Evidence map›Paper›PMID 35326744›Full record

ArticleCancers2022

Pterygium and Ocular Surface Squamous Neoplasia: Optical Biopsy Using a Novel Autofluorescence Multispectral Imaging Technique.

Abbas Habibalahi, Alexandra Allende, Jesse Michael, Ayad G Anwer, Jared Campbell, Saabah B Mahbub, Chandra Bala, Minas T Coroneo, Ewa M Goldys

Abstract read
In one paragraph

Article in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

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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.

Abbas HabibalahiARC Centre of Excellence for Nanoscale Biophotonics, University of New South Wales, Sydney, NSW 2032, Australia.
Alexandra AllendeDouglass Hanly Moir Pathology, Macquarie Park, NSW 2113, Australia.
Jesse MichaelARC Centre of Excellence for Nanoscale Biophotonics, University of New South Wales, Sydney, NSW 2032, Australia.
Ayad G AnwerARC Centre of Excellence for Nanoscale Biophotonics, University of New South Wales, Sydney, NSW 2032, Australia.ORCID 0000-0002-2029-1023
Jared CampbellARC Centre of Excellence for Nanoscale Biophotonics, University of New South Wales, Sydney, NSW 2032, Australia.
Saabah B MahbubARC Centre of Excellence for Nanoscale Biophotonics, University of New South Wales, Sydney, NSW 2032, Australia.ORCID 0000-0002-3320-2499
Chandra BalaDepartment of Ophthalmology, Faculty of Medicine and Health Sciences, Macquarie University, Sydney, NSW 2109, Australia.
Minas T CoroneoDepartment of Ophthalmology, University of New South Wales at Prince of Wales Hospital, High Street, Randwick, NSW 2031, Australia.ORCID 0000-0002-3061-2011
Ewa M GoldysARC Centre of Excellence for Nanoscale Biophotonics, University of New South Wales, Sydney, NSW 2032, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this study, differentiation of pterygium vs. ocular surface squamous neoplasia based on multispectral autofluorescence imaging technique was investigated. Fifty (N = 50) patients with histopathological diagnosis of pterygium (PTG) and/or ocular surface squamous neoplasia (OSSN) were recruited. Fixed unstained biopsy specimens were imaged by multispectral microscopy. Tissue autofluorescence images were obtained with a custom-built fluorescent microscope with 59 spectral channels, each with specific excitation and emission wavelength ranges, suitable for the most abundant tissue fluorophores such as elastin, flavins, porphyrin, and lipofuscin. Images were analyzed using a new classification framework called fused-classification, designed to minimize interpatient variability, as an established support vector machine learning method. Normal, PTG, and OSSN regions were automatically detected and delineated, with accuracy evaluated against expert assessment by a specialist in OSSN pathology. Signals from spectral channels yielding signals from elastin, flavins, porphyrin, and lipofuscin were significantly different between regions classified as normal, PTG, and OSSN (p < 0.01). Differential diagnosis of PTG/OSSN and normal tissue had accuracy, sensitivity, and specificity of 88 ± 6%, 84 ± 10% and 91 ± 6%, respectively. Our automated diagnostic method generated maps of the reasonably well circumscribed normal/PTG and OSSN interface. PTG and OSSN margins identified by our automated analysis were in close agreement with the margins found in the H&E sections. Such a map can be rapidly generated on a real time basis and potentially used for intraoperative assessment.

Indexed as

autofluorescenceboundary detectionmachine learningocular surface squamous neoplasiapterygium

Identifiers

PMID35326744
PMCPMC8946656

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LicenceCC BY
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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.