Diagnosing the GOSE: Structural and Psychometric Properties Using Item Response Theory, a TRACK-TBI Pilot Study
Jana Ranson, Brooke E Magnus, Nancy Temkin, Sureyya Dikmen, Joseph T Giacino, David O Okonkwo, Alex B Valadka, Geoffrey T Manley, Lindsay D Nelson, TRACK-TBI Investigators, Shelly R Cooper, Kristen Dams-O'Connor, Wayne A Gordon, Andrew I R Maas, David K Menon, Pratik Mukherjee, Ava M Puccio, Mary J Vassar, John K Yue, Esther L Yuh, Jana Ranson, Brooke E Magnus, Nancy Temkin, Sureyya Dikmen, Joseph T Giacino, David O Okonkwo, Alex B Valadka, Geoffrey T Manley, Lindsay D Nelson, TRACK-TBI Investigators, Shelly R Cooper, Kristen Dams-O'Connor, Wayne A Gordon, Andrew I R Maas, David K Menon, Pratik Mukherjee, Ava M Puccio, Mary J Vassar, John K Yue, Esther L Yuh
Abstract
The Glasgow Outcome Scale-Extended (GOSE) was designed to assess global outcome after traumatic brain injury (TBI). Since its introduction, several empirically founded criticisms of the GOSE have been raised, including poor reliability; an insensitivity to small, but potentially meaningful, changes; a tendency to produce ceiling effects; inconsistent associations with neurocognitive, psychological, and quality-of-life measures; and an inability to assess the multi-dimensional nature of TBI outcome. The current project took a diagnostic approach to identifying the underlying causes of reported limitations by exploring the internal construct validity of the GOSE at 3 and 6 months post-injury using item response theory (IRT) techniques. Data were from the TRACK-TBI Pilot Study, a large (N = 586), prospective, multi-site project that included TBI cases of all injury severity levels. To assess the level of latent functional "impairment" captured by GOSE items independent of the assigned outcome category or GOSE total score, items were modified so that higher scores reflected greater impairment. Results showed that although the GOSE's items capture varying levels of impairment across a broad disability spectrum at 3 and 6 months, there was also evidence at each time point of item redundancy (multiple items capturing similar levels of impairment), item deficiency (lack of items capturing lower levels of impairment), and item inefficiency (items only capturing minimal impairment information). The findings illustrate the value of IRT to illuminate strengths and weaknesses of clinical outcome assessment measures and provide a framework for future measure refinement.
Trial registration: ClinicalTrials.gov NCT01565551.
Keywords: Glasgow Outcome Scale–Extended; item response theory; outcome assessment; psychometrics; traumatic brain injury.
Conflict of interest statement
Dr. Temkin reports grants from the Department of Defense, NIH, NIDILRR, and CDC during the conduct of the study. Dr. Dikmen reports grants from NIH and NIDILRR during the conduct of the study. Dr. Giacino reports grants from the Department of Defense, NIH, NIDILRR, James S. McDonnell Foundation, and other support from the Barbara Epstein Foundation during the conduct of the study. Dr. Okonkwo reports grants from NIH and the Department of Defense during the conduct of the study. Dr. Manley reports grants from the Department of Defense, NIH, and other support from One Mind, Palantir, and Johnson & Johnson Family of Companies/DePuySynthes/Codman Neuro during the conduct of the study. Dr. Nelson reports grants from NIH and the Medical College of Wisconsin's Center for Patient Care and Outcomes Research, Clinical and Translational Science Institute, and Advancing a Healthier Wisconsin Endowment during the conduct of the study.
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Source: PubMed