Home Medicine The effect of 150 and 80 mg doses of aspirin on preventing preterm birth in high-risk pregnant women
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The effect of 150 and 80 mg doses of aspirin on preventing preterm birth in high-risk pregnant women

  • Maryam Kasraeian , Nasrin Asadi , Homeira Vafaei , Mahin Tazang , Azam Faraji , Neda Rahimirad , Sedighe Yousofi , Seyedeh Fatemeh Khaleghi and Marjan Zare ORCID logo EMAIL logo
Published/Copyright: May 27, 2022

Abstract

Objectives

Preterm birth (PTB) is the common cause of neonatal mortality nationwide. The present study aimed to evaluate the efficacy of different doses of aspirin in preventing PTB in high-risk pregnant women. As secondary outcomes, other perinatal complications were compared.

Methods

This double-blind randomized clinical trial was conducted on high-risk pregnant women with impaired placental perfusion diagnosed in the first trimester of pregnancy referring to the perinatal centers affiliated to Shiraz university of Medical Sciences between February 2020 and March 2021. The subjects were randomly divided in two groups administered with 150 or 80 mg aspirin every night from 11 to 13+6 weeks until 36 weeks or delivery. This study is registered in the Iranian Registry of Clinical Trials (IRCT20140317017035N6; http://www.irct.ir/). Univariate and multiple logistic regressions were applied using SPSS 22.

Results

A total of 101 subjects received 80 mg aspirin and 89 ones received 150 mg aspirin. The results of multiple analysis revealed a significantly lower odds of PTB (OR 0.4 (0.19, 0.99)) in the 150 mg group compared to the 80 mg group. As secondary outcomes, preeclampsia (PEC) and PEC with severe features (PECsf) were lower (OR 0.2 (0.06, 0.82) and 0.1 (0.01, 0.92), respectively); however, fetal age and neonatal weight were higher in the 150 mg group (OR 1.2 (1.04, 1.33) and 1.001 (1–1.001), respectively).

Conclusions

The study findings indicated that, compared with 80 mg of aspirin, taking 150 mg of aspirin reduced PTB and perinatal complications in high risk pregnant women.


Corresponding author: Marjan Zare, Maternal-fetal medicine Research Center, Shiraz University of Medical Sciences, Shiraz, Iran, E-mail:

  1. Research funding: None declared.

  2. Author contributions: All authors have accepted responsibility for the entire content of this manuscript and approved its submission.

  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: All study steps were in agreement with the Helsinki Declaration 1964 (IR.SUMS.MED.REC.1398.512). The study was also registered in the Iranian Registry of Clinical Trials (IRCT20140317017035N6; http://www.irct.ir/).

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Supplementary Material

The online version of this article offers supplementary material (https://doi.org/10.1515/jpm-2021-0668).


Received: 2021-12-15
Revised: 2022-04-27
Accepted: 2022-04-30
Published Online: 2022-05-27
Published in Print: 2022-11-25

© 2022 Walter de Gruyter GmbH, Berlin/Boston

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