Use of the activated partial thromboplastin time for heparin monitoring

• Published in: American journal of clinical pathology 2001, Vol.115 (1), p.148-155
• Main Authors: SMYTHE, Maureen A, KOERBER, John M, WESTLEY, Susan J, NOWAK, Sandra N, BEGLE, Robert L, BALASUBRAMANIAM, Mamtha, MATTSON, Joan C
• Format: Article
• Language: English
• Subjects: Aged; Biological and medical sciences; Blood coagulation; Clinical Laboratory Techniques; Dose-Response Relationship, Drug; Drug Monitoring - methods; Female; Heparin - administration & dosage; Heparin - blood; Humans; Investigative techniques, diagnostic techniques (general aspects); Laboratories; Male; Medical sciences; Middle Aged; Osmolar Concentration; Partial Thromboplastin Time; Point-of-Care Systems; Prospective Studies
• ISSN: 0002-9173; 1943-7722
• DOI: 10.1309/n7ra-d6xn-9eqx-abj9

The objectives of the present study were to evaluate the relationship between heparin concentration and activated partial thromboplastin time (aPTT) results, define a heparin concentration-derived therapeutic range for each aPTT instrument, compare aPTT- and heparin concentration-guided dosage adjustment decisions, and compare laboratory- and bedside aPTT-guided decisions. In phase 1, 102 blood samples were analyzed for bedside and laboratory aPTTs and heparin concentration (used to establish aPTT therapeutic range). In phase 2, 100 samples were analyzed in the same manner. Correlations for aPTT compared with heparin ranged from 0.36 to 0.82. Dosage adjustment decisions guided by the aPTT agreed with those based on heparin concentration 63% to 80% of the time. Laboratory and bedside aPTT dosage adjustment decisions agreed 59% to 68% of the time. The correlation of aPTT with heparin concentration and agreement between aPTT- and heparin-guided decisions vary with the aPTT instrument. Decisions guided by laboratory aPTT results often disagree with decisions guided by bedside aPTT results.