Pub Date : 2026-01-25DOI: 10.3760/cma.j.cn112141-20250627-00301
L Ma, X Yang, R M Liu, H Wu, J Liu, C M Sun
<p><p><b>Objective:</b> To investigate the application of single nucleotide polymorphism array (SNP array) in the detection of fetal cardiac dysplasia and to explore the characteristics of chromosomal variants associated with fetal cardiac dysplasia in the local population. <b>Methods:</b> A total of 556 pregnant women who underwent SNP array examination in Yantai Yuhuangding Hospital Affiliated to Medical College of Qingdao University from January 2021 to December 2024 because of abnormal soft index or structural malformations of fetal heart development by ultrasound examination were collected. According to the results of fetal ultrasound examination, they were divided into single abnormal soft markers group (237 cases), multiple abnormal soft index group (232 cases), soft index combined with cardiac structural abnormalities group (24 cases), isolated cardiac structural abnormalities group (47 cases), and cardiac structural abnormalities combined with other systemic abnormalities group (16 cases). According to the age of pregnant women, they were divided into ≤25 years old group (20 cases), 26-29 years old group (155 cases), 30-34 years old group (190 cases), 35-39 years old group (149 cases) and ≥40 years old group (42 cases). The differences in the detection of chromosomal abnormalities in pregnant women with different echocardiographic results and different ages were compared. <b>Results:</b> (1) Among the 556 pregnant women who underwent SNP array for fetal cardiac anomalies, 110 cases of fetal chromosomal variations were detected, with a detection rate of 19.8% (110/556), including 72 cases of pathogenic variations (12.9%, 72/556) and 38 cases of variants of uncertain significance (VUS; 6.8%, 38/556). Pathogenic copy number variations (CNV) involved 9 chromosomes, with 3q29, 16p13.11, 17p13.3p13.2 and 22q11.21 being the most common. (2) Among the pregnant women with different ultrasound results, the highest detection rate of fetal chromosomal variation was in the group with cardiac structural abnormalities combined with other systemic abnormalities, with a detection rate of 10/16. The detection rates of single abnormal soft index group, multiple abnormal soft index group, soft index combined with cardiac structural abnormalities group and isolated cardiac structural abnormalities group were 17.3% (41/237), 18.1% (42/232), 41.7% (10/24) and 14.9% (7/47), respectively, and the differences were statistically significant (<i>χ</i><sup>2</sup>=27.680, <i>P</i><0.001). (3) In different age groups, the detection rate of chromosome aneuploidy increased with age, and the detection rate of ≥40 years old group (16.7%, 7/42) was the highest. There was no significant difference in the detection rate of pathogenic CNV, VUS and chromosomal abnormalities among different age groups (all <i>P</i>>0.05). <b>Conclusions:</b> SNP array technology has important application value in prenatal diagnosis of fetal cardiac anomalies. The study on the characteristics o
{"title":"[Detection of fetal cardiac dysgenesis by SNP array technology and the variation hotspots of the local population].","authors":"L Ma, X Yang, R M Liu, H Wu, J Liu, C M Sun","doi":"10.3760/cma.j.cn112141-20250627-00301","DOIUrl":"https://doi.org/10.3760/cma.j.cn112141-20250627-00301","url":null,"abstract":"<p><p><b>Objective:</b> To investigate the application of single nucleotide polymorphism array (SNP array) in the detection of fetal cardiac dysplasia and to explore the characteristics of chromosomal variants associated with fetal cardiac dysplasia in the local population. <b>Methods:</b> A total of 556 pregnant women who underwent SNP array examination in Yantai Yuhuangding Hospital Affiliated to Medical College of Qingdao University from January 2021 to December 2024 because of abnormal soft index or structural malformations of fetal heart development by ultrasound examination were collected. According to the results of fetal ultrasound examination, they were divided into single abnormal soft markers group (237 cases), multiple abnormal soft index group (232 cases), soft index combined with cardiac structural abnormalities group (24 cases), isolated cardiac structural abnormalities group (47 cases), and cardiac structural abnormalities combined with other systemic abnormalities group (16 cases). According to the age of pregnant women, they were divided into ≤25 years old group (20 cases), 26-29 years old group (155 cases), 30-34 years old group (190 cases), 35-39 years old group (149 cases) and ≥40 years old group (42 cases). The differences in the detection of chromosomal abnormalities in pregnant women with different echocardiographic results and different ages were compared. <b>Results:</b> (1) Among the 556 pregnant women who underwent SNP array for fetal cardiac anomalies, 110 cases of fetal chromosomal variations were detected, with a detection rate of 19.8% (110/556), including 72 cases of pathogenic variations (12.9%, 72/556) and 38 cases of variants of uncertain significance (VUS; 6.8%, 38/556). Pathogenic copy number variations (CNV) involved 9 chromosomes, with 3q29, 16p13.11, 17p13.3p13.2 and 22q11.21 being the most common. (2) Among the pregnant women with different ultrasound results, the highest detection rate of fetal chromosomal variation was in the group with cardiac structural abnormalities combined with other systemic abnormalities, with a detection rate of 10/16. The detection rates of single abnormal soft index group, multiple abnormal soft index group, soft index combined with cardiac structural abnormalities group and isolated cardiac structural abnormalities group were 17.3% (41/237), 18.1% (42/232), 41.7% (10/24) and 14.9% (7/47), respectively, and the differences were statistically significant (<i>χ</i><sup>2</sup>=27.680, <i>P</i><0.001). (3) In different age groups, the detection rate of chromosome aneuploidy increased with age, and the detection rate of ≥40 years old group (16.7%, 7/42) was the highest. There was no significant difference in the detection rate of pathogenic CNV, VUS and chromosomal abnormalities among different age groups (all <i>P</i>>0.05). <b>Conclusions:</b> SNP array technology has important application value in prenatal diagnosis of fetal cardiac anomalies. The study on the characteristics o","PeriodicalId":10050,"journal":{"name":"中华妇产科杂志","volume":"61 1","pages":"23-29"},"PeriodicalIF":0.0,"publicationDate":"2026-01-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146084436","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-25DOI: 10.3760/cma.j.cn112141-20250421-00161
A M Zhao, Y Wang, W W Yang, Z Q Liang, F J Shen, C Z Li, Z T Wei, X J Sheng, W Yuan, Q Li, F Ming, Y H Zheng, X Y Lu, H Ye, J J Li, B Lye, H J Ruan, Y Z Zhang, Y X Li, W R Li, H K Yang, Y L Zheng, X J Dong, H Lu, S Y Hou, P Yan, Y Q Ge, J L Kang, L N Wang, H Y Zhang, Y Hu, R F Zhao, Y L Wang, S Y Zhang, L P Han, L Sang, M H Cui, J J Zhai, D Lu, Y Zheng, Y Z Guo, M L Chen, L P Sun, J Lu, S J Guo, X H Zhang, W Feng, L H Yang
<p><p><b>Objective:</b> To evaluate the efficacy and safety of triptorelin acetate microspheres for injection compared with triptorelin acetate for injection in the treatment of endometriosis. <b>Methods:</b> A total of 392 patients with endometriosis were prospectively enrolled from 47 research centers across China between October 25, 2021, and February 14, 2023. Participants were randomly assigned in a 1∶1 ratio to either the experimental group (<i>n</i>=196) or the control group (<i>n</i>=196). Both groups received intramuscular injections of the respective drugs once every 4 weeks for a total of 6 doses. The primary efficacy endpoint was the percentage of subjects with suppressed estradiol levels after treatment. Secondary endpoints included pain relief, amenorrhea rate, changes in ovarian endometrioma diameter, and adverse drug reactions. <b>Results:</b> For the primary efficacy endpoint, the percentages of subjects with suppressed estradiol levels at week 12 in the experimental and control groups were 97.3% (177/182) and 98.4% (181/184), respectively. The rate difference was -1.1% (95%<i>CI</i>: -4.8% to 2.3%), the lower limit of the 95%<i>CI</i> for the rate difference was greater than the non-inferiority margin of -10%. Compared to baseline, visual analog scale (VAS) scores for dysmenorrhea and non-menstrual pelvic pain decreased at all post-treatment time points in both groups, with no statistically significant differences between two groups (all <i>P</i>>0.05). Estradiol, luteinizing hormone, and follicle stimulating hormone levels significantly decreased from baseline at all post-treatment time points in both groups (all <i>P</i><0.05), with no significant intergroup differences (all <i>P</i>>0.05). No significant differences were observed in amenorrhea rates between two groups at week 8, 12, and 24 post-treatment (all <i>P</i>>0.05). However, the time to menstruation recovery after drug discontinuation was significantly earlier in the experimental group than that in the control group (<i>P</i>=0.003). Carbohydrate antigen 125 levels significantly decreased from baseline at week 12 and 24 post-treatment in both groups (all <i>P</i><0.001), but no significant intergroup differences were found (all <i>P</i>>0.05). In the experimental group, only the diameter of the right ovarian endometrioma showed a significant decrease from baseline at week 24 post-treatment (<i>P</i>=0.016). In the control group, neither left nor right ovarian endometrioma diameters showed significant changes from baseline (all <i>P</i>>0.05). The overall incidence of adverse drug reactions was similar between the experimental and control groups [77.6% (152/196) vs 78.6% (154/196), respectively; <i>P</i>>0.05]. <b>Conclusions:</b> Triptorelin acetate microspheres for injection is an effective treatment for endometriosis. It could maintain low estrogen levels, consistently alleviate endometriosis-associated pain, achieve a high rate of amenorrhea during treatment, and
{"title":"[Efficacy and safety of triptorelin acetate microspheres for injection versus triptorelin acetate for injection in Chinese patients with endometriosis: a multicenter, randomized, double-blind, phase Ⅲ non-inferiority clinical trial].","authors":"A M Zhao, Y Wang, W W Yang, Z Q Liang, F J Shen, C Z Li, Z T Wei, X J Sheng, W Yuan, Q Li, F Ming, Y H Zheng, X Y Lu, H Ye, J J Li, B Lye, H J Ruan, Y Z Zhang, Y X Li, W R Li, H K Yang, Y L Zheng, X J Dong, H Lu, S Y Hou, P Yan, Y Q Ge, J L Kang, L N Wang, H Y Zhang, Y Hu, R F Zhao, Y L Wang, S Y Zhang, L P Han, L Sang, M H Cui, J J Zhai, D Lu, Y Zheng, Y Z Guo, M L Chen, L P Sun, J Lu, S J Guo, X H Zhang, W Feng, L H Yang","doi":"10.3760/cma.j.cn112141-20250421-00161","DOIUrl":"https://doi.org/10.3760/cma.j.cn112141-20250421-00161","url":null,"abstract":"<p><p><b>Objective:</b> To evaluate the efficacy and safety of triptorelin acetate microspheres for injection compared with triptorelin acetate for injection in the treatment of endometriosis. <b>Methods:</b> A total of 392 patients with endometriosis were prospectively enrolled from 47 research centers across China between October 25, 2021, and February 14, 2023. Participants were randomly assigned in a 1∶1 ratio to either the experimental group (<i>n</i>=196) or the control group (<i>n</i>=196). Both groups received intramuscular injections of the respective drugs once every 4 weeks for a total of 6 doses. The primary efficacy endpoint was the percentage of subjects with suppressed estradiol levels after treatment. Secondary endpoints included pain relief, amenorrhea rate, changes in ovarian endometrioma diameter, and adverse drug reactions. <b>Results:</b> For the primary efficacy endpoint, the percentages of subjects with suppressed estradiol levels at week 12 in the experimental and control groups were 97.3% (177/182) and 98.4% (181/184), respectively. The rate difference was -1.1% (95%<i>CI</i>: -4.8% to 2.3%), the lower limit of the 95%<i>CI</i> for the rate difference was greater than the non-inferiority margin of -10%. Compared to baseline, visual analog scale (VAS) scores for dysmenorrhea and non-menstrual pelvic pain decreased at all post-treatment time points in both groups, with no statistically significant differences between two groups (all <i>P</i>>0.05). Estradiol, luteinizing hormone, and follicle stimulating hormone levels significantly decreased from baseline at all post-treatment time points in both groups (all <i>P</i><0.05), with no significant intergroup differences (all <i>P</i>>0.05). No significant differences were observed in amenorrhea rates between two groups at week 8, 12, and 24 post-treatment (all <i>P</i>>0.05). However, the time to menstruation recovery after drug discontinuation was significantly earlier in the experimental group than that in the control group (<i>P</i>=0.003). Carbohydrate antigen 125 levels significantly decreased from baseline at week 12 and 24 post-treatment in both groups (all <i>P</i><0.001), but no significant intergroup differences were found (all <i>P</i>>0.05). In the experimental group, only the diameter of the right ovarian endometrioma showed a significant decrease from baseline at week 24 post-treatment (<i>P</i>=0.016). In the control group, neither left nor right ovarian endometrioma diameters showed significant changes from baseline (all <i>P</i>>0.05). The overall incidence of adverse drug reactions was similar between the experimental and control groups [77.6% (152/196) vs 78.6% (154/196), respectively; <i>P</i>>0.05]. <b>Conclusions:</b> Triptorelin acetate microspheres for injection is an effective treatment for endometriosis. It could maintain low estrogen levels, consistently alleviate endometriosis-associated pain, achieve a high rate of amenorrhea during treatment, and ","PeriodicalId":10050,"journal":{"name":"中华妇产科杂志","volume":"61 1","pages":"30-38"},"PeriodicalIF":0.0,"publicationDate":"2026-01-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146084400","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-25DOI: 10.3760/cma.j.cn112141-20250824-00395
W R Zheng, B E Huang, X R Yang, J Yan, H X Yang
Objective: To analyze the reproductive and psychological health status of pregnant women with placenta accreta spectrum disorders (PAS) after fertile-preserving surgery, and to follow up their subsequent pregnancy and delivery. Methods: A total of 269 cases of abnormally invasive placenta (AIP) who underwent pregnancy supervision and surgical treatment in Peking University First Hospital from January 2010 to August 2020 were collected as AIP group. A total of 300 pregnant women without other complications who underwent elective cesarean section due to cesarean section history in the same center and at the same time period were selected as the control group. Their clinical information was collected, and their menstruation, fertility and psychological health were followed up by telephone and online questionnaire. Results: (1) In AIP group, 222 (82.5%, 222/269) valid questionnaires were returned, of which 171 (77.0%, 171/222) completed the subjective scale. The control group returned 254 valid questionnaires (84.7%, 254/300), of which 191 (75.2%, 191/254) filled in the complete subjective scale. There was no significant difference in the demographic characteristics between AIP group and control group (all P>0.05), but the intraoperative blood loss, the incidence of short-term postoperative complications and the length of hospital stay in AIP group were higher than those in control group. (2) There were no differences in reproductive physiological health status, including the time to resume sexual life, menstruation, re-pregnancy, pelvic ultrasound manifestations and long-term complications between AIP group and control group. The fertility intention of AIP group was lower than that of control group [12.3% (25/204) vs 19.3% (49/254)]. (3) In AIP group, 17 women tried to get pregnant again, and 12 of them (12/17) had successful pregnancy and delivered, and no PAS occurred again. (4) FSFI scores of women undergoing hysterectomy (18 cases) were lower than those undergoing fertive-sparing surgery (204 cases) in AIP group, but there was no differences in the proportion of pelvic floor dysfunction and suspicious emotional disorder. Conclusions: The physiological function of pelvic organs in women with AIP can be restored after fertive-preserving surgery, which is similar to that of women with a history of cesarean section. The risk of pelvic floor dysfunction and emotional disorders is not significantly increased after hysterectomy, but the risk of sexual dysfunction is higher. Hysterectomy is not recommended as the first-line treatment for PAS. Women with fertility desire can get pregnant again and deliver by cesarean section, but PAS should be closely monitored for recurrence during pregnancy.
{"title":"[Analysis of reproductive and psychological health of pregnant women with placenta accreta spectrum disorders after fertility-preserving treatment].","authors":"W R Zheng, B E Huang, X R Yang, J Yan, H X Yang","doi":"10.3760/cma.j.cn112141-20250824-00395","DOIUrl":"https://doi.org/10.3760/cma.j.cn112141-20250824-00395","url":null,"abstract":"<p><p><b>Objective:</b> To analyze the reproductive and psychological health status of pregnant women with placenta accreta spectrum disorders (PAS) after fertile-preserving surgery, and to follow up their subsequent pregnancy and delivery. <b>Methods:</b> A total of 269 cases of abnormally invasive placenta (AIP) who underwent pregnancy supervision and surgical treatment in Peking University First Hospital from January 2010 to August 2020 were collected as AIP group. A total of 300 pregnant women without other complications who underwent elective cesarean section due to cesarean section history in the same center and at the same time period were selected as the control group. Their clinical information was collected, and their menstruation, fertility and psychological health were followed up by telephone and online questionnaire. <b>Results:</b> (1) In AIP group, 222 (82.5%, 222/269) valid questionnaires were returned, of which 171 (77.0%, 171/222) completed the subjective scale. The control group returned 254 valid questionnaires (84.7%, 254/300), of which 191 (75.2%, 191/254) filled in the complete subjective scale. There was no significant difference in the demographic characteristics between AIP group and control group (all <i>P</i>>0.05), but the intraoperative blood loss, the incidence of short-term postoperative complications and the length of hospital stay in AIP group were higher than those in control group. (2) There were no differences in reproductive physiological health status, including the time to resume sexual life, menstruation, re-pregnancy, pelvic ultrasound manifestations and long-term complications between AIP group and control group. The fertility intention of AIP group was lower than that of control group [12.3% (25/204) vs 19.3% (49/254)]. (3) In AIP group, 17 women tried to get pregnant again, and 12 of them (12/17) had successful pregnancy and delivered, and no PAS occurred again. (4) FSFI scores of women undergoing hysterectomy (18 cases) were lower than those undergoing fertive-sparing surgery (204 cases) in AIP group, but there was no differences in the proportion of pelvic floor dysfunction and suspicious emotional disorder. <b>Conclusions:</b> The physiological function of pelvic organs in women with AIP can be restored after fertive-preserving surgery, which is similar to that of women with a history of cesarean section. The risk of pelvic floor dysfunction and emotional disorders is not significantly increased after hysterectomy, but the risk of sexual dysfunction is higher. Hysterectomy is not recommended as the first-line treatment for PAS. Women with fertility desire can get pregnant again and deliver by cesarean section, but PAS should be closely monitored for recurrence during pregnancy.</p>","PeriodicalId":10050,"journal":{"name":"中华妇产科杂志","volume":"61 1","pages":"16-22"},"PeriodicalIF":0.0,"publicationDate":"2026-01-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146084438","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-25DOI: 10.3760/cma.j.cn112141-20250705-00310
W L Han, L Chen
Objective: To analyze the clinical characteristics, diagnosis and treatment of pregnancy complicated with diffuse uterine leiomyomatosis (DUL), and to explore the treatment strategies for its complications during pregnancy and perinatal period. Methods: The clinical data of 12 pregnant women with DUL who delivered in Peking University Third Hospital from May 2017 to October 2024 were collected, and their complications during pregnancy and perinatal period, radiological features, and treatment strategies were analyzed. Results: The median age of 12 pregnant women with DUL was 32 years (range: 28 to 38 years), and all of them were primiparas with singleton pregnancy. Among the 12 pregnant women, only 7 cases (7/12) were suspected of DUL by imaging examination during pregnancy. Five cases (5/12) only showed multiple uterine fibroids by ultrasound and magnetic resonance imaging during pregnancy, which were finally diagnosed according to intraoperative exploration. Five cases (5/12) of DUL had signs of threatened abortion or threatened preterm birth such as uterine contraction and bleeding during pregnancy, including 3 cases of preterm birth (2 cases of spontaneous preterm birth and 1 case of iatrogenic preterm birth due to prenatal hemorrhage). Among the 12 pregnant women with DUL, 2 cases (2/12) had abnormal fetal position, 3 cases (3/12) had placental adhesion, and 1 case (1/12) had fibroid degeneration. Among the 12 pregnant women with DUL, 9 cases (9/12) were delivered by cesarean section, of which 3 cases were converted to cesarean section because of failed trial of labor, and 6 cases were directly terminated by cesarean section because of abnormal fetal position or previous myomectomy history. Postpartum hemorrhage occurred in 5 cases (5/12), including 4 cases of severe postpartum hemorrhage, and uterine tamponade had good hemostatic effect. Three cases (3/12) had fever after operation or postpartum. All the 12 pregnant women were discharged in a stable condition. Among the 12 neonates, 2 (2/12) were transferred to the department of pediatrics due to premature birth and finally discharged smoothly. Conclusions: Pregnancy complicated with DUL is a high-risk pregnancy, which increases the risk of complications during gestation, delivery and postpartum. Uterine cavity compression hemostasis may be an effective measure to deal with postpartum hemorrhage.
{"title":"[Clinical analysis of 12 cases of pregnancy complicated with diffuse uterine leiomyomatosis].","authors":"W L Han, L Chen","doi":"10.3760/cma.j.cn112141-20250705-00310","DOIUrl":"https://doi.org/10.3760/cma.j.cn112141-20250705-00310","url":null,"abstract":"<p><p><b>Objective:</b> To analyze the clinical characteristics, diagnosis and treatment of pregnancy complicated with diffuse uterine leiomyomatosis (DUL), and to explore the treatment strategies for its complications during pregnancy and perinatal period. <b>Methods:</b> The clinical data of 12 pregnant women with DUL who delivered in Peking University Third Hospital from May 2017 to October 2024 were collected, and their complications during pregnancy and perinatal period, radiological features, and treatment strategies were analyzed. <b>Results:</b> The median age of 12 pregnant women with DUL was 32 years (range: 28 to 38 years), and all of them were primiparas with singleton pregnancy. Among the 12 pregnant women, only 7 cases (7/12) were suspected of DUL by imaging examination during pregnancy. Five cases (5/12) only showed multiple uterine fibroids by ultrasound and magnetic resonance imaging during pregnancy, which were finally diagnosed according to intraoperative exploration. Five cases (5/12) of DUL had signs of threatened abortion or threatened preterm birth such as uterine contraction and bleeding during pregnancy, including 3 cases of preterm birth (2 cases of spontaneous preterm birth and 1 case of iatrogenic preterm birth due to prenatal hemorrhage). Among the 12 pregnant women with DUL, 2 cases (2/12) had abnormal fetal position, 3 cases (3/12) had placental adhesion, and 1 case (1/12) had fibroid degeneration. Among the 12 pregnant women with DUL, 9 cases (9/12) were delivered by cesarean section, of which 3 cases were converted to cesarean section because of failed trial of labor, and 6 cases were directly terminated by cesarean section because of abnormal fetal position or previous myomectomy history. Postpartum hemorrhage occurred in 5 cases (5/12), including 4 cases of severe postpartum hemorrhage, and uterine tamponade had good hemostatic effect. Three cases (3/12) had fever after operation or postpartum. All the 12 pregnant women were discharged in a stable condition. Among the 12 neonates, 2 (2/12) were transferred to the department of pediatrics due to premature birth and finally discharged smoothly. <b>Conclusions:</b> Pregnancy complicated with DUL is a high-risk pregnancy, which increases the risk of complications during gestation, delivery and postpartum. Uterine cavity compression hemostasis may be an effective measure to deal with postpartum hemorrhage.</p>","PeriodicalId":10050,"journal":{"name":"中华妇产科杂志","volume":"60 12","pages":"926-933"},"PeriodicalIF":0.0,"publicationDate":"2025-12-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145848685","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-25DOI: 10.3760/cma.j.cn112141-20250529-00244
J H Lang, J H Leng, Q Yang, R Li, K Q Hua, G N Zhang, W W Cheng, C D Liu, S Z Yao, Y Dai, X L Fang, H Jiang, Z Q Liang, C Peng, R C Chian, G Y Wang, L J Wang, B R Xia, H Xu, T M Zhang, S M Zhou, Y F Xu, Y J Zhu, W Di
{"title":"[Chinese Expert Consensus on GnRH-a in Obstetrics and Gynecology].","authors":"J H Lang, J H Leng, Q Yang, R Li, K Q Hua, G N Zhang, W W Cheng, C D Liu, S Z Yao, Y Dai, X L Fang, H Jiang, Z Q Liang, C Peng, R C Chian, G Y Wang, L J Wang, B R Xia, H Xu, T M Zhang, S M Zhou, Y F Xu, Y J Zhu, W Di","doi":"10.3760/cma.j.cn112141-20250529-00244","DOIUrl":"https://doi.org/10.3760/cma.j.cn112141-20250529-00244","url":null,"abstract":"","PeriodicalId":10050,"journal":{"name":"中华妇产科杂志","volume":"60 12","pages":"913-925"},"PeriodicalIF":0.0,"publicationDate":"2025-12-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145849051","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-25DOI: 10.3760/cma.j.cn112141-20250428-00177
X Feng, X Qin, F Tan, D M Xu, Q H Qu, L J Hao
Objective: To investigate the risk factors of endometrial polyps (EP) in patients with endometriosis (EM) and to analyze the predictive value of body composition measurement for EP. Methods: From January 1st, 2022 to June 30th, 2024, patients with EM who underwent hysteroscopy combined with laparoscopy in Chongqing Health Center for Women and Children due to "infertility" were enrolled. According to whether they had EP or not, they were divided into EP group and non-EP group. The general data and body composition (including skeletal muscle mass, body fat mass, body fat percentage and visceral fat level, waist-to-hip ratio, neck circumference, chest circumference, arm circumference, thigh circumference, etc.) of the two groups were compared. Univariate and multivariate logistic regression were used to analyze the high-risk factors of EP in infertile patients with EM. Body type was classified according to body fat percentage combined with lean body mass index. Body type classification and normal weight obesity rate were compared between the EP group and the non-EP group. Results: (1) A total of 180 patients with EM were enrolled, including 77 patients (42.8%, 77/180) in the EP group and 103 (57.2%, 103/180) patients in the non-EP group. There were no significant differences in body mass index (BMI), fasting blood glucose and blood lipid levels between the two groups (all P>0.05). The incidence of primary infertility, body fat mass, body fat percentage, visceral fat level, and thigh circumference in the EP group were higher than those in the non-EP group, and the differences were statistically significant (all P<0.05). (2) Multivariate logistic regression analysis showed that age≥30 years old (OR=3.079, 95%CI: 1.594-5.947), primary infertility (OR=2.914, 95%CI: 1.482-5.729), visceral fat level ≥10 grade (OR=2.838, 95%CI: 1.584-5.729) were the risk factors of EP in infertile patients with EM (all P<0.05). (3) In the EP group, there were no significant differences in BMI and body composition between single and multiple polyps, and between the largest polyp diameter <1 cm and ≥1 cm (all P>0.05). (4) The proportion of obese and puffy type in the EP group was higher than that in the non-EP group, and the difference in body type classification between the two groups was statistically significant (P=0.026). The proportion of patients with normal weight obesity in the EP group was significantly higher than that in the non-EP group [92.1% (35/38) vs 64.3% (36/56); χ2=9.480, P=0.002]. Conclusions: The occurrence of EP in infertile patients with EM is closely related to the increase of body fat mass, body fat percentage and visceral fat level, but not to BMI. The measurement of body composition is of great value for assessing the hidden obesity in infertile patients with EM.
{"title":"[Analysis of body composition in infertile patients with endometriosis complicated with endometrial polyps].","authors":"X Feng, X Qin, F Tan, D M Xu, Q H Qu, L J Hao","doi":"10.3760/cma.j.cn112141-20250428-00177","DOIUrl":"https://doi.org/10.3760/cma.j.cn112141-20250428-00177","url":null,"abstract":"<p><p><b>Objective:</b> To investigate the risk factors of endometrial polyps (EP) in patients with endometriosis (EM) and to analyze the predictive value of body composition measurement for EP. <b>Methods:</b> From January 1st, 2022 to June 30th, 2024, patients with EM who underwent hysteroscopy combined with laparoscopy in Chongqing Health Center for Women and Children due to \"infertility\" were enrolled. According to whether they had EP or not, they were divided into EP group and non-EP group. The general data and body composition (including skeletal muscle mass, body fat mass, body fat percentage and visceral fat level, waist-to-hip ratio, neck circumference, chest circumference, arm circumference, thigh circumference, etc.) of the two groups were compared. Univariate and multivariate logistic regression were used to analyze the high-risk factors of EP in infertile patients with EM. Body type was classified according to body fat percentage combined with lean body mass index. Body type classification and normal weight obesity rate were compared between the EP group and the non-EP group. <b>Results:</b> (1) A total of 180 patients with EM were enrolled, including 77 patients (42.8%, 77/180) in the EP group and 103 (57.2%, 103/180) patients in the non-EP group. There were no significant differences in body mass index (BMI), fasting blood glucose and blood lipid levels between the two groups (all <i>P</i>>0.05). The incidence of primary infertility, body fat mass, body fat percentage, visceral fat level, and thigh circumference in the EP group were higher than those in the non-EP group, and the differences were statistically significant (all <i>P</i><0.05). (2) Multivariate logistic regression analysis showed that age≥30 years old (<i>OR</i>=3.079, 95%<i>CI</i>: 1.594-5.947), primary infertility (<i>OR</i>=2.914, 95%<i>CI</i>: 1.482-5.729), visceral fat level ≥10 grade (<i>OR</i>=2.838, 95%<i>CI</i>: 1.584-5.729) were the risk factors of EP in infertile patients with EM (all <i>P</i><0.05). (3) In the EP group, there were no significant differences in BMI and body composition between single and multiple polyps, and between the largest polyp diameter <1 cm and ≥1 cm (all <i>P</i>>0.05). (4) The proportion of obese and puffy type in the EP group was higher than that in the non-EP group, and the difference in body type classification between the two groups was statistically significant (<i>P</i>=0.026). The proportion of patients with normal weight obesity in the EP group was significantly higher than that in the non-EP group [92.1% (35/38) <i>vs</i> 64.3% (36/56); <i>χ</i><sup>2</sup>=9.480, <i>P</i>=0.002]. <b>Conclusions:</b> The occurrence of EP in infertile patients with EM is closely related to the increase of body fat mass, body fat percentage and visceral fat level, but not to BMI. The measurement of body composition is of great value for assessing the hidden obesity in infertile patients with EM.</p>","PeriodicalId":10050,"journal":{"name":"中华妇产科杂志","volume":"60 12","pages":"951-957"},"PeriodicalIF":0.0,"publicationDate":"2025-12-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145849056","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-25DOI: 10.3760/cma.j.cn112141-20250415-00149
X L Jiang, M Y Zhang, H N Su, X Yang
<p><p><b>Objective:</b> To evaluate the efficacy and safety of low-dose mifepristone (10-25 mg) in patients with thromboembolic disorders complicated by heavy menstrual bleeding (HMB). <b>Methods:</b> The data of 13 patients (median age:37 years) with thrombotic disorders and HMB treated with low-dose mifepristone in Peking University People's Hospital from January 2020 to March 2025 were retrospectively analyzed. The changes of acute bleeding control, menstrual blood loss [assessed by pictorial blood loss assessment chart (PBAC)], hemoglobin level, coagulation function and quality of life [assessed by menorrhagia multi-attribute scale (MMAS)] were evaluated. <b>Results:</b> (1) Among the 13 patients, venous thrombosis occurred in 8 cases (8/13), arterial thrombosis in 3 cases (3/13), and other types of thrombosis in 2 cases (2/13), including 1 case of local thrombosis after stent placement for anastomotic stenosis after renal transplantation, requiring long-term aspirin and clopidogrel, and 1 case of arteriovenous fistula thrombosis in a renal failure patient with long-term dialysis. (2) Nine patients (9/13) received antithrombotic medication, 1 patient (1/13) received inferior vena cava filter, and 3 patients (3/13) did not receive antithrombotic therapy due to platelet count <50×10⁹/L and high risk of bleeding. (3) Management of acute bleeding stage: 6 patients with massive vaginal bleeding in emergency department were treated with dose reduction or withdrawal of antithrombotic drugs, 5 cases were treated with intrauterine Foley balloon compression hemostasis combined with mifepristone, 1 case was treated with oral norethindrone combined with mifepristone, and the bleeding was successfully stopped, and the antithrombotic therapy was resumed after 1-2 days. (4) Mifepristone treatment (median course: 6 months): 7 patients without bleeding were treated with oral mifepristone directly. All patients had amenorrhea after 1 month of treatment, and PBAC score (1, 3, 6 months), hemoglobin level and quality of life were significantly improved (all <i>P</i><0.05). During the follow-up period, there was no recurrence or new onset of thrombosis, and there were no statistically significant differences in coagulation function indexes (including prothrombin time, activated partial thromboplastin time, fibrinogen) compared with those before treatment (all <i>P</i>>0.05). The level of D-dimer was lower than that before treatment, considering that it was related to the control of thrombotic diseases. Patients were subsequently transitioned to other modalities for long-term menstrual management. <b>Conclusions:</b> Low-dose mifepristone is a viable bridging therapy for patients with thromboembolic disorders and HMB. It effectively induces amenorrhea, enabling patients to safely navigate high-risk periods for both thrombosis and bleeding without significantly impacting coagulation function. This approach facilitates subsequent long-term menstrual management and tr
{"title":"[Efficacy of low-dose mifepristone in patients with thrombotic disorders complicated by heavy menstrual bleeding].","authors":"X L Jiang, M Y Zhang, H N Su, X Yang","doi":"10.3760/cma.j.cn112141-20250415-00149","DOIUrl":"https://doi.org/10.3760/cma.j.cn112141-20250415-00149","url":null,"abstract":"<p><p><b>Objective:</b> To evaluate the efficacy and safety of low-dose mifepristone (10-25 mg) in patients with thromboembolic disorders complicated by heavy menstrual bleeding (HMB). <b>Methods:</b> The data of 13 patients (median age:37 years) with thrombotic disorders and HMB treated with low-dose mifepristone in Peking University People's Hospital from January 2020 to March 2025 were retrospectively analyzed. The changes of acute bleeding control, menstrual blood loss [assessed by pictorial blood loss assessment chart (PBAC)], hemoglobin level, coagulation function and quality of life [assessed by menorrhagia multi-attribute scale (MMAS)] were evaluated. <b>Results:</b> (1) Among the 13 patients, venous thrombosis occurred in 8 cases (8/13), arterial thrombosis in 3 cases (3/13), and other types of thrombosis in 2 cases (2/13), including 1 case of local thrombosis after stent placement for anastomotic stenosis after renal transplantation, requiring long-term aspirin and clopidogrel, and 1 case of arteriovenous fistula thrombosis in a renal failure patient with long-term dialysis. (2) Nine patients (9/13) received antithrombotic medication, 1 patient (1/13) received inferior vena cava filter, and 3 patients (3/13) did not receive antithrombotic therapy due to platelet count <50×10⁹/L and high risk of bleeding. (3) Management of acute bleeding stage: 6 patients with massive vaginal bleeding in emergency department were treated with dose reduction or withdrawal of antithrombotic drugs, 5 cases were treated with intrauterine Foley balloon compression hemostasis combined with mifepristone, 1 case was treated with oral norethindrone combined with mifepristone, and the bleeding was successfully stopped, and the antithrombotic therapy was resumed after 1-2 days. (4) Mifepristone treatment (median course: 6 months): 7 patients without bleeding were treated with oral mifepristone directly. All patients had amenorrhea after 1 month of treatment, and PBAC score (1, 3, 6 months), hemoglobin level and quality of life were significantly improved (all <i>P</i><0.05). During the follow-up period, there was no recurrence or new onset of thrombosis, and there were no statistically significant differences in coagulation function indexes (including prothrombin time, activated partial thromboplastin time, fibrinogen) compared with those before treatment (all <i>P</i>>0.05). The level of D-dimer was lower than that before treatment, considering that it was related to the control of thrombotic diseases. Patients were subsequently transitioned to other modalities for long-term menstrual management. <b>Conclusions:</b> Low-dose mifepristone is a viable bridging therapy for patients with thromboembolic disorders and HMB. It effectively induces amenorrhea, enabling patients to safely navigate high-risk periods for both thrombosis and bleeding without significantly impacting coagulation function. This approach facilitates subsequent long-term menstrual management and tr","PeriodicalId":10050,"journal":{"name":"中华妇产科杂志","volume":"60 12","pages":"943-950"},"PeriodicalIF":0.0,"publicationDate":"2025-12-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145848854","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-25DOI: 10.3760/cma.j.cn112141-20250712-00320
X Z Zuo, X L Yang, X Mao, J R Yang, L R Lin, E Tian, X Xi, J Huang, L Y Wang, M F Zhou, Y Fan, P Yi, L L Yu
Objective: To summarize the clinical characteristics, management and short-term and long-term outcomes of pregnant women with chronic kidney disease (CKD) stage 4-5. Methods: The clinical data of pregnant women with CKD stage 4-5 admitted by the multidisciplinary team (MDT) of CKD pregnancy management in the Third Affiliated Hospital of Chongqing Medical University from September 2019 to July 2024 were collected and retrospectively analyzed, including medical history, laboratory examination, pregnancy outcome, treatment options, and renal function outcome. To summarize the experience of prenatal counseling, pregnancy management, dialysis indications and lifestyle intervention in pregnant women with CKD stage 4-5. Results: A total of 10 pregnant women with CKD stage 4-5 were enrolled, aged (29.0±4.2) years (range: 23 to 36 years). Among the 10 cases, 3 cases were induced abortion in the second trimester, 1 case had missed abortion in the first trimester, and 6 cases were finally delivered successfully. Renal biopsy was performed in 4 cases to determine the type of primary nephropathy, and genetic testing was performed in 4 cases to confirm the diagnosis of hereditary nephropathy. Among the six CKD stage 4-5 pregnant women who successfully delivered, three started dialysis treatment in the second and third trimesters of pregnancy, and the other three started dialysis treatment immediately, 5.5 months and 18.3 months after delivery, respectively. All pregnant women were terminated by cesarean section and none of them had postpartum hemorrhage. The gestational age at delivery was (33.8±1.1) weeks (range: 32+1 to 35+1 weeks). All neonates were premature, with no fetal death and neonatal death. Two cases were small for gestational age and the other four were appropriate for gestational age. The length of neonatal intensive care unit (NICU) stay was (23.0±11.0) days (range: 10 to 38 days). No serious complications occurred during NICU stay. All newborns grew and developed well during the follow-up period of 10-60 months. Conclusions: CKD stage 4-5 is not an absolute contraindication for pregnancy. Comprehensive evaluation of doctor-patient shared decision-making on the premise of sufficient doctor-patient communication, precise management of MDT, close maternal and fetal monitoring, lifestyle medical intervention and timely initiation of dialysis can help pregnant women with CKD stage 4-5 achieve safe pregnancy and good maternal and fetal outcomes.
{"title":"[Clinical characteristics and maternal and fetal outcomes of pregnancy complicated with chronic kidney disease stage 4-5].","authors":"X Z Zuo, X L Yang, X Mao, J R Yang, L R Lin, E Tian, X Xi, J Huang, L Y Wang, M F Zhou, Y Fan, P Yi, L L Yu","doi":"10.3760/cma.j.cn112141-20250712-00320","DOIUrl":"https://doi.org/10.3760/cma.j.cn112141-20250712-00320","url":null,"abstract":"<p><p><b>Objective:</b> To summarize the clinical characteristics, management and short-term and long-term outcomes of pregnant women with chronic kidney disease (CKD) stage 4-5. <b>Methods:</b> The clinical data of pregnant women with CKD stage 4-5 admitted by the multidisciplinary team (MDT) of CKD pregnancy management in the Third Affiliated Hospital of Chongqing Medical University from September 2019 to July 2024 were collected and retrospectively analyzed, including medical history, laboratory examination, pregnancy outcome, treatment options, and renal function outcome. To summarize the experience of prenatal counseling, pregnancy management, dialysis indications and lifestyle intervention in pregnant women with CKD stage 4-5. <b>Results:</b> A total of 10 pregnant women with CKD stage 4-5 were enrolled, aged (29.0±4.2) years (range: 23 to 36 years). Among the 10 cases, 3 cases were induced abortion in the second trimester, 1 case had missed abortion in the first trimester, and 6 cases were finally delivered successfully. Renal biopsy was performed in 4 cases to determine the type of primary nephropathy, and genetic testing was performed in 4 cases to confirm the diagnosis of hereditary nephropathy. Among the six CKD stage 4-5 pregnant women who successfully delivered, three started dialysis treatment in the second and third trimesters of pregnancy, and the other three started dialysis treatment immediately, 5.5 months and 18.3 months after delivery, respectively. All pregnant women were terminated by cesarean section and none of them had postpartum hemorrhage. The gestational age at delivery was (33.8±1.1) weeks (range: 32<sup>+1</sup> to 35<sup>+1</sup> weeks). All neonates were premature, with no fetal death and neonatal death. Two cases were small for gestational age and the other four were appropriate for gestational age. The length of neonatal intensive care unit (NICU) stay was (23.0±11.0) days (range: 10 to 38 days). No serious complications occurred during NICU stay. All newborns grew and developed well during the follow-up period of 10-60 months. <b>Conclusions:</b> CKD stage 4-5 is not an absolute contraindication for pregnancy. Comprehensive evaluation of doctor-patient shared decision-making on the premise of sufficient doctor-patient communication, precise management of MDT, close maternal and fetal monitoring, lifestyle medical intervention and timely initiation of dialysis can help pregnant women with CKD stage 4-5 achieve safe pregnancy and good maternal and fetal outcomes.</p>","PeriodicalId":10050,"journal":{"name":"中华妇产科杂志","volume":"60 12","pages":"934-942"},"PeriodicalIF":0.0,"publicationDate":"2025-12-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145848898","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-25DOI: 10.3760/cma.j.cn112141-20250423-00166
J Zhang, J Zhao, R R Cui, T T Wang, H Feng, J X Li, J X Dong, Y Zhang
<p><p><b>Objective:</b> To analyze the clinical outcomes of people with abnormal cervical cancer screening results but normal colposcopic findings, and explore the reasons for missed detection high-grade cervical intraepithelial neoplasia Ⅱ and worse (CINⅡ<sup>+</sup>). <b>Methods:</b> People who underwent colposcopy at the Department of Obstetrics and Gynecology, Peking University First Hospital from January 1st, 2019 to December 31st, 2019 were selected. Those with normal colposcopic findings were included, some of them underwent biopsy, others were followed up for one year. Data including thinprep cytologic test (TCT) and high-risk human papillomavirus (HR-HPV)screening results, colposcopic image characteristics, and histopathological outcomes were collected for statistical analysis. Based on cytology results, people with normal colposcopic findings were divided into two groups: the low-risk group [negative for intraepithelial lesion and malignancy (NILM), atypical squamous cell of undetermined signification (ASCUS), and low grade squamous intraepithelial lesion (LSIL)] and the high-risk group [high-grade squamous intraepithelial lesion (HSIL), atypical squamous cells cannot exclude high-grade lesion (ASC-H), and atypical glandular cells (AGC)]. The detection performance of normal colposcopic findings was evaluated by calculating sensitivity, specificity, positive predictive value, negative predictive value and overall accuracy. Furthermore, based on follow-up results, the missed detection rate of CINⅡ<sup>+</sup>in these people and the reasons for missed detection were analyzed. <b>Results:</b> A total of 1 584 women with normal colposcopic findings were included in this study; the median age was 39.0 years. Among them, 1 419 cases were in low-risk group, and 165 cases were in high-risk group. (1) All of the women in high-risk group underwent cervical biopsy, the CINⅡ<sup>+</sup> missed detection rate was 37.58% (62/165). In contrast, 133 cases in low-risk group underwent cervical biopsy, of which 14 cases were immediate missed detection, while 1 068 cases who did not undergo cervical biopsy completed one year of follow-up, 16 and 6 new cases of CINⅡ<sup>+</sup> were detected at 6 months and 1 year, respectively. Among the 16 new detected cases at 6 months, 12 of them were CINⅡ (1 was focal CINⅡ and 11 were multifocal CINⅡ) and 4 of them were CINⅢ. Among the 6 new detected cases at 1 year, 4 of them were CINⅡ (2 were focal CINⅡ and 2 were multifocal CINⅡ) and 2 of them were CINⅢ. (2) The immediate missed detection rate of CINⅡ<sup>+</sup> in low-risk group was 1.17% (14/1 201), and the cumulative missed detection rate at one year was 3.00% (36/1 021). Normal colposcopic findings demonstrated a high negative predictive value (92.83%) for identifying CINⅡ<sup>+</sup>, particularly in low-risk group (97.00%). However, the specificity was only 74.97%. (3) The TCT and HR-HPV results of women with missed detection of colposcopy were analyzed. All o
{"title":"[Clinical outcomes of people with abnormal cervical cancer screening results but normal colposcopy findings].","authors":"J Zhang, J Zhao, R R Cui, T T Wang, H Feng, J X Li, J X Dong, Y Zhang","doi":"10.3760/cma.j.cn112141-20250423-00166","DOIUrl":"https://doi.org/10.3760/cma.j.cn112141-20250423-00166","url":null,"abstract":"<p><p><b>Objective:</b> To analyze the clinical outcomes of people with abnormal cervical cancer screening results but normal colposcopic findings, and explore the reasons for missed detection high-grade cervical intraepithelial neoplasia Ⅱ and worse (CINⅡ<sup>+</sup>). <b>Methods:</b> People who underwent colposcopy at the Department of Obstetrics and Gynecology, Peking University First Hospital from January 1st, 2019 to December 31st, 2019 were selected. Those with normal colposcopic findings were included, some of them underwent biopsy, others were followed up for one year. Data including thinprep cytologic test (TCT) and high-risk human papillomavirus (HR-HPV)screening results, colposcopic image characteristics, and histopathological outcomes were collected for statistical analysis. Based on cytology results, people with normal colposcopic findings were divided into two groups: the low-risk group [negative for intraepithelial lesion and malignancy (NILM), atypical squamous cell of undetermined signification (ASCUS), and low grade squamous intraepithelial lesion (LSIL)] and the high-risk group [high-grade squamous intraepithelial lesion (HSIL), atypical squamous cells cannot exclude high-grade lesion (ASC-H), and atypical glandular cells (AGC)]. The detection performance of normal colposcopic findings was evaluated by calculating sensitivity, specificity, positive predictive value, negative predictive value and overall accuracy. Furthermore, based on follow-up results, the missed detection rate of CINⅡ<sup>+</sup>in these people and the reasons for missed detection were analyzed. <b>Results:</b> A total of 1 584 women with normal colposcopic findings were included in this study; the median age was 39.0 years. Among them, 1 419 cases were in low-risk group, and 165 cases were in high-risk group. (1) All of the women in high-risk group underwent cervical biopsy, the CINⅡ<sup>+</sup> missed detection rate was 37.58% (62/165). In contrast, 133 cases in low-risk group underwent cervical biopsy, of which 14 cases were immediate missed detection, while 1 068 cases who did not undergo cervical biopsy completed one year of follow-up, 16 and 6 new cases of CINⅡ<sup>+</sup> were detected at 6 months and 1 year, respectively. Among the 16 new detected cases at 6 months, 12 of them were CINⅡ (1 was focal CINⅡ and 11 were multifocal CINⅡ) and 4 of them were CINⅢ. Among the 6 new detected cases at 1 year, 4 of them were CINⅡ (2 were focal CINⅡ and 2 were multifocal CINⅡ) and 2 of them were CINⅢ. (2) The immediate missed detection rate of CINⅡ<sup>+</sup> in low-risk group was 1.17% (14/1 201), and the cumulative missed detection rate at one year was 3.00% (36/1 021). Normal colposcopic findings demonstrated a high negative predictive value (92.83%) for identifying CINⅡ<sup>+</sup>, particularly in low-risk group (97.00%). However, the specificity was only 74.97%. (3) The TCT and HR-HPV results of women with missed detection of colposcopy were analyzed. All o","PeriodicalId":10050,"journal":{"name":"中华妇产科杂志","volume":"60 12","pages":"958-967"},"PeriodicalIF":0.0,"publicationDate":"2025-12-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145848838","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-25DOI: 10.3760/cma.j.cn112141-20250603-00252
Q Sheng, S Q Zhang, T T Sha, Y Y Zhao, L Chen
<p><p><b>Objective:</b> To investigate the impact of bundled management of late-pregnancy induction strategies on induction time and maternal and perinatal clinical outcomes. <b>Methods:</b> This was a historical control study, including 61 pregnant women before the implementation of the bundled management strategies for induction protocol in September 2024, and 78 pregnant women after the implementation in December 2024, who received regular prenatal check-ups and finally admitted to Peking University Third Hospital for elective induction of labor at term. The rate of successful induction, the rate of reaching active phase, induction to labor length, duration of labor, hospital stay, and adverse maternal and preinatal outcomes and other information were compared between two groups. Logistic regression model was used to analyze the factors affecting the rates of successful labor induction and reaching active phase. Kaplan-Meier survival curves were plotted for induction to labor length and duration of labor, and the Cox proportional hazards regression model was used to analyze the impact of the bundled management strategies for induction strategies on the above indicators. <b>Results:</b> (1) Compared with the group before implementation, the group after implementation had a shorter induction to labor length (median: 47.4 vs 35.1 h), a shorter duration of labor (median: 14.0 vs 10.5 h), and a shorter hospital stay (median: 6 vs 4 d). The rate of successful induction increased [87% (53/61) vs 97% (76/78)], and the rate of reaching active phase increased [70% (43/61) vs 86% (67/78)]; the differences were statistically significant (all <i>P</i><0.05). (2) Multivariate logistic regression analysis showed that the implementation of the bundled management strategies promoted successful induction (<i>OR</i>=7.299, 95%<i>CI</i>: 1.189-44.800; <i>P</i>=0.032) and reaching active phase (<i>OR</i>=2.640, 95%<i>CI</i>: 1.003-6.951; <i>P</i>=0.049). A pre-pregnancy body mass index<18.5 kg/m² promoted successful induction (<i>OR</i>=9.142, 95%<i>CI</i>: 1.154-72.423; <i>P</i>=0.036). (3) Kaplan-Meier curve analysis indicated that compared with the group before the implementation, the group after the implementation had a significantly shorter induction to labor length (<i>χ</i><sup>2</sup>=13.883, <i>P</i><0.001) and a shorter duration of labor (<i>χ</i><sup>2</sup>=5.72, <i>P</i>=0.017). Cox proportional hazards regression analysis showed that the implementation of the bundled management strategies for induction protocol was a protective factor for shortening induction to labor length (<i>HR</i>=1.806, 95%<i>CI</i>: 1.186-2.749; <i>P</i>=0.006) and duration of labor (<i>HR</i>=1.677, 95%<i>CI</i>: 1.066-2.637; <i>P</i>=0.025). A cervical Bishop score >3 at admission was a protective factor for shortening the induction to labor length (<i>HR</i>=1.627, 95%<i>CI</i>: 1.110-2.384; <i>P</i>=0.013), and parity was a protective factor for shortening the duration of
目的:探讨妊娠晚期引产策略捆绑管理对引产时间及母婴临床结局的影响。方法:采用历史对照研究,选取2024年9月实施引产方案捆绑管理策略前的61例孕妇和2024年12月实施捆绑管理策略后的78例孕妇,定期进行产前检查,最终在北京大学第三医院足月择期引产。比较两组间引产成功率、进入活跃期率、引产时长、产程、住院时间、不良母婴结局等信息。采用Logistic回归模型分析影响引产成功率及进入活跃期的因素。绘制引产时间和产程的Kaplan-Meier生存曲线,采用Cox比例风险回归模型分析引产策略捆绑管理策略对上述指标的影响。结果:(1)与实施前组相比,实施后组诱导产程缩短(中位数:47.4 h vs 35.1 h),产程缩短(中位数:14.0 h vs 10.5 h),住院时间缩短(中位数:6 d vs 4 d)。诱导成功率提高[87% (53/61)vs 97%(76/78)],达到活性期率提高[70% (43/61)vs 86% (67/78)];差异有统计学意义(P= 7.299, 95%CI: 1.189 ~ 44.800; P=0.032),达到活动期(P= 2.640, 95%CI: 1.003 ~ 6.951; P=0.049)。A孕前体重指数or =9.142, 95%CI: 1.154 ~ 72.423;P = 0.036)。(3) Kaplan-Meier曲线分析显示,与实施前组相比,实施后组诱导产时明显缩短(χ2=13.883, Pχ2=5.72, P=0.017)。Cox比例风险回归分析显示,实施诱导方案捆绑管理策略是缩短引产时间(HR=1.806, 95%CI: 1.186 ~ 2.749; P=0.006)和缩短产程(HR=1.677, 95%CI: 1.066 ~ 2.637; P=0.025)的保护因素。入院时宫颈Bishop评分bbbb3是缩短引产时间的保护因素(HR=1.627, 95%CI: 1.110 ~ 2.384; P=0.013),胎次是缩短引产时间的保护因素(HR=3.370, 95%CI: 1.806 ~ 6.288)结论:实施捆绑式引产方案管理策略,可促进引产孕妇顺利引产,进入产程活动期。这种方法还缩短了引产时间和分娩持续时间,而不会增加产妇和围产期并发症的风险。
{"title":"[Practice effect of bundled management strategies for induction of labor: a single-center historical controlled study].","authors":"Q Sheng, S Q Zhang, T T Sha, Y Y Zhao, L Chen","doi":"10.3760/cma.j.cn112141-20250603-00252","DOIUrl":"https://doi.org/10.3760/cma.j.cn112141-20250603-00252","url":null,"abstract":"<p><p><b>Objective:</b> To investigate the impact of bundled management of late-pregnancy induction strategies on induction time and maternal and perinatal clinical outcomes. <b>Methods:</b> This was a historical control study, including 61 pregnant women before the implementation of the bundled management strategies for induction protocol in September 2024, and 78 pregnant women after the implementation in December 2024, who received regular prenatal check-ups and finally admitted to Peking University Third Hospital for elective induction of labor at term. The rate of successful induction, the rate of reaching active phase, induction to labor length, duration of labor, hospital stay, and adverse maternal and preinatal outcomes and other information were compared between two groups. Logistic regression model was used to analyze the factors affecting the rates of successful labor induction and reaching active phase. Kaplan-Meier survival curves were plotted for induction to labor length and duration of labor, and the Cox proportional hazards regression model was used to analyze the impact of the bundled management strategies for induction strategies on the above indicators. <b>Results:</b> (1) Compared with the group before implementation, the group after implementation had a shorter induction to labor length (median: 47.4 vs 35.1 h), a shorter duration of labor (median: 14.0 vs 10.5 h), and a shorter hospital stay (median: 6 vs 4 d). The rate of successful induction increased [87% (53/61) vs 97% (76/78)], and the rate of reaching active phase increased [70% (43/61) vs 86% (67/78)]; the differences were statistically significant (all <i>P</i><0.05). (2) Multivariate logistic regression analysis showed that the implementation of the bundled management strategies promoted successful induction (<i>OR</i>=7.299, 95%<i>CI</i>: 1.189-44.800; <i>P</i>=0.032) and reaching active phase (<i>OR</i>=2.640, 95%<i>CI</i>: 1.003-6.951; <i>P</i>=0.049). A pre-pregnancy body mass index<18.5 kg/m² promoted successful induction (<i>OR</i>=9.142, 95%<i>CI</i>: 1.154-72.423; <i>P</i>=0.036). (3) Kaplan-Meier curve analysis indicated that compared with the group before the implementation, the group after the implementation had a significantly shorter induction to labor length (<i>χ</i><sup>2</sup>=13.883, <i>P</i><0.001) and a shorter duration of labor (<i>χ</i><sup>2</sup>=5.72, <i>P</i>=0.017). Cox proportional hazards regression analysis showed that the implementation of the bundled management strategies for induction protocol was a protective factor for shortening induction to labor length (<i>HR</i>=1.806, 95%<i>CI</i>: 1.186-2.749; <i>P</i>=0.006) and duration of labor (<i>HR</i>=1.677, 95%<i>CI</i>: 1.066-2.637; <i>P</i>=0.025). A cervical Bishop score >3 at admission was a protective factor for shortening the induction to labor length (<i>HR</i>=1.627, 95%<i>CI</i>: 1.110-2.384; <i>P</i>=0.013), and parity was a protective factor for shortening the duration of ","PeriodicalId":10050,"journal":{"name":"中华妇产科杂志","volume":"60 11","pages":"842-851"},"PeriodicalIF":0.0,"publicationDate":"2025-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145647662","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}