Prevalence of congenital malformation among neonates born after the use of progesterone for luteal support during IVF and ICSI cycles

Shuruq Alkhalaf, Nadeef Alqahtani, Amani AbuAlnaja, Saud Alhassoun, Alexandra Alkhatir, Dania Al-Jaroudi
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Abstract

Introduction: This study assessed the prevalence of congenital malformation among neonates born after using progesterone for luteal support in patients undergoing IVF and ICSI cycles. Methods: This retrospective cohort study was conducted in the Reproductive Endocrinology and Infertility Department of a tertiary hospital. Two groups were compared: one group received only Cyclogest or Crinone gel, and the other group received a combination of Cyclogest or Crinone gel with Proluton Depot injection Results: A total of 91 patients were included, all of whom took progesterone during their IVF and ICSI cycles. The minimum age of the participants was 21, and the maximum was 41. 16.5% (n=15) patients who received progesterone for luteal support during their IVF and ICSI cycles gave birth to infants with congenital malformation, while 76 (83.5%) did not. The most commonly observed congenital malformation was patent ductus arteriosus, observed in 5 cases (5.49%), followed by delayed speech observed in 2 (2.2%). Brachydactyly, Down syndrome, autism spectrum disorder, and a number of other conditions were observed at a rate of 1.1%. Ultimately, no significant association was found between the two groups and the incidence of congenital malformations (p = 0.121). Conclusion: Our review indicates that the incidence of congenital anomalies was similar across the different treatment groups.
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在IVF和ICSI周期中使用黄体酮支持黄体后出生的新生儿先天性畸形的患病率
本研究评估了在接受IVF和ICSI周期的患者中使用黄体激素支持后出生的新生儿先天性畸形的患病率。方法:回顾性队列研究在某三级医院生殖内分泌与不孕症科进行。比较两组患者:一组仅使用Cyclogest或crione凝胶,另一组使用Cyclogest或crione凝胶与Proluton Depot注射液联合使用。结果:共纳入91例患者,均在IVF和ICSI周期使用黄体酮。参与者的年龄最小为21岁,最大为41岁。16.5% (n=15)在IVF和ICSI周期中接受黄体激素支持的患者生下了先天性畸形婴儿,而76例(83.5%)没有。最常见的先天性畸形为动脉导管未闭5例(5.49%),其次为言语迟缓2例(2.2%)。短指畸形、唐氏综合症、自闭症谱系障碍和其他一些疾病的发生率为1.1%。最终,两组患儿先天性畸形发生率无显著相关性(p = 0.121)。结论:我们的综述表明,不同治疗组的先天性异常发生率相似。
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