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耳针疗法治疗疼痛的随机对照试验报告质量。

Quality of reporting on randomised controlled trials of auriculotherapy for pain.

机构信息

Department of Family Medicine, University of North Carolina, Chapel Hill, NC 27599-7595, USA.

出版信息

Acupunct Med. 2011 Jun;29(2):122-6. doi: 10.1136/aim.2010.003475. Epub 2011 Apr 12.

Abstract

OBJECTIVE

The authors investigated the quality of reporting for randomised controlled trials of auriculotherapy for pain before and after the implementation of the Consolidated Standards of Reporting Trials (CONSORT) and Standards for Reporting Interventions in Controlled Trials of Acupuncture (STRICTA) guidelines.

METHODS

The authors identified randomised controlled trials of auriculotherapy that measured pain or pain medication use as a primary outcome and were published in English in peer-reviewed journals. Proportions of studies that reported STRICTA and CONSORT items were compared for the years before and after implementation of STRICTA (2001) using Fisher's exact tests. Global differences across all study factors were investigated using hierarchical clustering and principle component analysis (PCA).

RESULTS

15 studies met our inclusion criteria. On average, 11 studies (74%) reported STRICTA items and eight studies (54%) reported CONSORT items. Differences in reporting between pre and post-STRICTA studies were found for two CONSORT items (randomised sequence and treatment provider) but no STRICTA items. However, the results of cluster analysis and PCA detected global differences over time for both STRICTA and CONSORT items.

CONCLUSION

Quality of reporting for studies of auriculotherapy for pain appears to have generally improved since the implementation of STRICTA and CONSORT guidelines.

摘要

目的

作者调查了耳针治疗疼痛的随机对照试验在实施 CONSORT(CONsolidated Standards of Reporting Trials)和 STRICTA(Standards for Reporting Interventions in Controlled Trials of Acupuncture)指南前后的报告质量。

方法

作者确定了以疼痛或疼痛药物使用为主要结局,并以英文在同行评议期刊上发表的耳针治疗疼痛的随机对照试验。使用 Fisher 精确检验比较 STRICTA(2001 年)实施前后年份报告 STRICTA 和 CONSORT 项目的研究比例。使用层次聚类和主成分分析(PCA)研究所有研究因素的全球差异。

结果

符合纳入标准的研究有 15 项。平均而言,有 11 项研究(74%)报告了 STRICTA 项目,8 项研究(54%)报告了 CONSORT 项目。在 STRICTA 前后研究中,有两个 CONSORT 项目(随机序列和治疗提供者)的报告存在差异,但没有 STRICTA 项目。然而,聚类分析和 PCA 的结果检测到 STRICTA 和 CONSORT 项目在时间上的总体差异。

结论

自 STRICTA 和 CONSORT 指南实施以来,耳针治疗疼痛的研究报告质量似乎普遍有所提高。

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