Literature DB >> 2732107

Chronic disease and its impact. The adolescent's perspective.

M Cappelli1, P J McGrath, C E Heick, N E MacDonald, W Feldman, P Rowe.   

Abstract

Although evidence suggests that adolescents with chronic illness are at a greater risk for psychosocial disability, little is known about the adolescent's perception of the impact of the disease on his or her day-to-day life. Standardized measures of coping strategies, mastery, self-efficacy, social support, depression, and a semistructured interview on everyday difficulties were administered to matched groups (sex and age) of 31 adolescents with cystic fibrosis, 31 adolescents with diabetes, and 31 healthy controls. No differences were found between control and adolescents with a chronic disease responses on the standardized measures. The semistructured interview, however, revealed that the adolescent's perception of his or her physical health and the reaction of other family members to the illness were important sources of stress. These findings suggest that, in general, adolescents with a chronic illness cope effectively with their disability but that parents and clinicians must be sensitive to the adolescents' feelings and concerns regarding their health and its impact on the family.

Entities:  

Mesh:

Year:  1989        PMID: 2732107     DOI: 10.1016/0197-0070(89)90058-2

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


  8 in total

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Authors: 
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3.  Sexuality of young women surviving leukaemia.

Authors:  L R Puukko; E Hirvonen; V Aalberg; L Hovi; J Rautonen; M A Siimes
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4.  Development of the Cystic Fibrosis Questionnaire (CFQ) for assessing quality of life in pediatric and adult patients.

Authors:  Bernadette Henry; Pierre Aussage; Cécile Grosskopf; Jean-Marie Goehrs
Journal:  Qual Life Res       Date:  2003-02       Impact factor: 4.147

Review 5.  Quality of life in cystic fibrosis.

Authors:  D E Tullis; G H Guyatt
Journal:  Pharmacoeconomics       Date:  1995-07       Impact factor: 4.981

6.  Comparative Analysis of the Quality of Life in Families with Children or Adolescents Having Congenital versus Acquired Neuropathology.

Authors:  Maria V Morcov; Liliana Pădure; Cristian G Morcov; Andrada Mirea; Marian Ghiță; Gelu Onose
Journal:  Children (Basel)       Date:  2022-05-12

7.  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

8.  Health outcomes related to early adolescent depression.

Authors:  Danielle Keenan-Miller; Constance L Hammen; Patricia A Brennan
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  8 in total

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