检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:李思琪 黄金狮 Li Siqi;Huang Jinshi(Department of Neonatal Surgery,Beijing Children′s Hospital,Capital Medical University,National Center for Children′s Health,Beijing 100045,China)
机构地区:[1]国家儿童医学中心,首都医科大学附属北京儿童医院新生儿外科,北京100045
出 处:《中华实用儿科临床杂志》2022年第1期67-70,共4页Chinese Journal of Applied Clinical Pediatrics
摘 要:先天性食管闭锁伴或不伴气管食管瘘是较常见且严重的先天性消化道畸形,通过手术修复,绝大多数患儿可实现长期生存,而随之产生的各种远期并发症会影响患儿的身心健康,造成生活质量下降。为进一步防治先天性食管闭锁术后远期并发症,现对其诊治现状和进展进行综述。Congenital esophageal atresia with or without tracheoesophageal fistula is a relatively common and serious congenital gastrointestinal anomaly,which can be surgically repaired to achieve long-term survival in the majority of patients.However,various consequent long-term complications would affect the physical and mental health of patients,thus inducing a decline in their quality of life.In this study,the present status and advances of diagnosis and treatment of these complications were reviewed,in an attempt to further explore the long-term complications after congenital esophageal atresia.
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.7