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抗分泌因子可能降低重度创伤性脑损伤患者的颅内压——病例系列研究

Antisecretory Factor May Reduce ICP in Severe TBI-A Case Series.

作者信息

Cederberg David, Hansson Hans-Arne, Visse Edward, Siesjö Peter

机构信息

Department of Neurosurgery, Skane University Hospital, Lund, Sweden.

Institute of Biomedicine, University of Gothenburg, Gothenburg, Sweden.

出版信息

Front Neurol. 2020 Mar 6;11:95. doi: 10.3389/fneur.2020.00095. eCollection 2020.

Abstract

Traumatic brain injury (TBI) constitutes a global epidemic. Overall outcome is poor, with mortality ranging from 10 to 70% and significant long-term morbidity. Several experimental reports have claimed effect on traumatic edema, but all clinical trials have failed. Antisecretory factor, an endogenous protein, is commercially available as Salovum®, which is classified as a medical food by the European Union and has been proven effective in experimental trauma models. It has, however, previously not been tested in humans with severe TBI. We hereby report a case series of five adult patients with severe TBI, treated with Salovum. The objective of the intervention was to evaluate safety and, if possible, its effect on intracranial pressure and outcome. Patients received 1 g Salovum per kilo of body weight divided into six doses per 24 h. Each dose was administered through the nasogastric tube. Patients were scheduled for 5 days of treatment with Salovum. Intracranial pressure was controlled in all patients. In three of five patients, intracranial pressure could be controlled with Salovum and deep sedation (no barbiturates), except during periods of gastroparesis. Five of five patients had a favorable short-term outcome, and four of five patients had a favorable long-term outcome. No toxicity was observed. We conclude that at least three of the five treated patients experienced an effect of Salovum with signs of reduction of intracranial pressure and signs of clinical benefit. In order to validate the potential of antisecretory factor in TBI, a prospective, randomized, double-blind, placebo-controlled trial with Salovum has been initiated. Primary outcome for the trial is 30-day mortality; secondary outcomes are treatment intensity level, intracranial pressure, and number of days at the neurointensive care unit.

摘要

创伤性脑损伤(TBI)是一种全球性的流行病。总体预后较差,死亡率在10%至70%之间,且长期发病率较高。多项实验报告称其对创伤性水肿有作用,但所有临床试验均告失败。抗分泌因子是一种内源性蛋白质,以Salovum®的商品名上市销售,欧盟将其归类为医用食品,并且已在实验性创伤模型中被证明有效。然而,此前尚未在重度TBI患者中进行过测试。我们在此报告一组五例接受Salovum治疗的成年重度TBI患者的病例系列。干预的目的是评估安全性,并在可能的情况下评估其对颅内压和预后的影响。患者每公斤体重接受1克Salovum,每24小时分为六剂。每剂通过鼻胃管给药。患者计划接受5天的Salovum治疗。所有患者的颅内压均得到控制。在五例患者中的三例中,除胃轻瘫期间外,Salovum联合深度镇静(不使用巴比妥类药物)可控制颅内压。五例患者中有五例短期预后良好,五例患者中有四例长期预后良好。未观察到毒性反应。我们得出结论,五例接受治疗的患者中至少有三例出现了Salovum的作用,表现为颅内压降低和临床获益迹象。为了验证抗分泌因子在TBI中的潜力,已启动一项使用Salovum的前瞻性、随机、双盲、安慰剂对照试验。该试验的主要结局是30天死亡率;次要结局是治疗强度水平、颅内压以及在神经重症监护病房的天数。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcc3/7067821/484db4c36db0/fneur-11-00095-g0001.jpg

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