首页> 外文期刊>Pediatric Pulmonology >Motor performance is better than normal in preschool children with cystic fibrosis.
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Motor performance is better than normal in preschool children with cystic fibrosis.

机译:在患有囊性纤维化的学龄前儿童中,运动表现比正常人好。

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The aim of the present study was to assess the motor performance in preschool children with a reliable and valid test battery developed to identify motor dysfunction and normal motor development in children aged from 4 to 6 years. Several aspects of motor performance were examined in 29 preschool children with cystic fibrosis (CF) age range 4-6 years (mean 5.2 +/- 0.8 years), FEV(1) 97.2 +/- 15.3pred and compared to with 22 healthy children of the same age 5.5 +/- 0.8 years. All children performed the "Motoriktest fuer 4-6jaehrige Kinder" (MOT) assessing seven different aspects of motor performance. Compared to healthy children, test score "Motor Quotient" (MQ) as the mean of all test items was significantly higher (P < 0.05) in children with CF (108.1 +/- 16 vs. 93.5 +/- 17.9). In both groups, the MQ can be classified as normal. Children with CF scored higher in MOT subtests "Agility and Coordination" (P < 0.05) and "Balance" (P < 0.01) than healthy children but not in the other subtests. We speculate that chest physiotherapy in preschool children with CF may have an effect on motor performance in general and in some aspects of motor performance.
机译:本研究的目的是通过开发可靠,有效的测试电池来评估学龄前儿童的运动能力,以鉴定4至6岁儿童的运动功能障碍和正常运动发育。在29名4-6岁(平均5.2 +/- 0.8岁)的囊性纤维化(CF)学龄前儿童,FEV(1)97.2 +/- 15.3pred的运动能力的几个方面进行了检查,并与22名健康儿童进行了比较年龄5.5 +/- 0.8岁。所有孩子都进行了“ Motoriktest fuer 4-6jaehrige Kinder”(MOT)评估运动能力的七个方面。与健康儿童相比,患有CF的儿童的所有项目的平均值“运动商”(MQ)均明显更高(P <0.05)(108.1 +/- 16 vs. 93.5 +/- 17.9)。在这两个组中,MQ都可以归类为正常。 CF儿童在MOT子测验“敏捷性和协调性”(P <0.05)和“平衡”(P <0.01)中的得分高于健康儿童,但在其他子测验中则没有。我们推测,在学龄前患有CF的儿童中进行胸部物理治疗可能会影响整体运动能力以及某些方面的运动能力。

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