Literature DB >> 3335473

The development of independence in adolescents with cystic fibrosis.

G Sinnema1, H C Bonarius, H Van der Laag, J W Stoop.   

Abstract

This study assessed the development of independence and its interaction with some biologic factors. Sixty-four adolescents with cystic fibrosis (CF) were compared with 36 adolescents with bronchial asthma, 47 healthy but small adolescents, and 71 normal healthy controls. A structured interview was designed to measure eight elements of independence. Adolescents with CF showed less responsibility for their own body hygiene and a delay in intimacy and sexuality, both correlated with puberty not yet having started. They also took less part in a number of social activities outside the home. There were minimal or no differences between ill and healthy adolescents for four elements. The results indicated that in future research, different types of independence should be taken into account. The correspondences between the chronically ill and the healthy adolescents prevailed over the differences. The main differences could be interpreted in terms of realistic coping with the illness and maintaining hope for the future.

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Mesh:

Year:  1988        PMID: 3335473     DOI: 10.1016/0197-0070(88)90020-4

Source DB:  PubMed          Journal:  J Adolesc Health Care        ISSN: 0197-0070


  4 in total

1.  Psychological, behavioural, and social adjustment in children and adolescents with juvenile chronic arthritis.

Authors:  A C Huygen; W Kuis; G Sinnema
Journal:  Ann Rheum Dis       Date:  2000-04       Impact factor: 19.103

2.  Guidance of children and adolescents with cystic fibrosis.

Authors:  J Gerritsen; H van der Laag; G Sinnema; K Knol
Journal:  Lung       Date:  1990       Impact factor: 2.584

3.  Attitudes to fertility issues among adults with cystic fibrosis in Scotland. The Collaborative Group of Scottish Adult CF Centres.

Authors:  A Fair; K Griffiths; L M Osman
Journal:  Thorax       Date:  2000-08       Impact factor: 9.139

4.  Psychosocial functioning of young adults with cystic fibrosis and their families.

Authors:  C Blair; A Cull; C P Freeman
Journal:  Thorax       Date:  1994-08       Impact factor: 9.139

  4 in total

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