Liver disease in pregnancy

被引:190
作者
Hay, J. Eileen [1 ]
机构
[1] Mayo Clin, Div Gastroenterol & Hepatol, Rochester, MN 55905 USA
关键词
D O I
10.1002/hep.22130
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Abnormal liver tests occur in 3%-5% of pregnancies, with many potential causes, including coincidental liver disease (most commonly viral hepatitis or gallstones) and underlying chronic liver disease. However, most liver dysfunction in pregnancy is pregnancy-related and caused by I of the 5 liver diseases unique to the pregnant state: these fall into 2 main categories depending on their association with or without preeclampsia. The preeclampsia-associated liver diseases are preeclampsia itself, the hemolysis (H), elevated liver tests (EL), and low platelet count (LP) (HELLP) syndrome, and acute fatty liver of pregnancy. Hyperemesis gravidarum and intrahepatic cholestasis of pregnancy have no relationship to preeclampsia. Although still enigmatic, there have been recent interesting advances in understanding of these unique pregnancy-related liver diseases. Hyperemesis gravidarum is intractable, dehydrating vomiting in the first trimester of pregnancy; 50% of patients with this condition have liver dysfunction. Intrahepatic cholestasis of pregnancy is pruritus and elevated bile acids in the second half of pregnancy, accompanied by high levels of aminotransferases and mild jaundice. Maternal management is symptomatic with ursodeoxycholic acid; for the fetus, however, this is a high-risk pregnancy requiring dose fetal monitoring and early delivery. Severe preeclampsia itself is the commonest cause of hepatic tenderness and liver dysfunction in pregnancy, and 2%-12% of cases are further complicated by hemolysis (H), elevated liver tests (EL), and low platelet count (LP) - the HELLP syndrome. Immediate delivery is the only definitive therapy, but many maternal complications can occur, including abruptio placentae, renal failure, subcapsular hematomas, and hepatic rupture. Acute fatty liver of pregnancy is a sudden catastrophic illness occurring almost exclusively in the third trimester; microvesicular fatty infiltration of hepatocytes causes acute liver failure with coagulopathy and encephalopathy. Early diagnosis and immediate delivery are essential for maternal and fetal survival.
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收藏
页码:1067 / 1076
页数:10
相关论文
共 37 条
[1]
Pregnancy after liver transplantation [J].
Armenti, Vincent T. .
LIVER TRANSPLANTATION, 2006, 12 (07) :1037-1039
[2]
Diagnosis and management of hemolysis, elevated liver enzymes, and low platelets syndrome [J].
Barton, JR ;
Sibai, BM .
CLINICS IN PERINATOLOGY, 2004, 31 (04) :807-+
[3]
HELLP syndrome: The state of the art [J].
Baxter, JSK ;
Weinstein, L .
OBSTETRICAL & GYNECOLOGICAL SURVEY, 2004, 59 (12) :838-845
[4]
Bellig Linda L, 2004, Adv Neonatal Care, V4, P26, DOI 10.1016/j.adnc.2003.12.001
[5]
Randomized prospective comparative study of ursodeoxycholic acid and S-adenosyl-L-methionine in the treatment of intrahepatic cholestasis of pregnancy [J].
Binder, Tomas ;
Salaj, Peter ;
Zima, Tomas ;
Vitek, Libor .
JOURNAL OF PERINATAL MEDICINE, 2006, 34 (05) :383-391
[6]
Fetal fatty acid oxidation defects and maternal liver disease in pregnancy [J].
Browning, MF ;
Levy, HL ;
Wilkins-Haug, LE ;
Larson, C ;
Shih, VE .
OBSTETRICS AND GYNECOLOGY, 2006, 107 (01) :115-120
[7]
Autoimmune hepatitis and pregnancy: A rheumatologist's dilemma [J].
Candia, L ;
Marquez, J ;
Espinoza, LR .
SEMINARS IN ARTHRITIS AND RHEUMATISM, 2005, 35 (01) :49-56
[8]
Prospective study of liver dysfunction in pregnancy in Southwest Wales [J].
Ch'ng, CL ;
Morgan, M ;
Hainsworth, I ;
Kingham, JGC .
GUT, 2002, 51 (06) :876-880
[9]
Glutathione S-transferase and liver function in intrahepatic cholestasis of pregnancy and pruritus gravidarum [J].
Dann, AT ;
Kenyon, AP ;
Seed, PT ;
Poston, L ;
Shennan, AH ;
Tribe, RM .
HEPATOLOGY, 2004, 40 (06) :1406-1414
[10]
Heterozygous MDR3 missense mutation associated with intrahepatic cholestasis of pregnancy:: evidence for a defect in protein trafficking [J].
Dixon, PH ;
Weerasekera, N ;
Linton, KJ ;
Donaldson, O ;
Chambers, J ;
Egginton, E ;
Weaver, J ;
Nelson-Piercy, C ;
de Swiet, M ;
Warnes, G ;
Elias, E ;
Higgins, CF ;
Johnston, DG ;
McCarthy, MI ;
Williamson, C .
HUMAN MOLECULAR GENETICS, 2000, 9 (08) :1209-1217