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一种用于纤维蛋白肽A的简单放射免疫测定法的性能特征

Performance characteristics of a simple radioimmunoassay for fibrinopeptide A.

作者信息

Walenga J M, Hoppensteadt D, Emanuele R M, Fareed J

出版信息

Semin Thromb Hemost. 1984 Oct;10(4):219-27. doi: 10.1055/s-2007-1004427.

Abstract

FPA, although identified 15 years ago, is now becoming an increasingly important diagnostic tool in the evaluation of the hemostatic process. Since this peptide is generated in very small amounts, only very sensitive methods, such as RIA, are useful for its quantitation. Measurement of this peptide allows for a most precise and reliable monitor of any ongoing thrombotic event in which thrombin is generated. Commercial kits have become available for fast and simple clinical evaluations of FPA. The Mallinckrodt RIA Quanti FPA kit has proved its reliability in precision, accuracy, fast turnaround time, and applicability to a routine laboratory setting. This assay kit was evaluated in our laboratory in various aspects. The following points summarize our finding: FPA is a useful diagnostic parameter to evaluate the activation of coagulation pathways in various pathologic states. A study of 170 normal plasma samples resulted in 1.7 +/- 0.5 ng/ml. No significant difference between males and females was noted. FPA levels are evaluated in patients with hypercoagulable states, DIC, and related thrombotic states. Our studies have shown that FPA levels are also elevated in certain cancers, postsurgical states, and certain other conditions in which the coagulation process is activated. During therapeutic heparinization, FPA levels are reduced; thus this form of therapy can be monitored using FPA levels. High-risk population (thrombotic) can be easily screened using FPA measurement. We propose that a multicenter study on FPA levels be conducted to prove its clinical relevance to other diseases.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

纤维蛋白肽A(FPA)尽管在15年前就已被发现,但如今在评估止血过程中正日益成为一种重要的诊断工具。由于这种肽的生成量极少,只有非常灵敏的方法,如放射免疫分析(RIA),才适用于对其进行定量测定。对这种肽的检测能够最精确、可靠地监测任何正在发生的有凝血酶生成的血栓形成事件。市面上已有用于快速、简便地临床评估FPA的试剂盒。马林克罗德特公司的RIA定量FPA试剂盒已在精密度、准确性、快速周转时间以及在常规实验室环境中的适用性等方面证明了其可靠性。我们实验室对该检测试剂盒进行了多方面评估。以下几点总结了我们的发现:FPA是评估各种病理状态下凝血途径激活情况的有用诊断参数。对170份正常血浆样本的研究结果为1.7±0.5纳克/毫升。未发现男性和女性之间有显著差异。对处于高凝状态、弥散性血管内凝血(DIC)及相关血栓形成状态的患者进行了FPA水平评估。我们的研究表明,在某些癌症、术后状态以及其他一些激活凝血过程的情况下,FPA水平也会升高。在进行肝素化治疗期间,FPA水平会降低;因此可以利用FPA水平来监测这种治疗方式。通过检测FPA能够轻松筛查出高风险(血栓形成)人群。我们建议开展一项关于FPA水平的多中心研究,以证明其与其他疾病的临床相关性。(摘要截选至250词)

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