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临床试验/NCT00456326
NCT00456326已完成不适用

A 3 Year Retrospective Heparin Induced Thrombocytopenia Registry (HIT) at Brigham and Women's Hospital.

Brigham and Women's Hospital1 个研究点 分布在 1 个国家目标入组 242 人开始时间: 2005年10月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
242
试验地点
1
主要终点
Incidence of HIT associated with UFH and LMWH

研究概览

简要总结

The purpose of the Heparin Induced Thrombocytopenia Registry is to explore the frequency of heparin-induced thrombocytopenia (HIT) at Brigham and Women's Hospital and to assess its mortality rate. Retrospective 3 years, looking forward prospectively.

详细描述

Heparin-induced thrombocytopenia (HIT) is an immune-mediated adverse drug reaction with potentially fatal complications of venous and arterial thrombosis.

HIT with thrombosis causes prolonged hospital length of stay and is associated with catastrophic outcomes such as extremity amputation as well as death. The fear of HIT has led to some proposals to minimize hospital use of unfractionated heparin (UFH) and low molecular weight heparin (LMWH) and to substitute other anticoagulants that have not been reported to cause HIT. Therefore, the frequency of confirmed HIT and the frequency of determining whether UFH or LMWH is the causative agent urgently require further investigation.

At BWH, we have placed patient safety at a premium. We have a Patient Safety Committee and a Patient Safety Officer. HIT has been identified as one of the primary problems requiring urgent policy decisions. Consequently, we have formed a multi-disciplinary team of physicians, pharmacists, nurses and physician's assistants to improve safe medication practices for patients receiving anticoagulation.

Our primary objectives are to establish an HIT registry which will provide information on:

  1. Incidence of HIT associated with UFH and LMWH
  2. Outcomes of patients with HIT
  3. Adverse events associated with alternative anticoagulants used to treat HIT

研究设计

研究类型
Observational
时间视角
Retrospective

入排标准

性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

结局指标

主要结局

Incidence of HIT associated with UFH and LMWH

时间窗: 30 Days

Outcomes of patients with HIT

时间窗: 30 Days

Adverse events associated with alternative anticoagulants used to treat HIT

时间窗: 30 Days

次要结局

  • Mortality(30 Days)
  • Hemorrhagic Events(30 Days)
  • Thrombotic Events(30 Days)

研究者

申办方类型
Other

研究点 (1)

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