评估格朗的报告质量随机对照试验摘要:当前状态和未来前景
Ana Vucinovic1, Josipa Bukic2, Doris Rusic2
1Department of Ophthalmology, University Hospital Centre Split, Spinciceva 1, 21000 Split, Croatia.
Life (Basel, Switzerland)
|January 23, 2024
概括
眼随机对照试验显示在摘要中对CONSORT报告标准的遵守不足,特别是在随机化和资金细节方面. 提高报告透明度对于临床实践至关重要.
科学领域:
- 眼科医生 眼科 眼科
- 临床试验 临床试验
- 医学研究报告报告 医学研究报告
背景情况:
- 临床试验报告综合标准 (CONSORT) 准则旨在提高临床试验报告的质量和透明度.
- 遵守CONSORT标准对于评估研究结果的可靠性和适用性至关重要.
研究的目的:
- 为了评估随机对照试验 (RCT) 的摘要中对CONSORT报告标准的遵守,重点是青光眼.
- 在这些摘要中确定非最佳报告的特定领域.
主要方法:
- 一项横截面的观察性研究分析了从2017年到2021年在MEDLINE/PubMed索引的302个玻璃眼RCT摘要.
- 摘要是根据CONSORT-摘要 (CONSORT-A) 项目进行评估的.
主要成果:
- 中位坚持得分为17分之8 (47.0%),表明报告不足最佳.
- 遵守率较低的关键领域包括试验设计 (20.5%),随机化 (6.0%) 和资金披露 (6.0%).
- 结构化摘要,多中心设置,行业资金,更大的参与者数量和更高的期刊影响因素与更好的成绩相关.
结论:
- 眼RCT摘要显示,对CONSORT-A报告标准的遵守程度较差,特别是在随机化和资金方面.
- 提高报告透明度是必要的,以改善试验质量的评估,并促进研究结果转化为临床实践.
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