Evidence map›Paper›PMID 29800941›Full record

ArticleJAMA ophthalmology2018

Multimodal Imaging and Spatial Analysis of Ebola Retinal Lesions in 14 Survivors of Ebola Virus Disease.

Paul J Steptoe, Fayiah Momorie, Alimamy D Fornah, Sahr P Komba, Elizabeth Emsley, Janet T Scott, Simon P Harding, Matthew J Vandy, Foday Sahr, Nicholas A V Beare and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in JAMA ophthalmology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

14 citing papers in PubMed, 25 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 4 institutions in 2 countries.

Paul J SteptoeInstitute of Translational Medicine, University of Liverpool, Liverpool, United Kingdom.
Fayiah Momorie34 Military Hospital, Freetown, Sierra Leone.
Alimamy D Fornah34 Military Hospital, Freetown, Sierra Leone.
Sahr P Komba34 Military Hospital, Freetown, Sierra Leone.
Elizabeth EmsleySt. Paul's Eye Unit, Royal Liverpool University Hospital, Liverpool, United Kingdom.
Janet T ScottInstitute of Translational Medicine, University of Liverpool, Liverpool, United Kingdom.
Simon P HardingSt. Paul's Eye Unit, Royal Liverpool University Hospital, Liverpool, United Kingdom.
Matthew J VandyConnaught Hospital, Freetown, Sierra Leone.
Foday Sahr34 Military Hospital, Freetown, Sierra Leone.
Nicholas A V BeareSt. Paul's Eye Unit, Royal Liverpool University Hospital, Liverpool, United Kingdom.
Malcolm G SempleInstitute of Translational Medicine, University of Liverpool, Liverpool, United Kingdom.
Sierra Leone Urban Research Centre · SLHealth Protection Research Unit in Emerging and Zoonotic Infections at University of Liverpool · GBRoyal Liverpool University Hospital · GBUniversity of Liverpool · GB

Funding

Medical Research Council MC_UU_12014/8Wellcome Trust 107779
6 · The paper itself

Abstract

Importance: Differentiation between Ebola retinal lesions and other retinal pathologies in West Africa is important, and the pathogenesis of Ebola retinal disease remains poorly understood. Objective: To describe the appearance of Ebola virus disease (EVD) retinal lesions using multimodal imaging to enable inferences on potential pathogenesis. Design, Setting, and Participants: This prospective case series study was carried out at 34 Military Hospital in Freetown, Sierra Leone. Ophthalmological images were analyzed from 14 consecutively identified survivors of EVD of Sierra Leonean origin who had identified Ebola retinal lesions. Main Outcomes and Measures: Multimodal imaging findings including ultra-widefield scanning laser ophthalmoscopy, fundus autofluorescence, swept-source optical coherence tomography (OCT), Humphrey visual field analysis, and spatial analysis. Results: The 14 study participants had a mean (SD) age of 37.1 (8.8) years; 6 (43%) were women. A total of 141 Ebola retinal lesions were observed in 22 of 27 eyes (81%) of these 14 survivors on ultra-widefield imaging. Of these, 41 lesions (29.1%) were accessible to OCT imaging. Retinal lesions were predominantly nonpigmented with a pale-gray appearance. Peripapillary lesions exhibited variable curvatures in keeping with the retinal nerve fiber layer projections. All lesions respected the horizontal raphe and spared the fovea. The OCT imaging demonstrated a V-shaped hyperreflectivity of the outer nuclear layer overlying discontinuities of the ellipsoid zone and interdigitation zone in the smaller lesions. Larger lesions caused a collapse of the retinal layers and loss of retinal thickness. Lesion shapes were variable, but sharp angulations were characteristic. Perilesional areas of dark without pressure (thinned ellipsoid zone hyporeflectivity) accompanied 125 of the 141 lesions (88.7%) to varying extents. Conclusions and Relevance: We demonstrate OCT evidence of localized pathological changes at the level of the photoreceptors in small lesions among survivors of EVD with retinal lesions. The relevance of associated areas of dark without pressure remains undetermined.

Indexed as

AdultEye Infections, ViralFemaleFluorescein AngiographyHemorrhagic Fever, EbolaHumansMaleMultimodal ImagingOphthalmoscopyProspective StudiesRetinal DiseasesSierra LeoneSurvivorsTomography, Optical CoherenceVisual AcuityVisual Fields

Identifiers

PMID29800941
PMCPMC6542654
OpenAlexW2802004259

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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.