M. Ikeda et al., SCLEROTHERAPY FOR VARICOSE-VEINS OF THE LOWER LEGS IN PATIENTS WITH DYSPLASMINOGENEMIA, SURGERY TODAY-THE JAPANESE JOURNAL OF SURGERY, 27(8), 1997, pp. 714-718
Sclerotherapy combined with ligation has become a widely accepted trea
tment for varicose veins; however, it is associated with some risk of
the serious complications of deep vein thrombosis (DVT). We investigat
ed the incidence of thrombophilia in 164 consecutive patients undergoi
ng treatment for varicose veins and determined the activities of antit
hrombin-In, protein C, and plasminogen. Of the 164 patients, 10 were d
iagnosed as having dysplasminogenemia (DPG), showing an incidence of 6
.1%, in accordance with previous reports. DVT was not found to be caus
ed by DPG in any patient, and no difference was found between patients
with and those without DPG, suggesting that DPG is not a risk factor
for varicose veins. We also investigated the activation of coagulation
by measuring the thrombin-antithrombin III complex (TAT). The activat
ion of coagulation after sclerotherapy was inhibited when ligation was
performed 1 month prior to sclerotherapy, whereas it was increased wh
en sclerotherapy and Ligation were performed simultaneously. Of the 10
patients with DPG, 5 were treated uneventfully, and their TAT level i
ncreased to 4.0 mu g/l, which was comparable to the level after sclero
therapy and ligation. These findings indicate that sclerotherapy can b
e performed safely in the majority of patients with DPG, and that the
temporal separation of sclerotherapy and surgery is an alternative for
these patients to prevent the activation of coagulation.