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两种复方激素避孕药的定期和不定期出血模式:标准化新建议的应用

Scheduled and unscheduled bleeding patterns with two combined hormonal contraceptives: application of new recommendations for standardization.

作者信息

Hampton Raymond Moss, Fisher Alan C, Pagano Susan, LaGuardia Katherine D

机构信息

Texas Tech University School of Medicine, Odessa, Texas, USA.

出版信息

Fertil Steril. 2009 Aug;92(2):434-40. doi: 10.1016/j.fertnstert.2008.07.010. Epub 2008 Oct 18.

Abstract

OBJECTIVE

To reassess and compare cycle control attained with two combined hormonal contraceptives, norgestimate (NGM)/ethinyl estradiol (EE) 25 microg and norethindrone acetate (NETA)/EE 20 microg, by new general criteria recommendations for all combined hormonal contraceptives.

DESIGN

Analysis of bleeding data for cycles 1-6 from a randomized, multicenter trial.

SETTING

221 North American centers.

PATIENT(S): Healthy, sexually active women (18-45 years old).

INTERVENTION(S): NETA/EE: 1 mg NETA/20 microg EE, days 1-21 of each cycle and 75 mg of ferrous fumarate, days 22-28; NGM/EE: triphasic NGM in 7-day increments (days 1-7: 180 microg; days 8-14: 215 microg; days 15-21: 250 microg) and 25 microg EE, placebo on days 22-28.

MAIN OUTCOME MEASURE(S): Cycle control evaluated from patients' daily diaries.

RESULT(S): For cycles 1-6, there was a statistically significant lower incidence of unscheduled bleeding/spotting with NGM/EE 25 microg (range 21.0%-34.4%) than with NETA/EE 20 microg (range 33.0%-46.6%). Of the women who had unscheduled bleeding/spotting, the mean number of days per cycle of bleeding/spotting was comparable. A statistically significant higher incidence of scheduled bleeding was seen with NGM/EE 25 microg (95.2%-97.5%) than with NETA/EE 20 microg (78.5%-84.2%).

CONCLUSION(S): The NGM/EE 25 microg has a lower incidence and comparable length of unscheduled bleeding and a higher incidence of scheduled bleeding than NETA/EE 20 microg in this post hoc analysis.

摘要

目的

根据针对所有复方激素避孕药的新通用标准建议,重新评估并比较两种复方激素避孕药炔诺孕酮(NGM)/炔雌醇(EE)25微克和醋酸炔诺酮(NETA)/EE 20微克所实现的周期控制情况。

设计

对一项随机多中心试验第1 - 6周期的出血数据进行分析。

地点

221个北美中心。

患者

健康、有性生活的女性(18 - 45岁)。

干预措施

NETA/EE:每个周期第1 - 21天服用1毫克NETA/20微克EE,第22 - 28天服用75毫克富马酸亚铁;NGM/EE:三相NGM,剂量以7天递增(第1 - 7天:180微克;第8 - 14天:215微克;第15 - 21天:250微克)和25微克EE,第22 - 28天服用安慰剂。

主要观察指标

根据患者的每日日记评估周期控制情况。

结果

在第1 - 6周期,与20微克NETA/EE(范围33.0% - 46.6%)相比,25微克NGM/EE出现非预期出血/点滴出血的发生率在统计学上显著更低(范围21.0% - 34.4%)。在出现非预期出血/点滴出血的女性中,每个周期出血/点滴出血的平均天数相当。与20微克NETA/EE(78.5% - 84.2%)相比,25微克NGM/EE出现预期出血的发生率在统计学上显著更高(95.2% - 97.5%)。

结论

在此事后分析中,与20微克NETA/EE相比,25微克NGM/EE出现非预期出血的发生率更低且持续时间相当,而出现预期出血的发生率更高。

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