Initiating intramuscular depot medroxyprogesterone acetate 24–48 hours after mifepristone administration does not affect success of early medical abortion

Author:

Lang Christina,Chen Zhong Eric,Johnstone Anne,Cameron Sharon

Abstract

ObjectivesThe primary objective of this study was to determine whether intramuscular depot medroxyprogesterone acetate (IM DMPA) given at the time of misoprostol administration, 24–48 hours after mifepristone, affects the rate of continuing pregnancy. In addition, the study explored factors predictive of continuing pregnancy.DesignCase-control study based on database review of women who underwent early medical abortion (EMA) over a 4-year period.SettingSingle abortion service in Scotland.Participants5122 women who underwent an EMA within the timeframe of this study.Main outcome measuresContinuing pregnancies among women receiving IM DMPA were compared with those choosing other hormonal methods of contraception, non-hormonal contraception or no contraception at the time of misoprostol administration. Logistic regression was performed to assess the effects of demographic characteristics, gestation at presentation and method of contraception provided, on outcome of pregnancy.ResultsA total of 4838 women with complete data were included, of which there were 20 continuing pregnancies (0.4%); 284 women were excluded due to missing data. There was no increased risk of a continuing pregnancy among women who initiated IM DMPA at the time of misoprostol administration (24–48 hours after mifepristone) compared with women who initiated no hormonal contraception at this time (RR 0.48; 95% CI 0.06 to 3.81). Gestation ≥8 weeks and previous terminations were factors associated with increased likelihood of continuing pregnancy.ConclusionsWomen choosing IM DMPA after EMA can be reassured that IM DMPA can be safely initiated at the time of misoprostol administration 24–48 hours after mifepristone without an increase in the risk of a continuing pregnancy. Both increasing gestation and previous termination were factors associated with an increased likelihood of continuing pregnancy following an EMA.

Publisher

BMJ

Subject

Obstetrics and Gynaecology,Reproductive Medicine

Reference19 articles.

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3. World Health Organisation. Safe abortion: technical and policy guidance for health care systems. 2nd edn. Geneva: WHO, 2012.

4. Faculty of Sexual & Reproductive Healthcare. Contraception after pregnancy. https://www.fsrh.org/standards-and-guidance/documents/contraception-after-pregnancy-guideline-january-2017/ (accessed 23 Jan 2018).

5. Royal College of Obstetricians and Gynaecologists. The care of women requesting induced abortion. Evidence-based Clinical Guideline No. 7. 2011 https://www.rcog.org.uk/globalassets/documents/guidelines/abortion-guideline_web_1.pdf (accessed 23 Jan 2018).

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1. Systemic hormonal contraception initiation after abortion: A systematic review and meta-analysis;Contraception;2021-05

2. Contraception After an Induced Abortion and Childbirth;Trends in Andrology and Sexual Medicine;2021

3. Contraception after pregnancy;Acta Obstetricia et Gynecologica Scandinavica;2019-05-13

4. Contraception after medication abortion should be determined by convenience and choice;BMJ Sexual & Reproductive Health;2018-10

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