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Haematologica 2004;89: supplement no. 8 - Supplements ...

Haematologica 2004;89: supplement no. 8 - Supplements ...

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66Oral Communicationsspontaneous recurrent VTE was <strong>no</strong>ticed in any groupin comparison with the reference individuals: thehazard ratio was 1.9 (95% CI 0.9-4.2) in the groupA (aPL), 1.2 (95% CI 0.8-1.8) in the group B (inheritedthrombophilia), and 0.8 (95% CI 0.2-2.8) in thegroup C (both aPL and inherited thrombophilia).Patients with aPL (group A), in spite of the observationtime shorter than that of the reference group D(median 2 years versus 4 years), showed a moderate1.9-fold increase in risk for recurrent VTE. However,the presence of aPL does <strong>no</strong>t seem to increase tendencytowards VTE among patients with inheritedthrombophilia.CO-0<strong>89</strong>D-DIMER AND VENOUS THROMBOTIC RESIDUE AREINDEPENDENT RISK FACTORS FOR RECURRENT VENOUSTHROMBOEMBOLISM AFTER ANTICOAGULATION WITHDRAWALCosmi B, Legnani C, Cini M, Guazzaloca G, Valdrè L,Brusi C, Palareti GDept. of Angiology & Blood Coagulation “Mari<strong>no</strong>Golinelli”, University Hospital S. Orsola-Malpighi,Bologna, ItalyIntroduction. D-dimer (D-d) and ve<strong>no</strong>us thromboticresidue (VTR) have been separately shown to berisk factors for recurrent VTE. Aims: to assess thepredictive value of the combination of D-d and VTRfor the development of recurrent VTE. Methods. 704consecutive symptomatic patients with a firstepisode of proximal deep vein thrombosis of the lowerlimbs were enrolled on the day of OAT withdrawal(T1). At T1 and three months afterwards (T3), D-dlevels were measured and VTR was determined bycompression ultraso<strong>no</strong>graphy. D-d was also measuredafter 30+10 days (T2). All the three availablemeasurements of D-d were considered to establish atrend (D-d trend): ab<strong>no</strong>rmal if D-d was persistentlyabove the cut-off value (75th percentile of the D-dvalues at T1 according to type of index event) at T1,T2 and T3 or if it increased above cut-off values atT2 and/or T3. Recurrences were diag<strong>no</strong>sed in case ofsymptoms of VTE by objective methods during a 2-year period. Results. Ab<strong>no</strong>rmal D-d trend was presentin 59.7% and VTR in 51.9% of patients. Ab<strong>no</strong>rmalD-d trend and VTR were associated with a multivariatehazard ratio for recurrence of 2.29 (95% CI:1.29-4.06; p=0.004) and 1.84 (95% CI: 1.15-2.95;p=0.011) respectively. When compared with patientswith <strong>no</strong>rmal D-d trend and absent VTR, the hazardratio for recurrence associated with ab<strong>no</strong>rmal D-dtrend and VTR was 6.36 (95% CI: 2.21-18.33; p=0.001) in all patients after adjustment for sex, age,OAT duration, thrombophilia, type of index event andcancer and 4.95 (95% CI: 1.45-16.<strong>89</strong>; p= 0.011) inpatients with an idiopathic DVT after adjustment forsex, age, OAT duration and thrombophilia. Conclusions:D-d and VTR are independent risk factors forrecurrent VTE.SISET PrizeCO-090RISK FACTORS AND RECURRENCE RATE OF PRIMARY DEEPVEIN THROMBOSIS OF THE UPPER EXTREMITIESBattaglioli T, Martinelli I, Bucciarelli P,Passamonti SM, Mannucci PMAngelo Bianchi Bo<strong>no</strong>mi Hemophilia and ThrombosisCenter, Department of Internal Medicine and Dermatology,IRCCS Maggiore Hospital, University ofMilan, ItalyOne third of cases of upper-extremity deep veinthrombosis (DVT) are primary, i.e, they occur in theabsence of central ve<strong>no</strong>us catheters or cancer. Riskfactors for primary upper-extremity DVT are <strong>no</strong>t wellestablished, and the recurrence rate is unk<strong>no</strong>wn. Westudied 115 primary upper-extremity DVT patientsand 797 healthy controls for the presence of thrombophiliadue to factor V Leiden, prothrombinG20210A, antithrombin, protein C, protein S deficiencyand hyperhomocysteinemia. Transient riskfactors for ve<strong>no</strong>us thromboembolism were recorded.Recurrent upper-extremity DVT was prospectivelyevaluated over a median period of 5.1 years of follow-up.The adjusted odds ratio for upper extremityDVT was 6.2 (95% CI 2.5-15.7) for factor V Leiden,5.0 (95% CI 2.0-12.2) for prothrombin G20210A and4.9 (95% CI 1.1-22.0) for the anticoagulant proteindeficiencies. Hyperhomocysteinemia and oral contraceptiveswere <strong>no</strong>t associated with upper-extremityDVT. However, in women with factor V Leiden orprothrombin G20210A taking oral contraceptives, theodds ratio for upper-extremity DVT was increased upto 13.6 (95% CI 2.7-67.3). The recurrence rate was4.4% patient-years in patients with and 1.6%patient-years in those without thrombophilia. Thehazard ratio for recurrent upper-extremity DVT inpatients with thrombophilia compared to thosewithout was 2.7 (95% CI 0.7-9.8). In conclusion,inherited thrombophilia is associated with anincreased risk of upper-extremity DVT. Oral contraceptivesincrease the risk only when combined withinherited thrombophilia. The recurrence rate of primaryupper-extremity DVT is low, but tends to behigher in patients with thrombophilia than in thosewithout.haematologica vol. <strong>89</strong>(suppl. n. 8):september <strong>2004</strong>

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