首页> 外文期刊>Research Journal of Biological Sciences >Congenital Heart Anomalies in Babies with Imperforate Anus and its Mortality
【24h】

Congenital Heart Anomalies in Babies with Imperforate Anus and its Mortality

机译:无孔肛门婴儿的先天性心脏异常及其死亡率

获取原文
       

摘要

Imperforate Anus (IA) is an abnormality of the anus and rectum that is present at birth. The infant is born without a normal rectal opening. Anorectal malformations occur in one in 5,000 live births. Anorectal and urogenital malformations are rarely fatal, although some associated anomalies (cardiac, renal) can be life threatening. The aim of this study is to determine congenital heart disease in babies with Imperforate Anus. Prospective study was carried out between February 1999 and January 2006 and it consisted of 93 consecutive children with IA. The study included children presenting with IA at the birth time. Echocardiography was done in all patients. Associated anomalies were studied and congenital heart anomalies were evaluated by Echocardiography. The study was undertaken in 93 patients with IA, 48(51.6%) boys and 44 girls. About 47(50.5%) of them had congenital heart anomalies. Echocardiography was performed in 87(93.5) of patients and were abnormal in 48.3% of studied cases. Mortality rate of studied patients with IA was 12.9%. Mean age of male patients was 1.02?0.146 day and Mean age of female patients was 1.02?1.51 day (p = 0.936). Mean age of died patients was 1.17?0.389 day and Mean age of improved patients was 1.02?1.51 day (p = 0.100). Atrial Septal Defect (ASD) was the most common associated cardiac anomaly. Associated anomalies such as congenital heart disease are present in a high percentage of patients with Anorectal malformations. Many of these associated anomalies are serious and long term prognosis of child with anorectal malformations more often depend on extent of these associated anomalies than on anorectal malformations itself. Systemic and radiological examination in neonatal period to detect associated anomalies at the earliest phase and should be managed immediately to prevent future morbidity and mortality.
机译:肛门无孔(IA)是在出生时出现的肛门和直肠异常。婴儿出生时没有正常的直肠开口。 5,000例活产中有1例发生肛肠畸形。肛门直肠和泌尿生殖道畸形很少致命,尽管某些相关异常(心脏,肾脏)可能危及生命。这项研究的目的是确定肛门闭孔婴儿的先天性心脏病。前瞻性研究在1999年2月至2006年1月之间进行,该研究由93名连续的IA儿童组成。该研究包括出生时患有IA的儿童。所有患者均进行了超声心动图检查。研究了相关异常,并通过超声心动图评估了先天性心脏异常。该研究在93例IA患者中进行,其中48名(51.6%)男孩和44名女孩。其中约47(50.5%)患有先天性心脏异常。超声心动图检查在87(93.5)位患者中进行,在48.3%的研究病例中异常。研究的IA患者的死亡率为12.9%。男性患者的平均年龄为1.02±0.146天,女性患者的平均年龄为1.02±1.51天(p = 0.936)。死亡患者的平均年龄为1.17?0.389天,病情好转的患者的平均年龄为1.02?1.51天(p = 0.100)。心房间隔缺损(ASD)是最常见的相关心脏异常。患有肛门直肠畸形的患者中,高比例存在先天性心脏病等相关异常。这些相关异常中的许多是严重的,直肠肛门畸形儿童的长期预后更多地取决于这些相关异常的程度,而不是取决于肛门直肠畸形本身。新生儿期的全身和放射学检查可尽早发现相关异常,应立即进行管理以防止将来发病和死亡。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号