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Gradual dosing of ursodeoxycholic acid in mothers with intrahepatic cholestasis of pregnancy may improve composite neonatal outcome.
Hamud, Amir; Cohen, Matan J; Hochner-Celnikier, Drorith; Bar-Oz, Benjamin; Ackerman, Zvi.
Afiliação
  • Hamud A; Department of Medicine, Hadassah-Hebrew University Medical Center and the Hebrew University-Hadassah Medical School, Jerusalem, Israel.
  • Cohen MJ; Clalit Health Services, Jerusalem District, affiliated to the Hebrew University-Hadassah Medical School, Jerusalem, Israel.
  • Hochner-Celnikier D; Department of Obstetrics and Gynecology, Hadassah-Hebrew University Medical Center and the Hebrew University-Hadassah Medical School, Jerusalem, Israel.
  • Bar-Oz B; Department of Neonatology, Hadassah-Hebrew University Medical Center and the Hebrew University-Hadassah Medical School, Jerusalem, Israel.
  • Ackerman Z; Department of Medicine, Hadassah-Hebrew University Medical Center and the Hebrew University-Hadassah Medical School, Jerusalem, Israel. Electronic address: zackerman@hadassah.org.il.
Ann Hepatol ; 29(3): 101490, 2024.
Article em En | MEDLINE | ID: mdl-38403070
ABSTRACT
INTRODUCTION AND

OBJECTIVES:

Intrahepatic cholestasis of pregnancy (ICP) is often accompanied by fetal and maternal complications. MATERIALS AND

METHODS:

Retrospective review of the clinical course of women with ICP and their neonates treated at our medical center over a 10-year period. Special attention was paid to the maternal and neonatal response to 2 different modes of ursodeoxycholic acid (UDCA) administration.

RESULTS:

Neonates of mothers with high total bile acid levels had a poorer composite neonatal outcome. Twenty-seven women who presented at an advanced stage of their pregnancies did not receive UDCA. UDCA was administered in 2 modes either a full dose at admission (76 women) or a gradually increasing dose until the desired dosage was reached (25 women). The mean gestational age at delivery for the 94 neonates that were exposed to full UDCA dose was the lowest (36±2.3 weeks for the full dose, 37±1.4 weeks for the 30 neonates from the gradually increasing dose, 38±1.6 weeks for the 29 neonates from the no treatment group, p<0.001). The group of neonates that were exposed to full UDCA dose had the highest rate of unfavorable composite neonatal outcome (53% for full dose, 30% for gradually increasing dose, 24% for the no treatment group, p=0.006).

CONCLUSIONS:

Compared to the administration of a full UDCA dose, the administration of a gradually increasing dose of UDCA may be associated with a greater gestational age at delivery and fewer events of unfavorable composite neonatal outcomes. These novel findings should be retested prospectively in a large cohort of patients.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Complicações na Gravidez / Ácido Ursodesoxicólico / Colagogos e Coleréticos / Colestase Intra-Hepática / Idade Gestacional Limite: Adult / Female / Humans / Newborn / Pregnancy Idioma: En Revista: Ann Hepatol Assunto da revista: GASTROENTEROLOGIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Israel

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Complicações na Gravidez / Ácido Ursodesoxicólico / Colagogos e Coleréticos / Colestase Intra-Hepática / Idade Gestacional Limite: Adult / Female / Humans / Newborn / Pregnancy Idioma: En Revista: Ann Hepatol Assunto da revista: GASTROENTEROLOGIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Israel