M. Decicco et al., ANTITHROMBIN-III DEFICIENCY AS A RISK FACTOR FOR CATHETER-RELATED CENTRAL VEIN-THROMBOSIS IN CANCER-PATIENTS, Thrombosis research, 78(2), 1995, pp. 127-137
The fibrin sleeve of venous catheters (VC) and parietal thrombi repres
ent frequent and dangerous side-effects of central venous catheterizat
ion (CVC), due to the risk of embolism. Reduced levels of coagulation
clotting factors inhibitors (such as Antithrombin III) are known to be
associated with increased thrombogenic risk. The aim of this study wa
s to evaluate the role of Antithrombin III (AT III) deficiency as a ri
sk factor for thrombosis in cancer patients undergoing CVC. The study
groups included patients with a reduced AT III activity (< 70%, 20 con
secutive patients) and with normal AT III values (> 70%, 20 randomly s
elected patients), requiring a VC for chemotherapy and/or total parent
eral nutrition. The study protocol included evaluation of Hb, PLTs, PT
(INR), aPTT, Fibrinogen and AT III at days 0, 1, 3 and 8 after CVC an
d upon VC removal. Peripheral and pullout phlebographies were performe
d in all patients on catheter withdrawal. A quantitative scale was dev
eloped to evaluate both VC and parietal thrombus degree in each cathet
er-containing venous segment (subclavian, innominate, superior vena ca
va); the sum of the mean values was defined as overall thrombus. The a
verage VC dwelling time was similar in both groups. There were no sign
ificant differences in Hb, PLTs, PT (INR), aPTT, Fibrinogen and in the
remaining parameters of the study between the two groups. The group w
ith AT III deficiency presented a higher degree of both parietal (p <
0.05) and overall thrombus (p < 0.02). Data showed a higher severity o
f CVC-related thrombosis in patients with AT III deficiency than in th
e control group. Further studies are needed to evaluate whether the th
erapeutically-induced normalization of AT III levels can reduce the th
rombosis degree.