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In Vivo CSF Shunt Hydrodynamics in Hydrocephalus

In Vivo CSF Shunt Hydrodynamics in Hydrocephalus
脑积水体内脑脊液分流流体动力学
批准号:
7569435
负责人:
MARVIN BERGSNEIDER
金额:
$33.8万
依托单位国家:
美国
项目类别:
财政年份:
2007
资助国家:
美国
项目状态:
已结题
起止时间:
2007-02-15 至 2011-01-31

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中文摘要
翻译
描述(由申请人提供):由于诊断不确定性和高治疗风险,正常压力脑积水(NPH)的管理具有挑战性。到目前为止,还没有针对这种疾病的循证治疗指南。我们的长期目标是通过降低与分流阀相关的并发症和增加我们对不同分流设计如何影响脑脊液(CSF)流体动力学的理解来改善NPH的结局。本研究采用三层共享受试者研究设计。具体目的是:1)确定两种可调节阀设计(一种带虹吸控制装置,另一种不带虹吸控制装置)中哪一种在降低并发症发生率方面上级于NPH治疗,2)比较标准压差阀(带和不带虹吸控制装置)在NPH治疗中的颅内压(ICP)生理反应,以及3)确定在分流手术之前和之后测量的颅内血液/流体动力学变量是否支持颅内压动力学的调谐动力学吸收器模型。我们假设虹吸控制装置增加了分流引流不足的发生率,表现为缺乏神经功能改善和脑室尺寸缩小。此外,我们假设目前的脑积水模型过于简单,分流诱导的流体动力学更好地建模的基础上ICP波形特征和新的动态模型的应用。所有研究都将作为前瞻性随机临床试验的一部分进行,该试验评估了两种现有的FDA批准的可调节瓣膜。结果分析将是有用的临床医生希望应用循证指南的管理NPH。从更好地理解CSF分流的ICP生理学的角度来看,综合流体动力学研究将提供有价值的信息,这些信息将有助于为个体患者选择最佳阀门压力或类型。此外,我们预计分流阀制造商将使用这些信息来改进当前的阀门设计。记录调谐动态吸收器模型的明确证据可能对所有ICP疾病产生根本影响。
英文摘要
DESCRIPTION (provided by applicant): The management of normal pressure hydrocephalus (NPH) is challenging due to diagnostic uncertainties and high treatment risks. To date, there are no evidence-based treatment guidelines for this disorder. Our long-term goal is to improve the outcome of NPH by lowering complications related to shunt valves and by increasing our understanding of how different shunt designs influence cerebrospinal fluid (CSF) hydrodynamics. This investigation uses a three-tiered shared-subject study design. The Specific Aims are to 1) determine which of two adjustable valve designs, one with a siphon control device and one without, is superior for the treatment of NPH with regard to lowering the complication rate, 2) compare the intracranial pressure (ICP) physiological response of a standard differential pressure valve, with and without a siphon control device, in the treatment of NPH, and 3) determine whether intracranial hemo/hydrodynamic variables, measured before and after a shunt operation, support the tuned-dynamic absorber model, of intracranial pressure dynamics. We hypothesize that siphon control devices increase the incidence of shunt under-drainage, manifesting as a lack of both neurological improvement and ventricular size reduction. Furthermore, we hypothesize that current hydrocephalus models are over- simplistic and that shunt-induced hydrodynamics are better modeled based on ICP waveform characteristics and the application of novel dynamic models. All of the studies will be performed as part of a prospective, randomized clinical trial assessing two existing, FDA-approved, adjustable valves. The outcome analysis will be useful for clinicians wishing to apply evidence-based guidelines in the management of NPH. From a viewpoint of better understanding the ICP physiology of CSF shunts, the comprehensive hydrodynamic studies will provide valuable information that will be useful in selecting the optimal valve pressure or type for individual patients. In addition, we foresee the information being used by shunt valve manufacturers to improve current valve designs. Documenting definitive evidence of the tuned-dynamic absorber model could have fundamental implications to all ICP disorders.
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