This study aimed to compare the axial cranial ultrasound images of normal and open neural tube defect (NTD) fetuses using a deep learning (DL) model and to assess its predictive accuracy in identifying open NTD.It was a prospective case-control study. Axial trans-thalamic fetal ultrasound images of participants with open fetal NTD and normal controls between 14 and 28 weeks of gestation were taken after consent. The images were divided into training, testing, and validation datasets randomly in the ratio of 70:15:15. The images were further processed and classified using DL convolutional neural network (CNN) transfer learning (TL) models. The TL models were trained for 50 epochs. The data was analyzed in terms of Cohen kappa score, accuracy score, area under receiver operating curve (AUROC) score, F1 score validity, sensitivity, and specificity of the test.A total of 59 cases and 116 controls were fully followed. Efficient net B0, Visual Geometry Group (VGG), and Inception V3 TL models were used. Both Efficient net B0 and VGG16 models gave similar high training and validation accuracy (100 and 95.83%, respectively). Using inception V3, the training and validation accuracy was 98.28 and 95.83%, respectively. The sensitivity and specificity of Efficient NetB0 was 100 and 89%, respectively, and was the best.The analysis of the changes in axial images of the fetal cranium using the DL model, Efficient Net B0 proved to be an effective model to be used in clinical application for the identification of open NTD. · Open spina bifida is often missed due to the nonrecognition of the lemon sign on ultrasound.. · Image classification using DL identified open spina bifida with excellent accuracy.. · The research is clinically relevant in low- and middle-income countries..
利用深度学习(DL)模型比较正常和开放神经管缺陷(NTD)胎儿的轴向颅超声图像,并评估其识别开放神经管缺陷(NTD)的预测准确性。这是一项前瞻性病例对照研究。经同意后,在14至28周妊娠期间,对开放性胎儿NTD和正常对照组的参与者进行轴向跨丘脑胎儿超声成像。将图像按70:15:15的比例随机分为训练、测试和验证数据集。使用DL卷积神经网络(CNN)迁移学习(TL)模型对图像进行进一步处理和分类。TL模型训练了50个epoch。根据Cohen kappa评分、准确性评分、受试者工作曲线下面积(AUROC)评分、F1评分效度、敏感性和特异性对数据进行分析。对59例病例和116例对照进行了全面随访。使用了Efficient net B0、Visual Geometry Group (VGG)和Inception V3 TL模型。Efficient net B0和VGG16模型均具有相似的高训练和验证准确率(分别为100%和95.83%)。使用inception V3,训练和验证准确率分别为98.28%和95.83%。有效率NetB0的敏感性为100%,特异度为89%,为最佳。利用DL模型对胎儿颅骨轴向图像的变化进行分析,证明Efficient Net B0是一种可用于临床诊断开放性NTD的有效模型。·开放性脊柱裂经常被遗漏,因为超声不能识别柠檬征。·使用深度学习图像分类识别开放性脊柱裂,准确率极高。·这项研究在低收入和中等收入国家具有临床意义。
{"title":"Use of Artificial Intelligence in Recognition of Fetal Open Neural Tube Defect on Prenatal Ultrasound.","authors":"Manisha Kumar, Urvashi Arora, Debarka Sengupta, Shilpi Nain, Deepika Meena, Reena Yadav, Miriam Perez","doi":"10.1055/a-2589-3554","DOIUrl":"10.1055/a-2589-3554","url":null,"abstract":"<p><p>This study aimed to compare the axial cranial ultrasound images of normal and open neural tube defect (NTD) fetuses using a deep learning (DL) model and to assess its predictive accuracy in identifying open NTD.It was a prospective case-control study. Axial trans-thalamic fetal ultrasound images of participants with open fetal NTD and normal controls between 14 and 28 weeks of gestation were taken after consent. The images were divided into training, testing, and validation datasets randomly in the ratio of 70:15:15. The images were further processed and classified using DL convolutional neural network (CNN) transfer learning (TL) models. The TL models were trained for 50 epochs. The data was analyzed in terms of Cohen kappa score, accuracy score, area under receiver operating curve (AUROC) score, F1 score validity, sensitivity, and specificity of the test.A total of 59 cases and 116 controls were fully followed. Efficient net B0, Visual Geometry Group (VGG), and Inception V3 TL models were used. Both Efficient net B0 and VGG16 models gave similar high training and validation accuracy (100 and 95.83%, respectively). Using inception V3, the training and validation accuracy was 98.28 and 95.83%, respectively. The sensitivity and specificity of Efficient NetB0 was 100 and 89%, respectively, and was the best.The analysis of the changes in axial images of the fetal cranium using the DL model, Efficient Net B0 proved to be an effective model to be used in clinical application for the identification of open NTD. · Open spina bifida is often missed due to the nonrecognition of the lemon sign on ultrasound.. · Image classification using DL identified open spina bifida with excellent accuracy.. · The research is clinically relevant in low- and middle-income countries..</p>","PeriodicalId":7584,"journal":{"name":"American journal of perinatology","volume":" ","pages":"56-63"},"PeriodicalIF":1.2,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143970303","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-01Epub Date: 2024-12-04DOI: 10.1055/a-2465-5163
Mary J Scourboutakos, Elenee H Harper, Michael T Kopec, Lauren Rose, Milena Forte
This study aimed to systematically document the reported omega-3 levels in commercially available prenatal supplements in the United States and Canada, and compare these levels to recommended intakes in pregnancy.Commercial prenatal supplements were identified using the Dietary Supplement Label Database (n = 50) and the Licensed Natural Health Products Database (n = 18). Mean omega-3 levels and the proportion of products meeting recommendations for pregnant women were tabulated.Average omega-3 levels were 368 ± 33 mg in the United States and 404 ± 72 mg in Canada. Seventy percent of products in the United States and 61% in Canada contained the amount of omega-3 levels recommended for pregnant women with sufficient intakes. Sixteen percent of products in the United States and 28% in Canada contained the dose recommended for pregnant women with insufficient intakes.These results illustrate that commercial prenatal supplements contain a wide variety of omega-3 fatty acid levels that may or may not be consistent with recommended intake levels. · most pregnant women consume inadequate amounts of omega-3 fatty acids.. · omega-3 fatty acids can help prevent preterm birth.. · new guidelines recommend increased intakes of omega-3 fatty acids during pregnancy.. · prenatal supplements contain a wide variety of omega-3 fatty acid levels.. · omega-3 levels in prenatal supplements may or may not be consistent with recommended intake levels..
{"title":"Omega-3 Levels in Prenatal Supplements.","authors":"Mary J Scourboutakos, Elenee H Harper, Michael T Kopec, Lauren Rose, Milena Forte","doi":"10.1055/a-2465-5163","DOIUrl":"10.1055/a-2465-5163","url":null,"abstract":"<p><p>This study aimed to systematically document the reported omega-3 levels in commercially available prenatal supplements in the United States and Canada, and compare these levels to recommended intakes in pregnancy.Commercial prenatal supplements were identified using the Dietary Supplement Label Database (<i>n</i> = 50) and the Licensed Natural Health Products Database (<i>n</i> = 18). Mean omega-3 levels and the proportion of products meeting recommendations for pregnant women were tabulated.Average omega-3 levels were 368 ± 33 mg in the United States and 404 ± 72 mg in Canada. Seventy percent of products in the United States and 61% in Canada contained the amount of omega-3 levels recommended for pregnant women with sufficient intakes. Sixteen percent of products in the United States and 28% in Canada contained the dose recommended for pregnant women with insufficient intakes.These results illustrate that commercial prenatal supplements contain a wide variety of omega-3 fatty acid levels that may or may not be consistent with recommended intake levels. · most pregnant women consume inadequate amounts of omega-3 fatty acids.. · omega-3 fatty acids can help prevent preterm birth.. · new guidelines recommend increased intakes of omega-3 fatty acids during pregnancy.. · prenatal supplements contain a wide variety of omega-3 fatty acid levels.. · omega-3 levels in prenatal supplements may or may not be consistent with recommended intake levels..</p>","PeriodicalId":7584,"journal":{"name":"American journal of perinatology","volume":" ","pages":"114-117"},"PeriodicalIF":1.2,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142779237","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-01Epub Date: 2025-01-09DOI: 10.1055/a-2512-9453
Yolanda Evong, Jiaxin Luo, Lingyun Ye, John Fahey, Janis L Breeze, Rebecca Attenborough, Kenny Wong, Joanne M Langley
From 2002 to 2023, palivizumab was the only intervention to reduce respiratory syncytial virus (RSV)-associated hospitalizations in high-risk infants in Canada but advances in RSV prevention are drastically changing this landscape. Eligibility criteria for this monoclonal antibody for preterm infants varied over time across each of 10 Canadian provinces and 3 territories. The National Professional Pediatric Association (Canadian Pediatric Society) revised its eligibility recommendations in 2015, removing access for preterm infants 30 to 32 weeks gestation (WG). The province of Nova Scotia followed these recommendations the next season. This study aimed to determine if the removal of access to palivizumab in these previously eligible infants was associated with a change in hospital admissions, deaths, or ambulatory visits associated with RSV.We identified a retrospective cohort of Nova Scotia infants born between 30 and 32 WG, without other risk factors for RSV-H, from April 2012 to September 2019 by linking six population-based provincial databases, and followed each infant through the first year of life. Episodes of RSV-associated hospitalization (RSV-H), ambulatory visits (RSV-A), or death were identified by the International Statistical Classification of Diseases and Related Health Disorders (ICD) RSV-associated diagnostic codes.Of 4,835 infants born during the study period, 250 were 30 to 32 WG and eligible for the cohort. RSV-H increased approximately 10-fold following restricted access to palivizumab (from no RSV-H (0/123) to 9.4%; 95% CI 5.0, 15.9; risk difference 9.4), but no RSV-associated deaths occurred. RSV-A also increased from 5.7 to 17.3% (risk difference 11.6).Discontinuation of access to a prophylactic anti-RSV monoclonal antibody in very preterm infants was associated with a higher risk of RSV-H and RSV-A. Evaluation of health care policy change on patient well-being is essential to assess the impact and guide future decision-making at the population level. · Discontinuation of access to a prophylactic anti-RSV monoclonal antibody in very preterm infants 30 to 32 WG was associated with a higher risk of RSV-H and RSV-A. Evaluation of changes to health care policy on patient well-being is essential to assess impact and guide future decision-making at the population level.. · Removing access to palivizumab led to higher RSV admissions in 30 to 32 WG infants.. · The effect of health care policy changes on child well-being should be assessed routinely.. · No deaths associated with RSV were identified prior to or after the policy change..
背景:从2002年到2023年,帕利珠单抗是加拿大减少RSV相关高危婴儿住院的唯一干预措施,但RSV预防的进展正在彻底改变这一现状。在加拿大10个省和3个地区,这种单克隆抗体用于早产儿的资格标准随着时间的推移而变化。国家儿科专业协会(加拿大儿科协会)于2015年修订了其资格建议,取消了妊娠30至32周的早产儿(WG)的准入。新斯科舍省(NS)在下一季遵循了这些建议。目的:确定在这些先前的婴儿中取消使用帕利珠单抗是否与与RSV相关的住院、死亡或门诊就诊的变化相关。方法:通过连接6个基于人口的省级数据库,我们确定了2012年4月至2019年9月期间出生年龄在30至32岁之间,无RSV-H其他危险因素的NS婴儿的回顾性队列,并对每个婴儿进行了第一年的随访。RSV相关住院、门诊就诊或死亡事件由国际疾病和相关健康障碍统计分类(ICD) RSV相关诊断代码确定。结果:在研究期间出生的4835名婴儿中,有250名30-32岁的婴儿符合队列条件。限制使用帕利珠单抗后,RSV-H增加了约10倍(0/123,至9.4%;(95% CI 5.0, 15.9,风险差9.4),但未发生与rsv相关的死亡。RSV-A也从5.7%增加到17.3%(风险差11.6)。结论:停止给予极早产儿预防性抗rsv单克隆抗体与RSV-H和RSV-A的高风险相关。评估医疗保健政策变化对患者福祉的影响,对于在人口层面评估影响和指导未来决策至关重要。
{"title":"Increased Respiratory Syncytial Virus-Associated Hospitalizations and Ambulatory Visits in Very Preterm Infants in the First Year of Life following Discontinuation of Access to Palivizumab.","authors":"Yolanda Evong, Jiaxin Luo, Lingyun Ye, John Fahey, Janis L Breeze, Rebecca Attenborough, Kenny Wong, Joanne M Langley","doi":"10.1055/a-2512-9453","DOIUrl":"10.1055/a-2512-9453","url":null,"abstract":"<p><p>From 2002 to 2023, palivizumab was the only intervention to reduce respiratory syncytial virus (RSV)-associated hospitalizations in high-risk infants in Canada but advances in RSV prevention are drastically changing this landscape. Eligibility criteria for this monoclonal antibody for preterm infants varied over time across each of 10 Canadian provinces and 3 territories. The National Professional Pediatric Association (Canadian Pediatric Society) revised its eligibility recommendations in 2015, removing access for preterm infants 30 to 32 weeks gestation (WG). The province of Nova Scotia followed these recommendations the next season. This study aimed to determine if the removal of access to palivizumab in these previously eligible infants was associated with a change in hospital admissions, deaths, or ambulatory visits associated with RSV.We identified a retrospective cohort of Nova Scotia infants born between 30 and 32 WG, without other risk factors for RSV-H, from April 2012 to September 2019 by linking six population-based provincial databases, and followed each infant through the first year of life. Episodes of RSV-associated hospitalization (RSV-H), ambulatory visits (RSV-A), or death were identified by the International Statistical Classification of Diseases and Related Health Disorders (ICD) RSV-associated diagnostic codes.Of 4,835 infants born during the study period, 250 were 30 to 32 WG and eligible for the cohort. RSV-H increased approximately 10-fold following restricted access to palivizumab (from no RSV-H (0/123) to 9.4%; 95% CI 5.0, 15.9; risk difference 9.4), but no RSV-associated deaths occurred. RSV-A also increased from 5.7 to 17.3% (risk difference 11.6).Discontinuation of access to a prophylactic anti-RSV monoclonal antibody in very preterm infants was associated with a higher risk of RSV-H and RSV-A. Evaluation of health care policy change on patient well-being is essential to assess the impact and guide future decision-making at the population level. · Discontinuation of access to a prophylactic anti-RSV monoclonal antibody in very preterm infants 30 to 32 WG was associated with a higher risk of RSV-H and RSV-A. Evaluation of changes to health care policy on patient well-being is essential to assess impact and guide future decision-making at the population level.. · Removing access to palivizumab led to higher RSV admissions in 30 to 32 WG infants.. · The effect of health care policy changes on child well-being should be assessed routinely.. · No deaths associated with RSV were identified prior to or after the policy change..</p>","PeriodicalId":7584,"journal":{"name":"American journal of perinatology","volume":" ","pages":"118-121"},"PeriodicalIF":1.2,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12688655/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142942631","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-01Epub Date: 2025-05-29DOI: 10.1055/a-2604-8329
Eva Senechal, Daniel Radeschi, Robert Kearney, Wissam Shalish, Guilherme Sant'Anna
This study aimed to assess the views of parents and neonatal intensive care unit (NICU) health care providers (HCPs) on current wired vital signs monitoring and future wireless alternatives.Prospective cross-sectional survey was conducted between March and July 2023, targeting three groups: (1) NICU parents, (2) physicians, and (3) nurses and respiratory therapists (RT) and physiotherapists (PT). A 17-question survey was developed to assess several perspectives with current vital signs monitoring and a possible wireless monitoring system. NICU parents completed paper surveys and HCPs participated via an anonymous electronic survey. The original English survey was tailored for different respondent groups, translated into French, Spanish, and Portuguese, and distributed through neonatal research networks. Responses from each group were analyzed as totals (%), with within-group comparisons assessed using the Wilcoxon signed-rank test. Additionally, between-group comparisons were conducted using the chi-square test of independence or Fisher's exact test, as appropriate.A total of 1,141 responses were included (25 parents, 438 physicians, and 678 nurses, RTs, and PTs). Only 52% of parents were satisfied with current wired systems; 68% reported wires hindered infant handling, and 52% cited interference with skin-to-skin care. Both physicians and HCPs expressed low satisfaction with the current system. Common concerns included tangling, skin irritation, and workload. Support for wireless technology introduction was high across all groups (parents = 60%, physicians = 91%, and nurses, RTs, and PTs = 87%), with main perceived benefits including improved kangaroo mother care (KMC), reduced patient discomfort, and enhanced bonding. All groups expressed accuracy, safety, battery life, and cost concerns of a possible wireless system.Parents and HCPs are generally dissatisfied with the current NICU vital signs monitoring systems, primarily due to concerns with wires and cables and interference with KMC. Wireless technologies were mostly supported, but data on reliability, safety, and economic feasibility will be critical for development and successful implementation. · Parents and HCPs dislike wired systems due to tangling, skin irritation, and interference with care.. · Support for wireless monitoring was viewed positively by parents and very positively by HCP.. · Wireless systems were seen as beneficial for KC, reducing patient discomfort, and improving bonding.. · However, each group expressed concerns about a potential future wireless monitoring system.. · Accuracy, battery life, radiation, and cost must be addressed before wireless systems can be adopted..
{"title":"Parents and Health Care Providers' Perspectives on Vital Signs Monitoring Technologies in the Neonatal Intensive Care Unit: An International Survey.","authors":"Eva Senechal, Daniel Radeschi, Robert Kearney, Wissam Shalish, Guilherme Sant'Anna","doi":"10.1055/a-2604-8329","DOIUrl":"10.1055/a-2604-8329","url":null,"abstract":"<p><p>This study aimed to assess the views of parents and neonatal intensive care unit (NICU) health care providers (HCPs) on current wired vital signs monitoring and future wireless alternatives.Prospective cross-sectional survey was conducted between March and July 2023, targeting three groups: (1) NICU parents, (2) physicians, and (3) nurses and respiratory therapists (RT) and physiotherapists (PT). A 17-question survey was developed to assess several perspectives with current vital signs monitoring and a possible wireless monitoring system. NICU parents completed paper surveys and HCPs participated via an anonymous electronic survey. The original English survey was tailored for different respondent groups, translated into French, Spanish, and Portuguese, and distributed through neonatal research networks. Responses from each group were analyzed as totals (%), with within-group comparisons assessed using the Wilcoxon signed-rank test. Additionally, between-group comparisons were conducted using the chi-square test of independence or Fisher's exact test, as appropriate.A total of 1,141 responses were included (25 parents, 438 physicians, and 678 nurses, RTs, and PTs). Only 52% of parents were satisfied with current wired systems; 68% reported wires hindered infant handling, and 52% cited interference with skin-to-skin care. Both physicians and HCPs expressed low satisfaction with the current system. Common concerns included tangling, skin irritation, and workload. Support for wireless technology introduction was high across all groups (parents = 60%, physicians = 91%, and nurses, RTs, and PTs = 87%), with main perceived benefits including improved kangaroo mother care (KMC), reduced patient discomfort, and enhanced bonding. All groups expressed accuracy, safety, battery life, and cost concerns of a possible wireless system.Parents and HCPs are generally dissatisfied with the current NICU vital signs monitoring systems, primarily due to concerns with wires and cables and interference with KMC. Wireless technologies were mostly supported, but data on reliability, safety, and economic feasibility will be critical for development and successful implementation. · Parents and HCPs dislike wired systems due to tangling, skin irritation, and interference with care.. · Support for wireless monitoring was viewed positively by parents and very positively by HCP.. · Wireless systems were seen as beneficial for KC, reducing patient discomfort, and improving bonding.. · However, each group expressed concerns about a potential future wireless monitoring system.. · Accuracy, battery life, radiation, and cost must be addressed before wireless systems can be adopted..</p>","PeriodicalId":7584,"journal":{"name":"American journal of perinatology","volume":" ","pages":"245-256"},"PeriodicalIF":1.2,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12768579/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144180589","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-01Epub Date: 2025-03-04DOI: 10.1055/a-2550-5306
Susan McAnany, Gangaram Akangire, Ashley Sherman, Venkatesh Sampath, Winston Manimtim
This study aimed to compare the accuracy of three newly proposed definitions of bronchopulmonary dysplasia (BPD) in predicting outcomes, and to investigate the impact of large airway versus parenchymal versus vascular BPD phenotypes on BPD outcomes.Retrospective chart review of 100 infants with severe BPD discharged from a Children's hospital between 2020 and 2021. Multivariable models evaluated the associations between BPD definitions and phenotypes with tracheostomy and death at 6 months and 1 year after NICU discharge. Secondary outcomes included the need for respiratory support, the use of pulmonary medications, and the need for long-term gastrostomy feeding.Neonatal research network (NRN) and BPD collaborative criteria best-predicted outcomes associated with tracheostomy and/or death (p < 0.001). Among the three BPD phenotypes, large airway disease was independently associated with death or tracheostomy (odds ratios [OR]: 10.5; 95% confidence interval [CI]: 1.6, 68.1). The combination of all three phenotypes was also associated with death or tracheostomy (OR: 9.8; 95% CI: 1.0, 93.5). Both NRN and BPD collaborative definitions showed an association with the need for respiratory support, medication use, and need for long-term gastrostomy tube feeding. Among the 29 infants for whom complete information was available, 18 (62%), 20 (69%), and 18 (62%) had parenchymal, central airway and pulmonary vascular phenotype, respectively.Our results indicate that newer definitions of BPD may better predict the severity of BPD and the need for long-term invasive ventilation support compared with the 2001 National Institute of Health definition of BPD phenotypes impacting mortality and short-term outcomes. These data may be useful for counseling families and developing phenotype-based individualized treatment plans. · The current definition of BPD has limitations.. · New definitions of BPD better predict outcomes.. · BPD phenotypes can better predict outcomes..
目的:比较支气管肺发育不良(BPD)的三种新定义在预测预后方面的准确性,并探讨大气道、实质和血管型BPD表型对BPD预后的影响。研究设计:对2020-2021年间某儿童医院出院的100例重度BPD患儿进行回顾性分析。多变量模型评估了新生儿重症监护病房出院后6个月和1年BPD定义和表型与气管切开术和死亡之间的关系。次要结局包括需要呼吸支持、使用肺部药物和需要长期胃造口喂养。结果:NRN和BPD联合标准最能预测与气管切开术和/或死亡相关的预后(p < 0.001)。在三种BPD表型中,大气道疾病与死亡或气管切开术独立相关(or 10.5, 95% CI 1.6, 68.1)。所有三种表型的组合也与死亡或气管切开术相关(or 9.8, 95% CI 1.0, 93.5)。NRN和BPD的协同定义都显示与呼吸支持、药物使用和长期胃造口管喂养的需要有关。在29例可获得完整信息的婴儿中,分别有18例(62%)、20例(69%)和18例(62%)具有实质、中央气道和肺血管表型。结论:我们的研究结果表明,与2001年NIH定义的BPD表型影响死亡率和短期预后的定义相比,BPD的新定义可以更好地预测BPD的严重程度和长期有创通气支持的需要。这些数据可能对家庭咨询和制定基于表型的个体化治疗计划有用。
{"title":"Predicting Clinical Outcomes of Severe Bronchopulmonary Dysplasia through New Definitions and Phenotypes.","authors":"Susan McAnany, Gangaram Akangire, Ashley Sherman, Venkatesh Sampath, Winston Manimtim","doi":"10.1055/a-2550-5306","DOIUrl":"10.1055/a-2550-5306","url":null,"abstract":"<p><p>This study aimed to compare the accuracy of three newly proposed definitions of bronchopulmonary dysplasia (BPD) in predicting outcomes, and to investigate the impact of large airway versus parenchymal versus vascular BPD phenotypes on BPD outcomes.Retrospective chart review of 100 infants with severe BPD discharged from a Children's hospital between 2020 and 2021. Multivariable models evaluated the associations between BPD definitions and phenotypes with tracheostomy and death at 6 months and 1 year after NICU discharge. Secondary outcomes included the need for respiratory support, the use of pulmonary medications, and the need for long-term gastrostomy feeding.Neonatal research network (NRN) and BPD collaborative criteria best-predicted outcomes associated with tracheostomy and/or death (<i>p</i> < 0.001). Among the three BPD phenotypes, large airway disease was independently associated with death or tracheostomy (odds ratios [OR]: 10.5; 95% confidence interval [CI]: 1.6, 68.1). The combination of all three phenotypes was also associated with death or tracheostomy (OR: 9.8; 95% CI: 1.0, 93.5). Both NRN and BPD collaborative definitions showed an association with the need for respiratory support, medication use, and need for long-term gastrostomy tube feeding. Among the 29 infants for whom complete information was available, 18 (62%), 20 (69%), and 18 (62%) had parenchymal, central airway and pulmonary vascular phenotype, respectively.Our results indicate that newer definitions of BPD may better predict the severity of BPD and the need for long-term invasive ventilation support compared with the 2001 National Institute of Health definition of BPD phenotypes impacting mortality and short-term outcomes. These data may be useful for counseling families and developing phenotype-based individualized treatment plans. · The current definition of BPD has limitations.. · New definitions of BPD better predict outcomes.. · BPD phenotypes can better predict outcomes..</p>","PeriodicalId":7584,"journal":{"name":"American journal of perinatology","volume":" ","pages":"257-265"},"PeriodicalIF":1.2,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143555484","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-01Epub Date: 2025-05-01DOI: 10.1055/a-2597-8542
Kazuma Onishi, Tetsuya Kawakita
This study aimed to determine optimal gestational weight gain (GWG) considering adverse infant and maternal outcomes among individuals with obesity, with detailed classification for body mass index (BMI) of 40 kg/m2 or higher.This study was a population-based retrospective cohort study, using U.S. birth certificate data from 2017 to 2021. We included nulliparous individuals with singleton pregnancies delivering live births between 370/7 and 416/7 weeks' gestation, excluding those with pregestational diabetes or hypertension, gestational diabetes, preeclampsia, major fetal anomalies, or chromosomal disorders. The study focused on three main outcomes: primary cesarean delivery, small for gestational age (SGA), and large for gestational age (LGA). GWG was evaluated in 2-kg increments, from weight loss >8 kg to gains ≥28 kg. Prepregnancy BMI was stratified into four categories: BMI of 30 to <35, 35 to <40, 40 to <50, and ≥50 kg/m2. Odds ratios and absolute risk reduction were used to identify GWG ranges with balanced risks for three outcomes within each BMI category.Among 1,677,968 individuals with obesity, increased GWG was associated with higher absolute risks of cesarean delivery and LGA and lower risk of SGA across all BMI categories. Optimal GWG ranges varied by prepregnancy BMI: >12 to ≤14 kg for BMI of 30 to <35 kg/m2; >10 to ≤12 kg for BMI of 35 to <40 kg/m2; >6 to ≤10 kg for BMI of 40 to <50 kg/m2; >0 to ≤8 kg for BMI of 50 kg/m2 or higher.We identified higher upper and lower GWG limits for individuals with BMI of 30 to 50 kg/m2, and lower limits for those with BMI ≥50 kg/m2, compared with the guidelines recommended by the U.S. National Academy of Medicine. These findings suggest the need to tailor GWG recommendations based on the severity of obesity. · Optimal GWG varies by obesity class, requiring tailored guidelines.. · Those with BMI ≥50 kg/m may need lower target for gestational gain than current recommendation.. · The optimal GWG range could be changed based on the outcomes of interest..
{"title":"Association of Gestational Weight Gain with Adverse Pregnancy Outcomes in Individuals with Obesity.","authors":"Kazuma Onishi, Tetsuya Kawakita","doi":"10.1055/a-2597-8542","DOIUrl":"10.1055/a-2597-8542","url":null,"abstract":"<p><p>This study aimed to determine optimal gestational weight gain (GWG) considering adverse infant and maternal outcomes among individuals with obesity, with detailed classification for body mass index (BMI) of 40 kg/m<sup>2</sup> or higher.This study was a population-based retrospective cohort study, using U.S. birth certificate data from 2017 to 2021. We included nulliparous individuals with singleton pregnancies delivering live births between 37<sup>0/7</sup> and 41<sup>6/7</sup> weeks' gestation, excluding those with pregestational diabetes or hypertension, gestational diabetes, preeclampsia, major fetal anomalies, or chromosomal disorders. The study focused on three main outcomes: primary cesarean delivery, small for gestational age (SGA), and large for gestational age (LGA). GWG was evaluated in 2-kg increments, from weight loss >8 kg to gains ≥28 kg. Prepregnancy BMI was stratified into four categories: BMI of 30 to <35, 35 to <40, 40 to <50, and ≥50 kg/m<sup>2</sup>. Odds ratios and absolute risk reduction were used to identify GWG ranges with balanced risks for three outcomes within each BMI category.Among 1,677,968 individuals with obesity, increased GWG was associated with higher absolute risks of cesarean delivery and LGA and lower risk of SGA across all BMI categories. Optimal GWG ranges varied by prepregnancy BMI: >12 to ≤14 kg for BMI of 30 to <35 kg/m<sup>2</sup>; >10 to ≤12 kg for BMI of 35 to <40 kg/m<sup>2</sup>; >6 to ≤10 kg for BMI of 40 to <50 kg/m<sup>2</sup>; >0 to ≤8 kg for BMI of 50 kg/m<sup>2</sup> or higher.We identified higher upper and lower GWG limits for individuals with BMI of 30 to 50 kg/m<sup>2</sup>, and lower limits for those with BMI ≥50 kg/m<sup>2</sup>, compared with the guidelines recommended by the U.S. National Academy of Medicine. These findings suggest the need to tailor GWG recommendations based on the severity of obesity. · Optimal GWG varies by obesity class, requiring tailored guidelines.. · Those with BMI ≥50 kg/m may need lower target for gestational gain than current recommendation.. · The optimal GWG range could be changed based on the outcomes of interest..</p>","PeriodicalId":7584,"journal":{"name":"American journal of perinatology","volume":" ","pages":"172-179"},"PeriodicalIF":1.2,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143964261","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-01Epub Date: 2025-05-01DOI: 10.1055/a-2597-8735
Ann M Bruno, Amanda A Allshouse, Christine M Warrick, Torr D Metz
This study aimed to evaluate trends in the frequency of pharmacologic prophylaxis following the implementation of a postpartum venous thromboembolism (VTE) prevention protocol. Secondarily, to evaluate the association between protocol implementation and incidence of VTE and complications.Retrospective cohort of patients delivering from 2015 to 2022 at a single academic institution. Those with an antepartum VTE or receiving therapeutic anticoagulation were excluded. An inpatient thromboprophylaxis protocol was implemented in January 2017 and further updated in July 2020 to expand risk factors to qualify for prophylaxis and extend the length of therapy to the outpatient setting (total 14 days). The cohort was divided into three time periods: preimplementation (January 1, 2025-December 31, 2016), initial protocol (January 1, 2017-June 30, 2020), and updated (July 1, 2020-December 31, 2022) protocol. The primary outcome was the receipt of inpatient heparin-based pharmacologic prophylaxis. Secondary outcomes included filling an outpatient pharmacologic prophylaxis prescription, VTE, and wound complications observed through 6 weeks postpartum. Baseline characteristics and outcomes were compared across the three protocol periods. Logistic regression modeling estimated the association between outcomes and the updated protocol period compared with prior periods.Overall, 22.6% (95% confidence interval [CI]: 22.1-23.0) of 34,217 included deliveries received inpatient pharmacologic prophylaxis: 7.7% (7.1-8.2%) preimplementation, 15.8% (15.2-16.4%) initial protocol, and 41.2% (40.4-42.1%) during the updated protocol period. The rates of inpatient and outpatient prophylaxis increased significantly over time (p < 0.001 test of trend). Delivery in the updated protocol period was not associated with differences in VTE (pre: 0.1%, initial: 0.2%, and updated: 0.1%) nor wound complications (pre: 3.4%, initial: 2.7%, and updated: 2.7%).Single-center implementation of a postpartum prophylaxis protocol resulted in increased use of inpatient and outpatient pharmacologic prophylaxis without changes in rates of VTE or wound complications. · Implementation of a postpartum thromboprophylaxis protocol resulted in increased rates of pharmacologic prophylaxis.. · No differences in wound complications were observed by the protocol period.. · Rates of VTE did not change over time..
背景:评估实施产后静脉血栓栓塞(VTE)预防方案后药物预防频率的趋势。其次,评估方案实施与静脉血栓栓塞和并发症发生率之间的关系。方法:对2015-2022年在单一学术机构分娩的患者进行回顾性队列研究。排除产前静脉血栓栓塞或接受治疗性抗凝治疗的患者。2017年1月实施了住院血栓预防方案,并于2020年7月进一步更新,以扩大有资格进行预防的风险因素,并将治疗时间延长到门诊(总共14天)。该队列被分为三个时间段:实施前(1/1/15 - 12/31/16),初始方案(1/1/17 - 6/30/20)和更新(7/1/20 - 12/31/22)方案。主要结局是住院患者接受以肝素为基础的药物预防。次要结果包括填写门诊药物预防处方、静脉血栓栓塞和产后6周观察的伤口并发症。在三个方案期间比较基线特征和结果。逻辑回归模型估计了结果与更新后的方案周期之间的关联。结果:总体而言,在34,217例纳入的分娩中,22.6% (95% CI 22.1-23.0%)接受了住院药物预防:7.7%(7.1-8.2%)实施前,15.8%(15.2-16.4%)初始方案,41.2%(40.4-42.1%)在更新方案期间。住院和门诊预防率随着时间的推移显著增加(结论:单中心实施产后预防方案导致住院和门诊药物预防使用率增加,而静脉血栓栓塞或伤口并发症的发生率没有变化。
{"title":"Single Center Implementation of a Postpartum Pharmacologic Thromboprophylaxis Protocol.","authors":"Ann M Bruno, Amanda A Allshouse, Christine M Warrick, Torr D Metz","doi":"10.1055/a-2597-8735","DOIUrl":"10.1055/a-2597-8735","url":null,"abstract":"<p><p>This study aimed to evaluate trends in the frequency of pharmacologic prophylaxis following the implementation of a postpartum venous thromboembolism (VTE) prevention protocol. Secondarily, to evaluate the association between protocol implementation and incidence of VTE and complications.Retrospective cohort of patients delivering from 2015 to 2022 at a single academic institution. Those with an antepartum VTE or receiving therapeutic anticoagulation were excluded. An inpatient thromboprophylaxis protocol was implemented in January 2017 and further updated in July 2020 to expand risk factors to qualify for prophylaxis and extend the length of therapy to the outpatient setting (total 14 days). The cohort was divided into three time periods: preimplementation (January 1, 2025-December 31, 2016), initial protocol (January 1, 2017-June 30, 2020), and updated (July 1, 2020-December 31, 2022) protocol. The primary outcome was the receipt of inpatient heparin-based pharmacologic prophylaxis. Secondary outcomes included filling an outpatient pharmacologic prophylaxis prescription, VTE, and wound complications observed through 6 weeks postpartum. Baseline characteristics and outcomes were compared across the three protocol periods. Logistic regression modeling estimated the association between outcomes and the updated protocol period compared with prior periods.Overall, 22.6% (95% confidence interval [CI]: 22.1-23.0) of 34,217 included deliveries received inpatient pharmacologic prophylaxis: 7.7% (7.1-8.2%) preimplementation, 15.8% (15.2-16.4%) initial protocol, and 41.2% (40.4-42.1%) during the updated protocol period. The rates of inpatient and outpatient prophylaxis increased significantly over time (<i>p</i> < 0.001 test of trend). Delivery in the updated protocol period was not associated with differences in VTE (pre: 0.1%, initial: 0.2%, and updated: 0.1%) nor wound complications (pre: 3.4%, initial: 2.7%, and updated: 2.7%).Single-center implementation of a postpartum prophylaxis protocol resulted in increased use of inpatient and outpatient pharmacologic prophylaxis without changes in rates of VTE or wound complications. · Implementation of a postpartum thromboprophylaxis protocol resulted in increased rates of pharmacologic prophylaxis.. · No differences in wound complications were observed by the protocol period.. · Rates of VTE did not change over time..</p>","PeriodicalId":7584,"journal":{"name":"American journal of perinatology","volume":" ","pages":"164-171"},"PeriodicalIF":1.2,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143952081","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-01Epub Date: 2025-05-08DOI: 10.1055/a-2586-3520
Michael Andrew Assaad, Yasmine Khouzam
This study aimed to identify the neonatal training needs of levels I and II community health centers (CHCs).We conducted a mixed-methods study involving a questionnaire, focus groups (FG), and an audit of neonatal transport data. The questionnaire assessed the felt needs of CHC staff, FGs identified normative needs with an expert neonatal transport team, and the audit captured expressed needs using data from the Canadian neonatal transport network.A total of 158 respondents from 12 CHCs completed the questionnaire (98% completeness rate). Key findings indicated significant challenges in human resources, procedural training, management of critical situations including neonatal resuscitation, nutrition, and neurodevelopmental care (NDC), and crisis resource management. Simulation emerged as the preferred training modality. FGs (three sessions, 17 participants) emphasized the importance of regular, multidisciplinary simulation-based training and stress management. The audit (947 means of transport, 2017-2020) revealed frequent respiratory, neurological, and surgical diagnoses, reinforcing the need for advanced training in respiratory support, neonatal resuscitation, and select high-acuity-specific pathologies.Targeted outreach education is essential to address the identified training needs in neonatal care at CHCs. Key components should include simulation-based training, comprehensive procedural modules, and specialized modules on extreme prematurity, pneumothorax, hypoxic-ischemic encephalopathy/seizures, and surgical conditions. Enhanced training in nutrition and NDC is also critical for community health practitioners. · CHC lack neonatal care training.. · In situ simulation training is the preferred modality of CHC.. · Key training gaps include resuscitation and ventilation.. · Crisis resource management and stress management are key team training components.. · Training must cover prematurity, respiratory, neurological, and surgical conditions..
{"title":"Neonatal Outreach Training: Identifying Needs in the Community.","authors":"Michael Andrew Assaad, Yasmine Khouzam","doi":"10.1055/a-2586-3520","DOIUrl":"10.1055/a-2586-3520","url":null,"abstract":"<p><p>This study aimed to identify the neonatal training needs of levels I and II community health centers (CHCs).We conducted a mixed-methods study involving a questionnaire, focus groups (FG), and an audit of neonatal transport data. The questionnaire assessed the felt needs of CHC staff, FGs identified normative needs with an expert neonatal transport team, and the audit captured expressed needs using data from the Canadian neonatal transport network.A total of 158 respondents from 12 CHCs completed the questionnaire (98% completeness rate). Key findings indicated significant challenges in human resources, procedural training, management of critical situations including neonatal resuscitation, nutrition, and neurodevelopmental care (NDC), and crisis resource management. Simulation emerged as the preferred training modality. FGs (three sessions, 17 participants) emphasized the importance of regular, multidisciplinary simulation-based training and stress management. The audit (947 means of transport, 2017-2020) revealed frequent respiratory, neurological, and surgical diagnoses, reinforcing the need for advanced training in respiratory support, neonatal resuscitation, and select high-acuity-specific pathologies.Targeted outreach education is essential to address the identified training needs in neonatal care at CHCs. Key components should include simulation-based training, comprehensive procedural modules, and specialized modules on extreme prematurity, pneumothorax, hypoxic-ischemic encephalopathy/seizures, and surgical conditions. Enhanced training in nutrition and NDC is also critical for community health practitioners. · CHC lack neonatal care training.. · In situ simulation training is the preferred modality of CHC.. · Key training gaps include resuscitation and ventilation.. · Crisis resource management and stress management are key team training components.. · Training must cover prematurity, respiratory, neurological, and surgical conditions..</p>","PeriodicalId":7584,"journal":{"name":"American journal of perinatology","volume":" ","pages":"32-42"},"PeriodicalIF":1.2,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143956235","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-01Epub Date: 2025-05-12DOI: 10.1055/a-2592-0565
John Ibrahim, Abeer Azzuqa, Jennifer Kloesz, Arcangela Balest
The aim of this study is to provide an extensive review of the published literature regarding the use of nasogastric (NG) feeds at discharge in the neonatal population as well as our experience with the implementation of an NG feeds at discharge program in our level IV neonatal intensive care unit.We reviewed and compared the use of NG tubes at discharge and gastrostomy tubes in the neonatal population. We provide an extensive review of previous publications regarding programs of NG feeds at discharge in neonates across the United States and Europe including preterm neonates, neonates with chronic lung disease, and neurological injury. We also reviewed parents' perspectives on NG use at discharge in the neonatal population as well as the use of telehealth in remote monitoring of neonates discharged on NG feeds. We reviewed the economic benefits of such programs. We finally provide our center's algorithm and workflow as well as our center's experience.Twenty-five patients have been discharged so far from this program since its implementation in December 2020. Only 1 patient of the 25 patients discharged on NG tube feeds required gastrostomy tube placement.Discharge with NG tube feeds in a carefully selected population is safe, and feasible and can lead to increased parent satisfaction, besides offering a developmental advantage for the neonates when the only remaining inpatient need is achieving full oral feeds. · Discharge with NG tube feeds in a carefully selected neonatal population is safe and feasible.. · Nasogastric feeds at discharge can lead to increased parent satisfaction and a developmental advantage for the neonates when the only remaining inpatient need is achieving full oral feeds.. · Carefully structured education at discharge, as well as follow-up programs in place can ensure adequate parental support during this process.. · Telehealth can play a key role in implementation of such programs..
{"title":"Implementation of Nasogastric Tube Feedings at Discharge in a Large Quaternary NICU: A Literature Review, Proposed Algorithm, and Our Center Experience.","authors":"John Ibrahim, Abeer Azzuqa, Jennifer Kloesz, Arcangela Balest","doi":"10.1055/a-2592-0565","DOIUrl":"10.1055/a-2592-0565","url":null,"abstract":"<p><p>The aim of this study is to provide an extensive review of the published literature regarding the use of nasogastric (NG) feeds at discharge in the neonatal population as well as our experience with the implementation of an NG feeds at discharge program in our level IV neonatal intensive care unit.We reviewed and compared the use of NG tubes at discharge and gastrostomy tubes in the neonatal population. We provide an extensive review of previous publications regarding programs of NG feeds at discharge in neonates across the United States and Europe including preterm neonates, neonates with chronic lung disease, and neurological injury. We also reviewed parents' perspectives on NG use at discharge in the neonatal population as well as the use of telehealth in remote monitoring of neonates discharged on NG feeds. We reviewed the economic benefits of such programs. We finally provide our center's algorithm and workflow as well as our center's experience.Twenty-five patients have been discharged so far from this program since its implementation in December 2020. Only 1 patient of the 25 patients discharged on NG tube feeds required gastrostomy tube placement.Discharge with NG tube feeds in a carefully selected population is safe, and feasible and can lead to increased parent satisfaction, besides offering a developmental advantage for the neonates when the only remaining inpatient need is achieving full oral feeds. · Discharge with NG tube feeds in a carefully selected neonatal population is safe and feasible.. · Nasogastric feeds at discharge can lead to increased parent satisfaction and a developmental advantage for the neonates when the only remaining inpatient need is achieving full oral feeds.. · Carefully structured education at discharge, as well as follow-up programs in place can ensure adequate parental support during this process.. · Telehealth can play a key role in implementation of such programs..</p>","PeriodicalId":7584,"journal":{"name":"American journal of perinatology","volume":" ","pages":"89-105"},"PeriodicalIF":1.2,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143963674","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-01Epub Date: 2025-05-06DOI: 10.1055/a-2586-3568
Jason G Bunn, Albert Tang, Kristen Warncke, Saron Gilazgi, Donald D Mcintire, David B Nelson, Catherine Y Spong, J Seth Hawkins
This study aimed to determine if the rate of hysterotomy extensions increases with increasing cervical dilation in unscheduled cesarean deliveries, and to develop a measure of the severity of hysterotomy extension for quantifying morbidity.This is a retrospective study of unscheduled cesarean deliveries relating to labor dystocia and/or nonreassuring tracings from January 1, 2021, to December 31, 2021. Severe extension was defined as bilateral or adjacent to a structure such as the uterine artery, broad ligament, or cervix, and was compared with uterine artery extensions alone.There were 990 unscheduled cesarean deliveries included. Extensions (n = 233) significantly increased with increasing cervical dilation (p < 0.0001), complicating more than 30 and 50% at 6 and 10 cm of cervical dilation, respectively. Apart from this trend, a logistic regression analysis indicated cervical dilation was an independent risk factor for extension. Transfusions of at least 2 units of blood were five times (26 vs. 5%) more likely for patients with severe extensions than no extension (p < 0.0001).Hysterotomy extensions significantly increase with increasing cervical dilation, and cervical dilation is an independent risk factor for extension. A composite measure of severity accounts for different types of extension when quantifying morbidity, but uterine artery extension is the primary driver of maternal morbidity in cases without hysterectomy. · We report higher than previously published rates of extension, in our study of unscheduled cesareans.. · Extension rates rise with cervical dilation-33% at 6 cm, over 50% at 10 cm.. · Cervical dilation is an independent risk factor for extension.. · Severe extensions were fivefold more likely to be transfused two units than no extension.. · The composite measure for severity was driven by uterine artery extensions..
{"title":"Analysis of Hysterotomy Extension at Unscheduled Cesarean Delivery.","authors":"Jason G Bunn, Albert Tang, Kristen Warncke, Saron Gilazgi, Donald D Mcintire, David B Nelson, Catherine Y Spong, J Seth Hawkins","doi":"10.1055/a-2586-3568","DOIUrl":"10.1055/a-2586-3568","url":null,"abstract":"<p><p>This study aimed to determine if the rate of hysterotomy extensions increases with increasing cervical dilation in unscheduled cesarean deliveries, and to develop a measure of the severity of hysterotomy extension for quantifying morbidity.This is a retrospective study of unscheduled cesarean deliveries relating to labor dystocia and/or nonreassuring tracings from January 1, 2021, to December 31, 2021. Severe extension was defined as bilateral or adjacent to a structure such as the uterine artery, broad ligament, or cervix, and was compared with uterine artery extensions alone.There were 990 unscheduled cesarean deliveries included. Extensions (<i>n</i> = 233) significantly increased with increasing cervical dilation (<i>p</i> < 0.0001), complicating more than 30 and 50% at 6 and 10 cm of cervical dilation, respectively. Apart from this trend, a logistic regression analysis indicated cervical dilation was an independent risk factor for extension. Transfusions of at least 2 units of blood were five times (26 vs. 5%) more likely for patients with severe extensions than no extension (<i>p</i> < 0.0001).Hysterotomy extensions significantly increase with increasing cervical dilation, and cervical dilation is an independent risk factor for extension. A composite measure of severity accounts for different types of extension when quantifying morbidity, but uterine artery extension is the primary driver of maternal morbidity in cases without hysterectomy. · We report higher than previously published rates of extension, in our study of unscheduled cesareans.. · Extension rates rise with cervical dilation-33% at 6 cm, over 50% at 10 cm.. · Cervical dilation is an independent risk factor for extension.. · Severe extensions were fivefold more likely to be transfused two units than no extension.. · The composite measure for severity was driven by uterine artery extensions..</p>","PeriodicalId":7584,"journal":{"name":"American journal of perinatology","volume":" ","pages":"23-31"},"PeriodicalIF":1.2,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143957247","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}