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. 2008 Jun;25(6):641-51.
doi: 10.1089/neu.2007.0510.

Effects of Glasgow Outcome Scale misclassification on traumatic brain injury clinical trials

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Effects of Glasgow Outcome Scale misclassification on traumatic brain injury clinical trials

Juan Lu et al. J Neurotrauma. 2008 Jun.

Abstract

The Glasgow Outcome Scale (GOS) is the primary endpoint for efficacy analysis of clinical trials in traumatic brain injury (TBI). Accurate and consistent assessment of outcome after TBI is essential to the evaluation of treatment results, particularly in the context of multicenter studies and trials. The inconsistent measurement or interobserver variation on GOS outcome, or for that matter, on any outcome scales, may adversely affect the sensitivity to detect treatment effects in clinical trial. The objective of this study is to examine effects of nondifferential misclassification of the widely used five-category GOS outcome scale and in particular to assess the impact of this misclassification on detecting a treatment effect and statistical power. We followed two approaches. First, outcome differences were analyzed before and after correction for misclassification using a dataset of 860 patients with severe brain injury randomly sampled from two TBI trials with known differences in outcome. Second, the effects of misclassification on outcome distribution and statistical power were analyzed in simulation studies on a hypothetical 800-patient dataset. Three potential patterns of nondifferential misclassification (random, upward and downward) on the dichotomous GOS outcome were analyzed, and the power of finding treatments differences was investigated in detail. All three patterns of misclassification reduce the power of detecting the true treatment effect and therefore lead to a reduced estimation of the true efficacy. The magnitude of such influence not only depends on the size of the misclassification, but also on the magnitude of the treatment effect. In conclusion, nondifferential misclassification directly reduces the power of finding the true treatment effect. An awareness of this procedural error and methods to reduce misclassification should be incorporated in TBI clinical trials.

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Figures

FIG. 1.
FIG. 1.
(A) Effect of random misclassification pattern on the power. The solid line presents the correlation between the power and the expected treatment effect, and dashed lines present the correlation between the random misclassified treatment effect and power according to the symbol key. For example, for the case of a 10% treatment effect, a 20% up and down random misclassification would result in a reduction of power from 82% (point a) to 49% (point b) thereby rendering the trial non-significant. (B) Effect of upward misclassification pattern on the power. The solid line represents the correlation between the power and the expected treatment effect, and dashed lines represent the correlation between the upward misclassified treatment effect and power according to the symbol key. For example, for the case of a 10% treatment effect, a 20% up and 10% down (lowest dashed line) misclassification results in a reduction of power from 82% (point a) to 60% (point b). (C) Effect of downward misclassification pattern on the power. The solid line represents the correlation between the power and the expected treatment effect, and dashed lines represent the correlation between the downward misclassified treatment effect and power according to the symbol key. For example, for the case of a 10% treatment effect, a 10% up and 20% down (lowest dashed line) misclassification results in a reduction of power from 82% (point a) to 55% (point b).
FIG. 2.
FIG. 2.
Reduction of treatment effect by upward outcome misclassification. The solid line represents the expected treatment effect, and dashed lines represent the reduction of treatment effect by the upward misclassifications according to the symbol key. For example, for the case of a 10% treatment effect, a 30% up (lowest dashed line) misclassification results in a reduction of treatment effect to 7.6%, which is a 2.4% reduction from the expected 10% treatment effect.

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