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Development and external validation of a new PTA assessment scale

BACKGROUND: Post-traumatic amnesia (PTA) is a key symptom of traumatic brain injury (TBI). Accurate assessment of PTA is imperative in guiding clinical decision making. Our aim was to develop and externally validate a short, examiner independent and practical PTA scale, by selecting the most discrim...

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Autores principales: Jacobs, Bram, van Ekert, Janneke, Vernooy, Lotje PL, Dieperink, Peter, Andriessen, Teuntje MJC, Hendriks, Marc PH, van Vugt, Arie B, Emons, Marjolein AA, Borm, George F, Vos, Pieter E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3447645/
https://www.ncbi.nlm.nih.gov/pubmed/22873279
http://dx.doi.org/10.1186/1471-2377-12-69
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author Jacobs, Bram
van Ekert, Janneke
Vernooy, Lotje PL
Dieperink, Peter
Andriessen, Teuntje MJC
Hendriks, Marc PH
van Vugt, Arie B
Emons, Marjolein AA
Borm, George F
Vos, Pieter E
author_facet Jacobs, Bram
van Ekert, Janneke
Vernooy, Lotje PL
Dieperink, Peter
Andriessen, Teuntje MJC
Hendriks, Marc PH
van Vugt, Arie B
Emons, Marjolein AA
Borm, George F
Vos, Pieter E
author_sort Jacobs, Bram
collection PubMed
description BACKGROUND: Post-traumatic amnesia (PTA) is a key symptom of traumatic brain injury (TBI). Accurate assessment of PTA is imperative in guiding clinical decision making. Our aim was to develop and externally validate a short, examiner independent and practical PTA scale, by selecting the most discriminative items from existing scales and using a three-word memory test. METHODS: Mild, moderate and severe TBI patients and control subjects were assessed in two separate cohorts, one for derivation and one for validation, using a questionnaire comprised of items from existing PTA scales. We tested which individual items best discriminated between TBI patients and controls, represented by sensitivity and specificity. We then created our PTA scale based on these results. This new scale was externally evaluated for its discriminative value using Receiver Operating Characteristic (ROC) analysis and compared to existing PTA scales. RESULTS: The derivation cohort included 126 TBI patients and 31 control subjects; the validation cohort consisted of 132 patients and 30 controls. A set of seven items was eventually selected to comprise the new PTA scale: age, name of hospital, time, day of week, month, mode of transport and recall of three words. This scale demonstrated adequate discriminative values compared to existing PTA scales on three consecutive administrations in the validation cohort. CONCLUSION: We introduce a valid, practical and examiner independent PTA scale, which is suitable for mild TBI patients at the emergency department and yet still valuable for the follow-up of more severely injured TBI patients.
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spelling pubmed-34476452012-09-21 Development and external validation of a new PTA assessment scale Jacobs, Bram van Ekert, Janneke Vernooy, Lotje PL Dieperink, Peter Andriessen, Teuntje MJC Hendriks, Marc PH van Vugt, Arie B Emons, Marjolein AA Borm, George F Vos, Pieter E BMC Neurol Research Article BACKGROUND: Post-traumatic amnesia (PTA) is a key symptom of traumatic brain injury (TBI). Accurate assessment of PTA is imperative in guiding clinical decision making. Our aim was to develop and externally validate a short, examiner independent and practical PTA scale, by selecting the most discriminative items from existing scales and using a three-word memory test. METHODS: Mild, moderate and severe TBI patients and control subjects were assessed in two separate cohorts, one for derivation and one for validation, using a questionnaire comprised of items from existing PTA scales. We tested which individual items best discriminated between TBI patients and controls, represented by sensitivity and specificity. We then created our PTA scale based on these results. This new scale was externally evaluated for its discriminative value using Receiver Operating Characteristic (ROC) analysis and compared to existing PTA scales. RESULTS: The derivation cohort included 126 TBI patients and 31 control subjects; the validation cohort consisted of 132 patients and 30 controls. A set of seven items was eventually selected to comprise the new PTA scale: age, name of hospital, time, day of week, month, mode of transport and recall of three words. This scale demonstrated adequate discriminative values compared to existing PTA scales on three consecutive administrations in the validation cohort. CONCLUSION: We introduce a valid, practical and examiner independent PTA scale, which is suitable for mild TBI patients at the emergency department and yet still valuable for the follow-up of more severely injured TBI patients. BioMed Central 2012-08-08 /pmc/articles/PMC3447645/ /pubmed/22873279 http://dx.doi.org/10.1186/1471-2377-12-69 Text en Copyright ©2012 Jacobs et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Jacobs, Bram
van Ekert, Janneke
Vernooy, Lotje PL
Dieperink, Peter
Andriessen, Teuntje MJC
Hendriks, Marc PH
van Vugt, Arie B
Emons, Marjolein AA
Borm, George F
Vos, Pieter E
Development and external validation of a new PTA assessment scale
title Development and external validation of a new PTA assessment scale
title_full Development and external validation of a new PTA assessment scale
title_fullStr Development and external validation of a new PTA assessment scale
title_full_unstemmed Development and external validation of a new PTA assessment scale
title_short Development and external validation of a new PTA assessment scale
title_sort development and external validation of a new pta assessment scale
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3447645/
https://www.ncbi.nlm.nih.gov/pubmed/22873279
http://dx.doi.org/10.1186/1471-2377-12-69
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