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[婴儿短肠综合征的管理——三例辅助性手术治疗经验]

[Management of short bowel syndrome in infants--experience of adjunctive surgical therapy in three cases].

作者信息

Tsuda M, Nagaya M, Esaki M, Harada T, Aono S

机构信息

Department of Pediatric Surgery, Aichi Prefectural Colony, Kasugai, Japan.

出版信息

Nihon Geka Gakkai Zasshi. 1988 Sep;89(9):1387-90.

PMID:3147367
Abstract

During the past nine years period, we managed 7 cases with short bowel syndrome resulting from massive intestinal resection in the neonatal period. Six children, aged 2 to 8 years are alive, and one died from cardiomyopathy caused by selenium deficiency at the age of one year. The carbohydrate-free milk was used for initial enteral nutrition, and the result was encouraging in 4 cases. In 3 cases in which residual small bowel varied between 6.5 to 18 cm, the enteral feeding was not incapable. These cases underwent adjunctive surgical therapy. Tailoring jejunoplasty was performed in the first case, and bowel lengthening in the second case. In both cases enteral nutrition was advanced postoperatively. The third patient who had rapid intestinal transit time underwent isoperistaltic colon interposition. Intestinal transit time was increased and enteral nutrition was advanced gradually.

摘要

在过去九年期间,我们诊治了7例因新生儿期大量肠切除导致短肠综合征的病例。6名年龄在2至8岁的儿童存活,1名在1岁时死于硒缺乏引起的心肌病。最初的肠内营养采用无碳水化合物牛奶,4例效果令人鼓舞。在3例残留小肠长度在6.5至18厘米之间的病例中,肠内喂养并非不可行。这些病例接受了辅助手术治疗。第一例进行了定制空肠成形术,第二例进行了肠延长术。两例术后均推进了肠内营养。第三例肠道传输时间较快的患者接受了等蠕动结肠间置术。肠道传输时间增加,肠内营养逐渐推进。

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