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使用常规快速肝素中和法检测未诊断出的凝血病。

Detection of undiagnosed coagulopathies using routine rapid heparin neutralization.

作者信息

Burns E R, Lee V, Wenz B

机构信息

Department of Laboratory Medicine, Albert Einstein College of Medicine, Bronx, New York 10461, USA.

出版信息

Clin Lab Sci. 1995 Mar-Apr;8(2):113-6.

Abstract

OBJECTIVE

To determine the most frequent clinical causes of a prolonged activated partial thromboplastin time (APTT) result, and to determine whether a new heparin-removal device (the Hepchek, Pall Biomedical, Glen Cove, NY 11542) is capable of efficiently detecting the causes of these values.

DESIGN

A combination of chart review and laboratory testing comparing the criterion standard--the heparin chromogenic substrate assay--with the Hepchek. Laboratory investigations were blinded and controlled.

SETTING

Inpatient, acute-care hospital.

PATIENTS

A total of 1,000 hospital patients with a variety of hemostatic disorders.

MAIN OUTCOME MEASURE

The extent to which the Hepchek accurately identified the etiology of a prolonged APTT result.

RESULTS

The APTT was prolonged in 25.2% of samples. The presence of heparin in the sample was confirmed by chromogenic assay or by using the Hepchek heparin-removal filter. The presence of heparin was confirmed in 12.8% of all samples and in more than 50% of all abnormal samples. The cause of the abnormal APTT was often unappreciated by the clinician. Bayesian analysis of the Hepchek's ability to diagnose heparin correctly as the cause of the abnormal APTT showed a sensitivity of 100% and specificity of 99.9%.

CONCLUSION

Use of the Hepchek in the routine clinical laboratory is an efficient and rapid method of detecting heparin as a cause of isolated prolonged APTT results, and should reduce demands for unwarranted coagulation analyses and inappropriate treatment with blood products.

摘要

目的

确定活化部分凝血活酶时间(APTT)结果延长最常见的临床原因,并确定一种新型肝素去除装置(Hepchek,颇尔生物医学公司,纽约州格伦科夫11542)能否有效检测出导致这些数值的原因。

设计

采用图表回顾和实验室检测相结合的方法,将标准检测方法——肝素显色底物法——与Hepchek进行比较。实验室检测采用盲法且进行了对照。

地点

急性护理住院医院。

患者

共1000例患有各种止血障碍的住院患者。

主要观察指标

Hepchek准确识别APTT结果延长病因的程度。

结果

25.2%的样本APTT延长。通过显色测定或使用Hepchek肝素去除过滤器确认样本中存在肝素。在所有样本的12.8%以及所有异常样本的50%以上中确认存在肝素。临床医生常常未认识到异常APTT的原因。对Hepchek正确诊断肝素为异常APTT病因的能力进行贝叶斯分析,结果显示灵敏度为100%,特异性为99.9%。

结论

在常规临床实验室中使用Hepchek是检测肝素导致孤立性APTT结果延长的一种高效、快速的方法,应可减少不必要的凝血分析需求以及血液制品的不当使用。

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