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DOI: 10.1055/s-0037-1607356
Social Morbidity in Relation to Bowel Functional Outcomes and Quality of Life in Anorectal Malformations and Hirschsprung's Disease
Funding This work was supported by a grant from the Finnish Foundation for Pediatric Research.Publication History
21 July 2017
15 September 2017
Publication Date:
23 October 2017 (online)
Abstract
Background Anorectal malformations (ARMs) and Hirschsprung's disease (HD) are chronic bowel conditions associated with varying degrees of fecal incontinence. We aimed to discuss the contemporary status of social morbidity associated with ARMs and HD in the long term after contemporary treatments.
Materials and Methods The bowel functional outcomes of our recent institutional series up to adulthood were reviewed and compared for ARMs and HD. The Rintala score was used to evaluate bowel function, which includes an assessment of the social effects of the condition. In this study, the social outcomes in our population of patients with ARMs and HD were specifically analyzed in relation to the surveyed functional outcomes, our previously collected data on quality of life (QoL) and the current literature.
Results Mild ARMs were associated with a minimal risk of social morbidity consistent with good outcomes. In severe ARMs and HD, social problems were reported steadily among all age groups studied. Impairment of domains of fecal control were present among 53 to 89% of patients with social problems, including frequent symptoms (>1/week) in up to 39%. Involuntary gas leakage contributed to social morbidity in 15 to 27%. Comparison with QoL data suggested that social morbidity experienced during childhood may continue to affect emotional domains of QoL in later life, despite improvements in bowel function by adulthood.
Conclusion Patients with severe ARMs and HD are at risk of social restrictions from impairment of bowel function despite contemporary surgical treatments. However, the QoL outcomes in adulthood may be more influenced by self-perceptions of illness formed from childhood than disease-specific factors. Strategies to reduce the psychological morbidity associated with these conditions that includes parental involvement from the outset may improve outcomes.
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References
- 1 Hartman EE, Oort FJ, Aronson DC, Sprangers MA. Quality of life and disease-specific functioning of patients with anorectal malformations or Hirschsprung's disease: a review. Arch Dis Child 2011; 96 (04) 398-406
- 2 Iwai N, Fumino S. Surgical treatment of anorectal malformations. Surg Today 2013; 43 (09) 955-962
- 3 Hamid CH, Holland AJ, Martin HC. Long-term outcome of anorectal malformations: the patient perspective. Pediatr Surg Int 2007; 23 (02) 97-102
- 4 Grano C, Fernandes M, Aminoff D, Bucci S, Lucidi F, Violani C. The role of coping strategies on health-related quality of life in adults with anorectal malformations. Pediatr Surg Int 2016; 32 (08) 759-765
- 5 Kyrklund K, Pakarinen MP, Koivusalo A, Rintala RJ. Long-term bowel functional outcomes in rectourethral fistula treated with PSARP: controlled results after 4-29 years of follow-up: a single-institution, cross-sectional study. J Pediatr Surg 2014; 49 (11) 1635-1642
- 6 Neuvonen MI, Kyrklund K, Rintala RJ, Pakarinen MP. Bowel function and quality of life after transanal endorectal pull-through for Hirschsprung disease: controlled outcomes up to adulthood. Ann Surg 2017; 265 (03) 622-629
- 7 Rintala RJ, Lindahl H. Is normal bowel function possible after repair of intermediate and high anorectal malformations?. J Pediatr Surg 1995; 30 (03) 491-494
- 8 Rintala RJ. Congenital cloaca: long-term follow-up results with emphasis on outcomes beyond childhood. Semin Pediatr Surg 2016; 25 (02) 112-116
- 9 Grano C, Aminoff D, Lucidi F, Arpante A, Violani C. Self-efficacy, postoperative care satisfaction, body image and sexual functioning in ARM patients. Pediatr Surg Int 2008; 24 (11) 1201-1205
- 10 Kyrklund K, Pakarinen MP, Taskinen S, Rintala RJ. Bowel function and lower urinary tract symptoms in females with anterior anus treated conservatively: controlled outcomes into adulthood. J Pediatr Surg 2015; 50 (07) 1168-1173
- 11 Kyrklund K, Pakarinen MP, Taskinen S, Rintala RJ. Bowel function and lower urinary tract symptoms in males with low anorectal malformations: an update of controlled, long-term outcomes. Int J Colorectal Dis 2015; 30 (02) 221-228
- 12 Kyrklund K, Pakarinen MP, Koivusalo A, Rintala RJ. Bowel functional outcomes in females with perineal or vestibular fistula treated with anterior sagittal anorectoplasty: controlled results into adulthood. Dis Colon Rectum 2015; 58 (01) 97-103
- 13 Kyrklund K, Koivusalo A, Rintala RJ, Pakarinen MP. Evaluation of bowel function and fecal continence in 594 Finnish individuals aged 4 to 26 years. Dis Colon Rectum 2012; 55 (06) 671-676
- 14 Kyrklund K, Taskinen S, Rintala RJ, Pakarinen MP. Sexual function, fertility and quality of life after modern treatment of anorectal malformations. J Urol 2016; 196 (06) 1741-1746
- 15 Neuvonen M, Kyrklund K, Taskinen S, Koivusalo A, Rintala RJ, Pakarinen MP. Lower urinary tract symptoms and sexual functions after endorectal pull-through for Hirschsprung disease: controlled long-term outcomes. J Pediatr Surg 2017; 52 (08) 1296-1301
- 16 Pakarinen MP, Rintala RJ. Management and outcome of low anorectal malformations. Pediatr Surg Int 2010; 26 (11) 1057-1063
- 17 Kyrklund K, Pakarinen MP, Rintala RJ. Manometric findings in relation to functional outcomes in different types of anorectal malformations. J Pediatr Surg 2017; 52 (04) 563-568
- 18 Okada A, Kamata S, Imura K. , et al. Anterior sagittal anorectoplasty for rectovestibular and anovestibular fistula. J Pediatr Surg 1992; 27 (01) 85-88
- 19 deVries PA, Peña A. Posterior sagittal anorectoplasty. J Pediatr Surg 1982; 17 (05) 638-643
- 20 Levitt MA, Peña A. Outcomes from the correction of anorectal malformations. Curr Opin Pediatr 2005; 17 (03) 394-401
- 21 Peña A, Hong A. Advances in the management of anorectal malformations. Am J Surg 2000; 180 (05) 370-376
- 22 Rintala RJ, Pakarinen MP. Imperforate anus: long- and short-term outcome. Semin Pediatr Surg 2008; 17 (02) 79-89
- 23 Rintala RJ. Congenital anorectal malformations: anything new?. J Pediatr Gastroenterol Nutr 2009; 48 (Suppl. 02) S79-S82
- 24 Yeung CK, Kiely EM. Low anorectal anomalies: a critical appraisal. Pediatr Surg Int 1991; 6: 333-335
- 25 Pakarinen MP, Koivusalo A, Lindahl H, Rintala RJ. Prospective controlled long-term follow-up for functional outcome after anoplasty in boys with perineal fistula. J Pediatr Gastroenterol Nutr 2007; 44 (04) 436-439
- 26 Rintala RJ, Pakarinen MP. Outcome of anorectal malformations and Hirschsprung's disease beyond childhood. Semin Pediatr Surg 2010; 19 (02) 160-167
- 27 Ieiri S, Nakatsuji T, Akiyoshi J. , et al. Long-term outcomes and the quality of life of Hirschsprung disease in adolescents who have reached 18 years or older--a 47-year single-institute experience. J Pediatr Surg 2010; 45 (12) 2398-2402
- 28 Kumar B, Kandpal DK, Sharma SB, Agrawal LD, Jhamariya VN. Single-stage repair of vestibular and perineal fistulae without colostomy. J Pediatr Surg 2008; 43 (10) 1848-1852
- 29 Menon P, Rao KL. Primary anorectoplasty in females with common anorectal malformations without colostomy. J Pediatr Surg 2007; 42 (06) 1103-1106
- 30 Kiesewetter WB, Chang JH. Imperforate anus: a five to thirty year follow-up perspective. Prog Pediatr Surg 1977; 10: 111-120
- 31 Templeton Jr JM, Ditesheim JA. High imperforate anus--quantitative results of long-term fecal continence. J Pediatr Surg 1985; 20 (06) 645-652
- 32 Rintala RJ, Lindahl H, Louhimo I. Anorectal malformations – results of treatment and follow-up of 208 patients. Pediatr Surg Int 1991; 6: 36-41
- 33 Stenström P, Kockum CC, Benér DK, Ivarsson C, Arnbjörnsson E. Adolescents with anorectal malformation: physical outcome, sexual health and quality of life. Int J Adolesc Med Health 2014; 26 (01) 49-59
- 34 Rintala RJ, Lindahl HG. Fecal continence improves in patients having undergone posterior sagittal anorectoplasty procedure for a high anorectal malformation improves at adolescence, as constipation disappears. J Pediatr Surg 2001; 36 (08) 1218-1221
- 35 Stensrud KJ, Emblem R, Bjørnland K. Anal endosonography and bowel function in patients undergoing different types of endorectal pull-through procedures for Hirschsprung disease. J Pediatr Surg 2015; 50 (08) 1341-1346
- 36 Jarvi K, Laitakari EM, Koivusalo A, Rintala RJ, Pakarinen MP. Bowel function and gastrointestinal quality of life among adults operated for Hirschsprung disease during childhood: a population-based study. Ann Surg 2010; 252 (06) 977-981
- 37 Heikkinen M, Rintala R, Luukkonen P. Long-term anal sphincter performance after surgery for Hirschsprung's disease. J Pediatr Surg 1997; 32 (10) 1443-1446
- 38 Diseth TH, Bjørnland K, Nøvik TS, Emblem R. Bowel function, mental health, and psychosocial function in adolescents with Hirschsprung's disease. Arch Dis Child 1997; 76 (02) 100-106
- 39 Hartman EE, Oort FJ, Sprangers MA. , et al. Factors affecting quality of life of children and adolescents with anorectal malformations or Hirschsprung disease. J Pediatr Gastroenterol Nutr 2008; 47 (04) 463-471
- 40 Faugli A, Bjørnland K, Emblem R, Nøvik TS, Diseth TH. Mental health and psychosocial functioning in adolescents with esophageal atresia. J Pediatr Surg 2009; 44 (04) 729-737
- 41 Hartman EE, Oort FJ, Aronson DC. , et al. Explaining change in quality of life of children and adolescents with anorectal malformations or Hirschsprung disease. Pediatrics 2007; 119 (02) e374-e383
- 42 Hartman EE, Oort FJ, Aronson DC. , et al. Critical factors affecting quality of life of adult patients with anorectal malformations or Hirschsprung's disease. Am J Gastroenterol 2004; 99 (05) 907-913
- 43 Cushing CC, Martinez-Leo B, Bischoff A. , et al. Health-related quality of life and parental stress in children with fecal incontinence: a normative comparison. J Pediatr Gastroenterol Nutr 2016; 63 (06) 633-636
- 44 Versteegh HP, van den Hondel D, IJsselstijn H, Wijnen RM, Sloots CE, de Blaauw I. Cloacal malformation patients report similar quality of life as female patients with less complex anorectal malformations. J Pediatr Surg 2016; 51 (03) 435-439
- 45 Ludman L, Spitz L, Tsuji H, Pierro A. Hirschsprung's disease: functional and psychological follow up comparing total colonic and rectosigmoid aganglionosis. Arch Dis Child 2002; 86 (05) 348-351
- 46 Lane VA, Nacion KM, Cooper JN, Levitt MA, Deans KJ, Minneci PC. Determinants of quality of life in children with colorectal diseases. J Pediatr Surg 2016; 51 (11) 1843-1850
- 47 Dellenmark-Blom M, Chaplin JE, Jönsson L, Gatzinsky V, Quitmann JH, Abrahamsson K. Coping strategies used by children and adolescents born with esophageal atresia - a focus group study obtaining the child and parent perspective. Child Care Health Dev 2016; 42 (05) 759-767
- 48 Beardslee WR, Gladstone TR, Wright EJ, Cooper AB. A family-based approach to the prevention of depressive symptoms in children at risk: evidence of parental and child change. Pediatrics 2003; 112 (02) e119-e131
- 49 Muise ED, Cowles RA. Transition of care in pediatric surgical patients with complex gastrointestinal disease. Semin Pediatr Surg 2015; 24 (02) 65-68