Skip to main content

CORRECTION article

Front. Med.
Sec. Obstetrics and Gynecology
Volume 12 - 2025 | doi: 10.3389/fmed.2025.1561413

Corrigendum: Progesterone, cerclage, pessary, or acetylsalicylic acid for prevention of preterm birth in singleton and multifetal pregnancies -A systematic review and meta-analyses

Provisionally accepted
Ulla-Britt Wennerholm Ulla-Britt Wennerholm *Lina Bergman Lina Bergman Bo Jacobsson Bo Jacobsson Annika Strandell Annika Strandell
  • Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden

The final, formatted version of the article will be published soon.

    In the published article, there was an error. "[This concerns the results of the meta-analyses, which have marginally changed after exclusion of an article that has been retracted and was included in several meta-analyses: Cetingoz E et al. Progesterone effects on preterm birth in high-risk pregnancies: a randomized placebo-controlled trial. Arch Gynecol Obstet. 2011 Mar;283(3):423-9. We observed a retraction note for this article that was published in: Arch Gynecol Obstet. 2024 Sep;310(3):1777. The scientific conclusions of our systematic review will not be changed.]" This sentence previously stated: "[Low risk of bias trials showed an overall effect of progesterone to reduce the risk of preterm birth (Table 2 and Figure 2A). A reduction of any preterm birth was demonstrated for <37 gestational weeks (26.8% vs. 30.2%, RR 0.82; 95% CI 0.71 to 0.95) and <34 gestational weeks (11.7% vs. 15.2%, RR 0.78; 95% CI 0.68 to 0.89) for any administration route (high certainty of evidence).]"The corrected sentence appears below: "[Low risk of bias trials showed an overall effect of progesterone to reduce the risk of preterm birth (Table 2 andFigure 2A). A reduction of any preterm birth was demonstrated for <37 gestational weeks (26.7% vs. 30.3%, RR 0.82; 95% CI 0.71 to 0.96) and <34 gestational weeks (11.8% vs. 15.4%, RR 0.78; 95% CI 0.67 to 0.89) for any administration route (high certainty of evidence).]" A correction has been made to [Results], [Progesterone, Preterm birth across gestational weeks in multifetal pregnancies]. This sentence previously stated: "[Low risk of bias trials demonstrated no effect of progesterone (any administration route) on the risk of any preterm birth <37 gestational weeks (58.3% vs. 57.2%, RR 1.01; 95% CI 0.95 to 1.08) (moderate certainty of evidence), and <34 gestational weeks (22.4% vs. 21.6%, RR 1.02; 95% CI 0.92 to 1.12) (high certainty of evidence), neither on < 35, <32, <28 gestational weeks (high certainty of evidence), nor on the risk of spontaneous preterm birth (low to moderate certainty of evidence)]."The corrected sentence appears below: "[Low risk of bias trials demonstrated no effect of progesterone (any administration route) on the risk of any preterm birth <37 gestational weeks (58.5% vs. 56.6%, RR 1.03; 95% CI 0.97 to 1.08) (moderate certainty of evidence), and <34 gestational weeks (22.8% vs. 21.5%, RR 1.02; 95% CI 0.93 to 1.13) (high certainty of evidence), neither on < 35, <32, <28 gestational weeks (high certainty of evidence), nor on the risk of spontaneous preterm birth (low to moderate certainty of evidence)]."The authors apologize for this error and state that this does not change the scientific conclusions of the article in any way.

    Keywords: acetylsalicylic acid, Cerclage, perinatal morbidity and mortality, Pessary, Preterm Birth, Progesterone, Systematic review

    Received: 15 Jan 2025; Accepted: 27 Jan 2025.

    Copyright: © 2025 Wennerholm, Bergman, Jacobsson and Strandell. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

    * Correspondence: Ulla-Britt Wennerholm, Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden

    Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.