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Decompressive craniectomy in traumatic brain injury: usage and clinical outcome in a single centre
BACKGROUND: Two randomised controlled trials (RCTs) of decompressive craniectomy (DC) in traumatic brain injury (TBI) have shown poor outcome, but there are considerations of how these protocols relate to real practice. The aims of this study were to evaluate usage and outcome of DC and thiopental i...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Vienna
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5766728/ https://www.ncbi.nlm.nih.gov/pubmed/29234973 http://dx.doi.org/10.1007/s00701-017-3418-3 |
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author | Wettervik, Teodor Svedung Lenell, Samuel Nyholm, Lena Howells, Tim Lewén, Anders Enblad, Per |
author_facet | Wettervik, Teodor Svedung Lenell, Samuel Nyholm, Lena Howells, Tim Lewén, Anders Enblad, Per |
author_sort | Wettervik, Teodor Svedung |
collection | PubMed |
description | BACKGROUND: Two randomised controlled trials (RCTs) of decompressive craniectomy (DC) in traumatic brain injury (TBI) have shown poor outcome, but there are considerations of how these protocols relate to real practice. The aims of this study were to evaluate usage and outcome of DC and thiopental in a single centre. METHOD: The study included all TBI patients treated at the neurointensive care unit, Akademiska sjukhuset, Uppsala, Sweden, between 2008 and 2014. Of 609 patients aged 16 years or older, 35 treated with DC and 23 treated with thiopental only were studied in particular. Background variables, intracranial pressure (ICP) measures and global outcome were analysed. RESULTS: Of 35 DC patients, 9 were treated stepwise with thiopental before DC, 9 were treated stepwise with no thiopental before DC and 17 were treated primarily with DC. Six patients received thiopental after DC. For 23 patients, no DC was needed after thiopental. Eighty-eight percent of our DC patients would have qualified for the DECRA study and 38% for the Rescue-ICP trial. Favourable outcome was 44% in patients treated with thiopental before DC, 56% in patients treated with DC without prior thiopental, 29% in patients treated primarily with DC and 52% in patients treated with thiopental with no DC. CONCLUSIONS: The place for DC in TBI management must be evaluated better, and we believe it is important that future RCTs should have clearer and less permissive ICP criteria regarding when thiopental should be followed by DC and DC followed by thiopental. |
format | Online Article Text |
id | pubmed-5766728 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Springer Vienna |
record_format | MEDLINE/PubMed |
spelling | pubmed-57667282018-01-25 Decompressive craniectomy in traumatic brain injury: usage and clinical outcome in a single centre Wettervik, Teodor Svedung Lenell, Samuel Nyholm, Lena Howells, Tim Lewén, Anders Enblad, Per Acta Neurochir (Wien) Original Article - Brain Injury BACKGROUND: Two randomised controlled trials (RCTs) of decompressive craniectomy (DC) in traumatic brain injury (TBI) have shown poor outcome, but there are considerations of how these protocols relate to real practice. The aims of this study were to evaluate usage and outcome of DC and thiopental in a single centre. METHOD: The study included all TBI patients treated at the neurointensive care unit, Akademiska sjukhuset, Uppsala, Sweden, between 2008 and 2014. Of 609 patients aged 16 years or older, 35 treated with DC and 23 treated with thiopental only were studied in particular. Background variables, intracranial pressure (ICP) measures and global outcome were analysed. RESULTS: Of 35 DC patients, 9 were treated stepwise with thiopental before DC, 9 were treated stepwise with no thiopental before DC and 17 were treated primarily with DC. Six patients received thiopental after DC. For 23 patients, no DC was needed after thiopental. Eighty-eight percent of our DC patients would have qualified for the DECRA study and 38% for the Rescue-ICP trial. Favourable outcome was 44% in patients treated with thiopental before DC, 56% in patients treated with DC without prior thiopental, 29% in patients treated primarily with DC and 52% in patients treated with thiopental with no DC. CONCLUSIONS: The place for DC in TBI management must be evaluated better, and we believe it is important that future RCTs should have clearer and less permissive ICP criteria regarding when thiopental should be followed by DC and DC followed by thiopental. Springer Vienna 2017-12-12 2018 /pmc/articles/PMC5766728/ /pubmed/29234973 http://dx.doi.org/10.1007/s00701-017-3418-3 Text en © The Author(s) 2017 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Article - Brain Injury Wettervik, Teodor Svedung Lenell, Samuel Nyholm, Lena Howells, Tim Lewén, Anders Enblad, Per Decompressive craniectomy in traumatic brain injury: usage and clinical outcome in a single centre |
title | Decompressive craniectomy in traumatic brain injury: usage and clinical outcome in a single centre |
title_full | Decompressive craniectomy in traumatic brain injury: usage and clinical outcome in a single centre |
title_fullStr | Decompressive craniectomy in traumatic brain injury: usage and clinical outcome in a single centre |
title_full_unstemmed | Decompressive craniectomy in traumatic brain injury: usage and clinical outcome in a single centre |
title_short | Decompressive craniectomy in traumatic brain injury: usage and clinical outcome in a single centre |
title_sort | decompressive craniectomy in traumatic brain injury: usage and clinical outcome in a single centre |
topic | Original Article - Brain Injury |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5766728/ https://www.ncbi.nlm.nih.gov/pubmed/29234973 http://dx.doi.org/10.1007/s00701-017-3418-3 |
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