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对巨结肠症的杜哈梅尔手术的批判性评估。

A critical evaluation of the Duhamel operation for Hirschsprung's disease.

作者信息

Grosfeld J L, Ballantine V N, Csicsko J F

出版信息

Arch Surg. 1978 Apr;113(4):454-60. doi: 10.1001/archsurg.1978.01370160112019.

Abstract

Eighty-nine patients with Hirschsprung's disease were treated from 1972 to 1977. Of the patients, 70 were boys, 85 were the result of full-term pregnancy, and four had Down's syndrome. There were 23 children, 32 infants, and 34 neonates including seven (20%) with enterocolitis. Early mortality was 8.8% in neonates and 3% in infants. After initial diversion (colostomy or enterostomy), 66 patients had "classic" (ten), modified (52), or "long" (four) Duhamel pull-through procedures at age 1 year. Operative mortality was zero. Three late deaths occurred; two of them were mongols. Fecaloma occurred in eight of ten classic cases that required revision. Postoperative enterocolitis occurred in three of four long procedures done for total colonic aganglionosis. The modified Duhamel procedure was associated with a low complication rate and good function. There were no instances of anastomotic leak, anal stricture, or genitourinary problems. These data indicate that the modified Duhamel operation is a highly acceptable procedure in the management of Hirsch sprung's disease.

摘要

1972年至1977年期间,对89例先天性巨结肠患者进行了治疗。其中,70例为男孩,85例为足月妊娠的结果,4例患有唐氏综合征。有23名儿童、32名婴儿和34名新生儿,其中7例(20%)患有小肠结肠炎。新生儿早期死亡率为8.8%,婴儿为3%。在最初的造瘘术(结肠造口术或肠造口术)后,66例患者在1岁时接受了“经典”(10例)、改良(52例)或“长”(4例)Duhamel拖出术。手术死亡率为零。发生了3例晚期死亡;其中2例为蒙古人。在10例需要进行修复的经典病例中,有8例出现粪瘤。在为全结肠无神经节症进行的4例长手术中,有3例发生术后小肠结肠炎。改良Duhamel手术并发症发生率低且功能良好。没有吻合口漏、肛门狭窄或泌尿生殖系统问题的病例。这些数据表明,改良Duhamel手术是治疗先天性巨结肠的一种高度可接受的手术方法。

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