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首页> 外文期刊>Archives of disease in childhood. Fetal and neonatal edition >Neurodevelopmental outcome descriptions in cohorts of extremely preterm children
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Neurodevelopmental outcome descriptions in cohorts of extremely preterm children

机译:极早产儿队列的神经发育结果描述

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Background and objectives Caregivers and clinicians of extremely preterm infants (born before 26 weeks' gestation) depend on long-term follow-up research to inform clinical decision-making. The completeness of outcome reporting in this area is unknown. The objective of this study was to evaluate the reporting of outcome definitions, selection, measurement and analysis in existing cohort studies that report on neurodevelopmental outcomes of children born extremely preterm. Methods We evaluated the completeness of reporting of 'cognitive function' and 'cerebral palsy' in prospective cohort studies summarised in a meta-analysis that assessed the effect of preterm birth on school-age neurodevelopment. Outcome reporting was evaluated using a checklist of 55 items addressing outcome selection, definition, measurement, analysis, presentation and interpretation. Reporting frequencies were calculated to identify strengths and deficiencies in outcome descriptions. Results All 14 included studies reported 'cognitive function' as an outcome; nine reported both 'cognitive function' and 'cerebral palsy' as outcomes. Studies reported between 26 and 46 of the 55 outcome reporting items assessed; results were similar for 'cognitive function' and 'cerebral palsy' (on average 34 and 33 of items reported, respectively). Key methodological concepts often omitted included the reporting of masking of outcome assessors, methods used to handle missing data and stakeholder involvement in outcome selection. Conclusions The reporting of neurodevelopmental outcomes in cohort studies of infants born extremely preterm is variable and often incomplete. This may affect stakeholders' interpretation of study results, impair knowledge synthesis efforts and limit evidence-based decision-making for this population.
机译:背景和目标 极早产儿(妊娠 26 周前出生)的照料者和临床医生依靠长期随访研究为临床决策提供信息。该领域结局报告的完整性尚不清楚。本研究的目的是评估现有队列研究中结局定义、选择、测量和分析的报告,这些研究报告了极早产儿的神经发育结局。方法 我们评估了前瞻性队列研究中“认知功能”和“脑瘫”报告的完整性,该研究总结在一项荟萃分析中,该分析评估了早产对学龄神经发育的影响。使用包含55个项目的清单对结果报告进行评估,这些项目涉及结果选择、定义、测量、分析、呈现和解释。计算报告频率以确定结果描述的优势和不足。结果 所有14项纳入的研究都报告了“认知功能”作为结局;9项报告“认知功能”和“脑瘫”作为结局。研究报告了评估的55个结局报告项目中的26%至46%;“认知功能”和“脑瘫”的结果相似(平均分别为34%和33%)。经常被忽略的关键方法概念包括报告结果评估人员的掩蔽、用于处理缺失数据的方法以及利益攸关方参与结果选择。结论 极早产儿队列研究中神经发育结局的报告是可变的,而且往往不完整。这可能会影响利益相关者对研究结果的解释,损害知识综合工作,并限制该人群的循证决策。

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