Early hydroxychloroquine retinopathy: optical coherence tomography abnormalities preceding Humphrey visual field defects.


Journal

The British journal of ophthalmology
ISSN: 1468-2079
Titre abrégé: Br J Ophthalmol
Pays: England
ID NLM: 0421041

Informations de publication

Date de publication:
11 2019
Historique:
received: 09 10 2018
revised: 02 01 2019
accepted: 04 01 2019
pubmed: 2 3 2019
medline: 30 5 2020
entrez: 2 3 2019
Statut: ppublish

Résumé

Hydroxychloroquine (HCQ) retinopathy may result in severe and irreversible vision loss, emphasising the importance of screening and early detection. The purpose of this study is to report the novel finding of early optical coherence tomography (OCT) abnormalities due to HCQ toxicity that may develop in the setting of normal Humphrey visual field (HVF) testing. Data from patients with chronic HCQ exposure was obtained from seven tertiary care retina centres. Ten patients with HCQ-associated OCT abnormalities and normal HVF testing were identified. Detailed analysis of the OCT findings and ancillary tests including colour fundus photography, fundus autofluorescence, multifocal electroretinography and microperimetry was performed in these patients. Seventeen eyes from 10 patients illustrated abnormalities with OCT and normal HVF testing. These OCT alterations included (1) attenuation of the parafoveal ellipsoid zone and (2) loss of a clear continuous interdigitation zone. Several eyes progressed to advanced parafoveal outer retinal disruption and/or paracentral visual field defects. Patients with high risk HCQ exposure and normal HVF testing may develop subtle but characteristic OCT abnormalities. This novel finding indicates that, in some cases of early HCQ toxicity, structural alterations may precede functional impairment. It is therefore important to employ a screening approach that includes OCT to assess for these early findings. Ancillary testing should be considered in cases with suspicious OCT changes and normal HVFs.

Sections du résumé

BACKGROUND/AIMS
Hydroxychloroquine (HCQ) retinopathy may result in severe and irreversible vision loss, emphasising the importance of screening and early detection. The purpose of this study is to report the novel finding of early optical coherence tomography (OCT) abnormalities due to HCQ toxicity that may develop in the setting of normal Humphrey visual field (HVF) testing.
METHODS
Data from patients with chronic HCQ exposure was obtained from seven tertiary care retina centres. Ten patients with HCQ-associated OCT abnormalities and normal HVF testing were identified. Detailed analysis of the OCT findings and ancillary tests including colour fundus photography, fundus autofluorescence, multifocal electroretinography and microperimetry was performed in these patients.
RESULTS
Seventeen eyes from 10 patients illustrated abnormalities with OCT and normal HVF testing. These OCT alterations included (1) attenuation of the parafoveal ellipsoid zone and (2) loss of a clear continuous interdigitation zone. Several eyes progressed to advanced parafoveal outer retinal disruption and/or paracentral visual field defects.
CONCLUSION
Patients with high risk HCQ exposure and normal HVF testing may develop subtle but characteristic OCT abnormalities. This novel finding indicates that, in some cases of early HCQ toxicity, structural alterations may precede functional impairment. It is therefore important to employ a screening approach that includes OCT to assess for these early findings. Ancillary testing should be considered in cases with suspicious OCT changes and normal HVFs.

Identifiants

pubmed: 30819690
pii: bjophthalmol-2018-313350
doi: 10.1136/bjophthalmol-2018-313350
doi:

Substances chimiques

Antirheumatic Agents 0
Hydroxychloroquine 4QWG6N8QKH

Types de publication

Case Reports Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1600-1604

Informations de copyright

© Author(s) (or their employer(s)) 2019. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: NKW is a consultant for Optovue and receives research support from Carl Zeiss Meditec, Topcon Medical Systems and Nidek Medical Products. JSD is a consultant for and receives research support from Carl Zeiss Meditec and Optovue. EHS is a consultant for Novartis, Bayer Schering Pharma, Allergan Inc. and Farmila-Thea. KBF is a consultant to Genentech, Allergan, Optos, Optovue, Zeiss, Heidelberg Engineering and Novartis. He receives research funding from Genentech/Roche. DS is a consultant for Amgen, Bayer, Genentech, Novartis and Optovue and receives research funding from Genentech, Heidelberg, Optovue and Regeneron. All other authors have no conflict of interest to declare.

Auteurs

Sean T Garrity (ST)

New England Eye Center, Tufts Medical Center, Boston, Massachusetts, USA.

Joo Yeon Jung (JY)

David Geffen School of Medicine at UCLA, University of California Los Angeles, Stein Eye Institute, Los Angeles, California, USA.

Olivia Zambrowski (O)

Department of Ophthalmology, University Paris Est Créteil, Centre Hospitalier Intercommunal de Créteil, Créteil, France.

Francesco Pichi (F)

Cleveland Clinic Abu Dhabi Eye Institute, Abu Dhabi, United Arab Emirates.
Cleveland Clinic Lerner College of Medicine, Case Western Reserve University, Cleveland, Ohio, USA.

Daniel Su (D)

Mid Atlantic Retina, Retina Service of Wills Eye Hospital, Philadelphia, Pennsylvania, USA.

Malvika Arya (M)

New England Eye Center, Tufts Medical Center, Boston, Massachusetts, USA.

Nadia K Waheed (NK)

New England Eye Center, Tufts Medical Center, Boston, Massachusetts, USA.

Jay S Duker (JS)

New England Eye Center, Tufts Medical Center, Boston, Massachusetts, USA.

Yaïr Chetrit (Y)

Department of Ophthalmology, Assistance Publique - Hôpitaux de Paris, Pitié Salpêtrière University Hospital, Pierre et Marie Curie University Paris VI, Paris, France.

Elisabetta Miserocchi (E)

Ocular Immunology and Uveitis Service, Department of Ophthalmology, San Raffaele Scientific Institute, Milano, Italy.

Chiara Giuffrè (C)

Ocular Immunology and Uveitis Service, Department of Ophthalmology, San Raffaele Scientific Institute, Milano, Italy.

Talia R Kaden (TR)

Vitreous Retina Macula Consultants of New York, New York City, New York, USA.
LuEsther T Mertz Retinal Research Center, Manhattan Eye, Ear and Throat Hospital, New York City, New York, USA.
Department of Ophthalmology, School of Medicine, New York University, New York City, New York, USA.
Department of Ophthalmology, Manhattan Eye Ear and Throat Hospital, New York City, New York, USA.

Giuseppe Querques (G)

Department of Ophthalmology, University Vita-Salute, IRCCS Ospedale San Raffaele, Milano, Italy.

Eric H Souied (EH)

Department of Ophthalmology, University Paris Est Créteil, Centre Hospitalier Intercommunal de Créteil, Créteil, France.
Clinical Research Center and Biological Resources Center, GRC Macula, Centre Hospitalier Intercommunal de Créteil, Créteil, France.

K Bailey Freund (KB)

Vitreous Retina Macula Consultants of New York, New York City, New York, USA.
LuEsther T Mertz Retinal Research Center, Manhattan Eye, Ear and Throat Hospital, New York City, New York, USA.
Department of Ophthalmology, School of Medicine, New York University, New York City, New York, USA.

David Sarraf (D)

David Geffen School of Medicine at UCLA, University of California Los Angeles, Stein Eye Institute, Los Angeles, California, USA dsarraf@ucla.edu.
Greater Los Angeles VA Healthcare Center, Los Angeles, California, USA.

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Classifications MeSH