TY - JOUR PY - 2003// TI - Systematic bias in traumatic brain injury outcome studies because of loss to follow-up JO - Archives of physical medicine and rehabilitation A1 - Corrigan, John D. A1 - Harrison-Felix, Cynthia L. A1 - Bogner, Jennifer A. A1 - Dijkers, Marcel A1 - Terrill, Melissa Sendroy A1 - Whiteneck, Gale Gibson SP - 153 EP - 160 VL - 84 IS - 2 N2 - OBJECTIVE: To identify potential sources of selection bias created by subjects lost to follow-up in studies of traumatic brain injury (TBI). DESIGN: Demographic, premorbid, injury-related, and hospital course characteristics were compared for subjects lost and found for 1- and 2-year postinjury follow-ups by using bivariate tests and logistic regression analysis. SETTING: Three prospective, longitudinal data sets-a single center, a multicenter, and a statewide incidence surveillance system and follow-up registry. PARTICIPANTS: Adolescents and adults hospitalized with a diagnosis of TBI. INTERVENTIONS: Not applicable. MAIN OUTCOME MEASURES: Subjects were considered lost when no information was collected from the person with TBI or only limited information could be obtained from a proxy, for any reason, including death, refusal, inability to locate, and inability to interview. RESULTS: At year 1 follow-up, 58.0% to 58.6% of subjects were found; 39.7% to 42.0% of subjects were found by year 2. Variables most frequently associated with loss to follow-up were cause of injury, blood alcohol level, motor function, hospital payer source, and race and ethnicity. CONCLUSIONS: TBI follow-up studies may experience selective attrition of subjects who (1) are socioeconomically disadvantaged, (2) have a history of substance abuse, and (3) have violent injury etiologies. These phenomena are mitigated for those with more severe motor deficits. Loss to follow-up may be a problem inherent to this population; however, the high rate and its selective nature are problematic for outcome studies.

Language: en

LA - en SN - 0003-9993 UR - http://dx.doi.org/10.1053/apmr.2003.50093 ID - ref1 ER -