按常见疾病亚型划分的青少年特发性关节炎儿童生物心理社会特征的比较。

IF 1.3 Q3 PEDIATRICS
Seher Şener, Nur Banu Karaca, Kutay Kaşlı, Aykut Özçadırcı, Ezgi Deniz Batu, Özge Başaran, Yelda Bilginer, Seza Özen, Edibe Ünal
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引用次数: 0

摘要

目的:在本研究中,我们根据疾病亚型评估了青少年特发性关节炎(JIA)患者的功能和生物心理社会特征。材料与方法:采用儿童健康评估问卷(CHAQ)、青少年关节炎活动评分71(JADAS-71)和青少年关节炎生物心理社会问卷(JAB-Q)量表对304例JIA患者进行调查,并对其家庭进行JAB-Q量表。结果:JIA患者诊断时的中位年龄为7.9(5.5-13)岁(女性/男性=1.3)。大多数患者正在接受治疗(68.7%),患有非活动性疾病(69.3%)。虽然根据JIA亚型的JADAS-71评分之间没有显著差异,多关节型JIA患者的CHAQ总分高于系统性JIA患者(P=.005)。与系统性JJIA患者相比,焓相关关节炎(ERA)患者的JAB-Q疲劳总分更高(P=.001)。青少年关节炎生物心理社会问卷儿童心理社会状态分在多关节型JIA患者中高于少关节型和系统性JIA患者(分别为P=0.004和P=0.003),并且他们的JAB-Q儿童形式总分高于系统性JIA患者(P=0.006)。此外,系统性JIA患者的父母与少关节型JIA患者父母相比,其JAB-Q家庭总分更高(P=0.03)。结论:我们的结果表明,多关节型JIA患者具有更高的CHAQ、,ERA患者的JAB-Q疲劳评分较高。此外,系统性JIA患者父母的JAB-Q父母评分较高。应评估JIA患者及其父母的生物心理社会特征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparison of Biopsychosocial Characteristics of Children with Juvenile Idiopathic Arthritis According to Common Disease Subtypes.

Objective: In this study, we assessed the functional and biopsychosocial characteristics of juvenile idiopathic arthritis (JIA) patients according to disease subtypes.

Materials and methods: Child Health Assessment Questionnaire (CHAQ), Juvenile Arthritis Disease Activity Score-71 (JADAS-71), and Juvenile Arthritis Biopsychosocial Questionnaire (JAB-Q) scales were administered to 304 JIA patients, and the subscale of JAB-Q was administered to their families.

Results: The median age of JIA patients at diagnosis was 7.9 (5.5-13) years (female/male = 1.3). Most patients were under treatment (68.7%) and had inactive disease (69.3%). While there was no significant difference between JADAS-71 scores according to the JIA subtypes, total CHAQ scores in polyarticular JIA patients were higher than in systemic JIA patients (P = .005). Enthesitis-related arthritis (ERA) patients had higher JAB-Q fatigue total scores compared to systemic JJIA patients (P = .001). Juvenile Arthritis Biopsychosocial Questionnaire-child psychosocial status scores were higher in polyarticular JIA patients than oligoarticular and systemic JIA patients (P = .004 and P = .003, respectively), and they had higher JAB-Q child form total scores than systemic JIA patients (P = .006). In addition, systemic JIA patients' parents had higher JAB-Q family total scores compared to oligoarticular JIA patients' parents (P = .03).

Conclusion: Our results suggest that polyarticular JIA patients had higher CHAQ, JAB-Q psychosocial status, and child form total scores, and the JAB-Q fatigue score was higher in ERA patients. Also, JAB-Q-parent scores were higher in systemic JIA patients' parents. Biopsychosocial characteristics should be evaluated in both JIA patients and their parents.

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