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止血方面的质量保证:来自美国病理学家学会能力验证计划的视角

Quality assurance in hemostasis: the perspective from the College of American Pathologists proficiency testing program.

作者信息

Cunningham Mark T, Brandt John T, Chandler Wayne L, Eby Charles S, Hayes Timothy E, Krishnan Jayashree, Lefkowitz Jerry B, Olson John D, Stasik Christopher J, Teruya Jun, Van Cott Elizabeth M

机构信息

Department of Pathology, University of Kansas Medical Center, Kansas City, Kansas 66160, USA.

出版信息

Semin Thromb Hemost. 2007 Apr;33(3):250-8. doi: 10.1055/s-2007-971811.

Abstract

External quality assurance (EQA) is an important component of the total quality assurance program of a clinical hemostasis laboratory. The College of American Pathologists (CAP) helps meet this requirement by providing a proficiency testing program that evaluates a broad range of hemostasis methods and analytes. This article reviews the published experience of the CAP proficiency testing program in hemostasis. The purpose is to formulate general conclusions about the benefits of EQA. Between 1963 and 2006, the performance characteristics of a variety of tests have been evaluated, including the prothrombin time, activated partial thromboplastin time, coagulation factor activity assays (e.g., fibrinogen, factor [F] VIII, FIX, FXI), von Willebrand factor assays, unfractionated heparin monitoring, lupus anticoagulant testing, and platelet function. Based on the results of these evaluations, the major benefits of EQA are to (1) enhance patient care and safety through improved laboratory testing; (2) characterize test accuracy and precision across multiple methods; (3) correlate specific method variables with accuracy and precision; (4) identify interfering substances and quantify their effects across multiple methods; (5) identify clinical laboratories that are at risk for poor performance so that their performance can improve; and (6) satisfy accreditation and regulatory requirements.

摘要

外部质量保证(EQA)是临床止血实验室全面质量保证计划的重要组成部分。美国病理学家学会(CAP)通过提供一项能力验证计划来满足这一要求,该计划评估广泛的止血方法和分析物。本文回顾了CAP止血能力验证计划已发表的经验。目的是就EQA的益处得出一般性结论。在1963年至2006年期间,已对多种检测的性能特征进行了评估,包括凝血酶原时间、活化部分凝血活酶时间、凝血因子活性测定(如纤维蛋白原、因子[F]VIII、FIX、FXI)、血管性血友病因子测定、普通肝素监测、狼疮抗凝物检测以及血小板功能。基于这些评估结果,EQA的主要益处在于:(1)通过改进实验室检测提高患者护理质量和安全性;(2)表征多种方法的检测准确性和精密度;(3)将特定方法变量与准确性和精密度相关联;(4)识别干扰物质并在多种方法中量化其影响;(5)识别性能不佳风险较高的临床实验室,以便其性能能够得到改善;(6)满足认证和监管要求。

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