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Optical Brain Biopsy with a Fluorescence and Vessel Tracing Probe
BACKGROUND: Accurate stereotactic biopsies of brain tumors are imperative for diagnosis and tailoring of the therapy. Repetitive needle insertions enhance risks of brain lesioning, hemorrhage, and complications due to prolonged procedure. OBJECTIVE: To investigate clinical benefits of a combined 5-a...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8440062/ https://www.ncbi.nlm.nih.gov/pubmed/34192763 http://dx.doi.org/10.1093/ons/opab216 |
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author | Richter, Johan Haj-Hosseini, Neda Milos, Peter Hallbeck, Martin Wårdell, Karin |
author_facet | Richter, Johan Haj-Hosseini, Neda Milos, Peter Hallbeck, Martin Wårdell, Karin |
author_sort | Richter, Johan |
collection | PubMed |
description | BACKGROUND: Accurate stereotactic biopsies of brain tumors are imperative for diagnosis and tailoring of the therapy. Repetitive needle insertions enhance risks of brain lesioning, hemorrhage, and complications due to prolonged procedure. OBJECTIVE: To investigate clinical benefits of a combined 5-aminolaevulinic acid (5-ALA) fluorescence and laser Doppler flowmetry system for the detection of malignant brain tumor and blood vessels in stereotactic biopsies. METHODS: Planning of targets and trajectories was followed by optical measurements in 20 patients, using the Leksell Stereotactic System and a manual insertion device. Fluorescence spectra, microvascular blood flow, and tissue grayness were recorded each millimeter along the paths. Biopsies were taken at preplanned positions. The diagnoses were compared with the fluorescence signals. The recordings were plotted against measurement positions and compared. Sites indicating a risk of hemorrhage were counted as well as the time for the procedures. RESULTS: Signals were recorded along 28 trajectories, and 78 biopsies were collected. The final diagnosis showed 17 glioblastomas, 2 lymphomas, and 1 astrocytoma grade III. Fluorescence was seen along 23 of the paths with 4 having the peak of 5-ALA fluorescence 3 mm or more from the precalculated target. There was increased microcirculation in 40 of 905 measured positions. The measurement time for each trajectory was 5 to 10 min. CONCLUSION: The probe provided direct feedback of increased blood flow along the trajectory and of malignant tissue in the vicinity of the target. The method can increase the precision and the safety of the biopsy procedure and reduce time. |
format | Online Article Text |
id | pubmed-8440062 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-84400622021-09-15 Optical Brain Biopsy with a Fluorescence and Vessel Tracing Probe Richter, Johan Haj-Hosseini, Neda Milos, Peter Hallbeck, Martin Wårdell, Karin Oper Neurosurg (Hagerstown) Concepts, Innovations and Techniques BACKGROUND: Accurate stereotactic biopsies of brain tumors are imperative for diagnosis and tailoring of the therapy. Repetitive needle insertions enhance risks of brain lesioning, hemorrhage, and complications due to prolonged procedure. OBJECTIVE: To investigate clinical benefits of a combined 5-aminolaevulinic acid (5-ALA) fluorescence and laser Doppler flowmetry system for the detection of malignant brain tumor and blood vessels in stereotactic biopsies. METHODS: Planning of targets and trajectories was followed by optical measurements in 20 patients, using the Leksell Stereotactic System and a manual insertion device. Fluorescence spectra, microvascular blood flow, and tissue grayness were recorded each millimeter along the paths. Biopsies were taken at preplanned positions. The diagnoses were compared with the fluorescence signals. The recordings were plotted against measurement positions and compared. Sites indicating a risk of hemorrhage were counted as well as the time for the procedures. RESULTS: Signals were recorded along 28 trajectories, and 78 biopsies were collected. The final diagnosis showed 17 glioblastomas, 2 lymphomas, and 1 astrocytoma grade III. Fluorescence was seen along 23 of the paths with 4 having the peak of 5-ALA fluorescence 3 mm or more from the precalculated target. There was increased microcirculation in 40 of 905 measured positions. The measurement time for each trajectory was 5 to 10 min. CONCLUSION: The probe provided direct feedback of increased blood flow along the trajectory and of malignant tissue in the vicinity of the target. The method can increase the precision and the safety of the biopsy procedure and reduce time. Oxford University Press 2021-06-30 /pmc/articles/PMC8440062/ /pubmed/34192763 http://dx.doi.org/10.1093/ons/opab216 Text en © Congress of Neurological Surgeons 2021. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Concepts, Innovations and Techniques Richter, Johan Haj-Hosseini, Neda Milos, Peter Hallbeck, Martin Wårdell, Karin Optical Brain Biopsy with a Fluorescence and Vessel Tracing Probe |
title | Optical Brain Biopsy with a Fluorescence and Vessel Tracing Probe |
title_full | Optical Brain Biopsy with a Fluorescence and Vessel Tracing Probe |
title_fullStr | Optical Brain Biopsy with a Fluorescence and Vessel Tracing Probe |
title_full_unstemmed | Optical Brain Biopsy with a Fluorescence and Vessel Tracing Probe |
title_short | Optical Brain Biopsy with a Fluorescence and Vessel Tracing Probe |
title_sort | optical brain biopsy with a fluorescence and vessel tracing probe |
topic | Concepts, Innovations and Techniques |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8440062/ https://www.ncbi.nlm.nih.gov/pubmed/34192763 http://dx.doi.org/10.1093/ons/opab216 |
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