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Can trial sequential monitoring boundaries reduce spurious inferences from meta-analyses?
Author(s) -
Kristian Thorlund,
P.J. Devereaux,
Jørn Wetterslev,
Gordon Guyatt,
John P. A. Ioannidis,
Lehana Thabane,
Lise Lotte Gluud,
Bodil AlsNielsen,
Christian Gluud
Publication year - 2008
Publication title -
international journal of epidemiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.406
H-Index - 208
eISSN - 1464-3685
pISSN - 0300-5771
DOI - 10.1093/ije/dyn179
Subject(s) - spurious relationship , meta analysis , medicine , inference , medline , econometrics , statistics , computer science , mathematics , artificial intelligence , biology , biochemistry
Results from apparently conclusive meta-analyses may be false. A limited number of events from a few small trials and the associated random error may be under-recognized sources of spurious findings. The information size (IS, i.e. number of participants) required for a reliable and conclusive meta-analysis should be no less rigorous than the sample size of a single, optimally powered randomized clinical trial. If a meta-analysis is conducted before a sufficient IS is reached, it should be evaluated in a manner that accounts for the increased risk that the result might represent a chance finding (i.e. applying trial sequential monitoring boundaries).

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