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Original Contribution
April 2006

Brain Response to One's Own Name in Vegetative State, Minimally Conscious State, and Locked-in Syndrome

Author Affiliations

Author Affiliations: Université Claude Bernard Lyon 1–CNRS, Lyon, France (Dr Perrin); Centre de Recherches du Cyclotron (Drs Perrin, Schabus, Degueldre, Luxen, Maquet, and Laureys and Ms Schnakers) and Départements des Sciences Cognitives (Dr Brédart), Anesthésiologie et des Soins Intensifs (Drs Faymonville and Lamy), and Neurologie (Drs Moonen and Laureys), Université de Liège, Liège, Belgium; Department of Physiological Psychology, University of Salzburg, Salzburg, Austria (Dr Schabus); and Unité TEP/Cyclotron Biomédical, Hôpital Erasme, Université Libre de Bruxelles, Brussels, Belgium (Dr Goldman).

Arch Neurol. 2006;63(4):562-569. doi:10.1001/archneur.63.4.562
Abstract

Background  A major challenge in the management of severely brain-injured patients with altered states of consciousness is to estimate their residual perception of the environment.

Objective  To investigate the integrity of detection of one's own name in patients in a behaviorally well-documented vegetative state (VS), patients in a minimally conscious state (MCS), and patients with locked-in syndrome.

Design  We recorded the auditory evoked potentials to the patient's own name and to 7 other equiprobable first names in 15 brain-damaged patients.

Results  A P3 component was observed in response to the patient's name in all patients with locked-in syndrome, in all MCS patients, and in 3 of 5 patients in a VS. P3 latency was significantly (P<.05) delayed for MCS and VS patients compared with healthy volunteers.

Conclusions  These results suggest that partially preserved semantic processing could be observed in noncommunicative brain-damaged patients, notably for the detection of salient stimuli, such as the subject's own name. This function seems delayed in MCS and (if present) in VS patients. More important, a P3 response does not necessarily reflect conscious perception and cannot be used to differentiate VS from MCS patients.

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