CLSI Publishes Guideline for One-Stage Prothrombin Time (PT) Test and Activated Partial Thromboplastin Time (APTT) Test.WAYNE, Pa. -- The PT and APTT APTT, aPTT activated partial thromboplastin time. APTT activated partial thromboplastin time. are important screening tests used in laboratory evaluation of patients suspected to have disorders of blood coagulation, including the presence of circulating coagulation coagulation (kōăg'y lā`shən), the collecting into a mass of minute particles of a solid dispersed throughout a liquid (a sol), usually followed by the precipitation or inhibitors. Clinical and Laboratory Standards Institute (CLSI) recently
published an updated document, One-Stage Prothrombin Time one-stage prothrombin timesee prothrombin time test. (PT) Test and Activated Partial Thromboplastin Time Activated partial thromboplastin time Partial thromboplastin time test that uses activators to shorten the clotting time, making it more useful for heparin monitoring. (APTT) Test; Approved Guideline--Second Edition (H47-A2), which provides guidelines for performing the PT and APTT tests in the clinical laboratory, for reporting results, and for identifying sources of error. Richard A. Marlar, PhD, Professor of Pathology, Chief, Clinical Pathology, University of Oklahoma University of Oklahoma, abbreviated OU, is a coeducational public research university located in the U.S. state of Oklahoma. Founded in 1890, it existed in Oklahoma Territory near Indian Territory 17 years before the two became the state of Oklahoma. Health Sciences Center, and Chairholder of subcommittee that developed the document, says, "The PT and PTT (1) (Postal, Telegraph & Telephone) The governmental agency responsible for combined postal, telegraph and telephone services in many European countries. (2) See push-to-talk. PTT - Post, Telephone and Telegraph administration assays are two of the most utilized and perhaps versatile tests in the clinical laboratory. Performing them correctly and in the appropriate setting can be a difficult task. H47-A2 presents the state of the art using evidence-based methods and criteria for performing these assays. This document was designed to provide all sizes and complexities of laboratories to use the PT and PTT correctly for the diagnosis and treatment of coagulation disorders." The objective of the guideline is to improve test reproducibility through standardization of technique and ensure clinical relevance by setting test performance goals. The document also highlights the international effort for standardization of the PT using the international normalized ratio International Normalized Ratio Hematology A method of reporting prothrombin time–PT results for Pts receiving oral anticoagulant therapy; the INR is defined by the formula, PTPatient/PTMNPT (INR INR In currencies, this is the abbreviation for the Indian Rupee. Notes: The currency market, also known as the Foreign Exchange market, is the largest financial market in the world, with a daily average volume of over US $1 trillion. ). This document is a revision of H47-A, which was published in 1996 and includes the following updates: * validating and calibrating PT reagents; * local system calibration; * PT mixing studies; * APTT mixing studies; * monitoring direct thrombin inhibitors; * establishing heparin therapeutic ranges; and * factor sensitivity determination. The document is written for laboratory and/or clinical personnel responsible for the performance, quality control, and reporting of the PT and APTT tests, as well as for manufacturers of coagulation instruments and reagents who are responsible for maintaining appropriate performance standards. For additional information on CLSI or for further information regarding this release, visit our website at www.clsi.org or call +610.688.0100. CLSI, formerly NCCLS, is a global, nonprofit, membership-based organization dedicated to developing standards and guidelines for the health care and medical testing community. CLSI's unique consensus process facilitates the creation of standards and guidelines that are reliable, practical, and achievable for an effective quality system. |
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