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复方庚酸炔诺酮注射液在早孕药物流产后即刻应用临床效果评价:基于子宫恢复与获益的前瞻性队列研究
高靖然, 孟文戈, 孙航宇, 杨舒棋, 王安冉, 姚晓英
中国实用妇科与产科杂志 ›› 2026, Vol. 42 ›› Issue (9) : 919-924.
PDF(932 KB)
PDF(932 KB)
复方庚酸炔诺酮注射液在早孕药物流产后即刻应用临床效果评价:基于子宫恢复与获益的前瞻性队列研究
Clinical efficacy evaluation of compound norethisterone enanthate injection immediately after medical abortion in early pregnancy:a prospective cohort study based on uterine recovery and benefit
目的 探讨早孕药物流产后即刻应用复方庚酸炔诺酮注射液对子宫恢复相关结局的影响。方法 采用双中心前瞻性队列研究设计,纳入2025年1月至2026年1月于复旦大学附属妇产科医院及徐州市妇幼保健院接受早孕药物流产且符合纳排标准的妇女139例。其中观察组69例,于药物流产后即刻注射复方庚酸炔诺酮注射液2 mL;对照组70例,流产后不使用任何激素避孕方法。比较两组药物流产后阴道流血持续时间、首次月经恢复时间、药物流产后2周及经后宫腔残留情况和清宫率。对药物流产后2周仍存在平均直径≤3 cm残留者进行亚组分析,并采用多因素logistic回归评估其转归的相关因素。结果 两组患者基线特征差异均无统计学意义。观察组首次月经恢复时间明显早于对照组[(25.51±6.77)d vs.(33.80±7.71)d,P<0.001]。观察组阴道流血持续时间≤2周的比例高于对照组(97.1% vs. 84.3%,P=0.021)。药物流产后2周复查时,观察组无宫腔残留比例高于对照组(44.9% vs. 27.1%,P=0.038),宫腔残留体积更小。经后复查,观察组无宫腔残留率显著高于对照组(76.8% vs. 55.7%,P=0.011)。观察组清宫率低于对照组(1.4% vs. 7.1%),但差异无统计学意义。在药物流产后2周仍存在平均直径≤3 cm残留者中,经后复查,观察组和对照组组内转阴率差异均有统计学意义(P<0.05);随访结束时,观察组宫腔恢复正常比例高于对照组(59.5% vs. 43.5%)。多因素分析显示,阴道流血持续时间>2周与平均直径≤3 cm残留转阴概率降低相关(aOR 0.08,95%CI 0.01~0.68,P=0.021)。结论 早孕药物流产后即刻应用复方庚酸炔诺酮注射液,阴道流血持续时间短、月经恢复快、宫腔残留更小、经后宫腔恢复正常比例更高。在落实流产后避孕的同时,该方案可能对药物流产后的宫腔恢复具有额外获益。
Objective To investigate the effect of immediate administration of compound norethisterone enanthate injection after medical abortion in early pregnancy on uterine recovery-related outcomes. Methods A dual-center,prospective cohort study design was adopted,enrolling 139 patients who underwent early-pregnancy medical abortion at the Obstetrics and Gynecology Hospital of Fudan University and Xuzhou Maternal and Child Health Hospital between January 2025 and January 2026 and met the inclusion and exclusion criteria. The observation group(n=69)received 2 mL of compound norethisterone enanthate injection immediately after medical abortion;the control group(n=70)did not use any hormonal contraception after abortion. The duration of vaginal bleeding after medical abortion,time to first menstruation,residual uterine tissue at 2 weeks after medical abortion,and curettage rate were compared between the two groups. Subgroup analysis was performed on patients with residual tissue of average diameter ≤3 cm at 2 weeks after-abortion,and multivariate logistic regression was used to assess the relevant factors for their outcome. Results There were no statistically significant differences in baseline characteristics between the two groups. The first menstrual period returned significantly earlier in the observation group than in the control group [(25.51±6.77)days vs.(33.80±7.71)days,P<0.001]. The proportion of vaginal bleeding lasting ≤2 weeks was higher in the observation group than in the control group(97.1% vs. 84.3%,P=0.021). At the 2-week follow-up after medical abortion,the proportion of no retained products of conception was higher in the observation group than in the control group(44.9% vs. 27.1%,P=0.038),and the retained product volume was smaller. At the post-menstrual follow-up,the rate of no retained products of conception was significantly higher in the observation group than in the control group(76.8% vs. 55.7%,P=0.011). The curettage rate was lower in the observation group than in the control group(1.4% vs. 7.1%),but the difference was not statistically significant. In patients with residual tissue of average diameter ≤3 cm at two weeks after medical abortion,the negative conversion rate was statistically significant in both the observation and control groups upon follow-up(P<0.05). At the end of follow-up,the proportion of patients with normal uterine cavity recovery was higher in the observation group than in the control group(59.5% vs. 43.5%). Multivariate analysis showed that vaginal bleeding duration >2 weeks was associated with a decreased probability of negative conversion of residual tissue of average diameter ≤3 cm(aOR 0.08,95%CI 0.01-0.68,P=0.021). Conclusions Immediate administration of compound norethisterone enanthate injection in early pregnancy after medical abortion results in shorter duration of vaginal bleeding,faster menstrual recovery,smaller residual tissue,and a higher proportion of normal uterine cavity recovery after menstruation. This regimen may provide additional benefits to uterine cavity recovery after medical abortion in addition to implementing post-abortion contraception.
药物流产 / 流产后避孕 / 复方庚酸炔诺酮注射液 / 宫腔残留 / 前瞻性队列研究
medical abortion / post-abortion contraception / compound norethisterone enanthate injection / residual tissue / prospective cohort study
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Medication abortion, also referred to as medical abortion, is a safe and effective method of providing abortion. Medication abortion involves the use of medicines rather than uterine aspiration to induce an abortion. The U.S. Food and Drug Administration (FDA)-approved medication abortion regimen includes mifepristone and misoprostol. The purpose of this document is to provide updated evidence-based guidance on the provision of medication abortion up to 70 days (or 10 weeks) of gestation. Information about medication abortion after 70 days of gestation is provided in other ACOG publications (1).
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Numerous studies have been performed assessing optimal treatment regimens for evacuating (retained) products of conception from the uterus, but standardized criteria for diagnosing retained products of conception (RPOC) are still lacking. We aim to provide an overview of diagnostic criteria in current literature, used to diagnose RPOC after induced first‐trimester abortion or early pregnancy loss.
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Medical abortion (using mifepristone followed by misoprostol to end an early pregnancy) is a more accessible and less invasive option than surgical termination and can be provided in primary care settings. However, few general practitioners (GPs) currently provide this service, and there remains great inequity in access to abortion across Australia, particularly for young women and those living in rural and remote area.The aim of this article is to help Australian GPs better understand the practical and legal considerations of providing medical abortion to patients.Provision of medical abortion is well within the scope of community general practice and improves the comprehensiveness of women's sexual and reproductive health services that GPs can deliver. This article will help GPs to better understand the process involved in providing medical abortion, including the practical considerations for patients; be better equipped to support patients who have decided that medical abortion is an appropriate choice for them; and make an informed decision as to whether to become a provider of medical abortion.
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To clarify the natural history of retained products of conception (RPOC) following abortion at less than 22 weeks of gestation, and those who show major bleeding during course observation.We retrospectively reviewed 640 patients who had spontaneous or artificial abortion at less than 22 weeks of gestation between January 2011 and August 2019 in our institute. Of those, patients with RPOC were included. The maternal background, RPOC characteristics, and subsequent complications including additional interventions were reviewed.Fifty-four patients with RPOC were included. The incidence of RPOC was 6.7 %. The median (interquartile range: IQR) RPOC length was 29 (20-38) mm. RPOC hypervascularity was observed in 26 (48 %) patients. The median (IQR) periods of RPOC flow disappearance and RPOC disappearance on ultrasound from abortive treatment were 50 (28-76) and 84 (50-111) days, respectively. Of the 54, 44 patients were selected for expectant management. Of the 44, 34 (77 %) patients were observed without intervention (recovery group); the other 10 (23 %) patients required additional interventions associated with subsequent bleeding (intervention group). Compared with the recovery group, heavy bleeding (> 500 mL) at abortion (6/10: 60 %) and RPOC hypervascularity (8/10: 80 %) were more frequently observed in the intervention group.Expectant management was successful in almost 80 % of patients with RPOC following abortion. The additional interventions were required in patients with heavy bleeding at abortion and RPOC hypervascularity.Copyright © 2021 Elsevier B.V. All rights reserved.
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