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超声监测与超声联合激素水平监测体外受精-胚胎移植周期的比较:一项前瞻性、多中心、随机研究。

Monitoring of in vitro fertilization-embryo transfer cycles by ultrasound versus by ultrasound and hormonal levels: a prospective, multicenter, randomized study.

作者信息

Lass Amir

机构信息

Bourn Hall Clinic, Cambridge, United Kingdom.

出版信息

Fertil Steril. 2003 Jul;80(1):80-5. doi: 10.1016/s0015-0282(03)00558-2.

Abstract

OBJECTIVE

To determine whether cycle monitoring using both serum E(2) and ultrasound findings yields superior clinical pregnancy rates during IVF-embryo transfer (ET) compared to monitoring with ultrasound alone.

DESIGN

Prospective, randomized, multicenter, patient-blinded study.

SETTING

Four assisted conception units in the United Kingdom.

PATIENT(S): Two hundred ninety-seven women believed to be normal responders undergoing IVF treatment.

INTERVENTION(S): Patients were randomly allocated on day 7 of stimulation to one of the two hCG administration criteria: [1] the E(2)-to-follicle > or =11 mm ratio was between 250 and 500 pmol/L/follicle and at least 2 follicles reached a mean diameter of 18 mm or [2] at least 2 follicles reached a mean diameter of 18 mm and the endometrium thickness was > or =8 mm.

MAIN OUTCOME MEASURE(S): Duration and cumulative dose of recombinant human FSH, total number of growing follicles, oocytes retrieved, number and quality of embryos, pregnancy rates, and ovarian hyperstimulation syndrome (OHSS) rates.

RESULT(S): Two hundred ninety-seven patients were randomized to one of the two criteria groups. Of these, 288 (97%) received urinary (u)-hCG (143 in group A and 145 in group B). One hundred three women in group A (72%) met both criteria for hCG administration. Pregnancy and OHSS rates were similar (34.3% vs. 31.4% and 4.9% vs. 4.1%, respectively).

CONCLUSION(S): The addition of E(2)/follicle criteria to ultrasound monitoring of IVF cycles in normal responders seldom changes the timing of hCG, and does not increase pregnancy rates or the risk of OHSS.

摘要

目的

确定在体外受精 - 胚胎移植(ET)过程中,与仅使用超声监测相比,同时使用血清E₂和超声检查结果进行周期监测是否能产生更高的临床妊娠率。

设计

前瞻性、随机、多中心、患者盲法研究。

地点

英国的四个辅助受孕单位。

患者

297名被认为是正常反应者且正在接受体外受精治疗的女性。

干预措施

在刺激的第7天,患者被随机分配到两种hCG给药标准中的一种:[1] E₂与平均直径≥11mm卵泡的比值在250至500pmol/L/卵泡之间,且至少有2个卵泡平均直径达到18mm,或[2] 至少有2个卵泡平均直径达到18mm,且子宫内膜厚度≥8mm。

主要观察指标

重组人促卵泡激素的使用时长和累积剂量、生长卵泡总数、获取的卵母细胞、胚胎数量和质量、妊娠率以及卵巢过度刺激综合征(OHSS)发生率。

结果

297名患者被随机分配到两个标准组中的一组。其中,288名(97%)接受了尿源性(u)-hCG(A组143名,B组145名)。A组中有103名女性(72%)符合两种hCG给药标准。妊娠率和OHSS发生率相似(分别为34.3%对31.4%和4.9%对4.1%)。

结论

在正常反应者的体外受精周期超声监测中增加E₂/卵泡标准很少改变hCG的给药时机,也不会提高妊娠率或增加OHSS的风险。

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