N-of-1 Trials in the Medical Literature A Systematic Review

被引:166
作者
Gabler, Nicole B. [1 ,2 ]
Duan, Naihua [3 ,4 ,5 ]
Vohra, Sunita [6 ]
Kravitz, Richard L. [7 ,8 ]
机构
[1] Univ Penn, Sch Med, Ctr Clin Epidemiol & Biostat, Philadelphia, PA 19104 USA
[2] Univ Penn, Sch Med, Dept Biostat & Epidemiol, Philadelphia, PA 19104 USA
[3] New York State Psychiat Inst & Hosp, New York, NY 10032 USA
[4] Columbia Univ, Dept Psychiat, New York, NY USA
[5] Columbia Univ, Dept Biostat, New York, NY USA
[6] Univ Alberta, Dept Pediat, CARE Program, Edmonton, AB, Canada
[7] Univ Calif Davis, Dept Internal Med, Davis, CA 95616 USA
[8] Univ Calif Davis, Ctr Healthcare Policy & Res, Davis, CA 95616 USA
关键词
n-of-1; trials; evidence-based medicine; clinical trials; systematic review; RANDOMIZED CONTROLLED TRIALS; CLINICAL-USEFULNESS; INDIVIDUAL PATIENTS; PATIENT; PARACETAMOL; AMITRIPTYLINE; HETEROGENEITY; PERSPECTIVES; CHEMOTHERAPY; FIBROMYALGIA;
D O I
10.1097/MLR.0b013e318215d90d
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Background: N-of-1 trials (multiple crossover studies conducted in single individuals) may be ideal for determining individual treatment effects and as a tool to estimate heterogeneity of treatment effects (HTE) in a population. However, comprehensive data on n-of-1 trial methodology and analysis is lacking. We performed this study to describe n-of-1 trial characteristics, examine treatment changes resulting from n-of-1 trial participation, and to determine if trial reporting is adequate for estimating HTE. Methods: We undertook a systematic review of n-of-1 trials published between 1985 and December 2010. Included trials were those having individual treatment episodes as the unit of randomization and reporting individual-specific treatment effects. We abstracted trial characteristics, treatment change information, and analytic methods. Results: We included 108 trials reporting on 2154 participants. Approximately half (49%) of the trials used a statistical cutoff to determine a superior treatment, whereas the remainder used a graphical comparison (25%) or a clinical significance cutoff (20%). Sixty-seven trials, reporting on 488 people, provided treatment change information: 54% of participants had subsequent treatment decisions consistent with the results of the trial, 8% had decisions inconsistent with trial results, and 38% had ambiguous results. Less than half of the trials (45%) reported adequate information to facilitate the calculation of HTE. Conclusion: N-of-1 trials are a useful tool for enhancing therapeutic precision in a range of conditions and should be conducted more often. To facilitate future meta-analysis, and the estimation of HTE, researchers reporting n-of-1 trial results should clearly describe individual data.
引用
收藏
页码:761 / 768
页数:8
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