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Correction: Impact of HIV infection on cervical intraepithelial neoplasia detection in pregnant and non-pregnant women in Germany: a cross-sectional study. 更正:HIV感染对德国孕妇和非孕妇宫颈上皮内瘤变检测的影响:一项横断面研究。
IF 2.5 3区 医学 Q2 OBSTETRICS & GYNECOLOGY Pub Date : 2025-12-01 DOI: 10.1007/s00404-025-08217-x
Irena Rohr, Anna Sophie Skof, Michaela Heinrich-Rohr, Fabian Weiss, Jan-Peter Siedentopf, Katharina von Weizsäcker, Irene Alba Alejandre, Wolfgang Henrich, Jalid Sehouli, Charlotte K Metz
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引用次数: 0
Association between hysterectomy, oophorectomy, and risk of breast cancer: a meta-analysis 子宫切除术、卵巢切除术与乳腺癌风险之间的关系:一项荟萃分析。
IF 2.5 3区 医学 Q2 OBSTETRICS & GYNECOLOGY Pub Date : 2025-11-29 DOI: 10.1007/s00404-025-08179-0
Bing Wang, Meng Wang, Huili Xu, Yu Liu, Tengteng Kang, Yang Cao

Objectives

This meta-analysis seeks to clarify the relationship between hysterectomy, oophorectomy, and the subsequent risk of developing breast cancer.

Methods

A comprehensive literature search was conducted across PubMed, the Cochrane Library, and Embase to identify relevant studies. The quality of the included studies was assessed using the Newcastle–Ottawa Scale (NOS). Statistical analyses were performed using Stata software (version 14.0), with hazard ratios (HRs) and their corresponding 95% confidence intervals (CIs) calculated. Publication bias was assessed using funnel plots and Egger’s test.

Results

A total of 12 studies were included, comprising 9 cohort studies and 3 case–control studies, with publication years ranging from 1988 to 2023, involving 5,868,660 participants, predominantly from the United States. The analysis revealed that both hysterectomy and oophorectomy are associated with a reduced risk of breast cancer, lowering the risk by 16% (HR 0.84; 95% CI: 0.76–0.92; I2 = 76.5%; P < 0.001). Standalone hysterectomy was associated with a 13% reduction in breast cancer risk (HR 0.87; 95% CI: 0.77–0.99; I2 = 82.3%; P = 0.033), while bilateral oophorectomy reduced the risk by approximately 19% (HR 0.81; 95% CI: 0.68–0.96; I2 = 61.7%; P = 0.016). In contrast, unilateral oophorectomy did not significantly affect the risk of breast cancer (HR 0.89; 95% CI: 0.71–1.11; I2 = 45.5%; P = 0.288). Patients who underwent bilateral oophorectomy and received hormone therapy experienced a 20% reduction in breast cancer risk (HR 0.80; 95% CI: 0.68–0.93; I2 = 38.5%; P = 0.005), whereas those who did not receive hormone therapy showed no significant risk reduction (HR 0.87; 95% CI: 0.69–1.10; I2 = 48.5%; P = 0.254). Premenopausal bilateral oophorectomy was associated with a 13% decrease in breast cancer incidence risk (HR 0.87; 95% CI: 0.79–0.96; I2 = 0%; P = 0.004), while postmenopausal bilateral oophorectomy had no significant impact (HR 0.95; 95% CI: 0.88–1.03; I2 = 1.2%; P = 0.196).

Conclusions

This meta-analysis suggests that both hysterectomy and oophorectomy are significantly associated with a reduction in breast cancer risk. The effectiveness of bilateral oophorectomy appears to be modulated by hormone therapy and menopausal status. Further research is needed to clarify these associations and to explore the underlying biological mechanisms.

目的:本荟萃分析旨在阐明子宫切除术、卵巢切除术与随后发生乳腺癌风险之间的关系。方法:通过PubMed、Cochrane图书馆和Embase进行全面的文献检索,以确定相关研究。纳入研究的质量采用纽卡斯尔-渥太华量表(NOS)进行评估。采用Stata软件(14.0版)进行统计分析,计算风险比(hr)及其相应的95%置信区间(ci)。采用漏斗图和Egger检验评估发表偏倚。结果:共纳入12项研究,包括9项队列研究和3项病例对照研究,发表年份从1988年到2023年,涉及5,868,660名受试者,主要来自美国。分析显示,子宫切除术和卵巢切除术与乳腺癌风险降低相关,风险降低16% (HR 0.84; 95% CI: 0.76-0.92; I2 = 76.5%; P = 82.3%; P = 0.033),而双侧卵巢切除术风险降低约19% (HR 0.81; 95% CI: 0.68-0.96; I2 = 61.7%; P = 0.016)。相比之下,单侧卵巢切除术对乳腺癌的风险无显著影响(HR 0.89; 95% CI: 0.71-1.11; I2 = 45.5%; P = 0.288)。接受双侧卵巢切除术并接受激素治疗的患者乳腺癌风险降低20% (HR 0.80; 95% CI: 0.68-0.93; I2 = 38.5%; P = 0.005),而未接受激素治疗的患者风险无显著降低(HR 0.87; 95% CI: 0.69-1.10; I2 = 48.5%; P = 0.254)。绝经前双侧卵巢切除术与乳腺癌发病率降低13%相关(HR 0.87; 95% CI: 0.79-0.96; I2 = 0%; P = 0.004),而绝经后双侧卵巢切除术无显著影响(HR 0.95; 95% CI: 0.88-1.03; I2 = 1.2%; P = 0.196)。结论:这项荟萃分析表明,子宫切除术和卵巢切除术与乳腺癌风险的降低显著相关。双侧卵巢切除术的有效性似乎受到激素治疗和绝经状态的调节。需要进一步的研究来澄清这些关联并探索潜在的生物学机制。
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引用次数: 0
AXINEO: AXIllary response to NEOadjuvant chemotherapy for breast cancer: can we predict response based on a biomarker panel? AXINEO:腋窝对乳腺癌新辅助化疗的反应:我们能基于生物标志物小组预测反应吗?
IF 2.5 3区 医学 Q2 OBSTETRICS & GYNECOLOGY Pub Date : 2025-11-18 DOI: 10.1007/s00404-025-08209-x
Franziska Fick, Florian Lenz, Verena-Wilbeth Sailer, Achim Rody, Nikolas Tauber, Kerstin Muras, Natalia Krawczyk, Julika Ribbat-Idel, Franziska Hemptenmacher, Maggie Banys-Paluchowski

Background

Up to 60% of breast cancer patients achieve pathological complete response (pCR) and factors associated with breast pCR have been extensively investigated. In patients with initially node-positive disease predicting axillary response to treatment remains challenging. Our study examines a biomarker panel assessed on core-biopsy lymph-node metastatic tissue with the goal to establish predictive markers for nodal positive breast cancer.

Materials and methods

Forty women with core biopsy-proven node-positive breast cancer scheduled to receive neoadjuvant treatment at the certified Breast Cancer Center of the University Hospital Schleswig–Holstein Campus Lübeck were included. The expressions of CAIX, PD-L1, TROP2, MSH2, MSH6, MLH1, and PMS2 as well as p53 mutation were assessed. Biomarkers were chosen based on their association with tumorigenesis and tumor progression. Statistical analysis was performed using SPSS 29. This investigator-initiated study was supported by a research grant from Gilead (Gilead Förderprogramm).

Results

Higher CAIX levels were associated with triple-negative and Her2-positive receptor status (p = 0.003), Ki67 ≥ 50% in breast core biopsy (p = 0.005), as well as postmenopausal status (p = 0.007). P53 mutation was more frequent in G3 tumors (p = 0.025). All lymph-node metastases were microsatellite stable (MSS). None of the markers could significantly predict pathological response (complete, breast, or nodal).

Conclusion

Our study shows upregulated CAIX in lymph-node metastasis frequently occurs in aggressive and highly proliferative tumors. However, none of the examined biomarkers could predict nodal response to therapy. Further research is necessary to better identify patients most likely to achieve nodal response through neoadjuvant chemotherapy.

背景:高达60%的乳腺癌患者达到病理完全缓解(pCR),与乳腺pCR相关的因素已被广泛研究。在最初淋巴结阳性疾病的患者中,预测腋窝对治疗的反应仍然具有挑战性。我们的研究对核心活检淋巴结转移组织的生物标志物进行了评估,目的是建立淋巴结阳性乳腺癌的预测标志物。材料和方法:纳入了40名核心活检证实的淋巴结阳性乳腺癌妇女,她们计划在石勒苏益格-荷尔斯泰因大学附属石勒苏益格-荷尔斯泰因校区贝克分校的认证乳腺癌中心接受新辅助治疗。检测CAIX、PD-L1、TROP2、MSH2、MSH6、MLH1、PMS2的表达及p53突变。生物标志物的选择是基于它们与肿瘤发生和肿瘤进展的关联。采用SPSS 29进行统计学分析。这项由研究者发起的研究得到了Gilead (Gilead Förderprogramm)的研究资助。结果:较高的CAIX水平与三阴性和her2阳性受体状态(p = 0.003)、乳房核心活检中Ki67≥50% (p = 0.005)以及绝经后状态(p = 0.007)相关。P53突变在G3肿瘤中更为常见(p = 0.025)。所有淋巴结转移均为微卫星稳定(MSS)。没有一种标志物能显著预测病理反应(完全、乳房或淋巴结)。结论:我们的研究表明,CAIX在淋巴结转移中的表达上调常见于侵袭性和高增生性肿瘤。然而,所检测的生物标志物都不能预测对治疗的淋巴结反应。需要进一步的研究来更好地识别最有可能通过新辅助化疗获得淋巴结反应的患者。
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引用次数: 0
Methotrexate plus low-dose prednisolone compared with high-dose corticosteroid therapy in the management of idiopathic granulomatous mastitis 甲氨蝶呤加低剂量强的松龙与高剂量皮质类固醇治疗特发性肉芽肿性乳腺炎的比较。
IF 2.5 3区 医学 Q2 OBSTETRICS & GYNECOLOGY Pub Date : 2025-11-18 DOI: 10.1007/s00404-025-08220-2
Leyla Shojaee, Nahid Nafissi, Fatemeh Niksolat Roodposhti, Kiana Shakeriastani, Kiarash Shakeriastani

Purpose

Idiopathic granulomatous mastitis (IGM) is a chronic, relapsing inflammatory breast disease of unknown etiology. Its unpredictable course and unclear pathogenesis have made treatment a persistent clinical challenge. This study aimed to evaluate treatment outcomes in patients with IGM, focusing on extending remission periods and reducing relapse rates after discontinuation of therapy.

Methods

This retrospective cohort study included 200 patients with histopathological confirmed idiopathic granulomatous mastitis who were referred to the Teaching and Therapeutic Center at the Central Hospital of Mazandaran University of Medical Sciences. Patient demographics, pathological characteristics, treatment regimens, remission duration, and recurrence rates were analyzed.

Results

From January 2018 to December 2024, a total of 200 patients were enrolled in the study, with a mean age of 33 years (range: 18–54 years) and a mean follow-up duration of 34 months (range: 8–51 months). Patients were divided into two treatment groups: Group A received high-dose prednisolone combined with abscess drainage (n = 99), while Group B received low-dose prednisolone, abscess drainage, and methotrexate (n = 101). Group B demonstrated a significantly shorter treatment duration (11.56 ± 2.15 months) compared to Group A (14.86 ± 3.42 months; P < 0.001). The mean time to follow-up was significantly longer in Group B (35.97 ± 6.96 months) than in Group A (20.00 ± 7.02 months; P < 0.001). The recurrence rate was lower in Group B (4.9%) than in Group A (23.2%), with the difference approaching statistical significance (P = 0.057). In addition, the mean time to relapse in Group B (34.46 ± 6.50 months) was significantly longer than that of Group A (16.96 ± 5.34 months), indicating that patients receiving the combined regimen of low-dose prednisolone, drainage, and methotrexate experienced a more sustained remission period.

Conclusions

According to the results, the treatment of idiopathic granulomatous mastitis, especially the moderate to severe form of the disease, using combination therapy with low-dose prednisolone and methotrexate can be associated with a reduction in treatment duration, and increase in remission duration, and a reduction in relapse, and drug side effects.

目的:特发性肉芽肿性乳腺炎(IGM)是一种病因不明的慢性、复发性炎性乳腺疾病。其不可预测的病程和不明确的发病机制使治疗成为一个持续的临床挑战。本研究旨在评估IGM患者的治疗结果,重点是延长缓解期和减少停药后的复发率。方法:本回顾性队列研究纳入200例组织病理学证实的特发性肉芽肿性乳腺炎患者,这些患者转介到马赞达兰医科大学中心医院的教学和治疗中心。分析患者人口统计学、病理特征、治疗方案、缓解持续时间和复发率。结果:2018年1月至2024年12月,共纳入200例患者,平均年龄33岁(范围18-54岁),平均随访时间34个月(范围8-51个月)。将患者分为两组,A组采用大剂量强的松龙联合脓肿引流(n = 99), B组采用小剂量强的松龙联合脓肿引流、甲氨蝶呤(n = 101)。B组治疗时间(11.56±2.15个月)明显短于a组(14.86±3.42个月);P结论:根据结果,治疗特发性肉芽肿性乳炎,特别是中重度疾病,采用低剂量强的松龙和甲氨蝶呤联合治疗可缩短治疗时间,延长缓解期,减少复发率,减少药物副作用。
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引用次数: 0
Prognostic factors for malignant tumors arising from mature cystic teratomas: a study involving the Kansai Clinical Oncology Group (KCOG-G1305s study) 成熟囊性畸胎瘤引起恶性肿瘤的预后因素:关西临床肿瘤组的一项研究(kcog - g135s研究)。
IF 2.5 3区 医学 Q2 OBSTETRICS & GYNECOLOGY Pub Date : 2025-11-17 DOI: 10.1007/s00404-025-08194-1
Fuminori Ito, Mototsugu Shimokawa, Atsushi Sugiura, Yoshio Itani, Atsushi Arakawa, Kayo Inoue, Mamiko Onuki, Tadahiro Shoji, Tomomi Egawa-Takata, Yuji Takei, Kazuhiro Takehara, Takashi Motohashi, Hiroaki Nagano, Toshiaki Nakamura, Satoru Munakata, Takashi Yamada, Naoto Furukawa, Tsunekazu Kita, Kimihiko Ito

Purpose

Current data regarding prognostic factors for malignant tumors arising from mature cystic teratomas (MT-MCTs) and effective treatments are insufficient. This study aimed to identify risk factors for MT-MCTs of the ovary.

Methods

Tumor samples diagnosed as MT-MCTs were collected from 13 institutions that participated in the Kansai Clinical Oncology Group. Based on the clinicopathological features and prognoses of the tumors, risk factors for progression and death were statistically assessed using univariable and multivariable analyses.

Results

Among the 60 tumor samples collected, 56 were diagnosed as MT-MCTs. Four samples were excluded based on the results of a central pathological review. Nine histological types, including squamous cell carcinoma, were diagnosed. Thirty of the 56 included samples were classified as International Federation of Gynecology and Obstetrics (FIGO) stage I, seven were classified as FIGO stage II, 18 were classified as FIGO stage III, and one was classified as FIGO stage IV. The 5-year progression-free survival and overall survival probabilities for stage I disease were significantly higher than those for stages II–IV disease (p < 0.001). In the multivariable analysis, surgery with residual tumor margins was a prognostic factor for progression, and FIGO stages I–IV and the absence of adjuvant therapy were prognostic factors for death.

Conclusion

Surgery without residual tumor margins and adjuvant therapy may be promising treatments for advanced-stage MT-MCTs.

目的:目前关于成熟囊性畸胎瘤(mt - mct)引起的恶性肿瘤的预后因素和有效治疗的数据不足。本研究旨在确定卵巢mt - mct的危险因素。方法:从关西临床肿瘤组参与的13家机构收集诊断为mt - mct的肿瘤样本。根据肿瘤的临床病理特征和预后,采用单变量和多变量分析对进展和死亡的危险因素进行统计学评估。结果:60例肿瘤中,56例诊断为mt - mct。根据中心病理检查的结果,排除了4个样本。诊断为9种组织学类型,包括鳞状细胞癌。56例纳入的病例中,30例为FIGO I期,7例为FIGO II期,18例为FIGO III期,1例为FIGO IV期。I期疾病的5年无进展生存率和总生存率显著高于II-IV期(p < 0.001)。在多变量分析中,肿瘤边缘残留的手术是进展的预后因素,FIGO I-IV期和缺乏辅助治疗是死亡的预后因素。结论:手术切除肿瘤边缘和辅助治疗可能是晚期mt - mct有希望的治疗方法。
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引用次数: 0
Management and natural course of CIN 1 and CIN 2 before and after implementation of the revised cervical cancer screening in Germany 德国修订宫颈癌筛查前后CIN 1和CIN 2的管理和自然病程。
IF 2.5 3区 医学 Q2 OBSTETRICS & GYNECOLOGY Pub Date : 2025-11-16 DOI: 10.1007/s00404-025-08190-5
T. Engler, M. Nägele, D. Dannehl, A. Englisch, S. Gerstner, M. Henes

Background

In 2020, Germany implemented a revised cervical cancer screening program, incorporating co-testing with cytology and human papillomavirus (HPV) testing for women aged 35 and older. This study describes patient characteristics, referral patterns, and follow-up outcomes of histologically confirmed cervical intraepithelial neoplasia (CIN) 1 and CIN 2 lesions before and after the introduction of the organized cervical cancer screening program in Germany.

Methods

In a hybrid prospective-retrospective study, we analyzed two consecutive cohorts of patients with histologically confirmed CIN 1 or CIN 2 at the Department of Women’s Health, University Hospital Tuebingen, between 2013 and 2022. Patient characteristics, referral indications, and follow-up outcomes were described and compared.

Results

Patients post-2020 were older (median 41 vs. 31 years), more often hrHPV-positive (93.4% vs. 63.3%), and more frequently presented with CIN 1 (62% vs. 51%). Immediate intervention was less common post-2020 (CIN 1: 7% vs. 25%; CIN 2: 37% vs. 67%). Among those followed, remission was higher in the post-2020 cohort (CIN 1: 63.5% vs. 42.2%; CIN 2: 61.6% vs. 41.0%). Progression to CIN 3 remained rare in both cohorts. Multivariable regression indicated that CIN 2 diagnosis and smoking reduced remission, while the post-2020 period was associated with increased remission odds.

Conclusion

The differences in remission and persistence between cohorts likely reflect changes in referral pathways, patient age rather than causal program effects. These data provide a descriptive benchmark for clinicians, supporting conservative management of CIN 1 and selected CIN 2 under the new screening program.

背景:2020年,德国实施了一项修订后的宫颈癌筛查计划,对35岁及以上的女性进行细胞学和人乳头瘤病毒(HPV)检测。本研究描述了在德国引入有组织的宫颈癌筛查项目前后组织学证实的宫颈上皮内瘤变(CIN) 1和CIN 2病变的患者特征、转诊模式和随访结果。方法:在一项混合前瞻性-回顾性研究中,我们分析了2013年至2022年在图宾根大学医院妇女健康部门连续两组组织学证实为CIN 1或CIN 2的患者。对患者特征、转诊指征和随访结果进行了描述和比较。结果:2020年后的患者年龄更大(中位年龄41岁对31岁),hrhpv阳性更常见(93.4%对63.3%),并且更频繁地出现CIN 1(62%对51%)。2020年后立即干预较少(CIN 1:7 % vs. 25%; CIN 2:37 % vs. 67%)。在随访中,2020年后队列的缓解率更高(CIN 1: 63.5%对42.2%;CIN 2: 61.6%对41.0%)。在这两个队列中进展到CIN 3的病例仍然很少见。多变量回归表明,CIN 2诊断和吸烟降低了缓解,而2020年后的时期与缓解的几率增加有关。结论:队列间缓解和持续性的差异可能反映了转诊途径、患者年龄的变化,而不是因果计划的影响。这些数据为临床医生提供了一个描述性的基准,支持在新的筛查方案下保守管理CIN 1和选择CIN 2。
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引用次数: 0
Chinese Expert Consensus on ultrasound anatomical examination of fetuses at 11 + 0 to 13 + 6 weeks of gestation based on the Delphi method 基于德尔菲法的妊娠11 + 0 ~ 13 + 6周胎儿超声解剖检查中国专家共识
IF 2.5 3区 医学 Q2 OBSTETRICS & GYNECOLOGY Pub Date : 2025-11-15 DOI: 10.1007/s00404-025-08231-z
Guorong Lyu, Ruibi Liao, Qiuxia Jiang, Xiaoqin He, Zongjie Weng
<div><h3>Objective</h3><p>First-trimester fetal malformation screening via ultrasound has become increasingly important. This study aims to establish a standardized expert consensus on the ultrasound anatomical examination of fetuses during the first trimester.</p><h3>Methods</h3><p>A comprehensive literature review was conducted on first-trimester fetal anatomical examinations and malformation screening. A draft of the <i>Chinese Expert Consensus on Fetal Anatomical Examination at 11</i> + <i>0 to 13</i> + <i>6 Weeks of Gestation</i> was initially prepared by eight core committee members. Using the Delphi method, three rounds of online voting were conducted by 35 expert panel members, and feedback was solicited from 122 experts across 27 representative medical institutions of various levels and regions in China. If three-fourths of the expert panel members agreed to categorize the first-trimester fetal anatomical ultrasound examination into three types, these classification methods were adopted. Similarly, if three-fourths of the experts agreed that a specific item or plane in the consensus should be a mandatory component of the examination, it was designated as a recommended item or plane; otherwise, it was classified as a suggested item or plane.</p><h3>Results</h3><p>This expert consensus categorizes the first-trimester fetal ultrasound anatomical examination into basic (Class I), detailed (Class II), and targeted (Class III) examinations. The examination includes one measurement item (with six sub-items) and nine anatomical examination items (with 26 sub-items). The basic and detailed fetal anatomical examinations involve largely consistent measurement parameters and target organs. However, the detailed examination includes a greater number of sub-items. In the basic examination, biometric parameters such as biparietal diameter (BPD), head circumference (HC), and abdominal circumference (AC) are considered suggested items (not mandatory). Similarly, sub-items such as the primary palate, kidneys, and genital tubercle are also classified as suggested items. In contrast, all of these parameters are regarded as recommended items (mandatory) in the detailed examination. Both the basic and detailed fetal anatomical examinations are indicated for low-risk pregnancies. The primary distinction between the two lies in the level of healthcare facility where they are conducted. Basic examinations are suitable for county-level hospitals with screening qualifications, whereas detailed examinations should be performed at municipal-level hospitals with equivalent screening credentials. In the targeted examination of the fetal central nervous system (FCNS), a total of 11 ultrasound planes are included. Among these, 4 are designated as recommended planes, and the remaining 7 as suggested planes. In the targeted fetal cardiac examination, 5 planes are evaluated, with 4 being recommended and the bilateral subclavian artery plane classified as a suggested plane.
目的:早期妊娠胎儿畸形超声筛查越来越重要。本研究旨在建立一个标准化的专家共识超声解剖检查胎儿在前三个月。方法:全面查阅有关妊娠早期胎儿解剖检查及畸形筛查的文献。《中国妊娠11 + 0 ~ 13 + 6周胎儿解剖检查专家共识》草案由8名核心委员初步起草。采用德尔菲法,由35名专家组成员进行三轮在线投票,并征求了来自中国27个各级、地区代表性医疗机构的122名专家的反馈意见。如果有四分之三的专家组成员同意将早期妊娠胎儿解剖超声检查分为三种类型,则采用这些分类方法。同样,如果有四分之三的专家同意协商一致意见中的某一特定项目或领域应成为审查的强制性组成部分,则指定该项目或领域为建议项目或领域;否则,它被归类为建议项目或平面。结果:本专家共识将妊娠早期胎儿超声解剖检查分为基础检查(I类)、详细检查(II类)和针对性检查(III类)。检查包括1个测量项目(6个分项)和9个解剖项目(26个分项)。基本和详细的胎儿解剖检查涉及基本一致的测量参数和靶器官。但是,详细审查包括更多的分项。在基础检查中,生物特征参数如双顶叶直径(BPD)、头围(HC)和腹围(AC)被认为是建议项目(非强制性)。类似地,子项目如主腭、肾脏和生殖器结节也被归类为建议项目。相反,在详细检查中,所有这些参数都被视为推荐项目(强制性)。对于低风险妊娠,应进行基本和详细的胎儿解剖检查。两者之间的主要区别在于进行治疗的保健设施的水平。基本检查适用于具有筛查资质的县级医院,而详细检查应在具有同等筛查资质的市级医院进行。在胎儿中枢神经系统(FCNS)的靶向检查中,共包括11个超声平面。其中4架被指定为推荐飞机,其余7架被指定为建议飞机。在胎儿心脏定向检查中,评估了5个平面,推荐4个平面,并将双侧锁骨下动脉平面列为建议平面。在唇腭裂妊娠早期筛查中,评估了5个层面,其中推荐层面3个,建议层面2个。有针对性的检查主要针对高危或疑似异常胎儿,应在合格的产前诊断中心由有资格的医生进行。结论:这一共识为不同水平和能力的医疗机构对妊娠早期胎儿的标准化超声解剖检查提供了一个强有力的框架。它还为未来的早期妊娠胎儿畸形筛查提供了循证支持。
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引用次数: 0
Isthmocele risk in repeated cesarean: the diagnostic and clinical role of morphometric parameters 重复剖宫产的峡部膨出风险:形态计量参数的诊断和临床作用。
IF 2.5 3区 医学 Q2 OBSTETRICS & GYNECOLOGY Pub Date : 2025-11-08 DOI: 10.1007/s00404-025-08238-6
Gülhan Özüm, Hakan Güraslan, Levent Deniz, Tuğba Demirtaş

Objective

This study aimed to evaluate the impact of repeated cesarean deliveries on isthmocele formation and to investigate the diagnostic value and clinical presentation of morphometric parameters, including niche depth, width, length, residual myometrial thickness (RMT), adjacent myometrial thickness (AMT), and the depth/AMT ratio.

Methods

A cross-sectional study was conducted with 116 symptomatic and asymptomatic women aged 18–45 years who had undergone one or more cesarean sections. The presence and dimensions of the isthmocele were assessed via transvaginal ultrasonography using Delphi consensus criteria. Morphometric and obstetric data were analyzed using descriptive statistics, correlation analysis, and binary logistic regression.

Results

Isthmocele was identified in 71.6% of participants, with prevalence rising from 42.9% after the first cesarean to 100% after the fourth. The isthmocele group had significantly higher gravidity, parity, and cesarean numbers (p < 0.001). Niche depth, length, and the depth/AMT ratio were significantly elevated, while RMT was reduced (p < 0.001). The number of cesareans showed a strong negative correlation with RMT (r = –0.499, p < 0.001) and a strong positive correlation with the depth/RMT ratio (r = 0.615, p < 0.001). Multivariate analysis identified having three or more cesareans as an independent predictor of isthmocele (OR = 15.6; 95% CI 3.27–74.4; p < 0.001). Niche length had the highest diagnostic accuracy for symptomatic isthmocele (AUC 0.700; 95% CI 0.589–0.796; cutoff 5 mm).

Conclusion

Repeated cesarean deliveries significantly increase both the risk and severity of isthmocele. In women with four cesareans, isthmocele was detected in 100% of cases. A niche length of ≥ 5 mm proved to be the most reliable morphometric marker in identifying symptomatic cases.

Implications for clinical practice

These findings emphasize the importance of routine transvaginal ultrasound screening post-cesarean—especially in women with multiple cesarean sections—and the incorporation of morphometric assessment (including RMT and depth/RMT ratio) into clinical decision-making.

目的:探讨反复剖宫产对峡部囊肿形成的影响,探讨形态计量学参数对峡部囊肿形成的诊断价值和临床表现,包括小位深度、宽度、长度、残余肌层厚度(RMT)、邻近肌层厚度(AMT)、深度/AMT比值。方法:横断面研究116例有症状和无症状的妇女,年龄18-45岁,接受过一次或多次剖宫产手术。峡部的存在和尺寸通过经阴道超声检查采用德尔菲共识标准进行评估。使用描述性统计、相关分析和二元逻辑回归分析形态计量学和产科数据。结果:71.6%的参与者发现峡部囊肿,患病率从第一次剖宫产后的42.9%上升到第四次剖宫产后的100%。结论:重复剖宫产明显增加了峡部囊肿的发生风险和严重程度。在四次剖宫产的妇女中,100%的病例检测到峡部囊肿。≥5mm的生态位长度被证明是识别有症状病例的最可靠的形态计量学标记。对临床实践的启示:这些发现强调了剖宫产后常规经阴道超声筛查的重要性,特别是对多次剖宫产的妇女,以及将形态计量学评估(包括RMT和深度/RMT比率)纳入临床决策。
{"title":"Isthmocele risk in repeated cesarean: the diagnostic and clinical role of morphometric parameters","authors":"Gülhan Özüm,&nbsp;Hakan Güraslan,&nbsp;Levent Deniz,&nbsp;Tuğba Demirtaş","doi":"10.1007/s00404-025-08238-6","DOIUrl":"10.1007/s00404-025-08238-6","url":null,"abstract":"<div><h3>Objective</h3><p>This study aimed to evaluate the impact of repeated cesarean deliveries on isthmocele formation and to investigate the diagnostic value and clinical presentation of morphometric parameters, including niche depth, width, length, residual myometrial thickness (RMT), adjacent myometrial thickness (AMT), and the depth/AMT ratio.</p><h3>Methods</h3><p>A cross-sectional study was conducted with 116 symptomatic and asymptomatic women aged 18–45 years who had undergone one or more cesarean sections. The presence and dimensions of the isthmocele were assessed via transvaginal ultrasonography using Delphi consensus criteria. Morphometric and obstetric data were analyzed using descriptive statistics, correlation analysis, and binary logistic regression.</p><h3>Results</h3><p>Isthmocele was identified in 71.6% of participants, with prevalence rising from 42.9% after the first cesarean to 100% after the fourth. The isthmocele group had significantly higher gravidity, parity, and cesarean numbers (<i>p</i> &lt; 0.001). Niche depth, length, and the depth/AMT ratio were significantly elevated, while RMT was reduced (<i>p</i> &lt; 0.001). The number of cesareans showed a strong negative correlation with RMT (<i>r</i> = –0.499, <i>p</i> &lt; 0.001) and a strong positive correlation with the depth/RMT ratio (<i>r</i> = 0.615, <i>p</i> &lt; 0.001). Multivariate analysis identified having three or more cesareans as an independent predictor of isthmocele (OR = 15.6; 95% CI 3.27–74.4; <i>p</i> &lt; 0.001). Niche length had the highest diagnostic accuracy for symptomatic isthmocele (AUC 0.700; 95% CI 0.589–0.796; cutoff 5 mm).</p><h3>Conclusion</h3><p>Repeated cesarean deliveries significantly increase both the risk and severity of isthmocele. In women with four cesareans, isthmocele was detected in 100% of cases. A niche length of ≥ 5 mm proved to be the most reliable morphometric marker in identifying symptomatic cases.</p><h3>Implications for clinical practice</h3><p>These findings emphasize the importance of routine transvaginal ultrasound screening post-cesarean—especially in women with multiple cesarean sections—and the incorporation of morphometric assessment (including RMT and depth/RMT ratio) into clinical decision-making.</p></div>","PeriodicalId":8330,"journal":{"name":"Archives of Gynecology and Obstetrics","volume":"312 6","pages":"2321 - 2332"},"PeriodicalIF":2.5,"publicationDate":"2025-11-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://link.springer.com/content/pdf/10.1007/s00404-025-08238-6.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145470352","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Ultrasound-guided ethanol sclerotherapy versus laparoscopic surgery for endometriomas: a randomized clinical trial in a real-world setting 超声引导乙醇硬化疗法与腹腔镜手术治疗子宫内膜异位瘤:一项现实世界环境下的随机临床试验。
IF 2.5 3区 医学 Q2 OBSTETRICS & GYNECOLOGY Pub Date : 2025-11-04 DOI: 10.1007/s00404-025-08205-1
Amparo García-Tejedor, Rodrigo Guevara-Peralta, Jose Manuel Martinez-Garcia, Shiana Corbalán, Mauricio Agüero, Maria Gomez-Romero, Marta Cararach, Marta Castellarnau, Mariví Rodríguez, Ana Cristina Lou-Mercadé, Laura Costa, Maria Jose Rodríguez, Eva Huguet, Manuel Carreras, Ana Belen Castel-Segui, Maria Font-Roig, Susana Royo, Nuria Sarasa, Beatriz Candas, Samuel Perez-Carton, Carlos Ortega, Maria Jesus Pla, Jordi Ponce

Purpose

To compare the efficacy of ultrasound-guided alcohol sclerotherapy versus laparoscopic cystectomy for the management of ovarian endometriomas, focusing on complications, recurrence, pain relief, and healthcare costs.

Methods

We conducted a multicentre, randomized clinical trial across 20 centers in Spain. A total of 167 women aged 18–40 years with ovarian endometriomas (35–100 mm) were recruited between June 2018 and June 2022. Participants were randomized to receive either ultrasound-guided aspiration with ethanol sclerotherapy or standard laparoscopic cystectomy. Complications were graded using the Clavien–Dindo classification. Pain was assessed using a visual analogue scale (VAS) before and six months after treatment. Recurrence was defined as the reappearance of a cystic lesion at the treated site and analyzed using Kaplan–Meier curves and log-rank tests. The primary analysis followed an intention-to-treat approach and included 158 patients (sclerotherapy: n = 84; cystectomy: n = 74). The per-protocol analysis included 92 patients (sclerotherapy: n = 57; cystectomy: n = 37). Direct hospital costs, complication rates, recurrence, and pain relief were compared between groups.

Results

Intention-to-treat analyses show that complications were low in both groups (12%), most of which were Grade I–II, although 4.1% were Grade III in the surgery group. The cost of sclerotherapy was significantly lower (€472 vs. €2128, p < 0.001). In per-protocol analyses, the cyst recurrence or reappearance was similar between the two groups, with rates of 25.7% (9 of 35) in the surgery group and 22.8% (13 of 57) in the sclerotherapy group (p = 0.16). Pain was improved or completely resolved in 49 of 55 cases (89.1%) in the sclerotherapy group and in 21 of 32 cases (65.7%) in the laparoscopic surgery group (p = 0.05).

Conclusions

Ultrasound-guided alcohol sclerotherapy is a safe, cost-effective alternative to laparoscopic cystectomy for the treatment of endometriomas, with comparable recurrence rates and pain relief. Clinical Trial Registration: https://clinicaltrials.gov/search?term=NCT03571776. Registered May 5, 2018.

目的:比较超声引导下酒精硬化疗法与腹腔镜膀胱切除术治疗卵巢子宫内膜异位瘤的疗效,重点关注并发症、复发、疼痛缓解和医疗费用。方法:我们在西班牙的20个中心进行了一项多中心随机临床试验。在2018年6月至2022年6月期间,共招募了167名年龄在18-40岁之间患有卵巢子宫内膜异位瘤(35-100毫米)的女性。参与者随机接受超声引导下的乙醇硬化疗法抽吸或标准腹腔镜膀胱切除术。采用Clavien-Dindo分级对并发症进行分级。在治疗前和治疗后6个月采用视觉模拟量表(VAS)评估疼痛。复发定义为治疗部位囊性病变的再次出现,并使用Kaplan-Meier曲线和log-rank检验进行分析。初步分析采用意向治疗方法,纳入158例患者(硬化治疗:n = 84;膀胱切除术:n = 74)。按方案分析包括92例患者(硬化治疗:n = 57;膀胱切除术:n = 37)。两组间直接住院费用、并发症发生率、复发率和疼痛缓解程度的比较。结果:意向治疗分析显示,两组并发症均较低(12%),其中大部分为I-II级,尽管手术组为4.1%的III级。结论:超声引导下的酒精硬化疗法是一种安全、经济的替代腹腔镜膀胱切除术治疗子宫内膜异位瘤的方法,其复发率和疼痛缓解程度相当。临床试验注册:https://clinicaltrials.gov/search?term=NCT03571776。2018年5月5日报名
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引用次数: 0
Can cell-free fetal DNA screening be utilized for the assessment of chromosomal abnormalities in fetuses with mildly increased nuchal translucency? 无细胞胎儿DNA筛查可用于评估轻度颈部半透明增加的胎儿染色体异常吗?
IF 2.5 3区 医学 Q2 OBSTETRICS & GYNECOLOGY Pub Date : 2025-11-04 DOI: 10.1007/s00404-025-08143-y
Linjuan Su, Wantong Zhao, Hailong Huang, Ying Li, Xiaorui Xie, Meiying Cai, Lin Zheng, Liangpu Xu, Xiaoqing Wu

Objectives

This article investigates the theoretical detection rate of non-invasive prenatal screening (NIPS) and the residual risk of copy-number variations (CNVs) after normal NIPS results, for fetuses with isolated mild increased nuchal translucency (ImiNT), compared to chromosomal microarray analysis (CMA).

Methods

A retrospective analysis was conducted on CMA results in a cohort with ImiNT (2.5 mm or 95th percentile ≤ NT < 3.5 mm). Theoretical detection rates and residual risk values were calculated for four NIPS panels—Basic NIPS-3, Basic NIPS-5, Expanded NIPS (ExpNIPS), and Genome-Wide (GW) NIPS—for common chromosomal aneuploidies and clinically significant CNVs.

Results

In a cohort of 936 fetuses with ImiNT, 44 cases had clinically significant CMA results. Basic NIPS-3 could detect 10 cases (9 trisomy 21 and 1 trisomy 18), leaving a residual risk of 3.63% (1/28). Basic NIPS-5 detected 17 cases, including 7 sex chromosome abnormalities, reducing the residual risk to 2.88% (1/35). ExpNIPS identified 18 cases, adding one microdeletion compared to Basic NIPS-5, with a residual risk of 2.78% (1/36). GW NIPS detected 22 cases, finding 5 additional CNVs > 10 Mb compared to Basic NIPS-5, lowering the residual risk to 2.35% (1/43).

Conclusion

Using NIPS as a substitute for invasive prenatal diagnosis in cases of ImiNT should still be approached with caution. Couples must be ensured to understand the advantages and limitations of both methods. They should also be informed about the residual risk, ranging from 2.35 (1/43) to 3.63% (1/28), even after normal NIPS results. This understanding will help couples make informed decisions.

目的:研究与染色体微阵列分析(CMA)相比,无创产前筛查(NIPS)的理论检出率和NIPS结果正常后拷贝数变异(CNVs)的残留风险。方法:回顾性分析ImiNT (2.5 mm或95百分位≤NT)队列CMA结果。结果:在936例ImiNT胎儿队列中,44例具有临床显著的CMA结果。基本NIPS-3检测10例(21三体9例,18三体1例),剩余风险为3.63%(1/28)。基本NIPS-5检测到17例,其中性染色体异常7例,剩余风险降低至2.88%(1/35)。ExpNIPS鉴定18例,与Basic NIPS-5相比增加1个微缺失,剩余风险为2.78%(1/36)。GW NIPS检测到22例,与Basic NIPS-5相比,发现了5个额外的CNVs bbb10 Mb,将剩余风险降低到2.35%(1/43)。结论:应用NIPS替代有创产前诊断治疗缺血性脑梗死仍需谨慎。必须确保夫妻了解这两种方法的优点和局限性。即使在NIPS结果正常之后,他们也应该被告知剩余风险,范围从2.35(1/43)到3.63%(1/28)。这种理解将有助于夫妻做出明智的决定。
{"title":"Can cell-free fetal DNA screening be utilized for the assessment of chromosomal abnormalities in fetuses with mildly increased nuchal translucency?","authors":"Linjuan Su,&nbsp;Wantong Zhao,&nbsp;Hailong Huang,&nbsp;Ying Li,&nbsp;Xiaorui Xie,&nbsp;Meiying Cai,&nbsp;Lin Zheng,&nbsp;Liangpu Xu,&nbsp;Xiaoqing Wu","doi":"10.1007/s00404-025-08143-y","DOIUrl":"10.1007/s00404-025-08143-y","url":null,"abstract":"<div><h3>Objectives</h3><p>This article investigates the theoretical detection rate of non-invasive prenatal screening (NIPS) and the residual risk of copy-number variations (CNVs) after normal NIPS results, for fetuses with isolated mild increased nuchal translucency (ImiNT), compared to chromosomal microarray analysis (CMA).</p><h3>Methods</h3><p>A retrospective analysis was conducted on CMA results in a cohort with ImiNT (2.5 mm or 95th percentile ≤ NT &lt; 3.5 mm). Theoretical detection rates and residual risk values were calculated for four NIPS panels—Basic NIPS-3, Basic NIPS-5, Expanded NIPS (ExpNIPS), and Genome-Wide (GW) NIPS—for common chromosomal aneuploidies and clinically significant CNVs.</p><h3>Results</h3><p>In a cohort of 936 fetuses with ImiNT, 44 cases had clinically significant CMA results. Basic NIPS-3 could detect 10 cases (9 trisomy 21 and 1 trisomy 18), leaving a residual risk of 3.63% (1/28). Basic NIPS-5 detected 17 cases, including 7 sex chromosome abnormalities, reducing the residual risk to 2.88% (1/35). ExpNIPS identified 18 cases, adding one microdeletion compared to Basic NIPS-5, with a residual risk of 2.78% (1/36). GW NIPS detected 22 cases, finding 5 additional CNVs &gt; 10 Mb compared to Basic NIPS-5, lowering the residual risk to 2.35% (1/43).</p><h3>Conclusion</h3><p>Using NIPS as a substitute for invasive prenatal diagnosis in cases of ImiNT should still be approached with caution. Couples must be ensured to understand the advantages and limitations of both methods. They should also be informed about the residual risk, ranging from 2.35 (1/43) to 3.63% (1/28), even after normal NIPS results. This understanding will help couples make informed decisions.</p></div>","PeriodicalId":8330,"journal":{"name":"Archives of Gynecology and Obstetrics","volume":"312 6","pages":"1977 - 1984"},"PeriodicalIF":2.5,"publicationDate":"2025-11-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://link.springer.com/content/pdf/10.1007/s00404-025-08143-y.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145437243","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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Archives of Gynecology and Obstetrics
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