Abstract
Survivors of Ebola virus disease (EVD) may experience ocular sequelae. Comparison with antibody-negative individuals from the local population is required to characterize the disease. To assess features of ophthalmic disease specific to EVD. This baseline cross-sectional analysis of survivors of EVD and their close contacts was conducted within PREVAIL III, a 5-year, longitudinal cohort study. Participants who enrolled at John F. Kennedy Medical Center in Liberia, West Africa from June 2015 to March 2016 were included in this analysis. Close contacts were defined as household members or sex partners of survivors of EVD. Data were analyzed from July 2016 to July 2020. All participants, both survivors and close contacts, underwent testing of IgG antibody levels against Ebola virus surface glycoprotein. Ocular symptoms, anterior and posterior ophthalmologic examination findings, and optical coherence tomography images were compared between antibody-positive survivors and antibody-negative close contacts. A total of 564 antibody-positive survivors (320 [56.7%] female; mean [SD] age, 30.3 [14.0] years) and 635 antibody-negative close contacts (347 [54.6%] female; mean [SD] age, 25.8 [15.5] years) were enrolled in this study. Survivors were more likely to demonstrate color vision deficit (28.9% vs 19.0%, odds ratio [OR], 1.6; 95% CI, 1.2-2.1) and lower intraocular pressure (12.4 vs 13.5 mm Hg; mean difference, -1.2 mm Hg; 95% CI, -1.6 to -0.8 mm Hg) compared with close contacts. Dilated fundus examination revealed a higher percentage of vitreous cells (7.8% vs 0.5%; OR, 16.6; 95% CI, 5.0-55.2) and macular scars (4.6% vs 1.6%; OR, 2.8; 95% CI, 1.4-5.5) in survivors than in close contacts. Uveitis was present in 26.4% of survivors and 12.1% of close contacts (OR, 2.4; 95% CI, 1.8-3.2). Among all participants with uveitis, survivors were more likely than close contacts to have intermediate uveitis (34.2% vs 6.5% of all cases; OR, 7.8; 95% CI, 3.1-19.7) and had thicker mean central subfield thickness on optical coherence tomography (222 vs 212 μm; mean difference, 14.4 μm; 95% CI, 1.9-26.9 μm). In this cross-sectional study, survivors of EVD had a distinct spectrum of ocular and neuro-ophthalmologic findings compared with close contacts that potentially require medical and surgical treatment.
Highlights
Zaire ebolavirus is a negative, single-stranded RNA virus associated with high rates of morbidity and mortality in infected humans
Dilated fundus examination revealed a higher percentage of vitreous cells (7.8% vs 0.5%; odds ratios (ORs), 16.6; 95% CI, 5.0-55.2) and macular scars (4.6% vs 1.6%; OR, 2.8; 95% CI, 1.4-5.5) in survivors than in close contacts
Uveitis was present in 26.4% of survivors and 12.1% of close contacts (OR, 2.4; 95% CI, 1.8-3.2)
Summary
Zaire ebolavirus is a negative, single-stranded RNA virus associated with high rates of morbidity and mortality in infected humans. Ocular symptoms can occur as part of the initial presentation of EVD or after resolution of the systemic illness.[2] Of 4 survivors with uveitis reported from the 1995 epidemic in Zaire ( named Democratic Republic of the Congo), all ocular symptoms occurred more than 40 days after onset of EVD symptoms, with the latest occurring 72 days after EVD onset.[3] In a patient with uveitis occurring after systemic convalescence during the West Africa epidemic, viable Ebola virus was detected in the aqueous humor 9 weeks after viremia resolved.[4] Polymerase chain reaction testing of tear samples has detected virus during active infection but not at 3 months.[4] To date, viral RNA has not been identified in samples of aqueous humor obtained from survivors undergoing cataract surgery more than 1 year after infection,[5] data are limited because eyes without inflammation are preferentially selected for surgery
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