Aims A novel sensitive method for analyses of soluble fibrin monomer antige
n was used to assess the predictive value of fibrin monomer when estimating
mortality after acute myocardial infarction.
Methods and Results Fibrin monomer was measured in plasma samples from 293
patients enrolled in a randomized clinical trial of low molecular weight he
parin (dalteparin) in acute myocardial infarction (the FRAMI trial). Sample
s taken on days 2 and 7 were analysed using the Enzymun-Test FM(R) (Boehrin
ger Mannheim, Germany). Non-survivors had significantly higher fibrin monom
er levels relative to survivors (day 2, median (min-max): 1.8 mg. l(-1) (<0
.01-73.1) vs 0.4 mg.l(-1) (<0.01-103.5), P<0.0001). Fibrin monomer levels w
ere significantly associated with congestive heart failure (P<0.001), enzym
atic infarct size (P<0.0001), dalteparin treatment (P<0.001), and thromboly
tic therapy (P=0.016). The relationship between fibrin monomer and mortalit
y remained statistically significant after adjustment for these variables.
In logistic regression analyses, fibrin monomer levels, age and congestive
heart failure were all independent predictors of fatal outcome.
Conclusions Increased fibrin monomer level is an independent predictor of m
ortality in patients with myocardial infarction. It allows further risk str
atification when combined with known risk factors such as age and presence
of congestive heart failure.