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人血白蛋白治疗蛛网膜下腔出血的研究:ALISAH 研究。原理与设计。

Treatment of subarachnoid hemorrhage with human albumin: ALISAH study. Rationale and design.

机构信息

Department of Neurology, Divisions Vascular Neurology and Neurocritical Care, Baylor College of Medicine, 6501 Fannin St, MS: NB320, Houston, TX 77030, USA.

出版信息

Neurocrit Care. 2010 Oct;13(2):263-77. doi: 10.1007/s12028-010-9392-8.

Abstract

The primary objective of this prospective dose-finding pilot study is to demonstrate the tolerability and safety of four dosages of 25% human albumin in patients with subarachnoid hemorrhage (SAH). For each dosage group, the study will enroll 20 patients who meet the eligibility criteria. The enrolled patients will undergo follow-up for 90 days post-treatment. The primary tolerability hypothesis is that intravenous 25% human albumin can be given without precipitating treatment related serious adverse events beyond expectations. The study will determine the maximum tolerated dosage of 25% human albumin therapy based on the rate of treatment related serious adverse events during treatment: severe or life-threatening heart failure. The secondary objectives are to obtain preliminary estimates of the albumin treatment effect using the incidence of neurological deterioration within 15 days after symptom onset. In addition, the incidence of rebleeding, hydrocephalus, seizures, delayed cerebral ischemia and the incidence of vasospasm (both symptomatic and by transcranial Doppler ultrasound criteria) within 15 days after symptom onset will be evaluated. Furthermore, the serum osmolality and serum albumin concentrations, serum magnesium concentration, blood pressure and heart rate within 15 days of symptom onset will also be observed. The Glasgow Outcome Scale, Barthel Index, modified Rankin Scale, NIH Stroke Scale, and Stroke Impact Scale will be performed 3 months after the onset of symptoms to assess residual neurological deficits.

摘要

本前瞻性剂量探索性研究的主要目的是在蛛网膜下腔出血(SAH)患者中,证明四种剂量的 25%人血白蛋白的耐受性和安全性。对于每个剂量组,研究将招募 20 名符合入选标准的患者。入组患者将在治疗后 90 天内进行随访。主要耐受性假设是静脉内给予 25%人血白蛋白不会引发预期之外的治疗相关严重不良事件。该研究将根据治疗期间治疗相关严重不良事件的发生率来确定 25%人血白蛋白治疗的最大耐受剂量:严重或危及生命的心衰。次要目标是通过症状出现后 15 天内神经功能恶化的发生率,初步评估白蛋白治疗效果。此外,还将评估症状出现后 15 天内再出血、脑积水、癫痫、迟发性脑缺血和血管痉挛(症状性和经颅多普勒超声标准)的发生率。此外,还将观察症状出现后 15 天内的血清渗透压和血清白蛋白浓度、血清镁浓度、血压和心率。格拉斯哥结局量表、巴氏指数、改良 Rankin 量表、NIH 中风量表和中风影响量表将在症状出现后 3 个月进行,以评估残留的神经功能缺损。

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