One-stage neonatal pull-through to treat Hirschsprung's disease

被引:33
作者
Wilcox, DT [1 ]
Bruce, J [1 ]
Bowen, J [1 ]
Bianchi, A [1 ]
机构
[1] ROYAL MANCHESTER CHILDRENS HOSP, MANCHESTER M27 1HA, LANCS, ENGLAND
关键词
Hirschsprung's disease; neonate; Swenson; Soave;
D O I
10.1016/S0022-3468(97)90187-1
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Introduction: Traditionally Hirschsprung's disease has been treated by a three-stage procedure. This approach has been associated with stoma problems, three episodes of hospitalization, and a theoretical disadvantage, because of the delayed passage of feces via the rectum, in controlling defecation. The aim of this study was to assess the results of one-stage neonatal pull-through for the treatment of Hirschsprung's disease. Methods: This was a 10-year retrospective review of all patients treated with a neonatal pull through for Hirschsprung's disease. information was obtained from the patients' records. All descriptive data are expressed as mean +/- standard deviation. Results: Fifty-one patients were treated in the 10-year period studied. The mean gestational age was 39.6 +/- 1.7 weeks, weight was 3.3 +/- 0.54 kg, with 76% being boys. The surgery was performed at 10.3 +/- 5.8 days of age. A Swenson procedure was carried out in 38 patients and a Soave in 13. The extent of the disease Was rectosigmoid in 39, and the remaining were sigmoid, descending colon, and total colonic. The mean length of the surgery was 181 +/- 40 minutes. Blood transfusions were required in 13 patients with a mean volume of 55 mL given. The complications observed were: an anastomotic leak in two cases, requiring laparotomy and colostomy (both in patients with Down's syndrome), and wound infection in three cases. There were two delayed deaths both associated with other congenital anomalies. In total, three patients required further surgery; two had colostomies, one requiring a redd pull-through and one had an ileostomy for enterocolitis. The total length of hospital stay was 20.4 +/- 11.2 days. Mean follow-up was 3.73 +/- 2.9 years. In 21 patients the follow-up was greater than 4 years End in this group none were totally incontinent. Four patients complained of soiling at least once a week; and 17 had normal bowel control. Conclusion: Hirschsprung's disease can be successfully treated in the neonatal period with a one-stage pull-through. The short- and long-term results are as good as those with the three-stage procedure, with the child usually benefitting by not having a stoma and a shorter hospital stay. Copyright (C) 1997 by W.B. Saunders Company.
引用
收藏
页码:243 / 247
页数:5
相关论文
共 11 条
[1]   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
[2]   PROLONGED SENSITIVITY TO MONOCULAR DEPRIVATION IN DARK-REARED CATS [J].
CYNADER, M ;
MITCHELL, DE .
JOURNAL OF NEUROPHYSIOLOGY, 1980, 43 (04) :1026-1040
[3]  
GILLEY RE, 1994, SURGERY, V115, P551
[4]   LONG-TERM ANORECTAL FUNCTION AFTER DUHAMEL OPERATION FOR HIRSCHSPRUNGS-DISEASE [J].
HEIJ, HA ;
DEVRIES, X ;
BREMER, I ;
EKKELKAMP, S ;
VOS, A .
JOURNAL OF PEDIATRIC SURGERY, 1995, 30 (03) :430-432
[5]   HIRSCHSPRUNGS-DISEASE - ONE SURGEONS EXPERIENCE IN ONE INSTITUTION [J].
JUNG, PM .
JOURNAL OF PEDIATRIC SURGERY, 1995, 30 (05) :646-651
[6]   RECTAL IRRIGATIONS FOR THE PREVENTION OF POSTOPERATIVE ENTEROCOLITIS IN HIRSCHSPRUNGS-DISEASE [J].
MARTY, TL ;
SEO, T ;
SULLIVAN, JJ ;
MATLAK, ME ;
BLACK, RE ;
JOHNSON, DG .
JOURNAL OF PEDIATRIC SURGERY, 1995, 30 (05) :652-654
[7]   THE INFLUENCE OF TRISOMY-21 ON OUTCOME IN CHILDREN WITH HIRSCHSPRUNGS-DISEASE [J].
QUINN, FMJ ;
SURANA, R ;
PURI, P .
JOURNAL OF PEDIATRIC SURGERY, 1994, 29 (06) :781-783
[8]  
SHANBHOGUE LKR, 1990, PEDIATR SURG INT, V5, P446
[9]   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
[10]  
SWENSON O, 1948, SURGERY, V24, P212