Am J Perinatol 2008; 25(6): 341-345
DOI: 10.1055/s-2008-1078756
© Thieme Medical Publishers

Pregnancy Outcomes during an Era of Aggressive Management for Intrahepatic Cholestasis of Pregnancy

Richard H. Lee1 , Kay May Kwok1 , Sue Ingles2 , Melissa L. Wilson2 , Patrick Mullin1 , Marc Incerpi1 , Bhuvan Pathak1 , T. Murphy Goodwin1
  • 1Department of Obstetrics and Gynecology, Los Angeles County-University of Southern California Medical Center, Los Angeles, California
  • 2Department of Preventive Medicine, Los Angeles County-University of Southern California Medical Center, Los Angeles, California
Further Information

Publication History

Publication Date:
28 May 2008 (online)

ABSTRACT

Our objective was to examine whether delivery at 37 weeks of gestation alters adverse pregnancy outcomes in Latina patients with intrahepatic cholestasis of pregnancy (ICP). We conducted a retrospective chart review of Latina patients who delivered at our institution coded with ICP between 2000 and 2007. During this time period it was our practice to offer delivery to patients with ICP at 37 weeks of gestation. Subjects were classified into three groups according to total bile acid (TBA) concentration: < 20 μmol/L (mild ICP), ≥ 20 μmol/L and < 40 μmol/L (moderate ICP), and ≥ 40 μmol/L (severe ICP). Meconium passage was observed in no births in patients with mild IC, but was found in 18% of deliveries with moderate/severe ICP. The risk of meconium passage increased linearly, with a 19.7% increased risk for each 10 μmol/L increase in TBA concentration (p = 0.001). There was no association with higher TBA concentration and other adverse outcomes. There was no difference in adverse outcomes between moderate and severe ICP. We concluded that in our Latina population with ICP, an association existed between meconium passage and moderate/severe ICP. Delivering at 37 weeks was associated with a low risk of adverse outcomes due to ICP among all patients, including those with higher TBA concentrations.

REFERENCES

  • 1 Fisk N M, Storey G N. Fetal outcome in obstetric cholestasis.  Br J Obstet Gynaecol. 1988;  95 1137-1143
  • 2 Rioseco A J, Ivankovic M B, Manzur A et al.. Intrahepatic cholestasis of pregnancy: a retrospective case-control study of perinatal outcome.  Am J Obstet Gynecol. 1994;  170 890-895
  • 3 Glantz A, Marschall H U, Mattsson L A. Intrahepatic cholestasis of pregnancy: Relationships between bile acid levels and fetal complication rates.  Hepatology. 2004;  40 467-474
  • 4 Alsulyman O M, Ouzounian J G, Ames-Castro M, Goodwin T M. Intrahepatic cholestasis of pregnancy: perinatal outcome associated with expectant management.  Am J Obstet Gynecol. 1996;  175 957-960
  • 5 Williamson C, Hems L M, Goulis D G et al.. Clinical outcome in a series of cases of obstetric cholestasis identified via a patient support group.  BJOG. 2004;  111 676-681
  • 6 Kenyon A P, Piercy C N, Girling J, Williamson C, Tribe R M, Shennan A H. Obstetric cholestasis, outcome with active management: a series of 70 cases.  BJOG. 2002;  109 282-288
  • 7 Mullally B A, Hansen W F. Intrahepatic cholestasis of pregnancy: review of the literature.  Obstet Gynecol Surv. 2002;  57 47-52
  • 8 Burrows R F, Clavisi O, Burrows E. Interventions for treating cholestasis in pregnancy.  Cochrane Database Syst Rev. 2001;  CD000493
  • 9 Sentilhes L, Verspyck E, Pia P, Marpeau L. Fetal death in a patient with intrahepatic cholestasis of pregnancy.  Obstet Gynecol. 2006;  107 458-460
  • 10 Londero F, San Marco L. Intrahepatic cholestasis of pregnancy: are we really able to predict fetal outcome?.  Am J Obstet Gynecol. 1997;  177 1274
  • 11 Andersen E, Karlaganis G, Sjovall J. Altered bile acid profiles in duodenal bile and urine in diabetic subjects.  Eur J Clin Invest. 1988;  18 166-172
  • 12 Fiorucci S, Rizzo G, Donini A, Distrutti E, Santucci L. Targeting farnesoid X receptor for liver and metabolic disorders.  Trends Mol Med. 2007;  13 298-309
  • 13 Oyelese Y, Culin A, Ananth C V, Kaminsky L M, Vintzileos A, Smulian J C. Meconium-stained amniotic fluid across gestation and neonatal acid-base status.  Obstet Gynecol. 2006;  108 345-349
  • 14 Campos G A, Guerra F A, Israel E J. Effects of cholic acid infusion in fetal lambs.  Acta Obstet Gynecol Scand. 1986;  65 23-26
  • 15 Rodrigues C M, Marin J J, Brites D. Bile acid patterns in meconium are influenced by cholestasis of pregnancy and not altered by ursodeoxycholic acid treatment.  Gut. 1999;  45 446-452

Richard H LeeM.D. 

Women's and Children's Hospital, 1240 N. Mission Road

Room 5K-40, Los Angeles, CA 90033; reprints not available from the author

    >