Stephenson Mary D, McQueen Dana, Winter Michelle, Kliman Harvey J
University of Illinois Recurrent Pregnancy Loss Program, Department of Obstetrics and Gynecology, University of Illinois at Chicago, Chicago, Illinois; University of Chicago, Chicago, Illinois.
University of Illinois Recurrent Pregnancy Loss Program, Department of Obstetrics and Gynecology, University of Illinois at Chicago, Chicago, Illinois.
Fertil Steril. 2017 Mar;107(3):684-690.e2. doi: 10.1016/j.fertnstert.2016.11.029. Epub 2017 Jan 9.
To assess the effectiveness of luteal start vaginal micronized P in a recurrent pregnancy loss (RPL) cohort.
Observational cohort study using prospectively collected data.
Not applicable.
PATIENT(S): Women seen between 2004 and 2012 with a history of two or more unexplained pregnancy losses <10 weeks in size; endometrial biopsy (EB) performed 9-11 days after LH surge; and one or more subsequent pregnancy(ies). Women were excluded if concomitant findings, such as endometritis, maturation delay, or glandular-stromal dyssynchrony, were identified on EB.
INTERVENTION(S): Vaginal micronized P was prescribed at a dose of 100-200 mg every 12 hours starting 3 days after LH surge (luteal start) if glandular epithelial nuclear cyclin E (nCyclinE) expression was elevated (>20%) in endometrial glands or empirically despite normal nCyclinE (≤20%). Women with normal nCyclinE (≤20%) who did not receive P were used as controls.
MAIN OUTCOME MEASURE(S): Pregnancy success was an ongoing pregnancy >10 weeks in size.
RESULT(S): One hundred sixteen women met the inclusion criteria, of whom 51% (n = 59) had elevated nCyclinE and 49% (n = 57) had normal nCyclinE. Pregnancy success in the 59 women with elevated nCyclinE significantly improved after intervention: 6% (16/255) in prior pregnancies versus 69% (57/83) in subsequent pregnancies. Pregnancy success in subsequent pregnancies was higher in women prescribed vaginal micronized P compared with controls: 68% (86/126) versus 51% (19/37); odds ratio = 2.1 (95% confidence interval, 1.0-4.4).
CONCLUSION(S): In this study, we found that the use of luteal start vaginal micronized P was associated with improved pregnancy success in a strictly defined cohort of women with RPL.
评估黄体期起始阴道用微粒化孕酮在复发性流产(RPL)队列中的有效性。
使用前瞻性收集数据的观察性队列研究。
不适用。
2004年至2012年间就诊的女性,有两次或更多次孕龄小于10周的不明原因流产史;在促黄体生成素(LH)峰后9 - 11天进行子宫内膜活检(EB);以及有一次或更多次后续妊娠。如果在EB中发现诸如子宫内膜炎、成熟延迟或腺-间质不同步等伴随发现,则将女性排除。
如果子宫内膜腺上皮细胞核周期蛋白E(nCyclinE)表达升高(>20%)或尽管nCyclinE正常(≤20%)但根据经验,在LH峰后3天(黄体期起始)开始每12小时阴道给予100 - 200mg微粒化孕酮。nCyclinE正常(≤20%)且未接受孕酮治疗的女性作为对照。
妊娠成功定义为孕龄大于10周的持续妊娠。
116名女性符合纳入标准,其中51%(n = 59)nCyclinE升高,49%(n = 57)nCyclinE正常。干预后,59名nCyclinE升高的女性的妊娠成功率显著提高:既往妊娠为6%(16/255),后续妊娠为69%(57/83)。与对照组相比,接受阴道微粒化孕酮治疗的女性后续妊娠的妊娠成功率更高:68%(86/126)对51%(19/37);优势比 = 2.1(95%置信区间,1.0 - 4.4)。
在本研究中,我们发现黄体期起始阴道用微粒化孕酮的使用与严格定义的RPL女性队列中妊娠成功率的提高相关。