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1.
Arch Med Sci ; 19(4): 1011-1015, 2023.
Article in English | MEDLINE | ID: mdl-37560726

ABSTRACT

Introduction: This study aims to explore the effects of combination of laparoscopy and hysteroscopy in pregnancy outcome in women diagnosed with congenital uterine malformation (CUM). The observation criteria include pregnancy rate, misdiagnosis rate, rate of spontaneous abortion and preterm birth rate. Material and methods: A total of 180 patients with congenital uterine malformation, who were treated in our hospital from January 2015 to June 2018, were enrolled in the study. Prior to hospitalization, all the patients had neither a history of genital tract surgery nor endocrine abnormalities, chromosomal abnormalities, immune abnormalities or other factors affecting pregnancy. Furthermore, the ovarian functions were normal, and there were no factors leading to infertility in the male partners. The diagnosis was mainly based on medical history, clinical manifestations, gynecological examinations, and ultrasonography including two-dimensional and three-dimensional ultrasonography, as well as hysterosalpingogram (HSG), magnetic resonance imaging (MRI), hysteroscopy, and/or laparoscopy or surgery. Patients were diagnosed and classified according to the Buttram classification. Results: Among these 180 patients, 37 patients were diagnosed with complete septate uterus, 96 patients had sub-septate uterus, 25 patients had unicornuate uterus, 11 patients were diagnosed with bicornuate uterus, and 11 patients had didelphic uterus. The total number of preoperative pregnancies was 112, including 106 spontaneous abortions, with an abortion rate of 94.64%, and 86 total postoperative pregnancies, among which spontaneous abortions occurred 11 times, with an abortion rate of 12.79%. The difference was statistically significant (p < 0.05). Conclusions: Uterine malformation surgery can significantly improve the reproductive prognosis in patients with CUM.

3.
BMC Womens Health ; 21(1): 88, 2021 03 01.
Article in English | MEDLINE | ID: mdl-33648484

ABSTRACT

BACKGROUND: The present study aims to provide a comparative analysis of the etiologies of female infertility between Dehong, on the Yunnan Frontier, and Kunming. METHODS: A retrospective study, which included 941 infertile females in Kunming who were treated in the First People's Hospital of Yunnan Province and infertile females who were treated in the local hospital in Dehong from January 2016 to November 2018, was conducted. A comparative analysis of the etiologies of infertility in the two regions was then carried out. RESULTS: In patients with primary infertility, ovulation disorder (15.03%) was the main cause of infertility in Kunming, and pelvic inflammatory disease (25.59%) was the main cause in Dehong. With regard to secondary infertility, although pelvic inflammatory disease was the main cause of infertility in both regions, the incidence of intrauterine adhesions in Kunming was significantly higher than in Dehong. CONCLUSIONS: The etiology of infertility showed different epidemiological characteristics depending on the region, hence individualized treatment should be given accordingly.


Subject(s)
Infertility, Female , Pelvic Inflammatory Disease , China/epidemiology , Female , Humans , Infertility, Female/epidemiology , Infertility, Female/etiology , Retrospective Studies , Tissue Adhesions
4.
BMC Pregnancy Childbirth ; 20(1): 644, 2020 Oct 22.
Article in English | MEDLINE | ID: mdl-33092547

ABSTRACT

BACKGROUND: This cross-sectional study aimed to evaluate the levels of tumor necrosis factor-alpha (TNF-ɑ), interleukin-8 (IL-8), interleukin-6 (IL-6), and transforming growth factor-beta 1 (TGF-ß1) in patients with primary and secondary tubal factor infertility (TFI) compared with fertile subjects, and to compare immune indexes in the serum and peritoneal fluid samples obtained from patients with TFI. METHODS: The pelvic fluid and peripheral blood of patients with TFI diagnosed by hysteroscopy and laparoscopy were taken as the study objects. The pelvic fluid and peripheral blood of patients who underwent hysteromyomectomy at the same time were taken as the control group. The contents of TNF-ɑ, IL-8, IL-6, and TGF-ß1 in serum and peritoneal fluid were determined by enzyme-linked immunosorbent assay, and the levels of these cytokines in serum and pelvic fluid were compared between the two groups. RESULTS: Patients with secondary TFI showed significantly higher levels of TNF-ɑ, IL-8, IL-6 and TGF-ß1 in the serum (26.15 ± 3.51 vs. 19.61 ± 0.157, 32.18 ± 15.13 vs. 5.73 ± 1.99, 38.84 ± 3.46 vs. 30.48 ± 0.61, and 38.37 ± 3.14 vs. 32.25 ± 1.69, respectively) and peritoneal fluid samples (129.73 ± 183.4 vs. 34.63 ± 0.56, 111.44 ± 207.42 vs. 15.34 ± 0.41, 80.01 ± 109.91 vs. 15.67 ± 0.52, and 82.54 ± 115.99 vs. 45.34 ± 0.41, respectively) compared with the control group. Patients with primary TFI exhibited significantly elevated concentration of TNF-α, IL-8, IL-6 and TGF-ß1 in the peritoneal fluid samples (36.88 ± 2.67 vs. 34.63 ± 0.56, 19.47 ± 3.51 vs. 15.34 ± 0.41, 80.01 ± 109.91 vs. 15.67 ± 0.52, and 82.54 ± 115.99 vs. 45.34 ± 0.41, respectively) when compared to the controls. In patients with secondary infertility, the levels of TNF-α (26.15 ± 3.51 vs. 129.73 ± 183.4), IL-8 (32.18 ± 15.13 vs. 111.44 ± 207.42), IL-6 (38.84 ± 3.46 vs. 80.01 ± 109.91) and TGF-ß1 (38.37 ± 3.14 vs. 82.54 ± 115.99) in the serum were significantly lower than those in the peritoneal fluid, whereas no significant difference was observed in the primary TFI group between the serum and peritoneal fluid cytokines levels. CONCLUSION: The expression of cytokines in the pelvic environment of patients with TFI is upregulated compared to patients who do not have infertility issues. The detection of cytokines TNF-ɑ, IL-6, IL-8, and TGF-ß1 in the pelvic fluid of tubal infertility patients can allow for further understanding of the etiology of TFI.


Subject(s)
Body Fluids/immunology , Cytokines/metabolism , Infertility, Female/immunology , Pelvis/pathology , Body Fluids/metabolism , Cross-Sectional Studies , Cytokines/analysis , Female , Humans , Hysteroscopy , Infertility, Female/diagnosis , Infertility, Female/pathology , Laparoscopy , Middle Aged , Pelvis/diagnostic imaging , Pregnancy , Up-Regulation/immunology
5.
Medicine (Baltimore) ; 97(48): e13307, 2018 Nov.
Article in English | MEDLINE | ID: mdl-30508919

ABSTRACT

The prognosis of right heart enlargement varies according to different etiologies. The purpose of this study was to investigate the characteristics of echocardiogram, surgical treatment, chromosome and prognosis for fetal right heart enlargement.The foetal echocardiogram was performed on 3987 pregnant women, and then 88 fetuses with right heart enlargement were identified. The data about prenatal and postnatal echocardiograms, postnatal cardiac surgical treatment, karyotype analysis and autopsy after induced labor were analyzed in the 88 fetuses.Except the 1111 cases that had loss of follow-up, 2876 cases had complete data. Among the 2876 cases, right heart enlargement was identified in 88 fetuses. Of the 88 fetuses, 15 had total atrioventricular septal defect (unbalanced type: right ventricular dominance), 15 Ebstein's anomaly, 18 fallot tetrad, 14 double outlet right ventricle, 13 total anomalous pulmonary venous drainage, and 13 premature closure of ductus arteriosus. Chromosomal abnormality was found in 12 cases.There are many etiological factors causing right heart enlargement. The prognosis is better in the fetuses with single heart malformation than in the fetuses who have extracardiac malformation or/and chromosomal abnormality besides heart malformation. Fetal echocardiography combined with karyotype analysis can provide important bases for evaluating the prognosis of fetuses with right heart enlargement.


Subject(s)
Cardiac Surgical Procedures , Echocardiography , Hypertrophy, Right Ventricular/diagnostic imaging , Hypertrophy, Right Ventricular/genetics , Ultrasonography, Prenatal , Adolescent , Adult , Chromosome Aberrations , Female , Follow-Up Studies , Heart Defects, Congenital/diagnostic imaging , Heart Defects, Congenital/genetics , Heart Defects, Congenital/surgery , Humans , Hypertrophy, Right Ventricular/etiology , Hypertrophy, Right Ventricular/surgery , Karyotype , Male , Middle Aged , Prognosis , Young Adult
6.
Org Biomol Chem ; 16(1): 130-139, 2017 Dec 19.
Article in English | MEDLINE | ID: mdl-29215122

ABSTRACT

Maleimide and benzene are employed as a dendron and a core, respectively, to construct two series of non-conjugate branched oligomers (B3G1 and B1G2) based on diarylmaleimide fluorophores by an alkylation reaction. Surface aryl groups are changed to tune the emissive color of branched oligomers from blue (λem = 480 nm) to red (λem = 651 nm), realizing full-color emission. The investigation on the photophysical properties of the oligomers indicates that they display intense emission in both solution and solid films, due to the suppression of intramolecular rotation and intermolecular interaction. Molecular simulation and natural transition orbital analysis show that the electron transition takes place in the individual arylmaleimide for the non-conjugate linkage of fluorophores in branched oligomers. It can avoid the unpredictability of the luminescence properties caused by the interaction of fluorophores. In addition, the good solubility, thermostability and oxidative stability of the branched oligomers make them have huge potential in the solution-processable photonic application. These results demonstrate that such a design strategy of non-conjugate branched oligomers is a very efficient and constructive method to obtain high-performance light-emitting materials in both solution and solid films.

7.
Phys Chem Chem Phys ; 19(20): 12642-12646, 2017 May 24.
Article in English | MEDLINE | ID: mdl-28489099

ABSTRACT

The non-emissive benzene ring and green-emissive arylmaleimide are employed as two independent cores to construct dual-core white star-shaped polymers (DC-PFMs). Due to the totally star-shaped structure, DC-PFMs display a higher quantum yield and electroluminescence efficiency for a more efficient energy transfer from the host to the guest than traditional single-core polymers (SC-PFMs).

8.
J Matern Fetal Neonatal Med ; 29(3): 493-503, 2016.
Article in English | MEDLINE | ID: mdl-25731651

ABSTRACT

OBJECTIVE: To provide a basis for evaluating the prognosis of small left heart system development in fetuses, we analyzed its related factors. METHODS: The fetal echocardiogram was performed in 3859 pregnant women, and then small left heart system development was identified in 69 fetuses. The data of prenatal and postnatal echocardiograms, postnatal cardiac surgical treatment, chromosome and autopsy after induced labor were analyzed in the 69 fetuses. RESULTS: Except 1320 cases losing follow-up, 2539 cases had complete data. Among the 2539 cases, small left heart system development was identified in 69 fetuses. Of the 69 fetuses, 12 had hypoplastic left heart syndrome, 20 premature closure of foramen ovale, 13 total anomalous pulmonary venous drainage, 2 common pulmonary vein lumen atresia, 21 aortic coarctation or interruption and 1 right pulmonary hypoplasia. Among the 69 fetuses, chromosome abnormality was found in 7. CONCLUSION: There are many etiological factors causing small left heart system development. The prognosis is poor in the fetuses with hypoplastic left heart syndrome, common pulmonary vein lumen atresia, pulmonary hypoplasia, other malformations or/and chromosome abnormality. Fetal echocardiography combined with chromosome examination can provide important bases for making diagnosis and evaluating the prognosis regarding small left heart system development.


Subject(s)
Fetal Diseases/etiology , Heart Defects, Congenital/etiology , Adolescent , Adult , Echocardiography , Female , Fetal Diseases/diagnostic imaging , Heart Defects, Congenital/diagnostic imaging , Humans , Karyotype , Middle Aged , Pregnancy , Prognosis , Prospective Studies , Reproducibility of Results , Ultrasonography, Prenatal , Young Adult
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