التفاصيل البيبلوغرافية
| العنوان: |
Incidence and risk factors of venous thromboembolism (VTD) in patients with amyloidosis. |
| المؤلفون: |
Srkalovic, Gordan1 gordan.srkalovic@sparrow.org, Cameron, Marte G.2 marteandlans@hotmail.com, Deitcher, Steven R.3 sdeitcher@nuvelo.com, Kattke-Marchant, Kandice4 marchak@ccf.org, Hussein, Mohamad A.5 mahhussein@runbox.us |
| المصدر: |
International Seminars in Surgical Oncology. 2005, Vol. 2, p17-7. 7p. 4 Charts. |
| مصطلحات موضوعية: |
*BLOOD coagulation, *AMYLOIDOSIS, *LYMPHOPROLIFERATIVE disorders, *VENOUS thrombosis, *THROMBOSIS, *DISEASE risk factors, *PATIENTS |
| مستخلص: |
Background: Coagulation problems in amyloidosis are historically associated with bleeding tendencies (mostly Factor X abnormalities). Increased clotting was observed in isolated cases diagnosed with low-grade disseminated intravascular coagulation (DIC). Problem of venous thromboembolic disaease (VTD) in amyloidosis was not systematically investigated. Methods: We evaluated frequency of VTD and risk factors for VTD in 56 consecutive amyloidosis patients with a documented disease evaluated and followed up at our Center from 1991-2001. Data was collected in 5 categories: (a) demographics, (b) disease and treatment, (c) thrombosis case information, (d) major risk factors for thrombosis and (e) baseline laboratory data. Univariable correlates of VTD were assessed using Kaplan-Meier analysis and Cox proportional hazards analysis. Results: Mean age of the patients was 67 (years range 21 - 83). Male/female percentage ratio was 70/30. 29 % of the patients had high creatinine level (> 1.4 mg/dl). Personal or family history of VTD was recorded in 2 and 0 % of patients, respectively. Known hypercoagulable state was present in 1 patient (2%). 8 % of patients were smokers. Of 56 patients, 6 developed VTD (11%). Median time from diagnosis of amyloidosis to VTD was 12.5 month (range 1-107). Treatment was given within a median of 1 month (range 0-4) from the development of thrombosis. Only sites of VTD were lower extremities. No cases were associated with I.V. line. 1 case (17 %) was identified postoperatively. We identified several univariable correlates of VTD in amyloid patients, including greater age at diagnosis (HR-2.99, P = .041), personal history of DVT (HR-47.7, P = .006) and immobility (HR-11.78, P = .006). Presence of circulating serum M-protein had protective role in our analysis (HR-.08, P = .031). There was no correlation with the type of treatment patients were receiving. Conclusion: Risk for thromboembolic diseases in patients with amyloidosis is similar to one previously described for multiple myeloma. Additional studies with higher number of thromboembolic events could help to further elucidate risk factors for VTD in this population of patients. [ABSTRACT FROM AUTHOR] |
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