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首页> 外文期刊>Contemporary Clinical Trials Communications >Study protocol for DICE trial: Video-assisted thoracoscopic surgery decortication versus interventional radiology guided chest tube insertion for the management of empyema
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Study protocol for DICE trial: Video-assisted thoracoscopic surgery decortication versus interventional radiology guided chest tube insertion for the management of empyema

机译:骰子试验研究方案:视频辅助胸腔镜手术截据与介入放射学引导胸管插入脓肿管理

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BackgroundEmpyema is a common thoracic surgery presentation, defined as pus in the pleural space. Despite the commonality of empyema, consensus on initial management remains ambiguous. Two standard of care treatment options include inserting a chest tube (thoracostomy) and the administration of intrapleural fibrinolytics, or an initial surgical approach, surgical decortication. Due to the complexity of this pleural space infection, often repeat interventions are required after initial management in order to achieve source control and resolution of clinical symptoms. This study aims to identify the most effective initial management option for empyema.Study designWe present a study protocol for a randomized control trial (RCT) comparing adult individuals with empyema to one of two standard of care initial management options. Participants will be randomized into either interventional radiology guided chest tube insertion with intrapleural fibrinolytics (Dornase 5?mg and Alteplase 10?mg intrapleural twice daily for three days) or video-assisted thoracoscopic surgery (VATS) decortication.MethodsAll adults with empyema meeting inclusion criteria will be invited to participate. They will be randomized into one of two intervention groups; interventional radiology guided chest tube insertion with fibrinolytics or initial VATS decortication. Each intervention will take place within 48?hours of randomization. The primary outcome will be the rate of re-intervention within 30 days. Re-intervention is defined as repeat chest tube insertion, VATS decortication, or decortication via thoracotomy. Secondary outcomes include a change in the size of empyema, length of stay, morbidity, as well as 30-day and 90-day mortality, as well as quality of life measurements.Anticipated impactThis study is aimed at identifying the most effective initial management option for individuals with empyema.
机译:Backgroundempyema是一种常见的胸部手术介绍,被定义为胸腔空间中的脓液。尽管Empyema的共同性,但对初始管理的共识仍然存在含糊不清。两种护理选项包括插入胸管(胸瘘)和牙周纤维蛋白溶解的给药,或初始手术方法,手术矫正。由于这种胸腔空间感染的复杂性,初始管理后经常需要重复干预,以实现临床症状的来源控制和解决。本研究旨在确定Empyema的最有效的初始管理选择.Study Designwe为随机控制试验(RCT)的研究协议将成年人与Empyema进行比较到两个护理初始管理方案之一。参与者将随机分为介入放射学引导胸管插入胸内纤维蛋白溶解剂(DORNASE 5?MG和Alteplase 10 -MG每日腹膜腹腔,每天两次)或视频辅助胸腔镜手术(VATS)抗束缚。与Empyema会议纳入标准的一体化成年人。将被邀请参加。它们将被随机分为两个干预组中的一个;介入放射学引导胸管插入纤维蛋白溶解或初始VATS矫正。每次干预将在48小时内进行随机化小时。主要结果将在30天内重新干预率。重复干预被定义为重复胸管插入,VATSθ或通过胸廓切开术次成。二次结果包括脓胸大小的变化,保持寿命长度,发病率,以及30天和90天的死亡率,以及生活质量测量。突破性的撞击研究旨在确定最有效的初始管理选择对于脓胸的个人。

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