Abstract

BackgroundWe aimed to describe the characteristics and outcomes in pregnant women with liver cirrhosis, and identify the predictors of adverse events of mother and fetus.MethodsRetrospectively collected mothers with liver cirrhosis in our center from 6/2010 to 6/2019. Women without liver cirrhosis were selected as a control in a 1:2 ratio. The primary assessment was the frequency of maternal and fetal adverse events. The secondary assessment was the adverse events in patients continuing pregnancy or not and the factors to predict the severe adverse events.ResultsOf 126 pregnancies enrolled, 29 pregnancies were terminated for worrying disease progression and 97 pregnancies continued. One hundred ninety-four pregnancies without liver cirrhosis were selected as control. At baseline, patients with liver cirrhosis have a lower level of platelet, hemoglobin, prothrombin activity, and a higher level of ALT, total Bilirubin, creatinine. Compared to control, patients with liver cirrhosis had a higher frequency of adverse events, including bleeding gums (7.2%vs. 1.0%), TBA elevation (18.6%vs.3.1%), infection (10.3%vs.0.5%), cesarean section (73.6%vs.49.5%), postpartum hemorrhage (13.8% vs 2.1%), blood transfusion (28.9% vs 2.1%), new ascites or aggravating ascites (6.2% vs.0%), MODS (7.2% vs.0.5%) and intensive care unit admissions (24.1% vs 1.1%). The incidence of severe maternal adverse events was also higher (32.0% vs 1.5%). Women who chose to terminated the pregnancy had less severe adverse events (3.4% vs.32.0%).A higher frequency of fetal/infants’ complications was observed in liver cirrhosis population than control, including newborn asphyxia (10.2% vs1.1%), low birth weight infant (13.6% vs. 2.6%). In patients who progressed into the third trimester, multivariable regression analysis demonstrated that severe adverse events were associated with a higher CTP score (OR 2.128, 95% CI [1.002, 4.521], p = 0.049). Wilson’s disease related liver cirrhosis has a better prognosis (OR = 0.009, 95% CI [0, 0.763], p = 0.038).ConclusionsThe incidence of the adverse events was significantly increased in pregnancies complicated by cirrhosis. The predictor of severe adverse events is higher CTP score. Wilson’s disease induced liver cirrhosis have a better prognosis. Timely termination of pregnancy during the first trimester may avoid the incidence of severe adverse events.

Highlights

  • We aimed to describe the characteristics and outcomes in pregnant women with liver cirrhosis, and identify the predictors of adverse events of mother and fetus

  • 1582 pregnancies were excluded for not progressing into liver cirrhosis (Fig. 1) and 126 pregnancies were diagnosed with liver cirrhosis before or during pregnancy

  • ALT Alanine aminotransferase; TBA Total bile acid; MODS Multiple organ dysfunction; ICU Intensive care unit. #continuous correction; ** Fisher’s test hypertension (8.2 vs.2.7, p = 0.065), gestational diabetes mellitus (20.7%vs. 14.4%, P = 0.187), placenta previa (4.6% vs. 1.1%, p = 0.155), poor wound healing (3.4% vs. 0.5%, p = 0.181) and less oligohydramnios (1.1% vs.6.4%, p = 0.057) seemed to be occurred in group A than group C, no statistical significance was found

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Summary

Introduction

We aimed to describe the characteristics and outcomes in pregnant women with liver cirrhosis, and identify the predictors of adverse events of mother and fetus. Pregnant women with advanced cirrhosis are associated with an increased risk of complications such as new-onset or deteriorated ascites for blood volume changes, bleeding from esophageal varices, liver failure, and hepatorenal syndrome [5, 6]. Besides the deteriorate complication of liver cirrhosis, adverse events of mothers and fetuses, such as spontaneous abortion, stillbirth, fetal or neonatal demise, placental abruption, preeclampsia, preterm delivery, small-for-gestational-age neonate, and postpartum hemorrhage are at an increased risk in women with cirrhosis [7]. Limited data exists regarding the negative maternal and fetal outcomes in mothers with liver cirrhosis. We evaluate the predictors and potential measures to improve the outcomes of the mother and fetus by comparing cirrhosis mothers with and those without adverse events

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