Ioannidis J P, Cappelleri J C, Lau J
National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20852, USA.
JAMA. 1998 Apr 8;279(14):1089-93. doi: 10.1001/jama.279.14.1089.
The extent of concordance between meta-analyses and large trials on the same topic has been investigated with different protocols. Inconsistent conclusions created confusion regarding the validity of these major tools of clinical evidence.
To evaluate protocols comparing meta-analyses and large trials in order to understand if and why they disagree on the concordance of these 2 clinical research methods.
Systematic comparison of protocol designs, study selection, definitions of agreement, analysis methods, and reported discrepancies between large trials and meta-analyses.
More discrepancies were claimed when large trials were selected from influential journals (which may prefer trials disagreeing with prior evidence) than from already performed meta-analyses (which may target homogeneous trials) and when both primary and secondary (rather than only primary) end points were considered. Depending on how agreement was defined, kappa coefficients varied from 0.22 (low agreement) to 0.72 (excellent agreement). The correlation of treatment effects between large trials and meta-analyses varied from -0.12 to 0.76, but was more similar (0.50-0.76) when only primary end points were considered. When both the magnitude and uncertainty of treatment effects were considered, large trials disagreed with meta-analyses 10% to 23% of the time. Discrepancies were attributed to different disease risks, variable protocols, quality, and publication bias.
Comparisons of large trials with meta-analyses may reach different conclusions depending on how trials and meta-analyses are selected and how end points and agreement are defined. Scrutiny of these 2 major research methods can enhance our appreciation of both for guiding medical practice.
已采用不同方案对同一主题的荟萃分析与大型试验之间的一致性程度进行了调查。结论不一致引发了关于这些临床证据主要工具有效性的困惑。
评估比较荟萃分析与大型试验的方案,以了解它们在这两种临床研究方法的一致性方面是否存在分歧以及原因。
对方案设计、研究选择、一致性定义、分析方法以及大型试验与荟萃分析之间报告的差异进行系统比较。
与从已完成的荟萃分析(可能针对同类试验)中选择大型试验相比,从有影响力的期刊(可能更倾向于与先前证据不一致的试验)中选择大型试验时,以及同时考虑主要和次要(而非仅主要)终点时,声称的差异更多。根据一致性的定义方式,kappa系数在0.22(低一致性)至0.72(极佳一致性)之间变化。大型试验与荟萃分析之间的治疗效果相关性在-0.12至0.76之间变化,但仅考虑主要终点时更为相似(0.50 - 0.76)。当同时考虑治疗效果的大小和不确定性时,大型试验与荟萃分析在10%至23%的时间内存在分歧。差异归因于不同的疾病风险、可变的方案、质量和发表偏倚。
大型试验与荟萃分析的比较可能会得出不同的结论,这取决于试验和荟萃分析的选择方式以及终点和一致性的定义方式。对这两种主要研究方法的审查可以增强我们对它们的理解,以指导医学实践。