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临床方案委员会报告:恶性肠梗阻随机试验的开展

Report of the clinical protocol committee: development of randomized trials for malignant bowel obstruction.

作者信息

Anthony Thomas, Baron Todd, Mercadante Sebastiano, Green Sylvan, Chi Dennis, Cunningham John, Herbst Anne, Smart Elizabeth, Krouse Robert S

机构信息

Department of Surgery, University of Texas, Southwestern Medical Center, and Veterans Affairs North Texas Health Care System, Dallas, Texas 75390-9155, USA.

出版信息

J Pain Symptom Manage. 2007 Jul;34(1 Suppl):S49-59. doi: 10.1016/j.jpainsymman.2007.04.011. Epub 2007 Jun 4.

Abstract

Malignant bowel obstruction (MBO) is a commonly encountered palliative care problem. There have been very few comparative trials in this area, and consequently there is very little clinical evidence upon which therapy can be rationally based. The purpose of this paper is to highlight the discussion and decision-making process that was undertaken by the Clinical Protocol Subcommittee during the development of a proposed clinical trial of best medical care versus surgical or endoscopic treatment for MBO. The development of the proposed clinical trials followed an orderly process. The first step taken was a discussion of a specific definition for MBO. Once agreed upon, this definition helped identify inclusion and exclusion criteria for the proposed trial. This was followed by an extensive literature review, which helped define both surgical and endoscopic approaches to MBO as well as what constituted best medical care. An extensive discussion was then undertaken concerning the best outcome measure of success for medical, surgical, and endoscopic interventions. All of the above steps culminated in two proposed protocols, one for MBO of the small intestine distal to the ligament of Treitz and a second for colonic obstructions. The small intestinal trial is designed to compare surgical intervention versus best medical care, whereas the colonic trial seeks to compare surgery with endoscopically-placed intraluminal stents coupled with best medical care.

摘要

恶性肠梗阻(MBO)是姑息治疗中常见的问题。该领域的比较试验极少,因此几乎没有可作为合理治疗依据的临床证据。本文旨在突出临床方案小组委员会在制定一项关于MBO最佳医疗护理与手术或内镜治疗对比的拟议临床试验过程中所进行的讨论和决策过程。拟议临床试验的开展遵循了有序的流程。第一步是对MBO的具体定义进行讨论。一旦达成共识,该定义有助于确定拟议试验的纳入和排除标准。接下来进行了广泛的文献综述,这有助于明确MBO的手术和内镜治疗方法以及最佳医疗护理的构成要素。随后就医疗、手术和内镜干预的最佳成功结局指标进行了广泛讨论。上述所有步骤最终形成了两项拟议方案,一项针对屈氏韧带远端小肠的MBO,另一项针对结肠梗阻。小肠试验旨在比较手术干预与最佳医疗护理,而结肠试验则旨在比较手术与内镜放置腔内支架联合最佳医疗护理。

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