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Correlation between ultrasonographic findings and histopathological and molecular characteristics in endometrial cancer: A multicenter study 子宫内膜癌超声表现与组织病理和分子特征的相关性:一项多中心研究
IF 1.9 4区 医学 Q2 OBSTETRICS & GYNECOLOGY Pub Date : 2025-12-18 DOI: 10.1016/j.ejogrb.2025.114900
Irene Colombi , Giuseppe Vizzielli , Eugenia Costantini , Silvia Pisaneschi , Federica Perelli , Anna Biasoli , Stefano Restaino , Francesca Ciccarone , Gabriele Centini , Francesco Giuseppe Martire , Martina Pacifici , Alberto Mattei , Errico Zupi , Lucia Lazzeri

Background

Accurate preoperative assessment of endometrial cancer is crucial for tailoring surgical and therapeutic management. Identifying correlations between ultrasonographic features and tumor histopathological and molecular profiles may help improve the accuracy of presurgical staging.

Objectives

This multicenter retrospective study aimed to evaluate the association between ultrasonographic features, histopathological characteristics and molecular profiles in endometrial cancer to improve preoperative assessment and risk stratification.

Study design

A total of 156 women from three Italian centers underwent standardized transvaginal or transrectal ultrasound following IETA criteria prior to hysterectomy. Ultrasonographic parameters, including endometrial thickness, echogenicity, junctional zone integrity, and vascularity assessed by Doppler, were analyzed. Postoperative histopathology and molecular classification (p53, MMR, POLE, NSMP) were performed. Statistical analyses evaluated correlations among ultrasound features, pathology, and molecular data.

Results

Endometrioid histotype was detected in 88.46 % of cases, mostly low-grade and early-stage. Cases in the early stage (i.e. lesions confined to the uterine corpus) accounted for 77.27 % of all cases. Ultrasound staging was consistent with the final staging in 65.5 % of cases, with errors primarily involving the overestimation of p53-abnormal tumors and the underestimation of MMRd tumors. Increased endometrial thickness was associated with a higher stage and grade (median 20 mm for stage III, p = 0.007). An irregular junctional zone was associated with high-grade tumors (p = 0.016). Complex and multifocal vascular patterns were significantly linked to advanced stages, high grade, and molecular aggressiveness, such as p53 mutations and MMR deficiency. Tumors with scattered vessels showed a higher risk of extensive lymphovascular space invasion.

Conclusions

Ultrasound features, particularly vascularity, junctional zone irregularity, and endometrial thickness, are significantly associated with tumor stage, grade, and molecular profiles. Incorporating detailed ultrasonographic assessment into preoperative evaluation can help identify high-risk endometrial cancers and guide personalized management strategies.
Larger prospective studies are needed to validate these findings.
背景准确的子宫内膜癌术前评估是调整手术和治疗管理的关键。确定超声特征与肿瘤组织病理学和分子特征之间的相关性有助于提高手术前分期的准确性。目的本多中心回顾性研究旨在探讨子宫内膜癌超声特征、组织病理特征和分子特征之间的关系,以改进术前评估和风险分层。研究设计来自意大利三个中心的156名妇女在子宫切除术前按照IETA标准接受了标准化的经阴道或经直肠超声检查。超声参数,包括子宫内膜厚度,回声性,连接区完整性和血管多普勒评估,进行分析。术后进行组织病理学检查和分子分型(p53、MMR、POLE、NSMP)。统计分析评估超声特征、病理和分子数据之间的相关性。结果88.46%的患者检出子宫内膜样组织型,多为低分级和早期。早期病变(即病变局限于子宫体)占77.27%。65.5%的病例超声分期与最终分期一致,错误主要包括高估p53-异常肿瘤和低估MMRd肿瘤。子宫内膜厚度增加与更高的分期和分级相关(III期中位数为20 mm, p = 0.007)。不规则交界区与高级别肿瘤相关(p = 0.016)。复杂和多灶性血管模式与晚期、高级别和分子侵袭性(如p53突变和MMR缺乏)显著相关。血管分散的肿瘤显示广泛淋巴血管浸润的风险较高。结论超声特征,特别是血管分布、连接带不规则性和子宫内膜厚度与肿瘤分期、分级和分子特征有显著相关性。在术前评估中结合详细的超声检查有助于识别高危子宫内膜癌,指导个性化的治疗策略。需要更大规模的前瞻性研究来验证这些发现。
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引用次数: 0
Current management and research priorities for second trimester pregnancy loss: a survey of healthcare professionals in the UK and Ireland (PASTeL-3) 妊娠中期流产的当前管理和研究重点:英国和爱尔兰医疗保健专业人员的调查(PASTeL-3)
IF 1.9 4区 医学 Q2 OBSTETRICS & GYNECOLOGY Pub Date : 2025-12-18 DOI: 10.1016/j.ejogrb.2025.114899
Andrea Woolner , Laura Linehan , Keelin O’Donoghue , Rosinder Kaur , Alexander E.P. Heazell

Background

Second trimester pregnancy loss (STPL) is under-researched. There are no published national or international guidelines. Yet evidence suggests this may be a high risk group. We hypothesised that the management of STPL varied across the UK and Ireland and we asked healthcare professionals’ views on current care and future priorities for STPL.

Methods

A prospective cross-sectional survey was conducted as part of the PASTeL-3 project. An electronic online survey was live between 19th November 2024 and 7th March 2025. Professionals working in maternity services in the UK and Ireland were invited to participate the survey via social media and email.

Findings

The definition of STPL varied between hospitals, with lack of consensus on the lower and upper gestational age limits. Care location for assessment and management of STPL differed between hospitals. 43 % of women could self-refer for assessment in the second trimester. Dosages of misoprostol used for STPL varied between hospitals from 50-400 µg, and 63 % of respondents reported uncertainty over the optimal dosage of misoprostol for STPL. Elective surgical management for STPL was rarely offered. Pharmacological management of the third stage of labour after STPL was largely based on oxytocics, with a minority using Misoprostol alone (10 %). Although almost all units reported consultant follow-up, only 45 % of respondents reported routine follow up took place in a dedicated pregnancy loss clinic. Only 52 % of respondents reported that post-mortem examination was routinely offered after STPL. Respondents reported antenatal care after a STPL was provided in a specialist pregnancy loss clinic (31 %) or preterm birth clinic (43 %); 80.1 % reported they felt confident caring for women in a asubsequent pregnancy after STPL. Respondents highlighted concerns with care locations for women with STPL under 16–18 weeks’ gestation and contingency locations where bereavement suites were in use. Highlighted research priorities included: optimising medical management of STPL for women with a scarred uterus, medical methods to reduce the risk of retained placenta after STPL, the impact of STPL on next pregnancies and investigations after STPL.

Interpretation

There is confusion over the definitions, appropriate location for care, optimal therapeutic options and follow up needed following STPL. High quality research for STPL should be prioritised to develop evidence-based clinical guidance to reduce variation in care.
孕中期妊娠丢失(STPL)的研究尚不充分。目前还没有出版的国家或国际指南。然而,有证据表明,这可能是一个高风险群体。我们假设STPL的管理在英国和爱尔兰各不相同,我们询问了医疗保健专业人员对STPL当前护理和未来优先事项的看法。方法采用前瞻性横断面调查作为PASTeL-3项目的一部分。一项电子在线调查于2024年11月19日至2025年3月7日进行。在英国和爱尔兰从事产科服务的专业人士被邀请通过社交媒体和电子邮件参与调查。研究结果:不同医院对STPL的定义不同,对胎龄下限和上限缺乏共识。评估和管理STPL的护理地点在医院之间存在差异。43%的女性在妊娠中期可以自我推荐进行评估。米索前列醇用于STPL的剂量因医院而异,从50µg到400µg不等,63%的受访者报告了米索前列醇用于STPL的最佳剂量的不确定性。选择性手术治疗STPL的机会很少。STPL后第三产程的药物管理主要基于催产素,少数单独使用米索前列醇(10%)。尽管几乎所有的单位都报告了顾问随访,但只有45%的受访者报告了在专门的流产诊所进行的常规随访。只有52%的受访者报告在STPL后常规提供尸检。应答者报告在STPL后在专科流产诊所(31%)或早产诊所(43%)提供产前护理;80.1%的人表示他们有信心照顾STPL后随后怀孕的妇女。受访者强调了对16-18周妊娠期STPL妇女的护理地点和使用丧亲套房的应急地点的关注。突出的研究重点包括:优化子宫瘢痕妇女STPL的医疗管理,减少STPL后胎盘残留风险的医学方法,STPL对下次妊娠的影响以及STPL后的调查。解释:在STPL的定义、适当的护理地点、最佳治疗选择和后续治疗方面存在混淆。应优先开展高质量的STPL研究,以制定循证临床指导,减少护理的差异。
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引用次数: 0
Association between severity of obstetric perineal tears and risk of levator ani avulsion – a systematic review 产科会阴撕裂严重程度与提肛肌撕脱伤风险之间的关系——一项系统综述。
IF 1.9 4区 医学 Q2 OBSTETRICS & GYNECOLOGY Pub Date : 2025-12-15 DOI: 10.1016/j.ejogrb.2025.114896
Line Norring Holst , Kathrine Perslev , Niels Klarskov , Hanna Jangö

Aim

The aim of this study was to investigate whether the incidence of levator ani avulsion (LAA) is associated with the degree of obstetric tear.

Methods

This systematic review was conducted in accordance with the PRISMA guidelines. A literature search was performed in PubMed, the Cochrane Library, and Embase. Articles were screened by two independent reviewers, and data were extracted on study characteristics, number of included women, degree of obstetric perineal tear, and the incidence of levator ani avulsion (LAA).

Results

A total of 13 studies were included, comprising 3,584 primiparous women. We found that the incidence of levator ani avulsion was 13 % (95 %CI: 10–17 %) in women without a perineal tear, 24% (95 %CI: 20–29 %) with a first-degree tear, 22 % (95 %CI: 18–25 %) with a spontaneous second-degree tear, 23 % (95 %CI: 17–29 %) with an episiotomy, and 35% (95 %CI: 30–40 %) with an obstetric anal sphincter injury (OASI). Additionally, some studies grouped women with no, first-, or second-degree tears together and here the incidence of LAA was 16% (95 %CI: 14–18 %).

Conclusion

LAA is common after vaginal delivery and is related to the degree of obstetric tear, ranging from 13 % in women without perineal tear to 35 % with OASI.
目的:本研究的目的是探讨提肛撕脱(LAA)的发生率是否与产科撕裂程度有关。方法:本系统评价按照PRISMA指南进行。在PubMed、Cochrane图书馆和Embase进行文献检索。文章由两名独立审稿人筛选,并提取研究特征、纳入妇女人数、产科会阴撕裂程度和提肛撕脱(LAA)发生率的数据。结果:共纳入13项研究,包括3584名初产妇。我们发现,在无会阴撕裂的女性中,提肛肌撕脱的发生率为13% (95% CI: 10- 17%),一级撕裂的发生率为24% (95% CI: 20- 29%),自发性二度撕裂的发生率为22% (95% CI: 18- 25%),会阴切开术的发生率为23% (95% CI: 17- 29%),产科肛门括约肌损伤(OASI)的发生率为35% (95% CI: 30- 40%)。此外,一些研究将没有、一度或二度撕裂的女性分组在一起,LAA的发生率为16% (95% CI: 14- 18%)。结论:LAA在阴道分娩后很常见,与产科撕裂程度有关,无会阴撕裂的妇女占13%,有OASI的妇女占35%。
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引用次数: 0
Diurnal variation in urine protein-to-creatinine ratio among pregnant women with and without hypertensive disorders: A retrospective clinical study 有或无高血压疾病孕妇尿蛋白与肌酐比值的日变化:一项回顾性临床研究。
IF 1.9 4区 医学 Q2 OBSTETRICS & GYNECOLOGY Pub Date : 2025-12-13 DOI: 10.1016/j.ejogrb.2025.114893
Cami Lehavi , Amir Naeh , Eiman Shalabna , Rinat Gabbay-Benziv , Esther Maor-Sagie

Objective

Physiological proteinuria occurs in approximately 8 % of normal pregnancies due to increased glomerular filtration and altered tubular reabsorption. Hypertensive disorders complicate 3–8 % of pregnancies and are associated with adverse outcomes. Although 24-hour urine collection is the traditional standard for assessing proteinuria, it is cumbersome and time-consuming. The urine protein-to-creatinine ratio (Upcr) has largely replaced it owing to its convenience and strong correlation with 24-hour values. However, Upcr relies on random sampling and may be influenced by diurnal variation. This study aimed to assess and compare Upcr diurnal variability in normotensive versus hypertensive singleton pregnancies.

Methods

A retrospective analysis was conducted of all Upcr tests performed between January 2021 and March 2024 at a single university-affiliated center. Tests were ordered following a positive urine dipstick during routine screening. Only the first test per pregnancy was included. Upcr values were compared by sampling time—day (07:00–22:59) versus night (23:00–06:59)—and by subsequent development of hypertensive disorders. Differences were analyzed using the Kruskal–Wallis test.

Results

Among 13,054 deliveries, 1,317 (10 %) underwent Upcr testing; 35.8 % developed hypertensive disorders. Most samples were collected during the day (1,121 vs. 196 at night). Hypertensive pregnancies exhibited higher Upcr levels regardless of sampling time. In this group, daytime Upcr values were significantly higher than nighttime values (0.75 vs. 0.39, p = 0.02), whereas no diurnal difference was observed in normotensive pregnancies.

Conclusions

Upcr demonstrates significant diurnal variation in hypertensive pregnancies. These findings support reevaluating current proteinuria thresholds and incorporating time-of-day considerations in Upcr interpretation.
目的:生理性蛋白尿发生在大约8%的正常妊娠,由于肾小球滤过增加和小管重吸收改变。高血压疾病使3- 8%的妊娠并发症,并伴有不良后果。虽然24小时尿液收集是评估蛋白尿的传统标准,但它既繁琐又耗时。尿蛋白与肌酐比值(Upcr)因其方便且与24小时值相关性强,已在很大程度上取代了尿蛋白与肌酐比值。然而,Upcr依赖于随机抽样,可能受到日变化的影响。本研究旨在评估和比较正常和高血压单胎妊娠的Upcr日变异性。方法:回顾性分析了2021年1月至2024年3月在一个大学附属中心进行的所有Upcr测试。在常规筛查中尿试纸呈阳性后,要求进行检查。只包括每次怀孕的第一次测试。Upcr值通过采样时间(白天(07:00-22:59)与夜晚(23:00-06:59)以及随后的高血压疾病发展情况进行比较。采用Kruskal-Wallis检验分析差异。结果:13054例分娩中,1317例(10%)接受了Upcr检测;35.8%发生高血压疾病。大多数样本是在白天收集的(1121对196)。高血压妊娠与采样时间无关,Upcr水平较高。在该组中,白天的Upcr值显著高于夜间的Upcr值(0.75 vs. 0.39, p = 0.02),而在正常血压的孕妇中没有观察到昼夜差异。结论:Upcr在高血压妊娠中显示出显著的日变化。这些发现支持重新评估当前的蛋白尿阈值,并在Upcr解释中纳入时间因素。
{"title":"Diurnal variation in urine protein-to-creatinine ratio among pregnant women with and without hypertensive disorders: A retrospective clinical study","authors":"Cami Lehavi ,&nbsp;Amir Naeh ,&nbsp;Eiman Shalabna ,&nbsp;Rinat Gabbay-Benziv ,&nbsp;Esther Maor-Sagie","doi":"10.1016/j.ejogrb.2025.114893","DOIUrl":"10.1016/j.ejogrb.2025.114893","url":null,"abstract":"<div><h3>Objective</h3><div>Physiological proteinuria occurs in approximately 8 % of normal pregnancies due to increased glomerular filtration and altered tubular reabsorption. Hypertensive disorders complicate 3–8 % of pregnancies and are associated with adverse outcomes. Although 24-hour urine collection is the traditional standard for assessing proteinuria, it is cumbersome and time-consuming. The urine protein-to-creatinine ratio (Upcr) has largely replaced it owing to its convenience and strong correlation with 24-hour values. However, Upcr relies on random sampling and may be influenced by diurnal variation. This study aimed to assess and compare Upcr diurnal variability in normotensive versus hypertensive singleton pregnancies.</div></div><div><h3>Methods</h3><div>A retrospective analysis was conducted of all Upcr tests performed between January 2021 and March 2024 at a single university-affiliated center. Tests were ordered following a positive urine dipstick during routine screening. Only the first test per pregnancy was included. Upcr values were compared by sampling time—day (07:00–22:59) versus night (23:00–06:59)—and by subsequent development of hypertensive disorders. Differences were analyzed using the Kruskal–Wallis test.</div></div><div><h3>Results</h3><div>Among 13,054 deliveries, 1,317 (10 %) underwent Upcr testing; 35.8 % developed hypertensive disorders. Most samples were collected during the day (1,121 vs. 196 at night). Hypertensive pregnancies exhibited higher Upcr levels regardless of sampling time. In this group, daytime Upcr values were significantly higher than nighttime values (0.75 vs. 0.39, <em>p</em> = 0.02), whereas no diurnal difference was observed in normotensive pregnancies.</div></div><div><h3>Conclusions</h3><div>Upcr demonstrates significant diurnal variation in hypertensive pregnancies. These findings support reevaluating current proteinuria thresholds and incorporating time-of-day considerations in Upcr interpretation.</div></div>","PeriodicalId":11975,"journal":{"name":"European journal of obstetrics, gynecology, and reproductive biology","volume":"318 ","pages":"Article 114893"},"PeriodicalIF":1.9,"publicationDate":"2025-12-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145767364","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
Reproductive factors, exogenous hormone use and risk of migraine among women: Results from UK Biobank 生殖因素,外源性激素的使用和女性偏头痛的风险:来自英国生物银行的结果。
IF 1.9 4区 医学 Q2 OBSTETRICS & GYNECOLOGY Pub Date : 2025-12-13 DOI: 10.1016/j.ejogrb.2025.114892
Nana Wang , Yongli Yang , Xiaocan Jia , Yuping Wang , Chaojun Yang , Jingwen Fan , Chenyu Zhao , Yacong Bo , Xuezhong Shi

Aims

The association between female reproductive factors and migraine risk remains inconclusive. This study aimed to investigate the association between reproductive factors and migraine.

Methods

This study included 268,440 female participants enrolled in the UK Biobank from 2006 to 2010. Cox proportional hazard models and restricted cubic spline were used for association analyses.

Results

With a median of 13.67 years follow-up, a total of 4,394 cases of migraine were documented. The adjusted HR (95 % CI) for menarche > 14 years was 1.16(1.04,1.28) compared with 12 to 14 years; 1.48(1.32,1.66) for menopause < 45 years compared with 45 to 55 years; 1.32 (1.18,1.48) for reproductive life expectancy < 33 years compared with 33 to 40 years; 1.60(1.43,1.79) for hysterectomy; 1.52(1.37,1.69) for oophorectomy; 1.31(1.19,1.45) for pregnant; 1.66(1.47,1.86) for first live birth < 22 years compared with > 27 years; 1.31(1.17,1.47) for last live birth < 27 years compared with > 33 years; 1.16(1.03,1.30), 1.16(1.06,1.27), and 1.17(1.05,1.29) for 1, 2, and 3 or more children compared with no children; 1.18(1.10,1.28) for miscarriages; 1.13(1.04,1.24) for abortions; 1.62(1.51,1.74) for using HRT. Age at menarche, age at first or last live birth, age started oral contraceptive pills, age started HRT, and HRT duration were nonlinearly associated with migraine risk (P < 0.001).

Discussion

Female reproductive factors, including gynecologic surgery, early first birth, and using HRT, were associated with incident migraine. The findings emphasize the need to incorporate reproductive history into clinical profiles and provide an evidence base for personalized prevention strategies in women.
目的:女性生殖因素与偏头痛风险之间的关系尚不明确。本研究旨在探讨生殖因素与偏头痛之间的关系。方法:本研究纳入了2006年至2010年在英国生物银行登记的268,440名女性受试者。关联分析采用Cox比例风险模型和受限三次样条。结果:在中位13.67年的随访中,共有4394例偏头痛被记录在案。与12 ~ 14年相比,14年初潮的调整HR (95% CI)为1.16(1.04,1.28);绝经27年为1.48(1.32,1.66);1.31(1.17,1.47)为最后一次活产33年;1.16(1.03,1.30)、1.16(1.06,1.27)、1.17(1.05,1.29);流产为1.18(1.10,1.28);堕胎1.13(1.04,1.24);1.62(1.51,1.74)。月经初潮年龄、首次或最后一次活产年龄、开始口服避孕药年龄、开始HRT年龄和HRT持续时间与偏头痛风险呈非线性相关(P < 0.001)。讨论:女性生殖因素,包括妇科手术、早产和使用激素替代疗法,与偏头痛的发生有关。研究结果强调了将生殖史纳入临床档案的必要性,并为女性的个性化预防策略提供了证据基础。
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引用次数: 0
Sexual function after female genital cosmetic surgery: A systematic review and meta-analysis 女性生殖器整形手术后的性功能:系统回顾和荟萃分析。
IF 1.9 4区 医学 Q2 OBSTETRICS & GYNECOLOGY Pub Date : 2025-12-13 DOI: 10.1016/j.ejogrb.2025.114894
Ebru Zulfikaroglu , Didem Kurban

Objectives

To evaluate postoperative sexual function after female genital cosmetic surgery (FGCS)—predominantly labia minora reduction with or without clitoral hood reduction (CHR)—and to contextualize safety, satisfaction, and technique-related signals.

Methods

We systematically searched MEDLINE, Embase, Scopus, and Cochrane (2015–2025). Eligible designs included randomized or nonrandomized studies and case series (n ≥ 5) reporting validated sexual outcomes. Two reviewers independently screened and extracted data; risk of bias was assessed with Cochrane Risk of Bias 2, the Newcastle–Ottawa Scale, and the JBI checklist. Random-effects meta-analysis was performed, with prespecified subgroups by technique (trim/edge, wedge, composite) and follow-up.

Results

Eleven studies met inclusion; six used the Female Sexual Function Index (FSFI) and were pooled quantitatively. In primarily uncontrolled pre–post cohorts, pooled standardized mean change in sexual function corresponded to a moderate improvement (standardized mean difference 0.52; 95 % confidence interval 0.38–0.65)., although the certainty of evidence was low due to nonrandomized single-arm designs and serious risk of bias. Studies using other validated instruments (Female Genital Self-Image Scale, Sexual Function Questionnaire-28, Sexual Quality of Life–Female, BODY-Q) demonstrated convergent gains in genital self-image and sexual well-being. Reported complications were uncommon and mostly minor, with infrequent revisions during follow-up. No technique showed clear superiority. One prospective cohort with standardized sensory testing found no reduction in clitoral or labial sensitivity after labiaplasty with CHR.

Conclusions

Observational pre–post data suggest that FGCS is associated with moderate short-term improvements in sexual function and genital self-image, but these findings are based on small, uncontrolled studies that are vulnerable to regression to the mean, expectancy effects, and natural recovery. High-quality controlled trials are needed to confirm the magnitude and durability of benefit. Benefits appear consistent across commonly used techniques, but technique-specific differences remain uncertain. Counseling should integrate validated patient-reported measures and realistic timelines for recovery and sexual resumption. Further comparative studies with standardized reporting and ≥12-month follow-up are needed.
目的:评估女性生殖器整形手术(FGCS)后的性功能-主要是小阴唇缩小伴有或不伴有阴蒂帽缩小(CHR)-并将安全性,满意度和技术相关信号纳入背景。方法:系统检索MEDLINE、Embase、Scopus和Cochrane(2015-2025)。符合条件的设计包括随机或非随机研究和病例系列(n≥5)报告证实的性结局。两名审稿人独立筛选和提取数据;采用Cochrane偏倚风险2、Newcastle-Ottawa量表和JBI检查表评估偏倚风险。随机效应荟萃分析进行,预先指定亚组的技术(修剪/边缘,楔形,复合)和随访。结果:11项研究符合纳入标准;6例采用女性性功能指数(FSFI)进行定量汇总。在主要不受控制的前后队列中,性功能的综合标准化平均变化对应于中度改善(标准化平均差0.52;95%可信区间0.38-0.65)。尽管由于非随机单臂设计和严重的偏倚风险,证据的确定性较低。使用其他有效工具(女性生殖器自我形象量表、性功能问卷-28、女性性生活质量、BODY-Q)的研究表明,生殖器自我形象和性幸福的收益趋同。报道的并发症不常见且大多轻微,随访期间很少进行修正。没有一种技术显示出明显的优势。一项标准化感觉测试的前瞻性队列研究发现,阴唇CHR成形术后阴蒂或阴唇敏感性没有降低。结论:术后观察性数据表明,FGCS与性功能和生殖器自我形象的中度短期改善有关,但这些发现是基于小型、不受控制的研究,容易受到回归均值、预期效应和自然恢复的影响。需要高质量的对照试验来确认获益的程度和持久性。在常用的技术中,益处似乎是一致的,但具体的技术差异仍然不确定。咨询应结合有效的病人报告的措施和现实的恢复和性恢复的时间表。需要标准化报告和≥12个月随访的进一步比较研究。
{"title":"Sexual function after female genital cosmetic surgery: A systematic review and meta-analysis","authors":"Ebru Zulfikaroglu ,&nbsp;Didem Kurban","doi":"10.1016/j.ejogrb.2025.114894","DOIUrl":"10.1016/j.ejogrb.2025.114894","url":null,"abstract":"<div><h3>Objectives</h3><div>To evaluate postoperative sexual function after female genital cosmetic surgery (FGCS)—predominantly labia minora reduction with or without clitoral hood reduction (CHR)—and to contextualize safety, satisfaction, and technique-related signals.</div></div><div><h3>Methods</h3><div>We systematically searched MEDLINE, Embase, Scopus, and Cochrane (2015–2025). Eligible designs included randomized or nonrandomized studies and case series (n ≥ 5) reporting validated sexual outcomes. Two reviewers independently screened and extracted data; risk of bias was assessed with Cochrane Risk of Bias 2, the Newcastle–Ottawa Scale, and the JBI checklist. Random-effects <em>meta</em>-analysis was performed, with prespecified subgroups by technique (trim/edge, wedge, composite) and follow-up.</div></div><div><h3>Results</h3><div>Eleven studies met inclusion; six used the Female Sexual Function Index (FSFI) and were pooled quantitatively. In primarily uncontrolled pre–post cohorts, pooled standardized mean change in sexual function corresponded to a moderate improvement (standardized mean difference 0.52; 95 % confidence interval 0.38–0.65)., although the certainty of evidence was low due to nonrandomized single-arm designs and serious risk of bias. Studies using other validated instruments (Female Genital Self-Image Scale, Sexual Function Questionnaire-28, Sexual Quality of Life–Female, BODY-Q) demonstrated convergent gains in genital self-image and sexual well-being. Reported complications were uncommon and mostly minor, with infrequent revisions during follow-up. No technique showed clear superiority. One prospective cohort with standardized sensory testing found no reduction in clitoral or labial sensitivity after labiaplasty with CHR.</div></div><div><h3>Conclusions</h3><div>Observational pre–post data suggest that FGCS is associated with moderate short-term improvements in sexual function and genital self-image, but these findings are based on small, uncontrolled studies that are vulnerable to regression to the mean, expectancy effects, and natural recovery. High-quality controlled trials are needed to confirm the magnitude and durability of benefit. Benefits appear consistent across commonly used techniques, but technique-specific differences remain uncertain. Counseling should integrate validated patient-reported measures and realistic timelines for recovery and sexual resumption. Further comparative studies with standardized reporting and ≥12-month follow-up are needed.</div></div>","PeriodicalId":11975,"journal":{"name":"European journal of obstetrics, gynecology, and reproductive biology","volume":"318 ","pages":"Article 114894"},"PeriodicalIF":1.9,"publicationDate":"2025-12-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145767360","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
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。
{"title":"Emotional freedom techniques-based counseling with breathing exercises in in vitro fertilization: effects on psychological distress and well-being","authors":"Merve Coşkun ,&nbsp;Ergül Aslan","doi":"10.1016/j.ejogrb.2025.114891","DOIUrl":"10.1016/j.ejogrb.2025.114891","url":null,"abstract":"<div><h3>Purpose</h3><div>To investigate whether psychosocial care during in vitro fertilization (IVF) treatment affects the emotional capacity and well-being of women undergoing fertility treatment.</div></div><div><h3>Methods</h3><div>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.</div></div><div><h3>Results</h3><div>Baseline characteristics did not differ between groups (p &gt; 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 &lt; 0.001), and increased acceptance (p &lt; 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 &lt; 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 &lt; 0.001; Cohen’s d = –1.71, 95 % CI [–2.20 to –1.22], p &lt; 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 &lt; 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.</div></div><div><h3>Conclusion</h3><div>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.</div></div>","PeriodicalId":11975,"journal":{"name":"European journal of obstetrics, gynecology, and reproductive biology","volume":"318 ","pages":"Article 114891"},"PeriodicalIF":1.9,"publicationDate":"2025-12-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145788925","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
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}
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European journal of obstetrics, gynecology, and reproductive biology
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