We enrolled 82 patients receiving oral anticoagulation in a pilot trial of
a point-of-care (POC) prothrombin time (PT) device in a patient self-testin
g (PST) application in 7 US and Canadian hospital-based anticoagulation cen
ters. The properly selected and suitably trained patients were given the PT
device to test at home for 6 weeks. Patients returned within 3 hours of th
e self-test to the hospital clinic where a repeated test was performed by a
health care professional using the patient's POC device (clinic). Blood sp
ecimens were obtained for routine laboratory PT determinations by the local
hospital laboratory (hospital) and a reference laboratory International No
rmalized Ratio agreement between the home test and the clinic test was exce
llent. Home results correlated well with reference laboratory results. Usin
g the I reference laboratory as a standard, 68% of hospital and 66% of home
results matched the patient's therapeutic range classification of the refe
rence laboratory result. Participants overwhelmingly reported satisfaction
and willingness to perform the self-test. Our results confirm the equivalen
ce of the PST PT and a reference laboratory result and suggest that PST PT
technology is an appropriate and useful adjunct to routine oral anticoagula
tion monitoring methods.