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Perinatal risk in singleton pregnancies after in vitro fertilization.

机译:体外受精后单胎妊娠的围产期风险。

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摘要

OBJECTIVE: To assess perinatal risks to singleton births after in vitro fertilization (IVF) versus spontaneous conception. DESIGN: Cross-sectional. SETTING: A 2006 registry database of the Japan Society of Obstetrics and Gynaecology (JSOG) capturing 5.8% of total births. PATIENT(S): 53,939 singleton births from spontaneous conceptions and 1,408 singletons after IVF. INTERVENTION(S): None. MAIN OUTCOME MEASURE(S): Perinatal death, low-birth weight (LBW), small for gestational age (SGA), congenital malformation, and sex ratio assessment based on singleton birth cases versus singleton live-born cases. RESULT(S): In this study, IVF may include intracytoplasmic sperm injection (ICSI), gamete intrafallopian transfer, or IVF followed by zygote intrafallopian transfer. In crude and adjusted analysis, perinatal death, SGA, congenital malformation, and sex ratio were not statistically significantly associated with IVF. The LBW rates were statistically significantly higher in IVF pregnancies, but the association statistically significantly decreased after adjusting for confounding factors. Placental previa, a maternal outcome, was found to be statistically significantly higher in IVF pregnancies. CONCLUSION(S): No evidence was implicated IVF procedures as dramatically increasing the adjusted risk of perinatal death, LBW, SGA, congenital malformation, or sex ratio when compared with spontaneous conceptions. However, because of sample size limitations, the study cannot exclude small to moderate increases in perinatal deaths or congenital malformations.
机译:目的:评估体外受精(IVF)与自然受孕后围产期单胎出生的风险。设计:横截面。地点:日本妇产科协会(JSOG)的2006年注册数据库,占总分娩的5.8%。患者:自发受孕53,939例单胎,IVF后1,408例单胎。干预措施:无。主要观察指标:围产期死亡,低出生体重(LBW),胎龄小(SGA),先天性畸形和基于单胎出生病例与单胎活产病例的性别比评估。结果:在这项研究中,IVF可能包括胞浆内精子注射(ICSI),配子输卵管内移植或IVF,然后进行合子输卵管内移植。在粗略和校正后的分析中,围产期死亡,SGA,先天性畸形和性别比与IVF无关。在试管婴儿中,LBW率在统计学上显着较高,但在校正混杂因素后,该协会在统计学上显着降低。在IVF怀孕中发现母体胎盘前置,在统计学上显着更高。结论:与自发性妊娠相比,没有证据表明IVF程序会显着增加围产期死亡,LBW,SGA,先天性畸形或性别比的调整风险。但是,由于样本量的限制,该研究不能排除围产期死亡或先天性畸形的小到中度增加。

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