Literature DB >> 29125516

Evaluation of spina bifida transitional care practices in the United States.

Maryellen S Kelly1, Judy Thibadeau2, Sara Struwe3, Lisa Ramen3, Lijing Ouyang2, Jonathan Routh1.   

Abstract

PURPOSE: Recent studies have revealed that the lack of continuity in preparing patients with spina bifida to transition into adult-centered care may have detrimental health consequences. We sought to describe current practices of transitional care services offered at spina bifida clinics in the US.
METHODS: Survey design followed the validated transitional care survey by the National Cystic Fibrosis center. Survey was amended for spina bifida. Face validity was completed. Survey was distributed to registered clinics via the Spina Bifida Association. Results were analyzed via descriptive means.
RESULTS: Total of 34 clinics responded. Over 90 characteristics were analyzed per clinic. The concept of transition is discussed with most patients. Most clinics discuss mobility, bowel and bladder management, weight, and education plans consistently. Most do not routinely evaluate their process or discuss insurance coverage changes with patients. Only 30% communicate with the adult providers. Sexuality, pregnancy and reproductive issues are not readily discussed in most clinics. Overall clinics self-rate themselves as a 5/10 in their ability to provide services for their patients during transition.
CONCLUSIONS: Characteristics of current transitional care services and formal transitional care programs at US clinics show wide variances in what is offered to patients and families.

Entities:  

Keywords:  Spina bifida; myelomeningocele; transitional care

Mesh:

Year:  2017        PMID: 29125516      PMCID: PMC5896760          DOI: 10.3233/PRM-170455

Source DB:  PubMed          Journal:  J Pediatr Rehabil Med        ISSN: 1874-5393


  18 in total

1.  A consensus statement on health care transitions for young adults with special health care needs.

Authors: 
Journal:  Pediatrics       Date:  2002-12       Impact factor: 7.124

2.  The Illness Management Survey: identifying adolescents' perceptions of barriers to adherence.

Authors:  Deirdre Logan; Nataliya Zelikovsky; Larissa Labay; Jonathan Spergel
Journal:  J Pediatr Psychol       Date:  2003-09

3.  Adult consequences of spina bifida: a cohort study.

Authors:  James W Roach; Barbara F Short; Hanna M Saltzman
Journal:  Clin Orthop Relat Res       Date:  2011-05       Impact factor: 4.176

4.  Improving transition from pediatric to adult cystic fibrosis care: lessons from a national survey of current practices.

Authors:  Suzanne Elizabeth McLaughlin; Marie Diener-West; Alka Indurkhya; Haya Rubin; Rebekah Heckmann; Michael Patrick Boyle
Journal:  Pediatrics       Date:  2008-05       Impact factor: 7.124

Review 5.  Transition to adult care for patients with spina bifida.

Authors:  Joan T Le; Shubhra Mukherjee
Journal:  Phys Med Rehabil Clin N Am       Date:  2015-02       Impact factor: 1.784

6.  Urologic problems in spina bifida patients transitioning to adult care.

Authors:  Stephen J Summers; Sean Elliott; Sean McAdams; Siam Oottamasathien; William O Brant; Angela P Presson; Joseph Fleck; Jeremy West; Jeremy B Myers
Journal:  Urology       Date:  2014-08       Impact factor: 2.649

7.  Long-term survival of individuals with myelomeningocele.

Authors:  Beth Ellen Davis; Colleen M Daley; David B Shurtleff; Sharon Duguay; Kristy Seidel; John D Loeser; Richard G Ellenbogan
Journal:  Pediatr Neurosurg       Date:  2005 Jul-Aug       Impact factor: 1.162

8.  Medication beliefs mediate between depressive symptoms and medication adherence in cystic fibrosis.

Authors:  Marisa E Hilliard; Michelle N Eakin; Belinda Borrelli; Angela Green; Kristin A Riekert
Journal:  Health Psychol       Date:  2014-08-11       Impact factor: 4.267

Review 9.  Cystic Fibrosis Transitions of Care: Lessons Learned and Future Directions for Cystic Fibrosis.

Authors:  Megumi J Okumura; Mary Ellen Kleinhenz
Journal:  Clin Chest Med       Date:  2015-12-23       Impact factor: 2.878

10.  Transition from pediatric to adult care for sickle cell disease: results of a survey of pediatric providers.

Authors:  Amy Sobota; Ellis J Neufeld; Philippa Sprinz; Matthew M Heeney
Journal:  Am J Hematol       Date:  2011-06       Impact factor: 10.047

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  3 in total

1.  The development of a lifetime care model in comprehensive spina bifida care.

Authors:  Betsy Hopson; Brandon G Rocque; David B Joseph; Danielle Powell; Amie B Jackson McLain; Richard D Davis; Tracey S Wilson; Michael J Conklin; Jeffrey P Blount
Journal:  J Pediatr Rehabil Med       Date:  2018

2.  Hospital and ED charges for spina bifida care in the United States between 2006 and 2014: Over $2 billion annually.

Authors:  Brian M Inouye; Ruiyang Jiang; M Hassan Alkazemi; Hsin-Hsiao S Wang; Steven Wolf; Gina-Maria Pomann; Rohit Tejwani; John S Wiener; J Todd Purves; Jonathan C Routh
Journal:  Disabil Health J       Date:  2019-01-21       Impact factor: 2.554

Review 3.  Research Needs for Effective Transition in Lifelong Care of Congenital Genitourinary Conditions: A Workshop Sponsored by the National Institute of Diabetes and Digestive and Kidney Diseases.

Authors:  Michael H Hsieh; Hadley M Wood; Brad E Dicianno; Nienke P Dosa; Veronica Gomez-Lobo; Tej K Mattoo; Rosalia Misseri; Jenna M Norton; Kathleen J Sawin; Peter Scal; James E Wright; Robert A Star; Tamara Bavendam
Journal:  Urology       Date:  2017-02-02       Impact factor: 2.649

  3 in total

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