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Risk of abnormal pregnancy outcomes after using Ondansetron during pregnancy: a systematic review and Meta-analysis
  • +4
  • xiao cao,
  • Mingyao Sun,
  • Qiuyu Yang,
  • Qi Wang,
  • Liangying Hou,
  • Long Ge,
  • Min Yin
xiao cao
Lanzhou University
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Mingyao Sun
Evidence-Based Nursing Centre, School of Nursing, Lanzhou University
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Qiuyu Yang
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Qi Wang
Department of Social Medicine and Health Management, and Evidence Based Social Science Research Centre, School of Public Health, Lanzhou University
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Liangying Hou
Department of Social Medicine and Health Management, and Evidence Based Social Science Research Centre, School of Public Health, Lanzhou University
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Long Ge
Key Laboratory of Evidence Based Medicine and Knowledge Translation of Gansu Province, Lanzhou, China

Corresponding Author:gelong2009@163.com

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Min Yin
International Health Examination Center of the First Hospital of Lanzhou University
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Abstract

Background Hyperemesis gravidarum (HG) is a severe complication of pregnancy affecting around 1% of pregnancies globally. Objective To investigate whether ondansetron use during pregnancy is associated with increased rates of abnormal pregnancy outcomes. Search strategy PubMed, Embase, the Cochrane Library, CINAHL, CNKI, CBM, WANFANG, and ClinicalTrials.gov were searched for citations published in any language from inception to 15 December 2021. Selection criteria Eligible studies included any observational study. Data collection and analysis We used odds ratios (ORs) and 95% confidence intervals (CIs) as a measure of the association between ondansetron and abnormal pregnancy outcomes. Main results Of 1,558 citations screened, 19 articles were included. No significant increased risk for overall congenital malformations (OR=1.10,95% CI:0.94–1.29, Low certainty), cleft palate (OR=0.78,95% CI:0.37–1.64, Very Low certainty), stillbirth (OR=0.60,95% CI:0.40–0.91, Low certainty) or preterm birth (OR=0.78,95% CI:0.37–1.64, Low certainty) were identified in our primary analysis. However, the results of our primary analysis indicated that ondansetron use during pregnancy was associated with significantly increased rates of heart defects (OR=1.06,95% CI:1.02–1.11, Moderate certainty) and other organ malformations (OR=1.09,95% CI:1.03–1.16, Moderate certainty) when exposed infants were compared with healthy or disease-matched controls. Conclusion Ondansetron use during pregnancy was associated with a significant increase in rate of some abnormal pregnancy outcomes in our primary analysis. In conclusion, our review found that ondansetron should not use as first-line treatment for NVP. But for sever and incurable NVP, clinician can consider use moderate amount ondansetron to treat NVP with close monitoring.