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Termination of pregnancy in the second trimester – the course of different therapy regimens

  • Jana Franzis Franke EMAIL logo , Kathrin Oelmeier , Mareike Möllers , Ute Möllmann , Janina Braun , Laura Kerschke , Helen Ann Köster , Walter Klockenbusch , Ralf Schmitz and Kerstin Hammer
Published/Copyright: May 10, 2022

Abstract

Objectives

To compare two prostaglandin analogs and two application intervals between mifepristone and the prostaglandin analog administration on the time to abortion in second trimester termination of pregnancy. Other endpoints were live birth rate and fetal lifetime after expulsion.

Methods

Retrospective data of 373 abortions performed were evaluated. Four medical induction subgroups and two feticide subgroups were considered. The definition criteria of the subgroups were the choice of administered prostaglandin analog (misoprostol vs. sulprostone) and the time interval between mifepristone and prostaglandin analog administration (48 vs. 24 h). The outcome parameters were the time to complete uterine evacuation (TCUE), the live birth rate and duration of fetal life.

Results

In the misoprostol subgroups, the median TCUE was 1.6 h longer in the 24-h group than in the 48-h group (p=0.950). In the sulprostone subgroups, the median TCUE was 1.9 h shorter in the 24-h group than in the 48-h group (p=0.950). The median TCUE was shorter for sulprostone than for misoprostol in all six subgroups (p<0.001). The rate of fetal live births ranged between 13.6 and 15.9% within the medical induction subgroups (p=0.969). The median fetal lifetime was slightly shorter in the sulprostone groups than in the misoprostol groups (p=0.563).

Conclusions

Both application intervals and prostaglandin analogs are similarly effective. The therapy regime should be adapted to the personal preferences of the woman, the situational and clinical conditions.


Corresponding author: Jana Franzis Franke, Department of Obstetrics and Gynecology, University Hospital Münster, Wermelingstraße 9, 48147 Münster, Germany, Phone: +49 17670918602, E-mail:

Acknowledgments

We thank everyone who voluntarily dedicated his or her time and effort.

  1. Research funding: None declared.

  2. Author contributions: All authors have accepted responsibility for the entire content of this manuscript and approved its submission. J.F. Franke: project development, data collection, and manuscript writing; K. Oelmeier, M. Möllers, U. Möllmann, J. Braun, H. Köster, and W. Klockenbusch: manuscript writing/editing; L. Kerschke: project development, data management, and data analysis; R. Schmitz and K. Hammer: project development, data management, and manuscript writing/editing.

  3. Competing interests: Authors state no conflict of interest.

  4. Informed consent: Informed consent was obtained from all individuals included in this study.

  5. Ethical approval: Research involving human subjects complied with all relevant national regulations, institutional policies and is in accordance with the tenets of the Helsinki Declaration (as revised in 2013), and has been approved by the authors’ Institutional Review Board.

  6. Data availability: The datasets generated during and/or analyzed during the current study are available from the corresponding author on reasonable request.

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Received: 2022-01-03
Accepted: 2022-04-24
Published Online: 2022-05-10
Published in Print: 2022-10-26

© 2022 Walter de Gruyter GmbH, Berlin/Boston

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