Literature DB >> 21881579

Prevention of gravidic endothelial hypertension by aspirin treatment administered from the 8th week of gestation.

Abdelouahab Bakhti1, Daniel Vaiman.   

Abstract

The aim of this study was to evaluate whether low doses of aspirin (100 mg per day) administered to a homogeneous population of women early (8-10 weeks) during their first pregnancy improved the outcome of gestation hypertensive disorders. This study was performed at the Blida Hospital, where many early deliveries and pregnancy complications are observed. A total of 164 women were either treated (82) or used as controls (82). Treatment increased the gestation length by 12 days on average, thus triggering an approximate 150-g increase in newborn weight. This consistently improved the outcome for all patients with respect to all parameters investigated. Overall, the relative risk of developing hypertensive disorders of gestation was reduced to 0.07 (confidence interval=0.01-0.51). In our series, we did not observe deleterious consequences for the fetus (teratogenicity and fetotoxicity) or adverse outcomes for the mothers. Despite the limited number of patients analyzed, the present study is one of the largest investigating early aspirin treatment of gestational hypertensive diseases. In addition, the time of aspirin administration is among the earliest yet examined. The data tend to confirm the results obtained from other cohorts on the overall benefit of aspirin treatment for gestational disorders. In the future, molecular or ultrasonographic markers of these diseases could help to screen patients before applying the treatment.

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Year:  2011        PMID: 21881579     DOI: 10.1038/hr.2011.111

Source DB:  PubMed          Journal:  Hypertens Res        ISSN: 0916-9636            Impact factor:   3.872


  8 in total

1.  Prediction and prevention of hypertensive disorders of pregnancy.

Authors:  Akihide Ohkuchi; Chikako Hirashima; Kayo Takahashi; Hirotada Suzuki; Shigeki Matsubara
Journal:  Hypertens Res       Date:  2016-08-18       Impact factor: 3.872

Review 2.  Extracellular Vesicles and Preeclampsia: Current Knowledge and Future Research Directions.

Authors:  Carlos Palma; Jessica Jellins; Andrew Lai; Alexis Salas; America Campos; Shayna Sharma; Gregory Duncombe; Jon Hyett; Carlos Salomon
Journal:  Subcell Biochem       Date:  2021

3.  The role of aspirin dose and initiation time in the prevention of preeclampsia and corresponding complications: a meta-analysis of RCTs.

Authors:  Ka Cheuk Yip; Ziyin Luo; Xiaman Huang; Weijen Lee; Layla Li; Chenyang Dai; Weiyu Zeng; Tsz Ngai Mok; Qiyu He; Ruiman Li
Journal:  Arch Gynecol Obstet       Date:  2022-01-09       Impact factor: 2.344

Review 4.  Aspirin vs Heparin for the Prevention of Preeclampsia.

Authors:  Vasiliki Katsi; Theoni Kanellopoulou; Thomas Makris; Petros Nihoyannopoulos; Efrosyni Nomikou; Dimitrios Tousoulis
Journal:  Curr Hypertens Rep       Date:  2016-07       Impact factor: 5.369

5.  Antiplatelet agents for preventing pre-eclampsia and its complications.

Authors:  Lelia Duley; Shireen Meher; Kylie E Hunter; Anna Lene Seidler; Lisa M Askie
Journal:  Cochrane Database Syst Rev       Date:  2019-10-30

6.  Medications for preventing hypertensive disorders in high-risk pregnant women: a systematic review and network meta-analysis.

Authors:  Tippawan Liabsuetrakul; Yoshiko Yamamoto; Chanon Kongkamol; Erika Ota; Rintaro Mori; Hisashi Noma
Journal:  Syst Rev       Date:  2022-07-01

7.  Low-dose aspirin at ≤16 weeks of gestation for preventing preeclampsia and its maternal and neonatal adverse outcomes: A systematic review and meta-analysis.

Authors:  Yuechong Cui; Bin Zhu; Fei Zheng
Journal:  Exp Ther Med       Date:  2018-03-20       Impact factor: 2.447

Review 8.  Molecular Targets of Aspirin and Prevention of Preeclampsia and Their Potential Association with Circulating Extracellular Vesicles during Pregnancy.

Authors:  Suchismita Dutta; Sathish Kumar; Jon Hyett; Carlos Salomon
Journal:  Int J Mol Sci       Date:  2019-09-05       Impact factor: 5.923

  8 in total

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