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Qualitative Assessment of Foetal Lung Size in Left Congenital Diaphragmatic Hernia Using Ultrasound and MRI: A Retrospective Cohort Study 利用超声和MRI定性评估左侧先天性膈疝胎儿肺大小:一项回顾性队列研究
IF 4.3 1区 医学 Q1 OBSTETRICS & GYNECOLOGY Pub Date : 2025-12-22 DOI: 10.1111/1471-0528.70120
Shiri Shinar, Dilkash Kajal, Sarah Johnson, Anna Otvodenko, Seungwoo Lee, Priscilla P. L. Chiu, Johannes Keunen, Tim Van Mieghem, Greg Ryan, Prakesh S. Shah, Nimrah Abbasi
<div> <section> <h3> Objective</h3> <p>To evaluate the reliability of qualitative foetal lung size assessments on ultrasound (US) and MRI in left congenital diaphragmatic hernia (CDH) and their correlation with quantitative metrics and neonatal mortality.</p> </section> <section> <h3> Design</h3> <p>Retrospective cohort study.</p> </section> <section> <h3> Setting</h3> <p>Single tertiary center, 2008–2020.</p> </section> <section> <h3> Population</h3> <p>A total of 103 cases of prenatally diagnosed isolated left CDH underwent postnatal active care.</p> </section> <section> <h3> Methods</h3> <p>Two independent reviewers performed qualitative foetal lung size assessments on US and MRI. Interrater agreement was assessed, and correlations were determined between qualitative assessments, quantitative metrics (observed-to-expected lung-to-head ratio [o/e LHR] and observed-to-expected total Foetal lung volume [o/e TFLV]), and neonatal mortality.</p> </section> <section> <h3> Main Outcome Measures</h3> <p>Interrater agreement and correlation between qualitative and quantitative assessments of lung size and neonatal mortality.</p> </section> <section> <h3> Results</h3> <p>A total of 74 cases with both US and MRI imaging were included. Interrater agreement for qualitative lung size assessment was strong for US (weighted kappa: 0.80, 95% CI 0.68–0.93) and moderate for MRI (Cohen's kappa: 0.48, 95% CI 0.30–0.66). Both modalities showed a strong correlation between qualitative and quantitative lung size assessments. On US, qualitative and quantitative assessments had similar associations with neonatal mortality (Spearman's correlation: 0.44 for each reviewer vs. 0.49). On MRI, quantitative metrics correlated more strongly with neonatal mortality than qualitative assessment (Cramér's V: 0.44 vs. 0.34–0.35).</p> </section> <section> <h3> Conclusions</h3> <p>Qualitative foetal lung size assessment, by US more so than MRI, is a reliable and reproducible tool that correlates with established quantitative metrics and neonatal mortality. These findings support its role as a complementary method for prenatal risk stratification in left CDH.</p> </section
目的评价超声(US)和MRI对左先天性膈疝(CDH)胎儿肺大小定性评估的可靠性及其与定量指标和新生儿死亡率的相关性。设计回顾性队列研究。2008-2020年单一三级中心。共有103例产前诊断为孤立性左CDH的患者接受了产后积极护理。方法两名独立审稿人通过超声和MRI对胎儿肺大小进行定性评估。评估了评估者间的一致性,并确定了定性评估、定量指标(观察到的与预期的肺头比[0 /e LHR]和观察到的与预期的总胎儿肺容量[0 /e TFLV])与新生儿死亡率之间的相关性。主要结果测量肺大小与新生儿死亡率定性和定量评估之间的一致性和相关性。结果本组共74例合并超声和MRI检查的病例。定性肺大小评估在US(加权kappa: 0.80, 95% CI 0.68-0.93)和MRI (Cohen’s kappa: 0.48, 95% CI 0.30-0.66)中具有较强的一致性。两种方法均显示定性和定量肺大小评估之间有很强的相关性。在美国,定性和定量评估与新生儿死亡率有相似的关联(Spearman相关性:每位评论者0.44比0.49)。在MRI上,定量指标与新生儿死亡率的相关性比定性评估更强(cramamer’s V: 0.44 vs. 0.34-0.35)。结论定性胎儿肺大小评估,通过US比MRI更可靠,是一个可重复的工具,与已建立的定量指标和新生儿死亡率相关。这些发现支持其作为左侧CDH产前风险分层的补充方法的作用。
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引用次数: 0
Incidence of Acne in Women Using the Levonorgestrel-Releasing Intrauterine Device: A Systematic Review and Meta-Analysis 使用左炔诺孕酮释放宫内节育器的女性痤疮发生率:一项系统综述和Meta分析
IF 4.3 1区 医学 Q1 OBSTETRICS & GYNECOLOGY Pub Date : 2025-12-22 DOI: 10.1111/1471-0528.70108
Elaine Cristina Fontes de Oliveira, Frederico Timm Rodrigues de Sousa, Felipe Augusto Oliveira Lemos, Ciro Peixoto Vasconcelos, Ana Luiza Lunardi Rocha

Background

The levonorgestrel-releasing intrauterine system (LNG-IUS) is a widely used long-term contraceptive with high continuation rates, but acne may lead to discontinuation.

Objectives

To evaluate the incidence of acne among LNG-IUS users.

Search Strategy

A systematic search was conducted in PubMed, Embase, and Cochrane Central from inception to September 2024.

Selection Criteria

Randomised clinical trials (RCTs) analysing patients of any age using LNG-IUS at 52 mg, 19.5 mg, or 13.5 mg, with acne reported as an outcome, were included.

Data Collection and Analysis

Statistical analyses were conducted using OpenMeta. Chi-square and Z-tests assessed differences between groups, and study quality was appraised using the ROB-2 tool.

Main Results

Of 587 studies identified, nine RCTs met inclusion criteria, comprising 6305 LNG-IUS users. The overall acne incidence was 15.0% (95% CI 9.8%–20.3%). Among 2295 users of LNG-IUS 52 mg, incidence reached 19.5% (95% CI 5.2%–33.7%), whereas in 2322 users of LNG-IUS 13.5 mg it was 13.1% (95% CI 8.3%–17.9%) (p < 0.001). Two trials evaluated the 19.5 mg device but data were insufficient for pooling. Studies enrolling younger women (mean age ~24 years) reported an incidence of 19.3% (95% CI 11.0%–27.5%). Excluding Suhonen et al. yielded pooled proportions of 11.9% (95% CI 1.1%–22.7%) for LNG-IUS 52 mg users, 10.8% (95% CI 6.1%–15.5%) when all dosages were combined, and 9.9% (95% CI 9.0%–10.9%) among young women. Heterogeneity remained substantial in the overall and dosage-specific analyses (I2≈95%–97%); it was eliminated in the young women subgroup (I2 = 0%).

Conclusions

LNG-IUS 52 mg users showed a higher incidence of acne compared with those using LNG-IUS 13.5 mg. Studies enrolling younger women also showed a higher incidence. These findings suggest that device dosage and age influence acne occurrence among LNG-IUS users.

Trial Registration

PROSPERO registration number: CRD42024588771

背景左炔诺孕酮释放宫内系统(LNG - IUS)是一种广泛使用的长期避孕药,具有较高的延续率,但痤疮可能导致停药。目的评估LNG - IUS服用者痤疮的发生率。系统检索PubMed, Embase, Cochrane Central从成立到2024年9月。纳入随机临床试验(rct),分析使用LNG - IUS剂量为52 mg、19.5 mg或13.5 mg的任何年龄患者,结果报告为痤疮。数据收集与分析使用OpenMeta进行统计分析。卡方检验和Z检验评估组间差异,并使用ROB‐2工具评估研究质量。在587项研究中,9项随机对照试验符合纳入标准,包括6305名LNG - IUS使用者。痤疮总发生率为15.0% (95% CI 9.8%-20.3%)。在2295名LNG - IUS 52 mg服用者中,发病率达到19.5% (95% CI 5.2%-33.7%),而在2322名LNG - IUS 13.5 mg服用者中,发病率为13.1% (95% CI 8.3%-17.9%) (p < 0.001)。两项试验评估了19.5 mg的装置,但数据不足以汇总。纳入年轻女性(平均年龄~24岁)的研究报告发病率为19.3% (95% CI 11.0%-27.5%)。排除Suhonen等人的结果,LNG - IUS 52 mg服用者的总比例为11.9% (95% CI 1.1%-22.7%),所有剂量联合使用时的总比例为10.8% (95% CI 6.1%-15.5%),年轻女性的总比例为9.9% (95% CI 9.0%-10.9%)。在总体和剂量特异性分析中,异质性仍然很大(I 2≈95%-97%);在年轻女性亚组中被排除(i2 = 0%)。结论:与使用LNG - IUS 13.5 mg的患者相比,使用LNG - IUS 52 mg的患者痤疮发生率更高。招募年轻女性的研究也显示出更高的发病率。这些发现表明,设备剂量和年龄影响LNG - IUS使用者痤疮的发生。普洛斯彼罗注册号:CRD42024588771
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引用次数: 0
Intrapartum Antibiotic Prophylaxis and Child Health Outcomes 产时抗生素预防和儿童健康结果
IF 4.3 1区 医学 Q1 OBSTETRICS & GYNECOLOGY Pub Date : 2025-12-22 DOI: 10.1111/1471-0528.70126
Tomi Kanninen

Linked article: This is a mini commentary on Moradi et al., pp. 577–588 in this issue. To view this article visit https://doi.org/10.1111/1471-0528.70015.

链接文章:这是对本期Moradi等人的577-588页的迷你评论。要查看本文,请访问https://doi.org/10.1111/1471-0528.70015。
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引用次数: 0
Adequacy of Prenatal Care and Ensuing Maternal and Neonatal Severe Morbidity and Mortality 产前护理的充分性和随后的孕产妇和新生儿严重发病率和死亡率
IF 4.3 1区 医学 Q1 OBSTETRICS & GYNECOLOGY Pub Date : 2025-12-17 DOI: 10.1111/1471-0528.70119
Zeenat Ladak, Jennifer A. Jairam, Sarah Swayze, Jennifer Shuldiner, Olesya Falenchuk, Richard Volpe, Noah M. Ivers, Joel G. Ray
<p>A mother or her infant may face life-threatening events during childbirth or shortly thereafter, which may be preventable [<span>1</span>]. Adequacy of prenatal care is one determinant of maternal and newborn outcomes [<span>2</span>]. This study assessed whether adequacy of prenatal care is associated with maternal and newborn morbidity and mortality after birth.</p><p>This population-based, retrospective cohort study was completed using deidentified healthcare datasets, linked using unique encoded identifiers at ICES (Table S1). Included were hospital-based singleton livebirths and stillbirths from 20 to 42 weeks' gestation, in Ontario, Canada, from April 1, 2012, to March 31, 2020 (Table S2).</p><p>Study variables were chosen a priori (Figure S1). The exposure was adequacy of prenatal care, determined using the Revised-Graduate Prenatal Care Utilisation Index (R-GINDEX), which includes the number of prenatal visits, newborn gestational age, and initiation of first-trimester care [<span>2</span>]. It reflects adequacy on a five-level scale: no care, inadequate, intermediate, adequate (reference), and intensive care. The primary maternal outcome was a validated composite of any severe <i>maternal</i> morbidity and mortality (SMM-M) from the mother's delivery hospitalisation date and up to 42 days thereafter [<span>3</span>]. The primary infant outcome was a validated composite of any severe <i>neonatal</i> morbidity and mortality (SNM-M) from the infant's birth and up to 27 days thereafter (Table 1) [<span>4</span>].</p><p>Mean values and proportions of baseline variables were contrasted using standardised differences. Modified Poisson regression with generalised estimating equations generated unadjusted and adjusted relative risks (aRR) for SMM-M and SNM-M, respectively, comparing the five-level exposure group of adequacy of prenatal care. The maternal assessment was among all livebirths and stillbirths, while the neonatal assessment was limited to livebirths. Additional analyses were conducted for the outcomes of non-fatal severe maternal morbidity (SMM) and severe neonatal morbidity (SNM), and also for maternal and neonatal mortality. Analyses were performed using SAS version 9.4 software.</p><p>Among 955 814 births, 950 757 (99.5%) were livebirths (Figure S2). A total of 924 773 (96.8%) pregnancies had sufficient prenatal care (mean age 30.9 years), while 31 041 (3.2%) did not (mean age 27.9 years) (Table S3 and Table S4).</p><p>SMM-M occurred among 27 757 (2.9%) women. Relative to receipt of adequate prenatal care, those with no care had an aRR of SMM-M of 1.42 (95% CI 1.13–1.77) (Table 1). Women with inadequate (aRR 1.08, 95% CI 1.01–1.15) and intensive (aRR 1.04, 95% CI 1.00–1.06) care also had a somewhat higher risk of SMM-M.</p><p>SNM-M occurred among 64 613 (6.8%) liveborn infants. Compared to newborns of women who received adequate care, those receiving no prenatal care had the greatest aRR of SNM-M (1.60, 95% CI 1.40–1.83) (Table
母亲或她的婴儿在分娩期间或分娩后不久可能面临危及生命的事件,这些事件是可以预防的。产前护理的充分性是孕产妇和新生儿结局的一个决定因素[b]。本研究评估了产前护理是否与产妇和新生儿出生后的发病率和死亡率有关。这项基于人群的回顾性队列研究是使用未识别的医疗数据集完成的,在ICES中使用唯一编码标识符进行连接(表S1)。其中包括2012年4月1日至2020年3月31日在加拿大安大略省住院的单胎活产和妊娠20至42周的死产(表S2)。研究变量的选择是先验的(图S1)。暴露是产前护理的充足性,使用修订毕业生产前护理利用指数(R-GINDEX)来确定,其中包括产前就诊次数、新生儿胎龄和妊娠早期护理的开始bb0。它反映了五个级别的适当性:无护理、不充分、中等、适当(参考)和重症监护。主要产妇结局是一项经过验证的综合指标,包括从产妇分娩住院之日起至产后42天内的任何严重产妇发病率和死亡率(SMM-M)。婴儿的主要结局是婴儿出生后27天内任何严重新生儿发病率和死亡率(SNM-M)的经过验证的综合结果(表1)。使用标准化差异对比基线变量的平均值和比例。使用广义估计方程的修正泊松回归分别为SMM-M和SNM-M产生未调整和调整的相对风险(aRR),比较产前护理充足性的五个水平暴露组。产妇评估包括所有活产和死产,而新生儿评估仅限于活产。对非致死性严重孕产妇发病率(SMM)和严重新生儿发病率(SNM)以及孕产妇和新生儿死亡率的结果进行了进一步分析。采用SAS 9.4版软件进行分析。在955814例出生中,950757例(99.5%)为活产(图S2)。共有924773例(96.8%)孕妇得到充分的产前护理(平均年龄30.9岁),而31041例(3.2%)孕妇没有得到充分的产前护理(平均年龄27.9岁)(表S3和表S4)。SMM-M发生在27757例(2.9%)女性中。相对于接受足够的产前护理,未接受护理者的aRR为1.42 (95% CI 1.13-1.77)(表1)。护理不充分(aRR 1.08, 95% CI 1.01-1.15)和强化(aRR 1.04, 95% CI 1.00-1.06)的妇女发生SMM-M的风险也较高。SNM-M发生在64 613例(6.8%)活产婴儿中。与接受充分护理的妇女的新生儿相比,未接受产前护理的妇女的SNM-M的aRR最高(1.60,95% CI 1.40-1.83)(表1)。非致命性SMM和SNM的结果与SMM- m和SNM- m的结果相似(表S5)。产妇和新生儿死亡率的结果也类似,但更为明显(表S6)。在具有完整人口数据集的全民医疗保健系统中,没有产前护理的妇女及其婴儿有更高的严重发病率和死亡风险。加拿大马尼托巴省的一项研究发现,产前护理不足与死产、早产、胎龄小出生体重和新生儿重症监护病房住院的几率较高有关。目前的研究表明,接受强化产前护理的妇女的相关发病率略高,但她们的婴儿没有。前者可能是由于适应症的混淆,因为高危妊娠更有可能接受多次产前护理,但可能仍然容易发生产妇并发症。在确定的高危妇女中,例如那些有孕前合并症的妇女,产前护理强度与SMM-M、SNM-M和其他结果之间的关系可以使用倾向评分加权分析来评估。使用R-GINDEX的产前护理主要基于产前就诊的次数,而不考虑护理的质量。潜在的混杂因素,包括肥胖和吸烟状况,都无法获得。此外,我们排除了20周前结束的妊娠,这可能与产前护理不足有关。危及生命的孕产妇和新生儿发病率在很少或没有产前护理的人群中更为明显。今后的研究和公共卫生方案应侧重于改善获得产前护理的机会和这种护理的质量。J.G.R.和N.M.I.对作品的构思和设计做出了贡献。z.l和S.S.对数据的获取、分析和清理做出了贡献。z.l起草了手稿。所有作者都对原稿进行了修改,并批准了最终版本的出版。由安大略省研究生奖学金资助。 这项研究得到了多伦多大学数据科学研究所(DSI-DAGY3R1P07)和ICES的支持,ICES由安大略省卫生部(MOH)和长期护理部(MLTC)的年度拨款资助。本文所报道的观点、结果和结论均为作者的观点、结果和结论,与资助来源无关。没有得到ICES、卫生部或MLTC的认可,也不应该推断。nmi得到了加拿大循证实践实施研究主席、女子学院医院家庭和社区医学部以及多伦多大学的支持。作者声明无利益冲突。本研究的数据集以编码形式安全地保存在ICES中。虽然国际数据中心与数据提供者(例如医疗保健组织和政府)之间的法律数据共享协议禁止国际数据中心公开提供数据集,但可以向符合预先规定的保密访问标准的人员授予访问权,可通过www.ices.on.ca/DAS(电子邮件:[email protected])获得。完整的数据集创建计划和底层分析代码可根据要求从作者处获得,理解计算机程序可能依赖于编码模板或宏,这些模板或宏是ICES独有的,因此,要么无法访问,要么可能需要修改。
{"title":"Adequacy of Prenatal Care and Ensuing Maternal and Neonatal Severe Morbidity and Mortality","authors":"Zeenat Ladak,&nbsp;Jennifer A. Jairam,&nbsp;Sarah Swayze,&nbsp;Jennifer Shuldiner,&nbsp;Olesya Falenchuk,&nbsp;Richard Volpe,&nbsp;Noah M. Ivers,&nbsp;Joel G. Ray","doi":"10.1111/1471-0528.70119","DOIUrl":"10.1111/1471-0528.70119","url":null,"abstract":"&lt;p&gt;A mother or her infant may face life-threatening events during childbirth or shortly thereafter, which may be preventable [&lt;span&gt;1&lt;/span&gt;]. Adequacy of prenatal care is one determinant of maternal and newborn outcomes [&lt;span&gt;2&lt;/span&gt;]. This study assessed whether adequacy of prenatal care is associated with maternal and newborn morbidity and mortality after birth.&lt;/p&gt;&lt;p&gt;This population-based, retrospective cohort study was completed using deidentified healthcare datasets, linked using unique encoded identifiers at ICES (Table S1). Included were hospital-based singleton livebirths and stillbirths from 20 to 42 weeks' gestation, in Ontario, Canada, from April 1, 2012, to March 31, 2020 (Table S2).&lt;/p&gt;&lt;p&gt;Study variables were chosen a priori (Figure S1). The exposure was adequacy of prenatal care, determined using the Revised-Graduate Prenatal Care Utilisation Index (R-GINDEX), which includes the number of prenatal visits, newborn gestational age, and initiation of first-trimester care [&lt;span&gt;2&lt;/span&gt;]. It reflects adequacy on a five-level scale: no care, inadequate, intermediate, adequate (reference), and intensive care. The primary maternal outcome was a validated composite of any severe &lt;i&gt;maternal&lt;/i&gt; morbidity and mortality (SMM-M) from the mother's delivery hospitalisation date and up to 42 days thereafter [&lt;span&gt;3&lt;/span&gt;]. The primary infant outcome was a validated composite of any severe &lt;i&gt;neonatal&lt;/i&gt; morbidity and mortality (SNM-M) from the infant's birth and up to 27 days thereafter (Table 1) [&lt;span&gt;4&lt;/span&gt;].&lt;/p&gt;&lt;p&gt;Mean values and proportions of baseline variables were contrasted using standardised differences. Modified Poisson regression with generalised estimating equations generated unadjusted and adjusted relative risks (aRR) for SMM-M and SNM-M, respectively, comparing the five-level exposure group of adequacy of prenatal care. The maternal assessment was among all livebirths and stillbirths, while the neonatal assessment was limited to livebirths. Additional analyses were conducted for the outcomes of non-fatal severe maternal morbidity (SMM) and severe neonatal morbidity (SNM), and also for maternal and neonatal mortality. Analyses were performed using SAS version 9.4 software.&lt;/p&gt;&lt;p&gt;Among 955 814 births, 950 757 (99.5%) were livebirths (Figure S2). A total of 924 773 (96.8%) pregnancies had sufficient prenatal care (mean age 30.9 years), while 31 041 (3.2%) did not (mean age 27.9 years) (Table S3 and Table S4).&lt;/p&gt;&lt;p&gt;SMM-M occurred among 27 757 (2.9%) women. Relative to receipt of adequate prenatal care, those with no care had an aRR of SMM-M of 1.42 (95% CI 1.13–1.77) (Table 1). Women with inadequate (aRR 1.08, 95% CI 1.01–1.15) and intensive (aRR 1.04, 95% CI 1.00–1.06) care also had a somewhat higher risk of SMM-M.&lt;/p&gt;&lt;p&gt;SNM-M occurred among 64 613 (6.8%) liveborn infants. Compared to newborns of women who received adequate care, those receiving no prenatal care had the greatest aRR of SNM-M (1.60, 95% CI 1.40–1.83) (Table ","PeriodicalId":50729,"journal":{"name":"Bjog-An International Journal of Obstetrics and Gynaecology","volume":"133 4","pages":"849-851"},"PeriodicalIF":4.3,"publicationDate":"2025-12-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://obgyn.onlinelibrary.wiley.com/doi/epdf/10.1111/1471-0528.70119","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145770802","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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IF 4.3 1区 医学 Q1 OBSTETRICS & GYNECOLOGY Pub Date : 2025-12-16 DOI: 10.1111/1471-0528.70113
Katy Vincent, Andrew Wemyss Horne
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引用次数: 0
Prediction of Adverse Perinatal Outcome in Monochorionic Twin Pregnancy Using Fetal Biometry and Doppler Data: A Multicentre Cohort Study 利用胎儿生物测量和多普勒数据预测单绒毛膜双胎妊娠不良围产期结局:一项多中心队列研究
IF 4.3 1区 医学 Q1 OBSTETRICS & GYNECOLOGY Pub Date : 2025-12-16 DOI: 10.1111/1471-0528.70116
Miriam Lopian, Veronica Giorgione, Mariarita Trapani, Mariafrancesca Brutto, Maria Giulia Ferrante, Amar Bhide, Jacques C. Jani, Dominique A. Badr, Tullio Ghi, Elisa Bevilacqua, Basky Thilaganathan, Alessandra Familiari

Objective

To assess whether combining estimated fetal weight (EFW) and fetal Doppler ultrasound parameters would provide information to optimize the timing of birth in monochorionic twin pregnancies and prevent adverse perinatal outcomes.

Study Design

Retrospective multicentre cohort study.

Setting

Three tertiary centres in the UK, Italy and Belgium.

Population

624 monochorionic twin pregnancies managed between 2013 and 2023.

Methods

Univariable and multivariable analyses assessed the association between EFW and Doppler indices taken within 2 weeks of birth.

Main Outcome Measures

Stillbirth at any gestation or iatrogenic preterm birth before 34 weeks for suspected fetal compromise.

Results

The primary outcome occurred in 143 (22.9%) pregnancies with 70 cases of early PTB for fetal reasons and 73 cases of at least one IUD. Significant associations between biometric and Doppler parameters and adverse perinatal outcomes were found. The best-performing prediction models incorporated EFW discordance and umbilical artery pulsatility index (UA PI) discordance, achieving an AUC of 0.85 (95% CI 0.78–0.91) and EFW discordance and absent or reverse end diastolic flow of UA PI with an AUC of 0.86 (95% CI 0.80–0.92). The model incorporating EFW and UA PI discordance could be applied to the largest proportion of pregnancies and outperformed the currently clinical sFGR classification in predicting adverse outcomes.

Conclusion

A model incorporating intertwin EFW discordance and UA PI discordance outperforms the current clinical classification for prediction of adverse perinatal outcomes in monochorionic pregnancies. If confirmed by further external validation studies, these findings could contribute to building a tailored risk assessment in these pregnancies.

目的探讨结合胎儿体重和胎儿多普勒超声参数对优化单绒毛膜双胎妊娠的分娩时机和预防围产期不良结局的影响。研究设计回顾性多中心队列研究。在英国、意大利和比利时设立了三个高等教育中心。2013年至2023年间,共有624名单绒毛膜双胞胎怀孕。方法采用单变量和多变量分析方法,评价新生儿出生2周内EFW与多普勒指数的相关性。主要观察指标任何妊娠期死产或医源性早产34周前疑似胎儿受损。结果143例(22.9%)妊娠发生了主要结局,其中70例为胎儿原因引起的早期PTB, 73例为至少一个宫内节育器。发现生物特征和多普勒参数与不良围产期结局之间存在显著关联。表现最好的预测模型包括EFW不一致和脐动脉搏动指数(UA PI)不一致,AUC为0.85 (95% CI 0.78-0.91), EFW不一致和UA PI缺失或反向舒张末期血流,AUC为0.86 (95% CI 0.80-0.92)。结合EFW和UA PI不一致的模型可以应用于最大比例的妊娠,并且在预测不良结局方面优于目前临床sFGR分类。结论结合双胎EFW不一致和UA PI不一致的模型在预测单绒毛膜妊娠不良围产期结局方面优于目前的临床分类。如果得到进一步的外部验证研究的证实,这些发现可能有助于在这些妊娠中建立量身定制的风险评估。
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IF 4.3 1区 医学 Q1 OBSTETRICS & GYNECOLOGY Pub Date : 2025-12-15 DOI: 10.1111/1471-0528.70114
Veronica Giorgione, Basky Thilaganathan, Alessandra Familiari, Elisa Bevilacqua
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Quality of Medication Abortion Services From Pharmacies and Drugstores in Ethiopia: A Two-Stage Study 埃塞俄比亚药房和药店的药物流产服务质量:两阶段研究。
IF 4.3 1区 医学 Q1 OBSTETRICS & GYNECOLOGY Pub Date : 2025-12-15 DOI: 10.1111/1471-0528.70110
Tesfaye Tufa, Stephanie Andrea Küng, Delayehu Bekele, Niguse Tadele, Mahari Yihdego, Kidist Lemma, Alice F. Cartwright
<div> <section> <h3> Objective</h3> <p>To assess the quality of medication abortion (MA) services provided in pharmacies and drugstores (‘pharmaceutical outlets’) in Ethiopia.</p> </section> <section> <h3> Design</h3> <p>A two-stage cross-sectional study.</p> </section> <section> <h3> Setting</h3> <p>Pharmaceutical outlets in Addis Ababa, Ethiopia.</p> </section> <section> <h3> Sample</h3> <p>Phase 1: 1696 pharmaceutical outlets listed in the Ethiopian Federal Ministry of Health Master Facility Registry, plus 187 additional outlets identified in the field. Phase 2: Selected 600 pharmaceutical outlets.</p> </section> <section> <h3> Methods</h3> <p>After assessing stock availability in phase 1, during phase 2, mystery clients (MCs) visited pharmaceutical outlets to evaluate service quality using an adapted version of the Abortion Care Quality (ACQ) Tool. Descriptive statistics were used to characterise the quality of services provided by the outlets.</p> </section> <section> <h3> Main Outcome Measures</h3> <p>The quality of abortion services provided by pharmaceutical outlets.</p> </section> <section> <h3> Results</h3> <p>Abortion medications were sold without prescriptions in 23.5% of MC visits. Among these sales, client respect (95.7%) and confidentiality (84.4%) were high. Additionally, 67.1% of staff gave correct instructions on dosage, timing, and administration of the medications. However, less than half of the MCs received adequate information on possible complications (36.4%). Almost all medications purchased were unexpired, packaged in aluminum, and of a known brand (96.5%); however, none were characterised as affordable.</p> </section> <section> <h3> Conclusions</h3> <p>Pharmaceutical outlets demonstrated moderate quality for MA services, yet there were notable gaps in counselling for physical side effects and complications, and affordability challenges. With appropriate policy adjustments and training interventions, there is potential to integrate pharmaceutical outlets into the abortion care service delivery infrastructure, ensuring equitable access to safe and effective abortion services in Ethiopia.</p> </section>
目的评价埃塞俄比亚药店(“药店”)提供的药物流产服务质量。设计:两阶段横断面研究。埃塞俄比亚亚的斯亚贝巴的医药销售点。sample1阶段:在埃塞俄比亚联邦卫生部总设施登记处列出的1696个药品销售点,加上在实地确定的187个其他销售点。第二阶段:选定600个医药网点。方法在第一阶段评估库存可用性后,在第二阶段,神秘客户(MCs)访问药店,使用人工流产护理质量(ACQ)工具评估服务质量。使用描述性统计来描述网点提供的服务质量。主要观察指标:药品网点人工流产服务质量。结果23.5%的医院就诊患者在无处方的情况下销售人工流产药物。在这些销售中,客户尊重(95.7%)和保密性(84.4%)较高。此外,67.1%的员工对药物的剂量、时间和给药给出了正确的指导。然而,不到一半的MCs(36.4%)获得了有关可能并发症的充分信息。几乎所有购买的药品都是未过期的、铝制包装的、知名品牌的(96.5%);然而,没有一个被认为是负担得起的。结论药店MA服务质量一般,但在身体不良反应和并发症咨询方面存在明显差距,价格存在挑战。通过适当的政策调整和培训干预,有可能将药品销售点纳入堕胎护理服务提供基础设施,确保在埃塞俄比亚公平获得安全和有效的堕胎服务。
{"title":"Quality of Medication Abortion Services From Pharmacies and Drugstores in Ethiopia: A Two-Stage Study","authors":"Tesfaye Tufa,&nbsp;Stephanie Andrea Küng,&nbsp;Delayehu Bekele,&nbsp;Niguse Tadele,&nbsp;Mahari Yihdego,&nbsp;Kidist Lemma,&nbsp;Alice F. Cartwright","doi":"10.1111/1471-0528.70110","DOIUrl":"10.1111/1471-0528.70110","url":null,"abstract":"&lt;div&gt;\u0000 \u0000 \u0000 &lt;section&gt;\u0000 \u0000 &lt;h3&gt; Objective&lt;/h3&gt;\u0000 \u0000 &lt;p&gt;To assess the quality of medication abortion (MA) services provided in pharmacies and drugstores (‘pharmaceutical outlets’) in Ethiopia.&lt;/p&gt;\u0000 &lt;/section&gt;\u0000 \u0000 &lt;section&gt;\u0000 \u0000 &lt;h3&gt; Design&lt;/h3&gt;\u0000 \u0000 &lt;p&gt;A two-stage cross-sectional study.&lt;/p&gt;\u0000 &lt;/section&gt;\u0000 \u0000 &lt;section&gt;\u0000 \u0000 &lt;h3&gt; Setting&lt;/h3&gt;\u0000 \u0000 &lt;p&gt;Pharmaceutical outlets in Addis Ababa, Ethiopia.&lt;/p&gt;\u0000 &lt;/section&gt;\u0000 \u0000 &lt;section&gt;\u0000 \u0000 &lt;h3&gt; Sample&lt;/h3&gt;\u0000 \u0000 &lt;p&gt;Phase 1: 1696 pharmaceutical outlets listed in the Ethiopian Federal Ministry of Health Master Facility Registry, plus 187 additional outlets identified in the field. Phase 2: Selected 600 pharmaceutical outlets.&lt;/p&gt;\u0000 &lt;/section&gt;\u0000 \u0000 &lt;section&gt;\u0000 \u0000 &lt;h3&gt; Methods&lt;/h3&gt;\u0000 \u0000 &lt;p&gt;After assessing stock availability in phase 1, during phase 2, mystery clients (MCs) visited pharmaceutical outlets to evaluate service quality using an adapted version of the Abortion Care Quality (ACQ) Tool. Descriptive statistics were used to characterise the quality of services provided by the outlets.&lt;/p&gt;\u0000 &lt;/section&gt;\u0000 \u0000 &lt;section&gt;\u0000 \u0000 &lt;h3&gt; Main Outcome Measures&lt;/h3&gt;\u0000 \u0000 &lt;p&gt;The quality of abortion services provided by pharmaceutical outlets.&lt;/p&gt;\u0000 &lt;/section&gt;\u0000 \u0000 &lt;section&gt;\u0000 \u0000 &lt;h3&gt; Results&lt;/h3&gt;\u0000 \u0000 &lt;p&gt;Abortion medications were sold without prescriptions in 23.5% of MC visits. Among these sales, client respect (95.7%) and confidentiality (84.4%) were high. Additionally, 67.1% of staff gave correct instructions on dosage, timing, and administration of the medications. However, less than half of the MCs received adequate information on possible complications (36.4%). Almost all medications purchased were unexpired, packaged in aluminum, and of a known brand (96.5%); however, none were characterised as affordable.&lt;/p&gt;\u0000 &lt;/section&gt;\u0000 \u0000 &lt;section&gt;\u0000 \u0000 &lt;h3&gt; Conclusions&lt;/h3&gt;\u0000 \u0000 &lt;p&gt;Pharmaceutical outlets demonstrated moderate quality for MA services, yet there were notable gaps in counselling for physical side effects and complications, and affordability challenges. With appropriate policy adjustments and training interventions, there is potential to integrate pharmaceutical outlets into the abortion care service delivery infrastructure, ensuring equitable access to safe and effective abortion services in Ethiopia.&lt;/p&gt;\u0000 &lt;/section&gt;\u0000 ","PeriodicalId":50729,"journal":{"name":"Bjog-An International Journal of Obstetrics and Gynaecology","volume":"133 4","pages":"796-804"},"PeriodicalIF":4.3,"publicationDate":"2025-12-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://obgyn.onlinelibrary.wiley.com/doi/epdf/10.1111/1471-0528.70110","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145752680","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"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
The Use of First-Void Urine to Screen Women Aged 60–79 for HPV in the UK: The Catch-Up Screen Study 在英国使用首次空尿筛查60-79岁女性HPV:追赶筛查研究
IF 4.3 1区 医学 Q1 OBSTETRICS & GYNECOLOGY Pub Date : 2025-12-15 DOI: 10.1111/1471-0528.70115
Christine Rake, Emma J. Davidson, Alex Young, Annelie Maskell, Jennifer C. Davies, Marina Flynn, Sofia Vidali, Hannah Mohy-Eldin, Jiexin Cao, Belinda Nedjai, Una Macleod, Julian Peto, Clare Gilham

Objective

Almost half the deaths from cervical cancer in the UK are among women aged over 65 who were already above the upper age of screening when primary HPV screening was introduced in the UK in 2019. Our aim is to test the feasibility of a national catch-up HPV testing programme.

Design

This first phase of the Catch-Up Screen study involved randomizing over 3000 invited participants to receive a urine HPV test and a follow-up telephone call or text message.

Setting

GP practices in Hull and Manchester, UK.

Population

Women aged 60–79 who have not undergone primary HPV screening.

Methods

Eligible women were selected from GP practice records, and 3074 were invited to provide an at-home first-void urine sample for HPV testing.

Main Outcome Measures

Uptake of at-home urine screening according to screening history, area-level index of deprivation, and randomised follow-up method.

Results

Overall, 59% (1816) of invited women returned a urine sample for HPV testing. Response varied by screening history and index of area-level deprivation, but 39% of those who declined their last invited NHS screen responded favorably and took part in Catch-Up Screen. Telephone reminders yielded a 5% absolute increase in response compared to the text message arm (p = 0.007).

Conclusions

An at-home first-void urine sample is a viable method for a national catch-up HPV test and has the potential to address decreasing national coverage among older women being invited for their last screen.

在英国,近一半死于宫颈癌的女性年龄在65岁以上,当2019年英国引入初级HPV筛查时,她们已经超过了筛查的年龄上限。我们的目的是测试国家追赶HPV检测规划的可行性。该研究的第一阶段包括随机抽取3000多名受邀参与者接受尿液HPV检测,并通过电话或短信随访。设置GP实践在赫尔和曼彻斯特,英国。年龄在60-79岁之间未接受过HPV初级筛查的女性。方法从全科医生执业记录中选择符合条件的妇女,并邀请3074名妇女提供家中首次空尿样本用于HPV检测。主要观察指标:根据筛查史、区域水平剥夺指数和随机随访方法进行家庭尿液筛查。结果总体而言,59%(1816)的受邀女性返回尿液样本进行HPV检测。反应因筛查历史和区域水平剥夺指数而异,但39%拒绝上次邀请的NHS筛查的人反应良好并参加了赶上筛查。与短信组相比,电话提醒组的反应绝对增加了5% (p = 0.007)。结论:家中首次空尿样本是一种可行的全国HPV检测方法,有可能解决全国老年妇女最后一次筛查覆盖率下降的问题。
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引用次数: 0
The Postnatal outcomES of Fetal Cortical mAlformations (PESCA) Study: A Multicentre Historical Cohort Study 胎儿皮质畸形的产后结局(PESCA)研究:一项多中心历史队列研究。
IF 4.3 1区 医学 Q1 OBSTETRICS & GYNECOLOGY Pub Date : 2025-12-15 DOI: 10.1111/1471-0528.70111
Natalia Abadia-Cuchi, Francesca Felici, Sophie Arulkumaran, Faraan Khan, Paolo Frassanito, Andrea Dall'Asta, Elvira di Pasquo, Elisa Bevilacqua, Amarnath Bhide, Tullio Ghi, Matia Martucci, Simona Gaudino, Basky Thilaganathan, Alessandra Familiari

Objectives

To provide further evidence on the outcomes associated with fetal malformations of cortical development (MCD), currently informed by data from symptomatic paediatric cohorts, this study provides a new classification system.

Design

Multicentre retrospective cohort study.

Setting

Fetal medicine units of three tertiary centres in the United Kingdom and Italy.

Population

118 foetuses diagnosed with MCD by ultrasound and/or magnetic resonance imaging included.

Methods

The cases were classified according to their presumed aetiology (genetic, haemorrhage, dysgenesis, infection) and imaging findings (focal, diffuse, mantle, sulcation). Neurodevelopmental delay was classified as mild, moderate or severe. Cases with missing information on postnatal outcome were excluded.

Main Outcome Measures

Postnatal neurodevelopmental outcome ascertained from the infant's neurological assessments according to international performance scales, depending on the age.

Results

There were 52/118 (44%) livebirths, 64/118 (54.2%) terminations of pregnancy (TOP) and 2/118 (1.6%) intrauterine demises. Twenty-five of 46 cases (54.3%, 95% CI 39–69.1) that survived the neonatal period had a normal or mildly delayed neurological development. The commonest aetiology was genetic, and the most frequent radiological finding was reduced sulcation. The best neurological outcome was found in children with focal lesions; those with diffuse hemispheric lesions had the worst one.

Conclusion

This is the largest cohort of foetuses diagnosed with MCDs systematically classified by aetiology and radiological findings. In this retrospective cohort of liveborn survivors, over half had normal or mildly abnormal neurodevelopmental outcomes. Prognosis varied according to lesion pattern and suspected aetiology. Fetal MCDs in this study had better neurodevelopmental outcomes than previously reported, though findings should be interpreted with caution given selection and follow-up limitations.

目的:为了提供胎儿皮质发育畸形(MCD)相关结果的进一步证据,本研究提供了一个新的分类系统。设计多中心回顾性队列研究。设置英国和意大利三所高等教育中心的胎儿医学单位。通过超声和/或磁共振成像诊断为MCD的胎儿包括118例。方法根据推测的病因(遗传、出血、发育不良、感染)和影像学表现(局灶性、弥漫性、套膜性、脉管性)对病例进行分类。神经发育迟缓分为轻度、中度和重度。排除了缺少产后结局信息的病例。主要结果测量:根据国际表现量表,根据婴儿的神经学评估确定出生后的神经发育结果,取决于年龄。结果活产52/118例(44%),终止妊娠64/118例(54.2%),宫内死亡2/118例(1.6%)。新生儿期存活的46例患者中有25例(54.3%,95% CI 39-69.1)神经发育正常或轻度延迟。最常见的病因是遗传,最常见的放射学发现是脉管减少。有局灶性病变的儿童神经学预后最好;弥漫性半球病变患者的症状最严重。结论:这是根据病因和放射学表现进行系统分类的最大的mcd胎儿队列。在这个活产幸存者的回顾性队列中,超过一半的神经发育结果正常或轻度异常。预后因病变类型和疑似病因而异。本研究中胎儿mcd的神经发育结果比先前报道的要好,尽管考虑到选择和随访的局限性,研究结果应谨慎解释。
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引用次数: 0
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Bjog-An International Journal of Obstetrics and Gynaecology
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