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中国药学(英文版) ›› 2017, Vol. 26 ›› Issue (3): 212-221.DOI: 10.5246/jcps.2017.03.022

• 【研究论文】 • 上一篇    下一篇

我国大陆期刊哮喘药学服务随机对照研究的质量评价

王利群, 谢晓慧*, 周瑞瑞   

  1. 北京大学医学部 药学院 药事管理与临床药学系, 北京 100191
  • 收稿日期:2016-11-02 修回日期:2016-12-27 出版日期:2017-03-30 发布日期:2017-01-20
  • 通讯作者: Tel.: +86-010-82805020, E-mail: xxhrenee@bjmu.edu.cn

Assessment of the quality of randomized controlled trials on pharmaceutical care for asthmatic patients in journals of mainland China

Liqun Wang, Xiaohui Xie*, Ruirui Zhou   

  1. Department of Pharmacy Administration and Clinical Pharmacy, School of Pharmaceutical Sciences, Peking University Health Science Center, Beijing 100191, China
  • Received:2016-11-02 Revised:2016-12-27 Online:2017-03-30 Published:2017-01-20
  • Contact: Tel.: +86-010-82805020, E-mail: xxhrenee@bjmu.edu.cn

摘要:

本文旨在评价我国药师开展的哮喘药学服务随机对照研究的质量, 指出当前研究存在的问题, 以期为进一步研究提供参考。检索中国期刊全文数据库(CNKI)、万方数据知识服务平台、维普数据库中我国药师开展的哮喘药学服务随机对照研究, 提取与研究设计和报道相关的信息并统计分析, 同时使用Cochrane偏倚风险评估工具对纳入研究进行偏倚风险评估。最终共纳入文献14篇。所有研究均未科学估算样本量; 所有研究均未具体报道科学的随机序列产生方法及分配隐藏; 2(14.3%)分别声明实施了单盲和双盲的方法, 但均未报道施盲的具体方法与过程; 所有文献均未报道对结局评价者施盲; 5(35.7%)统计方法声明不全或误用; 1(14.3%)声明有受试者的退出与失访但未进行意向性分析; 所有研究都不同程度地报道了受试者合格标准, 均涉及哮喘的诊断, 但仅有4(28.6%)涉及患者年龄、3(21.4%)涉及哮喘严重程度和分期; 9(64.3%)研究以文字形式而非表格呈现受试者基线资料, 13(92.9%)明确指出或能够推测出使用了显著性检验的方法比较了组间均衡性; 没有研究明确定义主要结局指标与次要结局指标; 2(14.3%)提及受试者知情同意, 所有研究均未提及取得伦理委员会批准。Cochrane偏倚风险评估结果显示不明确的偏倚风险所占比例最高。研究结果表明, 我国药师主导的哮喘药学服务的随机对照研究整体水平不高, 在研究设计和报道方面有较大提升空间。

关键词: 哮喘, 药学服务, 药师, 随机对照试验, 质量评价

Abstract:

The objective of this study was to assess the quality of randomized controlled trials (RCTs) on pharmaceutical care for asthmatic patients conducted by pharmacists in mainland China, to identify the problems in current studies, and to provide some references for further studies. The China National Knowledge Infrastructure (CNKI), Wanfang Database, and VIP Database were searched for randomized controlled trials on pharmaceutical care for asthmatic patients, and only those studies undertaken by pharmacists were included. Information about the study design and reporting of selected studies was extracted and collected to systematically analyze these studies. Meanwhile, the Cochrane Collaborations tool for assessing risk of bias was used to assess potential biases related to these studies. Ultimately, 14 articles were included in this study. No study determined the sample size in a scientific way. No article reported a scientific and detailed method of random sequence generation or allocation concealment. Two (14.3%) studies claimed to have implemented a double-blinding and a single-blinding respectively, but neither of them reported any details about how they performed the blinding. No study employed a blinding of outcome assessment. Five (35.7%) studies either stated statistical methods incompletely or used them incorrectly. One (7.1%) study reported an attrition without employing an intention-to-treat analysis. All studies reported eligibility criteria for participants to some extent, and all these criteria involved diagnosis of asthma, but only four (28.6%) of them reported patients ages and three (21.4%) described the severity and the stage of asthma. Nine (64.3%) reported baseline data in the text rather than in a table, and 13 (92.9%) involved comparisons between groups with significance tests either explicitly or implicitly. No report made a distinction between primary and secondary outcomes. Two (14.3%) mentioned informed consent of subjects, while no article reported ethical approval. “Unclear risk” made up the highest percentage of the studies analyzed according to the risk of bias assessment by the Cochrane Collaborations tool. Our study demonstrates that the quality of RCTs on pharmaceutical care for asthmatic patients conducted by Chinese pharmacists is suboptimal, especially with regards to study design and reporting.

Key words: Asthma, Pharmaceutical care, Pharmacist, Randomized controlled trial, Quality assessment

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