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运用 2020 年《牙髓随机对照试验报告的首选条目清单》(PRIRATE)质量标准检查表,对牙髓学领域随机试验的报告质量进行批判性分析。

Critical analysis of the reporting quality of randomized trials within Endodontics using the Preferred Reporting Items for RAndomized Trials in Endodontics (PRIRATE) 2020 quality standard checklist.

机构信息

Department of Preventive and Restorative Dentistry, College of Dental Medicine, University of Sharjah, Sharjah, UAE.

Department of Pathophysiology, School of Dental Medicine, University of Belgrade, Belgrade, Serbia.

出版信息

Int Endod J. 2021 Jul;54(7):1083-1104. doi: 10.1111/iej.13489. Epub 2021 Mar 5.

Abstract

AIM

To critically evaluate the reporting quality of a random sample of clinical trials published in Endodontics against the PRIRATE 2020 checklist and to analyse the association between the quality of reported trials and a variety of parameters.

METHODOLOGY

Fifty randomized clinical trials relating to Endodontics were randomly selected from the PubMed database from 2015 to 2019 and evaluated by two independent reviewers. For each trial, a score of '1' was awarded when it fully reported each item in the PRIRATE guidelines whereas a score of '0' was awarded when an item was not reported; when the item was reported inadequately a score of '0.5' was awarded. For the items that were not relevant to the trial, 'Not Applicable (NA)' was given. Based on the interquartile range of the overall scores received, trials were categorized into 'Low' (0-58.4%), 'Moderate' (58.5-72.8%) and 'High' (72.9-100%) quality. The associations between characteristics and quality of clinical trials were investigated. Descriptive statistics, frequency analysis and percentage analyses were used to describe the data. To determine the significance of categorical data, the chi-square test was used. The probability value 0.05 was considered as the level of significance.

RESULTS

Based on the overall scores, 13 (26%), 25(50%) and 12 (24%) of the reports of clinical trials were categorized as 'High', 'Moderate' and 'Low' quality, respectively. Three items (1b, 6d, 11e) were adequately reported in all manuscripts whilst two items (5k, 5m) were scored 'NA' in all the reports. The reports published from Europe had a significantly greater percentage of 'High'-quality scores, compared to Asia, Middle East, North America and South America (P = 0.0002). The 'High'-quality reports were published significantly more often in impact factor journals (P = 0.045). Reports of clinical trials published in journals that adhered to the CONSORT guidelines had significantly more 'High' scores compared to those that did not (P = 0.008). Clinical trials with protocols registered a priori had a significantly greater percentage of 'High' scores compared to the trials that were not registered in advance (P = 0.003). No significant difference occurred between the quality of clinical trials and the number of authors, journal (Endodontic specialty vs. Non-Endodontic specialty) or year of publication.

CONCLUSIONS

Reports of randomized clinical trials published in the speciality of Endodontics had a substantial number of deficiencies. To create high-quality reports of clinical trials, authors should comply with the PRIRATE 2020 guidelines.

摘要

目的

根据 PRIRATE 2020 清单,对发表在牙髓学杂志上的随机临床试验进行随机抽样,对其报告质量进行严格评估,并分析报告试验的质量与多种参数之间的关系。

方法

从 2015 年至 2019 年,从 PubMed 数据库中随机选择 50 项与牙髓学相关的随机临床试验,并由两名独立的审查员进行评估。对于每个试验,如果完全报告了 PRIRATE 指南中的每一项,则给予 1 分;如果未报告,则给予 0 分;如果报告不充分,则给予 0.5 分。对于与试验无关的项目,给予“不适用(NA)”。根据总分的四分位数范围,试验分为“低(0-58.4%)”、“中(58.5-72.8%)”和“高(72.9-100%)”质量。研究了临床试验特征与质量之间的关系。使用描述性统计、频率分析和百分比分析来描述数据。为了确定分类数据的显著性,使用卡方检验。概率值 0.05 被认为是显著性水平。

结果

根据总分,13 项(26%)、25 项(50%)和 12 项(24%)临床试验报告分别归类为“高”、“中”和“低”质量。所有手稿中均充分报告了 3 项(1b、6d、11e),而所有报告中均有 2 项(5k、5m)的评分“NA”。与亚洲、中东、北美和南美相比,来自欧洲的报告“高”质量评分显著更高(P=0.0002)。在影响因子较高的期刊上发表的“高”质量报告明显更多(P=0.045)。遵守 CONSORT 指南的期刊发表的临床试验报告的“高”评分明显高于不遵守的报告(P=0.008)。有预先注册方案的临床试验“高”评分的比例明显高于未预先注册的试验(P=0.003)。临床试验的质量与作者数量、期刊(牙髓学专业与非牙髓学专业)或出版年份之间没有显著差异。

结论

发表在牙髓学专业杂志上的随机临床试验报告存在大量缺陷。为了提高临床试验报告的质量,作者应遵守 PRIRATE 2020 指南。

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