Clifford K, Rai R, Watson H, Franks S, Regan L
Department of Obstetrics and Gynaecology, St. Mary's Hospital Medical School, London.
BMJ. 1996 Jun 15;312(7045):1508-11. doi: 10.1136/bmj.312.7045.1508.
To determine whether prepregnancy pituitary suppression of luteinising hormone secretion with a luteinising hormone releasing hormone analogue improves the outcome of pregnancy in ovulatory women with a history of recurrent miscarriage, polycystic ovaries, and hypersecretion of luteinising hormone.
Randomised controlled trial.
Specialist recurrent miscarriage clinic.
106 women with a history of three or more consecutive first trimester miscarriages, polycystic ovaries, and hypersecretion of luteinising hormone.
Women were randomised before conception to receive pituitary suppression with a luteinising hormone releasing hormone analogue followed by low dose ovulation induction and luteal phase progesterone (group 1) or were allowed to ovulate spontaneously and then given luteal phase progesterone alone or luteal phase placebo alone (group 2). No drugs were prescribed in pregnancy.
Conception and live birth rates over six cycles.
Conception rates in the pituitary suppression and luteal phase support groups were 80% (40/50 women) and 82% (46/56) respectively (NS). Live birth rates were 65% (26/40) and 76% (35/46) respectively (NS). In the luteal phase support group there was no difference in the outcome of pregnancy between women given progesterone and those given placebo pessaries. Live birth rates from an intention to treat analysis were 52% (26/50 pregnancies) in the group given pituitary suppression and 63% (35/56) in the controls (NS).
Prepregnancy suppression of high luteinising hormone concentrations in ovulatory women with recurrent miscarriage and hypersecretion of luteinising hormone does not improve the outcome of pregnancy. The outcome of pregnancy without pituitary suppression is excellent.
确定在有复发性流产、多囊卵巢和黄体生成素分泌过多病史的排卵女性中,妊娠前使用黄体生成素释放激素类似物抑制垂体黄体生成素分泌是否能改善妊娠结局。
随机对照试验。
复发性流产专科诊所。
106名有连续三次或更多次孕早期流产史、多囊卵巢和黄体生成素分泌过多病史的女性。
女性在受孕前被随机分组,一组接受黄体生成素释放激素类似物抑制垂体,随后进行低剂量促排卵和黄体期孕激素治疗(第1组);另一组允许自然排卵,然后单独给予黄体期孕激素或单独给予黄体期安慰剂(第2组)。孕期不使用任何药物。
六个周期内的受孕率和活产率。
垂体抑制组和黄体期支持组的受孕率分别为80%(50名女性中的40名)和82%(56名中的46名)(无显著性差异)。活产率分别为65%(40名中的26名)和76%(46名中的35名)(无显著性差异)。在黄体期支持组中,接受孕激素治疗的女性和接受安慰剂阴道栓剂治疗的女性的妊娠结局没有差异。意向性分析得出的活产率在接受垂体抑制治疗的组中为52%(50次妊娠中的26次),在对照组中为63%(56次中的35次)(无显著性差异)。
在有复发性流产和黄体生成素分泌过多的排卵女性中,妊娠前抑制高黄体生成素浓度并不能改善妊娠结局。不进行垂体抑制的妊娠结局良好。