Long-term functional outcomes and quality of life in patients with Hirschsprung's disease

Author:

Meinds R J1ORCID,van der Steeg A F W23,Sloots C E J4,Witvliet M J5,de Blaauw I6,van Gemert W G7,Trzpis M8,Broens P M A18

Affiliation:

1. Division of Paediatric Surgery, Department of Surgery, University of Groningen, University Medical Centre Groningen, Groningen, the Netherlands

2. Department of Paediatric Surgery, Emma Children's Hospital, Academic Medical Centre and VU University Medical Centre, Amsterdam, the Netherlands

3. Centre of Research on Psychology in Somatic Diseases, Tilburg University, Tilburg, the Netherlands

4. Department of Paediatric Surgery, Erasmus Medical Centre, Sophia Children's Hospital, Rotterdam, the Netherlands

5. Department of Paediatric Surgery, Wilhelmina Children's Hospital, University Medical Centre Utrecht, Utrecht, the Netherlands

6. Division of Paediatric Surgery, Department of Surgery, Radboudumc–Amalia Children's Hospital, Nijmegen, the Netherlands

7. Department of Paediatric Surgery, University Medical Centre Maastricht, University of Maastricht, Maastricht, the Netherlands

8. Anorectal Physiology Laboratory, Department of Surgery, University of Groningen, University Medical Centre Groningen, Groningen, the Netherlands

Abstract

Abstract Background It is unclear whether functional outcomes improve or deteriorate with age following surgery for Hirschsprung's disease. The aim of this cross-sectional study was to determine the long-term functional outcomes and quality of life (QoL) in patients with Hirschsprung's disease. Methods Patients with pathologically proven Hirschsprung's disease older than 7 years were included. Patients with a permanent stoma or intellectual disability were excluded. Functional outcomes were assessed according to the Rome IV criteria using the Defaecation and Faecal Continence questionnaire. QoL was assessed by means of the Child Health Questionnaire Child Form 87 or World Health Organization Quality of Life questionnaire 100. Reference data from healthy controls were available for comparison. Results Of 619 patients invited, 346 (55·9 per cent) responded, with a median age of 18 (range 8–45) years. The prevalence of constipation was comparable in paediatric and adult patients (both 22·0 per cent), and in patients and controls. Compared with controls, adults with Hirschsprung's disease significantly more often experienced straining (50·3 versus 36·1 per cent; P = 0·011) and incomplete evacuation (47·4 versus 27·2 per cent; P < 0·001). The prevalence of faecal incontinence, most commonly soiling, was lower in adults than children with Hirschsprung's disease (16·8 versus 37·6 per cent; P < 0·001), but remained higher than in controls (16·8 versus 6·1 per cent; P = 0·003). Patients with poor functional outcomes scored significantly lower in several QoL domains. Conclusion This study has shown that functional outcomes are better in adults than children, but symptoms of constipation and soiling persist in a substantial group of adults with Hirschsprung's disease. The persistence of defaecation problems is an indication that continuous care is necessary in this specific group of patients.

Publisher

Oxford University Press (OUP)

Subject

Surgery

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