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Child- and parent-reported quality of life trajectories in children with epilepsy: A prospective cohort study
被引:52
作者:
Ferro, Mark A.
[1
]
Avery, Lisa
[2
]
Fayed, Nora
[3
]
Streiner, David L.
[4
]
Cunningham, Charles E.
[4
]
Boyle, Michael H.
[4
]
Lach, Lucyna
[5
]
Glidden, Gina
[5
]
Rosenbaum, Peter L.
[6
]
Ronen, Gabriel M.
[6
]
机构:
[1] Univ Waterloo, Sch Publ Hlth & Hlth Syst, Waterloo, ON, Canada
[2] Avery Informat Serv, Orillia, ON, Canada
[3] Queens Univ, Sch Rehabil Therapy, Kingston, ON, Canada
[4] McMaster Univ, Dept Psychiat & Behav Neurosci, Hamilton, ON, Canada
[5] McGill Univ, Sch Social Work, Montreal, ON, Canada
[6] McMaster Univ, Dept Pediat, 1280 Main St West,MUMC Room 3A, Hamilton, ON, Canada
来源:
关键词:
Quality of life;
Patient-reported outcomes;
Adolescents;
Mental health;
Social support;
Longitudinal study;
HEALTH-RELATED QUALITY;
MATERNAL DEPRESSIVE SYMPTOMS;
RISK-FACTORS;
ADOLESCENTS;
PREDICTORS;
OUTCOMES;
ADULTS;
IMPACT;
SCALE;
D O I:
10.1111/epi.13774
中图分类号:
R74 [神经病学与精神病学];
学科分类号:
摘要:
ObjectiveTo describe the developmental trajectories of quality of life (QoL) in a large cohort of children with epilepsy, and to assess the relative contribution of clinical, psychosocial, and sociodemographic variables on QoL trajectories. MethodsFive assessments during a 28-month prospective cohort study were used to model trajectories of QoL. Participants were recruited with their parents from six Canadian tertiary centers. A convenience sample of 506 children aged 8-14 years with epilepsy and without intellectual disability or autism spectrum disorder were enrolled. A total of 894 children were eligible and 330 refused participation. Participating children were, on average, 11.4 years of age, and 49% were female. Nearly one third (32%) had partial seizures. At baseline, 479 and 503 child- and parent-reported questionnaires were completed. In total, 354 children (74%) and 366 parents (73%) completed the 28-month follow-up. QoL was measured using the child- and parent-reported version of the Childhood Epilepsy QoL scale (CHEQOL-25). ResultsChild-reported QoL was fitted best by a six-class model and parent-reported QoL by a five-class model. In both models, trajectories remained either stable or improved over 28 months. Of these children, 62% rated their QoL as high or moderately high, defined as at least one standard deviation above the average CHEQOL-25 score. Greater family, classmate, and peer social support, fewer symptoms of child and parent depression, and higher receptive vocabulary were identified as the most robust predictors of better QoL (all p < 0.001). SignificanceMost children with epilepsy and their parents reported relatively good QoL in this first joint self- and proxy-reported trajectory study. Findings confirm the heterogeneous QoL outcomes for children with epilepsy and the primary importance of psychosocial factors rather than seizure and AED-specific factors in influencing QoL. These predictors that are potentially amenable to change should now be the focus of specific intervention studies.
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页码:1277 / 1286
页数:10
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