Prediction of Functional Academic Outcomes by Fine Motor Skills in Individuals With Sickle Cell Disease.

IF 2.1 4区 医学 Q1 REHABILITATION American Journal of Occupational Therapy Pub Date : 2024-09-01 DOI:10.5014/ajot.2024.050684
Lakia Kearson, Christina Dandar, Catherine Hoyt, Jennifer Longoria, Victoria Okhomina, Darcy Raches, Brian Potter, Guolian Kang, Jane Hankins, Clifford Takemoto, Andrew Heitzer
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Abstract

Importance: Individuals with sickle cell disease (SCD) are at heightened risk of poor neurocognitive and academic outcomes. The relationship between fine motor skills and academic outcomes is not well understood.

Objective: To compare the fine motor skills of individuals with SCD with normative expectations, test whether demographic and medical factors are associated with fine motor performance, and determine the impact of fine motor performance on academic performance.

Design: Cross-sectional.

Setting: St. Jude Children's Research Hospital.

Participants: Individuals with SCD (N = 376; ages 8-24 yr).

Outcomes and measures: Fine motor outcomes included visual-motor integration, manual dexterity, and graphomotor speed. Academic outcomes included math fluency and word reading. Demographic and medical variables were obtained via medical records and interviews.

Results: Compared with normative expectations, the performance of individuals with SCD on all fine motor measures was lower than expected. Male sex, lower socioeconomic status, and lower oxygen saturation was associated with slower graphomotor speed. Lower socioeconomic status and older age were associated with lower visual-motor integration scores. Performance on all fine motor measures was positively associated with math fluency and word reading.

Conclusions and relevance: Individuals with SCD exhibited poorer than expected fine motor skills across multiple motor domains, and these deficits were associated with poorer academic outcomes. Early referral to intervention services for fine motor skills may facilitate improved academic outcomes for individuals with SCD. Plain-Language Summary: This study had three objectives: (1) Compare the fine motor skills of people with sickle cell disease (SCD) with normative expectations, (2) test whether demographic and medical factors are associated with fine motor performance, and (3) determine the impact of fine motor performance on academic performance. We found that SCD is a risk factor for lower than expected fine motor performance across multiple fine motor domains and that these deficits also affect functional academic skills.

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通过镰状细胞病患者的精细运动技能预测功能性学业成绩。
重要性:镰状细胞病(SCD)患者的神经认知能力和学习成绩较差的风险较高。精细运动技能与学习成绩之间的关系尚不十分清楚:将 SCD 患者的精细动作技能与标准期望值进行比较,检验人口统计学和医学因素是否与精细动作表现相关,并确定精细动作表现对学习成绩的影响:设计:横断面:圣犹达儿童研究医院:结果和测量指标:精细运动结果包括视觉运动整合、手部灵活性和图形运动速度。学习成绩包括数学流利程度和单词阅读能力。人口统计学和医学变量通过病历和访谈获得:结果:与常模相比,SCD 患者在所有精细动作测量中的表现均低于预期。男性、较低的社会经济地位和较低的血氧饱和度与图形运动速度较慢有关。社会经济地位较低和年龄较大与视觉运动整合得分较低有关。所有精细动作测量的成绩均与数学流畅性和单词阅读能力呈正相关:SCD 患儿在多个运动领域的精细运动技能均低于预期水平,这些缺陷与较差的学习成绩有关。早期转介到精细运动技能干预服务机构可能有助于改善 SCD 患者的学业成绩。通俗摘要:本研究有三个目标:(1)比较镰状细胞病(SCD)患者的精细动作技能与常模期望值;(2)检验人口和医疗因素是否与精细动作表现相关;(3)确定精细动作表现对学习成绩的影响。我们发现,在多个精细运动领域,SCD 是精细运动表现低于预期的一个风险因素,而这些缺陷也会影响功能性学业技能。
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来源期刊
CiteScore
3.10
自引率
10.30%
发文量
406
期刊介绍: The American Journal of Occupational Therapy (AJOT) is an official publication of the American Occupational Therapy Association, Inc. and is published 6 times per year. This peer reviewed journal focuses on research, practice, and health care issues in the field of occupational therapy. AOTA members receive 6 issues of AJOT per year and have online access to archived abstracts and full-text articles. Nonmembers may view abstracts online but must purchase full-text articles.
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