Pub Date : 2025-12-01Epub Date: 2025-06-02DOI: 10.1080/14767058.2025.2511092
Anna M Dueckelmann, Larry Hinkson, Malika Guggenberger, Thorsten Braun, Wolfgang Henrich
Objective: This retrospective analysis evaluates the safety and efficacy of the vaginal use of the chitosan covered gauze ("Celox™ PPH") in managing lower genital tract trauma with high blood loss, where conventional repair failed.
Methods: Data from patients receiving chitosan covered gauze intravaginally or locally at the vulva due to substantial blood loss because of birth injury were examined retrospectively, using data from a university hospital 2017-2024. Parameters included blood loss, anesthesia, transfusions, length of hospitalization, infection signs, need for intensive care, and tamponade success, defined as bleeding cessation within 5 min and no requirement of further operative intervention.
Results: Use of chitosan covered gauze effectively controlled bleeding in 26 severe birth injury cases except one. Seven women presented with bleeding due to vaginal tears, 2 with cervical tears, 14 with combined vaginal and perineal or cervical tears, 2 with clitoral lacerations and one with a paravaginal hematoma. In the single unsuccessful case the tamponade was applied late after initial suturing because of under-estimated blood loss, and a second subsequent surgery became necessary. In two women of the cohort the gauze was initially used as a bridging concept because of reduced surgical visibility. Median blood loss in the study cohort was 1000 ml resulting in a median hemoglobin-reduction of 3.65 g/dl. Four patients required blood transfusion and intensive care after the bleeding event. Tamponade application duration varied, ranging from 20 min to 24 h, with a median duration of 8.5 h. The median hospital stay was 3 days. Infection parameters were not elevated after gauze application, with no reported cases of postpartum fever nor signs of infection. Removal was uneventful in all patients, expulsion did not occur. Three successful pregnancies after the event have been reported so far.
Conclusion: Vaginal insertion of chitosan covered gauze proved to be safe and effective for the management of severe lacerations after vaginal birth in our retrospective cohort. Shorter application time may be sufficient for birth injuries.
{"title":"Safety and efficacy of the chitosan covered tamponade for the management of lower genital tract trauma during childbirth.","authors":"Anna M Dueckelmann, Larry Hinkson, Malika Guggenberger, Thorsten Braun, Wolfgang Henrich","doi":"10.1080/14767058.2025.2511092","DOIUrl":"https://doi.org/10.1080/14767058.2025.2511092","url":null,"abstract":"<p><strong>Objective: </strong>This retrospective analysis evaluates the safety and efficacy of the vaginal use of the chitosan covered gauze (\"Celox<sup>™</sup> PPH\") in managing lower genital tract trauma with high blood loss, where conventional repair failed.</p><p><strong>Methods: </strong>Data from patients receiving chitosan covered gauze intravaginally or locally at the vulva due to substantial blood loss because of birth injury were examined retrospectively, using data from a university hospital 2017-2024. Parameters included blood loss, anesthesia, transfusions, length of hospitalization, infection signs, need for intensive care, and tamponade success, defined as bleeding cessation within 5 min and no requirement of further operative intervention.</p><p><strong>Results: </strong>Use of chitosan covered gauze effectively controlled bleeding in 26 severe birth injury cases except one. Seven women presented with bleeding due to vaginal tears, 2 with cervical tears, 14 with combined vaginal and perineal or cervical tears, 2 with clitoral lacerations and one with a paravaginal hematoma. In the single unsuccessful case the tamponade was applied late after initial suturing because of under-estimated blood loss, and a second subsequent surgery became necessary. In two women of the cohort the gauze was initially used as a bridging concept because of reduced surgical visibility. Median blood loss in the study cohort was 1000 ml resulting in a median hemoglobin-reduction of 3.65 g/dl. Four patients required blood transfusion and intensive care after the bleeding event. Tamponade application duration varied, ranging from 20 min to 24 h, with a median duration of 8.5 h. The median hospital stay was 3 days. Infection parameters were not elevated after gauze application, with no reported cases of postpartum fever nor signs of infection. Removal was uneventful in all patients, expulsion did not occur. Three successful pregnancies after the event have been reported so far.</p><p><strong>Conclusion: </strong>Vaginal insertion of chitosan covered gauze proved to be safe and effective for the management of severe lacerations after vaginal birth in our retrospective cohort. Shorter application time may be sufficient for birth injuries.</p>","PeriodicalId":50146,"journal":{"name":"Journal of Maternal-Fetal & Neonatal Medicine","volume":"38 1","pages":"2511092"},"PeriodicalIF":1.7,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144210073","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}
Objectives: Acute leukemia (AL) presents significant health challenges, particularly in children, and iron plays a critical role in cellular processes that could influence cancer development. The study was motivated by the need to clarify the potential role of iron supplementation during pregnancy in influencing the risk of developing childhood leukemia.
Materials and methods: This meta-analysis adhered to PRISMA guidelines and systematically searched PubMed, Scopus, and Web of Science databases up to April 2024 for relevant observational studies. Inclusion criteria focused on case-control studies assessing the relationship between iron supplementation during pregnancy and leukemia risk, reporting odds ratios (ORs) with 95% confidence intervals (CIs). Data extraction and quality assessment were performed independently by two researchers using the Newcastle-Ottawa Scale (NOS). Statistical analysis involved calculating overall relative risk (RR) using a random-effects model and assessing heterogeneity through Cochran's Q test and the I2 statistic. Publication bias was evaluated using Egger's and Begg's tests.
Results: The study analyzed data from 9 studies with 12 data sets involving a total of 4281 participants (2327 cases and 1954 controls). The findings indicated no significant association between iron supplementation during pregnancy and the overall risk of childhood leukemia (OR:1.01; 95% CI: 0.84-1.21, I2 = 63.2%). Also, no relationship was found between receiving iron supplements during pregnancy and the risk of AML (OR:1.01; 95% CI: 0.84-1.21, I2 = 56.6%) and ALL (OR:1.00; 95% CI: 0.81-1.24, I2 = 67.3%).
Conclusion: This study found no significant association between iron supplementation during pregnancy and AL risk among case-control studies. Further research is needed to explore the potential influence of genetic and environmental factors on this relationship.
{"title":"The association between iron supplementation during pregnancy and the risk of childhood leukemia: a meta-analysis of case-control studies.","authors":"Mahsa Dabir, Pedram Pam, Mehrdad Jamali, Fakhredin Saba, Zohreh Ghoreishi","doi":"10.1080/14767058.2025.2474268","DOIUrl":"10.1080/14767058.2025.2474268","url":null,"abstract":"<p><strong>Objectives: </strong>Acute leukemia (AL) presents significant health challenges, particularly in children, and iron plays a critical role in cellular processes that could influence cancer development. The study was motivated by the need to clarify the potential role of iron supplementation during pregnancy in influencing the risk of developing childhood leukemia.</p><p><strong>Materials and methods: </strong>This meta-analysis adhered to PRISMA guidelines and systematically searched PubMed, Scopus, and Web of Science databases up to April 2024 for relevant observational studies. Inclusion criteria focused on case-control studies assessing the relationship between iron supplementation during pregnancy and leukemia risk, reporting odds ratios (ORs) with 95% confidence intervals (CIs). Data extraction and quality assessment were performed independently by two researchers using the Newcastle-Ottawa Scale (NOS). Statistical analysis involved calculating overall relative risk (RR) using a random-effects model and assessing heterogeneity through Cochran's Q test and the I<sup>2</sup> statistic. Publication bias was evaluated using Egger's and Begg's tests.</p><p><strong>Results: </strong>The study analyzed data from 9 studies with 12 data sets involving a total of 4281 participants (2327 cases and 1954 controls). The findings indicated no significant association between iron supplementation during pregnancy and the overall risk of childhood leukemia (OR:1.01; 95% CI: 0.84-1.21, I2 = 63.2%). Also, no relationship was found between receiving iron supplements during pregnancy and the risk of AML (OR:1.01; 95% CI: 0.84-1.21, I2 = 56.6%) and ALL (OR:1.00; 95% CI: 0.81-1.24, I2 = 67.3%).</p><p><strong>Conclusion: </strong>This study found no significant association between iron supplementation during pregnancy and AL risk among case-control studies. Further research is needed to explore the potential influence of genetic and environmental factors on this relationship.</p>","PeriodicalId":50146,"journal":{"name":"Journal of Maternal-Fetal & Neonatal Medicine","volume":"38 1","pages":"2474268"},"PeriodicalIF":1.6,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143568770","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 : 2025-12-01Epub Date: 2025-08-01DOI: 10.1080/14767058.2025.2540645
{"title":"Statement of Retraction: Impact of manual removal of the placenta and intrauterine cleaning during elective cesarean delivery on maternal infectious morbidity and blood loss.","authors":"","doi":"10.1080/14767058.2025.2540645","DOIUrl":"https://doi.org/10.1080/14767058.2025.2540645","url":null,"abstract":"","PeriodicalId":50146,"journal":{"name":"Journal of Maternal-Fetal & Neonatal Medicine","volume":"38 1","pages":"2540645"},"PeriodicalIF":1.6,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144762129","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 : 2025-12-01Epub Date: 2025-08-25DOI: 10.1080/14767058.2025.2546544
Ming Yang, Dajian Long, Yunxiu Li, Xiaozhu Liu, Zhi Bai, Zhongjun Li
Objective: Vaginal birth after cesarean section (VBAC) is recommended by obstetrical guidelines or expert consensuses. However, no valid tools can exactly predict who can have a vaginal birth among eligible candidates with one prior cesarean section. In recent years, machine learning (ML) is gradually used to develop predictive models in obstetrics and midwifery owing to its excellent performance. This study aimed to develop an explainable ML model to predict the chance of successful VBAC.
Methods: A total of 2438 pregnant women with trial of labor after cesarean (TOLAC) were analyzed from two tertiary hospitals in Guangdong province of China in the final cohort. The data were collected to establish seven predicting models. Training and internal validation data were collected from the First Dongguan Affiliated Hospital of Guangdong Medical University from January 2012 to December 2022. External validation data were collected from Shenzhen Longhua District Central Hospital from January 2011 to December 2017. Seven predicting models based on ML were developed and evaluated by area under the receiver operating characteristic (AUC) curve. The optimal one was picked out from seven models according to its AUC and other indices. The outcome of the predictive model was interpreted by Shapley Additive exPlanations (SHAP).
Results: The categorical boosting (CatBoost) model was selected as the predictive model with the greatest AUC for 0.767 (95% CI: 0.685-0.865), the accuracy for 0.652 (95% CI: 0.602-0.713), sensitivity 0.714 (95% CI: 0.576-0.840), and specificity 0.639 (95% CI: 0.574-0.70). Cervical Bishop score and interpregnancy interval showed the greatest impact on successful vaginal birth, according to SHAP results.
Conclusions: Models based on ML algorithms can be used to predict VBAC. The CatBoost model showed best performance in this study. Based on current evidence-based medical data, clinicians should provide systematic benefit-risk analysis and individualized assessment of VBAC to eligible pregnant women.
{"title":"An explainable machine learning model in predicting vaginal birth after cesarean section.","authors":"Ming Yang, Dajian Long, Yunxiu Li, Xiaozhu Liu, Zhi Bai, Zhongjun Li","doi":"10.1080/14767058.2025.2546544","DOIUrl":"https://doi.org/10.1080/14767058.2025.2546544","url":null,"abstract":"<p><strong>Objective: </strong>Vaginal birth after cesarean section (VBAC) is recommended by obstetrical guidelines or expert consensuses. However, no valid tools can exactly predict who can have a vaginal birth among eligible candidates with one prior cesarean section. In recent years, machine learning (ML) is gradually used to develop predictive models in obstetrics and midwifery owing to its excellent performance. This study aimed to develop an explainable ML model to predict the chance of successful VBAC.</p><p><strong>Methods: </strong>A total of 2438 pregnant women with trial of labor after cesarean (TOLAC) were analyzed from two tertiary hospitals in Guangdong province of China in the final cohort. The data were collected to establish seven predicting models. Training and internal validation data were collected from the First Dongguan Affiliated Hospital of Guangdong Medical University from January 2012 to December 2022. External validation data were collected from Shenzhen Longhua District Central Hospital from January 2011 to December 2017. Seven predicting models based on ML were developed and evaluated by area under the receiver operating characteristic (AUC) curve. The optimal one was picked out from seven models according to its AUC and other indices. The outcome of the predictive model was interpreted by Shapley Additive exPlanations (SHAP).</p><p><strong>Results: </strong>The categorical boosting (CatBoost) model was selected as the predictive model with the greatest AUC for 0.767 (95% CI: 0.685-0.865), the accuracy for 0.652 (95% CI: 0.602-0.713), sensitivity 0.714 (95% CI: 0.576-0.840), and specificity 0.639 (95% CI: 0.574-0.70). Cervical Bishop score and interpregnancy interval showed the greatest impact on successful vaginal birth, according to SHAP results.</p><p><strong>Conclusions: </strong>Models based on ML algorithms can be used to predict VBAC. The CatBoost model showed best performance in this study. Based on current evidence-based medical data, clinicians should provide systematic benefit-risk analysis and individualized assessment of VBAC to eligible pregnant women.</p>","PeriodicalId":50146,"journal":{"name":"Journal of Maternal-Fetal & Neonatal Medicine","volume":"38 1","pages":"2546544"},"PeriodicalIF":1.6,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144976970","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 : 2025-12-01Epub Date: 2025-09-21DOI: 10.1080/14767058.2025.2555477
Bo Ling, Xiao Zhang
Background: Advanced-maternal-age pregnancies carry a heightened risk of pre-eclampsia and fetal growth restriction (FGR), yet current first-trimester screening has limited predictive accuracy. We hypothesized that combining mid-pregnancy placental endocrine biomarkers with a Doppler-based vascular index would improve early identification of women at risk for these complications.
Methods: In a prospective cohort at Zibo Central Hospital (January 2022-June 2024), 420 singleton pregnancies in women ≥35 years (first antenatal visit <14 weeks) underwent serum assays for human chorionic gonadotrophin (hCG), pregnancy-associated plasma protein A (PAPP-A) and the soluble fms-like tyrosine kinase-1/placental growth factor ratio (sFlt-1/PlGF), plus transabdominal Doppler measurement of mean uterine-artery pulsatility index (UtA-PI) at 20-24 weeks. Sequential logistic-regression models-baseline clinical, + vascular (UtA-PI), + endocrine (biomarkers), and an integrated model-were internally validated with 1,000-bootstrap resampling; discrimination (AUC), calibration, net reclassification improvement (NRI) and decision-curve net benefit were assessed. The composite adverse pregnancy outcome (APO) was pre-eclampsia and/or SGA (defined post‑natally by INTERGROWTH‑21st birth‑weight standards).
Results: Eighty-three women (19.8%) developed the APO: 45 PE cases (10.7 %), 51 SGA cases (12.1%; 38 < 3rd centile, 13 3rd-< 10th centile + abnormal Doppler), including 13 concurrent PE +SGA. Compared with unaffected pregnancies, cases showed higher median hCG, lower PAPP-A, higher sFlt-1/PlGF ratio and elevated UtA-PI. Model AUC rose from 0.62 (baseline) to 0.70 (+vascular), 0.78 (+endocrine) and 0.80 (95% CI: 0.75-0.85) for the integrated model, with good calibration and NRI + 0.18. Decision-curve analysis showed the integrated model yielded the greatest net benefit across 5-25% risk thresholds; at a 10% threshold it correctly flagged nine additional high-risk pregnancies and avoided five unnecessary interventions per 100 women screened. Performance remained strong in women ≥40 years (AUC 0.78) and nulliparas (AUC 0.82).
Conclusion: Simultaneous mid-pregnancy assessment of endocrine (hCG, PAPP-A, sFlt-1/PlGF) and vascular (UtA-PI) placental function markedly improves prediction of pre-eclampsia and SGA in women of advanced maternal age, outperforming clinical or single-domain models and demonstrating practical decision-curve gains; integrating this dual-domain profile into routine prenatal care could facilitate targeted surveillance and prophylactic strategies to mitigate adverse outcomes.
背景:高龄妊娠具有较高的先兆子痫和胎儿生长受限(FGR)风险,但目前的妊娠早期筛查预测准确性有限。我们假设,将妊娠中期胎盘内分泌生物标志物与基于多普勒的血管指数相结合,可以提高对这些并发症风险女性的早期识别。方法:对淄博市中心医院(2022年1月- 2024年6月)的420例≥35岁的单胎妊娠(首次产前检查)进行前瞻性队列研究。结果:83例(19.8%)发生APO: PE 45例(10.7 %),SGA 51例(12.1%);38 结论:妊娠中期同时评估内分泌(hCG, PAPP-A, sFlt-1/PlGF)和血管(UtA-PI)胎盘功能可显著提高高龄产妇先兆子痫和SGA的预测,优于临床或单域模型,并显示出实用的决策曲线收益;将这种双域概况纳入常规产前护理可以促进有针对性的监测和预防策略,以减轻不良后果。
{"title":"Assessing placental endocrine and vascular function for prenatal prediction of adverse pregnancy outcomes in advanced‑maternal‑age pregnancies.","authors":"Bo Ling, Xiao Zhang","doi":"10.1080/14767058.2025.2555477","DOIUrl":"https://doi.org/10.1080/14767058.2025.2555477","url":null,"abstract":"<p><strong>Background: </strong>Advanced-maternal-age pregnancies carry a heightened risk of pre-eclampsia and fetal growth restriction (FGR), yet current first-trimester screening has limited predictive accuracy. We hypothesized that combining mid-pregnancy placental endocrine biomarkers with a Doppler-based vascular index would improve early identification of women at risk for these complications.</p><p><strong>Methods: </strong>In a prospective cohort at Zibo Central Hospital (January 2022-June 2024), 420 singleton pregnancies in women ≥35 years (first antenatal visit <14 weeks) underwent serum assays for human chorionic gonadotrophin (hCG), pregnancy-associated plasma protein A (PAPP-A) and the soluble fms-like tyrosine kinase-1/placental growth factor ratio (sFlt-1/PlGF), plus transabdominal Doppler measurement of mean uterine-artery pulsatility index (UtA-PI) at 20-24 weeks. Sequential logistic-regression models-baseline clinical, + vascular (UtA-PI), + endocrine (biomarkers), and an integrated model-were internally validated with 1,000-bootstrap resampling; discrimination (AUC), calibration, net reclassification improvement (NRI) and decision-curve net benefit were assessed. The composite adverse pregnancy outcome (APO) was pre-eclampsia and/or SGA (defined post‑natally by INTERGROWTH‑21st birth‑weight standards).</p><p><strong>Results: </strong>Eighty-three women (19.8%) developed the APO: 45 PE cases (10.7 %), 51 SGA cases (12.1%; 38 < 3rd centile, 13 3rd-< 10th centile + abnormal Doppler), including 13 concurrent PE +SGA. Compared with unaffected pregnancies, cases showed higher median hCG, lower PAPP-A, higher sFlt-1/PlGF ratio and elevated UtA-PI. Model AUC rose from 0.62 (baseline) to 0.70 (+vascular), 0.78 (+endocrine) and 0.80 (95% CI: 0.75-0.85) for the integrated model, with good calibration and NRI + 0.18. Decision-curve analysis showed the integrated model yielded the greatest net benefit across 5-25% risk thresholds; at a 10% threshold it correctly flagged nine additional high-risk pregnancies and avoided five unnecessary interventions per 100 women screened. Performance remained strong in women ≥40 years (AUC 0.78) and nulliparas (AUC 0.82).</p><p><strong>Conclusion: </strong>Simultaneous mid-pregnancy assessment of endocrine (hCG, PAPP-A, sFlt-1/PlGF) and vascular (UtA-PI) placental function markedly improves prediction of pre-eclampsia and SGA in women of advanced maternal age, outperforming clinical or single-domain models and demonstrating practical decision-curve gains; integrating this dual-domain profile into routine prenatal care could facilitate targeted surveillance and prophylactic strategies to mitigate adverse outcomes.</p>","PeriodicalId":50146,"journal":{"name":"Journal of Maternal-Fetal & Neonatal Medicine","volume":"38 1","pages":"2555477"},"PeriodicalIF":1.6,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145114651","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}
Objective: Fetal growth restriction (FGR) is a serious pathological complication associated with perinatal death and adverse pregnancy outcomes, which is largely related to placental dysfunction. This study aimed to identify FGR-related placenta transcriptomic features and provide insight into the pathologic mechanisms of FGR.
Methods: In this research, transcriptomic data were obtained by RNA sequencing on placenta samples from eight FGR patients and eight normal term-pregnant women. Differential expression analysis was used to identify the differentially expressed genes (DEGs) between groups, then function and pathway enrichment analysis by DEGs was performed. After correlation analysis between DEGs and clinical indicators of FGR, validation of DEGs by Gene Expression Omnibus (GEO) dataset was carried out. Receiver operating characteristic (ROC) analysis was used to calculate the diagnostic ability of DEG biomarkers.
Results: We identified seven candidate DEGs. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis revealed candidate DEGs primarily involved in chemokine activities and lymphocyte chemotaxis. Correlation analysis found that the expression level of DPPA4 and CTAG2 gene were significantly positively correlated with neonatal birth weight (p < 0.05). The expression level of IGSF21 was significantly negatively correlated with placenta weight, neonatal birth weight and neonatal birth weight percentile (p < 0.05). The expression level of CXCL11 showed a negative correlation with neonatal birth weight and neonatal birth weight percentile (p < 0.05). Additionally, the expression level of CXCL10 exhibited a negative correlation to neonatal birth weight percentile (p < 0.05). The expression level of HLA-DQA1, CXCL10 and CXCL11 in the GEO dataset were in good agreement with our results. We conducted the ROC analysis and found the area under the curve (AUC) values based on each DEG alone were 80% for HLA-DQA1, 79%f or CXCL11 and 76% for CXCL10, suggesting that the above three DEGs had potential significance for FGR diagnosis.
Conclusion: This study gives an insight into transcriptional features in FGR mechanism and discovers novel genes that may provide evidence for predicting and managing FGR.
{"title":"Placental transcriptomic profiling showed disturbance of chemokine activities and lymphocyte chemotaxis in pregnancy with fetal growth restriction.","authors":"Xiaohui Li, Xin He, Jiamei Tong, Yanan Hu, Zhengpeng Li, Yi Chen","doi":"10.1080/14767058.2025.2567473","DOIUrl":"https://doi.org/10.1080/14767058.2025.2567473","url":null,"abstract":"<p><strong>Objective: </strong>Fetal growth restriction (FGR) is a serious pathological complication associated with perinatal death and adverse pregnancy outcomes, which is largely related to placental dysfunction. This study aimed to identify FGR-related placenta transcriptomic features and provide insight into the pathologic mechanisms of FGR.</p><p><strong>Methods: </strong>In this research, transcriptomic data were obtained by RNA sequencing on placenta samples from eight FGR patients and eight normal term-pregnant women. Differential expression analysis was used to identify the differentially expressed genes (DEGs) between groups, then function and pathway enrichment analysis by DEGs was performed. After correlation analysis between DEGs and clinical indicators of FGR, validation of DEGs by Gene Expression Omnibus (GEO) dataset was carried out. Receiver operating characteristic (ROC) analysis was used to calculate the diagnostic ability of DEG biomarkers.</p><p><strong>Results: </strong>We identified seven candidate DEGs. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis revealed candidate DEGs primarily involved in chemokine activities and lymphocyte chemotaxis. Correlation analysis found that the expression level of <i>DPPA4</i> and <i>CTAG2</i> gene were significantly positively correlated with neonatal birth weight (<i>p</i> < 0.05). The expression level of <i>IGSF21</i> was significantly negatively correlated with placenta weight, neonatal birth weight and neonatal birth weight percentile (<i>p</i> < 0.05). The expression level of <i>CXCL11</i> showed a negative correlation with neonatal birth weight and neonatal birth weight percentile (<i>p</i> < 0.05). Additionally, the expression level of <i>CXCL10</i> exhibited a negative correlation to neonatal birth weight percentile (<i>p</i> < 0.05). The expression level of <i>HLA-DQA1</i>, <i>CXCL10</i> and <i>CXCL11</i> in the GEO dataset were in good agreement with our results. We conducted the ROC analysis and found the area under the curve (AUC) values based on each DEG alone were 80% for <i>HLA-DQA1</i>, 79%f or <i>CXCL11</i> and 76% for <i>CXCL10</i>, suggesting that the above three DEGs had potential significance for FGR diagnosis.</p><p><strong>Conclusion: </strong>This study gives an insight into transcriptional features in FGR mechanism and discovers novel genes that may provide evidence for predicting and managing FGR.</p>","PeriodicalId":50146,"journal":{"name":"Journal of Maternal-Fetal & Neonatal Medicine","volume":"38 1","pages":"2567473"},"PeriodicalIF":1.6,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145294262","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 : 2025-12-01Epub Date: 2025-12-03DOI: 10.1080/14767058.2025.2592375
Isaura Molina Stornelli, Nikolay Bliznyuk, Juan Carlos Roig, Josef Neu, Katherine Kisilewicz, Dhanashree Rajderkar, Livia Sura, Sujal Patel, Daniel Chong, Siena Vadakal, Taylor Edwards, Michael D Weiss
Background: Therapeutic hypothermia (TH) is standard of care for neonates ≥36 weeks with hypoxic-ischemic encephalopathy (HIE). Although intravenous fluid restriction is common, optimal strategies for parenteral and enteral nutrition remain unclear. This study evaluated the tolerance of parenteral nutrition (PN) and enteral feeding in neonates undergoing TH, as well as the impact of these interventions on clinical outcomes.
Methods: We retrospectively reviewed charts from the Florida Neonatal Neurologic Network (FN3) of neonates who underwent TH for HIE between 2012 and 2020. Collected data included demographics, neurologic assessments, nutritional strategies, laboratory values, and MRI findings. Statistical analysis was performed using one-way ANOVA, with results expressed as Kruskal-Wallis p-values.
Results: Of 170 neonates, 163 met inclusion criteria. Participants were categorized by nutritional approach: intravenous fluids (IVF), PN, or both. Neonates receiving PN had significantly higher blood urea nitrogen (BUN) during TH (p < 0.05), although values remained within acceptable limits. Lipid tolerance did not differ between groups. PN administration was associated with improved glucose regulation at 12 h (p < 0.05). Enteral feeding correlated with reduced brain injury on MRI and improved neurodevelopmental outcomes, including cognitive (p < 0.05) and motor (p < 0.05) function. Neonates receiving both PN and enteral feeding demonstrated significant recovery from malnutrition by the first outpatient follow-up (p < 0.05) and achieved full enteral feeds sooner (p < 0.05).
Conclusions: Early nutritional support, including PN and enteral feeding, appears to be well-tolerated in neonates undergoing TH for HIE. These findings suggest that providing early nutrition may enhance neurodevelopmental outcomes and promote growth during TH.
{"title":"Nutrition in infants with hypoxic-ischemic encephalopathy: insights from a single-center experience on parenteral and enteral feeding during therapeutic hypothermia.","authors":"Isaura Molina Stornelli, Nikolay Bliznyuk, Juan Carlos Roig, Josef Neu, Katherine Kisilewicz, Dhanashree Rajderkar, Livia Sura, Sujal Patel, Daniel Chong, Siena Vadakal, Taylor Edwards, Michael D Weiss","doi":"10.1080/14767058.2025.2592375","DOIUrl":"https://doi.org/10.1080/14767058.2025.2592375","url":null,"abstract":"<p><strong>Background: </strong>Therapeutic hypothermia (TH) is standard of care for neonates ≥36 weeks with hypoxic-ischemic encephalopathy (HIE). Although intravenous fluid restriction is common, optimal strategies for parenteral and enteral nutrition remain unclear. This study evaluated the tolerance of parenteral nutrition (PN) and enteral feeding in neonates undergoing TH, as well as the impact of these interventions on clinical outcomes.</p><p><strong>Methods: </strong>We retrospectively reviewed charts from the Florida Neonatal Neurologic Network (FN3) of neonates who underwent TH for HIE between 2012 and 2020. Collected data included demographics, neurologic assessments, nutritional strategies, laboratory values, and MRI findings. Statistical analysis was performed using one-way ANOVA, with results expressed as Kruskal-Wallis p-values.</p><p><strong>Results: </strong>Of 170 neonates, 163 met inclusion criteria. Participants were categorized by nutritional approach: intravenous fluids (IVF), PN, or both. Neonates receiving PN had significantly higher blood urea nitrogen (BUN) during TH (<i>p</i> < 0.05), although values remained within acceptable limits. Lipid tolerance did not differ between groups. PN administration was associated with improved glucose regulation at 12 h (<i>p</i> < 0.05). Enteral feeding correlated with reduced brain injury on MRI and improved neurodevelopmental outcomes, including cognitive (<i>p</i> < 0.05) and motor (<i>p</i> < 0.05) function. Neonates receiving both PN and enteral feeding demonstrated significant recovery from malnutrition by the first outpatient follow-up (<i>p</i> < 0.05) and achieved full enteral feeds sooner (<i>p</i> < 0.05).</p><p><strong>Conclusions: </strong>Early nutritional support, including PN and enteral feeding, appears to be well-tolerated in neonates undergoing TH for HIE. These findings suggest that providing early nutrition may enhance neurodevelopmental outcomes and promote growth during TH.</p>","PeriodicalId":50146,"journal":{"name":"Journal of Maternal-Fetal & Neonatal Medicine","volume":"38 1","pages":"2592375"},"PeriodicalIF":1.6,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145670785","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 : 2025-12-01Epub Date: 2025-11-02DOI: 10.1080/14767058.2025.2578576
Bridget Galati, Heather Jacobsen, Melissa Kraus, Melissa Mills, Brittaney Vaughn, Sam Williams, Michael Wenzinger, Cynthia Rogers, Nandini Raghuraman, Jeannie Kelly
<p><strong>Objective: </strong>The late postpartum period, defined as greater than 6 weeks to 12 months, is a high-risk time for individuals with opioid use disorder (OUD). Discontinuation rates of buprenorphine treatment for OUD during this period are high. Little is known about patients' subjective experience with buprenorphine treatment during this time. We sought to assess patient treatment experience, goals, facilitators and barriers to continued buprenorphine treatment throughout the extended postpartum period.</p><p><strong>Methods: </strong>We performed a cross-sectional survey of postpartum patients who received buprenorphine treatment, including sublingual and long-acting injectable formulations, in an interdisciplinary, wrap-around clinic for maternal OUD between February 2022 through May 2023. Individuals participated in a brief electronic questionnaire comprised of multiple choice, Likert scale and open-ended questions adapted from validated surveys. Individuals were recruited to participate at each of three separate time points postpartum; <6 weeks, ≥6 weeks to 3 months, and >3 months. Descriptive statistics, Fisher exact, the Cochran-Armitage trend and chi-squared tests were used to describe survey results.</p><p><strong>Results: </strong>Fifty individuals were approached to participate in the survey, of which 25 unique postpartum individuals participated. This captured a total of 37 responses amongst all three time points. At the time of final survey completion, the average individual was 10.68 months (SD ± 7.13) postpartum. 76% self-identified as white and 24% Black or African American. The majority (88%) were prescribed sublingual buprenorphine. Most (84%) had been prescribed buprenorphine for more than three months at the time of initial survey completion. The majority (89%) of responses across all time points reported being very satisfied or satisfied with their current treatment, being satisfied with the effectiveness of their buprenorphine in reducing opioid use (98%) and with the effectiveness at reducing other substance use (54%). Top motivators for continuing treatment included individual health, ability to care for child(ren), and social support of friends or family. No differences were detected across time points. Surprisingly, the most often reported treatment goal was to discontinue buprenorphine eventually (49% of all responses). Most strongly agreed or agreed with the following statements about social supports, including that they know they take buprenorphine (100%), support their decision to take buprenorphine (89%), believe it is treatment for OUD (78%), and want them to continue treatment (78%). However, fewer (41%) strongly agreed or agreed with the following statement: the people I am close to want me to continue buprenorphine treatment long term (i.e. several years). Less than half (46%) agreed with the statement, the people I am close to know what it takes to stay sober. Barriers to buprenorphine treatment we
{"title":"Buprenorphine treatment during the extended postpartum period: a survey of patient experiences.","authors":"Bridget Galati, Heather Jacobsen, Melissa Kraus, Melissa Mills, Brittaney Vaughn, Sam Williams, Michael Wenzinger, Cynthia Rogers, Nandini Raghuraman, Jeannie Kelly","doi":"10.1080/14767058.2025.2578576","DOIUrl":"https://doi.org/10.1080/14767058.2025.2578576","url":null,"abstract":"<p><strong>Objective: </strong>The late postpartum period, defined as greater than 6 weeks to 12 months, is a high-risk time for individuals with opioid use disorder (OUD). Discontinuation rates of buprenorphine treatment for OUD during this period are high. Little is known about patients' subjective experience with buprenorphine treatment during this time. We sought to assess patient treatment experience, goals, facilitators and barriers to continued buprenorphine treatment throughout the extended postpartum period.</p><p><strong>Methods: </strong>We performed a cross-sectional survey of postpartum patients who received buprenorphine treatment, including sublingual and long-acting injectable formulations, in an interdisciplinary, wrap-around clinic for maternal OUD between February 2022 through May 2023. Individuals participated in a brief electronic questionnaire comprised of multiple choice, Likert scale and open-ended questions adapted from validated surveys. Individuals were recruited to participate at each of three separate time points postpartum; <6 weeks, ≥6 weeks to 3 months, and >3 months. Descriptive statistics, Fisher exact, the Cochran-Armitage trend and chi-squared tests were used to describe survey results.</p><p><strong>Results: </strong>Fifty individuals were approached to participate in the survey, of which 25 unique postpartum individuals participated. This captured a total of 37 responses amongst all three time points. At the time of final survey completion, the average individual was 10.68 months (SD ± 7.13) postpartum. 76% self-identified as white and 24% Black or African American. The majority (88%) were prescribed sublingual buprenorphine. Most (84%) had been prescribed buprenorphine for more than three months at the time of initial survey completion. The majority (89%) of responses across all time points reported being very satisfied or satisfied with their current treatment, being satisfied with the effectiveness of their buprenorphine in reducing opioid use (98%) and with the effectiveness at reducing other substance use (54%). Top motivators for continuing treatment included individual health, ability to care for child(ren), and social support of friends or family. No differences were detected across time points. Surprisingly, the most often reported treatment goal was to discontinue buprenorphine eventually (49% of all responses). Most strongly agreed or agreed with the following statements about social supports, including that they know they take buprenorphine (100%), support their decision to take buprenorphine (89%), believe it is treatment for OUD (78%), and want them to continue treatment (78%). However, fewer (41%) strongly agreed or agreed with the following statement: the people I am close to want me to continue buprenorphine treatment long term (i.e. several years). Less than half (46%) agreed with the statement, the people I am close to know what it takes to stay sober. Barriers to buprenorphine treatment we","PeriodicalId":50146,"journal":{"name":"Journal of Maternal-Fetal & Neonatal Medicine","volume":"38 1","pages":"2578576"},"PeriodicalIF":1.6,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145432903","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}
Background: Postpartum psychiatric disorders (PPDs) have been deemed as a significant public health concern, affecting both maternal health and family dynamics. This study aimed to examine the current status of PPDs, identify the potential risk factors of PPDs, and further develop a clinical nomogram model for predicting PPDs in Chinese women.
Method: In this retrospective cohort study, 1418 postpartum women attending the routine postpartum examination at the 42nd day after delivery in Jiangsu Women and Children Health Hospital were recruited as participants from December 2020 to December 2022. The Symptom Checklist-90 (SCL-90) was utilized to assess the status of postpartum psychiatric disorders. A prediction model was constructed by multivariate logistic regression and presented as a nomogram. The performance of nomogram was measured by the receiver operating characteristic (ROC) curve, calibration curve, and decision curve analysis (DCA). The relationships between predictive factors of PPDs and SCL-90 were also evaluated using Pearson correlation analysis. The relationships between predictive factors of PPDs and SCL-90 were evaluated using Pearson correlation analysis.
Results: With the SCL-90 cutoff value of 160, the incidence of postpartum psychiatric disorders was 9.17% among Chinese urban women. The univariate and multivariate logistic regression analyses indicated that age ≤ 25 years old (OR = 10.07, 95%CI = 1.83-55.33), prenatal mood disorder (OR = 4.12, 95%CI = 1.99-8.53), invasive prenatal diagnostic procedures (OR = 4.39, 95%CI = 1.16-16.56), poor relationship with husband (OR = 2.86, 95%CI = 1.58-5.16) and poor relationship with mother-in-law (OR = 5.10, 95%CI = 2.70-9.64) were significantly associated with PPDs. A nomogram prediction model for PPDs was further constructed based on these five independent risk factors, and the area under the receiver operating characteristic curve (AUC) of the nomogram model was 0.823 (95% CI = 0.781-0.865). The calibration curves showed remarkable accuracy of the nomogram and the DCA exhibited high clinical net benefit of the nomogram. Besides, we also explored the relationships between the five risk factors and different symptom dimensions of PPDs and found that the five risk factors were almost associated with increased levels of all symptom dimensions.
Conclusions: Five psychosocial risk factors for PPDs were identified in Chinese women and the nomogram prediction model constructed based on these five risk factors could predict the risk of PPDs intuitively and individually. Systematic screening these risk factors and further conducting psychosocial interventions earlier during the pregnancy period are crucial to prevent PPDs. For future research, we intend to incorporate additional risk factors, including blood biomarkers and facial expression indicators, to refine our risk model.
{"title":"Risk factors and prediction model for postpartum psychiatric disorders: a retrospective cohort study of 1418 Chinese women from 2020 to 2022.","authors":"Wenxi Chen, Huan Ge, Jing Cong, Wenjie Zhou, Xiaoxia Chang, Xiaojie Quan, Jing Xia, Xincheng Tao, Danhua Pu, Jie Wu","doi":"10.1080/14767058.2024.2438756","DOIUrl":"10.1080/14767058.2024.2438756","url":null,"abstract":"<p><strong>Background: </strong>Postpartum psychiatric disorders (PPDs) have been deemed as a significant public health concern, affecting both maternal health and family dynamics. This study aimed to examine the current status of PPDs, identify the potential risk factors of PPDs, and further develop a clinical nomogram model for predicting PPDs in Chinese women.</p><p><strong>Method: </strong>In this retrospective cohort study, 1418 postpartum women attending the routine postpartum examination at the 42nd day after delivery in Jiangsu Women and Children Health Hospital were recruited as participants from December 2020 to December 2022. The Symptom Checklist-90 (SCL-90) was utilized to assess the status of postpartum psychiatric disorders. A prediction model was constructed by multivariate logistic regression and presented as a nomogram. The performance of nomogram was measured by the receiver operating characteristic (ROC) curve, calibration curve, and decision curve analysis (DCA). The relationships between predictive factors of PPDs and SCL-90 were also evaluated using Pearson correlation analysis. The relationships between predictive factors of PPDs and SCL-90 were evaluated using Pearson correlation analysis.</p><p><strong>Results: </strong>With the SCL-90 cutoff value of 160, the incidence of postpartum psychiatric disorders was 9.17% among Chinese urban women. The univariate and multivariate logistic regression analyses indicated that age ≤ 25 years old (OR = 10.07, 95%CI = 1.83-55.33), prenatal mood disorder (OR = 4.12, 95%CI = 1.99-8.53), invasive prenatal diagnostic procedures (OR = 4.39, 95%CI = 1.16-16.56), poor relationship with husband (OR = 2.86, 95%CI = 1.58-5.16) and poor relationship with mother-in-law (OR = 5.10, 95%CI = 2.70-9.64) were significantly associated with PPDs. A nomogram prediction model for PPDs was further constructed based on these five independent risk factors, and the area under the receiver operating characteristic curve (AUC) of the nomogram model was 0.823 (95% CI = 0.781-0.865). The calibration curves showed remarkable accuracy of the nomogram and the DCA exhibited high clinical net benefit of the nomogram. Besides, we also explored the relationships between the five risk factors and different symptom dimensions of PPDs and found that the five risk factors were almost associated with increased levels of all symptom dimensions.</p><p><strong>Conclusions: </strong>Five psychosocial risk factors for PPDs were identified in Chinese women and the nomogram prediction model constructed based on these five risk factors could predict the risk of PPDs intuitively and individually. Systematic screening these risk factors and further conducting psychosocial interventions earlier during the pregnancy period are crucial to prevent PPDs. For future research, we intend to incorporate additional risk factors, including blood biomarkers and facial expression indicators, to refine our risk model.</p>","PeriodicalId":50146,"journal":{"name":"Journal of Maternal-Fetal & Neonatal Medicine","volume":"38 1","pages":"2438756"},"PeriodicalIF":1.7,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142819873","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 : 2025-12-01Epub Date: 2024-12-10DOI: 10.1080/14767058.2025.2440150
{"title":"Statement of Retraction: A sandwich technique (N&H variation technique) to reduce blood loss during cesarean delivery for complete placenta previa: a randomized controlled trial.","authors":"","doi":"10.1080/14767058.2025.2440150","DOIUrl":"https://doi.org/10.1080/14767058.2025.2440150","url":null,"abstract":"","PeriodicalId":50146,"journal":{"name":"Journal of Maternal-Fetal & Neonatal Medicine","volume":"38 1","pages":"2440150"},"PeriodicalIF":1.7,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142808470","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}