4.5 Article

Potential Value of Coagulation Parameters for Suggesting Preeclampsia During the Third Trimester of Pregnancy

期刊

AMERICAN JOURNAL OF THE MEDICAL SCIENCES
卷 354, 期 1, 页码 39-43

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ELSEVIER SCIENCE INC
DOI: 10.1016/j.amjms.2017.03.012

关键词

Coagulation; Fibrinogen; Preeclampsia; Severe preeclampsia; Third trimester of pregnancy

资金

  1. Beijing Friendship Hospital of Capital Medical University, China

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ackground: Preeclampsia is a relatively common complication of pregnancy and considered to be associated with different degrees of coagulation dysfunction. This study was developed to evaluate the potential value of coagulation parameters for suggesting preeclampsia during the third trimester of pregnancy. Materials and Methods: Data from 188 healthy pregnant women, 125 patients with preeclampsia in the third trimester and 120 age-matched nonpregnant women were analyzed. Prothrombin time, prothrombin activity, activated partial thromboplastin time, fibrinogen (Fg), antithrombin, platelet count, mean platelet volume, platelet distribution width and plateletcrit were tested. Resuls: All parameters, excluding prothrombin time, platelet distribution width and plateletcrit, differed significantly between healthy pregnant women and those with preeclampsia. Platelet count, antithrombin and Fg were significantly lower and mean platelet volume and prothrombin activity were significantly higher in patients with preeclampsia (P < 0.001). Among these parameters, the largest area under the receiver operating characteristic curve for preeclampsia was 0.872 for Fg with an optimal cutoff value of <= 2.87 g/L (sensitivity = 0.68 and specificity = 0.98). For severe preeclampsia, the area under the curve for Fg reached up to 0.922 with the same optimal cutoff value (sensitivity = 0.84, specificity = 0.98, positive predictive value = 0.96 and negative predictive value = 0.93). Conclusions: Fg is a biomarker suggestive of preeclampsia in the third trimester of pregnancy, and our data provide a potential cutoff value of Fg <= 2.87 g/L for screening preeclampsia, especially severe preeclampsia.

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