Effect of analytic uncertainty of conventional and point-of-care assays of activated partial thromboplastin time on clinical decisions in heparin therapy.

The authors assessed the capability of assays of activated partial thromboplastin time (aPTT) for supporting clinical decision algorithms for heparin therapies of varying complexity. Blood samples were collected prospectively in three explicit management strategies from 100 sequential patients for whom heparin dosage was adjusted for therapeutic monitoring, femoral venous sheath removal after cardiac catheterization, or heparinization after thrombolytic therapy. In two- and three-way decision algorithms, conventional and point-of-care aPTT assays agreed with heparin assays in approximately two thirds of cases, and the two aPTT assays agreed in 80% or more of all cases. In six-way decision algorithms, the two aPTT assays agreed in only about half of all cases. The authors conclude that the reliability of point-of-care aPTT assays is similar to that of conventional assays. Both techniques can support two- and three-way decision algorithms but not some more complex patient classifications.

[1]  Frans Van de Werf,et al.  An international randomized trial comparing four thrombolytic strategies for acute myocardial infarction. , 1993, The New England journal of medicine.

[2]  J. Hirsh,et al.  A prospective study of the value of monitoring heparin treatment with the activated partial thromboplastin time. , 1972, The New England journal of medicine.

[3]  R. Baugh,et al.  Heparin monitoring in the coronary care unit after percutaneous transluminal coronary angioplasty. , 1990, Heart & lung : the journal of critical care.

[4]  C. Corke,et al.  A Comparison of Five Devices for the Bedside Monitoring of Heparin Therapy , 1991, Anaesthesia and intensive care.

[5]  A. R. Lea,et al.  Developments in near-patient testing. , 1990, Medical laboratory sciences.

[6]  G. Kost,et al.  New whole blood analyzers and their impact on cardiac and critical care. , 1993, Critical reviews in clinical laboratory sciences.

[7]  T. Bjornsson,et al.  Variability in heparin sensitivity of APTT reagents. , 1986, American journal of clinical pathology.

[8]  R. M. Greendyke Cost analysis. Bedside blood glucose testing. , 1992, American journal of clinical pathology.

[9]  B. Zanke,et al.  Comparison of two APTT methods of monitoring heparin therapy. APTT ratio and heparin response of pooled normal plasma. , 1990, American journal of clinical pathology.

[10]  G. Raskob,et al.  Optimal therapeutic level of heparin therapy in patients with venous thrombosis. , 1992, Archives of internal medicine.

[11]  D. Adler,et al.  Measurement of the activated partial thromboplastin time from a capillary (fingerstick) sample of whole blood. A new method for monitoring heparin therapy. , 1991, American journal of clinical pathology.

[12]  J. Hirsh Mechanism of Action and Monitoring of Anticoagulants , 1986, Seminars in thrombosis and hemostasis.

[13]  T. Baglin,et al.  Evaluation of the Ciba Corning Biotrack 512 coagulation monitor for the control of oral anticoagulation. , 1991, Journal of clinical pathology.

[14]  J. Hirsh,et al.  A standard heparin nomogram for the management of heparin therapy. , 1991, Archives of internal medicine.

[15]  E W Salzman,et al.  Management of heparin therapy: Controlled prospective trial. , 1975, The New England journal of medicine.

[16]  S. McCurdy,et al.  Accuracy and precision of a portable anticoagulation monitor in a clinical setting. , 1992, Archives of internal medicine.

[17]  E. Genton Drug Spotlight Program: Guidelines for Heparin Therapy , 1974 .

[18]  J. Vacek,et al.  Validation of a bedside method of activated partial thromboplastin time measurement with clinical range guidelines. , 1991, The American journal of cardiology.

[19]  C G Fraser,et al.  The application of theoretical goals based on biological variation data in proficiency testing. , 1988, Archives of pathology & laboratory medicine.

[20]  D. B. Tonks,et al.  A study of the accuracy and precision of clinical chemistry determinations in 170 Canadian laboratories. , 1963, Clinical chemistry.

[21]  K. High,et al.  Decentralized testing for prothrombin time and activated partial thromboplastin time using a dry chemistry portable analyzer. , 1993, Archives of pathology & laboratory medicine.

[22]  Campbell Bg Evaluation of two types of 'medically significant error limits' and two quality control procedures on a multichannel analyzer. , 1989 .

[23]  P. Bonini,et al.  Effect of clot-detection methods and reagents on activated partial thromboplastin time (APTT). Implications in heparin monitoring by APTT. , 1990, American journal of clinical pathology.

[24]  M. Lie,et al.  Evaluation of an amidolytic heparin assay method: increased sensitivity by adding purified antithrombin III. , 1977, Thrombosis research.

[25]  A. Shojania,et al.  The variations between heparin sensitivity of different lots of activated partial thromboplastin time reagent produced by the same manufacturer. , 1988, American journal of clinical pathology.

[26]  D. Mungall,et al.  A novel whole blood capillary technic for measuring the prothrombin time. , 1987, American journal of clinical pathology.