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Issue title: Spina Bifida, Part 2
Article type: Research Article
Authors: Webb, Thomas S.
Affiliations: Division of General Internal Medicine, University of Cincinnati College of Medicine, Cincinnati, OH, USA
Note: [] Address for correspondence: Thomas S. Webb, MD, MSc, Associate Professor of Clinical Medicine, Division of General Internal Medicine, University of Cincinnati College of Medicine, 231 Albert Sabin Way, ML 0535, Cincinnati, OH 45267, USA. Tel.: +1 513 636 8375; Fax: +1 513 803 0072; E-mail: [email protected]
Abstract: Survival into adulthood for individuals with spina bifida has significantly improved over the last 40 years. Health services research suggests the majority of patients with spina bifida are now over 18 years old. Adults with spina bifida have ongoing increased medical needs compared to the general population, including spina bifida-specific care, age-related secondary disabilities, and general adult medical needs. Unlike pediatric-aged patients, adults may not have access to multi-disciplinary spina bifida clinics and must often coordinate their own care with adult providers less familiar with spina bifida and the associated monitoring and treatment issues. This article will provide an overview of the medical issues of adults with spina bifida, highlighting areas that are different than pediatric care.
DOI: 10.3233/PRM-2009-0058
Journal: Journal of Pediatric Rehabilitation Medicine, vol. 2, no. 1, pp. 3-11, 2009
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