 Oct 1; 131 (4): 128112901281-1290.

    BackgroundCatheter-related thrombosis (CRT) is a serious complication of vascular catheters. Retrograde catheter insertion has been shown to decrease pericatheter hemostasis and thrombosis, but it is technically challenging. The current in silico trial is an analytical approach to evaluating different approaches to designing retrograde flow into a vascular catheter.MethodsThe novel catheter design aims to provide antistasis retrograde flow (ASRF) of fluid through multiple backward-directed side openings, with a self-closing terminal opening to facilitate standard insertion. Four different models of the catheter were evaluated by computational fluid dynamic studies, with retrograde-angled openings of 15°, 30°, 45°, and 60° to the long axis of the catheter.ResultsASRF successfully reduced the areas of fluid stagnation in models with 15° and 30° openings. Models with 45° and 60° did not significantly reduce stagnation. ASRF is reversed by the main bloodstream after a few millimeters. The novel catheter design achieved a slightly higher saline flow rate compared with the standard catheter (89.75, 91.72, 94.13, and 94.26 mL/min for 15°, 30°, 45°, and 60° designs, respectively, versus 86.93 mL/min for the standard catheter).ConclusionsThe novel ASRF vascular catheter reduces pericatheter fluid stasis and has the potential to reduce CRT. Further in vitro and in vivo trials are warranted to validate these findings and evaluate clinical efficacy.

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