Congenital Heart Disease最新文献_第4页

Having a Partner and Having Children: Comparisons of Adults with Congenital Heart Disease and the General Population: A 15-Year Case-Control Study 有伴侣和有孩子:患有先天性心脏病的成年人和一般人群的比较:一项为期15年的病例对照研究

IF 0.3 4区医学

Congenital Heart Disease Pub Date : 2023-01-01 DOI: 10.32604/chd.2023.028827

S. Geyer, C. Dellas, Thomas Paul, Matthias M黮ler, K. Norozi

{"title":"Having a Partner and Having Children: Comparisons of Adults with Congenital Heart Disease and the General Population: A 15-Year Case-Control Study","authors":"S. Geyer, C. Dellas, Thomas Paul, Matthias M黮ler, K. Norozi","doi":"10.32604/chd.2023.028827","DOIUrl":"https://doi.org/10.32604/chd.2023.028827","url":null,"abstract":"Objectives: To examine whether patients with congenital heart disease (CHD) are less likely to have a partner or children than individuals from the general population. Methods: Longitudinal study with two assessments of the same patients (n = 244) from a hospital population and controls (n = 238) from the German Socio-Economic Panel (GSOEP) using parental education, patients age, and sex as matching criteria. The ﬁ rst patient study was conducted between 5/2003 and 6/2004, the second one between 5/2017 and 4/2019. Controls were drawn from GSOEP-surveys 2004 and 2018. CHD-severity was classi ﬁ ed according to type of surgery: curative, reparative, or palliative. Living single was used as outcome measure, for offspring the outcome was having children or not. Results: Among women with CHD the rate of those living single was higher than among controls with the differences depending on disease complexity (curative: OR = 5.5; reparative: OR = 1.9; palliative: OR = 2.7). No statistically signi ﬁ cant differences between patients and controls emerged in the male study population. With respect to children a marked difference emerged between women with CHD and controls. Among patients the odds of having children were lower than among controls (curative: OR = 0.3; reparative: OR = 0.3; palliative: OR = 0.2). The rate of patients with children with CHD (women: 5.6%; men: 4.9%) was higher than expected (1%) if compared with the general population. Conclusions: Using partnership and children as outcome criteria, patients with CHD are disadvantaged if compared to subjects from the general population. In female patients the social consequences of the disease turned out as more pervasive than in women.","PeriodicalId":10666,"journal":{"name":"Congenital Heart Disease","volume":"1 1","pages":""},"PeriodicalIF":0.3,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"69720324","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}

引用次数: 0

The Prevalence of Congenital Heart Disease among School-Age Children in China: A Meta-Analysis and Systematic Review 中国学龄儿童先天性心脏病患病率:荟萃分析和系统评价

IF 0.3 4区医学

Congenital Heart Disease Pub Date : 2023-01-01 DOI: 10.32604/chd.2023.025616

Shuqin Zhang, Bin Zhang, Jianying Wu, Jin Luo, Haomin Shi, Jirong Qi, Han Yang

引用次数: 1

Transcatheter Ventricular Septal Defect Closure with Nit-Occlud Lê VSD Device—Five Years’ Experience and Literature Review 经导管镍闭塞Lê VSD装置封闭室间隔缺损- 5年经验及文献回顾

IF 0.3 4区医学

Congenital Heart Disease Pub Date : 2023-01-01 DOI: 10.32604/chd.2023.026533

Ivana B. Cerović, Vladislav A. Vukomanović, Jovan Lj. Košutić, Mila S. Stajević, Sanja S. Ninić, Saša S. Popović, Ivan D. Dizdarević, Staša D. Krasić, Sergej M. Prijić

引用次数: 0

Safety and Efficacy of Biodegradable Patent Foramen Ovale Occluder in Patients with Migraine: A Clinical Trial 可生物降解卵圆孔未闭封堵器治疗偏头痛的安全性和有效性:一项临床试验

IF 0.3 4区医学

Congenital Heart Disease Pub Date : 2023-01-01 DOI: 10.32604/chd.2023.028979

Xingbang Li, Xuan Zheng, B. Jin, Yun-yan Li, Yongyu Shao, Xiao-xian Deng, Dingyang Li, Shanshan Li, Hongmei Zhou, Jie Zhang, Xianya Zhang, Q. Shen, Gangcheng Zhang

引用次数: 0

Giant-Size Main Pulmonary Artery Aneurysm in an Adult Patient with Ebstein Anomaly and Dextrocardia 成人Ebstein异常伴右心的巨大肺动脉主动脉瘤1例

IF 0.3 4区医学

Congenital Heart Disease Pub Date : 2023-01-01 DOI: 10.32604/chd.2023.027453

K. Krželj, I. Ivanac Vranešić, Kristina Marić Bešić, Zeljko Durić, D. Anić

引用次数: 0

Transcatheter Closure vs. Surgical Ligation in Preterm Infants with Patent Ductus Arteriosus: A Systematic Review and Meta-Analysis 动脉导管未闭早产儿的经导管闭合与手术结扎:系统回顾和荟萃分析

IF 0.3 4区医学

Congenital Heart Disease Pub Date : 2023-01-01 DOI: 10.32604/chd.2023.027596

Rohan Suresh Daniel, Georgia K. Schmidt, H. Nakanishi, K. Smayra, Mariah N. Mascara, Dilip K. Vankayalapati, Reem H. Matar, Christian A. Than, George Shiakos, I. Tzanavaros

引用次数: 1

Intermediate and Long-Term Follow-Up of Transcatheter Closure of Congenital Coronary Cameral Fistulas in Infants and Children: Experience from a Single Center 婴儿和儿童先天性冠状动脉照相机瘘管经导管闭合的中期和长期随访:来自单一中心的经验

4区医学

Congenital Heart Disease Pub Date : 2023-01-01 DOI: 10.32604/chd.2023.029848

Yifan Li, Zewen Chen, Yumei Xie, Shushui Wang, Zhiwei Zhang

{"title":"Intermediate and Long-Term Follow-Up of Transcatheter Closure of Congenital Coronary Cameral Fistulas in Infants and Children: Experience from a Single Center","authors":"Yifan Li, Zewen Chen, Yumei Xie, Shushui Wang, Zhiwei Zhang","doi":"10.32604/chd.2023.029848","DOIUrl":"https://doi.org/10.32604/chd.2023.029848","url":null,"abstract":"Background: Limited data are available regarding intermediate and long-term outcomes of transcatheter closure (TCC) of coronary cameral fistulas (CCFs) in the pediatric patients. Methods: All pediatric patients diagnosed with CCFs who were scheduled to undergo TCC between 2005 and 2019 were retrospectively enrolled in the study. Results: A total of 66 patients (median age: 3.93 years, median weight: 15 kg) underwent attempted TCC of CCFs. Immediate successful device implantation was achieved in 62 patients, and immediate complete occlusion was achieved in 44 patients (44/62%, 71.0%). The closure procedure was waived in 2 patients due to anatomical factors. A total of 6 periprocedural complications occurred in 5 patients, including acute myocardial infarction (n = 3), procedure-related death (n = 1), device embolization (n = 1), and rupture of tricuspid chordae tendineae (n = 1). The acute procedural success rate was 89.4% (59/66), while the acute complication rate was 9.1% (6/66). Follow-up data were collected for 58 (93.5%) out of 62 patients at a median of 9.3 years (range: 3.0–15.7 years). 10 adverse events occurred in 9 patients, including 5 follow-up complications (1 aortic valve perforation, 1 coronary thrombosis, 1 progressive aneurysmal dilation after reintervention, and 2 cases of new-onset tricuspid valve prolapse with significant regurgitation), and 5 closure failure with large residual shunts. The intermediate and long-term adverse event rate was 17.2% (10/58). The anatomical features associated with both acute and follow-up adverse events were large CCFs (p = 0.005), and giant coronary artery aneurysms (CAAs) (p = 0.029). Conclusions: TCC of CCFs in infants and children appears to be effective and is associated with a relatively low complication rate. Large CCFs and giant CAAs represent a higher risk of both acute and intermediate and long-term adverse events after closure.","PeriodicalId":10666,"journal":{"name":"Congenital Heart Disease","volume":"4 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135400900","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}

引用次数: 0

Mortality Rates of Ventricular Septal Defect for Children in Kazakhstan: Spatio-Temporal Epidemiological Appraisal 哈萨克斯坦儿童室间隔缺损死亡率:时空流行病学评价

4区医学

Congenital Heart Disease Pub Date : 2023-01-01 DOI: 10.32604/chd.2023.028742

Akkerbez Adilbekova, Shukhrat Marassulov, Bakhytzhan Nurkeev, Saken Kozhakhmetov, Aikorkem Badambekova

引用次数: 0

Real-Time Remote-Mentored Echocardiography in Management of Newborns with Critical Congenital Heart Defects 实时远程监护超声心动图在新生儿危重先天性心脏缺陷治疗中的应用

4区医学

Congenital Heart Disease Pub Date : 2023-01-01 DOI: 10.32604/chd.2023.031537

H鍁ard Bjerkeseth Solvin, Simone Goa Diab, Ole Jakob Elle, Henrik Holmstr鴐, Henrik Brun

引用次数: 0

A New Three-Dimensional (3D) Printing Prepress Algorithm for Simulation of Planned Surgery for Congenital Heart Disease 一种新的三维(3D)印前算法用于模拟先天性心脏病计划手术

4区医学

Congenital Heart Disease Pub Date : 2023-01-01 DOI: 10.32604/chd.2023.030583

Vitaliy Suvorov, Olga Loboda, Maria Balakina, Igor Kulczycki

{"title":"A New Three-Dimensional (3D) Printing Prepress Algorithm for Simulation of Planned Surgery for Congenital Heart Disease","authors":"Vitaliy Suvorov, Olga Loboda, Maria Balakina, Igor Kulczycki","doi":"10.32604/chd.2023.030583","DOIUrl":"https://doi.org/10.32604/chd.2023.030583","url":null,"abstract":"Background: Three-dimensional printing technology may become a key factor in transforming clinical practice and in significant improvement of treatment outcomes. The introduction of this technique into pediatric cardiac surgery will allow us to study features of the anatomy and spatial relations of a defect and to simulate the optimal surgical repair on a printed model in every individual case. Methods: We performed the prospective cohort study which included 29 children with congenital heart defects. The hearts and the great vessels were modeled and printed out. Measurements of the same cardiac areas were taken in the same planes and points at multislice computed tomography images (group 1) and on printed 3D models of the hearts (group 2). Pre-printing treatment of the multislice computed tomography data and 3D model preparation were performed according to a newly developed algorithm. Results: The measurements taken on the 3D-printed cardiac models and the tomographic images did not differ significantly, which allowed us to conclude that the models were highly accurate and informative. The new algorithm greatly simplifies and speeds up the preparation of a 3D model for printing, while maintaining high accuracy and level of detail. Conclusions: The 3D-printed models provide an accurate preoperative assessment of the anatomy of a defect in each case. The new algorithm has several important advantages over other available programs. They enable the development of customized preliminary plans for surgical repair of each specific complex congenital heart disease, predict possible issues, determine the optimal surgical tactics, and significantly improve surgical outcomes.","PeriodicalId":10666,"journal":{"name":"Congenital Heart Disease","volume":"32 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135559350","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}

引用次数: 0