Quality of life of patients with Hirschsprung's disease at 5-20 years post pull-through operations

被引:35
作者
Niramis, R. [1 ,2 ]
Watanatittan, S. [1 ,2 ]
Anuntkosol, M. [1 ,2 ]
Buranakijcharoen, V. [1 ,2 ]
Rattanasuwan, T. [1 ,2 ]
Tongsin, A. [1 ,2 ]
Petlek, W. [1 ,2 ]
Mahatharadol, V. [1 ,2 ]
机构
[1] Childrens Hosp, Queen Sirikit Natl Inst Child Hlth, Dept Surg, Bangkok 10400, Thailand
[2] Rangsit Univ, Fac Med, Bangkok, Thailand
关键词
Hirschsprung's disease; quality of life; long-term follow-up; faecal continence;
D O I
10.1055/s-2008-1038325
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Purpose: The aim of this study was to evaluate the bowel habits and quality of life with respect to faecal continence of patients with Hirschsprung's disease (HD) who had undergone pull-through operations more than 5 years previously. Materials and Methods: Four hundred and sixty-seven patients who underwent pull-through operations for HD during the period of 1987-1999 were followed up for evaluation. A questionnaire including demographic data and a qualitative clinical scoring method as described by Holschneider was used for the evaluation of faecal continence. The scoring system did not require a physical examination. Outcomes of the 3 major procedures (Swenson, Duhamel and Soave technique) were analysed. The research was undertaken from October 2004 to September 2006. Patients with neurological defects and total colonic aganglionosis (TCA) were excluded from the analysis. Only patients with typical HD were evaluated, and they were divided into 3 groups based on the length of the period since surgery: 5-10 years in Group A; 10-15 years in Group 13; and 15-20 years in Group C. Results: Only 204 patients (male to female ratio: 169:35) returned to the Queen Sirikit National Institute of Child Health for evaluation. Twenty-six patients were excluded because of TCA in 13, Down's syndrome in 9 and cerebral palsy in 4. The remaining 178 patients were evaluated and divided into Group A (n=67), Group B (n=75) and Group C (n = 36). Excellent results (14 points), good results (10-13 points) and fair results (5-9 points) were noted in Group A in 52.2%, 34.3% and 7.5% of cases respectively, in Group B in 68%, 28% and 4% of cases, respectively, and in Group C in 88.9%, 11.1% and 0% of cases, respectively. Five cases (7.5%) in Group A and 3 cases (4%) in Group B with fair results still had problems such as constant soiling and an inability to hold back defecation. They experienced marked limitations in their social life because of their dependence on diapers and frustration because of teasing by their friends. Conclusion: Faecal incontinence still remains a problem in some patients with HD at 5-15 years after surgical correction. However, nearly all patients who were operated on more than 15 years previously had nearly normal faecal continence and a normal social life.
引用
收藏
页码:38 / 43
页数:6
相关论文
共 30 条
[11]   TOTAL COLONIC AGANGLIONOSIS WITH OR WITHOUT SMALL-BOWEL INVOLVEMENT - AN ANALYSIS OF 137 PATIENTS [J].
IKEDA, K ;
GOTO, S .
JOURNAL OF PEDIATRIC SURGERY, 1986, 21 (04) :319-322
[12]  
JASONNI V, 2000, HIRSCHSPRUNGS DIS AL, P336
[13]  
JOOSTEN KFM, 1988, PEDIATR SURG INT, V3, P204
[14]   HIRSCHSPRUNGS-DISEASE - SURVEY OF THE MEMBERS OF THE SURGICAL - SECTION OF THE AMERICAN-ACADEMY-OF-PEDIATRICS [J].
KLEINHAUS, S ;
BOLEY, SJ ;
SHERAN, M ;
SIEBER, WK .
JOURNAL OF PEDIATRIC SURGERY, 1979, 14 (05) :588-597
[15]   HIRSCHSPRUNGS-DISEASE - LONG-TERM RESULTS OF THE ORIGINAL DUHAMEL OPERATION [J].
LIVADITIS, A .
JOURNAL OF PEDIATRIC SURGERY, 1981, 16 (04) :484-486
[16]   GASTROINTESTINAL FUNCTION AFTER SURGICAL-CORRECTION OF HIRSCHSPRUNGS-DISEASE - LONG-TERM FOLLOW-UP IN 135 PATIENTS [J].
MARTY, TL ;
SEO, T ;
MATLAK, ME ;
SULLIVAN, JJ ;
BLACK, RE ;
JOHNSON, DG .
JOURNAL OF PEDIATRIC SURGERY, 1995, 30 (05) :655-658
[17]   POSTOPERATIVE FUNCTIONAL AND MANOMETRIC EVALUATION OF PATIENTS WITH HIRSCHSPRUNGS-DISEASE [J].
MISHALANY, HG ;
WOOLLEY, MM .
JOURNAL OF PEDIATRIC SURGERY, 1987, 22 (05) :443-446
[18]   Clinical outcome and long-term quality of life after surgical correction of Hirschsprung's disease [J].
Moore, SW ;
Albertyn, R ;
Cywes, S .
JOURNAL OF PEDIATRIC SURGERY, 1996, 31 (11) :1496-1502
[19]  
MOORE SW, 1998, SEMIN PEDIATR SURG, V17, P156
[20]   TOTAL COLONIC AGANGLIONOSIS (WITH OR WITHOUT ILEAL INVOLVEMENT) - A REVIEW OF 27 CASES [J].
NFEKETE, C ;
RICOUR, C ;
MARTELLI, H ;
JACOB, SL ;
PELLERIN, D .
JOURNAL OF PEDIATRIC SURGERY, 1986, 21 (03) :251-254