Summary
Laboratory monitoring is widely recommended to measure the anticoagulant effect of
unfractionated heparin and to adjust the dose to maintain levels in the target therapeutic
range.The most widely used laboratory assay for monitoring unfractionated heparin
therapy is the activated partial thromboplastin time (aPTT). A fixed therapeutic range
for the aPTT of 1.5 to 2.5 times the control value has become widely accepted,but
the evidence supporting this range is weak and the clinical validity of using the
aPTT for predicting thrombotic or bleeding events is questionable. The aPTT test is
also affected by numerous preanalytic and analytic variables that are unrelated to
the anticoagulant effect of unfractionated heparin, further eroding its potential
value for monitoring unfractionated heparin treatment. Unfractionated heparin dose
appears to be more important than the aPTT in predicting clinical efficacy. Despite
serious limitations,the reliance on the aPTT is likely to continue because of its
ready availability and familiarity of clinicians with the test. The focus of clinicians
who manage unfractionated heparin therapy should be to ensure that an adequate starting
dose of unfractionated heparin is used and that the aPTT method is standardized. Future
research efforts should be directed towards developing methods to improve standardization
of the aPTT assay for monitoring unfractionated heparin. Direct measures of the concentration
of unfractionated heparin in the blood are attractive because these assays are not
affected by many of the biologic variables that interfere with the aPTT and may be
suitable for automation. However, currently available unfractionated heparin assays
are much more expensive than the aPTT, are not widely available, and their validity
has not been adequately assessed in clinical outcome studies.
Keywords
Heparin - laboratory monitoring - aPTT