Evidence map›Paper›PMID 32798249›Full record

ArticleClinical & experimental ophthalmology2020

In vivo confocal microscopy and trachomatous conjunctival scarring: Predictors for clinical progression.

Jeremy J Hoffman, Patrick Massae, Helen A Weiss, William Makupa, Matthew J Burton, Victor H Hu

Open access · hybridAbstract read
In one paragraph

Article in Clinical & experimental ophthalmology, 2020. 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
0.4field-weighted citation impact, top 36% 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, 2 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

6 authors at 3 institutions in 2 countries.

Jeremy J HoffmanInternational Centre for Eye Health, London School of Hygiene and Tropical Medicine, London, UK.ORCID 0000-0001-9454-2131
Patrick MassaeDepartment of Ophthalmology, Kilimanjaro Christian Medical Centre, Moshi, Tanzania.
Helen A WeissMRC Tropical Epidemiology Group, London School of Hygiene & Tropical Medicine, London, UK.
William MakupaDepartment of Ophthalmology, Kilimanjaro Christian Medical Centre, Moshi, Tanzania.
Matthew J BurtonInternational Centre for Eye Health, London School of Hygiene and Tropical Medicine, London, UK.
Victor H HuInternational Centre for Eye Health, London School of Hygiene and Tropical Medicine, London, UK.
London School of Hygiene & Tropical Medicine · GBKilimanjaro Christian Medical Centre · TZUniversity of London · GB

Funding

Medical Research Council MR/R010161/1Wellcome Trust 080741Wellcome Trust 080741/Z/06/ZWellcome Trust 098481Wellcome Trust 098481/Z/12/ZWellcome Trust 207472
6 · The paper itself

Abstract

importanceIn vivo confocal microscopy (IVCM) provides high-resolution images of the ocular surface and has been validated in trachomatous conjunctival scarring.

backgroundThis study used IVCM to identify parameters associated with clinical scarring progression.

designProspective cohort study.

participantsA total of 800 participants in Northern Tanzania with trachomatous scarring.

methodsParticipants underwent clinical examination, photography and IVCM at baseline and 24-months. Clinical progression of scarring was defined by comparing baseline and 24-month photographs. Masked grading of IVCM images was used to identify scarring at both time points. Multivariable logistic regression was used to assess factors associated with clinical progression.

main outcome measuresRisk factors associated with clinical scarring progression.

resultsClinical and IVCM assessment of 800 participants were performed at baseline, with 617 (77.1%) seen at 24-months. Of these, 438 of 617 (71.0%) had gradable IVCM images at both time points and 342 of 438 (78.1%) of these could be graded as showing definite clinical progression or no progression on image comparison. Clinical progression was found to occur in 79 of 342 (23.1%). After adjusting for age and sex, clinical scarring progression was strongly associated with a high IVCM connective tissue organization score at both baseline (odds ratio [OR] = 1.84 for each increase in scarring category; P = .002) and 24-months (OR = 1.60; P = .02). Dendritiform cells present at 24-months were strongly associated with clinical scarring progression after adjustment (OR = 2.62; P = .03). CONCLUSIONS AND RELEVANCE: Quantitative IVCM parameters, including connective tissue organization score and the presence of dendritiform cells, are associated with disease progression and may be useful markers in trachoma and other conjunctival fibrotic diseases.

Indexed as

GonorrheaTrachomaCicatrixHumansMicroscopy, ConfocalProspective Studiesconfocal microscopyprogressionscarringtrachoma

Identifiers

PMID32798249
PMCPMC7618274
OpenAlexW2893080999

What OpenQuestion holds

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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.