Use of progestagens to preserve pregnancy: modern approaches

S. I. Zhuk, I. Us
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Abstract

Review objectives: to summarize current and clinical data on the role of progesterone support in women at risk of miscarriage and premature pregnancy according to the standards of evidence-based medicine. Control of plasma progesterone levels is a fundamental tool for managing the effectiveness of assisted reproductive technologies. The association of a low level of serum progesterone with lower rates of current pregnancy and live birth in cycles of assisted reproductive technologies was revealed. Patients with low serum progesterone on the day of embryo transfer need individualized support of the luteal phase, which involves adding additional doses of progesterone to standard regimens. Vaginal micronized progesterone is currently believed to be the only progestogen that increases the likelihood of a live birth in women with bleeding in early pregnancy which has one or more miscarriages. Vaginal progesterone can be considered for patients with a high risk of miscarriage in the following modes: with vaginal bleeding and a history of one or more miscarriages (threatened miscarriage) – 400 mg twice a day, starting with the detection of vaginal bleeding up to 16 full weeks of pregnancy; with a history of three or more pregnancy losses of unknown etiology (habitual miscarriage) – asymptomatic patients — 200 mg twice a day up to 12 full weeks of pregnancy; patients with vaginal bleeding – 400 mg 2 times a day up to 16 weeks of pregnancy. Currently, there is no evidence of the effectiveness other forms of progesterone and other doses. Conclusions. Vaginal micronized progesterone demonstrated: high efficiency as a standard of luteal phase support; increasing the chance of a live birth in women with a double risk factor for miscarriage (vaginal bleeding in the 1st trimester and ≥1 previous miscarriage); the absence of safety problems for the fetus and the health of newborns when used in the early and late stages of pregnancy.
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使用孕激素保胎:现代方法
综述目的:根据循证医学的标准,总结关于孕酮支持在流产和早孕风险妇女中的作用的当前和临床数据。控制血浆孕酮水平是管理辅助生殖技术有效性的基本工具。在辅助生殖技术周期中,血清孕酮水平低与当前妊娠率和活产率低有关。胚胎移植当天血清孕酮低的患者需要个性化的黄体期支持,这包括在标准方案的基础上增加额外剂量的孕酮。 目前,阴道微粒化黄体酮被认为是唯一一种能增加孕早期出血且有一次或多次流产的妇女活产可能性的孕激素。 在以下情况下,流产风险较高的患者可以考虑使用阴道黄体酮:阴道出血并有一次或多次流产史(威胁流产)--每天两次,每次 400 毫克,从发现阴道出血开始,直到怀孕满 16 周;有三次或三次以上不明原因的妊娠流产史(习惯性流产)--无症状患者 †"每天两次,每次 200 毫克,直到怀孕满 12 周;阴道出血患者--每天两次,每次 400 毫克,直到怀孕满 16 周。目前,还没有证据表明其他形式的黄体酮和其他剂量的黄体酮有效。 结论阴道用微粒化黄体酮证明了:作为黄体期支持的标准药物具有很高的效率;增加了具有流产双重危险因素(妊娠前三个月阴道出血和曾经流产过一次)的妇女活产的机会;在妊娠早期和晚期使用对胎儿和新生儿的健康没有安全问题。
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来源期刊
Reproductive Endocrinology
Reproductive Endocrinology Medicine-Obstetrics and Gynecology
CiteScore
0.50
自引率
0.00%
发文量
13
审稿时长
8 weeks
期刊最新文献
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