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临床试验/NCT01435304
NCT01435304已完成不适用

The Effect of the Hemobag® Ultrafiltration System on Blood Conservation and Coagulation After Cardiopulmonary Bypass

MaineHealth2 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2011年9月最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
MaineHealth
入组人数
100
试验地点
2
主要终点
Amount of Chest Catheter Drainage 24 Hours Postoperatively

研究概览

简要总结

This proposal is designed to mitigate hemodilution (blood diluted with an electrolyte solution) and loss of plasma proteins responsible for normal blood clotting as well as platelets at the completion of cardiopulmonary bypass (CPB). The Hemobag® system is a device qualified by the US Food and Drug Administration (FDA). Many cardiac centers, such as Englewood Hospital and Medical Center in Englewood NJ are using the Hemobag® system for Jehovah's witnesses and other patients who go to that center for bloodless cardiac surgery (cardiac surgery performed without the use of blood or blood products). The system is designed to filter excessive water from blood left in the heart lung machine (cardiopulmonary bypass) after it is separated from the patient during the performance of cardiac surgery. Consequently the likelihood of excessive post-operative bleeding and transfusion with allogeneic blood (blood bank blood from donors) is decreased.

详细描述

Background:

Cardiopulmonary bypass (CPB) consists of an extracorporeal (outside of the body) circuit which allows the circulation and oxygenation of blood during cardiac surgery. The circuit includes an oxygenator, a reservoir and tubing, all of which needs to be primed with a balanced electrolyte solution. Prior to initiating CPB, the venous and arterial ends of the CPB circuit are appropriately attached to the patient. The volume of the circuit is usually 1.5 liters which is equivalent to 30-38% of a typical patient's total blood volume that is generally between 4 and 5 liters.

When CPB is initiated, the patient's blood is mixed and diluted by the CPB priming fluid. Consequently, when the operation is completed and the CPB is discontinued, the content of the CPB circuit consists of the patient's diluted whole blood. The standard practice is to return as much of this hemodiluted CPB contents as the patient will accommodate and process the rest of the contents of the circuit with a cell washer and return packed red blood cells to the patient.

When the cell washer is used, plasma proteins, clotting factors and platelets are not returned to the patient. An alternate approach would be to use an ultrafiltration device to remove this non-cellular water and preserve proteins,

clotting factors and platelets as well as red blood cells that can then be returned to the patient. This alternate approach is the basic principle of the Hemobag®, an ultrafiltration technology and method.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
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

  • All adult cardiac surgery patients (age 18 or older) Cardiopulmonary bypass

排除标准

  • Patients under age 18 Off pump surgery

研究组 & 干预措施

Hemobag®

Experimental

Hemobag® method of returning residual CPB blood (study group)

干预措施: method of returning residual CPB blood ( Hemobag®) (Device)

cell saver

No Intervention

Standard method of returning the residual pump volume to the patient as washed, centrifuged cells (control group)

结局指标

主要结局

Amount of Chest Catheter Drainage 24 Hours Postoperatively

时间窗: Total amount for the first 24 hours postoperative

Chest catheters are placed in the mediastinum and sometimes pleural space(s) to collect shed mediastinal blood in the first 24 hours post operative cardiac surgery

次要结局

  • Number of Participants With Acute Kidney Injury (AKI)(All creatinines will be recorded and assessed during the entire index admission in order to compare postoperative to preoperative baseline creatinine, an expected average of 7 days.)
  • Number of Participants With a Mortality(Index admission postoperative until the time of discharge, an expected average of 7 days.)
  • Number of Participants With Stroke(Index admission postoperative until the time of discharge, an expected average of 7 days.)
  • Number of Participants on Vasoactive Drugs at 48 Hours Post op Point(Any intravenous vasoactive drug being used at the 48 hour time point postoperative)
  • Number of Participants Which Had Blood Products Transfused (RBC's, Platelets, FFP)(All blood products transfused during index admission, an expected average of 7 days, with the exception of preoperative transfusions.)

研究者

发起方
MaineHealth
申办方类型
Other
责任方
Principal Investigator
主要研究者

Robert Kramer, MD

Director of Research and Quality Improvement Division of Cardiothoracic Surgery

MaineHealth

研究点 (2)

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