作为哺乳期妇女避孕选择的只含屈螺酮的避孕药:关于使用者接受度和新生儿发育的首批数据。

IF 2 4区 医学 Q3 ENDOCRINOLOGY & METABOLISM Gynecological Endocrinology Pub Date : 2024-12-01 Epub Date: 2024-07-29 DOI:10.1080/09513590.2024.2382800
Pedro Antonio Regidor, Enrico Colli, Artur Jakimiuk
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引用次数: 0

摘要

背景:纯孕激素避孕药(POPs)多年来一直用于哺乳期妇女的避孕。现行指南允许使用这些避孕药物:方法:采用单次访问和回顾性数据审查的多中心研究。该研究涉及 100 名在哺乳期使用屈螺酮避孕药(DRSP)避孕至少 5 个月的妇女。研究旨在分析这些成功使用者对新生儿发育、出血情况的影响,并评估使用者的满意度:结果:对新生儿的分析表明,他们的身长和体重等生长参数都在标准发育的预期范围内。平均出生体重为 3368 克,最低为 2860 克,最高为 5040 克。新生儿身长的中位数为 55 厘米,从 35 厘米到 65 厘米不等。所有新生儿都在既定的百分位数范围内适当生长。出血情况的可接受性由 VAS 评分来评定:平均可接受性评分为 82.8 分。与年轻女性相比,35 岁或以上女性的可接受性明显更高(≥35 岁:平均值 = 88.4,标准差 = 16.5;P = 0.02)。61名患者(N = 61;61.0%;95% CI:50.7 - 70.4%)表示愿意在哺乳后继续使用 DRSP:结论:本研究表明,在继续使用 DRSP 单一药片 5 个月的患者中,新生儿没有受到任何负面影响,他们的发育也没有受到临床影响。此外,使用者对药片的出血情况表示非常满意:DRKS00028438 .
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The drospirenone only pill as a contraceptive option for breastfeeding women: First data on users' acceptability and newborn development.

Background: Progestin-only pills (POPs) have been used for contraception in breastfeeding women for years. The existing guidelines allow the use of these contraceptives.

Methods: Multicenter study with a single visit and retrospective data review. The study involved 100 women who used a drospirenone-only pill (DRSP) for contraception for at least 5 months during breastfeeding. The study aimed to analyze for those successful users the impact on new-born development, the bleeding profile and evaluate user satisfaction.

Results: Analysis of the newborns showed that their growth parameters length and weight, were within the expected range of standard development. The mean birth weight was 3368 g, with the lowest recorded weight being 2860 g and the highest 5040 g. The median length of the newborns was 55 cm, ranging from 35 to 65 cm. All new-borns demonstrated appropriate growth within the established percentiles. Acceptability with the bleeding profile was rated with a VAS score: the mean acceptability rating was 82.8. Women aged 35 years or older reported significantly higher acceptability compared to younger women (≥35 years: mean = 88.4, SD = 16.5; <35 years: mean = 80.3, SD = 20.2) (p = 0.02). Sixty-one patients (N = 61; 61.0%; 95% CI: 50.7 - 70.4%) expressed willingness to continue using DRSP after breastfeeding.

Conclusion: Among those patients who continued the use of the DRSP only-pill for 5 months, this study shows no negative impact for new-borns, with no clinical influence observed on their growth. Additionally, those users expressed high satisfaction with the bleeding profile of the pill.Clinical trial registration number: DRKS00028438 .

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来源期刊
Gynecological Endocrinology
Gynecological Endocrinology 医学-妇产科学
CiteScore
4.40
自引率
5.00%
发文量
137
审稿时长
3-6 weeks
期刊介绍: Gynecological Endocrinology , the official journal of the International Society of Gynecological Endocrinology, covers all the experimental, clinical and therapeutic aspects of this ever more important discipline. It includes, amongst others, papers relating to the control and function of the different endocrine glands in females, the effects of reproductive events on the endocrine system, and the consequences of endocrine disorders on reproduction
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