Papageorgiou Spyridon N, Koretsi Vasiliki, Jäger Andreas
Department of Orthodontics, School of Dentistry, University of Bonn, Germany,
Department of Oral Technology, School of Dentistry, University of Bonn, Germany, and.
Eur J Orthod. 2017 Feb;39(1):98-105. doi: 10.1093/ejo/cjw035. Epub 2016 Apr 29.
The validity of meta-analysis is dependent upon the quality of included studies. Here, we investigated whether the design of untreated control groups (i.e. source and timing of data collection) influences the results of clinical trials in orthodontic research.
This meta-epidemiological study used unrestricted literature searching for meta-analyses in orthodontics including clinical trials with untreated control groups. Differences in standardized mean differences (ΔSMD) and their 95% confidence intervals (CIs) were calculated according to the untreated control group through multivariable random-effects meta-regression controlling for nature of the interventional group and study sample size. Effects were pooled with random-effects synthesis, followed by mixed-effect subgroup and sensitivity analyses.
Studies with historical control groups reported deflated treatment effects compared to studies with concurrent control groups (13 meta-analyses; ΔSMD = -0.31; 95% CI = -0.53, -0.10; P = 0.004). Significant differences were found according to the type of historical control group (based either on growth study or clinical archive; 11 meta-analyses; ΔSMD = 0.40; 95% CI = 0.21, 0.59; P < 0.001).
The use of historical control groups in orthodontic clinical research was associated with deflation of treatment effects, which was independent from whether the interventional group was prospective or retrospective and from the study's sample size. Caution is warranted when interpreting clinical studies with historical untreated control groups or when interpreting systematic reviews that include such studies.
PROSPERO (CRD42015024179).
None.
荟萃分析的有效性取决于纳入研究的质量。在此,我们调查了未治疗对照组的设计(即数据收集的来源和时间)是否会影响正畸研究中临床试验的结果。
这项荟萃流行病学研究对正畸领域的荟萃分析进行了无限制文献检索,其中包括设有未治疗对照组的临床试验。通过多变量随机效应荟萃回归,根据未治疗对照组计算标准化均数差(ΔSMD)及其95%置信区间(CI),同时控制干预组的性质和研究样本量。采用随机效应合成法合并效应,随后进行混合效应亚组分析和敏感性分析。
与设有同期对照组的研究相比,设有历史对照组的研究报告的治疗效果较低(13项荟萃分析;ΔSMD = -0.31;95% CI = -0.53,-0.10;P = 0.004)。根据历史对照组的类型(基于生长研究或临床档案)发现了显著差异(11项荟萃分析;ΔSMD = 0.40;95% CI = 0.21,0.59;P < 0.001)。
正畸临床研究中使用历史对照组与治疗效果降低有关,这与干预组是前瞻性还是回顾性以及研究的样本量无关。在解释设有未治疗历史对照组的临床研究或包含此类研究的系统评价时,需要谨慎。
PROSPERO(CRD42015024179)。
无。