Venous Thromboembolism and Associated High Plasma Factor VIII Levels:Linked to Cytomegalovirus Infection?

2000 ◽  
Vol 83 (03) ◽  
pp. 510-511 ◽  
Author(s):  
K. Hinney ◽  
J. Gleixner ◽  
F. Keller ◽  
C. M. Schambeck
1977 ◽  
Author(s):  
H. Beeser ◽  
H. Eqli

Because of the well known wide normal range of the factor VIII activity between 60 to 170% I man, selecting of donors with high activity levels would be of advantaae for the preparation of factor VIII concentrates. This is especially true for preparing small-pool fractions, as for technical reasons the final product cannot be controlled for its factor VIII content. In preliminary investigations, we reported on elsewhere, high factor VIII activity in donors estimated before a donation had been rarely reproducible before a second donation after 8-12 weeks. So as a preliminary result of finding a donor’s factor VIII level varying from donation to donation selecting of plasmas with high factor VIII content for concentrate preparation could only be establishedby re-estimating the activity before each donation. Proceeding in this way would be much too troublesome. To get more reliable information whether a healthy subject’s high factor VIII plasma level is distinctly varying or rather constant we assayed the plasma of 200 donors with factor VIII activity > 120% two times more before donation. The results confirmed our preliminary findings, especially the fact that a high plasma factor VIII activity in experienced donors was rarely reproducible when re-estimated before a second and third donation. As a consequence selecting of donors with high factor VIII procoaqulant activity for preparing small-pool factor VIII concentrates is impracticable.


Author(s):  
Luis F. Bittar ◽  
Erich V. De Paula ◽  
Aline Barnabé ◽  
Bruna M. Mazetto ◽  
Kiara C. S. Zapponi ◽  
...  

2000 ◽  
Vol 343 (7) ◽  
pp. 457-462 ◽  
Author(s):  
Paul A. Kyrle ◽  
Erich Minar ◽  
Mirko Hirschl ◽  
Christine Bialonczyk ◽  
Milena Stain ◽  
...  

2004 ◽  
Vol 124 (4) ◽  
pp. 504-510 ◽  
Author(s):  
Legnani Cristina ◽  
Cosmi Benilde ◽  
Cini Michela ◽  
Frascaro Mirella ◽  
Guazzaloca Giuliana ◽  
...  

2020 ◽  
Vol 196 ◽  
pp. 349-354
Author(s):  
Victoria E. Castellón Rubio ◽  
Pedro Pérez- Segura ◽  
Andrés Muñoz ◽  
Antonio López Farré ◽  
Liliana Canosa Ruiz ◽  
...  

2006 ◽  
Vol 21 (4) ◽  
pp. 206-210 ◽  
Author(s):  
M. Dogan ◽  
A. Demirkazik ◽  
N. Konuk ◽  
B. Yalcin ◽  
A. Buyukcelik ◽  
...  

Background Venous thromboembolism (VT) increases mortality and morbidity in cancer patients. The primary aim of this study was to evaluate the effect of VT on the survival of cancer patients and its relationship with serum vascular endothelial growth factor (VEGF) and plasma factor VIII levels. Patients and methods Eighty-two patients with locally advanced or metastatic cancer were included in this study between September 2001 and March 2004, and 31 of them had VT. Fifty-one matched-paired cancer patients without VT were prospectively selected as a control group in the same period. Criteria for the selection of control group patients were having the same malignancy, stage, metastatic site, performance status and age (±5 years) as patients in the VT group. Results Plasma factor VIII and serum D-dimer levels in the VT group were significantly higher than those in the control group (p=0.030 and p=0.016, respectively). However, mean serum VEGF levels were similar in both groups (p=0.199). In the VT group, the median survival of patients who had higher serum VEGF levels (>150 pg/mL) was significantly shorter than that of patients in the same group with lower serum VEGF levels (p=0.005). The median survival of the VT group was 14 months, whereas it was 25 months in the control group (p=0.199). Conclusion There was a worse prognostic trend for cancer patients with VT. Nevertheless, the difference in survival was not statistically significant between the groups. Plasma factor VIII and serum D-dimer levels might have prognostic value in cancer patients with VT. Cancer patients with VT and higher serum VEGF levels had a significantly poorer prognosis.


Author(s):  
Taimur Saleem ◽  
Brandi Burr ◽  
Jerad Robinson ◽  
Kristen Degelman ◽  
Jenna Stokes

Author(s):  
Luis F. Bittar ◽  
Erich V. De Paula ◽  
Aline Barnabé ◽  
Bruna M. Mazetto ◽  
Kiara C. S. Zapponi ◽  
...  

1974 ◽  
Vol 31 (02) ◽  
pp. 328-338
Author(s):  
M. M. P Paulssen ◽  
H. L. M. A Vandenbussche-Scheffers ◽  
P. B Spaan ◽  
T de Jong ◽  
M. C Planje

SummaryFactor VIII occurs in the body in two different forms. In lymph factor VIII is bound to chylomicra. In plasma, factor VIII is bound to a protein.After delipidation of chylomicra we obtained a glycoprotein with a high polysaccharide content and a molecular weight of approx. 160,000.In plasma, factor VIII is attached to a protein which is present in normal concentrations in plasma of patients with haemophilia A and in serum (co-factor VIII).This factor is deficient in both the plasma and the serum of patients with von Willebrand’s disease.The binding between factor VIII and co-factor VIII is reversible.Some properties of these two factors are described.


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