Hrabovsky E E, Boyd J B, Savrin R A, Boles E T
Ann Surg. 1980 Aug;192(2):244-8. doi: 10.1097/00000658-198008000-00020.
Twenty-eight cases of gastroschisis have been treated over a five-year period. Twenty-two silos were placed and 19 infants had uncomplicated silo closure. Enlargement of the abdominal wall defect to allow optimum reduction of the edematous bowel was essential to closure in less than a week. Rapid removal of the prosthesis and strict adherence to aseptic technique prevented septic complications. Inability to return the bowel to the abdominal cavity within five to six days mandated re-exploration to determine the cause for failure to reduce the silo. Accordingly, three infants were re-explored. Two patients had unrecognized intestinal lesions and a third infant, whose defect had not been enlarged, had infarction of the midgut. Six infants underwent primary closure; two with preinatal evisceration and four who had concomminant cutaneous enterostomies performed for intestinal atresia. Intestinal atresia or stenosis occurred in 25% of these infants. Postoperative management was facilitated by insertion of a gastrostomy tube, early peripheral venous nutrition and later insertion of a central venous catheter for nutrition. The one postoperative death (3.5% mortality rate) resulted from failure to follow the principles of silo management as outlined in this report.
在五年期间共治疗了28例腹裂患儿。放置了22个肠袋,19例婴儿顺利关闭肠袋。腹壁缺损扩大以使水肿肠管能得到最佳复位,这对于在不到一周内完成关闭至关重要。迅速取出假体并严格遵守无菌技术可预防感染并发症。若在五至六天内无法将肠管回纳入腹腔,则需再次手术以确定肠袋复位失败的原因。因此,对三名婴儿进行了再次手术探查。两名患者存在未被识别的肠道病变,第三名婴儿的缺损未扩大,但发生了中肠梗死。六名婴儿接受了一期缝合;两名产前脏器外翻,四名因肠闭锁同时行了皮肤肠造口术。这些婴儿中有25%发生了肠闭锁或狭窄。通过插入胃造瘘管、早期外周静脉营养以及后期插入中心静脉导管进行营养支持,术后管理得以顺利进行。1例术后死亡(死亡率3.5%)是由于未遵循本报告所述的肠袋管理原则所致。