TY - JOUR
T1 - Health-related quality of life and psychosocial developmental trajectory in young female beneficiaries with JIA
AU - Haverman, Lotte
AU - Verhoof, Eefje J.
AU - Maurice-stam, Heleen
AU - Heymans, Hugo S.A.
AU - Gerlag, Daniëlle M.
AU - van Rossum, Marion A.J.
AU - Grootenhuis, Martha A.
N1 - Funding Information:
Funding: This work was supported by the Dutch Social Security Agency (UWV).
PY - 2012/2
Y1 - 2012/2
N2 - Objectives: It is generally recognized that for all children the fulfilling of age-specific psychosocial developmental tasks in childhood is of great importance to adjustment in adult life, including participation in society. For young adults with JIA this is more difficult. We assume that the achievement of psychosocial milestones while growing up (psychosocial developmental trajectory) is also related to labour participation. A proportion of all young adults with JIA have to apply for disability benefits. This study assessed the health-related quality of life (HRQOL) and the psychosocial developmental trajectory of young female beneficiaries with JIA compared with peers from the Dutch general population. Methods: Young females with disability benefits because of JIA completed the RAND-36 (HRQOL) and the Course of Life Questionnaire (psychosocial developmental trajectory). Differences between respondents and the peer group were tested using analysis of variance and logistic regression analysis by group and age. Results: The beneficiaries reported worse HRQOL than the peer group and achieved fewer milestones, or achieved the milestones at a later age than the peer group in the autonomy, social and psychosexual domain. Conclusions: Young females with JIA who have to apply for disability benefits are at risk for impaired HRQOL and a delay in their psychosocial developmental trajectory. Parents, physicians and other health-care providers should pay systematic attention to the development of social and independent functioning of children with JIA in order to optimize their adaptation to society at the time of transition to adulthood.
AB - Objectives: It is generally recognized that for all children the fulfilling of age-specific psychosocial developmental tasks in childhood is of great importance to adjustment in adult life, including participation in society. For young adults with JIA this is more difficult. We assume that the achievement of psychosocial milestones while growing up (psychosocial developmental trajectory) is also related to labour participation. A proportion of all young adults with JIA have to apply for disability benefits. This study assessed the health-related quality of life (HRQOL) and the psychosocial developmental trajectory of young female beneficiaries with JIA compared with peers from the Dutch general population. Methods: Young females with disability benefits because of JIA completed the RAND-36 (HRQOL) and the Course of Life Questionnaire (psychosocial developmental trajectory). Differences between respondents and the peer group were tested using analysis of variance and logistic regression analysis by group and age. Results: The beneficiaries reported worse HRQOL than the peer group and achieved fewer milestones, or achieved the milestones at a later age than the peer group in the autonomy, social and psychosexual domain. Conclusions: Young females with JIA who have to apply for disability benefits are at risk for impaired HRQOL and a delay in their psychosocial developmental trajectory. Parents, physicians and other health-care providers should pay systematic attention to the development of social and independent functioning of children with JIA in order to optimize their adaptation to society at the time of transition to adulthood.
KW - Health-related quality of life
KW - Juvenile idiopathic arthritis
KW - Psychosocial developmental trajectory
KW - Workforce
KW - Young adults
UR - http://www.scopus.com/inward/record.url?scp=84856110741&partnerID=8YFLogxK
U2 - 10.1093/rheumatology/ker378
DO - 10.1093/rheumatology/ker378
M3 - Article
C2 - 22179727
AN - SCOPUS:84856110741
SN - 1462-0324
VL - 51
SP - 368
EP - 374
JO - Rheumatology
JF - Rheumatology
IS - 2
M1 - ker378
ER -