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临床试验/NCT00237328
NCT00237328已完成不适用

The Incidence of Thromboembolic Events in Patients With Antibodies to Heparin-PF4 After Cardiac Bypass

Duke University4 个研究点 分布在 1 个国家目标入组 1,015 人开始时间: 2006年6月最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
1,015
试验地点
4
主要终点
Thrombotic events compatible with HIT

研究概览

简要总结

Heparin is a drug that is widely used to prevent and treat blood clotting. Individuals undergoing cardiopulmonary bypass surgery are administered high doses of heparin, and some of them develop antibodies to the drug. This immune response can lead to the formation of blood clots, setting the stage for a potential heart attack or stroke. The purpose of this study is to evaluate how often an immune response to heparin leads to the formation of blood clots in individuals who have had heart surgery.

详细描述

Heparin is a drug that is widely used to prevent and treat blood clotting. However, heparin can also cause serious adverse events. Individuals undergoing cardiopulmonary bypass surgery are administered and therefore exposed to high doses of heparin. Studies have shown that up to 61% of cardiac bypass patients develop elevated levels of antibodies to heparin-PF4 after surgery. This immune response may activate blood platelets, possibly resulting in a blood clot. These clots most often develop in the legs and lungs, and may lead to a heart attack or stroke. The frequency of such a reaction has yet to be determined definitively. This study will evaluate the incidence of an immune response to heparin-PF4 that leads to the formation of blood clots in individuals who have had heart surgery.

Participants in this study will be recruited prior to a scheduled cardiac bypass surgery. They will first complete a structured pre-operative interview to collect baseline measures on demographics, comorbidities, history of heparin exposures, and prior thromboembolic events. Immediately prior to surgery, a blood sample will be taken to assess the individual's platelet count and level of antibodies to heparin-PF4. Following the operation, participants will be followed daily to assess heparin exposure, platelet counts, and any blood clotting. Subsequent blood samples will be taken 5 days and 1 month following the surgery to again evaluate the individual's platelet count and level of heparin-PF4 antibodies. Additionally, participants will undergo a structured interview at 1 and 3 months post-surgery to evaluate the incidence of outcomes related to heparin-PF4 antibodies.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

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

  • Scheduled for cardiac bypass surgery at Duke University Hospital

排除标准

  • Plans to receive warfarin during the post-operative inpatient stay
  • Plans to receive a full anticoagulant dose of low-molecular weight heparin during the post-operative inpatient stay
  • Plans to receive a full anticoagulant dose of unfractionated heparin during the post-operative inpatient stay
  • Use of any drug other than unfractionated heparin for anticoagulation during cardiopulmonary bypass
  • Warfarin, heparin, or low-molecular weight heparin administered during a readmission to the hospital for a reason other than one of this study's outcomes does not constitute criteria for exclusion

结局指标

主要结局

Thrombotic events compatible with HIT

时间窗: one year

次要结局

  • antibody positibe status post operative day 5 and day 30(one year)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (4)

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