首页> 美国卫生研究院文献>British Medical Journal >Trial of support treatment with human chorionic gonadotrophin in the luteal phase after treatment with buserelin and human menopausal gonadotrophin in women taking part in an in vitro fertilisation programme.
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Trial of support treatment with human chorionic gonadotrophin in the luteal phase after treatment with buserelin and human menopausal gonadotrophin in women taking part in an in vitro fertilisation programme.

机译:在接受体外受精程序的女性中用布塞林和更年期促性腺激素治疗后在黄体期用人绒毛膜促性腺激素进行支持治疗的试验。

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摘要

OBJECTIVE--To evaluate the effect of support with human chorionic gonadotrophin in the luteal phase in women taking part in an in vitro fertilisation programme after buserelin and human menopausal gonadotrophin were used to hyperstimulate their ovaries. DESIGN--Controlled group comparison. SETTING--Outpatient department of a private hospital. PATIENTS--115 Women with indications for in vitro fertilisation, all of whom had at least one embryo transferred. INTERVENTIONS--After suppression of the pituitary with buserelin the ovaries of all the women were stimulated with human menopausal gonadotrophin on day 4 of the luteal phase. Human chorionic gonadotrophin (10,000 IU) was given to induce ovulation, and oocytes were recovered 34 hours later. Embryos were transferred 46 to 48 hours after insemination. Women who had received the 10,000 IU of human chorionic gonadotrophin on a date that was an uneven number (n = 61) were allocated to receive support doses of 2500 IU human chorionic gonadotrophin three and six days after that date. The remaining 54 women did not receive hormonal support. END POINT--Determination of the rates of pregnancy. MEASUREMENTS and main results--Support with human chorionic gonadotrophin did not significantly alter the progesterone or oestradiol concentrations in the early or mid-luteal phase. The mean (range) progesterone concentrations in the late luteal phase in women who did not become pregnant were, however, significantly higher in those who received support (16(9-110) nmol/l nu 8(4-46) nmol/l), and the luteal phase was significantly longer in this group (14 days nu 12 days). The rate of pregnancy was significantly higher in the women who received support than in those who did not (25/61 nu 8/54). CONCLUSIONS--When buserelin and human menopausal gonadotrophin are used to hyperstimulate ovaries support with human chorionic gonadotrophin in the luteal phase has a beneficial effect on in vitro fertilisation.
机译:目的-为了评估使用绒毛膜促性腺激素和绝经期人促性腺激素刺激卵巢功能后参与体外受精程序的妇女的黄体期绒毛膜促性腺激素的支持作用。设计-受控组比较。地点-私立医院的门诊部。患者-115有体外受精迹象的妇女,所有妇女均已转移至少一个胚胎。干预-在用黄体素抑制垂体后,在黄体期的第4天,用人类更年期促性腺激素刺激所有妇女的卵巢。给予人绒毛膜促性腺激素(10,000 IU)诱导排卵,并在34小时后恢复卵母细胞。授精后46至48小时转移胚胎。在日期不均匀(n = 61)的日期接受10,000 IU人绒毛膜促性腺激素的妇女被分配在该日期后三天和六天接受2500 IU人绒毛膜促性腺激素的支持剂量。其余54名妇女没有得到荷尔蒙支持。终点-妊娠率的测定。测量和主要结果-人绒毛膜促性腺激素的支持在黄体早期或中期没有明显改变孕酮或雌二醇的浓度。没有怀孕的妇女在黄体晚期黄体酮的平均(范围)孕激素浓度明显高于接受支持的妇女(16(9-110)nmol / l nu 8(4-46)nmol / l ),且该组的黄体期明显更长(14天至12天)。接受支持的妇女的妊娠率明显高于未接受支持的妇女(25/61 nu 8/54)。结论-当使用黄杨素和人更年期促性腺激素在黄体期用人绒毛膜促性腺激素来过度刺激卵巢支持时,对体外受精具有有益的作用。

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