Department of Clinical Sciences Lund, Division of Pediatrics, Lund University, Skåne University Hospital, Lund, 21185, Sweden.
Library and ICT, Faculty of Medicine, Lund University, Lund, Sweden.
Pediatr Res. 2024 Aug;96(3):643-653. doi: 10.1038/s41390-024-03197-1. Epub 2024 Apr 13.
Similar to systematic reviews (SRs) in clinical fields, preclinical SRs address a specific research area, furnishing information on current knowledge, possible gaps, and potential methodological flaws of study design, conduct, and report. One of the main goals of preclinical SRs is to identify aspiring treatment strategies and evaluate if currently available data is solid enough to translate to clinical trials or highlight the gaps, thus justifying the need for new studies. It is imperative to rigorously follow the methodological standards that are widely available. These include registration of the protocol and adherence to guidelines for assessing the risk of bias, study quality, and certainty of evidence. A special consideration should be made for pediatric SRs, clinical and preclinical, due to the unique characteristics of this age group. These include rationale for intervention and comparison of primary and secondary outcomes. Outcomes measured should acknowledge age-related physiological changes and maturational processes of different organ systems. It is crucial to choose the age of the animals appropriately and its possible correspondence for specific pediatric age groups. The findings of well-conducted SRs of preclinical studies have the potential to provide a reliable evidence synthesis to guide the design of future preclinical and clinical studies. IMPACT: This narrative review highlights the importance of rigorous design, conduct and reporting of preclinical primary studies and systematic reviews. A special consideration should be made for pediatric systematic reviews of preclinical studies, due to the unique characteristics of this age group.
与临床领域的系统评价 (SRs) 类似,临床前 SRs 针对特定的研究领域,提供当前知识、可能的差距以及研究设计、实施和报告的潜在方法学缺陷的信息。临床前 SRs 的主要目标之一是确定有前途的治疗策略,并评估当前可用数据是否足够扎实以转化为临床试验或突出差距,从而证明需要开展新的研究。严格遵循广泛可用的方法学标准至关重要。这些标准包括方案注册以及遵守评估偏倚风险、研究质量和证据确定性的指南。由于这个年龄组的独特特征,应特别考虑儿科临床前和临床 SRs。这些特征包括干预的理由以及主要和次要结局的比较。应考虑到与年龄相关的生理变化和不同器官系统的成熟过程来测量结果。选择适当的动物年龄及其与特定儿科年龄组的可能对应关系至关重要。精心设计的临床前研究的 SR 结果有可能提供可靠的证据综合,以指导未来的临床前和临床研究的设计。影响:本叙述性综述强调了严格设计、实施和报告临床前主要研究和系统评价的重要性。由于这个年龄组的独特特征,应特别考虑儿科临床前研究的系统评价。