Evidence map›Paper›PMID 39576825›Full record

ArticlePLoS neglected tropical diseases2024

Long-term visual outcomes and histopathologic findings after cataract surgery in Ebola virus disease survivors in the Ebola virus RNA persistence in ocular tissues and fluids (EVICT) study.

Caleb D Hartley, Lucas Kim, Tolulope Fashina, Jack Begley, John G Mattia, Matthew J Vandy, Lloyd C Harrison-Williams, Jalikatu Mustapha, Robert F Garry, John S Schieffelin and 10 more

Abstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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

What it found

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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

1 citing paper in PubMed.

  1. Review
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

20 authors.

Caleb D HartleyTruhlsen Eye Institute, Department of Ophthalmology, University of Nebraska Medical Center, Omaha, Nebraska, United States of America.ORCID https://orcid.org/0000-0002-8259-2518
Lucas KimTruhlsen Eye Institute, Department of Ophthalmology, University of Nebraska Medical Center, Omaha, Nebraska, United States of America.
Tolulope FashinaTruhlsen Eye Institute, Department of Ophthalmology, University of Nebraska Medical Center, Omaha, Nebraska, United States of America.
Jack BegleyTruhlsen Eye Institute, Department of Ophthalmology, University of Nebraska Medical Center, Omaha, Nebraska, United States of America.
John G MattiaNational Eye Programme, Ministry of Health and Sanitation, Freetown, Sierra Leone.
Matthew J VandyNational Eye Programme, Ministry of Health and Sanitation, Freetown, Sierra Leone.
Lloyd C Harrison-WilliamsNational Eye Programme, Ministry of Health and Sanitation, Freetown, Sierra Leone.
Jalikatu MustaphaNational Eye Programme, Ministry of Health and Sanitation, Freetown, Sierra Leone.
Robert F GarryTulane University School of Medicine, Tulane University, New Orleans, Louisiana, United States of America.
John S SchieffelinTulane University School of Medicine, Tulane University, New Orleans, Louisiana, United States of America.
Donald S GrantKenema Government Hospital, Lassa Hemorrhagic Fever Laboratory, Kenema, Sierra Leone.
Augustine GobaKenema Government Hospital, Lassa Hemorrhagic Fever Laboratory, Kenema, Sierra Leone.
Colleen S KraftEmory University School of Medicine, Emory University, Atlanta, Georgia, United States of America.
Brent R HayekNorth Georgia Eye Associates, Gainesville, Georgia, United States of America.
Gustavo PalaciosDepartment of Microbiology, Icahn School of Medicine at Mt. Sinai, New York, New York State, United States of America.
Jessica ShanthaFrancis I. Proctor Foundation for Ophthalmic Research, University of California San Francisco, San Francisco, California, United States of America.
Ian CrozierClinical Monitoring Research Program Directorate, Frederick National Laboratory for Cancer Research, Frederick, Maryland, United States of America.
Xiankun ZengUnited States Army Medical Research Institute of Infectious Diseases, Fort Detrick, Maryland, United States of America.
Steven YehTruhlsen Eye Institute, Department of Ophthalmology, University of Nebraska Medical Center, Omaha, Nebraska, United States of America.ORCID https://orcid.org/0000-0002-5417-7771
Ebola Virus Persistence in Ocular Tissues and Fluids (EVICT) Study Investigators

Funding

WORK ORDER 126643 B539 EXPAND IC SUITE75N91019D00024 · NIAID · LEIDOS BIOMEDICAL RESEARCH, INC. · PI BRISCOE, LYNN · 2019 to 2025
$3932.6M
Technology CoreU19AI135995 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI Laura D. Hughes · 2018 to 2026
$32.0M
Pathogenesis of Uveitis in Ebola Virus Disease SurvivorsR01EY029594 · NEI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI YEH, STEVEN · 2019 to 2023
$2.9M
Ophthalmic Disease and Laboratory Surveillance in a Viral Hemorrhagic Fever ZoneK23EY030158 · NEI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI SHANTHA, JESSICA · 2019 to 2023
$1.2M
NCI NIH HHS 75N91019D00024NEI NIH HHS K23 EY030158NEI NIH HHS R01 EY029594NIAID NIH HHS U19 AI135995
6 · The paper itself

Abstract

BACKGROUND/

objectivesEbola virus disease (EVD) survivors develop post-acute ophthalmic sequelae, including a high prevalence of uveitis that may be complicated by vision-threatening cataract. After the non-detection of Ebola virus (EBOV) RNA in sampled ocular fluid, vision impairment due to cataract can be treated safely and effectively via manual small incision cataract surgery (MSICS). However, the long-term ocular visual outcomes and assessment of ocular tissues, including for genomic RNA, have been infrequently or not reported in Western African survivors. SUBJECTS/

methodsA cohort of EVD survivors with visually significant cataract, in whom EBOV RNA was not detected by RT-PCR testing of ocular fluid sampled prior to MSICS, were followed for a year after intraocular lens replacement. Ophthalmic outcomes, including visual acuity (VA), adverse events, and follow-up examinations, were recorded. Ocular tissue specimens obtained at MSICS underwent histopathologic examination and in-situ hybridization (ISH) targeting EBOV genomic RNA.

resultsThirty-four EVD survivors underwent MSICS and were included for analysis. The median age of EVD survivors who underwent surgery at enrollment was 22.5 years (Interquartile range, IQR: 16.5-33) and the cohort was comprised of 20 females (58.8%). Median logMAR VA at preoperative baseline was 3 (IQR: 1-3) which improved to 0.4 (IQR: 0-0.6; n = 10; p = 0.002) and 0.6 (IQR: 0.18-0.78; n = 18; p < 0.0001) at 6- and 12-months following surgery, respectively. EBOV RNA was not detected in 7 cataract and capsular tissue specimens obtained at the time of MSICS.

conclusionsAfter MSICS, meaningful improvement in vision was maintained in EVD survivors at long-term follow-up. EBOV RNA was not detected in cataract and lens capsule specimens, providing additional reassurance of the low risk of EBOV RNA exposure during cataract surgery. Further study is needed to understand long-term ocular outcomes, including adverse events, in this population. AUTHOR SUMMARY: Ebola virus disease (EVD) survivors may develop several ophthalmic sequelae including uveitis and cataract that may lead to severe vision loss if left untreated. Manual small incision cataract surgery (MSICS) has been utilized to treat cataract in EVD survivors with encouraging short-term outcomes, but the long-term visual acuity outcomes and the potential for Ebola virus RNA to reside in cataract material is unknown. In this study, we reported long-term visual acuity outcomes following MSICS in a cohort of EVD survivors along with histopathology findings from materials collected during surgery. Visual acuity improved over 12-month follow-up with encouraging safety measures. Ebola virus RNA was not detected in cataract and lens capsular tissue analyzed from EVD survivors. This study provides additional assurance regarding the safety and efficacy of cataract surgery, with potential for improved vision for EVD survivors.

Indexed as

CataractCataract ExtractionEbolavirusHemorrhagic Fever, EbolaRNA, ViralSurvivorsVisual AcuityAdultCohort StudiesFemaleHumansMaleMiddle AgedUveitisYoung AdultRNA, Viral

Identifiers

PMID39576825
PMCPMC11623560

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