Literature DB >> 35367087

Moving up: Healthcare transition experiences of adolescents and young adults with cystic fibrosis.

Katherine South1, Maureen George2, Hossein Sadeghi3, Victoria Piane3, Arlene Smaldone2.   

Abstract

PURPOSE: The experience of healthcare transition from pediatric to adult care in cystic fibrosis (CF) remains poorly understood, particularly among racially and ethnically diverse adolescents and young adults (AYAs) with CF. The objective of this qualitative study was to explore the perspectives of a diverse sample of AYAs with CF at one urban academic medical center regarding healthcare transition. DESIGN AND METHODS: Guided by qualitative descriptive methodology, we purposively selected AYAs who represented the pre and post transition experience: some AYAs had experienced the transition preparation program CF R.I.S.E. Demographic information and responsibility for self-management behaviors were collected using an online survey. Semi-structured video interviews were conducted following an iterative interview guide. A codebook directed inductive coding. QSR NVivo Version 12 software was used to organize the data.
RESULTS: 12 AYAs with CF were enrolled (25% female, 25% Black AYA, 33% Hispanic/Latina/o AYA, 50% White AYA; mean age 20.8 years). Three themes were identified: independent care of the whole self, preparing for change and the unknown and transition experiences vary.
CONCLUSIONS: Not all participants experienced a smooth transition. Participants identified suggestions for the development of transition preparation interventions, specifically around involving AYAs in transition decisions and beginning transition preparation early in adolescence. PRACTICE IMPLICATIONS: Participants expressed uncertainty about transition when they felt little control over the process or lacked sufficient information about adult care. Therefore, comprehensive early transition preparation for all AYAs with CF with a focus on involving AYAs in transition decisions is recommended.
Copyright © 2022 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Adolescent; Chronic illness; Cystic fibrosis; Healthcare transition; Qualitative

Mesh:

Year:  2022        PMID: 35367087      PMCID: PMC9246909          DOI: 10.1016/j.pedn.2022.03.007

Source DB:  PubMed          Journal:  J Pediatr Nurs        ISSN: 0882-5963            Impact factor:   2.523


  37 in total

1.  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

2.  Applicability of the SMART Model of Transition Readiness for Sickle-Cell Disease.

Authors:  Siddika S Mulchan; Jessica M Valenzuela; Lori E Crosby; Claudia Diaz Pow Sang
Journal:  J Pediatr Psychol       Date:  2015-12-30

3.  The qualitative content analysis process.

Authors:  Satu Elo; Helvi Kyngäs
Journal:  J Adv Nurs       Date:  2008-04       Impact factor: 3.187

4.  Examining the Transition from Child to Adult Care in Chronic Kidney Disease: An Open Exploratory Approach.

Authors:  David B Nicholas; Miriam Kaufman; Maury Pinsk; Susan Samuel; Lorraine Hamiwka; Anita E Molzahn
Journal:  Nephrol Nurs J       Date:  2018 Nov-Dec       Impact factor: 0.959

5.  Motivating adherence among adolescents with cystic fibrosis: youth and parent perspectives.

Authors:  Gregory S Sawicki; Karen S Heller; Nathan Demars; Walter M Robinson
Journal:  Pediatr Pulmonol       Date:  2014-03-10

6.  Risk Factors for Gaps in Care during Transfer from Pediatric to Adult Cystic Fibrosis Programs in the United States.

Authors:  Gregory S Sawicki; Joshua Ostrenga; Kristofer Petren; Aliza K Fink; Emma D'Agostino; Camila Strassle; Michael S Schechter; Margaret Rosenfeld
Journal:  Ann Am Thorac Soc       Date:  2018-02

Review 7.  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

8.  Social and Psychological Factors Associated With Health Care Transition for Young Adults Living With Sickle Cell Disease.

Authors:  Dora Clayton-Jones; Nadine Matthie; Marsha Treadwell; Joshua J Field; Amy Mager; Rachel Sawdy; Safiya George Dalmida; Cynthia Leonard; Kathryn L Koch; Kristin Haglund
Journal:  J Transcult Nurs       Date:  2019-12-31       Impact factor: 1.959

9.  Factors influencing outcomes in cystic fibrosis: a center-based analysis.

Authors:  Charles Johnson; Steven M Butler; Michael W Konstan; Wayne Morgan; Mary Ellen B Wohl
Journal:  Chest       Date:  2003-01       Impact factor: 9.410

10.  Experiences and perspectives of the parents of emerging adults living with type 1 diabetes.

Authors:  Andrew Advani; Janet A Parsons; Cheryl Pritlove; Benjamin Markowitz; Geetha Mukerji
Journal:  BMJ Open Diabetes Res Care       Date:  2020-10
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