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Demographical and Clinical Characteristics of Women with Provoked Vestibulodynia in Israel. 以色列女性诱发性前庭痛的人口学和临床特征。
IF 1.8 Q3 OBSTETRICS & GYNECOLOGY Pub Date : 2025-10-09 eCollection Date: 2025-01-01 DOI: 10.1177/26884844251387013
Lea Tene, Adi Y Weintraub, Leonid Kalichman

Background: Provoked vestibulodynia (PVD) is a chronic pain condition affecting the vulvar vestibule, often triggered by minimal touch or pressure. It is underdiagnosed and poorly understood, leading to significant impacts on women's quality of life.

Objective: This study aims to identify the demographic and clinical characteristics of PVD among women in Israel.

Materials and methods: A cross-sectional study was conducted using an online questionnaire completed by a self-selected sample of adult women. Weighted estimates of vulvodynia prevalence and characteristics were determined.

Results: Out of 250 participants, 196 women (78%) met the diagnostic criteria for PVD. High rates of comorbid conditions were observed, including depression (33%), anxiety (43.3%), and other comorbidities (60%). The mean time from first consulting a physician to diagnosis was 2.5 years, with symptoms persisting for an average of 8 years. Physical therapy emerged as the most effective treatment modality.

Conclusions: PVD is a challenging condition to diagnose and treat, often leading to significant delays in diagnosis and prolonged suffering. The high prevalence of comorbid conditions underscores the need for comprehensive treatment approaches. Improved diagnostic protocols and more effective treatment options are essential to enhance the quality of life for women with PVD.

背景:诱发性前庭痛(PVD)是一种影响外阴前庭的慢性疼痛状况,通常由轻微的触摸或压力引起。该病未得到充分诊断和了解,导致对妇女生活质量产生重大影响。目的:本研究旨在确定以色列女性PVD的人口统计学和临床特征。材料和方法:横断面研究采用一份在线问卷,由自选的成年女性样本完成。确定外阴痛患病率和特征的加权估计。结果:在250名参与者中,196名女性(78%)符合PVD的诊断标准。观察到较高的合并症发生率,包括抑郁(33%)、焦虑(43.3%)和其他合并症(60%)。从第一次咨询医生到诊断的平均时间为2.5年,症状平均持续8年。物理治疗成为最有效的治疗方式。结论:PVD是一种诊断和治疗具有挑战性的疾病,经常导致诊断延误和延长痛苦。合并症的高患病率强调了综合治疗方法的必要性。改进诊断方案和更有效的治疗选择对于提高PVD妇女的生活质量至关重要。
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引用次数: 0
Real-World Safety and Effectiveness of Ganirelix for Ovarian Stimulation in Chinese Women: A Multicenter, Prospective, Single-Arm, Observational Study. Ganirelix用于中国女性卵巢刺激的安全性和有效性:一项多中心、前瞻性、单组、观察性研究。
IF 1.8 Q3 OBSTETRICS & GYNECOLOGY Pub Date : 2025-10-09 eCollection Date: 2025-01-01 DOI: 10.1177/26884844251387017
Jia Li, Fei Gong, Lihong Geng, Xiaohong Wang, Zhaolian Wei, Jianqiao Liu, Yong Zeng, Jue Wang, Keith Gordon, Sisi Chen, Rui Yang, Rong Li

Background: This study aimed to evaluate the safety and effectiveness of ganirelix acetate for Chinese women undergoing ovarian stimulation (OS) in real-world clinical practice.

Methods: This multicenter (16), prospective, single-arm, observational, post-authorization safety study included 1025 Chinese women receiving at least one dose of ganirelix during OS. Safety endpoints were collected until 5 weeks after embryo transfer. The investigator assessed the causality and seriousness of an adverse event (AE). Effectiveness and neonatal outcomes were collected from medical records and phone call follow-ups. The study had a probability of >95% to observe an AE occurring at 0.3% with a sample size of 1000.

Results: The occurrence of overall AEs, drug-related AEs, and serious AEs (SAEs) was 12.1% (124/1025), 1.3% (13/1025), and 2.4% (25/1025), respectively. None of the SAEs were drug related, according to the investigator. Two (0.2%) patients discontinued treatment due to an AE. The most reported AE was ovarian hyperstimulation syndrome (4.8%, 49/1025), among which 21 cases were reported as SAE. The proportion of patients with a premature luteinizing hormone (LH) rise >10 IU/L) was 2.5% (26/1025), and one patient had a premature ovulation. The live birth rate was 34.9% (358/1025) per start cycle with a cumulative live birth rate of 42.1% (432/1025). Neonatal malformations occurred in 1.3% (7/523) of the neonates.

Conclusions: This study indicates that the safety profile and effectiveness of ganirelix were clinically acceptable, and no new safety signals emerged in real-world clinical practice for Chinese women with OS. The study was registered on Chinadrugtrial.org (identifier: CTR20150284) (http://www.chinadrugtrials.org.cn) and ENCePP.eu (identifier: EUPAS8737) (https://catalogues.ema.europa.eu).

背景:本研究旨在评价醋酸甘尼瑞司用于卵巢刺激(OS)中国女性临床实践的安全性和有效性。方法:这项多中心(16)、前瞻性、单臂、观察性、授权后安全性研究包括1025名在OS期间接受至少一剂ganirelix的中国女性。安全终点收集至胚胎移植后5周。研究者评估了不良事件(AE)的因果关系和严重程度。从医疗记录和电话随访中收集有效性和新生儿结局。该研究在1000个样本量的情况下,观察到AE发生率为0.3%的概率为95%。结果:总不良事件发生率为12.1%(124/1025),药物相关不良事件发生率为1.3%(13/1025),严重不良事件发生率为2.4%(25/1025)。据调查人员称,所有的SAEs都与药物无关。2例(0.2%)患者因AE停止治疗。AE报告最多的是卵巢过度刺激综合征(4.8%,49/1025),其中SAE报告21例。黄体生成素(LH)过早升高(10 IU/L)的患者比例为2.5%(26/1025),1例患者出现早泄。每个起始周期的活产率为34.9%(358/1025),累计活产率为42.1%(432/1025)。新生儿畸形发生率为1.3%(7/523)。结论:本研究表明,ganirelix的安全性和有效性在临床上是可接受的,并且在现实世界的临床实践中没有出现新的安全性信号。本研究已在Chinadrugtrial.org(识别码:CTR20150284) (http://www.chinadrugtrials.org.cn)和ENCePP上注册。eu(标识符:EUPAS8737) (https://catalogues.ema.europa.eu)。
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引用次数: 0
Cannabis and Nicotine Substance Use Coercion During the Perinatal Period. 围产期大麻和尼古丁物质强制使用。
IF 1.8 Q3 OBSTETRICS & GYNECOLOGY Pub Date : 2025-10-08 eCollection Date: 2025-01-01 DOI: 10.1177/26884844251387024
Peyton Groves, Callie Laubacher, Yesmina Salib, Erin Mickievicz, Virginia Duplessis, Nicole Molinaro, Dara D Méndez, Katherine Guyon-Harris, Ruben G Martinez, Judy Chang, Natacha M De Genna, Maya I Ragavan

Introduction: Perinatal intimate partner violence (IPV) and perinatal cannabis and nicotine product use are common and associated with negative maternal-infant health outcomes. Substance use coercion (SUC), which involves abusive partners' controlling behaviors related to substance use, has not been studied for cannabis and nicotine products. Perinatal individuals may be particularly vulnerable to SUC, and this study aims to explore how cannabis and nicotine SUC manifests among perinatal survivors.

Methods: We conducted virtual, semi-structured, 45-minute retrospective interviews with 19 IPV advocates and 15 perinatal IPV survivors. Participants were recruited through local IPV agencies and an online recruitment repository. Audio-recorded interviews were transcribed and analyzed using a deductive-inductive thematic analysis approach. Two research team members individually coded each transcript and met to resolve discrepancies.

Results: Key themes emerged relating to survivors' use, interpersonal coercive tactics, and systems-level control. Specific findings included (1) survivors using substances to cope; (2) abusive partners coercing survivors through withholding, controlling, and punishing substance use; (3) shame and stigma are key drivers of coercion; (4) partners hinder cessation efforts; and (5) child protective services and health care are systems used by abusive partners to control and manipulate perinatal survivors of IPV.

Discussion: The findings demonstrate that cannabis and nicotine products are used to coerce and control survivors of IPV. Future work should focus on developing survivor-centered interventions within systems to better support perinatal IPV survivors using cannabis and nicotine products. This study highlights the impact of cannabis and nicotine SUC on perinatal individuals and underscores the need to consider SUC when providing resources or treatment.

围产期亲密伴侣暴力(IPV)和围产期大麻和尼古丁产品的使用是常见的,并与负面母婴健康结果相关。物质使用胁迫(SUC)涉及虐待伴侣对物质使用的控制行为,尚未对大麻和尼古丁产品进行研究。围产期个体可能特别容易受到SUC的影响,本研究旨在探讨大麻和尼古丁SUC在围产期幸存者中的表现。方法:我们对19名IPV倡导者和15名围产期IPV幸存者进行了虚拟的、半结构化的、45分钟的回顾性访谈。参与者是通过当地IPV机构和在线招聘库招募的。录音采访被转录和分析使用演绎-归纳主题分析方法。两名研究小组成员分别对每个转录本进行编码,并会面解决差异。结果:出现了与幸存者使用、人际胁迫策略和系统级控制有关的关键主题。具体发现包括:(1)幸存者使用物质来应对;(2)施虐伴侣通过扣留、控制和惩罚药物使用来胁迫幸存者;(3)羞耻和污名是胁迫的主要驱动因素;(4)伴侣阻碍戒烟努力;(5)儿童保护服务和卫生保健是施虐伴侣用来控制和操纵IPV围产期幸存者的系统。讨论:研究结果表明,大麻和尼古丁产品被用来胁迫和控制IPV幸存者。未来的工作应侧重于在系统内开发以幸存者为中心的干预措施,以更好地支持使用大麻和尼古丁产品的围产期IPV幸存者。本研究强调了大麻和尼古丁的SUC对围产期个体的影响,并强调了在提供资源或治疗时考虑SUC的必要性。
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引用次数: 0
Pressure and Pain: A Qualitative Pilot Study Describing the Complexity of Unhoused Women's Experiences with Reproductive Care. 压力和疼痛:定性试点研究描述的复杂性无住房妇女的经验与生殖保健。
IF 1.8 Q3 OBSTETRICS & GYNECOLOGY Pub Date : 2025-10-08 eCollection Date: 2025-01-01 DOI: 10.1177/26884844251387016
Casey C Woods, Anthony L Shanks, Niki Messmore, Krista J Longtin

Introduction: While there is extant literature surrounding barriers to reproductive care in the unhoused population-especially regarding access to contraception-little attention has been given to patient perspectives and the quality of care that is received. The unhoused population, which is disproportionately persons of color and low income, has a higher prevalence of psychiatric and physical disabilities. This is a population that has historically been a victim of eugenics and coercive practice.

Study objective: The purpose of the study is to qualitatively understand the experiences of currently unhoused women with pregnancy, birth control, and sterilization, as well as analyze their perspectives in their clinical encounters over their lifetime.

Materials and methods: Participants (n = 10) were recruited from two shelters in a midwestern city. The sample consisted of those assigned female at birth, are currently experiencing homelessness, and have experience with obstetrical and gynecological health care. A semistructured interview was conducted with each participant utilizing a question bank. Audio was recorded, transcribed, and coded for themes.

Results: The main themes coded from the interviews were negative birthing and/or sterilization experience, lack of shared decision-making for birth control and/or sterilization, pressure to undergo sterilization and/or go on birth control, the desire for a nonjudgmental provider, and sexual violence experience.

Conclusions/implications: Our data indicate that women experiencing homelessness (WEH) may prefer contraceptive conversations that are trauma-informed and rooted in a shared decision-making model, which in turn may help WEH develop more agency around their reproductive health care. This pilot study also emphasizes the need for more qualitative research to evaluate experiences directly in the population of interest.

导言:虽然现有文献围绕无住房人口生殖保健的障碍-特别是关于获得避孕措施-很少注意到病人的观点和所接受的护理质量。无住房人口主要是有色人种和低收入人群,他们患精神和身体残疾的比例更高。这一群体在历史上一直是优生学和强制实践的受害者。研究目的:本研究的目的是定性地了解目前无家可归的怀孕、节育和绝育妇女的经历,并分析她们一生中在临床遭遇中的观点。材料和方法:参与者(n = 10)从中西部城市的两个避难所招募。样本包括出生时被指定为女性、目前无家可归、有产科和妇科保健经验的人。采用半结构化访谈,每位参与者使用一个问题库。音频是为主题录制、转录和编码的。结果:从访谈中编码的主要主题是消极的生育和/或绝育经历,缺乏共同的节育和/或绝育决策,接受绝育和/或继续节育的压力,对非评判性提供者的渴望,以及性暴力经历。结论/启示:我们的数据表明,经历过无家可归的女性(WEH)可能更喜欢了解创伤并植根于共同决策模式的避孕对话,这反过来可能有助于WEH在其生殖保健方面建立更多的代理机构。这项初步研究还强调需要更多的定性研究来直接评价相关人群的经验。
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引用次数: 0
A Multilevel Framework for the Promotion of Maternal Mental Health and Well-Being During the Perinatal Period. 促进围产期产妇心理健康和福祉的多层次框架。
IF 1.8 Q3 OBSTETRICS & GYNECOLOGY Pub Date : 2025-10-08 eCollection Date: 2025-01-01 DOI: 10.1177/26884844251386007
Jenn A Leiferman, Jessica Walls Wilson, Charlotte V Farewell, Chelsea Walker-Mao, James F Paulson

Background: Depression and anxiety are prevalent in the perinatal period and may contribute to adverse maternal and child health outcomes. A focus on multilevel protective factors may be effective in promoting well-being and increasing quality of life (QOL) in the perinatal period while simultaneously reducing or preventing depression and anxiety symptoms. We tested a conceptual model that posits specific personal, social, and community factors affecting depression, anxiety, and QOL among pregnant and postpartum individuals.

Methods: Four hundred and thirty-eight pregnant or postpartum individuals completed a 121-item cross-sectional survey composed of validated tools that assessed multilevel protective factors, health behaviors, and mental health outcomes. Confirmatory factor analysis (CFA) was constructed to evaluate a 3-part conceptual model against measured indicators of well-being. A structural equation model (SEM) was then fit to test the pattern of associations between our latent structure and three end points: depression, anxiety, and QOL.

Results: The CFA fit the data well (comparative fit index [CFI] = 0.907, Tucker-Lewis index [TLI] = 0.876, root-mean-square error of approximation [RMSEA] = 0.092) supporting the proposed conceptual approach to measuring well-being. The SEM fit well (CFI = 0.964, TLI = 0.941, RMSEA = 0.059), and all three end points were predicted in the hypothesized direction. Social factors predicted reduced anxiety symptomatology, personal and community resources predicted reduced depressive symptomatology, and social resources predicted increased QOL. In addition, we found that collective community resources were associated with social and personal resources, and social resources directly affected personal resources, showing the benefit of multiple levels.

Conclusions: Our findings suggest that both the collection of and interplay between certain personal, social, and community-level resources may prevent and protect against depression and anxiety and promote QOL. Our conceptual model provides a framework to inform future interventions and clinical practice to better assess and promote maternal well-being during the perinatal period.

背景:抑郁和焦虑在围产期普遍存在,并可能导致不利的母婴健康结果。关注多层次的保护因素可能有效地促进围产期的健康和提高生活质量,同时减少或预防抑郁和焦虑症状。我们测试了一个概念模型,该模型假设了影响孕妇和产后个体抑郁、焦虑和生活质量的特定个人、社会和社区因素。方法:438名孕妇或产后个体完成了一项121项的横断面调查,该调查由经过验证的工具组成,评估了多层次的保护因素、健康行为和心理健康结果。验证性因子分析(CFA)被构建来评估一个由三部分组成的概念模型对幸福感的测量指标。然后拟合结构方程模型(SEM)来检验我们的潜在结构与三个终点之间的关联模式:抑郁、焦虑和生活质量。结果:CFA很好地拟合了数据(比较拟合指数[CFI] = 0.907, Tucker-Lewis指数[TLI] = 0.876,近似均方根误差[RMSEA] = 0.092),支持提出的概念方法来测量幸福感。SEM拟合良好(CFI = 0.964, TLI = 0.941, RMSEA = 0.059),三个终点均在假设方向预测。社会因素预测焦虑症状减轻,个人和社区资源预测抑郁症状减轻,社会资源预测生活质量提高。此外,我们发现集体社区资源与社会资源和个人资源存在关联,社会资源直接影响个人资源,呈现出多层次的效益。结论:我们的研究结果表明,某些个人、社会和社区层面的资源的收集和相互作用可以预防和保护抑郁和焦虑,并提高生活质量。我们的概念模型提供了一个框架,为未来的干预和临床实践提供信息,以更好地评估和促进围产期产妇的健康。
{"title":"A Multilevel Framework for the Promotion of Maternal Mental Health and Well-Being During the Perinatal Period.","authors":"Jenn A Leiferman, Jessica Walls Wilson, Charlotte V Farewell, Chelsea Walker-Mao, James F Paulson","doi":"10.1177/26884844251386007","DOIUrl":"10.1177/26884844251386007","url":null,"abstract":"<p><strong>Background: </strong>Depression and anxiety are prevalent in the perinatal period and may contribute to adverse maternal and child health outcomes. A focus on multilevel protective factors may be effective in promoting well-being and increasing quality of life (QOL) in the perinatal period while simultaneously reducing or preventing depression and anxiety symptoms. We tested a conceptual model that posits specific personal, social, and community factors affecting depression, anxiety, and QOL among pregnant and postpartum individuals.</p><p><strong>Methods: </strong>Four hundred and thirty-eight pregnant or postpartum individuals completed a 121-item cross-sectional survey composed of validated tools that assessed multilevel protective factors, health behaviors, and mental health outcomes. Confirmatory factor analysis (CFA) was constructed to evaluate a 3-part conceptual model against measured indicators of well-being. A structural equation model (SEM) was then fit to test the pattern of associations between our latent structure and three end points: depression, anxiety, and QOL.</p><p><strong>Results: </strong>The CFA fit the data well (comparative fit index [CFI] = 0.907, Tucker-Lewis index [TLI] = 0.876, root-mean-square error of approximation [RMSEA] = 0.092) supporting the proposed conceptual approach to measuring well-being. The SEM fit well (CFI = 0.964, TLI = 0.941, RMSEA = 0.059), and all three end points were predicted in the hypothesized direction. Social factors predicted reduced anxiety symptomatology, personal and community resources predicted reduced depressive symptomatology, and social resources predicted increased QOL. In addition, we found that collective community resources were associated with social and personal resources, and social resources directly affected personal resources, showing the benefit of multiple levels.</p><p><strong>Conclusions: </strong>Our findings suggest that both the collection of and interplay between certain personal, social, and community-level resources may prevent and protect against depression and anxiety and promote QOL. Our conceptual model provides a framework to inform future interventions and clinical practice to better assess and promote maternal well-being during the perinatal period.</p>","PeriodicalId":75329,"journal":{"name":"Women's health reports (New Rochelle, N.Y.)","volume":"6 1","pages":"1141-1152"},"PeriodicalIF":1.8,"publicationDate":"2025-10-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12549176/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145380194","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Two Decades and Counting Since the Abuja Summit: Where Do We Stand in the Fight Against HIV/AIDS-Related Maternal Mortality? 阿布贾首脑会议20年以来:我们在防治艾滋病毒/艾滋病相关孕产妇死亡率方面进展如何?
IF 1.8 Q3 OBSTETRICS & GYNECOLOGY Pub Date : 2025-10-08 eCollection Date: 2025-01-01 DOI: 10.1177/26884844251386289
Richmond Nketia, Austin Gideon Adobasom-Anane, Sandra Mensah, Faustina Ameyaa Marfo, Hannatu Favour Kachiro, Rostand Dimitri Messanga Bessala, Naomi Adotei, Abubakr Ahmed Farhan, Charles Limula, Ebenezer Gyamfi, Gideon Asamoah, Daniel Atta-Nyarko

Background: It is more than two decades since the Organisation of African Unity's historic Abuja Summit, yet the fight against human immunodeficiency virus/acquired immunodeficiency syndrome (HIV/AIDS)-related maternal deaths in the region remains as critical as ever. This study examined four key dimensions to inform future actions: cross-national comparison of current HIV/AIDS-related maternal deaths, temporal trends in mortalities (for pre- and post-Abuja periods), variations across age groups and birth cohorts, and potential policy levers to drive progress.

Methods: Poisson regression-based age-period-cohort models were fitted to the Global Burden of Disease Study 2021 (GBD 2021) data (1982-2021; N = 47,750 HIV/AIDS-aggravated maternal mortalities) to estimate age, calendar period, and birth cohort effects on mortalities for each of the 54 African countries.

Results: Notable variations in HIV/AIDS-aggravated maternal deaths were observed across Africa. In 2021, 16 of the 54 countries had age-standardized mortality rates near zero, while 38 countries reported rates ranging from 0.07 to 0.95 per 100,000 women. Mortality rates rose sharply from the early 1980s, peaked during the 1990s and early 2000s, and generally declined after the Abuja Summit; however, the trajectories varied considerably across the continent. Mortality also increased with age, with substantial heterogeneity in country-level patterns. In more than two-thirds of countries, cohort comparisons relative to a 1967 baseline showed marked increases in mortalities in recent birth cohorts.

Conclusions: Given the marked variations in HIV/AIDS-aggravated maternal mortality among African populations, this study advocates for context-specific, life-course strategies to drive progress toward universal health coverage and improved maternal health across Africa.

背景:非洲统一组织历史性的阿布贾首脑会议已经过去二十多年了,但本区域防治与人体免疫机能丧失病毒/后天免疫机能丧失综合症(艾滋病毒/艾滋病)有关的孕产妇死亡的斗争仍然一如既往地至关重要。这项研究审查了四个关键方面,为今后的行动提供信息:目前与艾滋病毒/艾滋病有关的孕产妇死亡的跨国比较、死亡率的时间趋势(阿布贾前后)、各年龄组和出生队列之间的差异以及推动进展的潜在政策杠杆。方法:将基于泊松回归的年龄-时期-队列模型拟合到全球疾病负担研究2021 (GBD 2021)数据中(1982-2021;N = 47,750例艾滋病毒/艾滋病加重的孕产妇死亡率),以估计54个非洲国家中年龄、自然期和出生队列对死亡率的影响。结果:非洲各地因艾滋病毒/艾滋病导致的孕产妇死亡情况存在显著差异。2021年,54个国家中有16个国家的年龄标准化死亡率接近于零,38个国家报告的死亡率在每10万名妇女0.07至0.95之间。死亡率从1980年代初开始急剧上升,在1990年代和2000年代初达到顶峰,在阿布贾首脑会议之后普遍下降;然而,整个非洲大陆的发展轨迹差异很大。死亡率也随着年龄的增长而增加,在国家一级的模式上存在很大的异质性。在超过三分之二的国家中,相对于1967年基线的队列比较显示,最近出生队列的死亡率显着增加。结论:鉴于非洲人口中艾滋病毒/艾滋病加剧的孕产妇死亡率存在显著差异,本研究主张采取针对具体情况的生命历程战略,以推动非洲全民健康覆盖和改善孕产妇健康。
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引用次数: 0
Real-World Outcomes of Brexanolone to Treat Postpartum Depression. 布雷沙诺酮治疗产后抑郁症的实际效果。
IF 1.8 Q3 OBSTETRICS & GYNECOLOGY Pub Date : 2025-10-06 eCollection Date: 2025-01-01 DOI: 10.1177/26884844251383702
Melanie Barrett, Jennifer Hettema, Constance Youngman, Samuel T Wilkinson, Rachel Dalthorp

Background: While the efficacy of brexanolone, a U.S. Food and Drug Administration-approved infusion treatment for postpartum depression (PPD), has been demonstrated in controlled trials, few reports are available describing its real-world effectiveness.

Methods: Leveraging real-world clinical data, the current report describes the characteristics and treatment outcomes of a sample of women (N = 150) receiving brexanolone treatment for PPD in a residential-style outpatient treatment center with up to 12 months of follow-up. The sample had a mean age of 30.0 years (SD = 4.5), with almost one-third (31.3%) on hormonal birth control, and most (91.3%) were taking concomitant psychiatric medications.

Results: Participants reported significant decreases in depression and anxiety symptoms from pretreatment to posttreatment that were sustained across a 12-month follow-up. Edinburgh postnatal depression scale (EPDS) scores decreased from pretreatment (M = 19.9, SD = 4.1) to posttreatment (M = 10.5, SD = 4.5, p < 0.001, within-group effect size [Cohen's d] of 2.2). At 12 months follow-up, EPDS scores remained significantly lower among the retained subset of patients (N = 64, M = 9.2, SD = 6.5). Among a subset who underwent formal assessments for anxiety, scores on the perinatal anxiety screening scale decreased from pretreatment (M = 60.1, SD = 17.1) to posttreatment (M = 33.3, SD = 22.1, p < 0.01, within-group effect size of 1.4). Response and remission rates for depression were 68.7% and 46.7%, respectively, posttreatment, and 73.4% and 60.9%, respectively, at 12-month follow-up. Importantly, 15 participants had a diagnosis of bipolar depression and were prescribed an antipsychotic or mood stabilizer at the time of treatment, there were no episodes of mania or hypomania reported during the follow-up period.

Conclusions: Given the shared mechanism of action between brexanolone and the recently approved oral medication for PPD, zuranolone, the applicability of findings and relevance to the more accessible oral drug, zuranolone, are explored.

背景:brexanolone是美国食品和药物管理局批准的一种用于产后抑郁症(PPD)输液治疗的药物,虽然其疗效已在对照试验中得到证实,但很少有报道描述其实际疗效。方法:利用真实世界的临床数据,本报告描述了一组妇女样本(N = 150)的特征和治疗结果,她们在一个住院式门诊治疗中心接受布雷沙诺酮治疗PPD,随访长达12个月。样本的平均年龄为30.0岁(SD = 4.5),几乎三分之一(31.3%)的人使用激素避孕,大多数(91.3%)的人同时服用精神药物。结果:参与者报告了从治疗前到治疗后抑郁和焦虑症状的显著减少,并持续了12个月的随访。爱丁堡产后抑郁量表(EPDS)评分从治疗前(M = 19.9, SD = 4.1)降至治疗后(M = 10.5, SD = 4.5, p < 0.001,组内效应量[Cohen's d]为2.2)。在12个月的随访中,保留的患者亚群的EPDS评分仍然明显较低(N = 64, M = 9.2, SD = 6.5)。在接受正式焦虑评估的子集中,围产期焦虑筛查量表得分从治疗前(M = 60.1, SD = 17.1)降至治疗后(M = 33.3, SD = 22.1, p < 0.01,组内效应量为1.4)。治疗后抑郁症的缓解率和缓解率分别为68.7%和46.7%,12个月随访时分别为73.4%和60.9%。重要的是,15名参与者被诊断为双相抑郁症,并在治疗期间服用抗精神病药或情绪稳定剂,在随访期间没有躁狂或轻躁狂发作的报告。结论:鉴于布雷沙诺酮与最近批准的PPD口服药物祖拉诺酮之间的共同作用机制,本研究探讨了研究结果的适用性及其与更容易获得的口服药物祖拉诺酮的相关性。
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引用次数: 0
Clinical Outcomes of Single-Port Versus Conventional Multiport Laparoscopic Myomectomy: A Retrospective Study. 单孔与常规多孔腹腔镜子宫肌瘤切除术的临床结果:回顾性研究。
IF 1.8 Q3 OBSTETRICS & GYNECOLOGY Pub Date : 2025-09-30 eCollection Date: 2025-01-01 DOI: 10.1177/26884844251383823
Yucui Zeng, Ping Li, Yushan Li, Wenwei Luo, Xiaoyan Guang

Introduction: To compare the clinical outcomes of laparoscopic myomectomy via single-port approach (SPLM) and conventional multiport laparoscopic myomectomy (MPLM).

Methods: A retrospective analysis was conducted on 149 patients with uterine fibroids, including 77 who underwent MPLM and 72 who underwent SPLM. Patient baseline characteristics and perioperative indicators were compared to evaluate surgical efficacy.

Results: No significant differences were observed between the two groups in demographic characteristics, fibroid number, or maximum fibroid diameter (p > 0.05). The SPLM group had a higher proportion of anterior wall fibroids (45.8% vs. 26.0%) and subserosal fibroids (38.9% vs. 18.2%) compared to the MPLM group (p < 0.05). The SPLM group showed significantly better outcomes in total operative time (99.85 ± 33.65 minutes vs. 120.91 ± 49.48 minutes), time to postoperative gastrointestinal recovery (1.40 ± 0.55 days vs. 1.69 ± 0.47 days), and 24-hour postoperative visual analog scale (VAS) score (2.33 ± 0.65 vs. 2.70 ± 0.84) (p < 0.05). No significant differences were found in intraoperative blood loss, postoperative complication rates, or hospital stay between the two groups in the overall analysis. However, based on the four influencing factors, further stratified analysis within each factor revealed that SPLM was more advantageous for treating single fibroids, fibroids less than 8 cm in diameter, and intramural fibroids, demonstrating significantly shorter operative times than MPLM (p < 0.05). Surgeon A demonstrated superior outcomes in both operative time and intraoperative blood loss when performing myomectomy via the single-port laparoscopic approach compared to the multiport technique (p ≤ 0.05).

Conclusion: SPLM is a safe and effective surgical approach. For single intramural fibroids less than 8 cm in diameter, it demonstrates superior operative efficiency compared to conventional MPLM, particularly regarding operative time. When performed by the senior surgeon, the advantages of SPLM become even more pronounced in both operative duration and intraoperative blood loss.

前言:比较单孔入路腹腔镜子宫肌瘤切除术(SPLM)与常规多孔腹腔镜子宫肌瘤切除术(MPLM)的临床效果。方法:对149例子宫肌瘤患者进行回顾性分析,其中MPLM 77例,SPLM 72例。比较患者的基线特征和围手术期指标,评估手术疗效。结果:两组在人口学特征、肌瘤数量、最大肌瘤直径方面无显著差异(p < 0.05)。SPLM组前壁肌瘤比例(45.8%比26.0%)和浆膜下肌瘤比例(38.9%比18.2%)高于MPLM组(p < 0.05)。SPLM组在总手术时间(99.85±33.65 min vs. 120.91±49.48 min)、术后胃肠恢复时间(1.40±0.55 d vs. 1.69±0.47 d)、术后24小时视觉模拟评分(VAS)(2.33±0.65 vs. 2.70±0.84)方面均显著优于SPLM组(p < 0.05)。在整体分析中,两组在术中出血量、术后并发症发生率或住院时间方面无显著差异。然而,基于四个影响因素,进一步对每个因素进行分层分析,发现SPLM更有利于治疗单个肌瘤、直径小于8cm的肌瘤和壁内肌瘤,且手术时间明显短于MPLM (p < 0.05)。外科医生A在单孔腹腔镜子宫肌瘤切除术的手术时间和术中出血量方面均优于多孔腹腔镜手术(p≤0.05)。结论:SPLM是一种安全有效的手术入路。对于直径小于8cm的单个壁内肌瘤,与传统MPLM相比,它显示出更高的手术效率,特别是在手术时间方面。当由资深外科医生实施时,SPLM在手术时间和术中出血量方面的优势更加明显。
{"title":"Clinical Outcomes of Single-Port Versus Conventional Multiport Laparoscopic Myomectomy: A Retrospective Study.","authors":"Yucui Zeng, Ping Li, Yushan Li, Wenwei Luo, Xiaoyan Guang","doi":"10.1177/26884844251383823","DOIUrl":"10.1177/26884844251383823","url":null,"abstract":"<p><strong>Introduction: </strong>To compare the clinical outcomes of laparoscopic myomectomy <i>via</i> single-port approach (SPLM) and conventional multiport laparoscopic myomectomy (MPLM).</p><p><strong>Methods: </strong>A retrospective analysis was conducted on 149 patients with uterine fibroids, including 77 who underwent MPLM and 72 who underwent SPLM. Patient baseline characteristics and perioperative indicators were compared to evaluate surgical efficacy.</p><p><strong>Results: </strong>No significant differences were observed between the two groups in demographic characteristics, fibroid number, or maximum fibroid diameter (<i>p</i> > 0.05). The SPLM group had a higher proportion of anterior wall fibroids (45.8% vs. 26.0%) and subserosal fibroids (38.9% vs. 18.2%) compared to the MPLM group (<i>p</i> < 0.05). The SPLM group showed significantly better outcomes in total operative time (99.85 ± 33.65 minutes vs. 120.91 ± 49.48 minutes), time to postoperative gastrointestinal recovery (1.40 ± 0.55 days vs. 1.69 ± 0.47 days), and 24-hour postoperative visual analog scale (VAS) score (2.33 ± 0.65 vs. 2.70 ± 0.84) (<i>p</i> < 0.05). No significant differences were found in intraoperative blood loss, postoperative complication rates, or hospital stay between the two groups in the overall analysis. However, based on the four influencing factors, further stratified analysis within each factor revealed that SPLM was more advantageous for treating single fibroids, fibroids less than 8 cm in diameter, and intramural fibroids, demonstrating significantly shorter operative times than MPLM (<i>p</i> < 0.05). Surgeon A demonstrated superior outcomes in both operative time and intraoperative blood loss when performing myomectomy <i>via</i> the single-port laparoscopic approach compared to the multiport technique (<i>p</i> ≤ 0.05).</p><p><strong>Conclusion: </strong>SPLM is a safe and effective surgical approach. For single intramural fibroids less than 8 cm in diameter, it demonstrates superior operative efficiency compared to conventional MPLM, particularly regarding operative time. When performed by the senior surgeon, the advantages of SPLM become even more pronounced in both operative duration and intraoperative blood loss.</p>","PeriodicalId":75329,"journal":{"name":"Women's health reports (New Rochelle, N.Y.)","volume":"6 1","pages":"1061-1069"},"PeriodicalIF":1.8,"publicationDate":"2025-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12549164/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145373241","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Level of Agreement Between a Modified, Three-Step Menstrual Cycle Tracking Method and a Female-Health Menstrual Cycle Tracking App. 改进的三步月经周期跟踪方法与女性健康月经周期跟踪应用程序之间的一致程度。
IF 1.8 Q3 OBSTETRICS & GYNECOLOGY Pub Date : 2025-09-30 eCollection Date: 2025-01-01 DOI: 10.1177/26884844251379415
Marissa L Doroshuk, Constance M Lebrun, Patricia K Doyle-Baker

Background: A need exists to incorporate evidence-based tracking methods that measure menstrual cycle (MC) variability to describe the data quality provided by an app. The study purpose was to assess the agreement between an app's cycle phase identifications and a modified version of the three-step method (m3stepMC) of hormone verification.

Materials and methods: Participants across Canada were recruited to track their MC over 3 months by entering data into a female-health MC tracking app (the app) while collecting measures of ovulation and salivary hormones around the late-follicular (FP) and mid-luteal (MLP) phases, respectively. Bland-Altman plots assessed the limits of agreement (LoA) between the identified days within each of the app's predetermined phases and the m3stepMC-identified days when MC dates aligned between the methods. Pearson's correlations (r) were used to examine the effect size of relationships between variables.

Results: Participants' (n = 25) mean age was 29.3 ± 4.24 with self-reported mean cycle lengths of 27.3 ± 2.38 days. The agreement between the app's estimated (1) end of phase one and the estimated start of the mid-FP was 0.6 ± 1.66 days (95% LoA: 2.65-3.85; r = 0.66), (2) end of phase two and the identified luteinizing hormone (LH) surge day and midpoint of phase three and the estimated 48-hour ovulatory window post-LH surge day were -0.6 ± 1.71 days (95% LoA: -3.95 to 2.75; r = 0.64), and (3) phase four and the estimated MLP day verified by salivary hormones and the start of the app's phase five and the estimated late-luteal midpoint day were -2.2 ± 0.97 (95% LoA: -4.13 to -0.32; r = 0.94).

Conclusion: This study describes the agreement between a m3stepMC tracking method and hormone measures and an app's predetermined MC phase system in eumenorrheic cycles when MC dates aligned between methods.

背景:需要采用基于证据的跟踪方法来测量月经周期(MC)可变性,以描述应用程序提供的数据质量。研究目的是评估应用程序的周期阶段识别与激素验证的三步法(m3stepMC)的修改版本之间的一致性。材料和方法:招募加拿大各地的参与者,通过将数据输入女性健康MC跟踪应用程序(该应用程序),同时分别收集卵泡晚期(FP)和黄体中期(MLP)前后的排卵和唾液激素测量,跟踪他们的MC超过3个月。Bland-Altman图评估了应用程序每个预定阶段内确定的天数与MC日期在两种方法之间一致的m3stepmc -确定的天数之间的一致性限制(LoA)。Pearson相关(r)用于检验变量间关系的效应大小。结果:参与者(n = 25)的平均年龄为29.3±4.24,自我报告的平均周期长度为27.3±2.38天。该应用程序估计的(1)第一阶段结束和估计的中期fp开始之间的一致性为0.6±1.66天(95% LoA: 2.65-3.85; r = 0.66),(2)第二阶段结束和确定的黄体生成素(LH)激增日和第三阶段中点与估计的48小时排卵窗口后LH激增日之间的一致性为-0.6±1.71天(95% LoA: -3.95至2.75;r = 0.64),(3)第四阶段和经唾液激素验证的估计MLP日,应用程序第五阶段开始和估计黄体晚期中点日为-2.2±0.97 (95% LoA: -4.13至-0.32;r = 0.94)。结论:本研究描述了m3stepMC跟踪方法与激素测量之间的一致性,以及应用程序在月经周期中预定的MC相位系统,当MC日期与方法一致时。
{"title":"Level of Agreement Between a Modified, Three-Step Menstrual Cycle Tracking Method and a Female-Health Menstrual Cycle Tracking App.","authors":"Marissa L Doroshuk, Constance M Lebrun, Patricia K Doyle-Baker","doi":"10.1177/26884844251379415","DOIUrl":"10.1177/26884844251379415","url":null,"abstract":"<p><strong>Background: </strong>A need exists to incorporate evidence-based tracking methods that measure menstrual cycle (MC) variability to describe the data quality provided by an app. The study purpose was to assess the agreement between an app's cycle phase identifications and a modified version of the three-step method (m3stepMC) of hormone verification.</p><p><strong>Materials and methods: </strong>Participants across Canada were recruited to track their MC over 3 months by entering data into a female-health MC tracking app (the app) while collecting measures of ovulation and salivary hormones around the late-follicular (FP) and mid-luteal (MLP) phases, respectively. Bland-Altman plots assessed the limits of agreement (LoA) between the identified days within each of the app's predetermined phases and the m3stepMC-identified days when MC dates aligned between the methods. Pearson's correlations (<i>r</i>) were used to examine the effect size of relationships between variables.</p><p><strong>Results: </strong>Participants' (<i>n</i> = 25) mean age was 29.3 ± 4.24 with self-reported mean cycle lengths of 27.3 ± 2.38 days. The agreement between the app's estimated (1) end of phase one and the estimated start of the mid-FP was 0.6 ± 1.66 days (95% LoA: 2.65-3.85; <i>r</i> = 0.66), (2) end of phase two and the identified luteinizing hormone (LH) surge day and midpoint of phase three and the estimated 48-hour ovulatory window post-LH surge day were -0.6 ± 1.71 days (95% LoA: -3.95 to 2.75; <i>r</i> = 0.64), and (3) phase four and the estimated MLP day verified by salivary hormones and the start of the app's phase five and the estimated late-luteal midpoint day were -2.2 ± 0.97 (95% LoA: -4.13 to -0.32; <i>r</i> = 0.94).</p><p><strong>Conclusion: </strong>This study describes the agreement between a m3stepMC tracking method and hormone measures and an app's predetermined MC phase system in eumenorrheic cycles when MC dates aligned between methods.</p>","PeriodicalId":75329,"journal":{"name":"Women's health reports (New Rochelle, N.Y.)","volume":"6 1","pages":"1070-1080"},"PeriodicalIF":1.8,"publicationDate":"2025-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12549177/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145373473","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Health Care Providers' Perspectives on Factors Influencing Diabetes Management Among Thai Pregnant Women. 卫生保健提供者对泰国孕妇糖尿病管理影响因素的看法。
IF 1.8 Q3 OBSTETRICS & GYNECOLOGY Pub Date : 2025-09-29 eCollection Date: 2025-01-01 DOI: 10.1177/26884844251383424
Jiraporn Lininger, Ratchanok Phonyiam, Sangthong Terathongkum

Background: Diabetes during pregnancy poses significant risks to maternal and fetal health. This study explores health care providers' perspectives on factors influencing pregnant women with type 2 diabetes management in Thailand.

Methods: A qualitative descriptive study based on the National Institute on Minority Health and Health Disparities (NIMHD) Research Framework. Semi-structured interviews were conducted with 13 physicians and nurses from two public hospitals (urban and rural areas). Directed content analysis was used to analyze the data, with themes and subthemes derived from initial codes based on the NIMHD framework.

Results: Thirteen health care providers participated, including 10 nurses and 3 physicians. Three major themes emerged. Each theme was categorized into NIMHD domains of influence, including biological, behavioral, physical/built environment, and sociocultural environment. Theme 1: Individual-level factors include biological vulnerability and mechanisms in diabetes risk, maternal and neonatal complications, unplanned pregnancy and unawareness of preexisting diabetes, lifestyle behavior factors contributing to diabetes risk, diabetes management during pregnancy, environmental and workplace adjustments for pregnant women, sociodemographic challenges in diabetes management during pregnancy, and culture and beliefs in pregnancy care. Theme 2: Interpersonal-level factors include maternal responsibility for a safe pregnancy, family involvement in pregnancy care, promoting diabetes awareness and healthy lifestyle in schools and workplaces, and the role of social media and digital platforms in maternal health. Theme 3: Community-level factors include the role of community functioning in maternal health, access to healthy and safe food in the community, and cultural shifts toward convenience food options.

Discussion: Emphasizing these factors requires a coordinated approach involving health care providers, families, communities, schools, workplaces, and policymakers. Tailored interventions promoting diabetes screening, healthy lifestyles, and supportive environments for pregnant women, particularly those from disadvantaged backgrounds, are crucial. Future research should focus on developing culturally sensitive, community-based strategies to overcome barriers to care and improve diabetes management during pregnancy.

背景:妊娠期糖尿病对孕产妇和胎儿健康构成重大风险。本研究探讨卫生保健提供者对泰国2型糖尿病孕妇管理影响因素的看法。方法:基于国家少数民族健康与健康差异研究所(NIMHD)研究框架进行定性描述性研究。对来自两家公立医院(城市和农村地区)的13名医生和护士进行了半结构化访谈。使用定向内容分析来分析数据,主题和子主题来源于基于NIMHD框架的初始代码。结果:13名医护人员参与,其中护士10名,医生3名。出现了三个主要主题。每个主题都被归类到NIMHD的影响领域,包括生物、行为、物理/建筑环境和社会文化环境。主题1:个人层面的因素包括糖尿病风险的生物脆弱性和机制、孕产妇和新生儿并发症、计划外妊娠和对既往糖尿病的不了解、导致糖尿病风险的生活方式行为因素、妊娠期糖尿病管理、孕妇的环境和工作场所调整、妊娠期糖尿病管理中的社会人口挑战,以及妊娠护理中的文化和信仰。主题2:人际层面的因素包括孕产妇对安全妊娠的责任、家庭参与妊娠护理、在学校和工作场所促进对糖尿病的认识和健康的生活方式,以及社交媒体和数字平台在孕产妇保健中的作用。主题3:社区层面的因素包括社区在孕产妇保健方面的作用、社区获得健康和安全食品的机会以及向方便食品选择的文化转变。讨论:强调这些因素需要一种涉及卫生保健提供者、家庭、社区、学校、工作场所和决策者的协调方法。促进糖尿病筛查、健康生活方式和为孕妇(特别是来自弱势背景的孕妇)提供支持性环境的量身定制的干预措施至关重要。未来的研究应侧重于发展具有文化敏感性的、基于社区的策略,以克服护理障碍并改善妊娠期间的糖尿病管理。
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引用次数: 0
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