Does ulipristal acetate emergency contraception (ella®) interfere with implantation?


Journal

Contraception
ISSN: 1879-0518
Titre abrégé: Contraception
Pays: United States
ID NLM: 0234361

Informations de publication

Date de publication:
11 2019
Historique:
received: 14 03 2019
revised: 15 07 2019
accepted: 18 07 2019
pubmed: 28 7 2019
medline: 2 10 2020
entrez: 28 7 2019
Statut: ppublish

Résumé

Ulipristal acetate (UPA) 30 mg (ella®, HRA-Pharma, Paris, France) acts as an emergency contraceptive (EC) by delaying ovulation. Because it is a selective progesterone receptor modulator, an additional effect on interfering with implantation has been suggested. This review discusses the evidence for, and against, an anti-implantation effect of UPA-EC. Primary research on the effect of UPA, at a relevant dose, on endometrium, implantation, efficacy and pregnancy outcome. UPA-EC does not appear to have a direct effect on the embryo. Changes in endometrial histology are small and not consistent, varying among studies. While UPA-EC affects the profile of gene expression in human endometrium, the findings vary between studies, and it is not clear that these changes affect endometrial receptivity or prevent implantation. UPA at pharmacological concentrations does not appear to have any inhibitory effect on embryo attachment in in vitro systems of human endometrium. UPA-EC is not more effective at preventing pregnancy than chance alone if used after ovulation and does not increase miscarriage rates. An anti-implantation effect of UPA is highly unlikely at the dose used for EC. Maintaining the warning on the FDA-approved label that "it may also work by preventing implantation to the uterus" might deter some women from using EC, leaving them no option to prevent unwanted pregnancy after unprotected sexual intercourse.

Sections du résumé

BACKGROUND
Ulipristal acetate (UPA) 30 mg (ella®, HRA-Pharma, Paris, France) acts as an emergency contraceptive (EC) by delaying ovulation. Because it is a selective progesterone receptor modulator, an additional effect on interfering with implantation has been suggested.
OBJECTIVE
This review discusses the evidence for, and against, an anti-implantation effect of UPA-EC.
SOURCES OF EVIDENCE
Primary research on the effect of UPA, at a relevant dose, on endometrium, implantation, efficacy and pregnancy outcome.
RESULTS
UPA-EC does not appear to have a direct effect on the embryo. Changes in endometrial histology are small and not consistent, varying among studies. While UPA-EC affects the profile of gene expression in human endometrium, the findings vary between studies, and it is not clear that these changes affect endometrial receptivity or prevent implantation. UPA at pharmacological concentrations does not appear to have any inhibitory effect on embryo attachment in in vitro systems of human endometrium. UPA-EC is not more effective at preventing pregnancy than chance alone if used after ovulation and does not increase miscarriage rates.
CONCLUSIONS
An anti-implantation effect of UPA is highly unlikely at the dose used for EC. Maintaining the warning on the FDA-approved label that "it may also work by preventing implantation to the uterus" might deter some women from using EC, leaving them no option to prevent unwanted pregnancy after unprotected sexual intercourse.

Identifiants

pubmed: 31351035
pii: S0010-7824(19)30368-3
doi: 10.1016/j.contraception.2019.07.140
pii:
doi:

Substances chimiques

Contraceptives, Postcoital 0
Norpregnadienes 0
ulipristal acetate YF7V70N02B

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

386-390

Informations de copyright

Copyright © 2019 Elsevier Inc. All rights reserved.

Auteurs

Hang Wun Raymond Li (HWR)

Department of Obstetrics and Gynaecology, The University of Hong Kong, Queen Mary Hospital, Hong Kong. Electronic address: raymondli@hku.hk.

Michele Resche-Rigon (M)

HRA Pharma, Châtillon, France.

Indrani C Bagchi (IC)

Department of Comparative Biosciences, University of Illinois, USA.

Kristina Gemzell-Danielsson (K)

Department of Women's and Children's Health, Division of Obstetrics and Gynaecology, Karolinska Institutet, and Karolinska University Hospital, 171 76 Stockholm, Sweden.

Anna Glasier (A)

Simpson Centre for Reproductive Health, The University of Edinburgh, Edinburgh, United Kingdom.

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Classifications MeSH