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[空肠上段闭锁:采用空肠切除、十二指肠塑形及十二指肠-空肠或回肠吻合术治疗。13例新生儿的治疗结果]

[Upper jejunal atresia: treatment using jejunal resection, duodenal modeling and duodeno-jejunal or ileal anastomosis. Results in 13 newborn infants].

作者信息

Kazandjian V, Aigrain Y, Enezian G, Guillaume M, Boige N, Amiel I, Weisgerber G, Boureau M

机构信息

Clinique Chirurgicale Infantile, Hôpital Robert-Debré, Paris.

出版信息

Chir Pediatr. 1989;30(5):191-5.

PMID:2515006
Abstract

13 high jejunal atresias, including 6 type IIIb apple peel small bowel deformities, have been treated by a one stage surgical procedure, including proximal jejunal resection, tapering duodenoplasty and end-to-end duodeno-jejunal or duodeno-ileal anastomosis. All 13 infants survived. There were no anastomotic leak or malfunction. 7 jejunal atresias with normal distal small bowel were fed a mean of 9 days post-operatively (range 4 to 12 days). Intra-venous fluids were discontinued at a mean of 18 days post-operatively (range 13 to 24 days). Patients, all premature babies, were discharged on the mean 30th post-operative day (range 24 to 40). 5 jejunal atresias with apple peel deformity were fed with an average post-operative delay of 21 days (range 12 to 24). All intra-venous fluids were discontinued at a mean of 48 days post-operatively (range 35 to 90). Average hospital stay was 78 days (45 to 120). In one case, an ileal diaphragm, unnoticed during the first operation was subsequently resected at age 45 days and an iterative tapering duodenoplasty was performed at the age of 8 months. Recovery was then uncomplicated and the child was discharged on a normal oral feeding at the age of 10 months. Functional obstruction of the intestine at the site of anastomosis often occurs in high jejunal atresias. 70% of mortality resulted from operative complications in atresias with apple peel deformity. Intestinal distension is the cause of anastomotic malfunction. After jejunal resection, the duodenum remains dilated and anastomosis cannot function properly.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

13例高位空肠闭锁,包括6例IIIb型苹果皮样小肠畸形,采用一期手术治疗,包括近端空肠切除、十二指肠缩窄成形术以及十二指肠空肠或十二指肠回肠端端吻合术。13例婴儿均存活。无吻合口漏或功能障碍。7例远端小肠正常的空肠闭锁患儿术后平均9天开始喂养(范围4至12天)。静脉补液平均在术后18天停止(范围13至24天)。所有患儿均为早产儿,术后平均第30天出院(范围24至40天)。5例苹果皮样畸形的空肠闭锁患儿术后平均延迟21天开始喂养(范围12至24天)。所有静脉补液平均在术后48天停止(范围35至90天)。平均住院时间为78天(45至120天)。1例患儿在首次手术时未发现回肠隔膜,45天时切除隔膜,8个月时再次行十二指肠缩窄成形术。此后恢复顺利,患儿10个月时正常经口喂养出院。高位空肠闭锁时,吻合口处常发生功能性肠梗阻。苹果皮样畸形闭锁患儿70%的死亡源于手术并发症。肠扩张是吻合口功能障碍的原因。空肠切除后,十二指肠仍扩张,吻合口无法正常发挥功能。(摘要截选至250词)

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