Objective: Plasma markers of coagulation and fibrinolysis have proved sensi
tive in the initial diagnosis of acute deep venous thrombosis (DVT). The pu
rpose of this study was to examine the evolution and utilitly of measuring
D-dimer and prothrombin fragment 1+2 (F 1+2) levels after an acute DVT.
Methods: Subjects with DVT confirmed by ultrasonography had quantitative pl
asma. D-dimer and F 1+2 levels determined before anticoagulation. Ultrasoun
d scan and coagulation studies were repeated at 3, 7, and 14 days; 1 month;
and every 3 months for 1 year.
Results: Sixty-one patients with a median initial thrombus score of 3 (inte
rquartile range, 2-7) were followed up for 266 days (interquartile range, 9
1.5-364 days). Initial D-dimer levels were elevated in 92.7% of patients an
d were associated with thrombus extent (P = .003), whereas F 1+2 levels wer
e increased in 94.5% of patients and were lower in patients with isolated c
alf vein thrombosis (P = .001). Initial D-dimer (P = .002) and F 1+2 levels
(P = .009) were significantly higher in the 26 (43%) patients with recurre
nt thrombosis during follow-up. Initial D-dimer levels of 2000 ng/mL or gre
ater were predictive of recurrent events after both proximal and isolated c
alf vein thrombosis. Although interval increases in these markers had littl
e value in detecting recurrent thrombotic events, D-dimer levels of 1000 ng
/mL or greater and 500 ng/mL or greater had respective sensitivities of 89.
3% and 100% in detecting early and late recurrences. Corresponding specific
ities were 35.6% and 53.9%.
Conclusions: Initial D-dimer levels are determined by total thrombus load a
nd remain elevated long after an acute DVT. F 1+2 levels are less sensitive
to thrombus score and return to baseline more quickly. Initial levels of t
hese markers may have some utility in predicting the risk of ultrasound sca
n-documented recurrences, whereas increased D-dimer levels are a sensitive
but nonspecific marker of these events.