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CRRTnet: a prospective, multi-national, observational study of continuous renal replacement therapy practices

机译:CRRTnet:连续肾脏替代疗法实践的前瞻性,多国,观察性研究

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Background Continuous renal replacement therapy (CRRT) is the recommended modality of dialysis for critically ill patients with hemodynamic instability. Yet there remains significant variability in how CRRT is prescribed and delivered, and limited evidence-basis to guide practice. Methods This is a prospective, multi-center observational study of patients undergoing CRRT. Initial enrollment phase will occur at 4 academic medical centers in North America over 5?years, with a target enrollment of 2000 patients. All adult patients (18–89?years of age) receiving CRRT will be eligible for inclusion; patients who undergo CRRT for less than 24?h will be excluded from analysis. Data collection will include patient characteristics at baseline and at time of CRRT initiation; details of CRRT prescription and delivery, including machine-generated treatment data; and patient outcomes. Discussion The goal of this study is to establish a large comprehensive registry of critically ill adults receiving CRRT. Specific aims include describing variations in CRRT prescription and delivery across quality domains; validating quality measures for CRRT care by correlating processes and outcomes; and establishing a large registry for use in quality improvement and benchmarking efforts. For initial analyses, some particular areas of interest are anticoagulation protocols; approach to fluid overload; CRRT-related workload; and patient safety. Trial registration Registered on ClinicalTrials.gov 1/10/2014: NCT02034448.
机译:背景技术连续肾脏替代疗法(CRRT)是血液动力学不稳定的重症患者的推荐透析方式。然而,CRRT的处方和交付方式仍存在很大差异,并且指导实践的证据基础有限。方法这是一项对接受CRRT的患者进行的前瞻性,多中心观察性研究。最初的招募阶段将在5年内在北美的4个学术医学中心进行,目标招募2000名患者。所有接受CRRT的成年患者(18-89岁)均符合纳入条件; CRRT少于24小时的患者将被排除在分析之外。数据收集将包括基线和CRRT启动时的患者特征; CRRT处方和交付的详细信息,包括机器生成的治疗数据;和患者的结果。讨论这项研究的目的是为接受CRRT的危重成年人建立一个大型综合登记册。具体目标包括描述CRRT处方和跨质量域交付的变化;通过关联过程和结果来验证CRRT护理的质量措施;并建立一个大型注册表,用于质量改进和基准测试。对于最初的分析,某些特定领域是抗凝方案。解决流体过载的方法;与CRRT相关的工作量;和患者安全。试验注册在ClinicalTrials.gov上注册的1/10/2014:NCT02034448。

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