Cholestasis of pregnancy
Revision as of 19:56, 21 August 2019 by ClaireLewis (talk | contribs)
Background
- Caused by combination of hormonal, genetic, and environmental factors --> impaired bile flow --> deposition of bile salts in skin and placenta
- May predispose mothers to vitamin K deficiency and increase risk of preterm delivery, IUFD, and neonatal respiratory distress syndrome[1]
Clinical Features
- Typically develops in late second and/or 3rd trimester
- Rapidly resolves after delivery
- Pruritus, starts and predominates on palms and soles
- RUQ pain
- Nausea
- Jaundice
Differential Diagnosis
- Liver disease in pregnancy:
- Acute fatty liver of pregnancy
- HELLP (hemolysis, elevated liver enzymes, and low platelets) syndrome
- Hyperemesis gravidarum
- Pregnancy-specific pruritus (see also: Rashes of pregnancy)
- Pruritus gravidarum
- Atopic eruption of pregnancy
- Polymorphic eruption of pregnancy
- Pemphigoid gestationis
- Prurigo of pregnancy
- Pruritic folliculitis of pregnancy
Evaluation
- CBC (rule out thrombocytopenia)
- LFTs
- Elevated total bile acid concentration
- Aminotransferases usually <2x upper limit of normal
- Alk phos and bili may be elevated
- GGT normal or modestly elevated
- RUQ US normal, no biliary duct dilation
Management
- Ursodeoxycholic acid (ursodiol) 300mg TID until delivery
- OBGYN follow-up
Disposition
- Discharge with OBGYN follow-up
See Also
External Links
References
https://www.uptodate.com/contents/intrahepatic-cholestasis-of-pregnancy
