Evidence map›Paper›PMID 31792293›Full record

ArticleScientific reports2019

Fluorescence imaging reversion using spatially variant deconvolution.

Maria Anastasopoulou, Dimitris Gorpas, Maximilian Koch, Evangelos Liapis, Sarah Glasl, Uwe Klemm, Angelos Karlas, Tobias Lasser, Vasilis Ntziachristos

Abstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Maria AnastasopoulouChair of Biological Imaging and TranslaTUM, Technical University Munich, Munich, 81675, Germany.
Dimitris GorpasChair of Biological Imaging and TranslaTUM, Technical University Munich, Munich, 81675, Germany.ORCID http://orcid.org/0000-0001-9576-8087
Maximilian KochChair of Biological Imaging and TranslaTUM, Technical University Munich, Munich, 81675, Germany.
Evangelos LiapisChair of Biological Imaging and TranslaTUM, Technical University Munich, Munich, 81675, Germany.
Sarah GlaslInstitute of Biological and Medical Imaging, Helmholtz Zentrum München, Neuherberg, 85764, Germany.
Uwe KlemmInstitute of Biological and Medical Imaging, Helmholtz Zentrum München, Neuherberg, 85764, Germany.
Angelos KarlasChair of Biological Imaging and TranslaTUM, Technical University Munich, Munich, 81675, Germany.
Tobias LasserComputer Aided Medical Procedures, Technical University Munich, Garching, 85748, Germany.ORCID http://orcid.org/0000-0001-5669-920X
Vasilis NtziachristosChair of Biological Imaging and TranslaTUM, Technical University Munich, Munich, 81675, Germany. v.ntziachristos@tum.de.ORCID http://orcid.org/0000-0002-9988-0233

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fluorescence imaging opens new possibilities for intraoperative guidance and early cancer detection, in particular when using agents that target specific disease features. Nevertheless, photon scattering in tissue degrades image quality and leads to ambiguity in fluorescence image interpretation and challenges clinical translation. We introduce the concept of capturing the spatially-dependent impulse response of an image and investigate Spatially Adaptive Impulse Response Correction (SAIRC), a method that is proposed for improving the accuracy and sensitivity achieved. Unlike classical methods that presume a homogeneous spatial distribution of optical properties in tissue, SAIRC explicitly measures the optical heterogeneity in tissues. This information allows, for the first time, the application of spatially-dependent deconvolution to correct the fluorescence images captured in relation to their modification by photon scatter. Using experimental measurements from phantoms and animals, we investigate the improvement in resolution and quantification over non-corrected images. We discuss how the proposed method is essential for maximizing the performance of fluorescence molecular imaging in the clinic.

Identifiers

PMID31792293
PMCPMC6889134

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.