论文部分内容阅读
目的分析总结先天性肠闭锁的临床诊断和治疗。方法对我院收治的60例先天性肠闭锁患儿的临床资料进行回顾性分析。结果 60例中55例经治疗病情治愈,其中包括二期手术治愈,术后恢复良好,5例因病情复杂、畸形重放弃治疗而死亡;合并并发症、低体重等情况对患儿预后有不良影响(P<0.05)。结论手术治疗先天性肠闭锁患儿的关键在于选择适宜的手术方式确保患儿吻合口畅通。合并并发症、低体重会影响患儿的预后效果。
Objective To analyze and summarize the clinical diagnosis and treatment of congenital intestinal atresia. Methods The clinical data of 60 cases of congenital intestinal obstruction admitted to our hospital were retrospectively analyzed. Results Of the 60 cases, 55 cases were cured after treatment, including the second stage of operation and good postoperative recovery. Five patients died of complex disease and deformity and abandonment of treatment. The complications such as complication and low body weight had a poor prognosis Influence (P <0.05). Conclusion The key to surgical treatment of children with congenital intestinal atresia is to choose the appropriate surgical approach to ensure that children anastomotic unimpeded. Combined complications, low weight will affect the prognosis of children.