Causal pathways to health-related quality of life in children with juvenile idiopathic arthritis: results from the ReACCh-Out cohort

被引:9
作者
Oen, Kiem [1 ]
Tian, Jiahao [2 ]
Loughin, Thomas M. [2 ]
Shiff, Natalie J. [3 ]
Tucker, Lori B. [4 ,5 ]
Huber, Adam M. [6 ,7 ]
Berard, Roberta A. [8 ]
Levy, Deborah M. [9 ,10 ]
Rumsey, Dax G. [11 ]
Tse, Shirley M. [9 ,10 ]
Chan, Mercedes [4 ,5 ]
Feldman, Brian M. [9 ,10 ,12 ,13 ]
Duffy, Ciaran M. [14 ,15 ]
Guzman, Jaime [4 ,5 ]
机构
[1] Univ Manitoba, Dept Pediat & Child Hlth, Winnipeg, MB, Canada
[2] Simon Fraser Univ, Dept Stat & Actuarial Sci, Burnaby, BC, Canada
[3] Univ Saskatchewan, Dept Community Hlth & Epidemiol, Saskatoon, SK, Canada
[4] British Columbia Childrens Hosp, Div Pediat Rheumatol, Vancouver, BC, Canada
[5] Univ British Columbia, Dept Pediat, Vancouver, BC, Canada
[6] IWK Hlth Ctr, Div Pediat Rheumatol, Halifax, NS, Canada
[7] Dalhousie Univ, Halifax, NS, Canada
[8] Childrens Hosp, London Hlth Sci Ctr, Pediat Rheumatol, London, England
[9] Univ Toronto, Hosp Sick Children, Div Rheumatol, Toronto, ON, Canada
[10] Univ Toronto, Dept Pediat, Toronto, ON, Canada
[11] Univ Alberta, Dept Pediat, Edmonton, AB, Canada
[12] Univ Toronto, Dept Med, Toronto, ON, Canada
[13] Univ Toronto, Inst Hlth Policy Management & Evaluat, Toronto, ON, Canada
[14] Univ Ottawa, Childrens Hosp Eastern Ontario, Ottawa, ON, Canada
[15] Univ Ottawa, Dept Pediat, Ottawa, ON, Canada
基金
加拿大健康研究院;
关键词
health-related quality of life; juvenile idiopathic arthritis; causal models; structural equation modelling; CONCEPTUAL-MODEL; CLASSIFICATION; QUESTIONNAIRE; DETERMINANTS; ORGANIZATION; ADOLESCENTS; VARIABLES; OUTCOMES;
D O I
10.1093/rheumatology/keab079
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective Structural equation modelling was applied to data from the Research in Arthritis in Canadian Children emphasizing Outcomes (ReACCh-Out) cohort to help elucidate causal pathways to decreased health-related quality of life (HRQoL) in children with JIA. Methods Based on published literature and clinical plausibility, a priori models were constructed with explicit root causes (disease activity, treatment intensity) and mediators (pain, disease symptoms, functional impairments) leading to HRQoL [measured by the Quality of my Life (QoML) scale and the Juvenile Arthritis Quality of Life Questionnaire (JAQQ)] at five disease stages: (i) diagnosis, (ii) 3-9 months after diagnosis, (iii) flare, (iv) remission on medications, (v) remission off medications. Following structural equation modelling, a posteriori models were selected based on data fit and clinical plausibility. Results We included 561, 887, 137, 186 and 182 patients at each stage, respectively. In a posteriori models for active disease stages, paths from disease activity led through pain, functional impairments, and disease symptoms, directly or through restrictions in participation, to decreased QoML scores. Treatment intensity had detrimental effects through psychosocial domains; while treatment side effects had a lesser role. Pathways were similar for QoML and JAQQ, but JAQQ models provided greater specificity. Models for remission stages were not supported by the data. Conclusion Our findings support disease activity and treatment intensity as being root causes of decreased HRQoL in children with JIA, with pain, functional impairments, and participation restrictions being mediators for disease activity; they support psychosocial effects and side effects as being mediators for treatment intensity.
引用
收藏
页码:4691 / 4702
页数:12
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