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Prednisone vs Placebo and Live Birth in Patients With Recurrent Implantation Failure Undergoing In Vitro Fertilization

医学 活产 强的松 胚胎移植 安慰剂 体外受精 随机对照试验 怀孕 妊娠期 相对风险 产科 妇科 内科学 置信区间 病理 替代医学 生物 遗传学
作者
Yun Sun,Linlin Cui,Yao Lu,Jichun Tan,Xi Dong,Tianxiang Ni,Junhao Yan,Yichun Guan,Guimin Hao,Jiayin Liu,Bo Zhang,Daimin Wei,Yan Hong,Yang He,Qi Jia,Bing Xu,Juanjuan Lu,Qian Zhang,Shanshan Zhao,Xiaowei Ji,Xiaofang Du,Jie Zhang,Jinyong Liu,Jing Wang,Yingqin Huang,Dongmei Huang,Yanzhi Du,Hugo Vankelecom,Heping Zhang,Zi‐Jiang Chen
出处
期刊:JAMA [American Medical Association]
卷期号:329 (17): 1460-1460 被引量:6
标识
DOI:10.1001/jama.2023.5302
摘要

Implantation failure remains a critical barrier to in vitro fertilization. Prednisone, as an immune-regulatory agent, is widely used to improve the probability of implantation and pregnancy, although the evidence for efficacy is inadequate.To determine the efficacy of 10 mg of prednisone compared with placebo on live birth among women with recurrent implantation failure.A double-blind, placebo-controlled, randomized clinical trial conducted at 8 fertility centers in China. Eligible women who had a history of 2 or more unsuccessful embryo transfer cycles, were younger than 38 years when oocytes were retrieved, and were planning to undergo frozen-thawed embryo transfer with the availability of good-quality embryos were enrolled from November 2018 to August 2020 (final follow-up August 2021).Participants were randomized (1:1) to receive oral pills containing either 10 mg of prednisone (n = 357) or matching placebo (n = 358) once daily, from the day at which they started endometrial preparation for frozen-thawed embryo transfer through early pregnancy.The primary outcome was live birth, defined as the delivery of any number of neonates born at 28 or more weeks' gestation with signs of life.Among 715 women randomized (mean age, 32 years), 714 (99.9%) had data available on live birth outcomes and were included in the primary analysis. Live birth occurred among 37.8% of women (135 of 357) in the prednisone group vs 38.8% of women (139 of 358) in the placebo group (absolute difference, -1.0% [95% CI, -8.1% to 6.1%]; relative ratio [RR], 0.97 [95% CI, 0.81 to 1.17]; P = .78). The rates of biochemical pregnancy loss were 17.3% in the prednisone group and 9.9% in the placebo group (absolute difference, 7.5% [95% CI, 0.6% to 14.3%]; RR, 1.75 [95% CI, 1.03 to 2.99]; P = .04). Of those in the prednisone group, preterm delivery occurred among 11.8% and of those in the placebo group, 5.5% of pregnancies (absolute difference, 6.3% [95% CI, 0.2% to 12.4%]; RR, 2.14 [95% CI, 1.00 to 4.58]; P = .04). There were no statistically significant between-group differences in the rates of biochemical pregnancy, clinical pregnancy, implantation, neonatal complications, congenital anomalies, other adverse events, or mean birthweights.Among patients with recurrent implantation failure, treatment with prednisone did not improve live birth rate compared with placebo. Data suggested that the use of prednisone may increase the risk of preterm delivery and biochemical pregnancy loss. Our results challenge the value of prednisone use in clinical practice for the treatment of recurrent implantation failure.Chinese Clinical Trial Registry Identifier: ChiCTR1800018783.
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