AI Article Synopsis

  • The study investigates the causes of anal incontinence (AI) and their link to symptom severity and surgical needs in a large group of patients.
  • Out of 1,046 patients analyzed, those with congenital, traumatic, and neurological causes exhibited the highest severity scores and a significant portion required surgical intervention.
  • The findings suggest that patients with AI linked to trauma or congenital issues are more likely to need surgery compared to those with other causes, while prolapse-related AI generally improves with treatment of the prolapse.

Article Abstract

Background: The etiology of anal incontinence (AI) is often multifactorial. There is little data on the relationship between the etiology of AI, symptom severity, and the need for surgery. The aim of our study was to investigate this association in a large number of unselected patients with AI referred to a tertiary specialist coloproctological practice.

Methods: Patients with AI seen at our unit between 1983 and 2008 were analyzed. The main etiologies were categorized as congenital, traumatic, neurologic, idiopathic, post-operative, post-obstetric, secondary to rectal prolapse, or inflammatory bowel disease. The severity of AI was graded using the validated Pescatori incontinence scale.

Results: Overall, 1,046 patients were studied. The AI score was higher in patients with congenital (4.7 ± 1.1), traumatic (4.6 ± 1.4), and neurological (4.4 ± 1.2) incontinence. Surgical treatment was indicated in 214 cases (20.5%). Patients with AI related to trauma and congenital anomalies required surgery in 43.5 and 31.4% of cases, respectively, a percentage significantly higher than that for patients with other etiologies (P = 0.002). Prolapse-related AI usually responded to correction of the prolapse.

Conclusions: Patients with congenital, traumatic, and neurological AI tend to have greater symptom severity. Traumatic, rectal prolapse-related, and congenital AI cases more often require surgery.

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Source
http://dx.doi.org/10.1007/s10151-011-0682-8DOI Listing

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