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Perihematomal diffusion restriction as a common finding in large intracerebral hemorrhages in the hyperacute phase
PURPOSE: There is growing evidence that a perihematomal area of restricted diffusion (PDR) exists in intraparenchymal hemorrhages (IPH) within 1 week of symptom onset (SO). Here, we study characteristics and the clinical impact of the PDR in patients with hyperacute (≤ 6 hours from SO) IPH by means...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5602530/ https://www.ncbi.nlm.nih.gov/pubmed/28922367 http://dx.doi.org/10.1371/journal.pone.0184518 |
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author | Schneider, Tanja Frieling, David Schroeder, Julian Regelsberger, Jan Schoen, Gerhard Fiehler, Jens Gellißen, Susanne |
author_facet | Schneider, Tanja Frieling, David Schroeder, Julian Regelsberger, Jan Schoen, Gerhard Fiehler, Jens Gellißen, Susanne |
author_sort | Schneider, Tanja |
collection | PubMed |
description | PURPOSE: There is growing evidence that a perihematomal area of restricted diffusion (PDR) exists in intraparenchymal hemorrhages (IPH) within 1 week of symptom onset (SO). Here, we study characteristics and the clinical impact of the PDR in patients with hyperacute (≤ 6 hours from SO) IPH by means of apparent diffusion coefficient (ADC). METHODS: This monocentric, retrospective study includes 83 patients with first-ever primary IPH from 09/2002-10/2015. 3D volumetric segmentation was performed for the IPH, PDR, and perihematomal edema (PHE) on fluid-attenuated inversion recovery, T2*/susceptibility weighted images, and ADC images. RESULTS: A PDR was seen in 56/83 patients (67.5%) presenting with hyperacute IPH. Multivariate logistic regression analysis revealed every 10-year increase of age (HR 1.929, 95% CI 1.047–3.552, P = .035) and male gender (HR 5.672, 95% CI 1.038–30.992, P = .045) as significant predictors of the presence of a PDR, but not IPH size, IPH location, nor National Institutes of Health Stroke Scale Score (NIHSS) at admission. We found no difference in NIHSS at discharge, hematoma removal, or mortality rate in PDR-positive patients. ADC values of the PDR show a step-wise normalization with increasing time from SO. CONCLUSIONS: Occurrence of a PDR is a common finding in supratentorial hyperacute IPH, but shows no adverse short-term clinical impact. It may represent transient oligemic and metabolic changes. |
format | Online Article Text |
id | pubmed-5602530 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-56025302017-09-22 Perihematomal diffusion restriction as a common finding in large intracerebral hemorrhages in the hyperacute phase Schneider, Tanja Frieling, David Schroeder, Julian Regelsberger, Jan Schoen, Gerhard Fiehler, Jens Gellißen, Susanne PLoS One Research Article PURPOSE: There is growing evidence that a perihematomal area of restricted diffusion (PDR) exists in intraparenchymal hemorrhages (IPH) within 1 week of symptom onset (SO). Here, we study characteristics and the clinical impact of the PDR in patients with hyperacute (≤ 6 hours from SO) IPH by means of apparent diffusion coefficient (ADC). METHODS: This monocentric, retrospective study includes 83 patients with first-ever primary IPH from 09/2002-10/2015. 3D volumetric segmentation was performed for the IPH, PDR, and perihematomal edema (PHE) on fluid-attenuated inversion recovery, T2*/susceptibility weighted images, and ADC images. RESULTS: A PDR was seen in 56/83 patients (67.5%) presenting with hyperacute IPH. Multivariate logistic regression analysis revealed every 10-year increase of age (HR 1.929, 95% CI 1.047–3.552, P = .035) and male gender (HR 5.672, 95% CI 1.038–30.992, P = .045) as significant predictors of the presence of a PDR, but not IPH size, IPH location, nor National Institutes of Health Stroke Scale Score (NIHSS) at admission. We found no difference in NIHSS at discharge, hematoma removal, or mortality rate in PDR-positive patients. ADC values of the PDR show a step-wise normalization with increasing time from SO. CONCLUSIONS: Occurrence of a PDR is a common finding in supratentorial hyperacute IPH, but shows no adverse short-term clinical impact. It may represent transient oligemic and metabolic changes. Public Library of Science 2017-09-18 /pmc/articles/PMC5602530/ /pubmed/28922367 http://dx.doi.org/10.1371/journal.pone.0184518 Text en © 2017 Schneider et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Schneider, Tanja Frieling, David Schroeder, Julian Regelsberger, Jan Schoen, Gerhard Fiehler, Jens Gellißen, Susanne Perihematomal diffusion restriction as a common finding in large intracerebral hemorrhages in the hyperacute phase |
title | Perihematomal diffusion restriction as a common finding in large intracerebral hemorrhages in the hyperacute phase |
title_full | Perihematomal diffusion restriction as a common finding in large intracerebral hemorrhages in the hyperacute phase |
title_fullStr | Perihematomal diffusion restriction as a common finding in large intracerebral hemorrhages in the hyperacute phase |
title_full_unstemmed | Perihematomal diffusion restriction as a common finding in large intracerebral hemorrhages in the hyperacute phase |
title_short | Perihematomal diffusion restriction as a common finding in large intracerebral hemorrhages in the hyperacute phase |
title_sort | perihematomal diffusion restriction as a common finding in large intracerebral hemorrhages in the hyperacute phase |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5602530/ https://www.ncbi.nlm.nih.gov/pubmed/28922367 http://dx.doi.org/10.1371/journal.pone.0184518 |
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