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人血红蛋白在白蛋白作为血浆置换替代溶液中存在。

Haptoglobin is present in albumin used as a replacement solution for plasma exchange.

机构信息

Apheresis Unit, Department of Hemotherapy-Hemostasis, University de Barcelona, Barcelona, Spain.

出版信息

Transfusion. 2013 Apr;53(4):757-60. doi: 10.1111/j.1537-2995.2012.03783.x. Epub 2012 Jul 15.

Abstract

BACKGROUND

Albumin is frequently used as replacement solution when performing plasma exchanges (PEs) and there are no previous data about the content of haptoglobin. The objective was to study the content of haptoglobin in albumin solution and the effect of PE on the removal of haptoglobin, a plasma protein often used for monitoring hemolytic conditions treated with PE.

STUDY DESIGN AND METHODS

Haptoglobin was measured in the 5% albumin replacement solution. It was also measured before and after performing 12 PEs using 5% albumin as a replacement solution on four patients. There were three patients with haptoglobin values within the reference range before starting PEs whereas one patient had low levels because of microangiopathic hemolytic anemia.

RESULTS

The mean content of haptoglobin in the 5% albumin replacement solution was 0.157±0.005g/L. Predicted removal according to the one-compartment model was 70% to 77%. Real removal (RR) of haptoglobin in patients with values within the reference range was 7% to 67%. The RR correlated with the value of haptoglobin before performing PE (r=0.709; r(2) =0.502; p=0.03). When haptoglobin levels were low before PE, the levels after the PE were those present in the albumin used as a replacement solution.

CONCLUSION

Albumin solution used for PE contained haptoglobin and it explained in part the kinetics removal of plasma haptoglobin observed in the patients.

摘要

背景

白蛋白在进行血浆置换(PE)时经常被用作替代溶液,目前尚无关于结合珠蛋白含量的相关数据。本研究旨在研究白蛋白溶液中结合珠蛋白的含量,以及 PE 对结合珠蛋白(一种常用于监测接受 PE 治疗的溶血性疾病的血浆蛋白)清除的影响。

研究设计和方法

在 5%白蛋白替代溶液中测量了结合珠蛋白的含量。还在 4 名患者中使用 5%白蛋白作为替代溶液进行 12 次 PE 前后测量了结合珠蛋白的含量。在开始进行 PE 之前,有 3 名患者的结合珠蛋白值在参考范围内,而 1 名患者由于微血管性溶血性贫血而出现低值。

结果

5%白蛋白替代溶液中结合珠蛋白的平均含量为 0.157±0.005g/L。根据单室模型预测的清除率为 70%至 77%。参考范围内患者的结合珠蛋白实际清除率(RR)为 7%至 67%。RR 与进行 PE 前的结合珠蛋白值相关(r=0.709;r²=0.502;p=0.03)。当 PE 前结合珠蛋白水平较低时,PE 后结合珠蛋白水平与白蛋白替代溶液中的水平一致。

结论

用于 PE 的白蛋白溶液中含有结合珠蛋白,这部分解释了患者中观察到的血浆结合珠蛋白的动力学清除。

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