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Intrahepatic cholestasis of pregnancy. Diagnosis. Maternal and fetal complications

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dc.contributor.author Butucel, Ana
dc.date.accessioned 2020-09-23T09:56:41Z
dc.date.available 2020-09-23T09:56:41Z
dc.date.issued 2020
dc.identifier.citation BUTUCEL, Ana. Intrahepatic cholestasis of pregnancy. Diagnosis. Maternal and fetal complications. In: MedEspera: the 8th Internat. Medical Congress for Students and Young Doctors: abstract book. Chișinău: S. n., 2020, p. 175-176. en_US
dc.identifier.uri http://repository.usmf.md/handle/20.500.12710/11750
dc.identifier.uri medespera.asr.md/wp-content/uploads/ABSTRACT-BOOK.pdf
dc.description Department of Obstetrics and Gynecology, Nicolae Testemitanu State University of Medicine and Pharmacy, Chisinau, Republic of Moldova, The 8th International Medical Congress for Students and Young Doctors, September 24-26, 2020 en_US
dc.description.abstract Introduction. Intrahepatic cholestasis of pregnancy (ICP) is a cholestatic disorder characterized by pruritus, elevated serum aminotransferases and bile acid levels with onset in the second or third trimester of pregnancy, and spontaneous relief of signs and symptoms within two to three weeks after delivery. ICP has been observed in almost all ethnic groups, but there is relevant geographical variation in the incidence of ICP varying from less than 1% to 27.6%. It is important to diagnose it in time because of its effects on pregnancy outcome.Aim of the study. This review was undertaken to find the criteria of diagnosis and to evaluate the possible maternal and fetal complications. Materials and methods. To identify relevant articles, NCBI and ScienceDirect databases were searched using the Key words: “intrahepatic cholestasis of pregnancy”, “Idiopathic jaundice of pregnancy”, “Pruritus gravidarum”, “diagnosis of intrahepatic cholestasis of pregnancy”, “outcome on intrahepatic cholestasis of pregnancy”. Results. This study concluded that Pruritus is the primary clinical symptom of ICP. It usually presents in the third trimester, after 30 weeks of gestation, but rare cases developing early. The diagnosis of ICP is based on pruritus of cholestasis, elevated fasting serum bile acids > 10 μmol/L (± and elevated serum transaminases), spontaneous relief of signs and symptoms within two to three weeks after delivery and absence of other diseases that cause pruritus and jaundice. Mild jaundice with serum levels of conjugated bilirubin only moderately elevated occurs in 10 to 15% of cases. ICP presents a greater risk to the fetus than to the mother. ICP increases the rate of preterm delivery with the associated mortality and morbidity, meconium-stained amniotic fluid. In addition, the fetus seems to be at an increased risk for stillbirth. The major concern for the mother is for postpartum hemorrhage if her vitamin K level is low, leading to an increase in prothrombin time. Also women with ICP are more likely to have gestational diabetes, pre-eclampsia, spontaneous and iatrogenic preterm delivery, with increased rates of induction of labour. Conclusions. ICP, especially severe ICP is associated with adverse pregnancy outcome. Pregnant women should be diagnosed in an efficient time for adopting the appropriate management to prevent complications as much as possible. en_US
dc.language.iso en en_US
dc.publisher MedEspera en_US
dc.subject intrahepatic cholestasis of pregnancy en_US
dc.subject idiopathic jaundice of pregnancy en_US
dc.subject pruritus gravidarum en_US
dc.subject diagnosis of intrahepatic cholestasis of pregnancy en_US
dc.subject outcome on intrahepatic cholestasis of pregnancy en_US
dc.title Intrahepatic cholestasis of pregnancy. Diagnosis. Maternal and fetal complications en_US
dc.type Article en_US


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  • MedEspera 2020
    The 8th International Medical Congress for Students and Young Doctors, September 24-26, 2020

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