Suppr超能文献

《Hepburn 研究:雾化肝素对比安慰剂治疗吸入性损伤烧伤患者的疗效和安全性:一项多中心随机对照试验研究方案》。

HEPBURN - investigating the efficacy and safety of nebulized heparin versus placebo in burn patients with inhalation trauma: study protocol for a multi-center randomized controlled trial.

机构信息

Laboratory of Experimental Intensive Care and Anesthesiology (L · E · I C · A), Department of Intensive Care Medicine, Academic Medical Center, M0-210, Meibergdreef 9, 1105 AZ Amsterdam, the Netherlands.

出版信息

Trials. 2014 Mar 25;15:91. doi: 10.1186/1745-6215-15-91.

Abstract

BACKGROUND

Pulmonary coagulopathy is a hallmark of lung injury following inhalation trauma. Locally applied heparin attenuates lung injury in animal models of smoke inhalation. Whether local treatment with heparin benefits patients with inhalation trauma is uncertain. The present trial aims at comparing a strategy using frequent nebulizations of heparin with standard care in intubated and ventilated burn patients with bronchoscopically confirmed inhalation trauma.

METHODS

The Randomized Controlled Trial Investigating the Efficacy and Safety of Nebulized HEParin versus Placebo in BURN Patients with Inhalation Trauma (HEPBURN) is an international multi-center, double-blind, placebo-controlled, two-arm study. One hundred and sixteen intubated and ventilated burn patients with confirmed inhalation trauma are randomized to nebulizations of heparin (the nebulized heparin strategy) or nebulizations of normal saline (the control strategy) every four hours for 14 days or until extubation, whichever comes first. The primary endpoint is the number of ventilator-free days, defined as days alive and breathing without assistance during the first 28 days, if the period of unassisted breathing lasts for at least 24 consecutive hours.

DISCUSSION

As far as the authors know, HEPBURN is the first randomized, placebo-controlled trial, powered to investigate whether local treatment with heparin shortens duration of ventilation of intubated and ventilated burn patients with inhalation trauma.

TRIAL REGISTRATION

NCT01773083 (http://www.clinicaltrials.gov), registered on 16 January 2013.Recruiting. Randomisation commenced on 1 January 2014.

摘要

背景

肺凝血功能障碍是吸入性损伤后肺部损伤的一个标志。局部应用肝素可减轻动物烟雾吸入模型中的肺损伤。局部应用肝素是否有益于吸入性损伤患者尚不确定。本试验旨在比较频繁雾化肝素与标准护理在有支气管镜证实的吸入性损伤的气管插管和机械通气烧伤患者中的作用。

方法

正在进行的随机对照试验调查了雾化肝素与烧伤患者吸入性损伤中的安慰剂(HEPBURN)的疗效和安全性,这是一项国际性的多中心、双盲、安慰剂对照、双臂研究。116 例经气管插管和机械通气且有吸入性损伤的烧伤患者随机分为两组:一组接受肝素雾化(雾化肝素组),另一组接受生理盐水雾化(对照组),每 4 小时雾化一次,持续 14 天,或直至拔管,以先发生者为准。主要终点是无呼吸机天数,定义为在第 28 天之前的存活天数和无辅助呼吸天数,如果无辅助呼吸持续至少 24 小时。

讨论

据作者所知,HEPBURN 是第一项随机、安慰剂对照试验,旨在研究局部应用肝素是否能缩短气管插管和机械通气的吸入性损伤烧伤患者的通气时间。

试验注册

NCT01773083(http://www.clinicaltrials.gov),于 2013 年 1 月 16 日注册。正在招募。随机化于 2014 年 1 月 1 日开始。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/47b3/3987885/5489b3b743c7/1745-6215-15-91-1.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验