Sarah Dowthwaite, Ann Quinton, Samantha Thomas, Timothy E Schlub, Jillian Clarke
Introduction: Women may need a surgical uterine evacuation for miscarriage, surgical termination, or retained products of conception. Previous research has indicated possible complications of uterine dilatation and curettage and potential benefits of an ultrasound-guided procedure. This study aimed to compare the rate of complications for uterine evacuation when performed blind or with ultrasound guidance, including whether the presence of patient risk factors determined the use of ultrasound guidance.
Material and methods: This retrospective cohort study included 733 cases in an Australian hospital between January 2019 and December 2023. Medical records, imaging, and surgical reports were searched for patient demographics, risk factors, and the presence of surgical complications. Primary outcomes were complications of uterine perforation, false passage, incomplete curettage, heavy blood loss, or laparoscopy. Secondary outcomes were patient demographics and potential presurgical complication factors. The study created two cohorts: patients receiving evacuation performed blind or with ultrasound guidance.
Results: The uterine evacuation was performed blind for 421/733 (57%) women and ultrasound-guided for 312/733 (43%) women. The ultrasound-guided group included higher gestational ages 8 [7-11] weeks vs blind 8 [7-9] weeks, more patients with risk factors (OR 1.7, CI: 1.3 to 2.3), more patients for surgical termination (OR 15.3, CI: 5.4 to 43.3), or postpartum RPOC removal (OR 2.3, CI: 1.3 to 3.9). The ultrasound group had lower overall blood loss (20 mLs vs 30 mL) and clinically significantly lower volumes of continuing retained products of conception, 0.66 cm3 [0.53-1.23] vs 8.35 cm3 [1.49-18.94]. There was no difference in complications between groups after adjusting for gestational age (OR 1.0, CI: 0.5 to 2.0).
Conclusions: There were low complication rates for blind and ultrasound-guided uterine evacuations. However, ultrasound guidance was utilized for higher-risk cases and significantly reduced the volume of retained tissue in complicated cases. The use of ultrasound guidance by doctors and sonographers for uterine evacuation is a compelling choice where available.
妇女可能需要手术子宫清除流产,手术终止,或保留的受孕产品。先前的研究表明子宫扩张和刮除可能的并发症以及超声引导手术的潜在益处。本研究旨在比较盲行和超声引导下子宫引流的并发症发生率,包括患者危险因素的存在是否决定了超声引导的使用。材料和方法:这项回顾性队列研究包括2019年1月至2023年12月期间澳大利亚一家医院的733例病例。我们检索了医疗记录、影像和手术报告,以确定患者的人口统计学特征、危险因素和手术并发症的存在。主要结局是并发症子宫穿孔,假通道,不完全刮除,大量失血,或腹腔镜检查。次要结局是患者人口统计学和潜在的手术前并发症因素。该研究创建了两个队列:接受盲式疏散的患者或在超声引导下接受疏散的患者。结果:733例女性中有421例(57%)采用盲子宫引流术,有312例(43%)采用超声引导下子宫引流术。超声引导组的孕周(8[7-11]周)高于盲组(8[7-9]周),存在危险因素的患者较多(OR为1.7,CI为1.3 - 2.3),手术终止的患者较多(OR为15.3,CI为5.4 - 43.3),或产后RPOC切除的患者较多(OR为2.3,CI为1.3 - 3.9)。超声组总失血量较低(20 mL vs 30 mL),妊娠产物持续保留体积临床上显著降低,为0.66 cm3 [0.53-1.23] vs 8.35 cm3[1.49-18.94]。调整胎龄后,两组间并发症发生率无差异(OR 1.0, CI: 0.5 ~ 2.0)。结论:超声引导下盲宫腔引流术并发症发生率低。然而,超声引导用于高风险病例,并显著减少复杂病例的保留组织体积。使用超声指导,由医生和超声医师子宫疏散是一个令人信服的选择,在可用的地方。
{"title":"Outcomes from blind versus ultrasound-guided uterine evacuation: A retrospective cohort analysis.","authors":"Sarah Dowthwaite, Ann Quinton, Samantha Thomas, Timothy E Schlub, Jillian Clarke","doi":"10.1111/aogs.70179","DOIUrl":"https://doi.org/10.1111/aogs.70179","url":null,"abstract":"<p><strong>Introduction: </strong>Women may need a surgical uterine evacuation for miscarriage, surgical termination, or retained products of conception. Previous research has indicated possible complications of uterine dilatation and curettage and potential benefits of an ultrasound-guided procedure. This study aimed to compare the rate of complications for uterine evacuation when performed blind or with ultrasound guidance, including whether the presence of patient risk factors determined the use of ultrasound guidance.</p><p><strong>Material and methods: </strong>This retrospective cohort study included 733 cases in an Australian hospital between January 2019 and December 2023. Medical records, imaging, and surgical reports were searched for patient demographics, risk factors, and the presence of surgical complications. Primary outcomes were complications of uterine perforation, false passage, incomplete curettage, heavy blood loss, or laparoscopy. Secondary outcomes were patient demographics and potential presurgical complication factors. The study created two cohorts: patients receiving evacuation performed blind or with ultrasound guidance.</p><p><strong>Results: </strong>The uterine evacuation was performed blind for 421/733 (57%) women and ultrasound-guided for 312/733 (43%) women. The ultrasound-guided group included higher gestational ages 8 [7-11] weeks vs blind 8 [7-9] weeks, more patients with risk factors (OR 1.7, CI: 1.3 to 2.3), more patients for surgical termination (OR 15.3, CI: 5.4 to 43.3), or postpartum RPOC removal (OR 2.3, CI: 1.3 to 3.9). The ultrasound group had lower overall blood loss (20 mLs vs 30 mL) and clinically significantly lower volumes of continuing retained products of conception, 0.66 cm<sup>3</sup> [0.53-1.23] vs 8.35 cm<sup>3</sup> [1.49-18.94]. There was no difference in complications between groups after adjusting for gestational age (OR 1.0, CI: 0.5 to 2.0).</p><p><strong>Conclusions: </strong>There were low complication rates for blind and ultrasound-guided uterine evacuations. However, ultrasound guidance was utilized for higher-risk cases and significantly reduced the volume of retained tissue in complicated cases. The use of ultrasound guidance by doctors and sonographers for uterine evacuation is a compelling choice where available.</p>","PeriodicalId":6990,"journal":{"name":"Acta Obstetricia et Gynecologica Scandinavica","volume":" ","pages":""},"PeriodicalIF":3.1,"publicationDate":"2026-03-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147368847","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Linda Hjertberg, Eva Uustal, Marie Blomberg, Sofia Pihl
Introduction: The aim of this study was to evaluate self-reported pelvic floor symptoms 12 months postpartum, in women after a first-time vaginal delivery complicated by an obstetric anal sphincter injury, according to body mass index. The hypothesis was that dyspareunia, urinary incontinence, and anal incontinence would be more common in overweight and obese women compared with normal weight women 12 months postpartum.
Material and methods: This is a population-based cohort study. Altogether, 6595 primiparous women with a first-time vaginal delivery complicated by an obstetric anal sphincter injury in Sweden between 2014 and 2019 were included in the Swedish Perineal Laceration Registry. Self-reported pre-pregnancy data and data from the 12-month follow-up questionnaire were retrieved from the Perineal Laceration Registry. Uni- and multivariate analyses were used to compare normal weight (BMI ≤ 24.9), overweight (25.0-29.9), and obese (≥30) women in regard to the self-reported prevalence of dyspareunia, urinary incontinence, and anal incontinence 12 months postpartum.
Results: Overweight and obese women had a decreased risk of dyspareunia compared with normal weight women, aOR 0.82 (CI = 0.68-0.98) and aOR 0.71 (CI = 0.54-0.93), respectively. The absolute rate of dyspareunia was 41% among normal weight women, 38% among overweight women, and 33% among the obese group. In the univariate analyses, episiotomy and the grade of anal sphincter injury did not affect the risk of dyspareunia. There was an increased risk of urinary incontinence among overweight (aOR = 1.51, CI = 1.11-2.04) and obese women (aOR = 2.82, CI = 1.94-4.12) compared with normal weight women. The risk of anal incontinence did not differ between the BMI groups.
Conclusions: Dyspareunia 12 months after an obstetric anal sphincter injury was less common among overweight and obese women than in normal-weight women. Self-reported anal incontinence one year after an obstetric anal sphincter injury was equally distributed over the BMI groups 12 months after delivery, which is a new finding and clinically relevant.
本研究的目的是根据体重指数评估首次阴道分娩并发产科肛门括约肌损伤的妇女产后12个月骨盆底症状的自我报告。假设是,产后12个月,超重和肥胖的女性比正常体重的女性更容易出现性交困难、尿失禁和肛门失禁。材料和方法:这是一项基于人群的队列研究。2014年至2019年期间,瑞典6595名首次阴道分娩并发产科肛门括约肌损伤的初产妇被纳入瑞典会阴撕裂伤登记处。自我报告的孕前数据和12个月随访问卷的数据从会阴撕裂伤登记处检索。采用单因素和多因素分析比较正常体重(BMI≤24.9)、超重(25.0-29.9)和肥胖(≥30)妇女产后12个月自我报告的性交困难、尿失禁和肛门失禁的发生率。结果:与正常体重的女性相比,超重和肥胖女性发生性交困难的风险降低,分别为aOR 0.82 (CI = 0.68-0.98)和aOR 0.71 (CI = 0.54-0.93)。正常体重女性发生性交困难的绝对比率为41%,超重女性为38%,肥胖组为33%。在单变量分析中,外阴切开术和肛门括约肌损伤程度不影响性交困难的风险。与正常体重的女性相比,超重女性(aOR = 1.51, CI = 1.11-2.04)和肥胖女性(aOR = 2.82, CI = 1.94-4.12)发生尿失禁的风险增加。肛门失禁的风险在BMI组之间没有差异。结论:产科肛门括约肌损伤后12个月的性交困难在超重和肥胖妇女中比在正常体重妇女中更少见。产科肛门括约肌损伤后1年自我报告的肛门失禁在分娩后12个月BMI组中分布均匀,这是一项新发现,具有临床相关性。
{"title":"Self-reported pelvic floor dysfunction 12 months after an obstetric anal sphincter injury in relation to maternal body mass index.","authors":"Linda Hjertberg, Eva Uustal, Marie Blomberg, Sofia Pihl","doi":"10.1111/aogs.70171","DOIUrl":"https://doi.org/10.1111/aogs.70171","url":null,"abstract":"<p><strong>Introduction: </strong>The aim of this study was to evaluate self-reported pelvic floor symptoms 12 months postpartum, in women after a first-time vaginal delivery complicated by an obstetric anal sphincter injury, according to body mass index. The hypothesis was that dyspareunia, urinary incontinence, and anal incontinence would be more common in overweight and obese women compared with normal weight women 12 months postpartum.</p><p><strong>Material and methods: </strong>This is a population-based cohort study. Altogether, 6595 primiparous women with a first-time vaginal delivery complicated by an obstetric anal sphincter injury in Sweden between 2014 and 2019 were included in the Swedish Perineal Laceration Registry. Self-reported pre-pregnancy data and data from the 12-month follow-up questionnaire were retrieved from the Perineal Laceration Registry. Uni- and multivariate analyses were used to compare normal weight (BMI ≤ 24.9), overweight (25.0-29.9), and obese (≥30) women in regard to the self-reported prevalence of dyspareunia, urinary incontinence, and anal incontinence 12 months postpartum.</p><p><strong>Results: </strong>Overweight and obese women had a decreased risk of dyspareunia compared with normal weight women, aOR 0.82 (CI = 0.68-0.98) and aOR 0.71 (CI = 0.54-0.93), respectively. The absolute rate of dyspareunia was 41% among normal weight women, 38% among overweight women, and 33% among the obese group. In the univariate analyses, episiotomy and the grade of anal sphincter injury did not affect the risk of dyspareunia. There was an increased risk of urinary incontinence among overweight (aOR = 1.51, CI = 1.11-2.04) and obese women (aOR = 2.82, CI = 1.94-4.12) compared with normal weight women. The risk of anal incontinence did not differ between the BMI groups.</p><p><strong>Conclusions: </strong>Dyspareunia 12 months after an obstetric anal sphincter injury was less common among overweight and obese women than in normal-weight women. Self-reported anal incontinence one year after an obstetric anal sphincter injury was equally distributed over the BMI groups 12 months after delivery, which is a new finding and clinically relevant.</p>","PeriodicalId":6990,"journal":{"name":"Acta Obstetricia et Gynecologica Scandinavica","volume":" ","pages":""},"PeriodicalIF":3.1,"publicationDate":"2026-03-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147363790","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Johanna Wagner Bjurström, Gisela Rickle, Maria Fogelberg, Frida Ekengård, Andreas Herbst
Introduction: Consensus is lacking regarding the upper limit for a safe contraction frequency during labor. We aimed to assess the association between different contraction frequencies and acidemia at birth, and whether an association was affected by oxytocin augmentation, concomitant cardiotocography (CTG) classification, and stage of labor.
Material and methods: This is a case-control study based on CTG traces from births in southern Sweden during 2012-2017. Cases (N = 364) had umbilical artery pH <7.1 if born by first-stage cesarean section and pH <7.05 if born vaginally or by second-stage cesarean. Controls were included with a 1:2 ratio (N = 728) and had pH ≥7.15. CTG traces from the hour prior to birth were assessed blinded to the clinical outcome. Logistic regression was used to estimate odds ratios (OR) with 95% confidence intervals (CI).
Results: After excluding insufficient topography traces, 328 cases and 677 controls remained for analysis. Contraction frequencies 5, 5-6, and ≥6 per 10 min occurred in 15.2%, 19.5%, and 29.6% of cases and in 15.1%, 16.5%, and 11.1% of controls, respectively. The OR (95% CI) for acidemia were 1.6 (1.1-2.4), 1.9 (1.3-2.7), and 4.3 (3.0-6.2), respectively, compared with a reference group of <5. When comparing two separate binary cut-offs of >5 and ≥5 contractions, similar strengths of association with acidemia were demonstrated with OR 2.7 (2.1-3.6) and 2.5 (1.9-3.3), respectively. The effect of contraction frequency >5 was similar in spontaneous (n = 586) and oxytocin-augmented (n = 419) labor (OR 2.5, 1.7-3.8 vs. OR 2.4, 1.6-3.6), and whether the CTG was normal, suspicious, or pathological according to the Swedish CTG template (OR 2.1, 1.3-3.3; OR 3.5, 1.6-7.6; and OR 2.6, 1.4-4.7, respectively). The study lacked power to study any association during the first stage of labor.
Conclusions: Increasing contraction frequency is incrementally associated with fetal acidemia. Although an increased risk of acidosis is evident at contraction frequencies as low as five, such frequencies are common while acidemia is uncommon, implying a poor positive predictive value. A contraction frequency of more than five is associated with acidemia in both spontaneous and oxytocin-augmented labor, and even when the fetal heart trace is normal.
导读:关于分娩时安全宫缩频率的上限,目前还缺乏共识。我们的目的是评估不同收缩频率与出生时酸血症之间的关系,以及这种关系是否受到催产素增强、伴随心脏造影(CTG)分类和产程的影响。材料和方法:这是一项基于2012-2017年瑞典南部出生CTG痕迹的病例对照研究。结果:在排除不充分的地形痕迹后,328例病例和677例对照留待分析。15.2%、19.5%和29.6%的病例以及15.1%、16.5%和11.1%的对照组分别出现5、5-6和≥6次/ 10min的收缩频率。与5次和≥5次宫缩的参照组相比,酸血症的OR (95% CI)分别为1.6(1.1-2.4)、1.9(1.3-2.7)和4.3(3.0-6.2),与酸血症相关的相似强度分别为2.7(2.1-3.6)和2.5(1.9-3.3)。收缩频率bbbb5对自然分娩(n = 586)和催产素增强(n = 419)的影响相似(OR 2.5, 1.7-3.8 vs. OR 2.4, 1.6-3.6),以及根据瑞典CTG模板判断CTG是否正常、可疑或病理(OR 2.1, 1.3-3.3; OR 3.5, 1.6-7.6; OR 2.6, 1.4-4.7)。这项研究没有能力研究分娩第一阶段的任何联系。结论:宫缩频率增加与胎儿酸血症呈递增关系。虽然在收缩频率低至5次时,酸中毒的风险明显增加,但这种频率很常见,而酸血症并不常见,这意味着阳性预测值很差。在自然分娩和催产素增强分娩中,甚至在胎心痕迹正常的情况下,超过5次的收缩频率都与酸血症有关。
{"title":"Contraction frequency and acidemia at birth: A case-control study.","authors":"Johanna Wagner Bjurström, Gisela Rickle, Maria Fogelberg, Frida Ekengård, Andreas Herbst","doi":"10.1111/aogs.70181","DOIUrl":"https://doi.org/10.1111/aogs.70181","url":null,"abstract":"<p><strong>Introduction: </strong>Consensus is lacking regarding the upper limit for a safe contraction frequency during labor. We aimed to assess the association between different contraction frequencies and acidemia at birth, and whether an association was affected by oxytocin augmentation, concomitant cardiotocography (CTG) classification, and stage of labor.</p><p><strong>Material and methods: </strong>This is a case-control study based on CTG traces from births in southern Sweden during 2012-2017. Cases (N = 364) had umbilical artery pH <7.1 if born by first-stage cesarean section and pH <7.05 if born vaginally or by second-stage cesarean. Controls were included with a 1:2 ratio (N = 728) and had pH ≥7.15. CTG traces from the hour prior to birth were assessed blinded to the clinical outcome. Logistic regression was used to estimate odds ratios (OR) with 95% confidence intervals (CI).</p><p><strong>Results: </strong>After excluding insufficient topography traces, 328 cases and 677 controls remained for analysis. Contraction frequencies 5, 5-6, and ≥6 per 10 min occurred in 15.2%, 19.5%, and 29.6% of cases and in 15.1%, 16.5%, and 11.1% of controls, respectively. The OR (95% CI) for acidemia were 1.6 (1.1-2.4), 1.9 (1.3-2.7), and 4.3 (3.0-6.2), respectively, compared with a reference group of <5. When comparing two separate binary cut-offs of >5 and ≥5 contractions, similar strengths of association with acidemia were demonstrated with OR 2.7 (2.1-3.6) and 2.5 (1.9-3.3), respectively. The effect of contraction frequency >5 was similar in spontaneous (n = 586) and oxytocin-augmented (n = 419) labor (OR 2.5, 1.7-3.8 vs. OR 2.4, 1.6-3.6), and whether the CTG was normal, suspicious, or pathological according to the Swedish CTG template (OR 2.1, 1.3-3.3; OR 3.5, 1.6-7.6; and OR 2.6, 1.4-4.7, respectively). The study lacked power to study any association during the first stage of labor.</p><p><strong>Conclusions: </strong>Increasing contraction frequency is incrementally associated with fetal acidemia. Although an increased risk of acidosis is evident at contraction frequencies as low as five, such frequencies are common while acidemia is uncommon, implying a poor positive predictive value. A contraction frequency of more than five is associated with acidemia in both spontaneous and oxytocin-augmented labor, and even when the fetal heart trace is normal.</p>","PeriodicalId":6990,"journal":{"name":"Acta Obstetricia et Gynecologica Scandinavica","volume":" ","pages":""},"PeriodicalIF":3.1,"publicationDate":"2026-03-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147353443","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Yuqi Li, Wei Shao, Xiaoxiao Gao, Yongxing Wang, Jinzhi Li, Liansuo Zhang, Yanyan Xing, Wentao Su, Yan Cheng, Li Wang, Songping Liu
Introduction: Endometriomsis (EMs) is a complex and chronic gynecological disease characterized by distressing symptoms. Its pathogenesis remains unknown, and there is no effective treatment. Therefore, establishing patient-derived models is crucial for elucidating disease mechanisms and identifying potential therapeutic agents. We developed a coculture system combining epithelial organoids and stromal cells, enabling the study of their dynamic interactions. Using this model, we assessed the therapeutic efficacy of dienogest, a drug clinically used for treating endometriomas.
Material and methods: The epithelial gland-like organoids and stromal cells derived from patients with endometriomas were isolated and cultured, respectively. Both of them were cocultured in matrix for partially mimicking in vivo pathological features. Immunohistochemical (IHC) assay was used to identify their biomarkers. Cell viability was quantitatively assessed using the CellTiter-Glo® assay following drug treatment.
Results: We successfully cultured patient-derived epithelial gland-like organoids and stromal cells derived from patients with endometriomas, a form of endometriosis characterized by ovarian cysts. Morphological and immunohistochemical analyses confirmed high consistency with native endometriotic lesions. These models exhibited comparable expression profiles for key biological markers, including estrogen receptors (ERs), progesterone receptors (PRs), E-cadherin, CD44, Intercellular Adhesion Molecule-1 (ICAM1), Integrin Beta 3 (ITGB3), Cytokeratin 7 (CK7), Matrix Metalloproteinase 2/9 (MMP2/9), Tissue Inhibitor of Metalloproteinases 1 (TIMP1), and TIMP2. Notably, drug responsiveness varied among the patient-derived models by coculturing two types of cells, indicating potential interpatient heterogeneity in treatment outcomes. We propose that this patient-specific endometriomas model serves as a valuable platform for investigating disease mechanisms and screening drug in endometriomas.
Conclusions: We established a novel coculture system integrating epithelial organoids and stromal cells to recapitulate the intricate cellular interactions within the endometriotic microenvironment, providing a more relevant in vitro representation of the disease. Upon evaluation with dienogest, a clinically used therapeutic agent for endometriomas, the patient-derived models exhibited heterogeneous drug responses.
{"title":"Three-dimensional patient-derived endometriosis model for drug evaluation.","authors":"Yuqi Li, Wei Shao, Xiaoxiao Gao, Yongxing Wang, Jinzhi Li, Liansuo Zhang, Yanyan Xing, Wentao Su, Yan Cheng, Li Wang, Songping Liu","doi":"10.1111/aogs.70146","DOIUrl":"https://doi.org/10.1111/aogs.70146","url":null,"abstract":"<p><strong>Introduction: </strong>Endometriomsis (EMs) is a complex and chronic gynecological disease characterized by distressing symptoms. Its pathogenesis remains unknown, and there is no effective treatment. Therefore, establishing patient-derived models is crucial for elucidating disease mechanisms and identifying potential therapeutic agents. We developed a coculture system combining epithelial organoids and stromal cells, enabling the study of their dynamic interactions. Using this model, we assessed the therapeutic efficacy of dienogest, a drug clinically used for treating endometriomas.</p><p><strong>Material and methods: </strong>The epithelial gland-like organoids and stromal cells derived from patients with endometriomas were isolated and cultured, respectively. Both of them were cocultured in matrix for partially mimicking in vivo pathological features. Immunohistochemical (IHC) assay was used to identify their biomarkers. Cell viability was quantitatively assessed using the CellTiter-Glo<sup>®</sup> assay following drug treatment.</p><p><strong>Results: </strong>We successfully cultured patient-derived epithelial gland-like organoids and stromal cells derived from patients with endometriomas, a form of endometriosis characterized by ovarian cysts. Morphological and immunohistochemical analyses confirmed high consistency with native endometriotic lesions. These models exhibited comparable expression profiles for key biological markers, including estrogen receptors (ERs), progesterone receptors (PRs), E-cadherin, CD44, Intercellular Adhesion Molecule-1 (ICAM1), Integrin Beta 3 (ITGB3), Cytokeratin 7 (CK7), Matrix Metalloproteinase 2/9 (MMP2/9), Tissue Inhibitor of Metalloproteinases 1 (TIMP1), and TIMP2. Notably, drug responsiveness varied among the patient-derived models by coculturing two types of cells, indicating potential interpatient heterogeneity in treatment outcomes. We propose that this patient-specific endometriomas model serves as a valuable platform for investigating disease mechanisms and screening drug in endometriomas.</p><p><strong>Conclusions: </strong>We established a novel coculture system integrating epithelial organoids and stromal cells to recapitulate the intricate cellular interactions within the endometriotic microenvironment, providing a more relevant in vitro representation of the disease. Upon evaluation with dienogest, a clinically used therapeutic agent for endometriomas, the patient-derived models exhibited heterogeneous drug responses.</p>","PeriodicalId":6990,"journal":{"name":"Acta Obstetricia et Gynecologica Scandinavica","volume":" ","pages":""},"PeriodicalIF":3.1,"publicationDate":"2026-03-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147343216","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-03-01Epub Date: 2026-01-28DOI: 10.1111/aogs.70137
Laura Nogué, Mar Bennasar, Laura Guirado, Felix Zölner, Justus Reitz, Roland Axt-Fliedner, María C Escobar-Díaz, Josep Maria Martínez, Eduard Gratacós, Fàtima Crispi, Olga Gómez
Introduction: Tetralogy of Fallot (ToF) shows variability in neonatal outcomes, and identifying reliable prenatal predictors is essential for optimizing perinatal management. The aim of this study was to determine the prognostic value of feto-placental data and prenatal echocardiography in the third trimester in ToF and to compare these findings with a matched control population.
Material and methods: Multicenter prospective cohort study (2011-2023) at two referral centers (BCNatal and University Hospital of Gießen and Marburg). The cohort included 63 fetuses with isolated ToF and 66 healthy controls. All fetuses underwent a third trimester ultrasound and comprehensive echocardiography with 2D speckle tracking. Severe small-for-gestational age (SGA) was defined as estimated fetal weight (EFW) below the third percentile. Adverse composite outcomes were defined as the need for prostaglandin infusion, surgery or ductal stenting, corrective surgery before 3 months, and/or neonatal intensive care unit stay ≥7 days. The association of feto-placental and cardiac data with adverse composite outcome was evaluated.
Results: Compared with controls, ToF fetuses showed higher rates of severe SGA (19% vs. 0%, p < 0.001). Cardiac findings showed mild biventricular concentric hypertrophy (relative wall thickness ToF 0.7 [0.5-0.9] vs. controls 0.5 [0.5-0.6], p = 0.001), and reduced deformation (right and left ventricular global longitudinal strain: ToF -17.3% ± 3.8 vs. controls -19.3% ± 3.1, p = 0.001; ToF -18.0% ± 3.8 vs. controls -20.9% ± 3.45, p < 0.001), regardless of placental dysfunction. The adverse composite outcome occurred in 29.3% of ToF cases with pulmonary stenosis. Within this group, EFW <3rd centile (adjusted OR 9.17) and PV peak systolic velocity (aOR 1.03) showed the strongest association with adverse outcomes. Their combined performance yielded an AUC of 0.734, with a predictive value of 71.4% at a 20% false-positive rate. Assessed individually, the AUC was 0.650 for PV peak systolic velocity and 0.639 for estimated fetal weight. Optimal PV Doppler cutoff values were >70 cm/s when EFW was <3rd centile, and >144 cm/s when EFW was above the 3rd centile.
Conclusions: Combining EFW with PV artery Doppler may allow identification of a high-risk subgroup of ToF-PS fetuses who may benefit from closer prenatal monitoring and prompt neonatal care.
简介:法洛四联症(ToF)显示新生儿结局的可变性,确定可靠的产前预测因子对于优化围产期管理至关重要。本研究的目的是确定胎儿胎盘数据和产前超声心动图在ToF妊娠晚期的预后价值,并将这些发现与匹配的对照人群进行比较。材料和方法:多中心前瞻性队列研究(2011-2023)在两个转诊中心(BCNatal和吉ßen和马尔堡大学医院)进行。该队列包括63例分离性ToF胎儿和66例健康对照。所有胎儿都进行了妊娠晚期超声检查和二维斑点跟踪的全面超声心动图检查。严重小胎龄(SGA)被定义为估计胎儿体重(EFW)低于第三个百分位数。不良综合结局定义为需要前列腺素输注、手术或导管支架置入术、3个月前进行矫正手术和/或新生儿重症监护病房住院≥7天。评估胎儿胎盘和心脏数据与不良综合结局的关系。结果:与对照组相比,ToF胎儿的严重SGA发生率更高(19% vs. 0%,当EFW大于3位时为70 cm/s,当EFW大于3位时为144 cm/s)。结论:结合EFW和PV动脉多普勒可以识别ToF-PS胎儿的高危亚群,这些胎儿可能受益于更密切的产前监测和及时的新生儿护理。
{"title":"Prognostic value of fetal growth and prenatal functional echocardiography in tetralogy of FALLOT.","authors":"Laura Nogué, Mar Bennasar, Laura Guirado, Felix Zölner, Justus Reitz, Roland Axt-Fliedner, María C Escobar-Díaz, Josep Maria Martínez, Eduard Gratacós, Fàtima Crispi, Olga Gómez","doi":"10.1111/aogs.70137","DOIUrl":"10.1111/aogs.70137","url":null,"abstract":"<p><strong>Introduction: </strong>Tetralogy of Fallot (ToF) shows variability in neonatal outcomes, and identifying reliable prenatal predictors is essential for optimizing perinatal management. The aim of this study was to determine the prognostic value of feto-placental data and prenatal echocardiography in the third trimester in ToF and to compare these findings with a matched control population.</p><p><strong>Material and methods: </strong>Multicenter prospective cohort study (2011-2023) at two referral centers (BCNatal and University Hospital of Gießen and Marburg). The cohort included 63 fetuses with isolated ToF and 66 healthy controls. All fetuses underwent a third trimester ultrasound and comprehensive echocardiography with 2D speckle tracking. Severe small-for-gestational age (SGA) was defined as estimated fetal weight (EFW) below the third percentile. Adverse composite outcomes were defined as the need for prostaglandin infusion, surgery or ductal stenting, corrective surgery before 3 months, and/or neonatal intensive care unit stay ≥7 days. The association of feto-placental and cardiac data with adverse composite outcome was evaluated.</p><p><strong>Results: </strong>Compared with controls, ToF fetuses showed higher rates of severe SGA (19% vs. 0%, p < 0.001). Cardiac findings showed mild biventricular concentric hypertrophy (relative wall thickness ToF 0.7 [0.5-0.9] vs. controls 0.5 [0.5-0.6], p = 0.001), and reduced deformation (right and left ventricular global longitudinal strain: ToF -17.3% ± 3.8 vs. controls -19.3% ± 3.1, p = 0.001; ToF -18.0% ± 3.8 vs. controls -20.9% ± 3.45, p < 0.001), regardless of placental dysfunction. The adverse composite outcome occurred in 29.3% of ToF cases with pulmonary stenosis. Within this group, EFW <3rd centile (adjusted OR 9.17) and PV peak systolic velocity (aOR 1.03) showed the strongest association with adverse outcomes. Their combined performance yielded an AUC of 0.734, with a predictive value of 71.4% at a 20% false-positive rate. Assessed individually, the AUC was 0.650 for PV peak systolic velocity and 0.639 for estimated fetal weight. Optimal PV Doppler cutoff values were >70 cm/s when EFW was <3rd centile, and >144 cm/s when EFW was above the 3rd centile.</p><p><strong>Conclusions: </strong>Combining EFW with PV artery Doppler may allow identification of a high-risk subgroup of ToF-PS fetuses who may benefit from closer prenatal monitoring and prompt neonatal care.</p>","PeriodicalId":6990,"journal":{"name":"Acta Obstetricia et Gynecologica Scandinavica","volume":"105 3","pages":"479-491"},"PeriodicalIF":3.1,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12942062/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147289004","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
While existing literature has compared the methodological strengths and limitations of randomized controlled trials (RCTs) and real-world data (RWD) in general medical research, two critical gaps remain unaddressed: (1) no prior communication papers have specifically examined this comparison in the context of maternity care where unique ethical and practical considerations exist, and (2) no studies have systematically compared cost-effectiveness analyses derived from RCTs versus RWD approaches-a crucial dimension for value-based maternity care decisions. This article examines how both approaches can strengthen the evidence base and support the delivery of value-based maternity care. We argue that neither RCTs nor RWD should be regarded as inherently superior in guiding decision-making. Each study design offers valuable insights, and their findings must be critically appraised in light of methodological rigor, context, and relevance, particularly when their results diverge.
{"title":"Beyond evidence hierarchies: Leveraging randomized controlled trials and real-world data to advance the value of maternity care.","authors":"Yanan Hu, Valerie Slavin, Joanne Enticott, Emily Callander","doi":"10.1111/aogs.70094","DOIUrl":"10.1111/aogs.70094","url":null,"abstract":"<p><p>While existing literature has compared the methodological strengths and limitations of randomized controlled trials (RCTs) and real-world data (RWD) in general medical research, two critical gaps remain unaddressed: (1) no prior communication papers have specifically examined this comparison in the context of maternity care where unique ethical and practical considerations exist, and (2) no studies have systematically compared cost-effectiveness analyses derived from RCTs versus RWD approaches-a crucial dimension for value-based maternity care decisions. This article examines how both approaches can strengthen the evidence base and support the delivery of value-based maternity care. We argue that neither RCTs nor RWD should be regarded as inherently superior in guiding decision-making. Each study design offers valuable insights, and their findings must be critically appraised in light of methodological rigor, context, and relevance, particularly when their results diverge.</p>","PeriodicalId":6990,"journal":{"name":"Acta Obstetricia et Gynecologica Scandinavica","volume":" ","pages":"395-402"},"PeriodicalIF":3.1,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12942053/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145942063","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-03-01Epub Date: 2025-12-29DOI: 10.1111/aogs.70132
Maria I Zervou, Theoni B Tarlatzi, Basil C Tarlatzis, George N Goulielmos
{"title":"Risk of cardiovascular disease and mortality among women with endometriosis: Genetic insights.","authors":"Maria I Zervou, Theoni B Tarlatzi, Basil C Tarlatzis, George N Goulielmos","doi":"10.1111/aogs.70132","DOIUrl":"10.1111/aogs.70132","url":null,"abstract":"","PeriodicalId":6990,"journal":{"name":"Acta Obstetricia et Gynecologica Scandinavica","volume":" ","pages":"553-554"},"PeriodicalIF":3.1,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12942065/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145852947","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-03-01Epub Date: 2026-01-26DOI: 10.1111/aogs.70149
Silje Marie Haga, Luisa Bergunde, Lara Seefeld, Susan Ayers, Malin Eberhard-Gran, Susan Garthus-Niegel
Introduction: Approximately 3%-4% of women experience childbirth-related posttraumatic stress disorder (CB-PTSD). The City Birth Trauma Scale (City BiTS) is a questionnaire developed to assess CB-PTSD, following the criteria outlined in the Diagnostic and Statistical Manual of Mental Disorders. The aim of the present study was to evaluate the psychometric properties of the Norwegian version of this questionnaire (City BiTS-Nor).
Material and methods: A community sample of 1079 mothers completed a cross-sectional online survey. The survey included questions on sociodemographic and obstetric characteristics, the City BiTS-Nor, the Impact of Event Scale-Revised, the Edinburgh Postnatal Depression Scale, the 10-item anxiety subscale of the Hopkins Symptom Checklist, and the Bergen Insomnia Scale.
Results: Confirmatory factor analysis supported a bifactor model comprising Birth-related Symptoms and General Symptoms in CB-PTSD, along with a General CB-PTSD factor that explained 58.4% of the variance. The study found high internal consistency (≥0.90), and good convergent and divergent validity were shown. Discriminant validity was evaluated by examining factors such as mode of birth, maternal complications, infant complications, parity, history of traumatic childbirth, and previous traumatic experiences. Higher General and Birth-related scores were observed in women who experienced emergency cesarean sections or instrumental vaginal births. This trend was observed in primiparous women, cases involving pregnancy and birth complications, and individuals with prior traumatic experiences.
Conclusions: The City BiTS-Nor presents appropriate psychometric properties for assessing CB-PTSD symptoms according to DSM-5 criteria. The findings suggest that using the total score, along with the individual subscale scores, is justified and enhances the comprehensive assessment of CB-PTSD symptoms. These findings support the clinical utility of the City BiTS-Nor as a screening tool for CB-PTSD, with potential to differentiate childbirth-related trauma from general psychopathology and to guide targeted interventions in perinatal care.
{"title":"Validation of the City Birth Trauma Scale in a sample of Norwegian mothers.","authors":"Silje Marie Haga, Luisa Bergunde, Lara Seefeld, Susan Ayers, Malin Eberhard-Gran, Susan Garthus-Niegel","doi":"10.1111/aogs.70149","DOIUrl":"10.1111/aogs.70149","url":null,"abstract":"<p><strong>Introduction: </strong>Approximately 3%-4% of women experience childbirth-related posttraumatic stress disorder (CB-PTSD). The City Birth Trauma Scale (City BiTS) is a questionnaire developed to assess CB-PTSD, following the criteria outlined in the Diagnostic and Statistical Manual of Mental Disorders. The aim of the present study was to evaluate the psychometric properties of the Norwegian version of this questionnaire (City BiTS-Nor).</p><p><strong>Material and methods: </strong>A community sample of 1079 mothers completed a cross-sectional online survey. The survey included questions on sociodemographic and obstetric characteristics, the City BiTS-Nor, the Impact of Event Scale-Revised, the Edinburgh Postnatal Depression Scale, the 10-item anxiety subscale of the Hopkins Symptom Checklist, and the Bergen Insomnia Scale.</p><p><strong>Results: </strong>Confirmatory factor analysis supported a bifactor model comprising Birth-related Symptoms and General Symptoms in CB-PTSD, along with a General CB-PTSD factor that explained 58.4% of the variance. The study found high internal consistency (≥0.90), and good convergent and divergent validity were shown. Discriminant validity was evaluated by examining factors such as mode of birth, maternal complications, infant complications, parity, history of traumatic childbirth, and previous traumatic experiences. Higher General and Birth-related scores were observed in women who experienced emergency cesarean sections or instrumental vaginal births. This trend was observed in primiparous women, cases involving pregnancy and birth complications, and individuals with prior traumatic experiences.</p><p><strong>Conclusions: </strong>The City BiTS-Nor presents appropriate psychometric properties for assessing CB-PTSD symptoms according to DSM-5 criteria. The findings suggest that using the total score, along with the individual subscale scores, is justified and enhances the comprehensive assessment of CB-PTSD symptoms. These findings support the clinical utility of the City BiTS-Nor as a screening tool for CB-PTSD, with potential to differentiate childbirth-related trauma from general psychopathology and to guide targeted interventions in perinatal care.</p>","PeriodicalId":6990,"journal":{"name":"Acta Obstetricia et Gynecologica Scandinavica","volume":" ","pages":"508-518"},"PeriodicalIF":3.1,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12942060/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146049918","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-03-01Epub Date: 2026-01-09DOI: 10.1111/aogs.70122
Eline E R Lust, Kim Bronsgeest, Lidewij Henneman, Neeltje M T H Crombag, Caterina M Bilardo, Robert-Jan H Galjaard, Esther Sikkel, Audrey B C Coumans, Ayten Elvan-Taşpınar, Sander Galjaard, Attie T J I Go, Gwendolyn T R Manten, Eva Pajkrt, Elisabeth van Leeuwen, Monique C Haak, Mireille N Bekker
Introduction: A frequently cited benefit of the first-trimester anomaly scan (FTAS) is that it reduces psychological impact by enabling earlier termination of pregnancy (TOP). However, the impact of early versus late TOP due to fetal anomalies remains unclear. This study evaluates the psychological impact and perspectives associated with early versus late TOP.
Material and methods: A prospective mixed methods study was conducted. The early group (TOP <18 weeks) included women with an abnormal FTAS; the late group (TOP 20-24 weeks) included women with an abnormal second-trimester scan (SAS), abnormal FTAS, or normal FTAS followed by abnormal SAS. Women completed questionnaires 2 (T1) and 6 months (T2) postpartum addressing psychological impact using validated scales (State-Trait Anxiety Inventory, Edinburgh Depression Scale, Impact of Event Scale, Perinatal Grief Scale) and study-specific questions. Semi-structured interviews were conducted with women and their partners 3-6 months after termination.
Results: 149 women with early TOP (15 + 2 weeks, range 14 + 4-16 + 1) and 129 with late TOP (22 + 0, 21 + 0-23 + 1) completed T1. In both groups, the majority had clinically relevant anxiety at T1 and T2 and moderate/severe distress at T1. The late TOP group had higher median depression and mean grief scores at T1 (5.0, range 3.0-8.0 vs. 4.0, range 2.0-7.0, p = 0.004) (85.9 ± 21.0 vs. 76.5 ± 22.4, p < 0.001) and at T2 (4.0, 1.0-7.0 vs. 3.0, 1.0-6.0, p = 0.043) (81.3 ± 22.9 vs. 70.8 ± 22.6, p < 0.001), respectively, and higher mean distress scores at T1 (33.8 ± 13.3 vs. 30.2 ± 14.7, p = 0.034). Of 51 interviews with women and partners (22 early, 29 late TOP), four themes were identified: fetal attachment, time pressure, grief, and reflections on gestational age. Most late TOP participants expressed strong fetal attachment; for early TOP participants, the experiences were more variable. Half of the late TOP participants reported time pressure due to the legal limit. Perceived grief and impact were substantial in both groups.
Conclusions: Our findings suggest that early TOP is associated with lower psychological impact compared to late TOP, mainly in the first months postpartum. This may reflect less intense fetal attachment and more time for reproductive decision-making for some parents, supporting the presumed benefit of earlier intervention. Nevertheless, TOP causes a significant emotional impact at any gestational age.
{"title":"Early versus late termination for fetal anomalies: Women's perspectives and psychological impact in a mixed methods study.","authors":"Eline E R Lust, Kim Bronsgeest, Lidewij Henneman, Neeltje M T H Crombag, Caterina M Bilardo, Robert-Jan H Galjaard, Esther Sikkel, Audrey B C Coumans, Ayten Elvan-Taşpınar, Sander Galjaard, Attie T J I Go, Gwendolyn T R Manten, Eva Pajkrt, Elisabeth van Leeuwen, Monique C Haak, Mireille N Bekker","doi":"10.1111/aogs.70122","DOIUrl":"10.1111/aogs.70122","url":null,"abstract":"<p><strong>Introduction: </strong>A frequently cited benefit of the first-trimester anomaly scan (FTAS) is that it reduces psychological impact by enabling earlier termination of pregnancy (TOP). However, the impact of early versus late TOP due to fetal anomalies remains unclear. This study evaluates the psychological impact and perspectives associated with early versus late TOP.</p><p><strong>Material and methods: </strong>A prospective mixed methods study was conducted. The early group (TOP <18 weeks) included women with an abnormal FTAS; the late group (TOP 20-24 weeks) included women with an abnormal second-trimester scan (SAS), abnormal FTAS, or normal FTAS followed by abnormal SAS. Women completed questionnaires 2 (T1) and 6 months (T2) postpartum addressing psychological impact using validated scales (State-Trait Anxiety Inventory, Edinburgh Depression Scale, Impact of Event Scale, Perinatal Grief Scale) and study-specific questions. Semi-structured interviews were conducted with women and their partners 3-6 months after termination.</p><p><strong>Results: </strong>149 women with early TOP (15 + 2 weeks, range 14 + 4-16 + 1) and 129 with late TOP (22 + 0, 21 + 0-23 + 1) completed T1. In both groups, the majority had clinically relevant anxiety at T1 and T2 and moderate/severe distress at T1. The late TOP group had higher median depression and mean grief scores at T1 (5.0, range 3.0-8.0 vs. 4.0, range 2.0-7.0, p = 0.004) (85.9 ± 21.0 vs. 76.5 ± 22.4, p < 0.001) and at T2 (4.0, 1.0-7.0 vs. 3.0, 1.0-6.0, p = 0.043) (81.3 ± 22.9 vs. 70.8 ± 22.6, p < 0.001), respectively, and higher mean distress scores at T1 (33.8 ± 13.3 vs. 30.2 ± 14.7, p = 0.034). Of 51 interviews with women and partners (22 early, 29 late TOP), four themes were identified: fetal attachment, time pressure, grief, and reflections on gestational age. Most late TOP participants expressed strong fetal attachment; for early TOP participants, the experiences were more variable. Half of the late TOP participants reported time pressure due to the legal limit. Perceived grief and impact were substantial in both groups.</p><p><strong>Conclusions: </strong>Our findings suggest that early TOP is associated with lower psychological impact compared to late TOP, mainly in the first months postpartum. This may reflect less intense fetal attachment and more time for reproductive decision-making for some parents, supporting the presumed benefit of earlier intervention. Nevertheless, TOP causes a significant emotional impact at any gestational age.</p>","PeriodicalId":6990,"journal":{"name":"Acta Obstetricia et Gynecologica Scandinavica","volume":" ","pages":"444-454"},"PeriodicalIF":3.1,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12942052/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145931819","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-03-01Epub Date: 2026-01-27DOI: 10.1111/aogs.70148
Laurel S Aberle, Katherine E Bayard, Kimberly M Juarez, Jennifer A Yao, Shinya Matsuzaki, Tatsuya Miyake, Aaron D Masjedi, Rachel S Mandelbaum, Caroline T Nguyen, Joseph G Ouzounian, Koji Matsuo
Introduction: Maternal outcomes of pregnancy with subclinical hypothyroidism continue to be active areas of research interest. The objective of this study was to compare severe maternal morbidity at delivery between pregnant patients with subclinical hypothyroidism and those with overt hypothyroidism.
Material and methods: This cross-sectional study queried the Healthcare Cost and Utilization Project's National Inpatient Sample. Study population included 11 620 hospital deliveries with a diagnosis code of subclinical hypothyroidism and 697 320 hospital deliveries with a diagnosis code of overt hypothyroidism. Main outcome was severe maternal morbidity per the Centers for Disease Control and Prevention definition (20 indicators), assessed with multivariable generalized linear model.
Results: Pregnancy with subclinical hypothyroidism was associated with a 54% higher rate of severe maternal morbidity at delivery compared with those with overt hypothyroidism (18.1 and 11.1 per 1000 deliveries, adjusted-incidence rate ratio [aIR] 1.54, 95% confidence interval [CI] 1.34-1.76). Among the individual severe maternal morbidity indicators, the incidence rate of eclampsia (2.2 versus 0.7 per 1000 deliveries, aIR 2.73, 95% CI: 1.83-4.09) was particularly higher among pregnancies with subclinical hypothyroidism compared with pregnancies with overt hypothyroidism. In an exploratory evaluation according to patient demographics, maternal age younger than 25 years (31.9 vs. 9.4 per 1000 deliveries, aIR 3.62, 95% CI: 2.62-5.01), Black individuals (55.2 vs. 24.7 per 1000 deliveries, aIR 2.21, 95% CI: 1.60-3.06), pregestational hypertension (70.2 vs. 27.2 per 1000 deliveries, aIR 2.20, 95% CI: 1.60-3.03), and obesity disorder (35.2 vs. 16.7 per 1000 deliveries, aIR 1.87, 95% CI: 1.48-2.35) were associated with higher rates of severe maternal morbidity for subclinical hypothyroidism compared with overt hypothyroidism. Severe maternal morbidity rates were more than twice as high for subclinical hypothyroidism compared with overt hypothyroidism among pregnant patients younger than 25 years with obesity disorder (79.4 vs. 10.1 per 1000 deliveries, aIR 7.89, 95% CI: 4.78-13.02), Black individuals with pregestational hypertension (157.9 vs. 40.2 per 1000 deliveries, aIR 3.15, 95% CI: 1.77-5.61), and Black individuals with obesity disorder (102.0 vs. 33.9 per 1000 deliveries, aIR 2.81, 95% CI: 1.83-4.32).
Conclusions: The results of this cross-sectional study suggest that subclinical hypothyroidism may be associated with higher rates of severe maternal morbidity at delivery compared with overt hypothyroidism.
{"title":"Comparison of severe maternal morbidity between pregnancy with subclinical hypothyroidism and overt hypothyroidism.","authors":"Laurel S Aberle, Katherine E Bayard, Kimberly M Juarez, Jennifer A Yao, Shinya Matsuzaki, Tatsuya Miyake, Aaron D Masjedi, Rachel S Mandelbaum, Caroline T Nguyen, Joseph G Ouzounian, Koji Matsuo","doi":"10.1111/aogs.70148","DOIUrl":"10.1111/aogs.70148","url":null,"abstract":"<p><strong>Introduction: </strong>Maternal outcomes of pregnancy with subclinical hypothyroidism continue to be active areas of research interest. The objective of this study was to compare severe maternal morbidity at delivery between pregnant patients with subclinical hypothyroidism and those with overt hypothyroidism.</p><p><strong>Material and methods: </strong>This cross-sectional study queried the Healthcare Cost and Utilization Project's National Inpatient Sample. Study population included 11 620 hospital deliveries with a diagnosis code of subclinical hypothyroidism and 697 320 hospital deliveries with a diagnosis code of overt hypothyroidism. Main outcome was severe maternal morbidity per the Centers for Disease Control and Prevention definition (20 indicators), assessed with multivariable generalized linear model.</p><p><strong>Results: </strong>Pregnancy with subclinical hypothyroidism was associated with a 54% higher rate of severe maternal morbidity at delivery compared with those with overt hypothyroidism (18.1 and 11.1 per 1000 deliveries, adjusted-incidence rate ratio [aIR] 1.54, 95% confidence interval [CI] 1.34-1.76). Among the individual severe maternal morbidity indicators, the incidence rate of eclampsia (2.2 versus 0.7 per 1000 deliveries, aIR 2.73, 95% CI: 1.83-4.09) was particularly higher among pregnancies with subclinical hypothyroidism compared with pregnancies with overt hypothyroidism. In an exploratory evaluation according to patient demographics, maternal age younger than 25 years (31.9 vs. 9.4 per 1000 deliveries, aIR 3.62, 95% CI: 2.62-5.01), Black individuals (55.2 vs. 24.7 per 1000 deliveries, aIR 2.21, 95% CI: 1.60-3.06), pregestational hypertension (70.2 vs. 27.2 per 1000 deliveries, aIR 2.20, 95% CI: 1.60-3.03), and obesity disorder (35.2 vs. 16.7 per 1000 deliveries, aIR 1.87, 95% CI: 1.48-2.35) were associated with higher rates of severe maternal morbidity for subclinical hypothyroidism compared with overt hypothyroidism. Severe maternal morbidity rates were more than twice as high for subclinical hypothyroidism compared with overt hypothyroidism among pregnant patients younger than 25 years with obesity disorder (79.4 vs. 10.1 per 1000 deliveries, aIR 7.89, 95% CI: 4.78-13.02), Black individuals with pregestational hypertension (157.9 vs. 40.2 per 1000 deliveries, aIR 3.15, 95% CI: 1.77-5.61), and Black individuals with obesity disorder (102.0 vs. 33.9 per 1000 deliveries, aIR 2.81, 95% CI: 1.83-4.32).</p><p><strong>Conclusions: </strong>The results of this cross-sectional study suggest that subclinical hypothyroidism may be associated with higher rates of severe maternal morbidity at delivery compared with overt hypothyroidism.</p>","PeriodicalId":6990,"journal":{"name":"Acta Obstetricia et Gynecologica Scandinavica","volume":" ","pages":"499-507"},"PeriodicalIF":3.1,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12942046/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146049923","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}