Suppr超能文献

早期预防危重症儿童导管相关性血栓形成的疗效:一项贝叶斯 2b 期随机临床试验。

Efficacy of Early Prophylaxis Against Catheter-Associated Thrombosis in Critically Ill Children: A Bayesian Phase 2b Randomized Clinical Trial.

机构信息

Department of Pediatrics, Yale School of Medicine, New Haven, CT.

Department of Pediatrics, Children's Hospital of Philadelphia, University of Pennsylvania, Philadelphia, PA.

出版信息

Crit Care Med. 2021 Mar 1;49(3):e235-e246. doi: 10.1097/CCM.0000000000004784.

Abstract

OBJECTIVES

We obtained preliminary evidence on the efficacy of early prophylaxis on the risk of central venous catheter-associated deep venous thrombosis and its effect on thrombin generation in critically ill children.

DESIGN

Bayesian phase 2b randomized clinical trial.

SETTING

Seven PICUs.

PATIENTS

Children less than 18 years old with a newly inserted central venous catheter and at low risk of bleeding.

INTERVENTION

Enoxaparin adjusted to anti-Xa level of 0.2-0.5 international units/mL started at less than 24 hours after insertion of central venous catheter (enoxaparin arm) versus usual care without placebo (usual care arm).

MEASUREMENTS AND MAIN RESULTS

At the interim analysis, the proportion of central venous catheter-associated deep venous thrombosis on ultrasonography in the usual care arm, which was 54.2% of 24 children, was significantly higher than that previously reported. This resulted in misspecification of the preapproved Bayesian analysis, reversal of direction of treatment effect, and early termination of the randomized clinical trial. Nevertheless, with 30.4% of 23 children with central venous catheter-associated deep venous thrombosis on ultrasonography in the enoxaparin arm, risk ratio of central venous catheter-associated deep venous thrombosis was 0.55 (95% credible interval, 0.24-1.11). Including children without ultrasonography, clinically relevant central venous catheter-associated deep venous thrombosis developed in one of 27 children (3.7%) in the enoxaparin arm and seven of 24 (29.2%) in the usual care arm (p = 0.02). Clinically relevant bleeding developed in one child randomized to the enoxaparin arm. Response profile of endogenous thrombin potential, a measure of thrombin generation, was not statistically different between trial arms.

CONCLUSIONS

These findings suggest the efficacy and safety of early prophylaxis that should be validated in a pivotal randomized clinical trial.

摘要

目的

我们获得了早期预防在危重症儿童中心静脉导管相关深静脉血栓形成风险和对凝血酶生成影响方面的疗效的初步证据。

设计

贝叶斯 2b 期随机临床试验。

设置

7 个 PICUs。

患者

年龄小于 18 岁、新插入中心静脉导管且出血风险低的儿童。

干预措施

在中心静脉导管插入后不到 24 小时,调整依诺肝素抗 Xa 水平至 0.2-0.5 国际单位/毫升(依诺肝素组),与未使用安慰剂的常规治疗(常规治疗组)相比。

测量和主要结果

在中期分析中,常规治疗组 24 名儿童中有 54.2%的超声检查显示中心静脉导管相关深静脉血栓形成,这一比例明显高于先前报道。这导致预批准的贝叶斯分析不精确,治疗效果方向逆转,以及随机临床试验提前终止。尽管如此,在依诺肝素组中,有 23 名儿童中有 30.4%的超声检查显示中心静脉导管相关深静脉血栓形成,中心静脉导管相关深静脉血栓形成的风险比为 0.55(95%可信区间,0.24-1.11)。包括未进行超声检查的儿童,在依诺肝素组中有 1 名(3.7%)儿童和常规治疗组中有 7 名(29.2%)儿童发生临床相关的中心静脉导管相关深静脉血栓形成(p=0.02)。有 1 名随机分配至依诺肝素组的儿童发生临床相关出血。内源凝血酶潜能(凝血酶生成的一种测量方法)的反应谱在试验组之间无统计学差异。

结论

这些发现提示早期预防有效且安全,应在一项关键性随机临床试验中得到验证。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/437a/7902342/3a8375d0ce54/nihms-1644059-f0001.jpg

相似文献

引用本文的文献

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验