SignificanceThe 5-aminolevulinic acid (5-ALA) fluorescence technique is now widely applied for intraoperative visualization of specific central nervous system (CNS) tumors. Previous technical implementations of this technique have relied on specifically modified surgical microscopes to visualize intratumoral fluorescent protoporphyrin (PpIX). While this approach evidently allows for reliable intraoperative tumor visualization, it requires the availability of specifically modified surgical microscopes and their use even in cases where the operating neurosurgeon would prefer to use surgical loupes. Recently, a novel loupe device was introduced that is also capable of visualizing 5-ALA fluorescence.AimThe aim of this study was therefore to compare the detected PpIX concentrations between the conventional fluorescence microscope and the novel loupe device.ApproachWe used fluorescence phantoms of different PpIX concentrations for comparison between a conventional fluorescence microscope and the novel loupe device. For this purpose, we created fluorescence images using the excitation light sources of the conventional fluorescence microscope and the loupe device with both available background illumination modes (low and high). Subsequently, the minimal detectable PpIX concentrations according to each technique were determined by five independent neurosurgeons.ResultsUsing the conventional fluorescence microscope, the median minimal detectable PpIX concentration was 0.16 μg / ml (range: 0.15 to 0.17 μg / ml). By the loupe device, the median minimal detectable PpIX concentration was 0.12 μg / ml (range: 0.10 to 0.12 μg / ml) and 0.08 μg / ml (range: 0.07 to 0.08 μg / ml) for the high- and low-modes, respectively. Altogether, the minimal detectable PpIX concentrations were significantly lower using the loupe device compared to the conventional fluorescence microscope (p = 0.007).ConclusionsOur data indicate that the novel loupe device is able to visualize 5-ALA fluorescence with high sensitivity and thus might serve as a powerful tool for visualization of specific CNS tumors in the future.
The fluorescent tracer 5-aminolevulinc acid was introduced to visualize brain tumors intraoperatively, but suffers from drawbacks such as limited sensitivity for certain tumor types. Optical coherence tomography (OCT) is a non-invasive imaging modality, which has recently found its application in neuroscience by contributing label-free tissue information. We present one of the first radiomics-based analyses to capture the form and texture of glioma samples resected during fluorescence-guided surgery in a large cohort of multimodal OCT-based microscopy (OCM) imaging data. Concluding, we report encouraging results for the prediction of tumor infiltration, entity and molecular biomarkers with accuracies as high as 96%.
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