Contraceptive vaginal ring-induced cholestasis in a patient with a history of intrahepatic cholestasis of pregnancy.


Journal

Clinics and research in hepatology and gastroenterology
ISSN: 2210-741X
Titre abrégé: Clin Res Hepatol Gastroenterol
Pays: France
ID NLM: 101553659

Informations de publication

Date de publication:
Jul 2021
Historique:
received: 22 05 2020
accepted: 01 06 2020
pubmed: 12 7 2020
medline: 11 1 2022
entrez: 12 7 2020
Statut: ppublish

Résumé

Intrahepatic cholestasis of pregnancy (ICP) is a heterogeneous group of liver disorders with a high recurrence rate. Patients with a history of ICP are at risk of developing contraceptive-induced cholestasis, especially if they harbour a biliary transporter mutation. We report the first case of drug-induced cholestasis associated with a contraceptive vaginal ring (CVR) in a patient with a prior history of ICP. Our patient was a women with a history of multiple pregnancies and spontaneous abortions and early and severe ICP. Two to four weeks after initiation of CVR, she developed signs and symptoms of cholestasis, which resolved after discontinuation of the CVR. A thorough investigation to exclude other plausible causes of cholestasis was performed, including a liver biopsy. Genetic testing revealed pathogenic mutations in both the ABCB11 and ABCB4 genes. Although a history of ICP used to be an absolute contraindication for oral contraceptive pills (OCP), recent studies suggest a lower risk of cholestasis associated with low-dose oestrogen pills (20-35 mcg compared to the original 50 mcg). No previous case report could confirm the theoretical risk associated with the use of a CVR, which delivers a very low estrogen dose (15 mcg). The two biliary transporter mutations identified in our case could potentially explain the patient's susceptibility to the cholestatic effect of oestrogen. This case illustrates that CVR can trigger drug-induced cholestasis in a susceptible patient. While such cases should not discourage the trial of low-dose hormonal contraception in women with prior ICP, an appropriate follow-up is necessary to ensure early detection and treatment of drug-induced cholestasis.

Identifiants

pubmed: 32651076
pii: S2210-7401(20)30170-4
doi: 10.1016/j.clinre.2020.06.002
pii:
doi:

Substances chimiques

ATP Binding Cassette Transporter, Subfamily B 0
Contraceptive Agents 0
Estrogens 0
Pharmaceutical Preparations 0

Types de publication

Case Reports

Langues

eng

Sous-ensembles de citation

IM

Pagination

101475

Informations de copyright

Copyright © 2020 Elsevier Masson SAS. All rights reserved.

Auteurs

Florence Perrault (F)

Department of Pathology, University of Sherbrooke, Centre hospitalier Universitaire de Sherbrooke (CHUS), Quebec, Canada. Electronic address: florence.perrault@usherbrooke.ca.

Philippe Echelard (P)

Department of Pathology, University of Sherbrooke, Centre hospitalier Universitaire de Sherbrooke (CHUS), Quebec, Canada.

Daniel Viens (D)

Department of Internal Medecine, Hôpital Sainte-Croix, Quebec, Canada.

Martin Borduas (M)

Department of Pathology, University of Sherbrooke, Centre hospitalier Universitaire de Sherbrooke (CHUS), Quebec, Canada.

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Classifications MeSH