Abstract
Purpose
Only a few patients with anorectal malformations (ARM) have satisfactory bowel functions. Studies of ARM have reported psychosocial problems in up to 73% of patients. The aim of the current study was to document the psychosocial needs of patients with ARM.
Methods
Between June 2004 and September 2005, 44 patients with ARM were treated; the sample included 30 patients (23 males and 7 females) aged 4–17. To focus on potential psychosocial strain, a comprehensive grading system with a sophisticated perspective of continence, associated malformations, number of surgical interventions and postoperative complications was introduced. For psychosocial screening, the following instruments were used: German “Basis-Dokumentation” (BADO), Impact on Family Scale (IFS), the Strengths and Difficulties Questionnaire (SDQ). All families assessed their own psychosocial needs. An extensive psychosocial programme was provided.
Results
Twenty-three patients were suffering severe burden according to the comprehensive grading system. Nearly half of the families reported increased financial stress, and one-third reported emotional or hyperactivity problems of the child. More than 70% confirmed psychosocial need.
Conclusions
Paediatric surgeons should promote psychosocial support for all patients who suffer severe forms of ARM or its numerous associated malformations as well as for patients undergoing numerous surgical interventions or having many postoperative complications.
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Acknowledgment
Our special thanks to Martina Pech for the assistance with the translation and to Dr. Med. E. Pfeiffer for critical assessment.
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The authors declare that they have no conflict of interest.
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Winter, S., Schmidt, D., Lenz, K. et al. Prospective evaluation of comorbidity and psychosocial need in children and adolescents with anorectal malformations. Part 2: Evaluation of psychosocial need. Pediatr Surg Int 25, 895–900 (2009). https://doi.org/10.1007/s00383-009-2441-8
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DOI: https://doi.org/10.1007/s00383-009-2441-8