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临床试验/NCT04628884
NCT04628884Unknown4 期

Comparison of Two Strategies for Protamine Dosing After Anticoagulation in Cardiovascular Surgery Regarding Postoperative Bleeding: Total Heparin Administered Versus Residual Heparin Determined by a Pharmacokinetic Model

Fundación Clínica Shaio1 个研究点 分布在 1 个国家目标入组 136 人开始时间: 2020年11月15日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
发起方
入组人数
136
试验地点
1
主要终点
postoperative mediastinal bleeding

研究概览

简要总结

In cardiovascular surgery, patients are anticoagulated with heparin during cardiopulmonary bypass, subsequently, anticoagulation is reversed with protamine to reduce bleeding due to residual heparin-induced coagulopathy, which can last more than four hours. Protamine reverses the effect of heparin by binding to each heparin molecule, therefore an amount of protamine equivalent to residual heparin is required at the time that anticoagulation is desired to be reversed, but generally, the dose of protamine is calculated from the total dose of heparin, ignoring that heparin is metabolized and cleared during of the extracorporeal circulation, this excess of protamine produces anticoagulant effects that increase postoperative bleeding. Residual heparin can be estimated from heparin pharmacokinetic models and therefore, from these models, a dose closer to the amount necessary to reverse the effect of heparin can be estimated, avoiding protamine excess. In this study, a protamine dosage strategy based on residual heparin determined by a pharmacokinetic model of heparin versus total administered heparin will be compared regarding bleeding and use of blood components in the postoperative period.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

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

  • Patients over 18 years of age who undergo scheduled cardiovascular surgery or scheduled urgency at the Shaio clinical foundation in the city of Bogotá, who require extracorporeal circulation.
  • ASA classification, between 1 - 4
  • Informed consent read and signed by the patient
  • No history of known blood dyscrasia, with INR values <1.5
  • Platelet count greater than 100,000
  • No history of heparin-induced thrombocytopenia
  • No history of adverse reaction to protamine
  • No use of dual anti-aggregation therapy acetylsalicylic acid (ASA) + ADP receptor inhibitors (Clopidogrel) at the time of surgery
  • Suspension of ADP receptor inhibitor drugs (Clopidogrel) according to institutional protocol.
  • No use of bridging therapy with tirofiban
  • Patient with chronic use of oral anticoagulants (warfarin, dabigatran), complete the suspension time according to the institutional protocol,
  • No requirement for renal replacement therapy in the last month
  • Patient with BMI between 18 - 41 kg / cm2
  • Not pregnant

排除标准

  • Emergency surgery
  • Anticoagulated patient at the time of the intervention
  • Procedure not performed under extracorporeal circulation.
  • Procedure requiring circulatory arrest and / or profound hypothermia
  • Intraoperative death before protamine administration
  • Inability to complete data collection.

研究组 & 干预措施

Protamine dosing according the total heparin administrated

Active Comparator

The protamine dose will be calculated according to the total heparin administered including the heparin dose add during the pump purge, 1 mg of protamine for each 100 IU of heparin

干预措施: Conventional dose (Drug)

Protamine dosing according the residual heparin determined by a pharmacokinetic model

Experimental

The protamine dose will be calculated according to the residual heparin estimated before the separation of the cardiopulmonary bypass using a pharmacokinetic model, 1 mg of protamine for each 100 IU of residual heparin

干预措施: Dosing according residual heparin (Drug)

结局指标

主要结局

postoperative mediastinal bleeding

时间窗: first 24 hours after surgery

total blood collected from the mediastinal chest tubes during the first 24 hours

次要结局

  • total blood products transfused(first 24 hours after surgery)

研究者

发起方
Fundación Clínica Shaio
申办方类型
Other
责任方
Sponsor

研究点 (1)

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