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临床试验/NCT05382481
NCT05382481招募中不适用

Effect of Anti Xa Monitoring Low Molecular Weight Heparin (LMWH) on Prevention of Venous Thromboembolism in Critically Ill Patients:A Randomized Controlled Trial

Xuanwu Hospital, Beijing1 个研究点 分布在 1 个国家目标入组 858 人开始时间: 2022年5月16日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
858
试验地点
1
主要终点
number of VTE

研究概览

简要总结

Venous thromboembolism (VTE), which includes deep vein thrombosis (DVT) and pulmonary embolism, is a common cardiovascular disease associated with significant morbidity ranging from painful leg swelling, chest pain, shortness of breath, and even death. About 50% of all VTE events occur as a result of a current or recent hospital admission for surgery or acute medical illness. Hospital-acquired VTE is preventable, with interventions including anticoagulants and mechanical measures, including compression stockings and intermittent pneumatic compression. Prevented hospital acquired VTE is the focus of health services and the strongest hospital strategy to improve patient health in the world.

详细描述

Low molecular weight heparins (LMWH) are commonly used injectable anticoagulants for venous thromboembolism (VTE) prophylaxis and treatment. LMWH forms an inhibitory complex with antithrombin to inactivate activated factor X (Xa). Due to the predictable pharmacokinetics and pharmacodynamics of LMWH, it is not necessary to routinely monitor anti-Xa levels. However, LMWH pharmacokinetics and pharmacodynamics may be less predictable in certain patient populations including renal impairment, obesity, malignancy, or pregnancy .

Both increased risk of bleeding and suboptimal efficacy are possible in obese patients. LMWHs distribute into lean body mass, therefore, obese patients with a lower proportion of lean body mass to adipose tissue receiving LMWH dosed according to actual body weight may achieve supratherapeutic drug concentrations which could increase bleeding risk . On the other hand, fixed-dose VTE prophylaxis regimens do not account for higher body weight associated with obesity potentially resulting in subtherapeutic drug concentrations increasing the risk for therapeutic failure.

As LMWH are primarily renally eliminated, impaired renal function can contribute to drug accumulation and increased risk of major bleeding.The prolonged LMWH monotherapy used in cancer-associated VTE treatment also raises concerns about drug accumulation and increased bleeding, especially in those with fluctuating renal function. In addition, pregnancy can potentially increase the clearance and volume of distribution of LMWH, increasing the potential for subtherapeutic anti-Xa levels. Thus, anti-Xa level assays are often performed for these specific patient populations in an attempt to provide optimal LMWH therapy.

Critically ill patients are higher risk populations of VTE and bleeding with complex conditions, for example sedation, mechanical ventilation, central venous catheter, and have severe infection, renal insufficiency/failure. So, the purpose of this RCT is to explore the effect of anti Xa monitoring LMWH in preventing VTE in critically ill patients and the optimal time of anti Xa monitoring, reduce mortality and serious adverse events.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Aged 18 years or older
  • No gender limited
  • Prospectively screened for risk and included if they received LMWH
  • The patient or his / her legal representative is able and willing to sign the informed consent

排除标准

  • History of hemorrhage or high risk of hemorrhage, including subarachnoid hemorrhage, cerebral hemorrhage, traumatic brain injury, blood system diseases, etc
  • Severe renal insufficiency before randomization (creatinine clearance rate (CCr) < 30mL/min)
  • Expected length of ICU stay less than 3 days
  • Known to be allergic to LMWH
  • Pregnancy
  • History of heparin induced thrombocytopenia
  • Patients with iliac vein compression syndrome
  • Receive non LMWH for prevention VTE according to the physician

结局指标

主要结局

number of VTE

时间窗: 14 days after randomization

VTE include symptomatic VTE or asymptomatic VTE at day 14

次要结局

  • number of all cause in-hospital death(14 days and in hospital)
  • number of targets reached of peak value or trough value of anti Xa for the first time(14 days after randomization)
  • number of hemorrhage(14 days after randomization)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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