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PROphylaxis for ThromboEmbolism in Critical Care Trial protocol and analysis plan.

机译:重症监护试验方案和分析计划中的血栓栓塞的预防。

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BACKGROUND: This article reports the preparatory studies as well as the design, implementation, and a priori analysis plans of PROphylaxis for ThromboEmbolism in Critical Care Trial (PROTECT) before dissemination of results. PROphylaxis for ThromboEmbolism in Critical Care Trial (NCT00182143) is a randomized, stratified, concealed international trial comparing subcutaneous injection of unfractionated heparin (UFH) 5000 IU or the low-molecular weight heparin (LMWH) dalteparin 5000 IU once daily plus once-daily placebo for the duration of the intensive care unit stay. METHODS: The objective of PROTECT is to examine, among medical-surgical critically ill patients, the effect of the LMWH vs heparin on the primary outcome of proximal leg deep vein thrombosis (DVT) and the following secondary outcomes: DVT elsewhere, pulmonary embolism, any venous thromboembolism (DVT or pulmonary embolism), the composite of venous thromboembolism or death, bleeding, and heparin-induced thrombocytopenia. Patients are followed up to death or hospital discharge. Venous thromboembolism events were included after intensive care unit discharge. All patients, families, clinicians, research personnel, and the trial biostatistician are blind to allocation. RESULTS: We describe the pilot work, large trial methodology, implementation methods, and the analytic plan. Patient recruitment is complete, but 2 patients remain in the hospital. The rigorous design of PROTECT suggests that the risk of systematic error will be low. The sample size suggests that the risk of random error will be low. PROTECT will be the largest investigator-initiated peer-review funded thromboprophylaxis trial in critical care in the world. CONCLUSIONS: If PROTECT shows that LMWH is more effective than UFH, this trial will change practice in that LMWH may be the anticoagulant thromboprophylaxis of choice for this population. If the results show that UFH is as effective or more effective than LMWH, intensivists in many parts of the world may continue to use UFH, whereas those currently using LMWH may reconsider and change to use UFH. Unfavorable consequences such as major bleeding, ease of use, and the costs of complications will also factor into such decisions.
机译:背景:本文报道了在结果发布前预防性治疗在重症监护试验中的血栓栓塞的准备研究以及设计,实施和先验分析计划。重症监护试验中的血栓栓塞预防(NCT00182143)是一项随机,分层,隐蔽的国际试验,比较皮下注射普通肝素(UFH)5000 IU或低分子量肝素(LMWH)达肝素5000 IU的情况,每天一次,每天一次,加安慰剂一次在重症监护病房住院期间。方法:PROTECT的目的是检查重症患者的LMWH与肝素对近端腿深静脉血栓形成(DVT)的主要结果以及以下继发性结果的影响:其他地方的DVT,肺栓塞,任何静脉血栓栓塞(DVT或肺动脉栓塞),静脉血栓栓塞或死亡,出血和肝素诱导的血小板减少症的综合。对患者进行随访直至死亡或出院。重症监护病房出院后包括静脉血栓栓塞事件。所有患者,家属,临床医生,研究人员和试验生物统计学家都不愿分配。结果:我们描述了试验工作,大型试验方法,实施方法和分析计划。患者招募完成,但仍有2名患者留在医院。 PROTECT的严格设计表明系统错误的风险将很低。样本数量表明,随机错误的风险会很低。 PROTECT将是世界上最大的由研究人员发起,由同行评审资助的栓塞预防试验。结论:如果PROTECT表明LMWH比UFH更有效,则该试验将改变实践,因为LMWH可能是该人群的首选抗凝血栓预防措施。如果结果表明UFH与LMWH一样有效或更有效,则世界许多地方的强化主义者可能会继续使用UFH,而目前正在使用LMWH的强化主义者可能会重新考虑并改用UFH。诸如严重出血,易用性和并发症成本等不利后果也将成为此类决策的因素。

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