Er. Burns et al., PARADOXIC EFFECT OF MULTIPLE MILD COAGULATION-FACTOR DEFICIENCIES ON THE PROTHROMBIN TIME AND ACTIVATED PARTIAL THROMBOPLASTIN TIME, American journal of clinical pathology, 100(2), 1993, pp. 94-98
Single coagulation factor deficiencies predictably prolong the prothro
mbin time (PT) and activated partial thromboplastin time (APTT) at lev
els below 35% of normal activity. Acquired coagulopathies generally ar
e characterized by multiple coagulation factor deficiencies. The effec
t was studied of such combined deficiencies on the PT/APTT using plasm
a from patients congenitally deficient in specific factors and pooled
normal plasma. The PT begins to lengthen when individual factor levels
fall below 25%. The APTT becomes prolonged when the levels of Factor
V fall below 45%; the levels of Factors II and XI fall below 40%; and
the levels of Factors I, V, VII, VIII, IX, and XII fall below 25% of n
ormal. When plasma samples containing 50% activity of a single factor
and 100% of all other factors were prepared by mixing the congenitally
deficient plasma samples with the normal pool, the resulting mixtures
had normal PT and APTT values. However, when two of these 50% factor-
deficient plasmas were combined so that the mixture contained 75% acti
vity of two coagulation factors and 100% of all other factors, the res
ulting PT and APTT were prolonged over the clotting times of either 50
% factor-deficient plasma. Similar findings were obtained in patients
with mild factor reductions caused by warfarin treatment. These data i
ndicate that prolongations of the PF and APTT in disorders of coagulat
ion affecting multiple factors represent less of a reduction in factor
levels than is generally appreciated. This may explain the poor clini
cal correlation between abnormalities in these test results and clinic
al bleeding in acquired disorders of hemostasis.