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Maternal serum uric acid concentration and pregnancy outcomes in women with pre‐eclampsia/eclampsia
Author(s) -
Le Tam M.,
Nguyen Long H.,
Phan Nam L.,
Le Duong D.,
Nguyen Huy V.Q.,
Truong Vinh Q.,
Cao Thanh N.
Publication year - 2019
Publication title -
international journal of gynecology and obstetrics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.895
H-Index - 97
eISSN - 1879-3479
pISSN - 0020-7292
DOI - 10.1002/ijgo.12697
Subject(s) - medicine , eclampsia , obstetrics , uric acid , maternal death , prospective cohort study , fetus , pregnancy , population , genetics , environmental health , biology
Abstract Objectives To determine the relationship between maternal serum uric acid levels and fetal/neonatal complications in women with pre‐eclampsia/eclampsia, and to establish a predictive threshold value. Methods A diagnostic test and historical cohort study conducted by prospective cross‐sectional data collection on pregnant women with pre‐eclampsia/eclampsia at Hue University Hospital, Vietnam, between March 2015 and July 2017. Pre‐eclampsia was diagnosed based on ACOG criteria. Serum uric acid levels were measured by enzymatic colorimetric testing using a Cobas c 501 analyzer (Roche Diagnostics, Mannheim, Germany). Fetal complications included intrauterine growth restriction, preterm delivery, fetal death, and neonatal death. Results There were 205 women enrolled. Serum uric acid at a cutoff of 393 μmol/L is a good predictor of fetal/neonatal complications ( AUC 0.752), with 64.4% sensitivity and 79.5% specificity. High uric acid level (≥393 μmol/L) resulted in increased risk of preterm birth ( OR 6.367, 95% CI 3.009–13.084), low Apgar scores ( OR 5.514, 95% CI 1.877–16.198), intrauterine growth restriction ( OR 7.188, 95% CI 3.592–14.382), and neonatal death ( OR 7.818, 95% CI 1.614–37.867). There was no relationship between uric acid level and fetal death ( OR 1.803, 95% CI 0.355–9.168). Conclusions Maternal serum uric acid concentration is a good predictor of fetal/neonatal outcomes in women with pre‐eclampsia/eclampsia.

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