Hemels Michiel E H, Vicente Colin, Sadri Hamid, Masson Mary Jane, Einarson Thomas R
Faculty of Pharmacology, University of Toronto, Canada.
Curr Med Res Opin. 2004 Apr;20(4):477-84. doi: 10.1185/030079904125003197.
Meta-analyses (MAs) of randomized controlled trials (RCTs) have the potential to provide the highest level of evidence, but the quality of published MAs has not been systematically assessed. Therefore, we determined reliability was significant (kappa = 0.89; p < 0.05). the quality of reporting in MAs of RCTs of pharmacotherapy for major depressive disorder (MDD) in adults (18-65 years) without comorbidities and examine trends over time.
MEDLINE, EMBASE, Healthstar, Psychlit and Cochrane databases were searched (1980-2002) by 4 independent reviewers for MAs of RCTs. Articles meeting inclusion criteria were blinded. Inter-rater reliability (kappa) was evaluated using a test-retest strategy on 4 articles. Quality was (p = 0.74) did not detect a difference in quality of assessed using the QUOROM checklist. Time trends were evaluated by calculating Spearman's rho.
One hundred articles were identified, 68 were excluded [co-morbidities (9), inappropriate comparator (13), inappropriate outcome (15), article not available (5), inappropriate patient population (15), and inappropriate study design (11)]; 32 were included. Initial kappa was 0.81 (p < 0.05). After resolution of disagreements, the test-retest The mean overall quality score was 50.2% (SD 15.8%, range = 16.7-88.9%). The overall score for Titles was very poor (22%), Abstracts (40%) and Methods (49%) were poor, while overall Results score was minimally acceptable (54%). Good quality scores were found for Introduction (91%) and Discussion (97%). No time trends were identified using Spearman's correlation analysis (rho 0.05; p = 0.79). The Mann-Whitney U test articles published before and after the QUOROM.
Despite quality guidelines, the average quality of published MAs of antidepressants is barely acceptable (50.2%). A need exists for adherence to standardized reporting and quality guidelines.
随机对照试验(RCT)的荟萃分析(MA)有潜力提供最高级别的证据,但已发表的MA的质量尚未得到系统评估。因此,我们确定了可靠性显著(kappa = 0.89;p < 0.05)。对18至65岁无合并症的成年人中重度抑郁症(MDD)药物治疗的RCT的MA报告质量进行评估,并研究随时间的趋势。
4名独立评审员在MEDLINE、EMBASE、Healthstar、Psychlit和Cochrane数据库中检索(1980 - 2002年)RCT的MA。符合纳入标准的文章进行盲法评审。使用重测策略对4篇文章评估评分者间信度(kappa)。使用QUOROM清单评估质量。通过计算Spearman秩相关系数评估时间趋势。
共识别出100篇文章,68篇被排除[合并症(9篇)、不适当的对照(13篇)、不适当的结局(15篇)、文章不可获取(5篇)、不适当的患者人群(15篇)和不适当的研究设计(11篇)];32篇被纳入。初始kappa为0.81(p < 0.05)。在解决分歧后,重测的平均总体质量得分是50.2%(标准差15.8%,范围 = 16.7 - 88.9%)。标题的总体得分非常差(22%),摘要(40%)和方法(49%)较差,而结果总体得分勉强可接受(54%)。引言(91%)和讨论(97%)的质量得分良好。使用Spearman相关分析未发现时间趋势(rho 0.05;p = 0.79)。采用Mann - Whitney U检验比较QUOROM发布前后发表的文章。
尽管有质量指南,但已发表的抗抑郁药物MA的平均质量勉强可接受(50.2%)。需要遵守标准化报告和质量指南。