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Published on: April 26, 2019
Defecation disorders in children after surgery for Hirschsprung disease
Bruno P Chumpitazi1, Samuel Nurko
1Center for Motility and Functional Gastrointestinal Disorders, Children's Hospital Boston, Boston, MA 02115, USA.
Insights
Children with Hirschsprung disease (HD) and defecation disorders (DDs) after surgery often improve with a systematic algorithm. This approach leads to favorable long-term outcomes for most pediatric patients.
Area of Science:
- Pediatric Surgery
- Gastroenterology
- Clinical Outcomes Research
Background:
- Hirschsprung disease (HD) frequently leads to persistent defecation disorders (DDs) post-corrective surgery (CS).
- These disorders include constipation, fecal incontinence, and enterocolitis, impacting quality of life.
Purpose of the Study:
- To determine diagnoses and therapies for protracted DDs in children with HD after CS.
- To evaluate long-term clinical outcomes using a systematic management algorithm.
Main Methods:
- Retrospective review of pediatric patients with HD and DDs after CS.
- Systematic algorithm application for diagnosis and treatment at a tertiary care center.
- Clinical outcomes categorized based on symptom severity and treatment response.
Main Results:
- Fifty-seven children were analyzed; 89.5% presented with obstructive symptoms or enterocolitis.
- Common etiologies included nonrelaxing anal sphincter (38.6%) and residual aganglionosis (15.8%).
- Overall, 66.7% achieved excellent or good clinical outcomes, with enterocolitis patients showing better results.
Conclusions:
- A systematic algorithm effectively manages protracted defecation disorders in children with HD post-surgery.
- Most children experience favorable long-term clinical outcomes with this structured approach.
Background And Objective:
The majority of children with Hirschsprung disease (HD) after corrective surgery (CS) develop protracted defecation disorders (DDs) such as constipation, fecal incontinence, and/or enterocolitis. The aim of this investigation was to determine the diagnoses, therapies, and long-term clinical outcomes using a systematic algorithm to address protracted DD in children with HD after CS.
Methods:
Retrospective review of children with HD after CS cared for using a systematic algorithm at a tertiary care center. Potential anatomic etiologies were evaluated for first. Clinical outcome was categorized into 4 groups based on symptom severity, time interval from last enterocolitis episode, laxative usage, and/or rectal therapies at the time of last follow-up.
Results:
Fifty-seven children were identified, of whom 51 (89.5%) had obstructive symptoms and/or enterocolitis and 6 (10.5%) had nonretentive fecal incontinence. Nonintractable constipation responsive to laxatives was identified in 10 (17.5%), colonic dysmotility in 4 (7.0%), nonrelaxing anal sphincter as a primary etiology in 22 (38.6%), bacterial overgrowth in 2 (3.5%), food intolerance in 2 (3.5%), and rapid transit in 2 (3.5%). Further surgical intervention was undertaken in 22 (38.6%), including 9 (15.8%) for residual aganglionosis. Mean follow-up was 41.4 ± 4.5 months. Clinical outcomes were excellent in 16 (28.1%), good in 22 (38.6%), fair in 1 (1.8%), and poor in 18 (31.6%). Children with enterocolitis were more likely to have an excellent or good clinical outcome.
Conclusions:
The majority of children with HD and protracted DD after CS have a favorable long-term clinical outcome when following a systematic algorithm.
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