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Emotional freedom techniques-based counseling with breathing exercises in in vitro fertilization: effects on psychological distress and well-being 基于情绪自由技术的体外受精呼吸练习咨询:对心理困扰和健康的影响
IF 1.9 4区 医学 Q2 OBSTETRICS & GYNECOLOGY Pub Date : 2025-12-13 DOI: 10.1016/j.ejogrb.2025.114891
Merve Coşkun , Ergül Aslan

Purpose

To investigate whether psychosocial care during in vitro fertilization (IVF) treatment affects the emotional capacity and well-being of women undergoing fertility treatment.

Methods

This randomized controlled, single-blind study was conducted between February 2020 and March 2021. A total of 112 women undergoing IVF were recruited based on predefined inclusion and exclusion criteria. After a 24.1 % loss to follow-up (n = 27), data from 85 participants (42 in the experimental group, 43 in the control group) were analyzed. The control group received routine care, while the intervention group attended a structured seven-session counseling program that included coping strategies such as Emotional Freedom Technique (EFT) and breathing exercises. Psychological outcomes were measured at three time points using Screening Tool on Distress in Fertility Treatment (SCREENIVF), Fertility Quality of Life Tool (FertiQol), COMPI Fertility Problem Stress Scales (COMPI-FPSS), and Subjective Units of Distress (SUD) scale. Group comparisons were analyzed with appropriate statistical methods.

Results

Baseline characteristics did not differ between groups (p > 0.05). The experimental group had a higher positive hCG rate on day + 13 of IVF (42.9 % vs. 18.6 %, p = 0.015). Post-intervention, they showed greater reductions in anxiety (Cohen’s d = –0.72, 95 % CI [–1.15 to –0.28], p = 0.001) and helplessness (Cohen’s d = 1.26, 95 % CI [0.79–1.72], p < 0.001), and increased acceptance (p < 0.001), while depression decreased non-significantly (p = 0.167). Personal and social stress decreased (Cohen’s d = –0.99, 95 % CI [–1.43 to –0.54], p < 0.001; social domain p = 0.003), but marital stress did not (p = 0.619). FertiQOL total and Treatment Environment scores improved (Cohen’s d = –1.89, 95 % CI [–2.39 to –1.39], p < 0.001; Cohen’s d = –1.71, 95 % CI [–2.20 to –1.22], p < 0.001), whereas Treatment Tolerance did not differ (p = 0.001). SUD scores decreased after sessions 2, 4, and 5 (r = –0.62 to –0.63, 95 % CI [–0.77 to –0.46], p < 0.001). Effect sizes indicate medium to large clinical relevance. Participants at risk per SCREENIVF showed marked stress reduction and improved quality of life, with referrals to mental health services as needed.

Conclusion

Psychosocial care during IVF treatment appears to reduces psychological distress and enhances treatment-related well-being in women undergoing fertility procedures. These findings support the incorporation of psychosocial interventions into standard fertility care.
目的探讨体外受精(IVF)治疗期间的心理社会护理是否会影响接受生育治疗的妇女的情绪能力和幸福感。方法本研究于2020年2月至2021年3月进行随机对照单盲研究。根据预先确定的纳入和排除标准,总共招募了112名接受体外受精的妇女。在随访损失24.1% (n = 27)后,对85名参与者(实验组42人,对照组43人)的数据进行分析。对照组接受常规护理,而干预组参加了一个结构化的七期咨询项目,包括情绪释放技巧(EFT)和呼吸练习等应对策略。在三个时间点使用生育治疗痛苦筛选工具(SCREENIVF)、生育生活质量工具(FertiQol)、COMPI生育问题压力量表(COMPI- fpss)和主观痛苦单位量表(SUD)测量心理结果。采用适当的统计学方法进行组间比较。结果两组患者基线特征无差异(p > 0.05)。试验组体外受精第13天hCG阳性率较高(42.9% vs. 18.6%, p = 0.015)。干预后,他们表现出焦虑(Cohen 's d = -0.72, 95% CI[-1.15至-0.28],p = 0.001)和无助(Cohen 's d = 1.26, 95% CI [0.79-1.72], p < 0.001)的显著减少,接受度增加(p < 0.001),而抑郁则无显著减少(p = 0.167)。个人和社会压力下降(Cohen 's d = -0.99, 95% CI [-1.43 ~ -0.54], p < 0.001;社会领域p = 0.003),但婚姻压力没有下降(p = 0.619)。FertiQOL总分和治疗环境评分均有改善(Cohen’s d = -1.89, 95% CI[-2.39至-1.39],p < 0.001; Cohen’s d = -1.71, 95% CI[-2.20至-1.22],p < 0.001),而治疗耐受性无差异(p = 0.001)。在第2、4和5次治疗后,SUD评分下降(r = -0.62至-0.63,95% CI[-0.77至-0.46],p < 0.001)。效应量表明中等到较大的临床相关性。每筛检试管婴儿风险的参与者表现出明显的压力减轻和生活质量提高,并根据需要转介到心理健康服务。结论体外受精治疗期间的社会心理护理似乎可以减少心理困扰,提高接受生育手术妇女的治疗相关幸福感。这些发现支持将社会心理干预纳入标准生育护理。
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引用次数: 0
Training and assessment of competencies in hysteroscopy – A systematic review 宫腔镜技能的培训和评估——系统综述。
IF 1.9 4区 医学 Q2 OBSTETRICS & GYNECOLOGY Pub Date : 2025-12-11 DOI: 10.1016/j.ejogrb.2025.114890
Karen Høgh Abrahamsen , Martine Siw Nielsen , Nicolaj Bruun Brandt , Anders Bo Nielsen , Lars Konge , Margit Dueholm , Pernille Ravn

Objective

Hysteroscopy is a core gynecological competence, acquired by training. Simulation training offers safe competence acquisition, but requires resource-efficient, clinically transferable approaches. Current hysteroscopic training curricula lack standardized assessment and validated pass-fail criteria. This review synthesizes evidence to inform optimized training and robust competency assessment.

Methods

Five databases were systematically searched on June 2nd 2025. Studies assessing hysteroscopy training and skills assessment were included without restrictions on population, study design, or publication year. Data extraction was performed using Covidence. Outcomes were evaluated with Kirkpatrick’s levels and quality assessment was evaluated with the Medical Education Research Study Quality Instrument (MERSQI).

Results

A total of 39 studies, 36 prospective cohort studies (92 %) and 3 RCTs (8 %), met the inclusion criteria. Studies used animal (13 %), inanimate (33 %), virtual reality (39 %), and combinations of models (15 %). Training approaches varied, with numbers-based training being most common (74 %). Outcomes were primarily evaluated with pre-post testing (41 %) and self-assessment (28 %). All studies reported improved performance, especially in novices, with either pre- and posttests or questionnaires. Study quality varied, with a mean MERSQI of 11.3 (range 5–16, of possible 5–18). Only one RCT showed clinical transferability.

Conclusion

Simulation-based training enhances hysteroscopic competencies. Despite methodological variability, evidence supports structured curricula combining theory, hands-on training, and pass-fail-based progression. A combination of virtual reality with tactile feedback seems optimal. Overall evidence failed to establish optimized training and robust competency assessment. Future research should include high-quality studies, patient-level outcomes, and updated validity frameworks to decide how to optimize training effectively.
目的:宫腔镜是一项核心的妇科技能,通过培训获得。模拟训练提供了安全的能力获取,但需要资源高效,临床可转移的方法。目前的宫腔镜培训课程缺乏标准化的评估和有效的及格-不及格标准。这篇综述综合证据,为优化培训和健全的能力评估提供信息。方法:于2025年6月2日系统检索5个数据库。评估宫腔镜培训和技能评估的研究纳入,不受人群、研究设计或发表年份的限制。使用Covidence进行数据提取。采用Kirkpatrick's水平评价结果,采用医学教育研究质量工具(MERSQI)评价质量评价。结果:共有39项研究,36项前瞻性队列研究(92%)和3项随机对照试验(8%)符合纳入标准。研究使用了动物(13%)、无生命(33%)、虚拟现实(39%)和模型组合(15%)。培训方法多种多样,以数字为基础的培训最为常见(74%)。结果主要通过前后测试(41%)和自我评估(28%)进行评估。通过前后测试或问卷调查,所有的研究都报告了表现的改善,尤其是在新手中。研究质量各不相同,平均MERSQI为11.3(范围5-16,可能为5-18)。只有一项RCT显示临床可转移性。结论:模拟训练增强了宫腔镜检查能力。尽管方法上存在差异,但证据支持将理论、实践训练和及格-不及格-递进相结合的结构化课程。虚拟现实与触觉反馈的结合似乎是最佳选择。总体证据未能建立优化的培训和健全的能力评估。未来的研究应包括高质量的研究、患者水平的结果和更新的效度框架,以决定如何有效地优化训练。
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引用次数: 0
Ferric carboxymaltose for third-trimester refractory anemia and perinatal outcomes: Retrospective cohort analysis 羧基麦芽糖铁治疗妊娠晚期难治性贫血和围产期结局:回顾性队列分析
IF 1.9 4区 医学 Q2 OBSTETRICS & GYNECOLOGY Pub Date : 2025-12-11 DOI: 10.1016/j.ejogrb.2025.114887
Şebnem Karagün , Hamza Yıldız , Yusuf Dal , Sefanur Gamze Karaca , Hatice Banu Atay , Mürşide Çevikoğlu Kıllı , Ayhan Coşkun

Background

Iron deficiency anemia (IDA) in the third trimester is associated with adverse perinatal outcomes, but data on intravenous ferric carboxymaltose (FCM) effects beyond hematologic response remain limited.

Methods

This retrospective cohort study, conducted at Mersin University Hospital (January 2019 – March 2024), included 311 pregnant women diagnosed with IDA in the third trimester who were clinically recommended FCM therapy due to inadequate response to oral ferrous sulfate. Among these, 206 accepted FCM treatment (in addition to continued oral iron) while 105 declined and received oral iron alone. Women were compared as two groups: those who received oral iron alone versus those who received oral iron plus a single-dose FCM in the third trimester,. At four timepoints (baseline, post-FCM, delivery, and postpartum), hemoglobin (Hgb), hematocrit, MCV, and MCHC levels were evaluated. The primary outcome was maternal perinatal hemoglobin response, while the secondary outcome was the investigation of its correlation with key neonatal outcomes following FCM administration. Repeated measures ANOVA, two-way ANOVA, and correlation analyses were used.

Results

The FCM group showed significantly higher Hgb levels at baseline, delivery, and postpartum (all p < 0.05). Birth weight (3164 ± 564 g vs. 2952 ± 691 g, p = 0.007), umblical cord blood pH (7.34 ± 0.04 vs. 7.28 ± 0.03, p < 0.001), and Apgar scores were also improved in the FCM group. Neonatal intensive care unit (NICU) admission was significantly reduced (20.9 % vs. 31.4 %, p = 0.041), as was the incidence of fetal growth restriction (16.5 % vs. 38.1 %, p < 0.001). In the FCM group, changes in Hgb from post-FCM to postpartum were positively correlated with 1-minute Apgar scores (r = 0.177, p = 0.011). Neonates requiring NICU admission showed an attenuated rise in Hgb across the same interval (p = 0.041), and women with adverse composite outcomes had greater Hgb fluctuation, particularly from delivery to postpartum (p = 0.020).

Conclusion

Third-trimester FCM therapy leads to superior hematologic correction and improved neonatal outcomes compared to oral iron alone. Hemoglobin recovery patterns after FCM may be predictive of neonatal adaptation and adverse outcomes, highlighting the broader perinatal significance of timely parenteral iron therapy in late pregnancy.
背景:妊娠晚期缺铁性贫血(IDA)与不良的围产期结局相关,但静脉注射羧基麦尔糖铁(FCM)除血液学反应外的影响数据仍然有限。该回顾性队列研究于2019年1月至2024年3月在梅尔辛大学医院进行,纳入了311名妊娠晚期诊断为IDA的孕妇,这些孕妇因口服硫酸亚铁反应不足,临床推荐FCM治疗。其中206例接受FCM治疗(外加继续口服铁),105例下降并仅接受口服铁治疗。将妇女分为两组进行比较:在妊娠晚期单独接受口服铁剂的妇女和接受口服铁剂加单剂量FCM的妇女。在四个时间点(基线、fcm后、分娩和产后),评估血红蛋白(Hgb)、红细胞压积、MCV和MCHC水平。主要结局是母体围产期血红蛋白反应,而次要结局是FCM给药后其与关键新生儿结局的相关性。采用重复测量方差分析、双向方差分析和相关分析。结果FCM组在基线、分娩和产后Hgb水平均显著升高(p < 0.05)。FCM组新生儿出生体重(3164±564 g比2952±691 g, p = 0.007)、脐带血pH值(7.34±0.04比7.28±0.03,p < 0.001)、Apgar评分均有改善。新生儿重症监护病房(NICU)住院率显著降低(20.9% vs. 31.4%, p = 0.041),胎儿生长受限发生率显著降低(16.5% vs. 38.1%, p < 0.001)。FCM组FCM后至产后Hgb变化与1分钟Apgar评分呈正相关(r = 0.177, p = 0.011)。需要入住NICU的新生儿Hgb在相同的时间间隔内上升减弱(p = 0.041),复合结局不良的妇女Hgb波动更大,特别是从分娩到产后(p = 0.020)。结论妊娠晚期FCM治疗与单纯口服铁相比,具有更好的血液学矫正和新生儿预后。FCM后血红蛋白恢复模式可能预测新生儿适应和不良结局,强调妊娠后期及时肠外铁治疗的围产期意义。
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引用次数: 0
Efficacy and safety of relugolix therapy for symptomatic uterine fibroids: a systematic review and meta-analysis 瑞路高利治疗症状性子宫肌瘤的疗效和安全性:一项系统综述和荟萃分析
IF 1.9 4区 医学 Q2 OBSTETRICS & GYNECOLOGY Pub Date : 2025-12-11 DOI: 10.1016/j.ejogrb.2025.114889
FNU Kalpina , Dinesh Kumar , Javeria Taj , Manal Kaleem , Tabia Shujaat , Maimoona Qayyum , Laiba Jabeen , Ahmed Raza , Muhammad Shaheer Bin Faheem

Introduction

Uterine fibroids are the most common benign tumors in premenopausal women and often necessitate fertility-sparing treatments. Relugolix, an oral GnRh antagonist has emerged as a promising non-surgical option. This systematic review and meta-analysis evaluate the efficacy and safety of relugolix for symptomatic uterine fibroids.

Methods

We searched PubMed, Embase, Cochrane CENTRAL, Scopus, and ClinicalTrials.gov through March 2025. Six studies (n = 511) were included in accordance with the PRISMA guidelines. Data were analysed using random-effects models in R (v4.5.0). Risk of Bias was assessed using ROB 2 tool. Continuous outcomes were reported as mean differences (MDs), dichotomous outcomes as odds ratios (ORs) or proportions, and heterogeneity using I2 statistics, with sensitivity analyses for I2 ≥ 50 %.

Results

Pooled analysis revealed a myoma volume reduction (MVR) of −30.18 %, with similar findings when compared to placebo (−28.50 %; p-value = 0.0070). Uterine volume decreased by −27.22 %. When compared with placebo, uterine volume significantly reduced by −30.31 (p-value = 0.0028). Amenorrhea was achieved by 63 % of patients, with relugolix-treated patients showing 31-fold higher odds versus controls (31.07 %; p-value < 0.0001). Haemoglobin levels improved in 46.3 % patients, while relugolix-treated patients achieved significant pain relief compared to controls (OR 9.02; p = value < 0.0001). Subgroup analyses showed that relugolix monotherapy produced greater reductions in myoma and uterine volumes than combination therapy, although both regimens were effective.
Treatment as generally well-tolerated, with hot flushes being the most common adverse event. A small proportion reported persistent menorrhagia without indicating treatment failure. Other adverse events, such as headache, were also reported, though discontinuation rates were comparable to controls.

Conclusion

Relugolix significantly reduces fibroid burden and symptoms with favourable safety profile. It offers a well-tolerated, fertility-preserving alternative to surgery. Further large-scale RCTs are needed to confirm these findings and optimize treatment protocols.
子宫肌瘤是绝经前妇女最常见的良性肿瘤,通常需要保留生育能力的治疗。口服GnRh拮抗剂Relugolix已成为一种有希望的非手术选择。本系统综述和荟萃分析评价了瑞路高利治疗症状性子宫肌瘤的疗效和安全性。方法:我们检索了PubMed、Embase、Cochrane CENTRAL、Scopus和ClinicalTrials.gov,检索截止日期为2025年3月。根据PRISMA指南纳入了6项研究(n = 511)。使用R (v4.5.0)中的随机效应模型分析数据。使用ROB 2工具评估偏倚风险。连续结果报告为平均差异(MDs),二分类结果报告为优势比(ORs)或比例,使用I2统计数据报告异质性,I2≥50%时进行敏感性分析。结果spoold分析显示,与安慰剂相比,肌瘤体积减少(MVR)为- 30.18%,结果相似(- 28.50%,p值= 0.0070)。子宫体积减少- 27.22%。与安慰剂组相比,子宫体积显著缩小- 30.31 (p值= 0.0028)。63%的患者实现了闭经,接受瑞路戈利斯治疗的患者的几率比对照组高31倍(31.07%;p值<; 0.0001)。46.3%的患者血红蛋白水平改善,而接受瑞路高利治疗的患者与对照组相比,疼痛得到显著缓解(OR 9.02; p = value < 0.0001)。亚组分析显示,瑞路高利单药治疗比联合治疗更能减少肌瘤和子宫体积,尽管两种治疗方案都有效。治疗一般耐受良好,潮热是最常见的不良事件。一小部分报告持续月经过多,但没有表明治疗失败。其他不良事件,如头痛,也有报道,尽管停药率与对照组相当。结论瑞路高利可显著减轻肌瘤负担和症状,且安全性良好。它提供了一种耐受良好、保留生育能力的手术替代方案。需要进一步的大规模随机对照试验来证实这些发现并优化治疗方案。
{"title":"Efficacy and safety of relugolix therapy for symptomatic uterine fibroids: a systematic review and meta-analysis","authors":"FNU Kalpina ,&nbsp;Dinesh Kumar ,&nbsp;Javeria Taj ,&nbsp;Manal Kaleem ,&nbsp;Tabia Shujaat ,&nbsp;Maimoona Qayyum ,&nbsp;Laiba Jabeen ,&nbsp;Ahmed Raza ,&nbsp;Muhammad Shaheer Bin Faheem","doi":"10.1016/j.ejogrb.2025.114889","DOIUrl":"10.1016/j.ejogrb.2025.114889","url":null,"abstract":"<div><h3>Introduction</h3><div>Uterine fibroids are the most common benign tumors in premenopausal women and often necessitate fertility-sparing treatments. Relugolix, an oral GnRh antagonist has emerged as a promising non-surgical option. This systematic review and meta-analysis evaluate the efficacy and safety of relugolix for symptomatic uterine fibroids.</div></div><div><h3>Methods</h3><div>We searched PubMed, Embase, Cochrane CENTRAL, Scopus, and <span><span>ClinicalTrials.gov</span><svg><path></path></svg></span> through March 2025. Six studies (n = 511) were included in accordance with the PRISMA guidelines. Data were analysed using random-effects models in R (v4.5.0). Risk of Bias was assessed using ROB 2 tool. Continuous outcomes were reported as mean differences (MDs), dichotomous outcomes as odds ratios (ORs) or proportions, and heterogeneity using I<sup>2</sup> statistics, with sensitivity analyses for I<sup>2</sup> ≥ 50 %.</div></div><div><h3>Results</h3><div>Pooled analysis revealed a myoma volume reduction (MVR) of −30.18 %, with similar findings when compared to placebo (−28.50 %; p-value = 0.0070). Uterine volume decreased by −27.22 %. When compared with placebo, uterine volume significantly reduced by −30.31 (p-value = 0.0028). Amenorrhea was achieved by 63 % of patients, with relugolix-treated patients showing 31-fold higher odds versus controls (31.07 %; p-value &lt; 0.0001). Haemoglobin levels improved in 46.3 % patients, while relugolix-treated patients achieved significant pain relief compared to controls (OR 9.02; p = value &lt; 0.0001). Subgroup analyses showed that relugolix monotherapy produced greater reductions in myoma and uterine volumes than combination therapy, although both regimens were effective.</div><div>Treatment as generally well-tolerated, with hot flushes being the most common adverse event. A small proportion reported persistent menorrhagia without indicating treatment failure. Other adverse events, such as headache, were also reported, though discontinuation rates were comparable to controls.</div></div><div><h3>Conclusion</h3><div>Relugolix significantly reduces fibroid burden and symptoms with favourable safety profile. It offers a well-tolerated, fertility-preserving alternative to surgery. Further large-scale RCTs are needed to confirm these findings and optimize treatment protocols.</div></div>","PeriodicalId":11975,"journal":{"name":"European journal of obstetrics, gynecology, and reproductive biology","volume":"318 ","pages":"Article 114889"},"PeriodicalIF":1.9,"publicationDate":"2025-12-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145735920","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Tubal patency testing in women with polycystic ovary syndrome − is it worth before ovarian induction: Cost-effectiveness analysis 多囊卵巢综合征妇女输卵管通畅检查-卵巢诱导前是否值得:成本-效果分析
IF 1.9 4区 医学 Q2 OBSTETRICS & GYNECOLOGY Pub Date : 2025-12-10 DOI: 10.1016/j.ejogrb.2025.114888
Magdalena Piróg , Bartosz Chrostowski , Robert Jach

Background

Polycystic ovarian syndrome (PCOS) is related to infertility due to anovulatory cycles. However, it is unknown whether women with PCOS are at higher risk of tubal factor of infertility.

Objectives

This study sought to investigate the diagnostic accuracy of hysterosalpingo-foam sonography (HyFoSy) in women with polycystic ovarian syndrome (PCOS) before initiation of ovarian induction (OI)?

Study design:

We studied 432 infertile women in two groups: 1) with PCOS (n = 216) and 2) without PCOS (n = 216) which served as the controls. Data analysis included basic clinical parameters, duration of infertility, history of previous abdominal surgeries, pelvic inflammatory disease (PID), ectopic pregnancy (EP) and smoking status. The primary outcome of this study was the evaluation of the tubal patency testing outcomes in women with PCOS and compare it to women without ovulatory disorders. Secondary outcome was a cost-effectiveness analysis focused on direct medical costs related to chosen therapeutic models: 1) primary 3 cycles of OI and 2) HyFoSy followed by 3 cycles of OI if at least one tube was patent.

Results

Women with PCOS had higher number of previous abdominal surgeries (+23.1 %) compared to the controls, with no differences in previously diagnosed either PID or EP and smoking. Bilateral tubal blockage was observed in 5 % of women with PCOS which was comparable to women without ovulatory disorders (4.2 %, p > 0.05). Regarding risk factors for blockage, among PCOS women at least one risk factor such as previous abdominal surgery, history of PID, EP or smoking were observed in 81.8 % (n = 9) participants with bilateral blocked tubes, 63.2 % (n = 12) in unilateral blocked group and 23.1 % (n = 43) participants with both patent tubes. The mean total costs per women were lower in Model 1 compared to Model 2 ($61 vs. $364, respectively). Implementation of HyFoSy in women with PCOS without risk factors of tubal blockage is not worth the extra cost and prolong the time to pregnancy.

Conclusion

A treatment model starting with OI before HyFoSY is cost-effective compared to the model with HyFoSY performed before OI. Tubal factor is present in 5% of woman with PCOS which is comparable to infertile women without ovulatory disorders.
背景:多囊卵巢综合征(PCOS)与无排卵周期导致的不孕有关。然而,目前尚不清楚患有多囊卵巢综合征的女性是否有更高的输卵管因素导致不孕的风险。目的探讨子宫输卵管泡沫超声(HyFoSy)在卵巢诱导(OI)前诊断多囊卵巢综合征(PCOS)的准确性。研究设计:我们将432名不孕妇女分为两组:1)有PCOS (n = 216)和2)无PCOS (n = 216)作为对照。数据分析包括基本临床参数、不孕持续时间、既往腹部手术史、盆腔炎(PID)、异位妊娠(EP)和吸烟状况。本研究的主要结果是评估多囊卵巢综合征女性的输卵管通畅测试结果,并将其与无排卵障碍的女性进行比较。次要结局是成本-效果分析,重点是与所选治疗模式相关的直接医疗费用:1)最初的3个成骨不全周期,2)如果至少有一个管是专利的,HyFoSy随后是3个成骨不全周期。结果与对照组相比,PCOS患者既往腹部手术次数较高(+ 23.1%),既往诊断的PID或EP和吸烟均无差异。5%的PCOS女性出现双侧输卵管阻塞,与无排卵障碍的女性相当(4.2%,p > 0.05)。关于阻塞的危险因素,在PCOS女性中,81.8% (n = 9)的双侧管道阻塞组,63.2% (n = 12)的单侧管道阻塞组和23.1% (n = 43)的双侧管道通畅组中至少有一项危险因素,如既往腹部手术,PID, EP或吸烟史。与模型2相比,模型1中每位女性的平均总成本更低(分别为61美元和364美元)。在没有输卵管堵塞危险因素的PCOS女性中实施HyFoSy并不值得额外的费用和延长怀孕时间。结论:与在成骨不全之前进行HyFoSY的治疗模式相比,在成骨不全之前进行HyFoSY的治疗模式更具成本效益。输卵管因子存在于5%的多囊卵巢综合征妇女中,与无排卵障碍的不孕妇女相当。
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引用次数: 0
Characteristics of ovarian stimulation in adolescents and young adults undergoing fertility preservation 保持生育能力的青少年和年轻成人卵巢刺激的特点。
IF 1.9 4区 医学 Q2 OBSTETRICS & GYNECOLOGY Pub Date : 2025-12-10 DOI: 10.1016/j.ejogrb.2025.114886
Tiffany Brun , Marie Sineux , Vincent Lavoué , Ludivine Dion , Jean Levêque , Solène Duros

Purpose

To compare the ovarian response to controlled ovarian hyperstimulation (COH) performed for fertility preservation (FP) in adolescents and young adults (AYA) aged ≤20 years with that of adult women aged 25–35 years.

Materials and Methods

This retrospective cohort study included 66 COH cycles in AYA patients (≤20 years) and 107 cycles in adults (25–35 years) treated between January 2014 and March 2022 for oocyte vitrification. Outcomes assessed included the number of mature oocytes vitrified, total oocytes retrieved, total rFSH dose, peak estradiol levels, maturation rate, and duration of stimulation.

Results

Groups were comparable regarding BMI, smoking status, AMH, stimulation protocol, and gonadotropin type. Median number of mature oocytes was not statistically different between groups: (9.5 (AYA) vs. 9.0 (A), p = 80.19). The maturation index was significantly lower in AYA (0.80 vs. 0.88, p = 80.02). Peak estradiol was lower in AYA (1267 pg/mL vs. 1582 pg/mL, p = 80.04). Other stimulation parameters were similar.

Conclusion

Fertility preservation through COH in adolescents and young adults appears as effective as in adult women in terms of mature oocyte yield. Nevertheless, AYA patients exhibit a lower oocyte maturation rate and lower peak estradiol levels. Larger studies are needed to confirm these findings and better characterise age-related physiological differences in ovarian response.
目的:比较年龄≤20岁的青少年和青壮年(AYA)与25-35岁成年女性为保持生育能力(FP)而进行的控制性卵巢过度刺激(COH)的卵巢反应。材料和方法:本回顾性队列研究包括2014年1月至2022年3月期间接受卵母细胞玻璃化治疗的AYA患者(≤20岁)66个COH周期和成人(25-35岁)107个周期。评估的结果包括玻璃化的成熟卵母细胞数量、回收的卵母细胞总数、rFSH总剂量、雌二醇峰值水平、成熟率和刺激持续时间。结果:各组在BMI、吸烟状况、AMH、刺激方案和促性腺激素类型方面具有可比性。两组成熟卵母细胞中位数差异无统计学意义:(9.5 (AYA) vs. 9.0 (A), p = 80.19)。成熟指数明显低于AYA (0.80 vs. 0.88, p = 80.02)。AYA组雌二醇峰值较低(1267 pg/mL vs. 1582 pg/mL, p = 80.04)。其他刺激参数相似。结论:就成熟卵母细胞产量而言,通过COH保存青少年和年轻成人的生育能力似乎与成年女性一样有效。然而,AYA患者表现出较低的卵母细胞成熟率和较低的雌二醇峰值水平。需要更大规模的研究来证实这些发现,并更好地描述卵巢反应中与年龄相关的生理差异。
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引用次数: 0
HPV awareness and vaccine decision-making: healthcare professionals vs social media in a cross-sectional study from Italy HPV意识和疫苗决策:医疗保健专业人员与社交媒体在意大利的横断面研究
IF 1.9 4区 医学 Q2 OBSTETRICS & GYNECOLOGY Pub Date : 2025-12-10 DOI: 10.1016/j.ejogrb.2025.114885
Cristina Lumia

Introduction

Social media is used increasingly as a source of health information. This study explored how women access information about human papillomavirus (HPV), and whether the use of social media influences vaccine decision-making.

Methods

A cross-sectional survey was conducted between October 2018 and March 2019 among 90 women aged 18-45 years attending the University Hospital of Palermo, Sicily (Italy). A 25-item questionnaire assessed sociodemographic characteristics, knowledge about HPV and vaccination, and sources of information. Descriptive statistics and odds ratios (OR) were calculated for behavioural risk factors associated with HPV infection.

Results

Overall, 89 % of women reported that they were aware of HPV, and 70 % had heard about HPV vaccination. Only 14 % were vaccinated. Physicians (34 %) and television (20 %) were the main sources of information, while the Internet accounted for 18 %, and social media was rarely used for HPV information (59 % of participants reported no use of social media for HPV information). Most participants (63 %) did not know how to access vaccination services. Risk factors significantly associated with HPV infection included early sexual debut [≤17 years; OR = 3.0, 95 % confidence interval (CI) 1.56-5.7], multiple partners in the past year (OR = 2.3, 95 % CI 1.6-2.5), and low educational level (OR = 2.8-3.1).

Discussion

Despite relatively high awareness of HPV, vaccination uptake was low, and social media played only a marginal role in shaping knowledge and decision-making among women. Healthcare professionals remained the main trusted source of information. The gap between awareness and actual vaccination highlights the need for targeted campaigns and easier access to vaccination services.

Conclusion

Strategies to increase HPV vaccine uptake should prioritize direct communication from healthcare providers and improve service accessibility, while social media currently appears to have limited influence.
社会媒体越来越多地被用作健康信息的来源。这项研究探讨了女性如何获取有关人乳头瘤病毒(HPV)的信息,以及社交媒体的使用是否会影响疫苗的决策。方法对2018年10月至2019年3月在意大利西西里岛巴勒莫大学医院就诊的90名18-45岁女性进行横断面调查。一份25项问卷评估了社会人口学特征、HPV和疫苗接种知识以及信息来源。计算与HPV感染相关的行为危险因素的描述性统计和比值比(OR)。结果总体而言,89%的妇女报告说她们知道HPV, 70%的人听说过HPV疫苗接种。只有14%的人接种了疫苗。医生(34%)和电视(20%)是主要的信息来源,而互联网占18%,社交媒体很少用于HPV信息(59%的参与者报告没有使用社交媒体获取HPV信息)。大多数参与者(63%)不知道如何获得疫苗接种服务。与HPV感染显著相关的危险因素包括过早性行为[≤17年;OR = 3.0, 95%可信区间(CI) 1.56 ~ 5.7],过去一年有多个伴侣(OR = 2.3, 95% CI 1.6 ~ 2.5),教育程度低(OR = 2.8 ~ 3.1)。尽管对HPV的认识相对较高,但疫苗接种率较低,社交媒体在塑造女性的知识和决策方面仅发挥了边缘作用。医疗保健专业人员仍然是主要的可信赖信息来源。认识和实际疫苗接种之间的差距突出表明,需要开展有针对性的运动,并更容易获得疫苗接种服务。结论提高HPV疫苗接种率的策略应优先考虑与卫生保健提供者的直接沟通并改善服务可及性,而社交媒体目前的影响似乎有限。
{"title":"HPV awareness and vaccine decision-making: healthcare professionals vs social media in a cross-sectional study from Italy","authors":"Cristina Lumia","doi":"10.1016/j.ejogrb.2025.114885","DOIUrl":"10.1016/j.ejogrb.2025.114885","url":null,"abstract":"<div><h3>Introduction</h3><div>Social media is used increasingly as a source of health information. This study explored how women access information about human papillomavirus (HPV), and whether the use of social media influences vaccine decision-making.</div></div><div><h3>Methods</h3><div>A cross-sectional survey was conducted between October 2018 and March 2019 among 90 women aged 18-45 years attending the University Hospital of Palermo, Sicily (Italy). A 25-item questionnaire assessed sociodemographic characteristics, knowledge about HPV and vaccination, and sources of information. Descriptive statistics and odds ratios (OR) were calculated for behavioural risk factors associated with HPV infection.</div></div><div><h3>Results</h3><div>Overall, 89 % of women reported that they were aware of HPV, and 70 % had heard about HPV vaccination. Only 14 % were vaccinated. Physicians (34 %) and television (20 %) were the main sources of information, while the Internet accounted for 18 %, and social media was rarely used for HPV information (59 % of participants reported no use of social media for HPV information). Most participants (63 %) did not know how to access vaccination services. Risk factors significantly associated with HPV infection included early sexual debut [≤17 years; OR = 3.0, 95 % confidence interval (CI) 1.56-5.7], multiple partners in the past year (OR = 2.3, 95 % CI 1.6-2.5), and low educational level (OR = 2.8-3.1).</div></div><div><h3>Discussion</h3><div>Despite relatively high awareness of HPV, vaccination uptake was low, and social media played only a marginal role in shaping knowledge and decision-making among women. Healthcare professionals remained the main trusted source of information. The gap between awareness and actual vaccination highlights the need for targeted campaigns and easier access to vaccination services.</div></div><div><h3>Conclusion</h3><div>Strategies to increase HPV vaccine uptake should prioritize direct communication from healthcare providers and improve service accessibility, while social media currently appears to have limited influence.</div></div>","PeriodicalId":11975,"journal":{"name":"European journal of obstetrics, gynecology, and reproductive biology","volume":"317 ","pages":"Article 114885"},"PeriodicalIF":1.9,"publicationDate":"2025-12-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145733942","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Prognostic factors for ovarian immature teratoma and significance of alpha-fetoprotein in recurrent cases 卵巢未成熟畸胎瘤的预后因素及复发病例中甲胎蛋白的意义
IF 1.9 4区 医学 Q2 OBSTETRICS & GYNECOLOGY Pub Date : 2025-12-09 DOI: 10.1016/j.ejogrb.2025.114882
Miaofen Hong , Kai Yang , Huijuan Ge , Jie Tang , Jin Li , Shanhui Liang

Objective

To analyze clinical characteristics of ovarian immature teratoma patients and to explore prognostic factors of recurrence-free survival.

Methods

Fifty-eight cases with ovarian immature teratoma who underwent surgery in Fudan University Shanghai Cancer Center from January 2008 to January 2023, were retrospectively analyzed. The potential risk factors of recurrence were investigated. Subgroup analysis was conducted in stage I patients and in recurrent cases.

Results

The median age of diagnosis was 24.5 years (range, 7∼40 years), twenty-eight patients relapsed after a median follow-up of 72.3 months, with a 5-year recurrence-free survival and disease-specific survival rate of 81.0 % and 89.7 %, respectively. Multivariate analysis showed that adjuvant chemotherapy (HR = −1.556, 95 %CI 0.056∼0.793, P = 0.021), stage II-III (HR = 1.549, 95 %CI 1.572∼14.086, P = 0.006) and unknown residual lesions (HR = 1.591 95 %CI 1.602∼15.039P = 0.005) were risk factors of recurrence. Subgroup analysis was conducted in 32 stage I patients, the recurrence-free survival rate between adjuvant chemotherapy and surveillance group were statistically significant (P < 0.05). There was significant difference in AFP level between 15 cases with immature recurrence and 10 cases with mature recurrence(P = 0.015), a cut-off value of 25.67 ng/ml was found to be predictive for immature recurrence of ovarian immature teratoma with an area under the curve of 0.793, sensitivity and specificity were 53.3 % and 100 %, respectively.

Conclusions

Adjuvant chemotherapy, stage II-III and unknown residual lesions were the prognostic factors for ovarian immature teratoma. Surveillance is not a substitute for adjuvant chemotherapy in stage I patients of any grade. Serum AFP level exceeding 25.67 ng/ml can be a predictor of immature recurrence.
目的分析卵巢未成熟畸胎瘤患者的临床特点,探讨影响其无复发生存的预后因素。方法回顾性分析2008年1月至2023年1月在复旦大学上海肿瘤中心行卵巢未成熟畸胎瘤手术的58例患者的资料。探讨复发的潜在危险因素。对I期患者和复发患者进行亚组分析。结果中位诊断年龄为24.5岁(范围7 ~ 40岁),28例患者在中位随访72.3个月后复发,5年无复发生存率和疾病特异性生存率分别为81.0%和89.7%。多因素分析显示,辅助化疗(HR =−1.556,95% CI 0.056 ~ 0.793, P = 0.021)、II-III期(HR = 1.549, 95% CI 1.572 ~ 14.086, P = 0.006)和未知残留病变(HR = 1.591, 95% CI 1.602 ~ 15.039P = 0.005)是复发的危险因素。对32例I期患者进行亚组分析,辅助化疗组与监测组无复发生存率比较,差异均有统计学意义(P < 0.05)。15例未成熟复发患者与10例成熟复发患者AFP水平差异有统计学意义(P = 0.015),预测卵巢未成熟畸胎瘤未成熟复发的临界值为25.67 ng/ml,曲线下面积为0.793,敏感性为53.3%,特异性为100%。结论辅助化疗、II-III期及未知残留病变是影响卵巢未成熟畸胎瘤预后的因素。在任何级别的I期患者中,监测都不能替代辅助化疗。血清AFP水平超过25.67 ng/ml可作为未成熟复发的预测因子。
{"title":"Prognostic factors for ovarian immature teratoma and significance of alpha-fetoprotein in recurrent cases","authors":"Miaofen Hong ,&nbsp;Kai Yang ,&nbsp;Huijuan Ge ,&nbsp;Jie Tang ,&nbsp;Jin Li ,&nbsp;Shanhui Liang","doi":"10.1016/j.ejogrb.2025.114882","DOIUrl":"10.1016/j.ejogrb.2025.114882","url":null,"abstract":"<div><h3>Objective</h3><div>To analyze clinical characteristics of ovarian immature teratoma patients and to explore prognostic factors of recurrence-free survival.</div></div><div><h3>Methods</h3><div>Fifty-eight cases with ovarian immature teratoma who underwent surgery in Fudan University Shanghai Cancer Center from January 2008 to January 2023, were retrospectively analyzed. The potential risk factors of recurrence were investigated. Subgroup analysis was conducted in stage I patients and in recurrent cases.</div></div><div><h3>Results</h3><div>The median age of diagnosis was 24.5 years (range, 7∼40 years), twenty-eight patients relapsed after a median follow-up of 72.3 months, with a 5-year recurrence-free survival and disease-specific survival rate of 81.0 % and 89.7 %, respectively. Multivariate analysis showed that adjuvant chemotherapy (HR = −1.556, 95 %CI 0.056∼0.793, <em>P</em> = 0.021), stage II-III (HR = 1.549, 95 %CI 1.572∼14.086, <em>P</em> = 0.006) and unknown residual lesions (HR = 1.591 95 %CI 1.602∼15.039<em>P</em> = 0.005) were risk factors of recurrence. Subgroup analysis was conducted in 32 stage I patients, the recurrence-free survival rate between adjuvant chemotherapy and surveillance group were statistically significant (<em>P</em> &lt; 0.05). There was significant difference in AFP level between 15 cases with immature recurrence and 10 cases with mature recurrence(<em>P</em> = 0.015), a cut-off value of 25.67 ng/ml was found to be predictive for immature recurrence of ovarian immature teratoma with an area under the curve of 0.793, sensitivity and specificity were 53.3 % and 100 %, respectively.</div></div><div><h3>Conclusions</h3><div>Adjuvant chemotherapy, stage II-III and unknown residual lesions were the prognostic factors for ovarian immature teratoma. Surveillance is not a substitute for adjuvant chemotherapy in stage I patients of any grade. Serum AFP level exceeding 25.67 ng/ml can be a predictor of immature recurrence.</div></div>","PeriodicalId":11975,"journal":{"name":"European journal of obstetrics, gynecology, and reproductive biology","volume":"317 ","pages":"Article 114882"},"PeriodicalIF":1.9,"publicationDate":"2025-12-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145733941","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Inside Back Cover - Editors with images 内封底-编辑与图像
IF 1.9 4区 医学 Q2 OBSTETRICS & GYNECOLOGY Pub Date : 2025-12-08 DOI: 10.1016/S0301-2115(25)01151-0
{"title":"Inside Back Cover - Editors with images","authors":"","doi":"10.1016/S0301-2115(25)01151-0","DOIUrl":"10.1016/S0301-2115(25)01151-0","url":null,"abstract":"","PeriodicalId":11975,"journal":{"name":"European journal of obstetrics, gynecology, and reproductive biology","volume":"316 ","pages":"Article 114875"},"PeriodicalIF":1.9,"publicationDate":"2025-12-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145733535","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The impact of early amniotomy on delivery outcomes in pregnancies with fetal macrosomia 早期羊膜切开对巨大儿妊娠分娩结局的影响
IF 1.9 4区 医学 Q2 OBSTETRICS & GYNECOLOGY Pub Date : 2025-12-08 DOI: 10.1016/j.ejogrb.2025.114881
Or Touval , Gal Cohen , Adi Koriat , Lior Heresco , Tal Biron-Shental , Michal Kovo , Hanoch Schreiber

Objective

To evaluate the effect of early versus late amniotomy on delivery outcomes in pregnancies complicated by fetal macrosomia.

Methods

A retrospective cohort study was conducted at a tertiary university-affiliated medical center between 2014 and 2020. The included patients admitted during the latent phase of labor (<6 cm cervical dilatation) who delivered neonates with birthweight ≥ 4,000 g. and underwent amniotomy during labor. Participants were classified into two groups according to cervical dilatation at the time of amniotomy: early amniotomy (≤4 cm) and late amniotomy (>4 cm). Delivery and neonatal outcomes were compared, and multivariable logistic regression was performed to adjust for potential confounders.

Results

A total of 789 patients were included (early amniotomy, n = 353; late amniotomy, n = 436). Baseline estimated fetal weights and neonatal birthweights were similar between groups. Compared with the late amniotomy group, the early amniotomy group had higher rates of nulliparity, diabetes, induction of labor (IOL), epidural use, and intrapartum fever.
In a multivariable analysis of the entire cohort, after adjusting for confounders, early amniotomy was independently associated with an increased risk of intrapartum cesarean delivery. However, sub analyses for induced vs. spontaneous labors revealed that this association was only observed in women undergoing IOL (14 % vs. 4 %, p = 0.009), whereas no significant difference was observed among women presenting in spontaneous labor (8.1 % vs. 5.2 %, p = 0.214).

Conclusions

In pregnancies with fetal macrosomia, early amniotomy was associated with an increased risk of intrapartum cesarean delivery among women undergoing induction of labor. The timing of amniotomy in this population should therefore be carefully considered.
目的探讨早期与晚期羊膜切开术对合并巨大儿妊娠分娩结局的影响。方法2014 - 2020年在某高校附属医学中心进行回顾性队列研究。纳入在分娩潜伏期(宫颈扩张6cm)分娩出生体重≥4000g并在分娩期间行羊膜切开术的患者。根据切开羊膜时宫颈扩张程度分为两组:早期切开羊膜(≤4cm)和晚期切开羊膜(≤4cm)。对分娩和新生儿结局进行比较,并进行多变量logistic回归以调整潜在的混杂因素。结果共纳入789例患者(早期羊膜切开353例,晚期羊膜切开436例)。基线估计的胎儿体重和新生儿出生体重在两组之间相似。与晚期羊膜切开组相比,早期羊膜切开组的无产率、糖尿病、人工引产(IOL)、硬膜外使用和产时发热的发生率较高。在对整个队列的多变量分析中,在调整混杂因素后,早期羊膜切开术与产时剖宫产风险增加独立相关。然而,对引产和自然分娩的亚组分析显示,这种关联仅在接受人工晶状体手术的妇女中观察到(14%对4%,p = 0.009),而在自然分娩的妇女中没有观察到显著差异(8.1%对5.2%,p = 0.214)。结论在有巨大儿的妊娠中,早期羊膜切开与引产妇女产时剖宫产的风险增加有关。因此,在这一人群中,应仔细考虑羊膜切开术的时机。
{"title":"The impact of early amniotomy on delivery outcomes in pregnancies with fetal macrosomia","authors":"Or Touval ,&nbsp;Gal Cohen ,&nbsp;Adi Koriat ,&nbsp;Lior Heresco ,&nbsp;Tal Biron-Shental ,&nbsp;Michal Kovo ,&nbsp;Hanoch Schreiber","doi":"10.1016/j.ejogrb.2025.114881","DOIUrl":"10.1016/j.ejogrb.2025.114881","url":null,"abstract":"<div><h3>Objective</h3><div>To evaluate the effect of early versus late amniotomy on delivery outcomes in pregnancies complicated by fetal macrosomia.</div></div><div><h3>Methods</h3><div>A retrospective cohort study was conducted at a tertiary university-affiliated medical center between 2014 and 2020. The included patients admitted during the latent phase of labor (&lt;6 cm cervical dilatation) who delivered neonates with birthweight ≥ 4,000 g. and underwent amniotomy during labor. Participants were classified into two groups according to cervical dilatation at the time of amniotomy: early amniotomy (≤4 cm) and late amniotomy (&gt;4 cm). Delivery and neonatal outcomes were compared, and multivariable logistic regression was performed to adjust for potential confounders.</div></div><div><h3>Results</h3><div>A total of 789 patients were included (early amniotomy, n = 353; late amniotomy, n = 436). Baseline estimated fetal weights and neonatal birthweights were similar between groups. Compared with the late amniotomy group, the early amniotomy group had higher rates of nulliparity, diabetes, induction of labor (IOL), epidural use, and intrapartum fever.</div><div>In a multivariable analysis of the entire cohort, after adjusting for confounders, early amniotomy was independently associated with an increased risk of intrapartum cesarean delivery. However, sub analyses for induced vs. spontaneous labors revealed that this association was only observed in women undergoing IOL (14 % vs. 4 %, p = 0.009), whereas no significant difference was observed among women presenting in spontaneous labor (8.1 % vs. 5.2 %, p = 0.214).</div></div><div><h3>Conclusions</h3><div>In pregnancies with fetal macrosomia, early amniotomy was associated with an increased risk of intrapartum cesarean delivery among women undergoing induction of labor. The timing of amniotomy in this population should therefore be carefully considered.</div></div>","PeriodicalId":11975,"journal":{"name":"European journal of obstetrics, gynecology, and reproductive biology","volume":"317 ","pages":"Article 114881"},"PeriodicalIF":1.9,"publicationDate":"2025-12-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145733939","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
European journal of obstetrics, gynecology, and reproductive biology
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