Pub Date : 2026-08-14DOI: 10.1016/j.gofs.2026.08.002
Alexa Miran, Thierry Brillac, Elodie Chantalat
Objective: The management of patients with endometriosis remains marked by a long, fragmented, and poorly coordinated care pathway, leading to significant diagnostic delay. In this context, the regional EndOccitanie network is being developed to improve the organization and quality of care. The aim of this study was to identify the expectations of patients regarding this network.
Methods: We conducted a descriptive epidemiological study using an online questionnaire administered through the LimeSurvey platform and distributed via the patient associations EndoFrance, Endomind, and the EndOccitanie network. Participants, all diagnosed with endometriosis, evaluated various aspects of their care pathway using a Likert scale.
Results: The results highlight several priority expectations: access to clear and reliable information, the implementation of a coordinated and accessible care pathway, and a comprehensive approach to the disease, including pain management, sexuality, and fertility.
Conclusion: These findings underscore the need to further strengthen the structuring of the EndOccitanie network in order to improve the accessibility, continuity, and quality of care. A future reassessment will help measure the impact of the actions implemented.
{"title":"[Evaluation of the expectations of patients with endometriosis regarding the EndOccitanie care network].","authors":"Alexa Miran, Thierry Brillac, Elodie Chantalat","doi":"10.1016/j.gofs.2026.08.002","DOIUrl":"https://doi.org/10.1016/j.gofs.2026.08.002","url":null,"abstract":"<p><strong>Objective: </strong>The management of patients with endometriosis remains marked by a long, fragmented, and poorly coordinated care pathway, leading to significant diagnostic delay. In this context, the regional EndOccitanie network is being developed to improve the organization and quality of care. The aim of this study was to identify the expectations of patients regarding this network.</p><p><strong>Methods: </strong>We conducted a descriptive epidemiological study using an online questionnaire administered through the LimeSurvey platform and distributed via the patient associations EndoFrance, Endomind, and the EndOccitanie network. Participants, all diagnosed with endometriosis, evaluated various aspects of their care pathway using a Likert scale.</p><p><strong>Results: </strong>The results highlight several priority expectations: access to clear and reliable information, the implementation of a coordinated and accessible care pathway, and a comprehensive approach to the disease, including pain management, sexuality, and fertility.</p><p><strong>Conclusion: </strong>These findings underscore the need to further strengthen the structuring of the EndOccitanie network in order to improve the accessibility, continuity, and quality of care. A future reassessment will help measure the impact of the actions implemented.</p>","PeriodicalId":56056,"journal":{"name":"Gynecologie Obstetrique Fertilite & Senologie","volume":" ","pages":""},"PeriodicalIF":1.0,"publicationDate":"2026-08-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148765348","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 : 2026-08-07DOI: 10.1016/j.gofs.2026.08.001
Marie Le Naelou, Thibault Thubert, Manon Degez, Maxime Chaillot
Objectives: Management of pregnancies of unknown location (PUL) relies on close monitoring with serial human chorionic gonadotropin (hCG) measurements and repeated ultrasound examinations to exclude ectopic pregnancy (EP). Although safe, this strategy leads to multiple consultations and significant organizational and economic burden. This paper aims to develop and preliminarily validate a simplified clinical algorithm to stratify the risk of EP in women presenting with PUL, in order to adapt follow-up frequency.
Methods: The prospective monocentric OPTIGLI study was conducted at Nantes University Hospital between May and September 2023. All women presenting with PUL were included after informed non-opposition. Fifteen clinical, biological, and ultrasound variables were analyzed using univariate and multivariate logistic regression. A composite predictive score was constructed from significant variables, and its positive predictive value (PPV) and negative predictive value (NPV) were calculated. Economic evaluation and patient satisfaction assessment were also performed.
Results: A total of 162 patients were included; the EP rate was 19.8%. Pregnancy occurring with a copper intrauterine device (IUD) was significantly associated with EP (p = 0.0089). The presence of a lateral uterine mass was associated with earlier EP diagnosis (p = 0.0169). The algorithm showed an NPV of 99.0% and a PPV of 22.0%, allowing reduced follow-up intensity in two-thirds of patients, with an estimated cost reduction of nearly euro10,000 over four months.
Conclusion: The OPTIGLI algorithm is a simple and safe tool for rationalizing PUL management. Multicenter validation is required to confirm its robustness and potential integration into national clinical protocols.
{"title":"[Optimizing follow-up of pregnancies of unknown location: a simplified clinical algorithm for ectopic pregnancy risk].","authors":"Marie Le Naelou, Thibault Thubert, Manon Degez, Maxime Chaillot","doi":"10.1016/j.gofs.2026.08.001","DOIUrl":"https://doi.org/10.1016/j.gofs.2026.08.001","url":null,"abstract":"<p><strong>Objectives: </strong>Management of pregnancies of unknown location (PUL) relies on close monitoring with serial human chorionic gonadotropin (hCG) measurements and repeated ultrasound examinations to exclude ectopic pregnancy (EP). Although safe, this strategy leads to multiple consultations and significant organizational and economic burden. This paper aims to develop and preliminarily validate a simplified clinical algorithm to stratify the risk of EP in women presenting with PUL, in order to adapt follow-up frequency.</p><p><strong>Methods: </strong>The prospective monocentric OPTIGLI study was conducted at Nantes University Hospital between May and September 2023. All women presenting with PUL were included after informed non-opposition. Fifteen clinical, biological, and ultrasound variables were analyzed using univariate and multivariate logistic regression. A composite predictive score was constructed from significant variables, and its positive predictive value (PPV) and negative predictive value (NPV) were calculated. Economic evaluation and patient satisfaction assessment were also performed.</p><p><strong>Results: </strong>A total of 162 patients were included; the EP rate was 19.8%. Pregnancy occurring with a copper intrauterine device (IUD) was significantly associated with EP (p = 0.0089). The presence of a lateral uterine mass was associated with earlier EP diagnosis (p = 0.0169). The algorithm showed an NPV of 99.0% and a PPV of 22.0%, allowing reduced follow-up intensity in two-thirds of patients, with an estimated cost reduction of nearly euro10,000 over four months.</p><p><strong>Conclusion: </strong>The OPTIGLI algorithm is a simple and safe tool for rationalizing PUL management. Multicenter validation is required to confirm its robustness and potential integration into national clinical protocols.</p>","PeriodicalId":56056,"journal":{"name":"Gynecologie Obstetrique Fertilite & Senologie","volume":" ","pages":""},"PeriodicalIF":1.0,"publicationDate":"2026-08-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148690347","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 : 2026-08-05DOI: 10.1016/j.gofs.2026.07.007
Philippe Bouhanna
{"title":"[Getting it right in fetal ultrasound: the demands of the scan, medico-legal responsibility, and humane disclosure].","authors":"Philippe Bouhanna","doi":"10.1016/j.gofs.2026.07.007","DOIUrl":"https://doi.org/10.1016/j.gofs.2026.07.007","url":null,"abstract":"","PeriodicalId":56056,"journal":{"name":"Gynecologie Obstetrique Fertilite & Senologie","volume":" ","pages":""},"PeriodicalIF":1.0,"publicationDate":"2026-08-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148681179","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 : 2026-07-27DOI: 10.1016/j.gofs.2026.07.005
Franck Perrotin, Amaury Poque, Amandine Le Bert, Alexander Pondaven
Apart from calcium supplementation, which is beneficial in women with inadequate intake, low-dose aspirin is the only drug with established efficacy for the primary prevention of preeclampsia. Its mechanism - restoration of the thromboxane A2 / prostacyclin balance through platelet cyclo-oxygenase-1 inhibition - accounts for its efficacy in placental vascular disease, and its benefit depends on a dose of 100 to 160 mg, evening intake and, above all, initiation before 16 weeks. The question is no longer whether it works, but in whom, and whether this can be known early enough. Three early identification strategies have been evaluated in turn. Clinical risk factors, used by the historical trials and then by Anglo-Saxon guidelines, are either too restrictive - a history of preeclampsia by construction excludes nulliparous women - or so broad that up to 85% of women would become eligible. First-trimester uterine artery Doppler, a direct reflection of trophoblastic invasion, offered an attractive pathophysiological rationale; the double-blind randomised trials nevertheless proved negative, including the French PERASTUN trial conducted in 1,104 nulliparous women selected on this criterion alone and treated with 160 mg before 16 weeks (16.0% vs 14.4%), Doppler alone lacking specificity and selecting a population with low absolute risk whose preeclampsia is mostly late - precisely where aspirin has no effect. Combined algorithms, associating maternal factors, mean arterial pressure, Doppler and PlGF, perform better: the ASPRE trial reduced preeclampsia before 37 weeks of gestation by 62%, though part of the benefit arose from women already identifiable by their history; the ongoing French RANSPRE trial randomises the screening strategy itself for the first time. This uncertainty about the target population explains the marked heterogeneity of international guidelines and bears directly on safety: while the fetal profile remains reassuring at antiplatelet doses, recent maternal data, including a French nationwide cohort of 5.8 million pregnancies, show an excess of haemorrhagic complications. Defining whom to treat is the condition for preserving a favourable benefit-risk balance.
除了补钙对摄入不足的妇女有益外,低剂量阿司匹林是唯一一种确定对子痫前期一级预防有效的药物。其机制-通过血小板环氧化酶-1抑制恢复血栓素A2 /前列环素平衡-解释了其对胎盘血管疾病的疗效,其益处取决于100至160毫克的剂量,晚上摄入,最重要的是,在16周之前开始。问题不再是它是否起作用,而是在谁身上起作用,以及能否及早发现。先后评价了三种早期识别策略。临床风险因素,由历史试验和盎格鲁撒克逊指导方针使用,要么过于严格——经构建的先兆子痫病史排除了未生育的妇女——要么太广泛,高达85%的妇女将符合条件。孕早期子宫动脉多普勒,滋养层浸润的直接反映,提供了一个有吸引力的病理生理理论基础;然而,双盲随机试验证明是阴性的,包括法国PERASTUN试验,该试验在1104名未生育妇女中进行,仅根据该标准选择,16周前服用160毫克(16.0% vs 14.4%),多普勒单独缺乏特异性,选择绝对风险低的人群,其先兆子痫大多发生在晚期-正是阿司匹林没有作用的时候。将母体因素、平均动脉压、多普勒和PlGF相关联的综合算法表现更好:ASPRE试验将妊娠37周前的子痫前期减少了62%,尽管部分益处来自于已经有病史的女性;正在进行的法国RANSPRE试验首次将筛查策略本身随机化。目标人群的这种不确定性解释了国际指南的显著异质性,并直接影响到安全性:虽然胎儿在抗血小板剂量下的情况仍然令人放心,但最近的产妇数据,包括法国全国580万例妊娠,显示出出血并发症过多。确定治疗对象是保持有利的利益-风险平衡的条件。
{"title":"[Aspirin and pregnancy in the era of early first-trimester screening: efficacy, indications and maternal-fetal safety].","authors":"Franck Perrotin, Amaury Poque, Amandine Le Bert, Alexander Pondaven","doi":"10.1016/j.gofs.2026.07.005","DOIUrl":"https://doi.org/10.1016/j.gofs.2026.07.005","url":null,"abstract":"<p><p>Apart from calcium supplementation, which is beneficial in women with inadequate intake, low-dose aspirin is the only drug with established efficacy for the primary prevention of preeclampsia. Its mechanism - restoration of the thromboxane A2 / prostacyclin balance through platelet cyclo-oxygenase-1 inhibition - accounts for its efficacy in placental vascular disease, and its benefit depends on a dose of 100 to 160 mg, evening intake and, above all, initiation before 16 weeks. The question is no longer whether it works, but in whom, and whether this can be known early enough. Three early identification strategies have been evaluated in turn. Clinical risk factors, used by the historical trials and then by Anglo-Saxon guidelines, are either too restrictive - a history of preeclampsia by construction excludes nulliparous women - or so broad that up to 85% of women would become eligible. First-trimester uterine artery Doppler, a direct reflection of trophoblastic invasion, offered an attractive pathophysiological rationale; the double-blind randomised trials nevertheless proved negative, including the French PERASTUN trial conducted in 1,104 nulliparous women selected on this criterion alone and treated with 160 mg before 16 weeks (16.0% vs 14.4%), Doppler alone lacking specificity and selecting a population with low absolute risk whose preeclampsia is mostly late - precisely where aspirin has no effect. Combined algorithms, associating maternal factors, mean arterial pressure, Doppler and PlGF, perform better: the ASPRE trial reduced preeclampsia before 37 weeks of gestation by 62%, though part of the benefit arose from women already identifiable by their history; the ongoing French RANSPRE trial randomises the screening strategy itself for the first time. This uncertainty about the target population explains the marked heterogeneity of international guidelines and bears directly on safety: while the fetal profile remains reassuring at antiplatelet doses, recent maternal data, including a French nationwide cohort of 5.8 million pregnancies, show an excess of haemorrhagic complications. Defining whom to treat is the condition for preserving a favourable benefit-risk balance.</p>","PeriodicalId":56056,"journal":{"name":"Gynecologie Obstetrique Fertilite & Senologie","volume":" ","pages":""},"PeriodicalIF":1.0,"publicationDate":"2026-07-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148610254","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 : 2026-07-24DOI: 10.1016/j.gofs.2026.07.004
Jérémy Boujenah
{"title":"[Paracetamol use during pregnancy and child neurodevelopmental disorders: what sibling studies add, and the limitations that suggest causal triangulation].","authors":"Jérémy Boujenah","doi":"10.1016/j.gofs.2026.07.004","DOIUrl":"https://doi.org/10.1016/j.gofs.2026.07.004","url":null,"abstract":"","PeriodicalId":56056,"journal":{"name":"Gynecologie Obstetrique Fertilite & Senologie","volume":" ","pages":""},"PeriodicalIF":1.0,"publicationDate":"2026-07-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148585870","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 : 2026-07-18DOI: 10.1016/j.gofs.2026.07.002
Valentine Cordonnier, Frédérique Forestier, Marie Gilles-Baray, Dragos Georgescu, Marie Ottaviani
Objective: The aim of this study is to evaluate the impact of outpatient management on the transfusion rate of blood products for post-mastectomy hematoma since the implementation of the Nursing Support and Post Ambulatory Follow-up Device at Home (DIASPAD).
Method: This is a retrospective monocentric observational study carried out January 1, 2011 and December 31, 2022, at the Henri Becquerel Center. It covers all adult women undergoing total mastectomy with or without associated axillary surgery, without breast reconstruction, who developed a hematoma requiring drainage within 30 days of the initial surgery. The study assesses the use of blood products during hematoma management and compares their use according to two distinct hospitalization modes: conventional hospitalization versus outpatient hospitalization.
Results: During the study period, 80 patients required revision surgery for post-mastectomy hematoma. Twenty-eight of them received a transfusion, i.e. 35%; with no significant difference between the two hospitalization groups: 37.1% in the outpatient group and 33.3% in the conventional group (P=0.72).
Conclusion: Performing mastectomies on an outpatient basis does not appear to have an impact on the utilization rate of blood products when complicated by hematoma.
{"title":"[Impact of outpatient management on the transfusion rate for post-mastectomy hematomas].","authors":"Valentine Cordonnier, Frédérique Forestier, Marie Gilles-Baray, Dragos Georgescu, Marie Ottaviani","doi":"10.1016/j.gofs.2026.07.002","DOIUrl":"10.1016/j.gofs.2026.07.002","url":null,"abstract":"<p><strong>Objective: </strong>The aim of this study is to evaluate the impact of outpatient management on the transfusion rate of blood products for post-mastectomy hematoma since the implementation of the Nursing Support and Post Ambulatory Follow-up Device at Home (DIASPAD).</p><p><strong>Method: </strong>This is a retrospective monocentric observational study carried out January 1, 2011 and December 31, 2022, at the Henri Becquerel Center. It covers all adult women undergoing total mastectomy with or without associated axillary surgery, without breast reconstruction, who developed a hematoma requiring drainage within 30 days of the initial surgery. The study assesses the use of blood products during hematoma management and compares their use according to two distinct hospitalization modes: conventional hospitalization versus outpatient hospitalization.</p><p><strong>Results: </strong>During the study period, 80 patients required revision surgery for post-mastectomy hematoma. Twenty-eight of them received a transfusion, i.e. 35%; with no significant difference between the two hospitalization groups: 37.1% in the outpatient group and 33.3% in the conventional group (P=0.72).</p><p><strong>Conclusion: </strong>Performing mastectomies on an outpatient basis does not appear to have an impact on the utilization rate of blood products when complicated by hematoma.</p>","PeriodicalId":56056,"journal":{"name":"Gynecologie Obstetrique Fertilite & Senologie","volume":" ","pages":""},"PeriodicalIF":1.0,"publicationDate":"2026-07-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148498560","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 : 2026-07-14DOI: 10.1016/j.gofs.2026.07.001
Franck Perrotin, Caroline Brisson
Maternal mobilisation and upright positions during labour are recommended by both the World Health Organization (WHO, 2018) and the French National Authority for Health (HAS, 2017) for low-risk women, and more recently by the 2025 SFAR-CARO-HAS guidelines on neuraxial analgesia. Physiologically, upright positions and postural changes optimise uterine dynamics through gravity, improve utero-placental perfusion by preventing aorto-caval compression, and take advantage of pelvic mobility which modifies the diameters of the pelvic inlet and outlet by several millimetres. Cochrane systematic reviews suggest that during the first stage of labour, upright positions and ambulation shorten labour duration and reduce the use of epidural analgesia, with moderate-quality evidence limited by methodological heterogeneity and risk of bias. During the second stage, upright positions shorten expulsion in women without epidural; the BUMPES trial and recent meta-analyses by Verastegui-Martín and Pan do not show a major clinical benefit of upright positions under low-dose epidural, although no detrimental effects are identified. According to the 2021 French Perinatal Survey, 82.7% of women received epidural analgesia and 74.2% used PCEA. Despite consistent guidelines, mobilisation remains underused. Barriers are organisational, technical (including the lack of one-to-one midwifery care), cultural and related to maternal preferences. Promoting a culture of mobility requires interprofessional training, suitable equipment and early antenatal information.
{"title":"[Benefits of maternal mobility during labour: Between international guidelines and clinical practice].","authors":"Franck Perrotin, Caroline Brisson","doi":"10.1016/j.gofs.2026.07.001","DOIUrl":"10.1016/j.gofs.2026.07.001","url":null,"abstract":"<p><p>Maternal mobilisation and upright positions during labour are recommended by both the World Health Organization (WHO, 2018) and the French National Authority for Health (HAS, 2017) for low-risk women, and more recently by the 2025 SFAR-CARO-HAS guidelines on neuraxial analgesia. Physiologically, upright positions and postural changes optimise uterine dynamics through gravity, improve utero-placental perfusion by preventing aorto-caval compression, and take advantage of pelvic mobility which modifies the diameters of the pelvic inlet and outlet by several millimetres. Cochrane systematic reviews suggest that during the first stage of labour, upright positions and ambulation shorten labour duration and reduce the use of epidural analgesia, with moderate-quality evidence limited by methodological heterogeneity and risk of bias. During the second stage, upright positions shorten expulsion in women without epidural; the BUMPES trial and recent meta-analyses by Verastegui-Martín and Pan do not show a major clinical benefit of upright positions under low-dose epidural, although no detrimental effects are identified. According to the 2021 French Perinatal Survey, 82.7% of women received epidural analgesia and 74.2% used PCEA. Despite consistent guidelines, mobilisation remains underused. Barriers are organisational, technical (including the lack of one-to-one midwifery care), cultural and related to maternal preferences. Promoting a culture of mobility requires interprofessional training, suitable equipment and early antenatal information.</p>","PeriodicalId":56056,"journal":{"name":"Gynecologie Obstetrique Fertilite & Senologie","volume":" ","pages":""},"PeriodicalIF":1.0,"publicationDate":"2026-07-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148450535","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 : 2026-07-07DOI: 10.1016/j.gofs.2026.06.007
Lisa Joulot, Jeanne Sibiude, Pierre Delorme, Anne Pinton
Objective: Historically used for screening gestational diabetes, testing for glycosuria during pregnancy is now controversial. Despite the low diagnostic performance of this test, the "Haute Autorité de Santé" (HAS) recommends performing it at each prenatal visit. However, this practice represents an estimated annual cost of 2 million euros in France. The aim of this study was to evaluate French practices regarding glycosuria prescription and the management adopted by practitioners in case of a positive result.
Materials and methods: An observational study was conducted using a questionnaire distributed to healthcare professionals in France between August 31, 2024, and April 1, 2025. A univariate comparative analysis was performed according to whether glycosuria was prescribed or not, and according to the management implemented in cases of positive glycosuria.
Results: A total of 1132 responses were collected. Glycosuria was prescribed by 62% of respondents during pregnancy follow-up. In the event of a positive result, 45% of practitioners took no action, 45% prescribed screening for gestational diabetes using fasting blood glucose or an oral glucose tolerance test (OGTT), and 10% reinforced dietary and lifestyle advice during the consultation. Glycosuria prescription was significantly more frequent among midwives (P=0.04), practitioners working in private practice (P=0.01), in private healthcare facilities (P=0.04), and in type 1 maternity units (P=0.01).
Conclusion: Glycosuria continues to be prescribed by the majority of practitioners, but with highly heterogeneous practices across France and without evaluation of its effectiveness. Glycosuria testing is costly, and its performance in screening for gestational diabetes has not been demonstrated. Reassessment of its role in prenatal care in France appears necessary.
{"title":"[Screening and management of monthly glycosuria in pregnancy follow-up: An overview of clinical practices in France].","authors":"Lisa Joulot, Jeanne Sibiude, Pierre Delorme, Anne Pinton","doi":"10.1016/j.gofs.2026.06.007","DOIUrl":"10.1016/j.gofs.2026.06.007","url":null,"abstract":"<p><strong>Objective: </strong>Historically used for screening gestational diabetes, testing for glycosuria during pregnancy is now controversial. Despite the low diagnostic performance of this test, the \"Haute Autorité de Santé\" (HAS) recommends performing it at each prenatal visit. However, this practice represents an estimated annual cost of 2 million euros in France. The aim of this study was to evaluate French practices regarding glycosuria prescription and the management adopted by practitioners in case of a positive result.</p><p><strong>Materials and methods: </strong>An observational study was conducted using a questionnaire distributed to healthcare professionals in France between August 31, 2024, and April 1, 2025. A univariate comparative analysis was performed according to whether glycosuria was prescribed or not, and according to the management implemented in cases of positive glycosuria.</p><p><strong>Results: </strong>A total of 1132 responses were collected. Glycosuria was prescribed by 62% of respondents during pregnancy follow-up. In the event of a positive result, 45% of practitioners took no action, 45% prescribed screening for gestational diabetes using fasting blood glucose or an oral glucose tolerance test (OGTT), and 10% reinforced dietary and lifestyle advice during the consultation. Glycosuria prescription was significantly more frequent among midwives (P=0.04), practitioners working in private practice (P=0.01), in private healthcare facilities (P=0.04), and in type 1 maternity units (P=0.01).</p><p><strong>Conclusion: </strong>Glycosuria continues to be prescribed by the majority of practitioners, but with highly heterogeneous practices across France and without evaluation of its effectiveness. Glycosuria testing is costly, and its performance in screening for gestational diabetes has not been demonstrated. Reassessment of its role in prenatal care in France appears necessary.</p>","PeriodicalId":56056,"journal":{"name":"Gynecologie Obstetrique Fertilite & Senologie","volume":" ","pages":""},"PeriodicalIF":1.0,"publicationDate":"2026-07-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148406996","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Objective: Since the LACC trial, the ESGO has favoured laparotomy over laparoscopy for radical hysterectomy in early-stage cervical cancer. The aim of our study was to compare recurrence-free survival (RFS) and morbidity between laparoscopy and laparotomy.
Materials and methods: A single-centre, retrospective observational study (2005-2024) of patients treated with type C radical hysterectomy for stage IA2-IIA1 cervical cancer. The use of an intrauterine manipulator without creating a vaginal collar was routine in laparoscopic surgery.
Results: One hundred and two female patients were included, 65 of whom underwent laparoscopic surgery and 37 laparotomy. With a mean follow-up of 6.2 years, no significant difference was observed in terms of disease-free survival (81.6% for laparoscopy vs 74.2% for laparotomy; P=0.24). After adjusting for stage and conisation, the hazard ratio for recurrence following laparotomy was 1.74 (95% CI: [0.67-4.51]). Long-term overall survival showed no difference between the surgical approaches. Laparoscopy offered significant advantages in terms of blood loss (140.6±264ml vs 228±229ml; P<0.05) and length of hospital stay (4.3±2.6 days vs 7.0±2.8 days; P<0.05). Major complications (Clavien-Dindo III-IV) were similar (7.7% with laparoscopy vs 5.4% with laparotomy; P=0.65).
Conclusion: When performed by surgeons trained to deal with tumours of a medium size (<2cm), laparoscopy did not compromise overall survival compared with laparotomy, whilst significantly reducing perioperative morbidity.
目的:自LACC试验以来,ESGO更倾向于剖腹手术而不是腹腔镜进行早期宫颈癌根治性子宫切除术。本研究的目的是比较腹腔镜和开腹手术的无复发生存率(RFS)和发病率。材料和方法:一项单中心、回顾性观察研究(2005-2024),对IA2-IIA1期宫颈癌患者行C型根治性子宫切除术。在腹腔镜手术中,使用宫内机械手而不制造阴道项圈是常规的。结果:纳入102例女性患者,其中腹腔镜手术65例,开腹手术37例。平均随访6.2年,无病生存率无显著差异(腹腔镜组为81.6%,开腹组为74.2%,p=0.24)。在调整分期和锥度后,剖腹手术后复发的风险比为1.74 (95% CI:[0.67-4.51])。两种手术入路的长期总生存率无差异。腹腔镜在失血量方面具有显著优势(140.6±264 ml vs 228±229 ml)。结论:当接受过中等大小肿瘤治疗训练的外科医生进行腹腔镜手术时(
{"title":"[Long-term oncological outcomes and morbidity and mortality associated with radical hysterectomy by laparoscopy versus laparotomy for early-stage cervical cancer].","authors":"Cristina Zabrian, Antoine Vanoost, Pierrick Theret, Albine Mancaux, Denis Chatelain, Fabrice Sergent","doi":"10.1016/j.gofs.2026.06.008","DOIUrl":"10.1016/j.gofs.2026.06.008","url":null,"abstract":"<p><strong>Objective: </strong>Since the LACC trial, the ESGO has favoured laparotomy over laparoscopy for radical hysterectomy in early-stage cervical cancer. The aim of our study was to compare recurrence-free survival (RFS) and morbidity between laparoscopy and laparotomy.</p><p><strong>Materials and methods: </strong>A single-centre, retrospective observational study (2005-2024) of patients treated with type C radical hysterectomy for stage IA2-IIA1 cervical cancer. The use of an intrauterine manipulator without creating a vaginal collar was routine in laparoscopic surgery.</p><p><strong>Results: </strong>One hundred and two female patients were included, 65 of whom underwent laparoscopic surgery and 37 laparotomy. With a mean follow-up of 6.2 years, no significant difference was observed in terms of disease-free survival (81.6% for laparoscopy vs 74.2% for laparotomy; P=0.24). After adjusting for stage and conisation, the hazard ratio for recurrence following laparotomy was 1.74 (95% CI: [0.67-4.51]). Long-term overall survival showed no difference between the surgical approaches. Laparoscopy offered significant advantages in terms of blood loss (140.6±264ml vs 228±229ml; P<0.05) and length of hospital stay (4.3±2.6 days vs 7.0±2.8 days; P<0.05). Major complications (Clavien-Dindo III-IV) were similar (7.7% with laparoscopy vs 5.4% with laparotomy; P=0.65).</p><p><strong>Conclusion: </strong>When performed by surgeons trained to deal with tumours of a medium size (<2cm), laparoscopy did not compromise overall survival compared with laparotomy, whilst significantly reducing perioperative morbidity.</p>","PeriodicalId":56056,"journal":{"name":"Gynecologie Obstetrique Fertilite & Senologie","volume":" ","pages":""},"PeriodicalIF":1.0,"publicationDate":"2026-07-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148407011","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}