Occult retinopathy following treatment of Hepatitis C with glecaprevir/pibrentasvir (Mavyret).

Doc Ophthalmol

Department of Ophthalmology and Visual Sciences, University of Illinois at Chicago, 1905 W. Taylor St, M/C 648, Chicago, IL, 60612, USA.

Published: April 2023

AI Article Synopsis

  • Medication-induced ocular toxicity can lead to unexplained visual disturbances, as seen in a case involving a 50-year-old man who experienced vision loss after starting Mavyret for Hepatitis C.
  • Despite extensive testing, including MRI and various imaging techniques, no traditional causes for the visual disturbance were identified, prompting further specialized assessments.
  • Ultimately, the findings suggested that Mavyret may cause a type of retinal toxicity that affects the visual function without visible structural damage, indicating a need for awareness around this potential side effect.

Article Abstract

Background/purpose: Medication-induced ocular toxicity is an important consideration in the differential diagnosis of unexplained visual disturbance. We present a case of visual disturbance after starting treatment with glecaprevir/pibrentasvir (Mavyret), a therapy for Hepatitis C virus approved by the FDA in 2017.

Methods: A 50-year-old male with no significant ocular history experienced bilateral visual disturbance, including visual field and acuity loss, shortly after initiating treatment with Mavyret for Hepatitis C. Examination of the anterior and posterior segments was unremarkable, and no abnormalities could be identified on multimodal imaging of the eye and brain, including MRI, SD-OCT, and fundus autofluorescence. Extensive testing for inflammatory, infectious, nutritional, and genetic etiologies for optic neuropathy and retinopathy was negative.

Results: Electrophysiology testing was pursued to narrow the broad differential diagnosis. Full-field electroretinography and multi-focal electroretinography detected deficiencies in the rod and cone visual pathways and attenuated electrophysiologic responses in the fovea. Pattern electroretinography and visually-evoked potentials demonstrated macula dysfunction. Taken together, electrophysiologic data suggested diffuse retinal dysfunction, which was most pronounced in the macula.

Conclusions: Given the temporal relationship between Mavyret administration and vision loss in our patient, and the absence of an underlying cause after extensive evaluation, we propose that Mavyret may be associated with a toxic occult retinopathy characterized by panretinal dysfunction without clinically apparent structural findings.

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Source
http://dx.doi.org/10.1007/s10633-023-09923-0DOI Listing

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