XVIII Congress of the Italian Society for Hemostasis and Thrombosis Research, Rome, Sept. 30-Oct. 3, <strong>2004</strong>161ment: surgery was performed in 20 cases (27%); 2patients underwent unsuccessful thrombolysis withrt-PA. 39% of pts were on oral anticoagulant therapyfor 6-12 months and showed 34% of recurrencesafter stopping warfarin. 28% of patients wereassigned to lifelong warfarin therapy, of which 2showed thrombosis progression into inferior cavalvein. CVT treatment: 92% of patients were on oralanticoagulant therapy for 3-12 months and showed2% of recurrences after stopping warfarin. 8% ofpatients were assigned to lifelong warfarin. Sevendeath were recorded in VVT group (death rate 5.5%per year). Acquired hypercoagulable states werefound during the follow-up: myeloproliferative disorders(15% of VVT), antiphospholipid syndrome(12% of VVT). Inherited thrombophilia was found in37% of VVT and in 33% of CVT pts: ATIII deficiency(2), protein C deficiency (3), protein S deficiency (5),factor V Leiden (9), prothrombin 20210 G/A mutation(7), hyperhomocysteinemia (9). Conclusions. In ourcase series, VVT and CVT were found to be commonlyrelated to inherited and acquired thrombophilicdisorders. VVT showed a high recurrency rate afterwithdrawal of antithrombotic therapy.PO-131GENETIC AND ACQUIRED THROMBOPHYLIC FACTORS INPATIENTS WITH UNUSUAL VENOUS THROMBOSISRupoli S, Pulini S, Barulli S, Da Lio L,° Logullo F,*Scortechini AR, Tassetti A, Ravaglia F,° Leoni PClinica Ematologica, *Clinica Neurologica, °LaboratorioAnalisi; Università Politecnica delle MarcheAzienda Ospedaliero Universitaria Ospedali RiunitiUmberto I-G.M. Lancisi-G. Salesi, Ancona, ItalyUnusual ve<strong>no</strong>us thrombosis are frequently associatedwith genetic and acquired risk factors. We evaluatedthe frequency of such factors in 6 patients(median age 38 years, range 26-56) with cerebralve<strong>no</strong>us thrombosis (CVT) and in 9 patients (medianage of 41 years, range 18-56) with splancnic veinthrombosis (SVT). Among the first group a completethrombophylic screening was performed in 5/6. Onlyone patient had <strong>no</strong> risk factors. The others presented,respectively: 1)APC resistance and high plasmalevels of coagulation factor VIII together with oralcontraceptive therapy (OCT); 2) LAC/ACA antibodies,factor V Leiden with OCT; 3)OCT and breast cancer;4)essential thrombocytemia (ET). Among the patientswith SVT only one patient had <strong>no</strong> risk factors. Threepatients presented a combination of genetic andacquired risk factors: factor V Leiden and OCT;G20210A prothrombin gene mutation and OCT;hyperhomocysteinemia and ET. A<strong>no</strong>ther woman, intherapy with OC, was diag<strong>no</strong>sed has having ET at thetime of SVT. With regards to the remaining patients,one had various genetic polymorphism of fibri<strong>no</strong>gen,PAI and coagulation factor XIII genes; one wasaffected by idiopathic myelofibrosis; one was affectedby ET and one by myelo-mo<strong>no</strong>citic chronicleukemia. The majority of these 15 patients wasquickly treated after diag<strong>no</strong>sis with LMWH and warfarin.The outcome of thrombosis was: complete resolutionin 10/13 valuable patients; an unfavourableresult in one; 2 patients are still in treatment; 2patients were lost at follow-up. At present <strong>no</strong> recurrenceshave been observed. Patients with unusualve<strong>no</strong>us thrombosis need an accurate research of anunderlying myeloproliferative disorder or othermalignancy in order to optimise treatment for boththe thrombosis and the baseline disorder. Despite thesmall sample size, our data suggest that geneticthrombophilias are often associated with predisposingfactors. xAmong them, OCT seems to be animportant determinant in the global thrombotic riskof CVT and SVT and chronic myeloproliferative disordersin the pathogenesis of SVT.PO-132VENOUS THROMBOEMBOLIC DISEASE: CLINICAL FEATURES OF1282 PROSPECTIVE CONSECUTIVE CASES AT ANGIOLOGY UNITOF REGGIO EMILIAGhirarduzzi A, Iotti M, Cattabiani L, Ieran M,Iorio A,* Silingardi M, Iori ISSD Angiologia and Thrombosis Centre, Dpt areaMedica 1^, Arcispedale Santa Maria Nuova,Reggio Emilia.*Dept Internal Medicine, Universitàdi Perugia, ItalyBackground. In the last decade the validation ofcompressive ultraso<strong>no</strong>graphy, D-dimer testing andpre-clinical probability assessment for the diag<strong>no</strong>sisand the availability of low molecular weight heparinfor the prophylaxis and initial treatment of ve<strong>no</strong>usthromboembolism (VTE), have both induced significantchanges in the management of proximal deepve<strong>no</strong>us thrombosis (DVT) and pulmonary embolism(PE). Aim of the study. We referred to the registriesof the Angiology Unit of Reggio Emilia, built up in1997, to trace the effect of the availability of preferreddiag<strong>no</strong>stic pathways, adoption and maintenanceof prophylaxis-therapeutic guidelines, progressiveincrease of home treatment and reductionlenght of hospital stay on the epidemiology and naturalhistory of VTE. Patients and methods. Wereviewed all the patients admitted for VTE to ourhospital between January 1997 and December 2003.Data were collected from Angiology Unit data baseand cross-matched with those of hospital data base(DRGs codes 451 and 411). All the patients with ahaematologica vol. <strong>89</strong>(suppl. n. 8):september <strong>2004</strong>
162Postersfirst VTE episode were enrolled and prospectively followed-upto estimate mortality, recurrences and longterm sequelae (pulmonary hypertension and postthromboticsyndrome). Results. 1282 patients wereenrolled (729 male / 553 female, mean age 70 years,range 18 – 96) with estimated incidence in the generalpopulation of 1.07 cases/1,000/year. The maincharacteristics of study population are shown in thetable.DVT DVT+PE Isolated Massive Unusual Idiopathic Surg/Orthp.PE PE Site VT VTE VTE(or RVD)558 210 448 97 66 610 358Cancer Intern./CO Recurrent Cr.Pulm. Fatal Total MajorVTE VTE VTE Hypert. PE Deaths Bleedings279 148/30 163 17 29 129 32Conclusions. During the seven years of follow-upwe observed a steadiness in VTE incidence rate, withsignificant reduction both in incidence and in deathrate massive-PE related. Cancer-VTE increased withconsistent effect on late recurrence, mortality andhemorrhagic events.PO-133INCIDENCE OF POSTOPERATIVE PULMONARY EMBOLISMDETECTED BY MULTI-SLICE COMPUTERIZED TOMOGRAPHYIN LUNG SURGERY FOR CANCERMilillo G, Daddi G, lupattelli L, Ragusa M, Lemmi A,Puma F, lomonaco A, Agnelli G for The PulmonaryEmbolism In Thoracic Surgery (PETS) Study GroupDivisions of Internal and CardiovascularMedicine,Thoracic Surgery and Radiology,University of Perugia, ItalyThe incidence of pulmonary embolism (PE) inpatients undergoing lung surgery for cancer remainsundefined. In these patients the risk for ve<strong>no</strong>us thromboembolismis potentially high due to the combinatio<strong>no</strong>f prothrombotic effects of cancer, extensivesurgery, prolonged immobilization and parietal andendothelial local alteration consequent to surgery. Theaim of this study was to assess the incidence of PEafter lung surgery for cancer using multi-slice computerizedtomography (MSCT). Methods: Consecutivepatients undergoing surgery for lung cancer wereincluded in this study. PE was detected by MSCT (GELight-Speed 4×1,25) scan performed 7-15 days aftersurgery. Diag<strong>no</strong>stic criteria for PE were complete orpartial intraluminal filling defect. Patients werescheduled to receive pharmacological prophylaxis forve<strong>no</strong>us thromboembolism with low-molecular-weightheparin (LMWH) starting the first post-operative dayand continued until discharge. Results: Fifty patientswere included in this study. The average age was 66,5(range 26 to 90). Diag<strong>no</strong>sis of cancer was confirmedin all except one patient found to be affected bytuberculosis. Thirty-six patients underwent lobectomy,11 pneumonectomy, and the remaining 3 patientswedge resection. Histology showed epidermoid carci<strong>no</strong>main 20 cases, ade<strong>no</strong>carci<strong>no</strong>ma in 15, anaplasticcarci<strong>no</strong>ma in 7, and other types in the remaining 8cases. All patients but two received prophylaxis forve<strong>no</strong>us thromboembolism. Seven patients (14%)showed PE at MSCT scan. Of the PE, 5 involved centralarteries (principal, lobar and segmentary) and 2subsegmentary arteries. Two of the patients withMSCT scan detected PE were symptomatic. PE is acommon complication in patients undergoing lungsurgery for cancer, despite antithrombotic prophylaxis.In such high-risk population prophylactic regimensshould be optimized.PO-134CARDIOVASCULAR RISK FACTORS AND THE RISK OF VENOUSTHROMBOEMBOLISMTufa<strong>no</strong> A, Varricchione N, Coppola A, Cirillo F,De Simone C, Meola M, Lombardini D,Sidiropulos M, Albisinni R, Cerbone AMRegional Reference Centre for Coagulation Disease,Dep. of Clinical and Experimental Medicine;Federico II University, Naples, ItalyThe association between established cardiovascularrisk factors and the risk of ve<strong>no</strong>us thromboembolism(VTE) is <strong>no</strong>t entirely understood. We havescreened for cigarette smoking, hypertension, hypercholesterolemia,diabetes mellitus, obesity, andhyperhomocysteinemia 397 consecutive patients(172 men and 225 women; 42.69±14.<strong>89</strong> yrs) referredto our Centre because of recently documented ve<strong>no</strong>usthromboembolic events (deep ve<strong>no</strong>us thrombosisand/or pulmonary embolism, and ve<strong>no</strong>us thrombosisin abdominal veins, and cerebral vein thrombosis). Asmany as 407 age- and sex-matched apparentlyhealthy subjects (164 men and 243 women;39.53±13.57 yrs), from the same ethnic backgroung,served as controls. Arterial hypertension was presentin 18.5% of VTE patients and in 12.8% of controls(p=0.026; OR 1.5, 95% CI 1.1-2.3). Hypercholesterolemia(total cholesterol levels >5.2 mmol/L inrepeated evaluations over a 1-yr period) was morecommon in VTE patients than in controls (53.6% vs.39.1%, p=0.001, OR 1.8, 95% CI 1.3-2.5), as was BMI>25 (59.5% vs 40.4%; p