Literature DB >> 21896381

Health care transition for adolescents with CKD-the journey from pediatric to adult care.

Lorraine E Bell1, Maria E Ferris, Nicole Fenton, Stephen R Hooper.   

Abstract

The design of Health Care Transition (HCT) services for adolescents and emerging adults with CKD or end-stage kidney disease (ESKD) needs to take into account patient cognition/developmental stage, family factors, and health resources within the hospital setting and community. Patient and family education is fundamental and teaching and learning tools must be literacy-accessible. Adolescents and emerging adults with CKD/ESDK have complex medical and dietary regimes, and therapeutic adherence is important for optimizing their health, quality of life, and longevity. Health providers need to identify ways of engaging them to become successful disease self-mangers. Interdisciplinary collaboration between the pediatric- and adult-focused health care teams and the services of a dedicated transition coordinator are paramount to ensure clear communication between the patient and the health professionals involved. Valid measurement tools to monitor and assess the HCT process and health outcomes need to be developed. The aims of planned HCT for adolescents and/or emerging adults with CKD/ESKD are anchored by the goals of optimizing health outcomes, health-related quality of life, and continuous quality improvement. The care of young people with CKD/ESKD can be both challenging and rewarding; we offer strategies for planned HCT services geared to these vulnerable patients.
Copyright © 2011 National Kidney Foundation, Inc. Published by Elsevier Inc. All rights reserved.

Entities:  

Mesh:

Year:  2011        PMID: 21896381     DOI: 10.1053/j.ackd.2011.04.003

Source DB:  PubMed          Journal:  Adv Chronic Kidney Dis        ISSN: 1548-5595            Impact factor:   3.620


  4 in total

1.  Pediatric kidney disease: tracking onset and improving clinical outcomes.

Authors:  Carlton M Bates; Jennifer R Charlton; Maria E Ferris; Friedhelm Hildebrandt; Deborah K Hoshizaki; Bradley A Warady; Marva M Moxey-Mims
Journal:  Clin J Am Soc Nephrol       Date:  2014-03-20       Impact factor: 8.237

Review 2.  In their own words: the value of qualitative research to improve the care of children with chronic kidney disease.

Authors:  Camilla S Hanson; Jonathan C Craig; Allison Tong
Journal:  Pediatr Nephrol       Date:  2016-10-15       Impact factor: 3.714

3.  Association between socioeconomic status and academic performance in children and adolescents with chronic kidney disease.

Authors:  Rabia Khalid; Anita Van Zwieten; Siah Kim; Madeleine Didsbury; Anna Francis; Steven Mctaggart; Amanda Walker; Fiona E Mackie; Chanel Prestidge; Armando Teixeira-Pinto; Belinda Barton; Jennifer Lorenzo; Suncica Lah; Kirsten Howard; Natasha Nassar; Eric Au; Allison Tong; Katrina Blazek; Jonathan C Craig; Germaine Wong
Journal:  Pediatr Nephrol       Date:  2022-03-30       Impact factor: 3.651

4.  Neurocognitive and Educational Outcomes in Children and Adolescents with CKD: A Systematic Review and Meta-Analysis.

Authors:  Kerry Chen; Madeleine Didsbury; Anita van Zwieten; Martin Howell; Siah Kim; Allison Tong; Kirsten Howard; Natasha Nassar; Belinda Barton; Suncica Lah; Jennifer Lorenzo; Giovanni Strippoli; Suetonia Palmer; Armando Teixeira-Pinto; Fiona Mackie; Steven McTaggart; Amanda Walker; Tonya Kara; Jonathan C Craig; Germaine Wong
Journal:  Clin J Am Soc Nephrol       Date:  2018-02-22       Impact factor: 8.237

  4 in total

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