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Issue title: Spina Bifida
Guest editors: Timothy Brei and Amy Houtrow
Article type: Research Article
Authors: Wiener, John S.a; * | Suson, Kristina D.b | Castillo, Jonathanc | Routh, Jonathan C.a | Tanaka, Stacyd | Liu, Tiebine | Ward, Elisabethf | Thibadeau, Judye | Joseph, Davidg | Registry, National Spina Bifida Patient
Affiliations: [a] Division of Urologic Surgery, Duke University Medical Center, Durham, NC, USA | [b] Department of Urology, Children’s Hospital of Michigan, Detroit, MI, USA | [c] Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA | [d] Department of Urology, Vanderbilt University, Nashville, TN, USA | [e] Centers for Disease Control and Prevention, Atlanta, GA, USA | [f] Carter Consulting, Inc., Consultant to CDC, Atlanta, GA, USA | [g] Department of Urology, University of Alabama at Birmingham, Birmingham, AL, USA
Correspondence: [*] Corresponding author: John S. Wiener, Section of Pediatric Urology, P.O. Box 3831, Duke University Medical Center, Durham, NC 27710, USA. Tel.: +1 919 684 6994; Fax: +1 919 681 5507; E-mail: [email protected].
Abstract: INTRODUCTION: Advances in care have allowed most children with spina bifida (SB) to live to adulthood. The majority have neuropathic bowel dysfunction (NBD), resulting in constipation, incontinence, and diminished quality of life. We sought to 1) describe contemporary NBD management and continence outcomes of adults with SB; 2) describe differences from younger patients; and 3) assess for association with socio-economic factors. METHODS: We analyzed data on NBD management and continence from the National Spina Bifida Patient Registry (NSBPR). Patients were segregated into young children (5–11 years), adolescents (12–19 years), and adults (20 years and older). A strict definition of continence was utilized. Statistical analysis compared cohorts by gender, ethnicity, SB type, lesion level, insurance status, educational attainment, employment status, and continence. RESULTS: A total of 5209 SB patients were included, of whom 1370 (26.3%) were adults. Management and continence varied by age and SB type. Oral medication use did not differ between groups (5.2–6.6%). Suppositories and rectal enemas were used only by 11.5% of adults, which was significantly less than among school-aged children. Antegrade enemas were used by 17.7% of adults which was significantly less than among adolescents (27.2%). Adults were more likely to use digital stimulation or disimpaction or have undergone a colostomy. Bowel continence was reported by 58.3% of overall adult cohort: 55.6% of adults with myelomeningocele and 74.9% with non-myelomeningocele. Bowel continence was significantly associated with employment (p= 0.0002), private insurance (p= 0.0098), non-myelomeningocele type of SB (p= 0.0216) and educational attainment (p= 0.0324) on univariate analysis but only with employment on multivariable logistic regression (p= 0.0027). CONCLUSIONS: Bowel management techniques differed between adults and younger patients with SB. Bowel continence was reported by over half of SB adults and was associated with socio-economic factors.
Keywords: Neurogenic bowel, spina bifida, fecal incontinence
DOI: 10.3233/PRM-170466
Journal: Journal of Pediatric Rehabilitation Medicine, vol. 10, no. 3-4, pp. 335-343, 2017
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