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达那唑与炔雌醇/炔诺孕酮组合用作性交后避孕药的一种可能作用机制。

A possible mechanism of action of danazol and an ethinylestradiol/norgestrel combination used as postcoital contraceptive agents.

作者信息

Rowlands S, Kubba A A, Guillebaud J, Bounds W

出版信息

Contraception. 1986 Jun;33(6):539-45. doi: 10.1016/0010-7824(86)90042-9.

Abstract

Twenty-seven women requesting postcoital contraception were randomly allocated to take an ethinylestradiol/dl-norgestrel combination or danazol. Urine specimens were assayed for luteinising hormone (LH) and pregnanediol-3-glucuronide (P3G) levels from the day of the postcoital treatment to the next period. In addition, the urine samples of these recruits and 12 additional women were assayed for the Beta-subunit of human chorionic gonadotropin (B-hCG). A consistent pattern of alteration in urinary steroids was lacking, indicating a heterogeneous effect on ovarian function. There was no evidence of early pregnancy in successfully treated cases. We suggest that the main mechanism of action of these drugs is at the endometrial level.

摘要

27名要求进行性交后避孕的女性被随机分配服用炔雌醇/左炔诺孕酮复方制剂或达那唑。从性交后治疗当天到下次月经期间,对尿液样本进行促黄体生成素(LH)和孕二醇-3-葡萄糖醛酸苷(P3G)水平检测。此外,对这些受试者以及另外12名女性的尿液样本进行人绒毛膜促性腺激素β亚基(β-hCG)检测。尿液甾体激素缺乏一致的变化模式,表明对卵巢功能有不同的影响。在成功治疗的病例中没有早期妊娠的迹象。我们认为这些药物的主要作用机制是在子宫内膜水平。

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