Literature DB >> 17333004

Adolescent dialysis patient transition to adult care: a cross-sectional survey.

Lorraine Bell1.   

Abstract

Adolescent dialysis patients transitioning to adult care are particularly vulnerable, dependent on complex, demanding and life-sustaining treatment. There is little published information on transition practices for this group. Therefore, a survey was carried out to assess the current status. Results are presented for 58 paediatric dialysis centres in North America and Europe. The majority of centres (53%) did not have a fixed cut-off age for transfer. For those that did, it ranged from 17 to 22 years, with the median 20.5 years and mean [+/- standard deviation (SD)] of 19.9 (+/-1.5) years. Only one third of centres reported a transition programme. Less than 20% of young adult patients were perceived to function autonomously at transfer. The paediatric centres had minimal knowledge of resources at the adult receiving sites. For the majority of programs there was a system in place to assist with application for social and health benefits (83%), an adult dialysis unit linked to the paediatric programme (62%) and an opportunity for patients to choose (78%) and visit (83%) the adult unit prior to transfer. Seventy-four percent of centres without a transition programme believed there was a need for one. This is an area clearly in need of attention.

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Year:  2007        PMID: 17333004     DOI: 10.1007/s00467-006-0404-z

Source DB:  PubMed          Journal:  Pediatr Nephrol        ISSN: 0931-041X            Impact factor:   3.714


  16 in total

1.  Health care transition: destinations unknown.

Authors:  John Reiss; Robert Gibson
Journal:  Pediatrics       Date:  2002-12       Impact factor: 7.124

2.  Transition to adult health care for adolescents and young adults with chronic conditions: position paper of the Society for Adolescent Medicine.

Authors:  David S Rosen; Robert W Blum; Maria Britto; Susan M Sawyer; David M Siegel
Journal:  J Adolesc Health       Date:  2003-10       Impact factor: 5.012

3.  Transition programs in cystic fibrosis centers.

Authors:  Steven P Conway
Journal:  Pediatr Pulmonol       Date:  2004-01

Review 4.  Transitioning care of the pediatric recipient to adult caregivers.

Authors:  Janet E McDonagh; Deirdre A Kelly
Journal:  Pediatr Clin North Am       Date:  2003-12       Impact factor: 3.278

5.  Transition from child-centered to adult health-care systems for adolescents with chronic conditions. A position paper of the Society for Adolescent Medicine.

Authors:  R W Blum; D Garell; C H Hodgman; T W Jorissen; N A Okinow; D P Orr; G B Slap
Journal:  J Adolesc Health       Date:  1993-11       Impact factor: 5.012

6.  Transition to adulthood in congenital heart disease: missed adolescent milestones.

Authors:  Maureen E Lyon; Karen Kuehl; Robert McCarter
Journal:  J Adolesc Health       Date:  2006-07       Impact factor: 5.012

Review 7.  Success on the road to adulthood. Issues and hurdles for adolescents with disabilities.

Authors:  P H White
Journal:  Rheum Dis Clin North Am       Date:  1997-08       Impact factor: 2.670

8.  Current methods of transfer of young people with Type 1 diabetes to adult services.

Authors:  S Kipps; T Bahu; K Ong; F M Ackland; R S Brown; C T Fox; N K Griffin; A H Knight; N P Mann; H A W Neil; H Simpson; J A Edge; D B Dunger
Journal:  Diabet Med       Date:  2002-08       Impact factor: 4.359

9.  Prevalence and correlates of successful transfer from pediatric to adult health care among a cohort of young adults with complex congenital heart defects.

Authors:  Graham J Reid; M Jane Irvine; Brian W McCrindle; Renee Sananes; Paul G Ritvo; Samuel C Siu; Gary D Webb
Journal:  Pediatrics       Date:  2004-03       Impact factor: 7.124

Review 10.  Transition from paediatric to adult-orientated care for adolescents with cystic fibrosis.

Authors:  S P Conway
Journal:  Disabil Rehabil       Date:  1998 Jun-Jul       Impact factor: 3.033

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  8 in total

Review 1.  Moving on: transitioning young people with chronic kidney disease to adult care.

Authors:  Anna Francis; David W Johnson; Jonathan C Craig; Germaine Wong
Journal:  Pediatr Nephrol       Date:  2017-07-13       Impact factor: 3.714

Review 2.  Psychosocial considerations and recommendations for care of pediatric patients on dialysis.

Authors:  Michelle A Clementi; Cortney Taylor Zimmerman
Journal:  Pediatr Nephrol       Date:  2019-03-20       Impact factor: 3.714

3.  Comparative clinical outcomes between pediatric and young adult dialysis patients.

Authors:  Meredith A Atkinson; Rachel M Lestz; Barbara A Fivush; Douglas M Silverstein
Journal:  Pediatr Nephrol       Date:  2011-06-04       Impact factor: 3.714

4.  The problem of transition from pediatric to adult healthcare in patients with steroid-sensitive nephrotic syndrome (SSNS): a survey of the experts.

Authors:  Masataka Honda; Kazumoto Iijima; Kenji Ishikura; Kazunari Kaneko
Journal:  Clin Exp Nephrol       Date:  2014-02-02       Impact factor: 2.801

5.  Behavioral disorders and low quality of life in children and adolescents with chronic kidney disease.

Authors:  Renata C Marciano; Cristina M Bouissou Soares; José Silvério S Diniz; Eleonora M Lima; Jose Maria P Silva; Monica R Canhestro; Andrea Gazzinelli; Carla Cristina D Melo; Cristiane S Dias; Ana Cristina Simões e Silva; Humberto Correa; Eduardo A Oliveira
Journal:  Pediatr Nephrol       Date:  2010-11-26       Impact factor: 3.714

6.  National Estimates of Mental Health Needs Among Adults With Self-Reported CKD in the United States.

Authors:  Adam S Wilk; Ju-Chen Hu; Puneet Chehal; Courtney R Yarbrough; Xu Ji; Janet R Cummings
Journal:  Kidney Int Rep       Date:  2022-05-05

7.  Parents' perception of self-advocacy of children with myositis: an anonymous online survey.

Authors:  James D Katz; Gulnara Mamyrova; Shilpi Agarwal; Olcay Y Jones; Harriet Bollar; Adam M Huber; Lisa G Rider; Patience H White
Journal:  Pediatr Rheumatol Online J       Date:  2011-06-07       Impact factor: 3.054

8.  Shifting responsibilities: A qualitative study of how young people assume responsibility from their parents for self-management of their chronic kidney disease.

Authors:  Ruth Nightingale; Gretl A McHugh; Veronica Swallow; Sue Kirk
Journal:  Health Expect       Date:  2022-06-30       Impact factor: 3.318

  8 in total

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