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Impact of brain biopsy on management of nonneoplastic brain disease()
INTRODUCTION: Diagnostic yield of brain biopsy in neoplastic brain disease is high and its clinical impact is well established. In nonneoplastic brain disease with negative conventional investigation, decision to undergo invasive procedures is difficult due to its inherent risk and known lower diagn...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9560663/ https://www.ncbi.nlm.nih.gov/pubmed/36248174 http://dx.doi.org/10.1016/j.bas.2022.100863 |
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author | Santos, Mónica Roque, Rafael Rainha Campos, Alexandre Albuquerque, Luísa Pimentel, José |
author_facet | Santos, Mónica Roque, Rafael Rainha Campos, Alexandre Albuquerque, Luísa Pimentel, José |
author_sort | Santos, Mónica |
collection | PubMed |
description | INTRODUCTION: Diagnostic yield of brain biopsy in neoplastic brain disease is high and its clinical impact is well established. In nonneoplastic brain disease with negative conventional investigation, decision to undergo invasive procedures is difficult due to its inherent risk and known lower diagnostic yield. Research question: What is the clinical impact of brain biopsy results on management of nonneoplastic brain disease ? MATERIAL AND METHODS: A multidisciplinary team retrospectively reviewed and included all nonneoplastic brain disease cases submitted to biopsy between 2009 and 2019, in a tertiary hospital in Lisbon. Baseline characteristics were registered, including immunosuppression status, diagnostic workup, and treatment prior to biopsy. Diagnostic yield, clinical impact and in-hospital complication rates were assessed. RESULTS: Sixty-four patients were included, 20 (31.3%) of them immunosuppressed (15 HIV + patients). Thirty-five (67.7%) were previously treated with steroids or antiinfectious agents, with higher percentage (93.3%) in the immunosuppressed group. Biopsy results were diagnostic in 46 (71.9%) cases. More frequent diagnosis was infectious in 20 (31.2%), neoplastic in 12 (18.8%) and inflammatory diseases in 8 (12.5%). Brain biopsy resulted on impact on patient's clinical management in 56 (87.5%), of which 37(57.8%) were submitted to treatment change. In-hospital complications were registered in 4 (6.6%) patients. DISCUSSION AND CONCLUSION: Brain biopsy had clinical impact, including a change in treatment, in most patients studied, and may be considered a useful diagnostic option in nonneoplastic brain disease. However, associated complication rate is not negligible, and previous thorough workup, patient selection and risk-benefit assessment are important. |
format | Online Article Text |
id | pubmed-9560663 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-95606632022-10-14 Impact of brain biopsy on management of nonneoplastic brain disease() Santos, Mónica Roque, Rafael Rainha Campos, Alexandre Albuquerque, Luísa Pimentel, José Brain Spine Article INTRODUCTION: Diagnostic yield of brain biopsy in neoplastic brain disease is high and its clinical impact is well established. In nonneoplastic brain disease with negative conventional investigation, decision to undergo invasive procedures is difficult due to its inherent risk and known lower diagnostic yield. Research question: What is the clinical impact of brain biopsy results on management of nonneoplastic brain disease ? MATERIAL AND METHODS: A multidisciplinary team retrospectively reviewed and included all nonneoplastic brain disease cases submitted to biopsy between 2009 and 2019, in a tertiary hospital in Lisbon. Baseline characteristics were registered, including immunosuppression status, diagnostic workup, and treatment prior to biopsy. Diagnostic yield, clinical impact and in-hospital complication rates were assessed. RESULTS: Sixty-four patients were included, 20 (31.3%) of them immunosuppressed (15 HIV + patients). Thirty-five (67.7%) were previously treated with steroids or antiinfectious agents, with higher percentage (93.3%) in the immunosuppressed group. Biopsy results were diagnostic in 46 (71.9%) cases. More frequent diagnosis was infectious in 20 (31.2%), neoplastic in 12 (18.8%) and inflammatory diseases in 8 (12.5%). Brain biopsy resulted on impact on patient's clinical management in 56 (87.5%), of which 37(57.8%) were submitted to treatment change. In-hospital complications were registered in 4 (6.6%) patients. DISCUSSION AND CONCLUSION: Brain biopsy had clinical impact, including a change in treatment, in most patients studied, and may be considered a useful diagnostic option in nonneoplastic brain disease. However, associated complication rate is not negligible, and previous thorough workup, patient selection and risk-benefit assessment are important. Elsevier 2022-01-19 /pmc/articles/PMC9560663/ /pubmed/36248174 http://dx.doi.org/10.1016/j.bas.2022.100863 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Santos, Mónica Roque, Rafael Rainha Campos, Alexandre Albuquerque, Luísa Pimentel, José Impact of brain biopsy on management of nonneoplastic brain disease() |
title | Impact of brain biopsy on management of nonneoplastic brain disease() |
title_full | Impact of brain biopsy on management of nonneoplastic brain disease() |
title_fullStr | Impact of brain biopsy on management of nonneoplastic brain disease() |
title_full_unstemmed | Impact of brain biopsy on management of nonneoplastic brain disease() |
title_short | Impact of brain biopsy on management of nonneoplastic brain disease() |
title_sort | impact of brain biopsy on management of nonneoplastic brain disease() |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9560663/ https://www.ncbi.nlm.nih.gov/pubmed/36248174 http://dx.doi.org/10.1016/j.bas.2022.100863 |
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