Pub Date : 2025-01-22DOI: 10.1016/j.ajog.2025.01.022
Fang Jiang, Dong-Zhi Li
{"title":"Prevention of preeclampsia with aspirin: studies are needed to more fully understand the populations most likely to benefit from it.","authors":"Fang Jiang, Dong-Zhi Li","doi":"10.1016/j.ajog.2025.01.022","DOIUrl":"https://doi.org/10.1016/j.ajog.2025.01.022","url":null,"abstract":"","PeriodicalId":7574,"journal":{"name":"American journal of obstetrics and gynecology","volume":" ","pages":""},"PeriodicalIF":8.7,"publicationDate":"2025-01-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143035875","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-01-22DOI: 10.1016/j.ajog.2025.01.018
Ioannis Papastefanou, Vita Mesaric, Renata Gomes Castello, Kypros H Nicolaides, Marietta Charakida
Background: The role of maternal cardiac and hemodynamic assessment during normal and complicated pregnancies has gained attention during the last few years. Some researchers suggested that the manifestation of complications in pregnancy suffering from impaired placentation is mainly driven by pre-existing cardiac changes, identifiable at an early stage by echocardiographic and hemodynamic assessment. It is therefore of great importance to determine the link between placental perfusion and maternal cardiac function and hemodynamics. Also, the impact of maternal cardiac function on birth weight has not been thoroughly studied.
Objective: To elucidate the possible association of maternal cardiovascular indices with placental perfusion at mid-gestation and birthweight.
Methods: Prospective study on women with singleton pregnancies attending Kings' College Hospital, London, UK for a routine hospital visit at 19-24 weeks' gestation. We recorded maternal characteristics and medical history, measured mean arterial pressure (MAP), heart rate, uterine artery pulsatility index (UtA-PI), umbilical artery PI, middle cerebral artery PI, and serum placental growth factor (PlGF). We also performed maternal echocardiogram to assess cardiac output and peripheral vascular resistance as well as indices of diastolic and systolic cardiac function. Multivariable regression modeling was used.
Results: Our cohort included 4006 women. Higher UtA-PI values were associated with lower MAP, heart rate, and left ventricular systolic function, after adjustment for maternal characteristics and subsequent development of hypertensive disorders of pregnancy (HDP) and gestational diabetes mellitus (GDM). In a multivariable approach that explained 17.9% of the variance of the birthweight we found that some cardiovascular indices provided small but significant contribution to the model after accounting for maternal factors, and development of HDP and GDM, UtA-PI, and PlGF.
Conclusion: The findings of our study indicate a weak but significant association between maternal cardiovascular indices with placental perfusion at mid-gestation and birthweight. Our data would not support routine maternal cardiovascular assessment for predicting birthweight.
{"title":"At mid gestation, markers of placental function rather than maternal cardiac function are stronger determinants of birthweight.","authors":"Ioannis Papastefanou, Vita Mesaric, Renata Gomes Castello, Kypros H Nicolaides, Marietta Charakida","doi":"10.1016/j.ajog.2025.01.018","DOIUrl":"https://doi.org/10.1016/j.ajog.2025.01.018","url":null,"abstract":"<p><strong>Background: </strong>The role of maternal cardiac and hemodynamic assessment during normal and complicated pregnancies has gained attention during the last few years. Some researchers suggested that the manifestation of complications in pregnancy suffering from impaired placentation is mainly driven by pre-existing cardiac changes, identifiable at an early stage by echocardiographic and hemodynamic assessment. It is therefore of great importance to determine the link between placental perfusion and maternal cardiac function and hemodynamics. Also, the impact of maternal cardiac function on birth weight has not been thoroughly studied.</p><p><strong>Objective: </strong>To elucidate the possible association of maternal cardiovascular indices with placental perfusion at mid-gestation and birthweight.</p><p><strong>Methods: </strong>Prospective study on women with singleton pregnancies attending Kings' College Hospital, London, UK for a routine hospital visit at 19-24 weeks' gestation. We recorded maternal characteristics and medical history, measured mean arterial pressure (MAP), heart rate, uterine artery pulsatility index (UtA-PI), umbilical artery PI, middle cerebral artery PI, and serum placental growth factor (PlGF). We also performed maternal echocardiogram to assess cardiac output and peripheral vascular resistance as well as indices of diastolic and systolic cardiac function. Multivariable regression modeling was used.</p><p><strong>Results: </strong>Our cohort included 4006 women. Higher UtA-PI values were associated with lower MAP, heart rate, and left ventricular systolic function, after adjustment for maternal characteristics and subsequent development of hypertensive disorders of pregnancy (HDP) and gestational diabetes mellitus (GDM). In a multivariable approach that explained 17.9% of the variance of the birthweight we found that some cardiovascular indices provided small but significant contribution to the model after accounting for maternal factors, and development of HDP and GDM, UtA-PI, and PlGF.</p><p><strong>Conclusion: </strong>The findings of our study indicate a weak but significant association between maternal cardiovascular indices with placental perfusion at mid-gestation and birthweight. Our data would not support routine maternal cardiovascular assessment for predicting birthweight.</p>","PeriodicalId":7574,"journal":{"name":"American journal of obstetrics and gynecology","volume":" ","pages":""},"PeriodicalIF":8.7,"publicationDate":"2025-01-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143035871","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-01-22DOI: 10.1016/j.ajog.2025.01.021
Lakha Prasannan, Patricia Rekawek, Wendy L Kinzler, Martin R Chavez
{"title":"The Evolving Role of 3D Ultrasound in Evaluating Müllerian Anomalies During Pregnancy.","authors":"Lakha Prasannan, Patricia Rekawek, Wendy L Kinzler, Martin R Chavez","doi":"10.1016/j.ajog.2025.01.021","DOIUrl":"https://doi.org/10.1016/j.ajog.2025.01.021","url":null,"abstract":"","PeriodicalId":7574,"journal":{"name":"American journal of obstetrics and gynecology","volume":" ","pages":""},"PeriodicalIF":8.7,"publicationDate":"2025-01-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143035616","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-01-21DOI: 10.1016/j.ajog.2025.01.015
Sven Karstensen, Kirsten Jochumsen, Claus Høgdall, Estrid Høgdall, Niels Marcussen, Finn Friis Lauszus
<p><strong>Background: </strong>Sex cord-stromal cell tumors (SCST) are rare tumors of the ovary. Some of the SCSTs secrete hormone originating from the sex or stromal cell of the ovaries. Previous studies have indicated an increased risk of breast and endometrial cancers. However, these studies focused only on the SCST-subtype adult granulosa cell tumor, the estimates stem from selected cohorts and lack a well described cohort making it difficult to adjust for possible confounders.</p><p><strong>Objective: </strong>We examinined the incidence of other primary hormone sensitive cancers and comparing the risk to a matched cohort of women without SCST.</p><p><strong>Study design: </strong>This is a nested cohort study evaluating women diagnosed with sex cord-stromal cell tumors (SCSTs). We established the cohort of women diagnosed with SCSTs using Systematized Medical Nomenclature for Medicine (SNOMED) codes from the Danish Pathology Register. SCST diagnoses were considered valid if the primary diagnosis was established at a tertiary referral center or confirmed by at least two pathologists. A 1:10 matched control group, matched on birth year, was selected from national registries. Variables for follow up of cases and controls were drawn from national registries including assessment of rates of breast, ovarian and endometrial cancer, hormone use, Charlson Comorbidity Index and sociodemographics. Hazard ratios (HRs) for cancer rates were calculated using multivariate Cox proportional hazards models with SCST exposure estimated in early and delayed models to capture cancer rates over time. Standardized incidence ratios (SIRs) for very rare SCSTs were determined using log-linear Poisson models.</p><p><strong>Results: </strong>Among the 1,516 tumors assigned SNOMED codes for SCSTs, 1,387 met the inclusion criteria after pathologic chart review. The majority had benign tumors, primarily thecoma/fibrothecoma (66%), while 26% had adult granulosa cell tumors (aGCTs). Increased rates for breast cancer were found in thecomas (HR: 1.2; 95% CI 1.0-1.4). In the analysis of all SCSTs combined, an increased rate of synchronous endometrial cancer was found (HR: 3.3; 95% CI 2.7-4.1). In sub-group analysis, malignant and benign SCSTs showed significantly higher HRs for synchronous endometrial cancer, notably in aGCTs (HR: 10.7; 95% CI 5.7-20.1). In the model assessing the rates of endometrial cancer two months after surgical removal of the SCST, no increased rates were found. Sertoli cell tumors were linked to an increased incidence of breast cancer (SIR: 18.9; 95% CI 2.7-134). Both Sertoli and Leydig cell tumors were associated with a higher incidence of synchronous endometrial cancer, with SIRs of 41.4 (95% CI 10.4-166) and 44.9 (95% CI 18.7-108), respectively.</p><p><strong>Conclusion: </strong>In conclusion, women with SCSTs have an increased rate of synchronous endometrial cancer and women with benign SCSTs have an increased rate of synchronous ovarian cancer.
{"title":"Ovarian sex cord-stromal cell tumors and the risk of sex hormone-sensitive cancers.","authors":"Sven Karstensen, Kirsten Jochumsen, Claus Høgdall, Estrid Høgdall, Niels Marcussen, Finn Friis Lauszus","doi":"10.1016/j.ajog.2025.01.015","DOIUrl":"https://doi.org/10.1016/j.ajog.2025.01.015","url":null,"abstract":"<p><strong>Background: </strong>Sex cord-stromal cell tumors (SCST) are rare tumors of the ovary. Some of the SCSTs secrete hormone originating from the sex or stromal cell of the ovaries. Previous studies have indicated an increased risk of breast and endometrial cancers. However, these studies focused only on the SCST-subtype adult granulosa cell tumor, the estimates stem from selected cohorts and lack a well described cohort making it difficult to adjust for possible confounders.</p><p><strong>Objective: </strong>We examinined the incidence of other primary hormone sensitive cancers and comparing the risk to a matched cohort of women without SCST.</p><p><strong>Study design: </strong>This is a nested cohort study evaluating women diagnosed with sex cord-stromal cell tumors (SCSTs). We established the cohort of women diagnosed with SCSTs using Systematized Medical Nomenclature for Medicine (SNOMED) codes from the Danish Pathology Register. SCST diagnoses were considered valid if the primary diagnosis was established at a tertiary referral center or confirmed by at least two pathologists. A 1:10 matched control group, matched on birth year, was selected from national registries. Variables for follow up of cases and controls were drawn from national registries including assessment of rates of breast, ovarian and endometrial cancer, hormone use, Charlson Comorbidity Index and sociodemographics. Hazard ratios (HRs) for cancer rates were calculated using multivariate Cox proportional hazards models with SCST exposure estimated in early and delayed models to capture cancer rates over time. Standardized incidence ratios (SIRs) for very rare SCSTs were determined using log-linear Poisson models.</p><p><strong>Results: </strong>Among the 1,516 tumors assigned SNOMED codes for SCSTs, 1,387 met the inclusion criteria after pathologic chart review. The majority had benign tumors, primarily thecoma/fibrothecoma (66%), while 26% had adult granulosa cell tumors (aGCTs). Increased rates for breast cancer were found in thecomas (HR: 1.2; 95% CI 1.0-1.4). In the analysis of all SCSTs combined, an increased rate of synchronous endometrial cancer was found (HR: 3.3; 95% CI 2.7-4.1). In sub-group analysis, malignant and benign SCSTs showed significantly higher HRs for synchronous endometrial cancer, notably in aGCTs (HR: 10.7; 95% CI 5.7-20.1). In the model assessing the rates of endometrial cancer two months after surgical removal of the SCST, no increased rates were found. Sertoli cell tumors were linked to an increased incidence of breast cancer (SIR: 18.9; 95% CI 2.7-134). Both Sertoli and Leydig cell tumors were associated with a higher incidence of synchronous endometrial cancer, with SIRs of 41.4 (95% CI 10.4-166) and 44.9 (95% CI 18.7-108), respectively.</p><p><strong>Conclusion: </strong>In conclusion, women with SCSTs have an increased rate of synchronous endometrial cancer and women with benign SCSTs have an increased rate of synchronous ovarian cancer. ","PeriodicalId":7574,"journal":{"name":"American journal of obstetrics and gynecology","volume":" ","pages":""},"PeriodicalIF":8.7,"publicationDate":"2025-01-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143027463","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-01-21DOI: 10.1016/j.ajog.2025.01.017
Dan Liu, Lin Wu, Linan Zeng, Hailong Li, Yangyang Zhan, Lin Wang, Xu Zhang, Xuebin Li, Ya Ling, Peng Zhang, Huaiyu Su, Bing Peng, Lang Qin, Xiumei Liu, Jing Huang, Yun Teng, Lin Li, Aiyun Xing, Lingli Zhang
Background: While guidelines suggest administering antibiotics 12 to 18 hours after the rupture of membranes in term premature rupture of membranes (PROM) women, in practice, clinicians tend to initiate prophylactic antibiotics as soon as possible to avoid risk of infection.
Objective: This study aimed to assess whether early administration of prophylactic antibiotics for term premature rupture of membranes reduces the incidence of maternal and neonatal infections.
Study design: This multi-center, prospective cohort study included women with term premature rupture of membranes. Participants were divided into early and late administration groups according to the duration between membranes rupture and antibiotic use. The effectiveness outcomes included the incidence of puerperal infection, the incidence of total maternal infection, the rate of neonatal sepsis, among others; the safety outcomes included the incidence of adverse reactions; and Antibiotics Use Density was used to assess the antibiotic consumption. Propensity score matching method was used to control confounding.
Results: A total of 1099 women with term PROM were enrolled, 459 in the early group-6 hours (antibiotics administration within 6 hours) and 640 in the late group-6 hours (antibiotics administration after 6 hours); 707 in the early group-12 hours (antibiotics administration within 12 hours) and 392 in the late group-12 hours (antibiotics administration after 12 hours). After propensity score matching, there were 300 women in each of the 6-hour groups and 230 women in each of the 12-hour groups. Baseline characteristics showed no significant differences between matched groups (P>0.05). The early 6-hour and 12-hour groups had lower maternal C-reactive protein levels compared to the late groups (P<0.05), but no significant differences in other maternal and neonatal outcomes. Adverse reactions showed no statistical significance between early and late groups (P=1.000). Antibiotic use density was higher in the early treatment groups by 10.1 defined daily doses (DDDs) (6-hour) and 11.7 DDDs (12-hour).
Conclusion: There was no statistical difference in the efficacy and safety when antibiotics administered within 6-12 hours after rupture of membranes, compared to after 6-12 hours in women with term PROM. Meanwhile delayed use significantly reduces the antibiotic consumption.
{"title":"No Difference in Outcomes with Early vs. Late Antibiotic Prophylaxis for Term PROM: A Multi-Center Analysis.","authors":"Dan Liu, Lin Wu, Linan Zeng, Hailong Li, Yangyang Zhan, Lin Wang, Xu Zhang, Xuebin Li, Ya Ling, Peng Zhang, Huaiyu Su, Bing Peng, Lang Qin, Xiumei Liu, Jing Huang, Yun Teng, Lin Li, Aiyun Xing, Lingli Zhang","doi":"10.1016/j.ajog.2025.01.017","DOIUrl":"https://doi.org/10.1016/j.ajog.2025.01.017","url":null,"abstract":"<p><strong>Background: </strong>While guidelines suggest administering antibiotics 12 to 18 hours after the rupture of membranes in term premature rupture of membranes (PROM) women, in practice, clinicians tend to initiate prophylactic antibiotics as soon as possible to avoid risk of infection.</p><p><strong>Objective: </strong>This study aimed to assess whether early administration of prophylactic antibiotics for term premature rupture of membranes reduces the incidence of maternal and neonatal infections.</p><p><strong>Study design: </strong>This multi-center, prospective cohort study included women with term premature rupture of membranes. Participants were divided into early and late administration groups according to the duration between membranes rupture and antibiotic use. The effectiveness outcomes included the incidence of puerperal infection, the incidence of total maternal infection, the rate of neonatal sepsis, among others; the safety outcomes included the incidence of adverse reactions; and Antibiotics Use Density was used to assess the antibiotic consumption. Propensity score matching method was used to control confounding.</p><p><strong>Results: </strong>A total of 1099 women with term PROM were enrolled, 459 in the early group-6 hours (antibiotics administration within 6 hours) and 640 in the late group-6 hours (antibiotics administration after 6 hours); 707 in the early group-12 hours (antibiotics administration within 12 hours) and 392 in the late group-12 hours (antibiotics administration after 12 hours). After propensity score matching, there were 300 women in each of the 6-hour groups and 230 women in each of the 12-hour groups. Baseline characteristics showed no significant differences between matched groups (P>0.05). The early 6-hour and 12-hour groups had lower maternal C-reactive protein levels compared to the late groups (P<0.05), but no significant differences in other maternal and neonatal outcomes. Adverse reactions showed no statistical significance between early and late groups (P=1.000). Antibiotic use density was higher in the early treatment groups by 10.1 defined daily doses (DDDs) (6-hour) and 11.7 DDDs (12-hour).</p><p><strong>Conclusion: </strong>There was no statistical difference in the efficacy and safety when antibiotics administered within 6-12 hours after rupture of membranes, compared to after 6-12 hours in women with term PROM. Meanwhile delayed use significantly reduces the antibiotic consumption.</p>","PeriodicalId":7574,"journal":{"name":"American journal of obstetrics and gynecology","volume":" ","pages":""},"PeriodicalIF":8.7,"publicationDate":"2025-01-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143027421","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-01-21DOI: 10.1016/j.ajog.2025.01.019
Marisa R Imbroane, Felicia LeMoine, Christopher T Nau
Background: The use of glucagon-like-peptide-1 receptor agonists (GLP-1RAs) has greatly increased in patients of reproductive age within the past four years. However, there is minimal research into the long-term impact of these medications on future pregnancies.
Objectives: We aimed to evaluate the association between adverse obstetric outcomes and antecedent GLP-1RA use using a nationally representative database.
Study design: We conducted a retrospective cohort study of female patients age ≥ 18 using the United States Collaborative Network in TriNetX. We defined the exposure cohort as individuals who received a GLP-1RA prescription within 2 years preceding a pregnancy. The unexposed cohort comprised individuals with a history of pregnancy but no prior history of GLP-1RA use. Cohorts were matched for age, race, ethnicity, and history of co-morbid conditions. ICD-10 codes for hypertensive disorders of pregnancy (HDP), gestational diabetes mellitus (GDM), preterm delivery, and rates of Cesarean section (CD) were the primary outcomes of interest compared between the cohorts. Logistic regression was performed in TriNetX to determine odds ratios (OR) and 95% confidence intervals (CI).
Results: After matching, there were 4,267 individuals in each cohort. Individuals who had a prescription for GLP-1RA were less likely to develop GDM (15.2% versus 18.2%, OR 0.81 (95% CI 0.72,0.91)), HDP (19.9% versus 22.8%, OR 0.84 (0.76,0.94)), have a preterm delivery (3.0% vs 4.4%, OR 0.68 (0.54,0.85)), and undergo a CD (17.6% vs 19.7%, OR 0.89 (0.87,0.97)) compared to the unexposed cohort.
Conclusions: A prescription of a GLP-1RA within 24 months preceding pregnancy is associated with a reduced risk of several adverse obstetric outcomes, including GDM, HDP, preterm delivery, and CD. This is suggestive that use of a GLP-1RA may be a powerful tool to improve perinatal outcomes in high-risk populations, though future work is required to define how this class of medication is best incorporated clinically into preconception health optimization.
{"title":"Preconception GLP-1 Receptor Agonist Use Associated with Decreased Risk for Adverse Obstetric Outcomes.","authors":"Marisa R Imbroane, Felicia LeMoine, Christopher T Nau","doi":"10.1016/j.ajog.2025.01.019","DOIUrl":"https://doi.org/10.1016/j.ajog.2025.01.019","url":null,"abstract":"<p><strong>Background: </strong>The use of glucagon-like-peptide-1 receptor agonists (GLP-1RAs) has greatly increased in patients of reproductive age within the past four years. However, there is minimal research into the long-term impact of these medications on future pregnancies.</p><p><strong>Objectives: </strong>We aimed to evaluate the association between adverse obstetric outcomes and antecedent GLP-1RA use using a nationally representative database.</p><p><strong>Study design: </strong>We conducted a retrospective cohort study of female patients age ≥ 18 using the United States Collaborative Network in TriNetX. We defined the exposure cohort as individuals who received a GLP-1RA prescription within 2 years preceding a pregnancy. The unexposed cohort comprised individuals with a history of pregnancy but no prior history of GLP-1RA use. Cohorts were matched for age, race, ethnicity, and history of co-morbid conditions. ICD-10 codes for hypertensive disorders of pregnancy (HDP), gestational diabetes mellitus (GDM), preterm delivery, and rates of Cesarean section (CD) were the primary outcomes of interest compared between the cohorts. Logistic regression was performed in TriNetX to determine odds ratios (OR) and 95% confidence intervals (CI).</p><p><strong>Results: </strong>After matching, there were 4,267 individuals in each cohort. Individuals who had a prescription for GLP-1RA were less likely to develop GDM (15.2% versus 18.2%, OR 0.81 (95% CI 0.72,0.91)), HDP (19.9% versus 22.8%, OR 0.84 (0.76,0.94)), have a preterm delivery (3.0% vs 4.4%, OR 0.68 (0.54,0.85)), and undergo a CD (17.6% vs 19.7%, OR 0.89 (0.87,0.97)) compared to the unexposed cohort.</p><p><strong>Conclusions: </strong>A prescription of a GLP-1RA within 24 months preceding pregnancy is associated with a reduced risk of several adverse obstetric outcomes, including GDM, HDP, preterm delivery, and CD. This is suggestive that use of a GLP-1RA may be a powerful tool to improve perinatal outcomes in high-risk populations, though future work is required to define how this class of medication is best incorporated clinically into preconception health optimization.</p>","PeriodicalId":7574,"journal":{"name":"American journal of obstetrics and gynecology","volume":" ","pages":""},"PeriodicalIF":8.7,"publicationDate":"2025-01-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143027562","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-01-21DOI: 10.1016/j.ajog.2025.01.016
K Thevissen, J Cornette, L Bruckers, W Gyselaers
Objective: To investigate the association between functional parameters of the microcirculation and the systemic cardiovascular system in a population of pregnant women at risk for gestational hypertension disorders.
Study design: For this observational study, women at high cardiovascular risk according to maternal anthropometrics, obstetric and medical history, were recruited at random gestational age depending on time of referral to the outpatient clinic for high risk prenatal care at Ziekenhuis Oost Limburg, Genk Belgium. After birth, data of maternal and neonatal outcome were obtained from the hospital records: only women with normal pregnancy (n = 142) and with preeclampsia (n = 34) were included in this analysis. Nailfold video capillaroscopy measurements were performed in first and/or second and/or third trimester. Video magnification of 200x was used at all fingers except thumbs, and stored images were analyzed offline. Capillary density was counted (n/mm2), mean capillary diameter measured (μm) and capillary bed was calculated as density x diameter. Cardiac output and total peripheral resistance were measured using impedance cardiography, together with sphygmomanometric blood pressure measurement. Linear mixed model for repeated measures was employed to investigate the association between the microvascular and macrovascular parameters. No correction for multiple testing was used.
Results: In normal pregnancies, a positive association was observed between capillary bed and total vascular resistance (1.807, p =0.01), and a negative association between capillary density and cardiac output (-0.269, p =0.037). In preeclampsia, a negative association was observed between capillary density and mean arterial pressure (-0.5649, p = 0.010), and between capillary diameter and cardiac output (-0.165, p=0.032).
Conclusion: A reduction of capillary density with increase of blood pressure in preeclampsia is similar to observations in chronic hypertension. Here, this is considered the result of capillary closure after constriction of precapillary arterioles. In normal pregnancy however, the increase of the capillary bed with rising vascular resistance can only be explained by a primary role for the microcirculation, preventing capillary overflow via stimulation of arteriolar constriction. These observations enlighten the very first hemodynamic origins of hypertension at the level of the microcirculation in preeclampsia.
{"title":"The microcirculation : master in normal pregnancy, puppet in preeclampsia.","authors":"K Thevissen, J Cornette, L Bruckers, W Gyselaers","doi":"10.1016/j.ajog.2025.01.016","DOIUrl":"https://doi.org/10.1016/j.ajog.2025.01.016","url":null,"abstract":"<p><strong>Objective: </strong>To investigate the association between functional parameters of the microcirculation and the systemic cardiovascular system in a population of pregnant women at risk for gestational hypertension disorders.</p><p><strong>Study design: </strong>For this observational study, women at high cardiovascular risk according to maternal anthropometrics, obstetric and medical history, were recruited at random gestational age depending on time of referral to the outpatient clinic for high risk prenatal care at Ziekenhuis Oost Limburg, Genk Belgium. After birth, data of maternal and neonatal outcome were obtained from the hospital records: only women with normal pregnancy (n = 142) and with preeclampsia (n = 34) were included in this analysis. Nailfold video capillaroscopy measurements were performed in first and/or second and/or third trimester. Video magnification of 200x was used at all fingers except thumbs, and stored images were analyzed offline. Capillary density was counted (n/mm<sup>2</sup>), mean capillary diameter measured (μm) and capillary bed was calculated as density x diameter. Cardiac output and total peripheral resistance were measured using impedance cardiography, together with sphygmomanometric blood pressure measurement. Linear mixed model for repeated measures was employed to investigate the association between the microvascular and macrovascular parameters. No correction for multiple testing was used.</p><p><strong>Results: </strong>In normal pregnancies, a positive association was observed between capillary bed and total vascular resistance (1.807, p =0.01), and a negative association between capillary density and cardiac output (-0.269, p =0.037). In preeclampsia, a negative association was observed between capillary density and mean arterial pressure (-0.5649, p = 0.010), and between capillary diameter and cardiac output (-0.165, p=0.032).</p><p><strong>Conclusion: </strong>A reduction of capillary density with increase of blood pressure in preeclampsia is similar to observations in chronic hypertension. Here, this is considered the result of capillary closure after constriction of precapillary arterioles. In normal pregnancy however, the increase of the capillary bed with rising vascular resistance can only be explained by a primary role for the microcirculation, preventing capillary overflow via stimulation of arteriolar constriction. These observations enlighten the very first hemodynamic origins of hypertension at the level of the microcirculation in preeclampsia.</p>","PeriodicalId":7574,"journal":{"name":"American journal of obstetrics and gynecology","volume":" ","pages":""},"PeriodicalIF":8.7,"publicationDate":"2025-01-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143027596","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
BACKGROUNDA subgroup of patients with chronic pelvic pain (CPP) exhibit organ sensitization, whose origin and mechanism remains largely unknown. Changes in microbiota composition in pelvic organs have been found to be associated with various pelvic pathological conditions. Therefore, a comprehensive analysis of the gut and genito-urinary microbiota composition and interactions in women with CPP may be key to understanding their involvement in the sensitization processes.OBJECTIVETo identify pelvic organ microbiota signatures that are associated with organ hypersensitivity in CPP patients.STUDY DESIGNThis study involved women with high (S-CPP, n=14) and low (NS-CPP, n=14) pelvic sensitization scores according to the Convergences PP criteria. Pelvic organ sensitivity was assessed by rectal barostat, and noninvasive bladder, muscular and vulvar sensory tests. Quality of life, pelvic symptoms and psychological state were assessed. Using 16S rRNA gene sequencing, the gut, vaginal and urinary microbiota diversity and composition were analyzed and compared between S-CPP and NS-CPP women. Differentially abundant bacterial amplicon sequence variants (ASVs) between groups were associated with clinical characteristics and organ sensitivity. System biology approaches using Weighted Gene Correlation Network Analysis (WGCNA) were used to identify bacterial ASV modules associated with functional and clinical parameters.RESULTSPain pressure thresholds were significantly decreased in S-CPP women for the vulva and for the rectum, the bladder and the perineal muscles as compared to NS-CPP. However, pain intensity felt at rectal, muscular and bladder pain thresholds was significantly increased in S-CPP women. After stimulation, S-CPP women presented increased and prolonged pain in perineal muscles and bladder compared to NS-CPP women. Alpha and β-diversities were significantly increased in S-CPP women in vaginal and urinary but not in gut microbiota. Using, differential abundance analysis, we showed that 13 ASVs in the gut, 6 in the vagina and 2 in the bladder were differentially expressed between S-CPP and NS-CPP patients. More specifically, in vaginal microbiota, a significant increase of Streptococcus and Prevotella genera was observed in S-CPP as compared to NS-CPP. A significant increase in Clostridium sensu stricto 1 ASV was observed in urinary microbiota of S-CPP as compared to NS-CPP patients. Next, we found that 4 gut microbiota ASVs (belonging to Akkermansia, Desulfovibrio, Faecalibacterium and CAG-352) were correlated with pain intensity at maximal rectal distension threshold. We also identified an ASV (Blautia) which is increased in NS-CPP as being inversely correlated to several gut sensitization markers. In the vaginal microbiota, the Lactobacillus jensenii ASV was associated with less dysmenorrhea and an increased bladder capacity. Furthermore, we identified two vaginal ASVs belonging to Prevotella which are increased in S-CPP as being associated with
{"title":"GUT, VAGINAL AND URINARY MICROBIOTA AS POTENTIAL BIOMARKERS OF SENSITIZATION IN WOMEN WITH CHRONIC PELVIC PAIN.","authors":"Claire Cardaillac,Camille Trottier,Charlène Brochard,Philippe Aubert,Philippe Bordron,Marie-Aimée Perrouin-Verbe,Thibault Thubert,Samuel Chaffron,Amélie Levesque,Stéphane Ploteau,Justine Marchix,Michel Neunlist","doi":"10.1016/j.ajog.2025.01.013","DOIUrl":"https://doi.org/10.1016/j.ajog.2025.01.013","url":null,"abstract":"BACKGROUNDA subgroup of patients with chronic pelvic pain (CPP) exhibit organ sensitization, whose origin and mechanism remains largely unknown. Changes in microbiota composition in pelvic organs have been found to be associated with various pelvic pathological conditions. Therefore, a comprehensive analysis of the gut and genito-urinary microbiota composition and interactions in women with CPP may be key to understanding their involvement in the sensitization processes.OBJECTIVETo identify pelvic organ microbiota signatures that are associated with organ hypersensitivity in CPP patients.STUDY DESIGNThis study involved women with high (S-CPP, n=14) and low (NS-CPP, n=14) pelvic sensitization scores according to the Convergences PP criteria. Pelvic organ sensitivity was assessed by rectal barostat, and noninvasive bladder, muscular and vulvar sensory tests. Quality of life, pelvic symptoms and psychological state were assessed. Using 16S rRNA gene sequencing, the gut, vaginal and urinary microbiota diversity and composition were analyzed and compared between S-CPP and NS-CPP women. Differentially abundant bacterial amplicon sequence variants (ASVs) between groups were associated with clinical characteristics and organ sensitivity. System biology approaches using Weighted Gene Correlation Network Analysis (WGCNA) were used to identify bacterial ASV modules associated with functional and clinical parameters.RESULTSPain pressure thresholds were significantly decreased in S-CPP women for the vulva and for the rectum, the bladder and the perineal muscles as compared to NS-CPP. However, pain intensity felt at rectal, muscular and bladder pain thresholds was significantly increased in S-CPP women. After stimulation, S-CPP women presented increased and prolonged pain in perineal muscles and bladder compared to NS-CPP women. Alpha and β-diversities were significantly increased in S-CPP women in vaginal and urinary but not in gut microbiota. Using, differential abundance analysis, we showed that 13 ASVs in the gut, 6 in the vagina and 2 in the bladder were differentially expressed between S-CPP and NS-CPP patients. More specifically, in vaginal microbiota, a significant increase of Streptococcus and Prevotella genera was observed in S-CPP as compared to NS-CPP. A significant increase in Clostridium sensu stricto 1 ASV was observed in urinary microbiota of S-CPP as compared to NS-CPP patients. Next, we found that 4 gut microbiota ASVs (belonging to Akkermansia, Desulfovibrio, Faecalibacterium and CAG-352) were correlated with pain intensity at maximal rectal distension threshold. We also identified an ASV (Blautia) which is increased in NS-CPP as being inversely correlated to several gut sensitization markers. In the vaginal microbiota, the Lactobacillus jensenii ASV was associated with less dysmenorrhea and an increased bladder capacity. Furthermore, we identified two vaginal ASVs belonging to Prevotella which are increased in S-CPP as being associated with","PeriodicalId":7574,"journal":{"name":"American journal of obstetrics and gynecology","volume":"8 1","pages":""},"PeriodicalIF":9.8,"publicationDate":"2025-01-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142991701","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-01-15DOI: 10.1016/j.ajog.2025.01.012
Allison L Brodsky,Alejandra Flores Legarreta,Jeffrey A How,Veena Vuttaradhi,Anil K Sood,Lois M Ramondetta,David M Gershenson,R Tyler Hillman
BACKGROUNDAdult-type granulosa cell tumors are a rare form of ovarian cancer, 30% of which will recur. Cytoreductive surgery is often performed at the time of a first recurrence, but little is known about the impact of open versus minimally invasive surgical approaches on survival outcomes.OBJECTIVETo examine associations between surgical approach, clinical variables, and survival outcomes among patients with adult-type granulosa cell tumors who underwent cytoreductive surgery at the time of first recurrence.STUDY DESIGNThis is a retrospective cohort study of patients with adult-type granulosa cell tumors enrolled in the MD Anderson Rare Gynecologic Malignancy Registry as of April 2024. Included patients had at least one documented recurrence and underwent secondary cytoreductive surgery as part of their treatment plan. Patients were excluded if surgery was performed prior to January 1, 2000, or if surgery was not intra-abdominal. Demographics and clinical variables were compared using descriptive statistics. Surgical complexity was classified as either low, intermediate, or high based on procedures performed. Progression-free and overall survival outcomes were stratified by surgical approach and estimated using Kaplan-Meier curves. A multivariable Cox proportional hazards model was used to adjust progression-free survival at time of first recurrence for age, year of surgery, and extent of disease.RESULTS485 patients with adult granulosa cell tumors were identified, 108 met inclusion criteria. Seventy-eight (72%) had open and 30 (28%) had minimally invasive secondary cytoreductive surgery. Baseline characteristics, including initial stage, self-identified race, or age at diagnosis, did not differ between open and minimally invasive surgery groups. Patients undergoing minimally invasive surgery were significantly younger at the time of surgery than the open group, with a median age of 42 vs 49, respectively (p=0.03). For the open group, 33% of surgeries were considered intermediate complexity and 4% high complexity, compared to 7% and 0% in the MIS group, respectively (p=0.004). There was no difference in achieving optimal cytoreduction, 85% in the open group and 88% in the MIS group (p=0.68). Following secondary cytoreductive surgery, there was no difference in overall survival, median overall survival of 166 months in the open group and 94 months in the minimally invasive group (p=0.27), or progression-free survival after first recurrence, 26 months in the open group compared to 21 months in the minimally invasive group (p=0.42). The difference in progression-free survival after the first recurrence remained non-significant after adjustment for key potential variables, including age, surgical approach, year of surgery, and extent of disease. There was no difference in incisional or port site recurrences at the time of second recurrence among those undergoing open (8.3%) compared to minimally invasive surgery (7.4%) at time of first recurrence (p
{"title":"Survival outcomes comparing minimally invasive versus open cytoreductive surgery in recurrent adult-type granulosa cell tumors.","authors":"Allison L Brodsky,Alejandra Flores Legarreta,Jeffrey A How,Veena Vuttaradhi,Anil K Sood,Lois M Ramondetta,David M Gershenson,R Tyler Hillman","doi":"10.1016/j.ajog.2025.01.012","DOIUrl":"https://doi.org/10.1016/j.ajog.2025.01.012","url":null,"abstract":"BACKGROUNDAdult-type granulosa cell tumors are a rare form of ovarian cancer, 30% of which will recur. Cytoreductive surgery is often performed at the time of a first recurrence, but little is known about the impact of open versus minimally invasive surgical approaches on survival outcomes.OBJECTIVETo examine associations between surgical approach, clinical variables, and survival outcomes among patients with adult-type granulosa cell tumors who underwent cytoreductive surgery at the time of first recurrence.STUDY DESIGNThis is a retrospective cohort study of patients with adult-type granulosa cell tumors enrolled in the MD Anderson Rare Gynecologic Malignancy Registry as of April 2024. Included patients had at least one documented recurrence and underwent secondary cytoreductive surgery as part of their treatment plan. Patients were excluded if surgery was performed prior to January 1, 2000, or if surgery was not intra-abdominal. Demographics and clinical variables were compared using descriptive statistics. Surgical complexity was classified as either low, intermediate, or high based on procedures performed. Progression-free and overall survival outcomes were stratified by surgical approach and estimated using Kaplan-Meier curves. A multivariable Cox proportional hazards model was used to adjust progression-free survival at time of first recurrence for age, year of surgery, and extent of disease.RESULTS485 patients with adult granulosa cell tumors were identified, 108 met inclusion criteria. Seventy-eight (72%) had open and 30 (28%) had minimally invasive secondary cytoreductive surgery. Baseline characteristics, including initial stage, self-identified race, or age at diagnosis, did not differ between open and minimally invasive surgery groups. Patients undergoing minimally invasive surgery were significantly younger at the time of surgery than the open group, with a median age of 42 vs 49, respectively (p=0.03). For the open group, 33% of surgeries were considered intermediate complexity and 4% high complexity, compared to 7% and 0% in the MIS group, respectively (p=0.004). There was no difference in achieving optimal cytoreduction, 85% in the open group and 88% in the MIS group (p=0.68). Following secondary cytoreductive surgery, there was no difference in overall survival, median overall survival of 166 months in the open group and 94 months in the minimally invasive group (p=0.27), or progression-free survival after first recurrence, 26 months in the open group compared to 21 months in the minimally invasive group (p=0.42). The difference in progression-free survival after the first recurrence remained non-significant after adjustment for key potential variables, including age, surgical approach, year of surgery, and extent of disease. There was no difference in incisional or port site recurrences at the time of second recurrence among those undergoing open (8.3%) compared to minimally invasive surgery (7.4%) at time of first recurrence (p","PeriodicalId":7574,"journal":{"name":"American journal of obstetrics and gynecology","volume":"122 1","pages":""},"PeriodicalIF":9.8,"publicationDate":"2025-01-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142989718","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-01-10DOI: 10.1016/j.ajog.2025.01.010
Noelle E Younge, Shampa Saha, Jane E Brumbaugh, Jonathan M Klein, Edward F Bell, Tarah T Colaizy, Brenna L Hughes, William F Malcolm, Ronald N Goldberg, Myra H Wyckoff, Krisa P VAN Meurs, Abhik DAS, C Michael Cotten
Background: Preterm prelabor rupture of membranes (PPROM) before or around the limit of fetal viability is associated with serious maternal and neonatal complications including chorioamnionitis, extremely preterm birth, and pulmonary hypoplasia.
Objectives: To describe contemporary outcomes of extremely preterm infants born after prolonged periviable PPROM, and to identify perinatal factors associated with survival and survival without severe neurodevelopmental impairment (NDI).
Study design: Among actively treated infants born alive at <27 weeks' gestational age (GA) in centers of the Eunice Kennedy Shriver National Institute of Child Health and Human Development Neonatal Research Network from 2012 to 2018, the outcomes of survival and survival without severe NDI at 22-26 months' corrected age were compared between infants exposed to prolonged (≥120 hours) periviable (<24 weeks' GA) PPROM and unexposed infants born after rupture of membranes ≤18 hours before delivery or at delivery, adjusting for birth GA, sex, multiple gestation, antenatal steroids, small for gestational age (SGA), insurance, and center. Regression models were used to identify perinatal factors associated with survival and survival without severe NDI among the infants exposed to prolonged periviable PPROM.
Results: The analysis included 609 infants exposed to prolonged periviable PPROM and 4,489 unexposed infants. In the prolonged periviable PPROM group, 444/608 (73%) infants survived and 298/533 (56%) infants survived without severe NDI. Odds of survival (OR, 0.84; 95% CI, 0.68-1.05) and survival without severe NDI (OR, 0.91; 95% CI, 0.75-1.12) were not significantly different between prolonged periviable PPROM and unexposed groups. Variables associated with higher odds of survival without severe NDI were later GA at birth (OR, 1.37; 95% CI, 1.13-1.67), later GA at PPROM (OR 1.44; 95% CI, 1.26-1.63), and female sex (OR, 1.57; 95% CI, 1.06-2.34), while SGA infants had lower odds of survival without severe NDI (OR, 0.14; 95% CI, 0.04-0.51).
Conclusions: Odds of survival and survival without severe NDI among infants exposed to prolonged periviable PPROM were not significantly different from unexposed infants, but decreased with earlier GA at birth and PPROM.
{"title":"Outcomes of Extremely Preterm Infants Exposed to Prolonged Prelabor Rupture of Membranes before 24 Weeks of Gestation.","authors":"Noelle E Younge, Shampa Saha, Jane E Brumbaugh, Jonathan M Klein, Edward F Bell, Tarah T Colaizy, Brenna L Hughes, William F Malcolm, Ronald N Goldberg, Myra H Wyckoff, Krisa P VAN Meurs, Abhik DAS, C Michael Cotten","doi":"10.1016/j.ajog.2025.01.010","DOIUrl":"https://doi.org/10.1016/j.ajog.2025.01.010","url":null,"abstract":"<p><strong>Background: </strong>Preterm prelabor rupture of membranes (PPROM) before or around the limit of fetal viability is associated with serious maternal and neonatal complications including chorioamnionitis, extremely preterm birth, and pulmonary hypoplasia.</p><p><strong>Objectives: </strong>To describe contemporary outcomes of extremely preterm infants born after prolonged periviable PPROM, and to identify perinatal factors associated with survival and survival without severe neurodevelopmental impairment (NDI).</p><p><strong>Study design: </strong>Among actively treated infants born alive at <27 weeks' gestational age (GA) in centers of the Eunice Kennedy Shriver National Institute of Child Health and Human Development Neonatal Research Network from 2012 to 2018, the outcomes of survival and survival without severe NDI at 22-26 months' corrected age were compared between infants exposed to prolonged (≥120 hours) periviable (<24 weeks' GA) PPROM and unexposed infants born after rupture of membranes ≤18 hours before delivery or at delivery, adjusting for birth GA, sex, multiple gestation, antenatal steroids, small for gestational age (SGA), insurance, and center. Regression models were used to identify perinatal factors associated with survival and survival without severe NDI among the infants exposed to prolonged periviable PPROM.</p><p><strong>Results: </strong>The analysis included 609 infants exposed to prolonged periviable PPROM and 4,489 unexposed infants. In the prolonged periviable PPROM group, 444/608 (73%) infants survived and 298/533 (56%) infants survived without severe NDI. Odds of survival (OR, 0.84; 95% CI, 0.68-1.05) and survival without severe NDI (OR, 0.91; 95% CI, 0.75-1.12) were not significantly different between prolonged periviable PPROM and unexposed groups. Variables associated with higher odds of survival without severe NDI were later GA at birth (OR, 1.37; 95% CI, 1.13-1.67), later GA at PPROM (OR 1.44; 95% CI, 1.26-1.63), and female sex (OR, 1.57; 95% CI, 1.06-2.34), while SGA infants had lower odds of survival without severe NDI (OR, 0.14; 95% CI, 0.04-0.51).</p><p><strong>Conclusions: </strong>Odds of survival and survival without severe NDI among infants exposed to prolonged periviable PPROM were not significantly different from unexposed infants, but decreased with earlier GA at birth and PPROM.</p>","PeriodicalId":7574,"journal":{"name":"American journal of obstetrics and gynecology","volume":" ","pages":""},"PeriodicalIF":8.7,"publicationDate":"2025-01-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142969415","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}