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

被引:34
作者
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
[1] Univ Kansas, Med Ctr, Dept Pathol, Kansas City, KS 66160 USA
[2] Eli Lilly Corp Ctr, Indianapolis, IN USA
[3] Univ Washington, Dept Lab Med, Seattle, WA 98195 USA
[4] Washington Univ, Sch Med, Dept Pathol, St Louis, MO 63110 USA
[5] Maine Med Ctr, Dept Pathol & Lab Med, Portland, ME 04102 USA
[6] Washington Hosp Ctr, Dept Pathol, Washington, DC 20010 USA
[7] Univ Colorado, Hlth Sci Ctr, Dept Pathol, Aurora, CO USA
[8] Univ Texas, Hlth Sci Ctr, Dept Pathol, San Antonio, TX 78285 USA
[9] Texas Childrens Hosp, Baylor Coll Med, Dept Pathol, Houston, TX 77030 USA
[10] Massachusetts Gen Hosp, Dept Pathol, Boston, MA 02114 USA
关键词
coagulation; hemostasis testing; proficiency testing; quality assurance; quality control;
D O I
10.1055/s-2007-971811
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
引用
收藏
页码:250 / 258
页数:9
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