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Diagnosis and treatment of postoperative intestinal perforation in infants and young children with congenital heart disease: A report of three cases

机译:先天性心脏病婴幼儿术后肠穿孔的诊断和治疗:三种情况报告

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The aim of the present study was to analyze risk factors of intestinal perforation following surgery for the treatment of congenital heart disease in infants and young children, and to summarize experiences of diagnosis and treatment. A total of 3,270 children, who underwent congenital heart disease surgery under extracorporeal circulation from January 2010 to July 2015, were retrospectively analyzed. Among these children, three (0.09%) developed postoperative intestinal perforation. Primary diseases were Tetralogy of Fallot (two cases) and ventricular septal defect combined with atrial septal defect (one case). The age range of the children was 6-11 months and the weight range was 7.3-8.6 kg. Furthermore, these children underwent radical surgery under general anesthesia and extracorporeal circulation in low temperatures. Abdominal symptoms appeared 4-10 days after surgery, and included poor appetite, abdominal distension, intermittent vomiting, high fever, refractory irritability, crying and shortness of breath. One case was confirmed by routine abdominal puncture and the remaining two were confirmed by the detection of free gas under the diaphragm, as revealed by abdominal X-ray. Following the diagnosis of intestinal perforation, emergency intestinal fistula surgery was performed. At 3-5 days post-surgery, the patients underwent treatment by fasting and intravenously administered parenteral nutrition. Diet was increased following recovery of bowel function. All patients recovered following active treatment and 3-4 months following hospital discharge, the fistula was successfully closed. In conclusion, a concerted effort should be made to identify intestinal perforation in infants and young children with postoperative congenital heart disease during emergency surgery. Farly diagnosis and treatment may significantly improve prognosis and reduce mortality.
机译:本研究的目的是分析手术后患有先天性心脏病的肠穿孔的危险因素,并总结诊断和治疗的经验。回顾性分析了2010年1月至2015年7月,共有3,270名患有先天性心脏病手术的儿童。在这些孩子中,三种(0.09%)开发出术后肠道穿孔。原发性疾病是椎间盘突出的(两种情况)和心室间隔缺损与心房隔膜缺陷(一种情况)结合。儿童的年龄范围为6-11个月,重量范围为7.3-8.6千克。此外,这些儿童在一般麻醉下接受了激进的手术和低温下的体外循环。手术后腹部症状4-10天出现,包括差的食欲,腹胀,间歇性呕吐,高烧,耐火性烦躁,哭泣和呼吸急促。通过常规腹部穿刺证实了一种情况,并且通过检测隔膜下的游离气体确认剩余的两种情况,如腹部X射线所揭示的。在肠道穿孔诊断后,进行急诊肠瘘手术。在手术后3-5天,患者通过禁食和静脉内给药的肠胃外营养进行治疗。肠功能恢复后饮食增加。所有患者在活性治疗后恢复,医院排放后3-4个月,瘘管已成功关闭。总之,应在急诊手术期间患有术后先天性心脏病的婴儿和幼儿中的肠穿孔。令人惊异的诊断和治疗可能会显着提高预后和降低死亡率。

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