Pub Date : 2026-02-01Epub Date: 2025-05-19DOI: 10.1055/a-2615-5098
Alexandra D Forrest, Debra Eluobaju, Amanda Finney, Laura Prichett, Nicole R Gavin, Christopher Novak, Kristin Martin, Arthur Jason Vaught
Although cesarean hysterectomy (C-HYST) is standard management for placenta accreta spectrum (PAS), the type of hysterectomy performed, total abdominal (TAH), or supracervical (SCH), is left to surgeon discretion. TAH has been previously associated with higher estimated blood loss (EBL), transfusion requirements, and complications compared to SCH.This was a single-site retrospective cohort study examining outcomes of TAH compared to SCH for PAS performed from 2008 to 2023. PAS was confirmed by clinical and pathologic diagnoses. Cervical removal was confirmed by operative report, postoperative exam, and pathology. Associations were assessed using chi-square tests, Fisher's exact tests, Mann-Whitney U tests, or individual t-tests.During the study period, 90 TAH and 54 SCH were performed. There were no significant differences in patient demographics, except that planned C-HYST was more likely to be TAH. TAH was associated with significantly lower transfusion requirements. When unexpected hysterectomies were excluded, there was not a significant difference in blood products transfused between the TAH and SCH groups.In PAS, maternal outcomes after TAH are at least equivalent to SCH. The surgical approach for the management of PAS should be further explored. · In PAS, outcomes are at least equivalent between TAH and SCH.. · C-HYST is optimally performed in a planned manner with all multidisciplinary team members present.. · Vertical skin incision was significantly associated with TAH in this retrospective cohort study..
{"title":"Outcomes of Total Abdominal Hysterectomy Compared to Supracervical Hysterectomy for Management of Placenta Accreta Spectrum.","authors":"Alexandra D Forrest, Debra Eluobaju, Amanda Finney, Laura Prichett, Nicole R Gavin, Christopher Novak, Kristin Martin, Arthur Jason Vaught","doi":"10.1055/a-2615-5098","DOIUrl":"10.1055/a-2615-5098","url":null,"abstract":"<p><p>Although cesarean hysterectomy (C-HYST) is standard management for placenta accreta spectrum (PAS), the type of hysterectomy performed, total abdominal (TAH), or supracervical (SCH), is left to surgeon discretion. TAH has been previously associated with higher estimated blood loss (EBL), transfusion requirements, and complications compared to SCH.This was a single-site retrospective cohort study examining outcomes of TAH compared to SCH for PAS performed from 2008 to 2023. PAS was confirmed by clinical and pathologic diagnoses. Cervical removal was confirmed by operative report, postoperative exam, and pathology. Associations were assessed using chi-square tests, Fisher's exact tests, Mann-Whitney U tests, or individual <i>t</i>-tests.During the study period, 90 TAH and 54 SCH were performed. There were no significant differences in patient demographics, except that planned C-HYST was more likely to be TAH. TAH was associated with significantly lower transfusion requirements. When unexpected hysterectomies were excluded, there was not a significant difference in blood products transfused between the TAH and SCH groups.In PAS, maternal outcomes after TAH are at least equivalent to SCH. The surgical approach for the management of PAS should be further explored. · In PAS, outcomes are at least equivalent between TAH and SCH.. · C-HYST is optimally performed in a planned manner with all multidisciplinary team members present.. · Vertical skin incision was significantly associated with TAH in this retrospective cohort study..</p>","PeriodicalId":7584,"journal":{"name":"American journal of perinatology","volume":" ","pages":"333-337"},"PeriodicalIF":1.2,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144101181","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 : 2026-02-01Epub Date: 2025-05-27DOI: 10.1055/a-2622-2743
Nadine Sunji, Alyssa M Hernandez, Rachel Schmidt, Amy Y Pan, Nina Ayala, Margaret H Bublitz, Anna Palatnik
To estimate the association between maternal body mass index (BMI) at delivery, time from skin incision to infant delivery, and umbilical artery (UA) pH < 7.0.This was a secondary analysis of the Assessment of Perinatal Excellence, a multicenter observational study of an obstetrical cohort of individuals who delivered between 2008 and 2011 in the United States. This analysis included women who delivered via cesarean with known BMI at delivery, skin incision-to-delivery time, and UA pH. Multivariable linear regression assessed the association between BMI and time from skin incision to infant delivery while multivariable logistic regression estimated the associations of BMI and time from skin incision to delivery with UA pH < 7.0. An interaction between BMI and skin incision-to-delivery time was evaluated to examine their combined effect on UA pH < 7.0.A total of 16,723 women were included across five BMI groups. Increasing BMI was associated with longer time intervals from skin incision to delivery and higher rates of UA pH < 7.0. After controlling for potentially confounding factors, all BMI groups ≥25 kg/m2 were associated with longer time intervals from skin incision to delivery. Specifically, BMI groups of 40 to 49.9 and ≥50 kg/m2 had skin incision-to-delivery times that were 1.30 (95% confidence interval [CI]: 1.23-1.36) and 1.44 (95% CI: 1.34-1.55) times longer, respectively, compared with BMI < 25 kg/m2. In the multivariable logistic regression, BMI group ≥50 kg/m2 remained associated with higher odds of UA pH < 7.0. There was a significant interaction between BMI and time from skin incision to delivery regarding the risk of UA pH < 7.0 (p for the interaction term = 0.003).Maternal BMI ≥ 50 kg/m2 was associated with a longer time from skin incision to infant delivery and higher odds of UA pH < 7.0. BMI differentially impacted UA pH at different skin incision-to-delivery time intervals. · Maternal BMI ≥ 25 kg/m2 was associated with longer skin incision-to-delivery times.. · Maternal BMI ≥ 50 kg/m2 was associated with higher odds of UA pH < 7.0.. · The effect of maternal BMI on UA pH varied at different skin incision-to-delivery time intervals.. · Reducing skin incision-to-delivery time may mitigate the risk of UA pH <7.0 in women with BMI ≥50.
目的:评估分娩时产妇体重指数(BMI)、从皮肤切开到婴儿分娩的时间和脐带动脉(UA) pH值之间的关系研究设计:这是对围产期优生评估的二次分析,这是一项多中心观察性研究,研究对象是美国2008年至2011年间分娩的产科队列。该分析纳入了已知分娩时BMI、皮肤切口至分娩时间和UA pH的剖宫产妇女。多变量线性回归评估BMI与从皮肤切口至婴儿分娩时间之间的关系,而多变量logistic回归评估BMI和皮肤切口至分娩时间与UA pH之间的关系。结果:五个BMI组共纳入16,723名妇女。体重指数的增加与皮肤切口到分娩的时间间隔较长有关,较高的UA pH 2率与皮肤切口到分娩的时间间隔较长有关。具体来说,BMI为40-49.9 kg/m2和≥50 kg/m2组的皮肤切口到分娩时间分别是BMI 2组的1.30倍(95% CI 1.23-1.36)和1.44倍(95% CI 1.34-1.55)。在多变量logistic回归中,BMI≥50 kg/m2组仍与较高的UA pH几率相关。结论:母亲BMI≥50 kg/m2与较长的皮肤切口至婴儿分娩时间和较高的UA pH几率相关
{"title":"Association between Maternal Body Mass Index, Skin Incision-to-Delivery Time, and Umbilical Artery pH in Cesarean Deliveries.","authors":"Nadine Sunji, Alyssa M Hernandez, Rachel Schmidt, Amy Y Pan, Nina Ayala, Margaret H Bublitz, Anna Palatnik","doi":"10.1055/a-2622-2743","DOIUrl":"10.1055/a-2622-2743","url":null,"abstract":"<p><p>To estimate the association between maternal body mass index (BMI) at delivery, time from skin incision to infant delivery, and umbilical artery (UA) pH < 7.0.This was a secondary analysis of the Assessment of Perinatal Excellence, a multicenter observational study of an obstetrical cohort of individuals who delivered between 2008 and 2011 in the United States. This analysis included women who delivered via cesarean with known BMI at delivery, skin incision-to-delivery time, and UA pH. Multivariable linear regression assessed the association between BMI and time from skin incision to infant delivery while multivariable logistic regression estimated the associations of BMI and time from skin incision to delivery with UA pH < 7.0. An interaction between BMI and skin incision-to-delivery time was evaluated to examine their combined effect on UA pH < 7.0.A total of 16,723 women were included across five BMI groups. Increasing BMI was associated with longer time intervals from skin incision to delivery and higher rates of UA pH < 7.0. After controlling for potentially confounding factors, all BMI groups ≥25 kg/m<sup>2</sup> were associated with longer time intervals from skin incision to delivery. Specifically, BMI groups of 40 to 49.9 and ≥50 kg/m<sup>2</sup> had skin incision-to-delivery times that were 1.30 (95% confidence interval [CI]: 1.23-1.36) and 1.44 (95% CI: 1.34-1.55) times longer, respectively, compared with BMI < 25 kg/m<sup>2</sup>. In the multivariable logistic regression, BMI group ≥50 kg/m<sup>2</sup> remained associated with higher odds of UA pH < 7.0. There was a significant interaction between BMI and time from skin incision to delivery regarding the risk of UA pH < 7.0 (<i>p</i> for the interaction term = 0.003).Maternal BMI ≥ 50 kg/m<sup>2</sup> was associated with a longer time from skin incision to infant delivery and higher odds of UA pH < 7.0. BMI differentially impacted UA pH at different skin incision-to-delivery time intervals. · Maternal BMI ≥ 25 kg/m2 was associated with longer skin incision-to-delivery times.. · Maternal BMI ≥ 50 kg/m2 was associated with higher odds of UA pH < 7.0.. · The effect of maternal BMI on UA pH varied at different skin incision-to-delivery time intervals.. · Reducing skin incision-to-delivery time may mitigate the risk of UA pH <7.0 in women with BMI ≥50.</p>","PeriodicalId":7584,"journal":{"name":"American journal of perinatology","volume":" ","pages":"374-382"},"PeriodicalIF":1.2,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144155495","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 : 2026-02-01Epub Date: 2025-06-10DOI: 10.1055/a-2608-0889
Christine Stoops, Sofia I Perazzo, Jennifer A Rumpel, Tahagod Mohamed, Andrew M South, Mona Khattab, Catherine Joseph, Matthew W Harer, Cara L Slagle, Mary Revenis, John Daniel
In a survey conducted within the Children's Hospital Neonatal Consortium (CHNC), the Kidney Focus Group aimed to describe the resource and practice variations among participating level IV neonatal intensive care units.A 24-question survey was developed by neonatologists and pediatric nephrologists who belong to the Kidney Support Therapy (KST) subgroup of the CHNC Kidney Focus Group.The majority (89.5%) of responding centers offered some form of KST, with > 90% centers offered prenatal consultations. The most common KST modality offered were peritoneal dialysis (PD) and continuous renal replacement therapy (CRRT) while on ECMO. Prismaflex was the most common device used for stand-alone CRRT. The most common indication for KST initiation was fluid overload and body weight was indicated as the most common limiting factor with the majority of centers reporting weight limitation ≤ 1.5-2 kg.Advances in technology have made it possible to offer KST to a wider neonatal population than before. However, the availability of such technologies can vary significantly among institutions in addition to diversity of clinical experience and standardized protocols. This survey provides valuable insights into current KST practices across 19 level IV NICUs within the CHNC demonstrating expected practice variations amongst centers that may be dependent on location, center resources, and subspecialty providers, among others. · Considerable practice variation exists in KST among NICUs.. · Majority of NICUs utilize multi-disciplinary involvement, but subspecialties vary widely.. · The most common indication for KST initiation was fluid overload..
{"title":"Current Practice of Kidney Support Therapy in the NICU: Results from a CHNC Survey.","authors":"Christine Stoops, Sofia I Perazzo, Jennifer A Rumpel, Tahagod Mohamed, Andrew M South, Mona Khattab, Catherine Joseph, Matthew W Harer, Cara L Slagle, Mary Revenis, John Daniel","doi":"10.1055/a-2608-0889","DOIUrl":"10.1055/a-2608-0889","url":null,"abstract":"<p><p>In a survey conducted within the Children's Hospital Neonatal Consortium (CHNC), the Kidney Focus Group aimed to describe the resource and practice variations among participating level IV neonatal intensive care units.A 24-question survey was developed by neonatologists and pediatric nephrologists who belong to the Kidney Support Therapy (KST) subgroup of the CHNC Kidney Focus Group.The majority (89.5%) of responding centers offered some form of KST, with > 90% centers offered prenatal consultations. The most common KST modality offered were peritoneal dialysis (PD) and continuous renal replacement therapy (CRRT) while on ECMO. Prismaflex was the most common device used for stand-alone CRRT. The most common indication for KST initiation was fluid overload and body weight was indicated as the most common limiting factor with the majority of centers reporting weight limitation ≤ 1.5-2 kg.Advances in technology have made it possible to offer KST to a wider neonatal population than before. However, the availability of such technologies can vary significantly among institutions in addition to diversity of clinical experience and standardized protocols. This survey provides valuable insights into current KST practices across 19 level IV NICUs within the CHNC demonstrating expected practice variations amongst centers that may be dependent on location, center resources, and subspecialty providers, among others. · Considerable practice variation exists in KST among NICUs.. · Majority of NICUs utilize multi-disciplinary involvement, but subspecialties vary widely.. · The most common indication for KST initiation was fluid overload..</p>","PeriodicalId":7584,"journal":{"name":"American journal of perinatology","volume":" ","pages":"418-421"},"PeriodicalIF":1.2,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144265085","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 : 2026-02-01Epub Date: 2025-06-11DOI: 10.1055/a-2620-7882
Tamara Alexander, Lise DeShea, Leonard W Wilson, William H Beasley, Carol P Dionne, Edgardo Szyld, Birju A Shah
This study aimed to evaluate whether a custom warmer height improves the quality and consistency of chest compressions (CCs) compared with a standard warmer height during simulated neonatal resuscitation.Cross-over study using simulated neonatal resuscitation. A controlled research environment equipped with a 12-camera motion capture system, four in-floor multi-axis force plates, a neonatal manikin, and resuscitation equipment. Biomechanical assessments were recorded every 2 minutes during a 20-minute simulation for each condition. Twenty Neonatal Resuscitation Program (NRP)-trained providers. Each participant performed two 20-minute CC sessions-one with the warmer at the standard 100 cm height and one at a custom height selected by the participant. CC depth, force, and rate; participant back angle, heart rate, and self-reported exertion, were analyzed at 2-minute intervals.Compared with the standard height, the custom height resulted in greater and more consistent CC depth and force while maintaining compression rate. Participants also exhibited a greater back angle, and lower heart rate, and reported reduced exertion under the custom height condition.Allowing NRP-trained providers to adjust warmer heights led to improved CC quality and consistency, suggesting that customizable warmer heights may enhance neonatal resuscitation performance. KEY POINTS: · Custom warmer height chosen by NRP-trained providers resulted in more consistent and greater CC depth and force.. · It also was associated with less provider fatigue, compared with standard height.. · During neonatal resuscitation, frontline healthcare professionals changed.. · Participant heart rate was lower when using the custom versus standard height.. · Our findings support the need for guidelines on adjusting warmer height during neonatal cardiopulmonary resuscitation..
{"title":"Effect of Warmer Height (Standard versus Custom) on Neonatal Chest Compression Performance: A Cross-Over Simulation Study.","authors":"Tamara Alexander, Lise DeShea, Leonard W Wilson, William H Beasley, Carol P Dionne, Edgardo Szyld, Birju A Shah","doi":"10.1055/a-2620-7882","DOIUrl":"10.1055/a-2620-7882","url":null,"abstract":"<p><p>This study aimed to evaluate whether a custom warmer height improves the quality and consistency of chest compressions (CCs) compared with a standard warmer height during simulated neonatal resuscitation.Cross-over study using simulated neonatal resuscitation. A controlled research environment equipped with a 12-camera motion capture system, four in-floor multi-axis force plates, a neonatal manikin, and resuscitation equipment. Biomechanical assessments were recorded every 2 minutes during a 20-minute simulation for each condition. Twenty Neonatal Resuscitation Program (NRP)-trained providers. Each participant performed two 20-minute CC sessions-one with the warmer at the standard 100 cm height and one at a custom height selected by the participant. CC depth, force, and rate; participant back angle, heart rate, and self-reported exertion, were analyzed at 2-minute intervals.Compared with the standard height, the custom height resulted in greater and more consistent CC depth and force while maintaining compression rate. Participants also exhibited a greater back angle, and lower heart rate, and reported reduced exertion under the custom height condition.Allowing NRP-trained providers to adjust warmer heights led to improved CC quality and consistency, suggesting that customizable warmer heights may enhance neonatal resuscitation performance. KEY POINTS: · Custom warmer height chosen by NRP-trained providers resulted in more consistent and greater CC depth and force.. · It also was associated with less provider fatigue, compared with standard height.. · During neonatal resuscitation, frontline healthcare professionals changed.. · Participant heart rate was lower when using the custom versus standard height.. · Our findings support the need for guidelines on adjusting warmer height during neonatal cardiopulmonary resuscitation..</p>","PeriodicalId":7584,"journal":{"name":"American journal of perinatology","volume":" ","pages":"355-361"},"PeriodicalIF":1.2,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144273979","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 : 2026-02-01Epub Date: 2025-05-12DOI: 10.1055/a-2605-7721
Lauren C Sayres, Natalie T Simon, Virginia A Lijewski, Jeanelle Sheeder, Shane A Reeves
The goal of this study is to evaluate whether adjuvant progesterone following cerclage affords a reduction in the rate of preterm delivery.This is a retrospective cohort review of all individuals who underwent transvaginal cerclage placement at a tertiary care academic medical center between 2005 and 2021. The rate of delivery prior to 37 weeks and several secondary maternal and neonatal outcomes were compared between patients with and without progesterone supplementation after cerclage. Multivariable regression, subgroup, and matched pairs analyses were performed in order to account for the formulation of progesterone, indication for cerclage, and other potential confounding variables. The study was powered a priori to detect a difference in our primary outcome.Among 451 patients, there were 163 history-, 135 ultrasound-, and 153 examination-indicated cerclages. Overall, 284 (63%) received adjuvant progesterone. Adjuvant progesterone was associated with an increased rate of preterm delivery before 37 weeks (45 vs. 34%, p = 0.03) with an adjusted odds ratio of 1.78 (95% confidence interval: 1.14 and 2.80) in our multivariable model. The median latency from cerclage placement to delivery was shorter when progesterone was used (119 vs. 139 days, p < 0.001). There was no benefit of adjuvant progesterone when analyzed by formulation of progesterone or indication for cerclage or when analyzing pairs matched based on propensity score matching. There were no differences in secondary outcomes for pregnant patients or their offspring.Adjuvant progesterone does not decrease the preterm delivery rate and may in fact cause harm by decreasing latency from cerclage to delivery. Maternal and neonatal outcomes do not vary with supplemental progesterone after cerclage. Our data do not support a synergistic benefit of cerclage and postcerclage progesterone. · There are currently no guidelines for the use of progesterone after cerclage.. · Adjuvant progesterone does not decrease the preterm birth rate.. · Secondary maternal and neonatal outcomes do not improve with adjuvant progesterone..
目的本研究的目的是评估环扎术后辅助黄体酮是否能降低早产率。本研究是一项回顾性队列研究,纳入了2005年至2021年间在三级医疗学术中心接受阴道环切术的所有患者。37周前的分娩率和几个次要的产妇和新生儿结局比较了环扎术后补充和不补充黄体酮的患者。进行多变量回归、亚组和配对分析,以解释黄体酮的配方、环扎的适应症和其他潜在的混杂变量。这项研究是先验的,以检测我们的主要结果的差异。结果451例患者中,163例有病史,135例有超声,153例有检查指征。总的来说,284例(63%)接受了辅助黄体酮治疗。在我们的多变量模型中,辅助孕酮与37周前早产率增加相关(45% vs . 34%, p=0.03),校正优势比为1.78(95%可信区间1.14,2.80)。当使用黄体酮时,从环扎置入到分娩的中位潜伏期更短(119天vs 139天,p
{"title":"Progesterone Supplementation after Cerclage Does Not Improve the Preterm Birth Rate.","authors":"Lauren C Sayres, Natalie T Simon, Virginia A Lijewski, Jeanelle Sheeder, Shane A Reeves","doi":"10.1055/a-2605-7721","DOIUrl":"10.1055/a-2605-7721","url":null,"abstract":"<p><p>The goal of this study is to evaluate whether adjuvant progesterone following cerclage affords a reduction in the rate of preterm delivery.This is a retrospective cohort review of all individuals who underwent transvaginal cerclage placement at a tertiary care academic medical center between 2005 and 2021. The rate of delivery prior to 37 weeks and several secondary maternal and neonatal outcomes were compared between patients with and without progesterone supplementation after cerclage. Multivariable regression, subgroup, and matched pairs analyses were performed in order to account for the formulation of progesterone, indication for cerclage, and other potential confounding variables. The study was powered a priori to detect a difference in our primary outcome.Among 451 patients, there were 163 history-, 135 ultrasound-, and 153 examination-indicated cerclages. Overall, 284 (63%) received adjuvant progesterone. Adjuvant progesterone was associated with an increased rate of preterm delivery before 37 weeks (45 vs. 34%, <i>p</i> = 0.03) with an adjusted odds ratio of 1.78 (95% confidence interval: 1.14 and 2.80) in our multivariable model. The median latency from cerclage placement to delivery was shorter when progesterone was used (119 vs. 139 days, <i>p</i> < 0.001). There was no benefit of adjuvant progesterone when analyzed by formulation of progesterone or indication for cerclage or when analyzing pairs matched based on propensity score matching. There were no differences in secondary outcomes for pregnant patients or their offspring.Adjuvant progesterone does not decrease the preterm delivery rate and may in fact cause harm by decreasing latency from cerclage to delivery. Maternal and neonatal outcomes do not vary with supplemental progesterone after cerclage. Our data do not support a synergistic benefit of cerclage and postcerclage progesterone. · There are currently no guidelines for the use of progesterone after cerclage.. · Adjuvant progesterone does not decrease the preterm birth rate.. · Secondary maternal and neonatal outcomes do not improve with adjuvant progesterone..</p>","PeriodicalId":7584,"journal":{"name":"American journal of perinatology","volume":" ","pages":"291-299"},"PeriodicalIF":1.2,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143960941","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 : 2026-02-01Epub Date: 2025-07-17DOI: 10.1055/a-2657-6249
Jamie Kim, Marcia Chen, Robert S White
Microplastics have been detected in human placental and neural tissues, raising urgent concerns about their potential effects on maternal and fetal health. Emerging evidence links microplastics to systemic inflammation, neurotoxicity, and endocrine disruption, yet their impact on pregnancy outcomes and fetal development remains poorly understood. Given the placenta's central role in early-life health, perinatal researchers are uniquely positioned to lead investigations into this environmental threat. We call for collaborative, multidisciplinary research to better understand and mitigate the effects of microplastic exposure during pregnancy. · Microplastics can cross the placenta and blood-brain barrier, reaching fetal tissues.. · Microplastics trigger inflammation, oxidative stress, and endocrine disruption in human cells.. · Perinatal research should explore links between microplastics and fetal development risks..
{"title":"Microplastics and the Placenta: A Call to Action for Perinatal Research.","authors":"Jamie Kim, Marcia Chen, Robert S White","doi":"10.1055/a-2657-6249","DOIUrl":"10.1055/a-2657-6249","url":null,"abstract":"<p><p>Microplastics have been detected in human placental and neural tissues, raising urgent concerns about their potential effects on maternal and fetal health. Emerging evidence links microplastics to systemic inflammation, neurotoxicity, and endocrine disruption, yet their impact on pregnancy outcomes and fetal development remains poorly understood. Given the placenta's central role in early-life health, perinatal researchers are uniquely positioned to lead investigations into this environmental threat. We call for collaborative, multidisciplinary research to better understand and mitigate the effects of microplastic exposure during pregnancy. · Microplastics can cross the placenta and blood-brain barrier, reaching fetal tissues.. · Microplastics trigger inflammation, oxidative stress, and endocrine disruption in human cells.. · Perinatal research should explore links between microplastics and fetal development risks..</p>","PeriodicalId":7584,"journal":{"name":"American journal of perinatology","volume":" ","pages":"433-436"},"PeriodicalIF":1.2,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144658141","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 : 2026-02-01Epub Date: 2025-06-24DOI: 10.1055/a-2628-3904
Michelle C Starr, Abigail C Hardy, Paulomi Chaudhry, Cara L Slagle, Stephanie P Gilley, Danielle E Soranno
This study aimed to determine the association between food insecurity (FI) and short-term kidney outcomes in neonates.Single-site prospective cohort study of sequentially admitted neonates to two neonatal intensive care units (NICUs). We collected demographic characteristics and FI status on maternal-neonatal dyads using the Hunger Vital Signs tool. Kidney outcomes (acute kidney injury [AKI]) within the first 14 days, recovery from AKI, and serum creatinine (SCr) at day 14 of age) were compared by FI status.Of the 70 neonates in this study, 39% lived in FI households. Infants from FI households were more likely to have early AKI (56 vs. 14%, p = 0.002) and were more likely to have a slower recovery from AKI (66 vs. 17%, p = 0.035) than those from food-secure households. Neonates from FI households were also more likely to have an abnormally elevated SCr at 2 weeks of age (66 vs. 17%, p = 0.007).FI is common in families with neonates admitted to the NICU. Neonates born into FI households were more likely to have early AKI, slower AKI recovery, and elevated SCr at 2 weeks of age. Our findings emphasize the importance of FI screening and recognition as part of prenatal care and as an essential social determinant of health in studies investigating kidney outcomes. · FI is common in families with neonates admitted to the NICU.. · Neonates born into households with FI were more likely to have early AKI.. · They also had slower AKI recovery and elevated SCr at 2 weeks of age.. · Our findings emphasize the importance of FI screening and recognition as part of prenatal care.. · FI is an essential social determinant of health in studies investigating kidney outcomes..
{"title":"Association of Food Insecurity and Short-Term Kidney Outcomes in Neonates.","authors":"Michelle C Starr, Abigail C Hardy, Paulomi Chaudhry, Cara L Slagle, Stephanie P Gilley, Danielle E Soranno","doi":"10.1055/a-2628-3904","DOIUrl":"10.1055/a-2628-3904","url":null,"abstract":"<p><p>This study aimed to determine the association between food insecurity (FI) and short-term kidney outcomes in neonates.Single-site prospective cohort study of sequentially admitted neonates to two neonatal intensive care units (NICUs). We collected demographic characteristics and FI status on maternal-neonatal dyads using the Hunger Vital Signs tool. Kidney outcomes (acute kidney injury [AKI]) within the first 14 days, recovery from AKI, and serum creatinine (SCr) at day 14 of age) were compared by FI status.Of the 70 neonates in this study, 39% lived in FI households. Infants from FI households were more likely to have early AKI (56 vs. 14%, <i>p</i> = 0.002) and were more likely to have a slower recovery from AKI (66 vs. 17%, <i>p</i> = 0.035) than those from food-secure households. Neonates from FI households were also more likely to have an abnormally elevated SCr at 2 weeks of age (66 vs. 17%, <i>p</i> = 0.007).FI is common in families with neonates admitted to the NICU. Neonates born into FI households were more likely to have early AKI, slower AKI recovery, and elevated SCr at 2 weeks of age. Our findings emphasize the importance of FI screening and recognition as part of prenatal care and as an essential social determinant of health in studies investigating kidney outcomes. · FI is common in families with neonates admitted to the NICU.. · Neonates born into households with FI were more likely to have early AKI.. · They also had slower AKI recovery and elevated SCr at 2 weeks of age.. · Our findings emphasize the importance of FI screening and recognition as part of prenatal care.. · FI is an essential social determinant of health in studies investigating kidney outcomes..</p>","PeriodicalId":7584,"journal":{"name":"American journal of perinatology","volume":" ","pages":"425-429"},"PeriodicalIF":1.2,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12458895/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144482791","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 : 2026-02-01Epub Date: 2025-05-12DOI: 10.1055/a-2605-7786
Alexis C Gimovsky, Silas Monje, Jack Dunn, Jordan Levine
<p><p>Counseling patients who are considering a trial of labor after cesarean (TOLAC) is a challenging task given the risks and benefits of either approach. While calculators exist to give patients an idea of their likelihood of having a successful vaginal birth after cesarean (VBAC), their validity is limited by outdated mathematical methods used to develop them. Most importantly, current VBAC calculators only offer insight into the chance of successful VBAC, without any ability to predict the risk of adverse outcomes relevant to both the patient and neonate. The objective of this study is to develop a prediction model for individualized risks and benefits of a TOLAC using modern mathematical techniques.This was a secondary analysis of the Cesarean Registry database, the same database used in developing the Maternal-Fetal Medicine Units (MFMU) VBAC calculator. The primary outcome was the prediction of the success of VBAC. Secondary outcomes were the prediction of uterine rupture, maternal complications, and neonatal complications. Inclusion criteria were term, singleton gestation, and cephalic presentation pregnancies with one prior low transverse cesarean delivery (CD). Exclusion criteria included intrauterine fetal demise, planned cesarean, and prior myomectomy. Univariate comparisons identified variables that were independently associated with VBAC. An optimal decision tree was used to create a prediction model. A test set was withheld for validation. A risk calculator tool was developed for the prediction of successful VBAC and adverse perinatal outcomes. Adverse maternal outcomes: uterine dehiscence, hysterectomy, postpartum hemorrhage, endometritis, intensive care unit admission, thromboembolic event, readmission, and organ injury. Adverse neonatal outcomes: hypoxic-ischemic encephalopathy, respiratory distress, seizures, apnea, respirator use, death, and cord blood pH < 7.1.The study population included 73,262 deliveries of which 12,942 patients met inclusion and exclusion criteria. After removing cases for the test set, the included patients were 8,078 patients, of which 5,970 people had a successful VBAC (73.9%). Parity, number of years since prior CD, prepregnancy body mass index (BMI), delivery BMI, maternal age, and previous VBAC were associated with successful VBAC. A risk predictor calculator was created, and a receiver operator characteristic curve was developed with an area under the curve of 0.72. The tool was also developed to identify a person's risk of uterine rupture, composite maternal morbidity, and neonatal morbidity.VBAC for patients with term, cephalic, singleton gestation was associated with several variables. This advanced calculator tool will facilitate shared decision-making about the value of a TOLAC regarding the personalized risks of maternal and neonatal morbidity. By using more advanced mathematical models, this tool allows providers to predict not only the likelihood of successful VBAC but also the risk of mat
{"title":"A Novel and Modern Calculator to Predict Vaginal Birth after Cesarean Delivery.","authors":"Alexis C Gimovsky, Silas Monje, Jack Dunn, Jordan Levine","doi":"10.1055/a-2605-7786","DOIUrl":"10.1055/a-2605-7786","url":null,"abstract":"<p><p>Counseling patients who are considering a trial of labor after cesarean (TOLAC) is a challenging task given the risks and benefits of either approach. While calculators exist to give patients an idea of their likelihood of having a successful vaginal birth after cesarean (VBAC), their validity is limited by outdated mathematical methods used to develop them. Most importantly, current VBAC calculators only offer insight into the chance of successful VBAC, without any ability to predict the risk of adverse outcomes relevant to both the patient and neonate. The objective of this study is to develop a prediction model for individualized risks and benefits of a TOLAC using modern mathematical techniques.This was a secondary analysis of the Cesarean Registry database, the same database used in developing the Maternal-Fetal Medicine Units (MFMU) VBAC calculator. The primary outcome was the prediction of the success of VBAC. Secondary outcomes were the prediction of uterine rupture, maternal complications, and neonatal complications. Inclusion criteria were term, singleton gestation, and cephalic presentation pregnancies with one prior low transverse cesarean delivery (CD). Exclusion criteria included intrauterine fetal demise, planned cesarean, and prior myomectomy. Univariate comparisons identified variables that were independently associated with VBAC. An optimal decision tree was used to create a prediction model. A test set was withheld for validation. A risk calculator tool was developed for the prediction of successful VBAC and adverse perinatal outcomes. Adverse maternal outcomes: uterine dehiscence, hysterectomy, postpartum hemorrhage, endometritis, intensive care unit admission, thromboembolic event, readmission, and organ injury. Adverse neonatal outcomes: hypoxic-ischemic encephalopathy, respiratory distress, seizures, apnea, respirator use, death, and cord blood pH < 7.1.The study population included 73,262 deliveries of which 12,942 patients met inclusion and exclusion criteria. After removing cases for the test set, the included patients were 8,078 patients, of which 5,970 people had a successful VBAC (73.9%). Parity, number of years since prior CD, prepregnancy body mass index (BMI), delivery BMI, maternal age, and previous VBAC were associated with successful VBAC. A risk predictor calculator was created, and a receiver operator characteristic curve was developed with an area under the curve of 0.72. The tool was also developed to identify a person's risk of uterine rupture, composite maternal morbidity, and neonatal morbidity.VBAC for patients with term, cephalic, singleton gestation was associated with several variables. This advanced calculator tool will facilitate shared decision-making about the value of a TOLAC regarding the personalized risks of maternal and neonatal morbidity. By using more advanced mathematical models, this tool allows providers to predict not only the likelihood of successful VBAC but also the risk of mat","PeriodicalId":7584,"journal":{"name":"American journal of perinatology","volume":" ","pages":"300-306"},"PeriodicalIF":1.2,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143960927","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 : 2026-02-01Epub Date: 2025-05-14DOI: 10.1055/a-2607-2619
Kaitlyn G Jackson, Alana C Sampson, Kenji M Cunnion, Zachary A Vesoulis, Neel K Krishna
Perinatal hypoxic-ischemic encephalopathy (HIE) is a major contributor to infant death and neurological injury worldwide. Both neuroglia and infiltrating peripheral immune cells contribute to inflammation and oxidative stress, which leads to neuronal loss and cerebral tissue necrosis in neonates with HIE. To date, there are no approved pharmacological interventions to treat inflammatory responses in infants affected by HIE. Therapeutic hypothermia (TH) remains the only effective treatment option. Therefore, novel pharmacotherapeutics that interrupt immune-mediated brain inflammation in HIE represent a promising target for intervention. To meet this unmet need, this study tested the hypothesis that a novel anti-inflammatory peptide, RLS-0071 (pegtarazimod), could modulate neuroinflammation in a neonatal rat model of HIE.RLS-0071 was evaluated in the acute stages of hypoxic-ischemic injury utilizing the well-established Vannucci rat pup model of HIE. Rat pups subject to hypoxia-ischemic brain insult received three interventions: normothermia, hypothermia, and RLS-0071. Histopathological effects were assessed via fluorescence microscopy of the hypoxic-ischemic induced cerebral infarct in the cortex at 24 and 48 hours after controlled oxygen deprivation.Increased surviving neurons were seen at 48 hours for RLS-0071 treatment compared with hypothermia treatment as assessed by neuronal nuclear protein (NeuN) staining. Ionized calcium-binding adaptor molecule 1 (Iba1)-positive microglial recruitment was reduced by fourfold in RLS-0071 treatment or hypothermia-treated rats between 24 and 48 hours, compared to normothermia controls. Likewise, myeloperoxidase (MPO) staining showed a twofold decrease in RLS-0071 or hypothermia-treated rats between 24 and 48 hours compared to normothermia controls.Our findings suggest that RLS-0071 decreases immune cell recruitment and oxidative damage to levels comparable to TH in an animal model of HIE. · No pharmacologic interventions for HIE currently exist.. · TH is the current standard of care.. · RLS-0071 increases neuron survival and lowers microglial cell influx in a HIE rat model.. · RLS-0071 limits oxidative damage in a HIE rat model.. · RLS-0071 may provide an orthogonal treatment for HIE..
{"title":"The Anti-inflammatory Peptide RLS-0071 Reduces Immune Cell Recruitment and Oxidative Damage in a Neonatal Rat Model of Hypoxic-Ischemic Encephalopathy.","authors":"Kaitlyn G Jackson, Alana C Sampson, Kenji M Cunnion, Zachary A Vesoulis, Neel K Krishna","doi":"10.1055/a-2607-2619","DOIUrl":"10.1055/a-2607-2619","url":null,"abstract":"<p><p>Perinatal hypoxic-ischemic encephalopathy (HIE) is a major contributor to infant death and neurological injury worldwide. Both neuroglia and infiltrating peripheral immune cells contribute to inflammation and oxidative stress, which leads to neuronal loss and cerebral tissue necrosis in neonates with HIE. To date, there are no approved pharmacological interventions to treat inflammatory responses in infants affected by HIE. Therapeutic hypothermia (TH) remains the only effective treatment option. Therefore, novel pharmacotherapeutics that interrupt immune-mediated brain inflammation in HIE represent a promising target for intervention. To meet this unmet need, this study tested the hypothesis that a novel anti-inflammatory peptide, RLS-0071 (pegtarazimod), could modulate neuroinflammation in a neonatal rat model of HIE.RLS-0071 was evaluated in the acute stages of hypoxic-ischemic injury utilizing the well-established Vannucci rat pup model of HIE. Rat pups subject to hypoxia-ischemic brain insult received three interventions: normothermia, hypothermia, and RLS-0071. Histopathological effects were assessed via fluorescence microscopy of the hypoxic-ischemic induced cerebral infarct in the cortex at 24 and 48 hours after controlled oxygen deprivation.Increased surviving neurons were seen at 48 hours for RLS-0071 treatment compared with hypothermia treatment as assessed by neuronal nuclear protein (NeuN) staining. Ionized calcium-binding adaptor molecule 1 (Iba1)-positive microglial recruitment was reduced by fourfold in RLS-0071 treatment or hypothermia-treated rats between 24 and 48 hours, compared to normothermia controls. Likewise, myeloperoxidase (MPO) staining showed a twofold decrease in RLS-0071 or hypothermia-treated rats between 24 and 48 hours compared to normothermia controls.Our findings suggest that RLS-0071 decreases immune cell recruitment and oxidative damage to levels comparable to TH in an animal model of HIE. · No pharmacologic interventions for HIE currently exist.. · TH is the current standard of care.. · RLS-0071 increases neuron survival and lowers microglial cell influx in a HIE rat model.. · RLS-0071 limits oxidative damage in a HIE rat model.. · RLS-0071 may provide an orthogonal treatment for HIE..</p>","PeriodicalId":7584,"journal":{"name":"American journal of perinatology","volume":" ","pages":"314-324"},"PeriodicalIF":1.2,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144075371","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 : 2026-02-01Epub Date: 2025-05-28DOI: 10.1055/a-2622-3839
Adrienne Pahl, Zhuopei Hu, Leslie W Young, Kara Wong Ramsey, Bonny L Whalen, Akshatha Akshatha, Kristen L Benninger, Camille M Fung, Meghan P Howell, Sofia Markee, Abhik Das, Margaret M Crawford, Lillian Trochinski, Rachel G Greenberg, Brian Smith, Songthip T Ounpraseuth, Stephanie L Merhar, Lori A Devlin, Kathryn Dee L MacMillan
Determine the relationship between maternal Social Deprivation Index (SDI), a composite measure of area-level deprivation, and maternal characteristics and infant outcomes for mother-infant dyads with perinatal opioid exposure.Post hoc secondary analysis of 1,298 mother-infant dyads in the ESC-NOW study, a multicenter, stepped-wedge cluster-randomized controlled trial (2020-2022) conducted at 26 U.S. study hospitals. The 2016 American Community Survey was used to develop SDI scores based on the maternal zip code of residence at the time of delivery. Outcomes evaluated included receipt of pharmacologic treatment for neonatal opioid withdrawal syndrome (PT), receipt of breastmilk during hospital stay, direct breastfeeding at discharge, discharge disposition, and length of stay for infants who received PT (length of hospital stay, LOS).The median SDI score was 62 on a scale of 100. The high SDI group, with a score above the SDI median and more social deprivation, was less likely to receive adequate prenatal care or medication for opioid use disorder and more likely to be Black and/or Hispanic. The mean proportion of infants in the high SDI group was 6.2% points (relative risk [RR]: 0.89; 95% confidence interval [CI]: 0.80, 0.98) less likely to receive breastmilk during the newborn hospitalization and 7.3% points (RR: 0.91; 95% CI: 0.87, 0.96) less likely to be discharged home with a biological parent. There was no difference between the high and low SDI groups in receipt of PT, direct breastfeeding at discharge, or LOS.Mothers from high SDI communities with opioid exposure during pregnancy were less likely to receive the established standard of care and more likely to be Black and/or Hispanic. Infants born to these mothers were less likely to receive breastmilk and/or to be discharged home with a biological parent. Targeting interventions to mitigate the impact of social deprivation in high SDI communities may improve outcomes for opioid-exposed infants and their mothers. · Living in an area with high social deprivation was associated with differences in health outcomes.. · Mothers were more likely to be Black and/or Hispanic.. · Mothers were less likely to receive the standard of care during pregnancy.. · Infants were less likely to receive breastmilk and/or be discharged home with a biological parent.. · Interventions designed to address community social deprivation may improve outcomes..
{"title":"Maternal Area of Residence and Outcomes for Mother-Infant Dyads with Perinatal Opioid Exposure.","authors":"Adrienne Pahl, Zhuopei Hu, Leslie W Young, Kara Wong Ramsey, Bonny L Whalen, Akshatha Akshatha, Kristen L Benninger, Camille M Fung, Meghan P Howell, Sofia Markee, Abhik Das, Margaret M Crawford, Lillian Trochinski, Rachel G Greenberg, Brian Smith, Songthip T Ounpraseuth, Stephanie L Merhar, Lori A Devlin, Kathryn Dee L MacMillan","doi":"10.1055/a-2622-3839","DOIUrl":"10.1055/a-2622-3839","url":null,"abstract":"<p><p>Determine the relationship between maternal Social Deprivation Index (SDI), a composite measure of area-level deprivation, and maternal characteristics and infant outcomes for mother-infant dyads with perinatal opioid exposure.Post hoc secondary analysis of 1,298 mother-infant dyads in the ESC-NOW study, a multicenter, stepped-wedge cluster-randomized controlled trial (2020-2022) conducted at 26 U.S. study hospitals. The 2016 American Community Survey was used to develop SDI scores based on the maternal zip code of residence at the time of delivery. Outcomes evaluated included receipt of pharmacologic treatment for neonatal opioid withdrawal syndrome (PT), receipt of breastmilk during hospital stay, direct breastfeeding at discharge, discharge disposition, and length of stay for infants who received PT (length of hospital stay, LOS).The median SDI score was 62 on a scale of 100. The high SDI group, with a score above the SDI median and more social deprivation, was less likely to receive adequate prenatal care or medication for opioid use disorder and more likely to be Black and/or Hispanic. The mean proportion of infants in the high SDI group was 6.2% points (relative risk [RR]: 0.89; 95% confidence interval [CI]: 0.80, 0.98) less likely to receive breastmilk during the newborn hospitalization and 7.3% points (RR: 0.91; 95% CI: 0.87, 0.96) less likely to be discharged home with a biological parent. There was no difference between the high and low SDI groups in receipt of PT, direct breastfeeding at discharge, or LOS.Mothers from high SDI communities with opioid exposure during pregnancy were less likely to receive the established standard of care and more likely to be Black and/or Hispanic. Infants born to these mothers were less likely to receive breastmilk and/or to be discharged home with a biological parent. Targeting interventions to mitigate the impact of social deprivation in high SDI communities may improve outcomes for opioid-exposed infants and their mothers. · Living in an area with high social deprivation was associated with differences in health outcomes.. · Mothers were more likely to be Black and/or Hispanic.. · Mothers were less likely to receive the standard of care during pregnancy.. · Infants were less likely to receive breastmilk and/or be discharged home with a biological parent.. · Interventions designed to address community social deprivation may improve outcomes..</p>","PeriodicalId":7584,"journal":{"name":"American journal of perinatology","volume":" ","pages":"383-395"},"PeriodicalIF":1.2,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12246980/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144172343","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}