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Systematic review of the clinimetric properties of laboratory- and field-based aerobic and anaerobic fitness measures in children with cerebral palsy

机译:对脑性麻痹儿童的实验室和野外有氧和无氧健身措施的临床特性的系统评价

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Objective: To systematically evaluate the level of evidence of the clinimetric properties of measures of aerobic and anaerobic capacity used for children with cerebral palsy (CP). Data Sources: A systematic search of databases PubMed, Embase, SPORTDiscus, and PsycINFO through April 2011 was performed. Study Selection: Two independent raters identified and examined studies that reported laboratory- or field-based measures of maximal aerobic or anaerobic capacity in children with CP aged 5 to 14 years. Data Extraction: The COnsensus-based Standards for the selection of health status Measurement INstruments (COSMIN) checklist was used by 2 independent raters to evaluate the methodologic quality of the included clinimetric studies and to identify measures used in these studies. Data Synthesis: Twenty-four studies that used a maximal aerobic or anaerobic capacity measure were identified. Five studies reported clinimetric properties for 5 measures (2 aerobic and 3 anaerobic measures). Methodologic quality was excellent in 3 studies, showing good validity and reliability of field-based aerobic (Shuttle Run Test) and anaerobic (Muscle Power Sprint Test) measures. The studies on laboratory-based measures were rated fair, mainly because of inadequate statistics. The level of evidence was strong for good validity and reliability of the field-based tests. The level of evidence was unknown for validity and low to moderate for good reliability of laboratory-based tests. Conclusions: There is a paucity of research on the clinimetric properties of measurement instruments to assess aerobic and anaerobic capacity for children with CP. Further clinimetric studies of laboratory-based measures in children with CP at all Gross Motor Function Classification System (GMFCS) levels, and clinimetric studies of field-based measures in children who are classified as GMFCS levels III to V are required.
机译:目的:系统评估用于儿童脑瘫(CP)的有氧和无氧能力量度的临床检验证据水平。数据来源:截至2011年4月,系统搜索了PubMed,Embase,SPORTDiscus和PsycINFO数据库。研究选择:两名独立的评估者确定并检查了研究,这些研究报告了基于实验室或野外测量的5至14岁CP儿童最大有氧或无氧能力。数据提取:2名独立评估者使用基于COnsensus的健康状况测量仪器(COSMIN)选择清单标准来评估所包括的斜度研究的方法学质量,并确定这些研究中使用的措施。数据综合:鉴定了二十一项使用最大有氧或无氧能力量度的研究。五项研究报告了五项措施(两项有氧措施和三项厌氧措施)的斜度特性。在3项研究中,方法学质量非常出色,显示了基于野外的有氧运动(Shuttle Run Test)和无氧运动(Muscle Power Sprint Test)的良好有效性和可靠性。实验室措施的研究被评为公平,主要是因为统计不足。有力的证据证明现场测试的有效性和可靠性。有效性的证据水平未知,而基于实验室的测试的良好可靠性则证据等级低至中等。结论:目前尚缺乏用于评估CP儿童有氧和无氧能力的测量仪器的斜度特性的研究。需要对在所有大运动功能分类系统(GMFCS)级别上的CP儿童进行基于实验室的措施的进一步临床检验,以及对被分类为GMFCS III至V级的儿童进行基于实地的临床检验。

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