Detection of additional abnormalities or co-morbidities in women with suspected intrahepatic cholestasis of pregnancy.

Cholestasis pregnancy

Journal

Obstetric medicine
ISSN: 1753-495X
Titre abrégé: Obstet Med
Pays: England
ID NLM: 101464191

Informations de publication

Date de publication:
Dec 2020
Historique:
received: 25 06 2019
accepted: 19 07 2019
entrez: 21 12 2020
pubmed: 22 12 2020
medline: 22 12 2020
Statut: ppublish

Résumé

Current guidelines recommend viral, autoimmune, coagulation and liver ultrasound testing in intrahepatic cholestasis of pregnancy to exclude alternative diagnoses. Electronic health records were searched for investigations and diagnoses in women with raised bile acid concentrations (>10 µmol/L) between January 2016 and December 2017 at two UK maternity units. Five hundred and thirty-one women had a raised bile acid concentration (median (IQR): 18 (13-32 µmol/L)) at a median gestation of 35.1 (IQR 31.8-37.0) weeks. Out of 531 women, 250 (47.1%) had full virology, autoimmune and ultrasound tests, and 348 (65.5%) had coagulation performed. Positive hepatitis B and C results were previously known. No new Epstein-Barr virus, cytomegalovirus or hepatitis A diagnoses were made. There were 11 positive autoimmune results, but no new diagnoses. No woman had an unexplained prolonged prothrombin time. No ultrasound liver ( Intrahepatic cholestasis of pregnancy investigations provided no new diagnoses that influenced clinical management during pregnancy.

Sections du résumé

BACKGROUND BACKGROUND
Current guidelines recommend viral, autoimmune, coagulation and liver ultrasound testing in intrahepatic cholestasis of pregnancy to exclude alternative diagnoses.
METHODS METHODS
Electronic health records were searched for investigations and diagnoses in women with raised bile acid concentrations (>10 µmol/L) between January 2016 and December 2017 at two UK maternity units.
RESULTS RESULTS
Five hundred and thirty-one women had a raised bile acid concentration (median (IQR): 18 (13-32 µmol/L)) at a median gestation of 35.1 (IQR 31.8-37.0) weeks. Out of 531 women, 250 (47.1%) had full virology, autoimmune and ultrasound tests, and 348 (65.5%) had coagulation performed. Positive hepatitis B and C results were previously known. No new Epstein-Barr virus, cytomegalovirus or hepatitis A diagnoses were made. There were 11 positive autoimmune results, but no new diagnoses. No woman had an unexplained prolonged prothrombin time. No ultrasound liver (
CONCLUSION CONCLUSIONS
Intrahepatic cholestasis of pregnancy investigations provided no new diagnoses that influenced clinical management during pregnancy.

Identifiants

pubmed: 33343695
doi: 10.1177/1753495X19868873
pii: 10.1177_1753495X19868873
pmc: PMC7726172
doi:

Types de publication

Journal Article

Langues

eng

Pagination

185-191

Subventions

Organisme : Department of Health
ID : 12/164/16
Pays : United Kingdom
Organisme : Department of Health
ID : RP-2014-05-019
Pays : United Kingdom

Informations de copyright

© The Author(s) 2019.

Déclaration de conflit d'intérêts

Declaration of conflicting interests: The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

Références

Am J Med. 2013 Apr;126(4):342-8
pubmed: 23395534
Ethn Health. 1999 Feb-May;4(1-2):35-7
pubmed: 10887460
Clin Res Hepatol Gastroenterol. 2016 Apr;40(2):141-53
pubmed: 26823041
Gut. 1971 Feb;12(2):145-52
pubmed: 5548561
Hepatology. 1997 Aug;26(2):358-64
pubmed: 9252146
Sci Rep. 2017 Sep 18;7(1):11823
pubmed: 28924228
Obstet Med. 2010 Mar;3(1):25-9
pubmed: 27582836
Expert Rev Gastroenterol Hepatol. 2015;9(10):1273-9
pubmed: 26313609
Obstet Gynecol. 1999 Aug;94(2):189-93
pubmed: 10432125
BJOG. 2002 Mar;109(3):282-8
pubmed: 11950183
Clin Dermatol. 2016 May-Jun;34(3):327-34
pubmed: 27265070

Auteurs

Frances Conti-Ramsden (F)

Department of Women and Children's Health, School of Life Course Sciences, King's College London, London, UK.

Michael McEwan (M)

West Middlesex University Hospital, Chelsea and Westminster Hospital NHS Foundation Trust, London, UK.

Rachel Hill (R)

Department of Women and Children's Health, School of Life Course Sciences, King's College London, London, UK.

Julie Wade (J)

Department of Women and Children's Health, School of Life Course Sciences, King's College London, London, UK.

Georgina Abraham (G)

Department of Women and Children's Health, School of Life Course Sciences, King's College London, London, UK.

Olivia Buckeldee (O)

West Middlesex University Hospital, Chelsea and Westminster Hospital NHS Foundation Trust, London, UK.

Catherine Williamson (C)

Department of Women and Children's Health, School of Life Course Sciences, King's College London, London, UK.

Caroline L Knight (CL)

Department of Women and Children's Health, School of Life Course Sciences, King's College London, London, UK.

Joanna Girling (J)

West Middlesex University Hospital, Chelsea and Westminster Hospital NHS Foundation Trust, London, UK.

Lucy C Chappell (LC)

Department of Women and Children's Health, School of Life Course Sciences, King's College London, London, UK.

Classifications MeSH