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Comparison of the Glasgow Coma Scale and the Reaction Level Scale for assessment of cerebral responsiveness in the critically ill

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Abstract

Objective

The Glasgow Coma Scale (GCS) is a well-known source of error in outcome prediction models. We compared assessment of cerebral responsiveness with the GCS and the Reaction Level Scale (RLS) in two otherwise similar outcome prediction models.

Design and setting

Prospective, observational study in a general intensive care unit.

Patients and participants

All admissions of patients with or at risk of developing impaired brain function between 1997 and 1998 (n=534).

Measurements and results

Admissions were scored by RLS and APACHE II (includes scoring with the GCS). The RLS scores were transformed to APACHE II central nervous system scores according to a predetermined protocol. APACHE II estimated probability of death was calculated conventionally with the GCS and the RLS. Vital status 90 days after admission was secured from a national database. Bias and precision was 0.5% and 16.6%, respectively. The area under receiver operating characteristic curves was slightly but significantly greater with the RLS-based APACHE II model than with the GCS-based model (0.92 vs. 0.90). Discrimination was improved primarily in admissions with low and intermediate probability of death.

Conclusions

Scoring of cerebral responsiveness with the RLS instead of the GCS was associated with minimal bias of the APACHE II probability of death estimate. Assessment of consciousness in critically ill with the RLS deserves further evaluation

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Acknowledgements

This work was performed at the Intensive Care Unit, Department of Anesthesia and Intensive Care, Norrköping Hospital, Norrköping, Sweden. The research was supported by a grant from the Norrköping Hospital Research Board.

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Correspondence to Sten M. Walther.

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Walther, S.M., Jonasson, U. & Gill, H. Comparison of the Glasgow Coma Scale and the Reaction Level Scale for assessment of cerebral responsiveness in the critically ill. Intensive Care Med 29, 933–938 (2003). https://doi.org/10.1007/s00134-003-1757-4

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  • DOI: https://doi.org/10.1007/s00134-003-1757-4

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