scholarly journals Tissue factor pathway inhibitor 2 as a serum marker for diagnosing asymptomatic venous thromboembolism in patients with epithelial ovarian cancer and positive D‑dimer results

2021 ◽  
Vol 16 (2) ◽  
Author(s):  
Ryuta Miyake ◽  
Yuki Yamada ◽  
Shoichiro Yamanaka ◽  
Ryuji Kawaguchi ◽  
Norihisa Ootake ◽  
...  
CHEST Journal ◽  
2016 ◽  
Vol 149 (4) ◽  
pp. A287
Author(s):  
Chaosheng Deng ◽  
Xiaoming Cao ◽  
Qi-Chang Lin ◽  
Zhihua Huang ◽  
Haibo Ding ◽  
...  

2013 ◽  
Vol 23 (1) ◽  
pp. 65-72 ◽  
Author(s):  
Xiangxiang Wu ◽  
Xiang Xue ◽  
Jie Tang ◽  
Xi Cheng ◽  
Wenjuan Tian ◽  
...  

ObjectiveVenous thromboembolism (VTE) is a life-threatening complication that often occurs in ovarian tumors. However, the risk factors for VTE are still undetermined.MethodsWe retrospectively analyzed VTE occurrence and its potential risk factors in 254 Chinese patients with ovarian tumor at Fudan University Cancer Hospital from July 2007 to June 2011.ResultsThe VTE incidence was 7.1% (13/183) in epithelial ovarian cancer (EOC), and no VTE was found in ovarian borderline or benign tumor. D-dimer levels were significantly higher in EOC than in ovarian benign and borderline tumors. Furthermore, D-dimer levels increased with the advancement of EOC stages. Correlation analysis suggested that D-dimer levels were well correlated with platelet counting (PLT), prothrombin time (PT), white blood cell counting (WBC), cancer antigen (CA) 125, and CA153. Univariate logistic regression analysis found that D-dimer levels greater than 788 μg/L, PLT levels greater than 261 × 109/L, PT greater than 11.7 seconds, CA125 greater than 760 U/mL, and ascites greater than 1500 mL are risk factors for VTE in EOC. Moreover, multivariate analysis grouped primary EOC, low differentiated grade, D-dimer greater than 788 μg/L, PT greater than 11.7 seconds, and CA125 greater than 760 U/mL as prediction factors for VTE.ConclusionsIn addition to D-dimer and ascites, high levels of PLT, PT, and CA125, which are highly correlated with D-dimer, are independent risk factors for VTE


2011 ◽  
Vol 127 ◽  
pp. S149
Author(s):  
F. Abu Saadeh ◽  
L. Norris ◽  
S. O'Toole ◽  
N. Gleeson

Author(s):  
Matthias Hoke ◽  
Paul A. Kyrle ◽  
Erich Minar ◽  
Christine Bialonzcyk ◽  
Mirko Hirschl ◽  
...  

2013 ◽  
Vol 132 (5) ◽  
pp. 627-634 ◽  
Author(s):  
Feras Abu Saadeh ◽  
Lucy Norris ◽  
Sharon O’Toole ◽  
Bashir M. Mohamed ◽  
Ream Langhe ◽  
...  

2010 ◽  
Vol 104 (08) ◽  
pp. 207-212 ◽  
Author(s):  
Pamela Lutsey ◽  
Aaron Folsom ◽  
Susan Heckbert ◽  
Mary Cushman ◽  
Neil Zakai

SummaryTissue factor pathway inhibitor (TFPI) inhibits tissue factor, a potent coagulation initiator. Limited evidence suggests that low TFPI levels are associated with increased risk of venous thromboembolism (VTE). We measured total TFPI in a nested case-control study in the Longitudinal Investigation of Thromboembolism Etiology. Control subjects were frequency matched 2:1 to cases on age, sex, race, and cohort. Odds ratios (ORs) for VTE by TFPI levels were computed using logistic regression models adjusting for age, race, sex, coagulation factors (factors VII, VIII, IX, XI, D-dimer), and body mass index (BMI). To evaluate for greater than additive interactions, we calculated the percent relative excess risk due to interaction between TFPI and other VTE risk factors. A total of 534 cases of VTE occurred and matched to 1,091 controls. Mean baseline TFPI in ng/ml (standard deviation) in those who developed VTE and controls was 36.4 (12.8) and 35.0 (11.1), respectively. Higher TFPI was associated with male sex, age, BMI, factors VII, VIII, IX, XI, and D-dimer. TFPI level did not differ by ethnicity, factor V Leiden, or pro-thrombin G20210A. Compared with those in the upper 95%, the bottom 5% of TFPI had an age-, sex-, race-, and study-adjusted OR (95% CI) of 1.35 (0.86, 2.12) for VTE. Adjusting for factors VII, VIII, IX, and XI the OR was 1.93 (1.05, 3.53). Further addition of D-dimer and BMI to this model decreased the OR to 1.70 (0.98, 2.93). Low TFPI did not demonstrate greater than additive interaction with other VTE risk factors.


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