TY - JOUR
T1 - Intrahepatic cholestasis of pregnancy
AU - Roediger, Rebecca
AU - Fleckenstein, Jaquelyn
N1 - Publisher Copyright:
© 2024 American Association for the Study of Liver Diseases.
PY - 2024/2
Y1 - 2024/2
N2 - ICP presents as pruritus typically in the third trimester and is associated with adverse fetal outcomes such as preterm labor, meconium-stained amniotic fluid, and stillbirth.[7] The risk of these adverse fetal outcomes is correlated with peak bile acid levels.[6] The risk of preterm labor and meconium-stained amniotic fluid is associated with peak BA > 40, and the risk of stillbirth is associated with peak BA > 100.[4] UDCA is beneficial for the treatment of pruritus, and data suggests it lowers the risk of spontaneous preterm birth and meconium-stained amniotic fluid.[4] To reduce the risk of stillbirth, guidelines have recommended early delivery for women with ICP.[1] Many of the reported adverse perinatal outcomes associated with ICP are actually complications of preterm birth, such as low birth weight and NICU utilization.[1] Newer guidelines recommend stratifying early delivery based on peak bile acid level to balance the risks of iatrogenic preterm birth with risks of adverse fetal effects from ICP (Figure 1).
AB - ICP presents as pruritus typically in the third trimester and is associated with adverse fetal outcomes such as preterm labor, meconium-stained amniotic fluid, and stillbirth.[7] The risk of these adverse fetal outcomes is correlated with peak bile acid levels.[6] The risk of preterm labor and meconium-stained amniotic fluid is associated with peak BA > 40, and the risk of stillbirth is associated with peak BA > 100.[4] UDCA is beneficial for the treatment of pruritus, and data suggests it lowers the risk of spontaneous preterm birth and meconium-stained amniotic fluid.[4] To reduce the risk of stillbirth, guidelines have recommended early delivery for women with ICP.[1] Many of the reported adverse perinatal outcomes associated with ICP are actually complications of preterm birth, such as low birth weight and NICU utilization.[1] Newer guidelines recommend stratifying early delivery based on peak bile acid level to balance the risks of iatrogenic preterm birth with risks of adverse fetal effects from ICP (Figure 1).
UR - https://www.scopus.com/pages/publications/85199004433
U2 - 10.1097/CLD.0000000000000119
DO - 10.1097/CLD.0000000000000119
M3 - Review article
C2 - 38379768
AN - SCOPUS:85199004433
SN - 2046-2484
VL - 23
JO - Clinical Liver Disease
JF - Clinical Liver Disease
IS - 1
M1 - e0119
ER -