Association between Genitourinary and Congenital Heart Defects: A 52-year Case-Control Study of the Latin American Collaborative Study of Congenital Malformations (ECLAMC)

Nicolás Fernández, Daniela Varela, J. Villanueva, J. L. López Camelo, I. Zarante
{"title":"Association between Genitourinary and Congenital Heart Defects: A 52-year Case-Control Study of the Latin American Collaborative Study of Congenital Malformations (ECLAMC)","authors":"Nicolás Fernández, Daniela Varela, J. Villanueva, J. L. López Camelo, I. Zarante","doi":"10.1055/s-0042-1746203","DOIUrl":null,"url":null,"abstract":"Abstract Background  Congenital urological anomalies are present in 4.3/10 thousand newborns, and their association with other anomalies may increase the overall mortality and disability. The present study establishes the risk of having congenital urological anomalies presenting associated cardiopathies . Methods  We conducted a retrospective case-control study using the Latin American Collaborative Study of Congenital Malformations (Estudio Colaborativo Latino Americano de Malformaciones Congénitas, ECLAMC, in Spanish). The analysis included all registered cases of congenital urological malformation from 1967 to 2019. Patients with or without associated heart defects were included for the statistical analysis. Odds ratios (ORs) were calculated using a 95% confidence interval (95% CI). We compared the variables with the Chi-squared test and analysis of variance (ANOVA). The statistical analysis was performed using the Statistical Package for the Social Sciences (IBM SPSS Statistics for Windows, IBM Corp., Armonk, NY, United States) software, version 27.0. Values of p  < 0.05 were considered statistically significant. Results  A total of 7,767,161 newborns were evaluated, and 17,834 genital and upper urinary tract malformations were identified. Of these, 64.2% were genital anomalies, and 35.8% were abnormalities of the upper urinary tract. Genitourinary malformations and concomitant congenital heart defects (GU + C) were observed in 3.5% of the cases. Subjects with GU + C had a higher number of malformations (4.59 ± 2.3) than patients without heart defects (1.53 ± 1.58) ( p  < 0.000). The OR was of 3.61 (range: 1.86–7.00) for cloacal exstrophy, of 4.01 (range: 3.14–5.12) for imperforate anus, of 5.52 (range: 3.92–7.78) for horseshoe kidney, and of 13.7 (range: 6.65–28.22) for trisomy 21 (Down syndrome) with malformations of the upper urinary tract. Conclusion  The association of congenital heart defects with urological anomalies is higher for complex congenital anomalies such as imperforate anus, cloacal exstrophy, and horseshoe kidney. Patients with urological abnormalities and Down syndrome have the highest likelihood.","PeriodicalId":38070,"journal":{"name":"Urologia Colombiana","volume":"31 1","pages":"e143 - e148"},"PeriodicalIF":0.0000,"publicationDate":"2022-01-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Urologia Colombiana","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1055/s-0042-1746203","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

Abstract

Abstract Background  Congenital urological anomalies are present in 4.3/10 thousand newborns, and their association with other anomalies may increase the overall mortality and disability. The present study establishes the risk of having congenital urological anomalies presenting associated cardiopathies . Methods  We conducted a retrospective case-control study using the Latin American Collaborative Study of Congenital Malformations (Estudio Colaborativo Latino Americano de Malformaciones Congénitas, ECLAMC, in Spanish). The analysis included all registered cases of congenital urological malformation from 1967 to 2019. Patients with or without associated heart defects were included for the statistical analysis. Odds ratios (ORs) were calculated using a 95% confidence interval (95% CI). We compared the variables with the Chi-squared test and analysis of variance (ANOVA). The statistical analysis was performed using the Statistical Package for the Social Sciences (IBM SPSS Statistics for Windows, IBM Corp., Armonk, NY, United States) software, version 27.0. Values of p  < 0.05 were considered statistically significant. Results  A total of 7,767,161 newborns were evaluated, and 17,834 genital and upper urinary tract malformations were identified. Of these, 64.2% were genital anomalies, and 35.8% were abnormalities of the upper urinary tract. Genitourinary malformations and concomitant congenital heart defects (GU + C) were observed in 3.5% of the cases. Subjects with GU + C had a higher number of malformations (4.59 ± 2.3) than patients without heart defects (1.53 ± 1.58) ( p  < 0.000). The OR was of 3.61 (range: 1.86–7.00) for cloacal exstrophy, of 4.01 (range: 3.14–5.12) for imperforate anus, of 5.52 (range: 3.92–7.78) for horseshoe kidney, and of 13.7 (range: 6.65–28.22) for trisomy 21 (Down syndrome) with malformations of the upper urinary tract. Conclusion  The association of congenital heart defects with urological anomalies is higher for complex congenital anomalies such as imperforate anus, cloacal exstrophy, and horseshoe kidney. Patients with urological abnormalities and Down syndrome have the highest likelihood.
泌尿生殖系统与先天性心脏缺陷的关系:拉丁美洲先天性畸形合作研究(ECLAMC)的52年病例对照研究
摘要背景 先天性泌尿系统异常存在于4.3/10万新生儿中,它们与其他异常的关联可能会增加总死亡率和残疾率。本研究确定了先天性泌尿系统异常伴发心脏病的风险。方法 我们使用拉丁美洲先天性畸形合作研究(Estudio Colaborative o Latino Americano de Malformaciones Congénitas,ECLAMC,西班牙语)进行了一项回顾性病例对照研究。该分析包括1967年至2019年所有登记的先天性泌尿系统畸形病例。将有或没有相关心脏缺陷的患者纳入统计分析。使用95%置信区间(95%CI)计算比值比(OR)。我们将这些变量与卡方检验和方差分析(ANOVA)进行了比较。使用社会科学统计软件包(IBM SPSS Statistics for Windows,IBM Corp.,Armonk,NY,United States)软件27.0版进行统计分析。p的值 < 0.05被认为具有统计学意义。后果 共对7767161名新生儿进行了评估,发现17834例生殖器和上尿路畸形。其中,64.2%为生殖器异常,35.8%为上尿路异常。泌尿生殖系统畸形和伴随的先天性心脏缺陷(GU + C) 在3.5%的病例中观察到。GU受试者 + C的畸形率较高(4.59 ± 2.3)比没有心脏缺陷的患者(1.53 ± 1.58)(p < 泄殖腔外翻的OR为3.61(范围:1.86–7.00),肛门闭锁的OR为4.01(范围为3.14–5.12),马蹄肾的OR为5.52(范围:3.92–7.78),21三体(唐氏综合征)伴上尿路畸形的OR为13.7(范围:6.65–28.22)。结论 对于复杂的先天性异常,如肛门闭锁、泄殖腔膨出和马蹄肾,先天性心脏缺陷与泌尿系统异常的相关性更高。泌尿系统异常和唐氏综合症患者的可能性最高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Urologia Colombiana
Urologia Colombiana Medicine-Urology
CiteScore
0.30
自引率
0.00%
发文量
26
期刊介绍: Urología Colombiana is the serial scientific publication of the Colombian Society of Urology at intervals of three issues per year, in which the results of original research, review articles and other research designs that contribute to increase knowledge in medicine and particularly in the specialty of urology.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信