Evidence map›Paper›PMID 24893592›Full record

ArticleJournal of visualized experiments : JoVE2014

Diagnosis of neoplasia in Barrett's esophagus using vital-dye enhanced fluorescence imaging.

Daniel P Perl, Neil Parikh, Shannon Chang, Paul Peng, Nadhi Thekkek, Michelle H Lee, Alexandros D Polydorides, Josephine Mitcham, Rebecca Richards-Kortum, Sharmila Anandasabapathy

Open access · bronzeAbstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.3field-weighted citation impact, top 37% of its field
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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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

10 authors at 2 institutions in 1 country.

Daniel P PerlDepartment of Gastroenterology, Icahn School of Medicine at Mount Sinai.
Neil ParikhDepartment of Gastroenterology, Icahn School of Medicine at Mount Sinai.
Shannon ChangDepartment of Gastroenterology, Icahn School of Medicine at Mount Sinai.
Paul PengDepartment of Gastroenterology, Icahn School of Medicine at Mount Sinai.
Nadhi ThekkekDepartment of Bioengineering, Rice University.
Michelle H LeeDepartment of Gastroenterology, Icahn School of Medicine at Mount Sinai.
Alexandros D PolydoridesDepartment of Pathology, Icahn School of Medicine at Mount Sinai.
Josephine MitchamDepartment of Gastroenterology, Icahn School of Medicine at Mount Sinai.
Rebecca Richards-KortumDepartment of Bioengineering, Rice University.
Sharmila AnandasabapathyDepartment of Gastroenterology, Icahn School of Medicine at Mount Sinai; sharmila.anandasabapathy@mountsinai.org.
Icahn School of Medicine at Mount Sinai · USRice University · US

Funding

Academic-Industrial Partnership to Develop & Test Esophageal Cancer Imaging ToolsR01CA140257 · NCI · RICE UNIVERSITY · PI ANANDASABAPATHY, SHARMILA, CALDER, GREGORY A · 2010 to 2014
$3.4M
NCI NIH HHS R01 CA140257NCI NIH HHS R01 CA140257-01
6 · The paper itself

Abstract

The ability to differentiate benign metaplasia in Barrett's Esophagus (BE) from neoplasia in vivo remains difficult as both tissue types can be flat and indistinguishable with white light imaging alone. As a result, a modality that highlights glandular architecture would be useful to discriminate neoplasia from benign epithelium in the distal esophagus. VFI is a novel technique that uses an exogenous topical fluorescent contrast agent to delineate high grade dysplasia and cancer from benign epithelium. Specifically, the fluorescent images provide spatial resolution of 50 to 100 μm and a field of view up to 2.5 cm, allowing endoscopists to visualize glandular morphology. Upon excitation, classic Barrett's metaplasia appears as continuous, evenly-spaced glands and an overall homogenous morphology; in contrast, neoplastic tissue appears crowded with complete obliteration of the glandular framework. Here we provide an overview of the instrumentation and enumerate the protocol of this new technique. While VFI affords a gastroenterologist with the glandular architecture of suspicious tissue, cellular dysplasia cannot be resolved with this modality. As such, one cannot morphologically distinguish Barrett's metaplasia from BE with Low-Grade Dysplasia via this imaging modality. By trading off a decrease in resolution with a greater field of view, this imaging system can be used at the very least as a red-flag imaging device to target and biopsy suspicious lesions; yet, if the accuracy measures are promising, VFI may become the standard imaging technique for the diagnosis of neoplasia (defined as either high grade dysplasia or cancer) in the distal esophagus.

Indexed as

Barrett EsophagusEsophageal NeoplasmsHumansOptical Imaging

Identifiers

PMID24893592
PMCPMC4089432
OpenAlexW2064643934

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.