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Optic nerve sonography in the diagnostic evaluation of adult brain injury

INTRODUCTION: The optic nerve sheath diameter (ONSD) may be increased in brain-injured patients, especially children, with intracranial hypertension. We investigated whether measurements of ONSD correlated with simultaneous noninvasive and invasive measurements of the intracranial pressure (ICP) in...

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Autores principales: Soldatos, Theodoros, Karakitsos, Dimitrios, Chatzimichail, Katerina, Papathanasiou, Matilda, Gouliamos, Athanasios, Karabinis, Andreas
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2481450/
https://www.ncbi.nlm.nih.gov/pubmed/18477382
http://dx.doi.org/10.1186/cc6897
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author Soldatos, Theodoros
Karakitsos, Dimitrios
Chatzimichail, Katerina
Papathanasiou, Matilda
Gouliamos, Athanasios
Karabinis, Andreas
author_facet Soldatos, Theodoros
Karakitsos, Dimitrios
Chatzimichail, Katerina
Papathanasiou, Matilda
Gouliamos, Athanasios
Karabinis, Andreas
author_sort Soldatos, Theodoros
collection PubMed
description INTRODUCTION: The optic nerve sheath diameter (ONSD) may be increased in brain-injured patients, especially children, with intracranial hypertension. We investigated whether measurements of ONSD correlated with simultaneous noninvasive and invasive measurements of the intracranial pressure (ICP) in brain-injured adults. METHODS: Seventy-six critical care patients (58 males; 47 ± 18 years old) were included in the study. Fifty patients suffered from brain injury, whereas 26 had no intracranial pathology and served as control individuals. Initially, brain-injured patients were evaluated clinically (Glasgow Coma Scale) and using a semiquantitative (I to VI) neuroimaging scale (Marshall Scale). Thereafter, the patients were divided into those with moderate (Marshall Scale = I and Glasgow Coma Scale > 8 [n = 18]) and severe (Marshall Scale = II to VI and Glasgow Coma Scale ≤8 [n = 32]) brain injury. All patients underwent noninvasive measurement of the ICP (estimated ICP) by transcranial Doppler sonography, and synchronous ONSD measurements by optic nerve sonography. Finally, invasive ICP measurement using an intraparenchymal catheter was performed in patients with severe brain injury. RESULTS: ONSD and estimated ICP were both significantly increased (6.1 ± 0.7 mm and 26.2 ± 8.7 mmHg, respectively; P < 0.0001) in patients with severe brain injury as compared with patients with moderate brain injury (4.2 ± 1.2 mm and 12.0 ± 3.6 mmHg) and compared with control individuals (3.6 ± 0.6 mm and 10.3 ± 3.1 mmHg). Furthermore, in patients with severe brain injury the ONSD measurements were strongly correlated with estimated ICP values (r = 0.80, P < 0.0001) as well as with the neuroimaging scale results (r = 0.82, P < 0.001). In the patients with severe brain injury, ONSD measurements correlated with invasive ICP values (r = 0.68, P = 0.002). The best cut-off value of ONSD for predicting elevated ICP was 5.7 mm (sensitivity = 74.1% and specificity = 100%). CONCLUSION: ONSD measurements correlate with noninvasive and invasive measurements of the ICP, and with head computed tomography scan findings in brain-injured adults. Hence, optic nerve sonography may serve as an additional diagnostic tool that could alert clinicians to the presence of elevated ICP, whenever invasive ICP evaluation is contraindicated and/or is not available. This trial is International Standard Randomised Controlled Trial Number registered (ISRCTN 91941687).
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spelling pubmed-24814502008-07-24 Optic nerve sonography in the diagnostic evaluation of adult brain injury Soldatos, Theodoros Karakitsos, Dimitrios Chatzimichail, Katerina Papathanasiou, Matilda Gouliamos, Athanasios Karabinis, Andreas Crit Care Research INTRODUCTION: The optic nerve sheath diameter (ONSD) may be increased in brain-injured patients, especially children, with intracranial hypertension. We investigated whether measurements of ONSD correlated with simultaneous noninvasive and invasive measurements of the intracranial pressure (ICP) in brain-injured adults. METHODS: Seventy-six critical care patients (58 males; 47 ± 18 years old) were included in the study. Fifty patients suffered from brain injury, whereas 26 had no intracranial pathology and served as control individuals. Initially, brain-injured patients were evaluated clinically (Glasgow Coma Scale) and using a semiquantitative (I to VI) neuroimaging scale (Marshall Scale). Thereafter, the patients were divided into those with moderate (Marshall Scale = I and Glasgow Coma Scale > 8 [n = 18]) and severe (Marshall Scale = II to VI and Glasgow Coma Scale ≤8 [n = 32]) brain injury. All patients underwent noninvasive measurement of the ICP (estimated ICP) by transcranial Doppler sonography, and synchronous ONSD measurements by optic nerve sonography. Finally, invasive ICP measurement using an intraparenchymal catheter was performed in patients with severe brain injury. RESULTS: ONSD and estimated ICP were both significantly increased (6.1 ± 0.7 mm and 26.2 ± 8.7 mmHg, respectively; P < 0.0001) in patients with severe brain injury as compared with patients with moderate brain injury (4.2 ± 1.2 mm and 12.0 ± 3.6 mmHg) and compared with control individuals (3.6 ± 0.6 mm and 10.3 ± 3.1 mmHg). Furthermore, in patients with severe brain injury the ONSD measurements were strongly correlated with estimated ICP values (r = 0.80, P < 0.0001) as well as with the neuroimaging scale results (r = 0.82, P < 0.001). In the patients with severe brain injury, ONSD measurements correlated with invasive ICP values (r = 0.68, P = 0.002). The best cut-off value of ONSD for predicting elevated ICP was 5.7 mm (sensitivity = 74.1% and specificity = 100%). CONCLUSION: ONSD measurements correlate with noninvasive and invasive measurements of the ICP, and with head computed tomography scan findings in brain-injured adults. Hence, optic nerve sonography may serve as an additional diagnostic tool that could alert clinicians to the presence of elevated ICP, whenever invasive ICP evaluation is contraindicated and/or is not available. This trial is International Standard Randomised Controlled Trial Number registered (ISRCTN 91941687). BioMed Central 2008 2008-05-13 /pmc/articles/PMC2481450/ /pubmed/18477382 http://dx.doi.org/10.1186/cc6897 Text en Copyright © 2008 Soldatos 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
Soldatos, Theodoros
Karakitsos, Dimitrios
Chatzimichail, Katerina
Papathanasiou, Matilda
Gouliamos, Athanasios
Karabinis, Andreas
Optic nerve sonography in the diagnostic evaluation of adult brain injury
title Optic nerve sonography in the diagnostic evaluation of adult brain injury
title_full Optic nerve sonography in the diagnostic evaluation of adult brain injury
title_fullStr Optic nerve sonography in the diagnostic evaluation of adult brain injury
title_full_unstemmed Optic nerve sonography in the diagnostic evaluation of adult brain injury
title_short Optic nerve sonography in the diagnostic evaluation of adult brain injury
title_sort optic nerve sonography in the diagnostic evaluation of adult brain injury
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2481450/
https://www.ncbi.nlm.nih.gov/pubmed/18477382
http://dx.doi.org/10.1186/cc6897
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