利用手写速度的详细评估，研究幼年特发性关节炎患者的手写速度。

IF 2.8 3区医学 Q1 PEDIATRICS

Pediatric Rheumatology Pub Date : 2024-08-15 DOI:10.1186/s12969-024-01013-y

C A Marchak, S James, I Davidson, J Brown, K Houghton

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引用次数: 0

摘要

背景：手写是幼年特发性关节炎（JIA）患儿常见的功能障碍。本研究旨在评估 JIA 儿童的书写能力：12名JIA患儿（平均年龄13.0岁，SD=1.9；年龄范围9.1至15.6岁）完成了手写速度详细评估（DASH）。此外，还对手部和腕部关节炎、握力、残疾、疼痛和生活质量（QOL）进行了评估。平均 DASH 得分为 34.5 百分位数（SD = 22.5）。八人（75%）的得分低于第 50 百分位数。DASH得分与握力呈负相关（r = -0.31）：结论：手写困难在JIA患儿中很常见。结论：手写困难在JIA患儿中很常见，手写评估可能有助于指导治疗，并为学校提供支持和便利。

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Handwriting speed in juvenile idiopathic arthritis using the detailed assessment of speed of handwriting.

Background: Handwriting is a commonly reported functional limitation for children with juvenile idiopathic arthritis (JIA). The aim of this study was to evaluate handwriting in children with JIA.

Findings: Twelve children (mean age 13.0 years, SD = 1.9; range 9.1 to 15.6 years) with JIA completed the Detailed Assessment of Speed of Handwriting (DASH). The presence of hand and wrist arthritis, grip strength, disability, pain, and quality of life (QOL) was also assessed. The mean DASH score was 34.5th percentile (SD = 22.5). Eight (75%) scored below the 50th centile. DASH scores were negatively associated with grip strength (r = -0.31).

Conclusions: Handwriting difficulties are common in children with JIA. Handwriting assessment may be helpful to direct treatments, and advocate for support and accommodations in school.

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来源期刊

Pediatric Rheumatology PEDIATRICS-RHEUMATOLOGY

CiteScore

4.10

自引率

8.00%

发文量

审稿时长

>12 weeks

期刊介绍： Pediatric Rheumatology is an open access, peer-reviewed, online journal encompassing all aspects of clinical and basic research related to pediatric rheumatology and allied subjects. The journal’s scope of diseases and syndromes include musculoskeletal pain syndromes, rheumatic fever and post-streptococcal syndromes, juvenile idiopathic arthritis, systemic lupus erythematosus, juvenile dermatomyositis, local and systemic scleroderma, Kawasaki disease, Henoch-Schonlein purpura and other vasculitides, sarcoidosis, inherited musculoskeletal syndromes, autoinflammatory syndromes, and others.