Clemens Birkenmaier, Tamara Steiger, A. Philipp, K. Lehle, L. Krenkel
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引用次数: 0
摘要
背景:在体外膜氧合(ECMO)治疗过程中,剪切诱导的血管性血液病因子(vWF)构象改变可能是导致膜氧合器(MOs)内凝血障碍和血栓形成的原因。目的:确定临床使用的MOs内的vWF结构,并利用计算流体动力学验证相应的流动条件。方法:采用免疫荧光技术对MOs气体交换膜(GEM)样品进行vWF和p选择素阳性血小板的积累分析。采用层流稳定的reynolds - average - navier - stokes方法计算了GEMs周围流动的流线和剪切率。结果:大多数样品定植均匀分布的白细胞,整合成薄的蛛网状vwf结构。只有25%的样品显示vWF的延长积累。计算的流线显示在相互连接的相邻通道之间有相当大的交叉流动。滞止点不对称,接触面被紧密地冲刷。发生的最大剪切速率范围为2500 ~ 3000 1/s。结论:如果存在明显的vWF结构,其形状和范围与流动计算相匹配。由于不正确的粘度模型,计算出的剪切速率具有临界程度的不确定性。如果MO内部的流动条件足以影响vWF,则应该存在更一致的vWF在样品中的分布。
Flow-Induced Accumulations of Von Willebrand Factor Inside Oxygenators During Extracorporeal Life Support Therapy
BACKGROUND: Shear-induced conformational changes of von Willebrand factor (vWF) may be responsible for coagulation disorder and clot formation inside membrane oxygenators (MOs) during extracorporeal membrane oxygenation (ECMO) therapy. OBJECTIVE: The aim was to identify vWF structures inside clinically used MOs and employ computational fluid dynamics to verify the corresponding flow conditions. METHODS: Samples from gas exchange membranes (GEM) from MOs were analysed for accumulations of vWF and P-selectin-positive platelets using immunofluorescence techniques. Streamlines and shear rates of the flow around GEMs were computed using a laminar steady Reynolds-Averaged-Navier-Stokes approach. RESULTS: Most samples were colonized with equally distributed leukocytes, integrated in thin cobweb-like vWF-structures. Only 25 % of the samples showed extended accumulations of vWF. Computed streamlines showed considerable cross flow between interconnected neighbouring channels. Stagnation points were non-symmetric and contact faces were washed around closely. The occurring maximum shear rates ranged from 2,500 to 3,000 1/s. CONCLUSIONS: If pronounced vWF structures are present, shape and extent match the flow computations well. Computed shear rates bear a critical degree of uncertainty due to the improper viscosity model. If flow conditions inside the MO were sufficient to affect vWF, a more consistent distribution of vWF across the samples should be present.