Selvaag Anne M, Lien Gunhild, Sørskaar Dag, Vinje Odd, Førre Øystein, Flatø Berit
Department of Rheumatology, Rikshospitalet University Hospital, Oslo, Norway.
J Rheumatol. 2005 Jun;32(6):1122-30.
. To describe the 3 year disease course in early juvenile rheumatoid arthritis (JRA) and juvenile spondyloarthropathy (JSpA), to compare the health status after 3 years of followup with that of normal controls, and to investigate the relationship between physical function at followup and disease characteristics recorded during the first 6 months.
One hundred and ninety-seven children (median age 6:6 yrs) with JRA and JSpA and disease duration <1.5 years were examined by a pediatric rheumatologist every 6 months for a median of 3.1 years. Controls were randomly selected from the National Population Register. Physical and psychosocial health was assessed by means of the Child Health Questionnaire and the Childhood Health Assessment Questionnaire (CHAQ). Disease course was analyzed by analysis of variance for repeated measurements.
Health status and disease activity improved over time. Treatment with disease modifying antirheumatic drugs was started in 58% of the patients at baseline. Patients with persistent oligoarthritis had the most favorable disease course. The patients with juvenile ankylosing spondylitis (JAS), syndrome of seronegative enthesopathy and arthropathy (SEA), and rheumatoid factor (RF) positive polyarthritis had the poorest health status. A significant improvement for the whole group was observed after 3 years in all measures of disease activity and health status, except pain. Patients had poorer physical function and general health and more pain than controls. Predictors of reduced physical function at followup were a high CHAQ disability index and a poor well-being assessed during the first 6 months.
Health status and disease activity improved over time in patients under medical treatment. The patients with JAS/SEA and RF positive polyarthritis had poorer health than the patients in other subtypes. A high disability index and a poor well-being at baseline predicted reduced physical function after 3 years.
描述幼年类风湿关节炎(JRA)和幼年脊柱关节炎(JSpA)的3年病程,比较3年随访后的健康状况与正常对照组,并研究随访时的身体功能与最初6个月记录的疾病特征之间的关系。
197名JRA和JSpA且病程<1.5年的儿童(中位年龄6:6岁)由儿科风湿病学家每6个月检查一次,中位检查时间为3.1年。对照组从国家人口登记册中随机选取。通过儿童健康问卷和儿童健康评估问卷(CHAQ)评估身体和心理社会健康状况。采用重复测量方差分析对疾病病程进行分析。
健康状况和疾病活动随时间改善。58%的患者在基线时开始使用改善病情抗风湿药物治疗。持续性少关节炎患者的疾病病程最为有利。幼年强直性脊柱炎(JAS)、血清阴性附着点病和关节病综合征(SEA)以及类风湿因子(RF)阳性多关节炎患者的健康状况最差。除疼痛外,3年后观察到全组在所有疾病活动和健康状况指标上均有显著改善。患者的身体功能、总体健康状况较对照组差,疼痛更多。随访时身体功能下降的预测因素是CHAQ残疾指数高以及最初6个月评估的幸福感差。
接受治疗的患者健康状况和疾病活动随时间改善。JAS/SEA和RF阳性多关节炎患者的健康状况比其他亚型患者差。基线时高残疾指数和幸福感差预示3年后身体功能下降。