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Radiological Parameters to Predict Hemorrhagic Progression of Traumatic Contusional Brain Injury
INTRODUCTION: Traumatic intracerebral contusion is a frequent factor culminating in death and disability, and its progression relates to unfavorable outcome. We evaluated the radiological factors associated with hemorrhagic progression of contusions (HPC). MATERIALS AND METHODS: Two hundred and fort...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6454978/ https://www.ncbi.nlm.nih.gov/pubmed/31001007 http://dx.doi.org/10.4103/jnrp.jnrp_335_18 |
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author | Rehman, Lal Afzal, Ali Aziz, Hafiza Fatima Akbar, Sana Abbas, Asad Rizvi, Raza |
author_facet | Rehman, Lal Afzal, Ali Aziz, Hafiza Fatima Akbar, Sana Abbas, Asad Rizvi, Raza |
author_sort | Rehman, Lal |
collection | PubMed |
description | INTRODUCTION: Traumatic intracerebral contusion is a frequent factor culminating in death and disability, and its progression relates to unfavorable outcome. We evaluated the radiological factors associated with hemorrhagic progression of contusions (HPC). MATERIALS AND METHODS: Two hundred and forty-six patients were enrolled in this prospective cohort over a period of 1 year. Contusion volume was quantified using the “ABC/2” technique, whereas progression was considered as >30% increase in the initial volume. Univariate and multivariate statistics were used to examine the correlation between the risk factors of interest and HPC. RESULTS: HPC was seen in 110 (44.7%) patients. Binary logistic regression showed in the final adjusted model that multiplicity (relative risk [RR]: 2.24, 95% confidence limit [CL]: 1.00–5.48), bilateral lesions (RR: 2.99, 95% CL: 1.08–8.25), initial volume of contusion (RR: 4.96, 95% CL: 1.87–13.13), frontal location (RR: 1.42, 95% CL: 1.08–3.56), and presence of concomitant intracranial hematoma (extradural-RR: 3.90, 95% CL: 1.51–10.01, subdural-RR: 2.91, 95% CL: 1.26–6.69, and subarachnoid-RR: 2.27, 95% CL: 1.01–5.80) were significantly associated with HPC. The overall mortality was 18.7% and was almost equal among patients with and without HPC. Mortality was significantly associated with Glasgow Coma Scale on admission (adjusted RR: 12.386, 95% CL: 4.789–32.035) and presence of comorbid conditions (adjusted RR: 0.313, 95% CL: 0.114–0.860). CONCLUSION: Initial computed tomography scan is a good predictor of high-risk group for HPC. |
format | Online Article Text |
id | pubmed-6454978 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-64549782019-04-18 Radiological Parameters to Predict Hemorrhagic Progression of Traumatic Contusional Brain Injury Rehman, Lal Afzal, Ali Aziz, Hafiza Fatima Akbar, Sana Abbas, Asad Rizvi, Raza J Neurosci Rural Pract Original Article INTRODUCTION: Traumatic intracerebral contusion is a frequent factor culminating in death and disability, and its progression relates to unfavorable outcome. We evaluated the radiological factors associated with hemorrhagic progression of contusions (HPC). MATERIALS AND METHODS: Two hundred and forty-six patients were enrolled in this prospective cohort over a period of 1 year. Contusion volume was quantified using the “ABC/2” technique, whereas progression was considered as >30% increase in the initial volume. Univariate and multivariate statistics were used to examine the correlation between the risk factors of interest and HPC. RESULTS: HPC was seen in 110 (44.7%) patients. Binary logistic regression showed in the final adjusted model that multiplicity (relative risk [RR]: 2.24, 95% confidence limit [CL]: 1.00–5.48), bilateral lesions (RR: 2.99, 95% CL: 1.08–8.25), initial volume of contusion (RR: 4.96, 95% CL: 1.87–13.13), frontal location (RR: 1.42, 95% CL: 1.08–3.56), and presence of concomitant intracranial hematoma (extradural-RR: 3.90, 95% CL: 1.51–10.01, subdural-RR: 2.91, 95% CL: 1.26–6.69, and subarachnoid-RR: 2.27, 95% CL: 1.01–5.80) were significantly associated with HPC. The overall mortality was 18.7% and was almost equal among patients with and without HPC. Mortality was significantly associated with Glasgow Coma Scale on admission (adjusted RR: 12.386, 95% CL: 4.789–32.035) and presence of comorbid conditions (adjusted RR: 0.313, 95% CL: 0.114–0.860). CONCLUSION: Initial computed tomography scan is a good predictor of high-risk group for HPC. Wolters Kluwer - Medknow 2019 /pmc/articles/PMC6454978/ /pubmed/31001007 http://dx.doi.org/10.4103/jnrp.jnrp_335_18 Text en Copyright: © 2019 Journal of Neurosciences in Rural Practice http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Rehman, Lal Afzal, Ali Aziz, Hafiza Fatima Akbar, Sana Abbas, Asad Rizvi, Raza Radiological Parameters to Predict Hemorrhagic Progression of Traumatic Contusional Brain Injury |
title | Radiological Parameters to Predict Hemorrhagic Progression of Traumatic Contusional Brain Injury |
title_full | Radiological Parameters to Predict Hemorrhagic Progression of Traumatic Contusional Brain Injury |
title_fullStr | Radiological Parameters to Predict Hemorrhagic Progression of Traumatic Contusional Brain Injury |
title_full_unstemmed | Radiological Parameters to Predict Hemorrhagic Progression of Traumatic Contusional Brain Injury |
title_short | Radiological Parameters to Predict Hemorrhagic Progression of Traumatic Contusional Brain Injury |
title_sort | radiological parameters to predict hemorrhagic progression of traumatic contusional brain injury |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6454978/ https://www.ncbi.nlm.nih.gov/pubmed/31001007 http://dx.doi.org/10.4103/jnrp.jnrp_335_18 |
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