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[卵巢活动、周期行为与低剂量口服避孕药耐受性:一项对比研究]

[Ovarian activity, cycle behavior and tolerance of low dosage oral contraceptives: a comparative study].

作者信息

Rossmanith W G, Wirth U, Gasser S, Thun B, Steffens D

机构信息

Universitäts-Frauenklinik Ulm.

出版信息

Zentralbl Gynakol. 1997;119(11):538-44.

PMID:9480608
Abstract

In a double-blind randomized study, the suppression of ovarian activity, the effects on the cervix and endometrium, menstrual bleeding patterns and overall tolerance were assessed during administration of two low-dose oral contraceptives (20 micrograms ethinylestradiol EE, 500 micrograms norethisterone--Eve 20, Grünenthal, Aachen; 20 micrograms EE, 150 micrograms Desogestrel--Lovelle, Organon, Munich), 118 healthy women (ages: 18 to 35 years) with comparable bioprofiles (height, weight, menstrual cycle patterns) were studied in 10 investigation centres during medication with either Eve 20 (n = 59) or Lovelle (n = 59). During 3 treatment cycles, ovarian activity was evaluated by sonographic determination of follicular size and by simultaneous assessment of serum endocrine profiles (gonadotropins LH and FSH, ovarian steroids estradiol [E2] and progesterone [P]). Treatment cycles 4 to 6 served to evaluate the patterns of menstrual bleeding and the overall subjective tolerance on each contraceptive. While on the preparations, no ovarian activity (as judged by a lack of follicular growth and suppressed sex steroid levels) was found in over 90% of all investigated cycles. Follicular activity and/or cyst formation were detected in 18 of 173 cycles (Eve 20) and in 5 of 175 cycles (Lovelle) respectively. Gonadotropin levels were suppressed (LH < 6 IU/l, FSH < 8 IU/l) in most treatment cycles (Eve 20: 76.6% vs. Lovelle: 84.8%). Serum E2 concentrations exceeding 0.1 nmol/l indicated residual follicular activity in 19.3% (Eve 20) vs. 12.2% (Lovelle) of all cycles. As estimated by serum P levels over 5 nmol/l, ovulation had presumably occurred in 4.1% (Eve 20) vs. 2.9% (Lovelle) of treatments respectively. However, when the sonographic and endocrinological data were combined, no ovulation was documented in any treatment cycle. In addition, the quality of the cervical mucus was minimal and a low endometrial thickness was found in the majority of women, indicating strong progestogen effects of both contraceptives. Menstrual irregularities (intermenstrual spotting, break-through bleeding) occurred initially on each preparation, but were mostly resolved when the pills were continued. The acceptance of each investigated drug was rated as very good or good by most subjects. These observations allow us to conclude that the rate of ovarian suppression with inhibition of follicular activity is high under low-dose oral contraceptives. The different progestogens as components of these contraceptive pills display equally good anti-conceptive effects on both the cervix and the endometrium. Furthermore, the rate of irregular menstrual bleeding is acceptable for these low-dose contraceptives. The high acceptance of each preparation suggests that such agents will have a high rate of acceptability in clinical use.

摘要

在一项双盲随机研究中,对两种低剂量口服避孕药(20微克炔雌醇[EE]、500微克炔诺酮——Eve 20,德国亚琛的格伦泰公司;20微克EE、150微克去氧孕烯——Lovelle,德国慕尼黑的欧加农公司)给药期间的卵巢活动抑制情况、对子宫颈和子宫内膜的影响、月经出血模式及总体耐受性进行了评估。在10个研究中心,118名具有相似生物特征(身高、体重、月经周期模式)的健康女性(年龄:18至35岁)在服用Eve 20(n = 59)或Lovelle(n = 59)期间接受了研究。在3个治疗周期中,通过超声测定卵泡大小并同时评估血清内分泌指标(促性腺激素LH和FSH、卵巢甾体激素雌二醇[E2]和孕酮[P])来评估卵巢活动。第4至6个治疗周期用于评估每种避孕药的月经出血模式和总体主观耐受性。服用这些制剂期间,在所有研究周期中超过90%未发现卵巢活动(根据卵泡无生长及性甾体激素水平受抑制判断)。分别在Eve 20组的173个周期中的18个以及Lovelle组的175个周期中的5个检测到卵泡活动和/或囊肿形成。在大多数治疗周期中促性腺激素水平受到抑制(LH < 6 IU/l,FSH < 8 IU/l)(Eve 20组:76.6%,Lovelle组:84.8%)。血清E2浓度超过0.1 nmol/l表明在所有周期中分别有19.3%(Eve 20组)和12.2%(Lovelle组)存在残余卵泡活动。根据血清P水平超过5 nmol/l估计,分别在4.1%(Eve 20组)和2.9%(Lovelle组)的治疗中有排卵可能发生。然而,当将超声和内分泌学数据综合起来时,在任何治疗周期中均未记录到排卵。此外,大多数女性的宫颈黏液质量极低且子宫内膜厚度较薄,表明两种避孕药均有较强的孕激素作用。最初在每种制剂上均出现月经不规律(经间期点滴出血、突破性出血),但继续服药时大多可缓解。大多数受试者对每种研究药物的接受度评价为非常好或良好。这些观察结果使我们得出结论,低剂量口服避孕药抑制卵泡活动的卵巢抑制率较高。这些避孕药丸中不同的孕激素对子宫颈和子宫内膜均显示出同样良好的避孕效果。此外,这些低剂量避孕药的月经不规则出血率是可接受的。每种制剂的高接受度表明此类药物在临床使用中将具有较高的接受率。

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