Abstract

BackgroundBlood removal from cerebrospinal fluid (CSF) in post-subarachnoid hemorrhage patients may reduce the risk of related secondary brain injury. We formulated a computational fluid dynamics (CFD) model to investigate the impact of a dual-lumen catheter-based CSF filtration system, called Neurapheresis™ therapy, on blood removal from CSF compared to lumbar drain.MethodsA subject-specific multiphase CFD model of CSF system-wide solute transport was constructed based on MRI measurements. The Neurapheresis catheter geometry was added to the model within the spinal subarachnoid space (SAS). Neurapheresis flow aspiration and return rate was 2.0 and 1.8 mL/min, versus 0.2 mL/min drainage for lumbar drain. Blood was modeled as a bulk fluid phase within CSF with a 10% initial tracer concentration and identical viscosity and density as CSF. Subject-specific oscillatory CSF flow was applied at the model inlet. The dura and spinal cord geometry were considered to be stationary. Spatial–temporal tracer concentration was quantified based on time-average steady-streaming velocities throughout the domain under Neurapheresis therapy and lumbar drain. To help verify CFD results, an optically clear in vitro CSF model was constructed with fluorescein used as a blood surrogate. Quantitative comparison of numerical and in vitro results was performed by linear regression of spatial–temporal tracer concentration over 24-h.ResultsAfter 24-h, tracer concentration was reduced to 4.9% under Neurapheresis therapy compared to 6.5% under lumbar drain. Tracer clearance was most rapid between the catheter aspiration and return ports. Neurapheresis therapy was found to have a greater impact on steady-streaming compared to lumbar drain. Steady-streaming in the cranial SAS was ~ 50× smaller than in the spinal SAS for both cases. CFD results were strongly correlated with the in vitro spatial–temporal tracer concentration under Neurapheresis therapy (R2 = 0.89 with + 2.13% and − 1.93% tracer concentration confidence interval).ConclusionA subject-specific CFD model of CSF system-wide solute transport was used to investigate the impact of Neurapheresis therapy on tracer removal from CSF compared to lumbar drain over a 24-h period. Neurapheresis therapy was found to substantially increase tracer clearance compared to lumbar drain. The multiphase CFD results were verified by in vitro fluorescein tracer experiments.

Highlights

  • Blood removal from cerebrospinal fluid (CSF) in post-subarachnoid hemorrhage patients may reduce the risk of related secondary brain injury

  • Neurapheresis therapy was found to clear tracer from the CSF more rapidly than lumbar drain with most of the clearance occurring within the thoracic subarachnoid space (SAS) after 1-h of treatment

  • After 24-h, tracer concentration was reduced to 4.9% under Neurapheresis therapy compared to 6.5% under lumbar drain

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Summary

Introduction

Blood removal from cerebrospinal fluid (CSF) in post-subarachnoid hemorrhage patients may reduce the risk of related secondary brain injury. A detailed understanding of cerebrospinal fluid (CSF) physiologic function may help improve treatment of CSFrelated central nervous system (CNS) diseases and debilitating neurological conditions. CSF is a clear, colorless fluid that occupies the subarachnoid space (SAS) and the ventricular system within the brain [1]. CSF is believed to be primarily produced within the ventricles of the brain by secretory epithelial cells which form the choroid plexuses and absorbed at the arachnoid granulations located in the SAS on the surface of the superior sagittal sinus [2]. CSF moves with a net flow direction outward from the ventricles to the SAS and multi-directionally with an oscillatory motion, driven by cardiac and respiratoryrelated pressure fluctuations and other transient maneuvers [3]. Some of the roles of CSF include: (1) suspension of the delicate brain tissue by the Archimedes principle making the brain tissue nearly neutrally buoyant, (2) damping of forces that act on the brain tissue due to transient impact [4], (3) providing immunological and biochemical homeostasis for the CNS [5], and (4) delivery of metabolites and micronutrients to the CNS [1, 6]

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