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COBI(颅脑损伤患者持续高渗治疗)试验方案:一项多中心随机开放标签试验,主要结局设盲裁定。

COBI (COntinuous hyperosmolar therapy for traumatic Brain-Injured patients) trial protocol: a multicentre randomised open-label trial with blinded adjudication of primary outcome.

机构信息

Anaesthesia Intensive Care Unit, Centre Hospitalier Universitaire, Nantes, France.

Anaesthesia Intensive Care Unit, Centre Hospitalier Universitaire, Angers, France.

出版信息

BMJ Open. 2017 Sep 24;7(9):e018035. doi: 10.1136/bmjopen-2017-018035.

Abstract

INTRODUCTION

Traumatic brain injury (TBI) is a major cause of death and severe prolonged disability. Intracranial hypertension (ICH) is a critical risk factor of bad outcomes after TBI. Continuous infusion of hyperosmolar therapy has been proposed for the prevention and the treatment of ICH. Whether an early administration of continuous hyperosmolar therapy improves long-term outcomes of patients with TBI is uncertain. The aim of the COBI study (number clinicaltrial.gov 03143751, pre-results stage) is to assess the efficiency and the safety of continuous hyperosmolar therapy in patients with TBI.

METHODS AND ANALYSIS

The COBI (COntinuous hyperosmolar therapy in traumatic Brain-Injured patients) trial is a multicentre, randomised, controlled, open-label, two-arms study with blinded adjudication of primary outcome. Three hundred and seventy patients hospitalised in intensive care unit with a TBI (Glasgow Coma Scale ≤12 and abnormal brain CT scan) are randomised in the first 24 hours following trauma to standard care or continuous hyperosmolar therapy (20% NaCl) plus standard care. Continuous hyperosmolar therapy is maintained for at least 48 hours in the treatment group and continued for as long as is necessary to prevent ICH. The primary outcome is the score on the Extended Glasgow Outcome Scale at 6 months. The treatment effect is estimated with ordinal logistic regression adjusted for prespecified prognostic factors and expressed as a common OR.

ETHICS AND DISSEMINATION

The COBI trial protocol has been approved by the ethics committee of Paris Ile de France VIII and will be carried out according to the principles of the Declaration of Helsinki and the Good Clinical Practice guidelines. The results of this study will be disseminated through presentation at scientific conferences and publication in peer-reviewed journals. The COBI trial is the first randomised controlled trial powered to investigate whether continuous hyperosmolar therapy in patients with TBI improve long-term recovery.

TRIAL REGISTRATION NUMBER

Trial registration number is NCT03143751.

摘要

简介

创伤性脑损伤(TBI)是死亡和严重长期残疾的主要原因。颅内高压(ICH)是 TBI 后不良结局的关键危险因素。已经提出持续输注高渗治疗以预防和治疗 ICH。TBI 患者早期给予持续高渗治疗是否能改善长期预后尚不确定。COBI 研究(clinicaltrial.gov 编号 03143751,预结果阶段)的目的是评估 TBI 患者持续高渗治疗的有效性和安全性。

方法和分析

COBI(创伤性脑损伤患者连续高渗治疗)试验是一项多中心、随机、对照、开放标签、双臂研究,主要结局采用盲法判断。370 名入住重症监护病房的 TBI 患者(格拉斯哥昏迷量表≤12 分且异常脑 CT 扫描)在创伤后 24 小时内随机分为标准治疗组或持续高渗治疗(20%NaCl)加标准治疗组。治疗组持续至少 48 小时进行高渗治疗,以防止 ICH 发生。主要结局为 6 个月时扩展格拉斯哥预后量表评分。治疗效果采用有序逻辑回归调整预设预后因素进行估计,并表示为通用比值比。

伦理和传播

COBI 试验方案已获得巴黎法兰西岛八区伦理委员会的批准,并将按照赫尔辛基宣言和良好临床实践指南的原则进行。本研究结果将通过在科学会议上的演讲和同行评议期刊上的发表进行传播。COBI 试验是第一项针对 TBI 患者持续高渗治疗是否能改善长期恢复的随机对照试验。

试验注册号

NCT03143751。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0795/5623466/99eca8a5fae2/bmjopen-2017-018035f01.jpg

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