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Optimization of magnetic resonance imaging protocol for the diagnosis of transient global amnesia

OBJECTIVE: To emphasize the most appropriate magnetic resonance imaging (MRI) diffusion protocol for the detection of lesions that cause transient global amnesia, in order to perform an accurate examination, as well as to determine the ideal time point after the onset of symptoms to perform the exam...

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Autores principales: de Abreu Junior, Luiz, de Godoy, Laiz Laura, Vaz, Luciana Pinheiro dos Santos, Torres, André Evangelista, Wolosker, Angela Maria Borri, Torres, Ulysses Santos, Borri, Maria Lucia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Colégio Brasileiro de Radiologia e Diagnóstico por Imagem 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6561356/
https://www.ncbi.nlm.nih.gov/pubmed/31210688
http://dx.doi.org/10.1590/0100-3984.2018.0028
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author de Abreu Junior, Luiz
de Godoy, Laiz Laura
Vaz, Luciana Pinheiro dos Santos
Torres, André Evangelista
Wolosker, Angela Maria Borri
Torres, Ulysses Santos
Borri, Maria Lucia
author_facet de Abreu Junior, Luiz
de Godoy, Laiz Laura
Vaz, Luciana Pinheiro dos Santos
Torres, André Evangelista
Wolosker, Angela Maria Borri
Torres, Ulysses Santos
Borri, Maria Lucia
author_sort de Abreu Junior, Luiz
collection PubMed
description OBJECTIVE: To emphasize the most appropriate magnetic resonance imaging (MRI) diffusion protocol for the detection of lesions that cause transient global amnesia, in order to perform an accurate examination, as well as to determine the ideal time point after the onset of symptoms to perform the examination. MATERIALS AND METHODS: We evaluated five patients with a diagnosis of transient global amnesia treated between 2012 and 2015. We analyzed demographic characteristics, clinical data, symptom onset, diffusion techniques, and radiological findings. Examination techniques included a standard diffusion sequence (b value = 1000 s/mm(2); slice thickness = 5 mm) and a optimized diffusion sequence (b value = 2000 s/mm(2); slice thickness = 3 mm). RESULTS: Brain MRI was performed at 24 h or 36 h after symptom onset, except in one patient, in whom it was performed at 12 h after (at which point no changes were seen) and repeated at 36 h after symptom onset (at which point it showed alterations in the right hippocampus). The standard and optimized diffusion sequences were both able to demonstrate focal changes in the hippocampi in all of the patients but one, in whom the changes were demonstrated only in the optimized sequence. CONCLUSION: MRI can confirm a clinical hypothesis of transient global amnesia. Knowledge of the optimal diffusion parameters and the ideal timing of diffusion-weighted imaging (> 24 h after symptom onset) are essential to improving diagnostic efficiency.
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spelling pubmed-65613562019-06-17 Optimization of magnetic resonance imaging protocol for the diagnosis of transient global amnesia de Abreu Junior, Luiz de Godoy, Laiz Laura Vaz, Luciana Pinheiro dos Santos Torres, André Evangelista Wolosker, Angela Maria Borri Torres, Ulysses Santos Borri, Maria Lucia Radiol Bras Original Articles OBJECTIVE: To emphasize the most appropriate magnetic resonance imaging (MRI) diffusion protocol for the detection of lesions that cause transient global amnesia, in order to perform an accurate examination, as well as to determine the ideal time point after the onset of symptoms to perform the examination. MATERIALS AND METHODS: We evaluated five patients with a diagnosis of transient global amnesia treated between 2012 and 2015. We analyzed demographic characteristics, clinical data, symptom onset, diffusion techniques, and radiological findings. Examination techniques included a standard diffusion sequence (b value = 1000 s/mm(2); slice thickness = 5 mm) and a optimized diffusion sequence (b value = 2000 s/mm(2); slice thickness = 3 mm). RESULTS: Brain MRI was performed at 24 h or 36 h after symptom onset, except in one patient, in whom it was performed at 12 h after (at which point no changes were seen) and repeated at 36 h after symptom onset (at which point it showed alterations in the right hippocampus). The standard and optimized diffusion sequences were both able to demonstrate focal changes in the hippocampi in all of the patients but one, in whom the changes were demonstrated only in the optimized sequence. CONCLUSION: MRI can confirm a clinical hypothesis of transient global amnesia. Knowledge of the optimal diffusion parameters and the ideal timing of diffusion-weighted imaging (> 24 h after symptom onset) are essential to improving diagnostic efficiency. Colégio Brasileiro de Radiologia e Diagnóstico por Imagem 2019 /pmc/articles/PMC6561356/ /pubmed/31210688 http://dx.doi.org/10.1590/0100-3984.2018.0028 Text en http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
de Abreu Junior, Luiz
de Godoy, Laiz Laura
Vaz, Luciana Pinheiro dos Santos
Torres, André Evangelista
Wolosker, Angela Maria Borri
Torres, Ulysses Santos
Borri, Maria Lucia
Optimization of magnetic resonance imaging protocol for the diagnosis of transient global amnesia
title Optimization of magnetic resonance imaging protocol for the diagnosis of transient global amnesia
title_full Optimization of magnetic resonance imaging protocol for the diagnosis of transient global amnesia
title_fullStr Optimization of magnetic resonance imaging protocol for the diagnosis of transient global amnesia
title_full_unstemmed Optimization of magnetic resonance imaging protocol for the diagnosis of transient global amnesia
title_short Optimization of magnetic resonance imaging protocol for the diagnosis of transient global amnesia
title_sort optimization of magnetic resonance imaging protocol for the diagnosis of transient global amnesia
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6561356/
https://www.ncbi.nlm.nih.gov/pubmed/31210688
http://dx.doi.org/10.1590/0100-3984.2018.0028
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