Renal and Metabolic, The George Institute for Global Health, UNSW, Newtown, New South Wales, Australia.
Neurology, Prince of Wales Clinical School, UNSW, Sydney, New South Wales, Australia.
BMJ Open. 2019 Jan 15;9(1):e023736. doi: 10.1136/bmjopen-2018-023736.
The majority of patients undergoing haemodialysis (HD) show evidence of uraemic neuropathy, a condition with no known disease-modifying treatments. The pathogenesis of uraemic neuropathy is poorly understood, but may be related to cumulative exposure to middle molecules or other solutes such as potassium. It is not known whether haemodiafiltration (HDF) reduces the progression of uraemic neuropathy.
Filtration In the Neuropathy of End-Stage kidney disease Symptom Evolution (FINESSE) is a multicentre, randomised, open-label, blinded endpoint assessment, controlled trial designed to assess the impact of HDF versus HD on uraemic neuropathy. Maintenance HD patients will be randomised in a 1:1 ratio to receive HDF or HD with high-flux membranes for 4 years. The primary endpoint is the difference in the mean change in Total Neuropathy Score (TNS)-a measure of peripheral neuropathy combining symptoms, signs and nerve conduction velocity-over the study period. Secondary outcomes include change at annual timepoints in the TNS and the Neuropathy Symptom Score; and in morbidity, mortality and safety events.
The FINESSE trial has been approved by the Ethics Review Committee of the Sydney South West Area Health Service (HREC/09/RPAH/268) and of Adventist HealthCare Limited (2012-027). When published in a peer-reviewed journal, it will be the largest and longest reported randomised trial aimed at reducing the incidence and severity of uraemic neuropathy. It will advance the understanding of the natural history of uraemic neuropathy and the influence of convective therapies on both neurophysiological and clinical outcomes. It will also allow refinement of current hypotheses surrounding the pathogenesis of uraemic neuropathy and, most importantly, may lead to improvements in the lives of the many patients affected by this debilitating condition.
ACTRN12609000615280.
大多数接受血液透析(HD)的患者都有证据表明存在尿毒症性神经病变,这是一种没有已知的疾病修饰治疗方法的疾病。尿毒症性神经病变的发病机制尚不清楚,但可能与中分子或其他溶质(如钾)的累积暴露有关。目前尚不清楚血液透析滤过(HDF)是否能减缓尿毒症性神经病变的进展。
在终末期肾病症状演变中的过滤神经病变(FINESSE)是一项多中心、随机、开放标签、盲终点评估、对照试验,旨在评估 HDF 与 HD 对尿毒症性神经病变的影响。维持性 HD 患者将以 1:1 的比例随机分为 HDF 组或 HD 组,接受高通量膜治疗 4 年。主要终点是研究期间总神经病变评分(TNS)-一种结合症状、体征和神经传导速度的周围神经病变测量-的平均变化差异。次要结局包括 TNS 和神经病变症状评分在年度时间点的变化;发病率、死亡率和安全性事件。
FINESSE 试验已获得悉尼西南地区卫生服务伦理审查委员会(HREC/09/RPAH/268)和 Adventist HealthCare Limited(2012-027)的批准。在同行评议期刊上发表时,它将是最大和最长的报告随机试验,旨在降低尿毒症性神经病变的发生率和严重程度。它将推进对尿毒症性神经病变自然史的理解,以及对流式治疗对神经生理学和临床结局的影响。它还将完善围绕尿毒症性神经病变发病机制的现有假设,最重要的是,可能会改善许多受这种衰弱性疾病影响的患者的生活。
ACTRN12609000615280。