Protocol for the Catheter-Related Early Thromboprophylaxis With Enoxaparin (CRETE) Studies.

IF 4 2区 医学 Q1 CRITICAL CARE MEDICINE Pediatric Critical Care Medicine Pub Date : 2024-11-19 DOI:10.1097/PCC.0000000000003648
E Vincent S Faustino, Sarah B Kandil, Matthew K Leroue, Anthony A Sochet, Michele Kong, Jill M Cholette, Marianne E Nellis, Matthew G Pinto, Madhuradhar Chegondi, Michelle Ramirez, Hilary Schreiber, Elizabeth W J Kerris, Christie L Glau, Amanda Kolmar, Teddy M Muisyo, Anjali Sharathkumar, Lee Polikoff, Cicero T Silva, Lauren Ehrlich, Oscar M Navarro, Philip C Spinella, Leslie Raffini, Sarah N Taylor, Tara McPartland, Veronika Shabanova
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引用次数: 0

Abstract

Objectives: In post hoc analyses of our previous phase 2b Bayesian randomized clinical trial (RCT), prophylaxis with enoxaparin reduced central venous catheter (CVC)-associated deep venous thrombosis (CADVT) in critically ill older children but not in infants. The goal of the Catheter-Related Early Thromboprophylaxis with Enoxaparin (CRETE) Studies is to investigate this newly identified age-dependent heterogeneity in the efficacy of prophylaxis with enoxaparin against CADVT in critically ill children.

Design: Two parallel, multicenter Bayesian superiority explanatory RCTs, that is, phase 3 for older children and phase 2b for infants, and an exploratory mechanistic nested case-control study (Trial Registration ClinicalTrials.gov NCT04924322, June 7, 2021).

Setting: At least 15 PICUs across the United States.

Patients: Older children 1-17 years old ( n = 90) and infants older than 36 weeks corrected gestational age younger than 1 year old ( n = 168) admitted to the PICU with an untunneled CVC inserted in the prior 24 hours. Subjects with or at high risk of clinically relevant bleeding will be excluded.

Interventions: Prophylactic dose of enoxaparin starting at 0.5 mg/kg then adjusted to anti-Xa range of 0.2-0.5 international units (IU)/mL for older children and therapeutic dose of enoxaparin starting at 1.5 mg/kg then adjusted to anti-Xa range of greater than 0.5-1.0 IU/mL or 0.2-0.5 IU/mL for infants while CVC is in situ.

Measurements and main results: Randomization is 2:1 to enoxaparin or usual care (no enoxaparin) for older children and 1:1:1 to either of 2 anti-Xa ranges of enoxaparin or usual care for infants. Ultrasonography will be performed after removal of CVC to assess for CADVT. Subjects will be monitored for bleeding. Platelet poor plasma will be analyzed for markers of thrombin generation. Samples from subjects with CADVT will be counter-matched 1:1 to subjects without CADVT from the opposite trial arm. Institutional Review Board approved the "CRETE Studies" on July 1, 2021. Enrollment is ongoing with planned completion in July 2025 for older children and July 2026 for infants.

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依诺肝素导管相关早期血栓预防疗法(CRETE)研究方案。
研究目的在对我们之前的 2b 期贝叶斯随机临床试验 (RCT) 进行的事后分析中,使用依诺肝素进行预防可减少重症大龄儿童中中心静脉导管 (CVC) 相关性深静脉血栓 (CADVT) 的发生,但对婴儿却没有效果。依诺肝素导管相关早期血栓预防(CRETE)研究的目的是调查依诺肝素预防重症儿童CADVT疗效中新发现的年龄依赖性异质性:设计:两项平行、多中心贝叶斯优势解释性 RCT,即针对年长儿童的第 3 阶段和针对婴儿的第 2b 阶段,以及一项探索性机理嵌套病例对照研究(试验注册 ClinicalTrials.gov,NCT04924322,2021 年 6 月 7 日):地点:全美至少 15 个 PICU:患者:1-17 岁的大龄儿童(90 人)和胎龄大于 36 周但小于 1 岁的婴儿(168 人),这些儿童和婴儿在入住 PICU 之前的 24 小时内插入了未经管道的 CVC。有临床相关出血或高风险的受试者将被排除在外:干预措施:预防剂量的依诺肝素从 0.5 mg/kg 开始,然后调整到抗 Xa 范围为 0.2-0.5 国际单位 (IU)/mL(较大儿童);治疗剂量的依诺肝素从 1.5 mg/kg 开始,然后调整到抗 Xa 范围大于 0.5-1.0 IU/mL 或 0.2-0.5 IU/mL(婴儿),同时 CVC 处于原位:大龄儿童按 2:1 随机分配到依诺肝素或常规护理(无依诺肝素),婴儿按 1:1:1 随机分配到两种抗 Xa 范围的依诺肝素或常规护理。拔除 CVC 后将进行超声波检查,以评估是否存在 CADVT。受试者将接受出血监测。将对贫血小板血浆进行凝血酶生成标记物分析。患有 CADVT 的受试者样本将与来自相反试验组的无 CADVT 的受试者样本进行 1:1 的反匹配。机构审查委员会于 2021 年 7 月 1 日批准了 "CRETE 研究"。目前正在进行注册,计划于 2025 年 7 月完成年龄较大儿童的注册,2026 年 7 月完成婴儿的注册。
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来源期刊
Pediatric Critical Care Medicine
Pediatric Critical Care Medicine 医学-危重病医学
CiteScore
7.40
自引率
14.60%
发文量
991
审稿时长
3-8 weeks
期刊介绍: Pediatric Critical Care Medicine is written for the entire critical care team: pediatricians, neonatologists, respiratory therapists, nurses, and others who deal with pediatric patients who are critically ill or injured. International in scope, with editorial board members and contributors from around the world, the Journal includes a full range of scientific content, including clinical articles, scientific investigations, solicited reviews, and abstracts from pediatric critical care meetings. Additionally, the Journal includes abstracts of selected articles published in Chinese, French, Italian, Japanese, Portuguese, and Spanish translations - making news of advances in the field available to pediatric and neonatal intensive care practitioners worldwide.
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