Initial experience with one-stage endorectal pull-through procedures for Hirschsprung's disease

被引:3
作者
Skarsgard, ED [1 ]
Superina, RA [1 ]
Shandling, B [1 ]
Wesson, DE [1 ]
机构
[1] HOSP SICK CHILDREN, DEPT SURG, TORONTO, ON M5G 1X8, CANADA
关键词
Hirschsprung's disease; endorectal pull-through; one-stage;
D O I
暂无
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
To evaluate our experience with one-stage endorectal pull-through (ERPT) procedures (without colostomy) for Hirschsprung's disease (HD), we compared 7 such patients to a cohort of 20 consecutive patients undergoing ERPT following colostomy. Reasons for exclusion from the cohort group included: (1) bowel obstruction requiring operation before 1 month of age; (2) presentation with enterocolitis (EC), intestinal perforation, or massive fecal distension; (3) long-segment disease; or (4) severe associated anomalies. The 7 male patients in the single-stage ERPT group first presented at a median ape of 16 days (4 days-2.5 years) and were managed by regular digital dilation or colonic irrigation for between 1 and 6 months (median 2 months) prior to surgery. Single-stage procedures were performed at a median age and weight of 4 months (2 months-2.5 years) and 6.4 kg (4.5-13.8 kg), respectively. Median hospitalization for these patients was 9 days. Postoperative complications occurred in 2 patients (29%), and included anastomotic stricture requiring outpatient dilation, and 1 case of recurrent EC that responded to a course of anal dilations. The cohort group (14 M, 6 F) presented at a median of 15 months. All underwent colostomy as a primary procedure. ERPT was deferred until a median age of 21 months, and the hospitalization after pull-through averaged 10 days (20 days including stay after colostomy). Four patient (20%) developed complications requiring reoperation following the initial colostomy. Complications after ERPT occurred in 5 patients (25%) and included 1 death from fulminant Hirschsprung's EC. Other complications included 1 anastomotic stricture and 2 mucosal prolapses requiring anoplasty. Long-term functional results were similar in both groups. Despite our limited experience, we conclude that one-stage ERPT can be safely performed in infants, including those under 3 months of age, with rectosigmoid HD. Total duration of hospitalization is reduced and colostomy complications are avoided. Functional outcome appears to be comparable between patients treated in one or two stages.
引用
收藏
页码:480 / 482
页数:3
相关论文
共 10 条
[1]  
BOLEY SJ, 1964, SURGERY, V56, P1015
[2]   MANAGEMENT OF HIRSCHSPRUNGS-DISEASE - CURATIVE SURGERY BEFORE 3 MONTHS OF AGE [J].
CARCASSONNE, M ;
GUYS, JM ;
MORISSONLACOMBE, G ;
KREITMANN, B .
JOURNAL OF PEDIATRIC SURGERY, 1989, 24 (10) :1032-1034
[4]  
FREEMAN NV, 1980, Z KINDERCHIR, V31, P22
[5]  
GILLEY RE, 1994, SURGERY, V115, P551
[6]  
REHBEIN F, 1958, CHIRURG, V29, P336
[7]   PUNCH BIOPSY OF RECTUM FOR DIAGNOSIS OF HIRSCHSPRUNGS DISEASE [J].
SHANDLING, B ;
AULDIST, AW .
JOURNAL OF PEDIATRIC SURGERY, 1972, 7 (05) :546-+
[8]   ENDORECTAL PULL-THROUGH WITHOUT PRELIMINARY COLOSTOMY IN NEONATES WITH HIRSCHSPRUNGS-DISEASE [J].
SO, HB ;
SCHWARTZ, DL ;
BECKER, JM ;
DAUM, F ;
SCHNEIDER, KM .
JOURNAL OF PEDIATRIC SURGERY, 1980, 15 (04) :470-471
[9]   HIRSCHSPRUNGS DISEASE - NEW SURGICAL TECHNIQUE [J].
SOAVE, F .
ARCHIVES OF DISEASE IN CHILDHOOD, 1964, 39 (204) :116-&
[10]  
SWENSON O, 1948, SURGERY, V24, P212