Literature DB >> 19637994

What is the perceived nature of parental care and support for young people with cystic fibrosis as they enter adult health services?

Nicola Iles1, Karen Lowton.   

Abstract

The majority of those diagnosed with cystic fibrosis (CF) now live to adulthood. In response to increased survival age, transition services have been developed to ensure smooth transfer from paediatric to adult specialist healthcare, although the majority of treatment and care continues to be delivered in the home. However, little is known about how young adults and staff conceptualise the nature of the parental role after young people have left paediatric care. The aim of this study is to explore the nature of parental support that is perceived to be available at this time. As part of a larger study of transitional care, semi-structured interviews were conducted with 50 young people with CF aged 13-24 years (32 with experience of transition and/or adult CF services) and 23 specialist healthcare professionals (14 working in adult care) across two CF centres in Southeast England. Interviews took place in young people's homes or within CF services, using a topic guide and were recorded, transcribed and analysed thematically. Four domains of perceived parental support were identified by the young people interviewed, with varying degrees of continuity into adult care: (1) Providing non-clinical practical and emotional support; (2) Acting as 'troubleshooters' in times of health-related crisis; (3) Working in partnership with offspring in ongoing disease management in the home and clinic; (4) Acting as 'protectors' of their children. Young people and service staff expressed tensions in managing parental involvement in post-paediatric consultations and the degree to which parents should be aware of their offspring's deteriorating health and social concerns. Parental anxiety and over-involvement was perceived by many young people and staff as unsupportive. We suggest that although health and social care providers are mindful of the tensions that arise for those leaving paediatric services, the place of parental support in adult care is currently contentious for these 'new' ageing populations.

Entities:  

Mesh:

Year:  2009        PMID: 19637994     DOI: 10.1111/j.1365-2524.2009.00871.x

Source DB:  PubMed          Journal:  Health Soc Care Community        ISSN: 0966-0410


  8 in total

1.  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

2.  Parents' Role in Adolescent Depression Care: Primary Care Provider Perspectives.

Authors:  Ana Radovic; Kerry Reynolds; Heather L McCauley; Gina S Sucato; Bradley D Stein; Elizabeth Miller
Journal:  J Pediatr       Date:  2015-07-02       Impact factor: 4.406

3.  Longevity of patients with cystic fibrosis in 2000 to 2010 and beyond: survival analysis of the Cystic Fibrosis Foundation patient registry.

Authors:  Todd MacKenzie; Alex H Gifford; Kathryn A Sabadosa; Hebe B Quinton; Emily A Knapp; Christopher H Goss; Bruce C Marshall
Journal:  Ann Intern Med       Date:  2014-08-19       Impact factor: 25.391

4.  Transition to adult care: systematic assessment of adolescents with chronic illnesses and their medical teams.

Authors:  Jeannie S Huang; Michael Gottschalk; Mark Pian; Lindsay Dillon; Daniela Barajas; Leona Kay Bartholomew
Journal:  J Pediatr       Date:  2011-07-23       Impact factor: 4.406

5.  Flying the nest: a challenge for young adults with cystic fibrosis and their parents.

Authors:  Vibeke Bregnballe; Kirsten A Boisen; Peter Oluf Schiøtz; Tacjana Pressler; Kirsten Lomborg
Journal:  Patient Prefer Adherence       Date:  2017-02-13       Impact factor: 2.711

Review 6.  The use of the concept of transition in different disciplines within health and social welfare: An integrative literature review.

Authors:  Ulrika Lindmark; Pia H Bülow; Jan Mårtensson; Helén Rönning
Journal:  Nurs Open       Date:  2019-03-06

7.  "We Sometimes Hold on to Ours" - Professionals' Views on Factors that both Delay and Facilitate Transition to Adult Care.

Authors:  Susie Aldiss; Hilary Cass; Judith Ellis; Faith Gibson
Journal:  Front Pediatr       Date:  2016-11-24       Impact factor: 3.418

8.  Chronological age when healthcare transition skills are mastered in adolescents/young adults with inflammatory bowel disease.

Authors:  Natalie Stollon; Yi Zhong; Maria Ferris; Suneet Bhansali; Brian Pitts; Eniko Rak; Maureen Kelly; Sandra Kim; Miranda A L van Tilburg
Journal:  World J Gastroenterol       Date:  2017-05-14       Impact factor: 5.742

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.