RETINAL VASCULITIS OR VASCULAR OCCLUSION AFTER BROLUCIZUMAB FOR NEOVASCULAR AGE-RELATED MACULAR DEGENERATION

Author:

Wykoff Charles C.1ORCID,Matsumoto Hidetaka2,Barakat Mark R.3,Karcher Helene4,Lozama Anthony5,Mayhook Andrew6,Oshagbemi Olorunfemi A.4,Zorina Olessia4,Hassan Tarek S.7,Khanani Arshad M.8,Heier Jeffrey S.9

Affiliation:

1. Retina Consultants of Texas, Houston and Blanton Eye Institute, Houston Methodist Hospital, Houston, Texas

2. Department of Ophthalmology, Gunma University Graduate School of Medicine, Gunma, Japan;

3. Retinal Consultants of Arizona, Phoenix and University of Arizona College of Medicine, Phoenix, Arizona

4. Novartis Pharma AG, Basel, Switzerland;

5. Novartis Pharmaceuticals Corporation, Minneapolis, Minnesota

6. Oxford PharmaGenesis, Oxford, UK;

7. Associated Retinal Consultants P.C., Royal Oak and Oakland University William Beaumont School of Medicine, Royal Oak, Michigan

8. Sierra Eye Associates, Reno and University of Nevada, Reno School of Medicine, Reno, Nevada

9. Ophthalmic Consultants of Boston, Boston, Massachusetts

Abstract

Purpose: Retinal vasculitis or vascular occlusion (RV/RO) have been reported after brolucizumab for neovascular age-related macular degeneration. This systematic literature review evaluated RV/RO events after brolucizumab in real-world practice. Methods: Systematic literature searches identified 89 publications; 19 were included. Results: Publications described 63 patients (70 eyes) with an RV/RO event following brolucizumab. Mean age was 77.6 years and 77.8% of patients were women; 32 eyes (45.7%) received one brolucizumab injection before RV/RO. Mean (range) time to event from last brolucizumab injection was 19.4 (0–63) days, with 87.5% of events occurring within 30 days. Among eyes with preevent and postevent visual acuity (VA) assessments, 22/42 eyes (52.4%) showed unchanged (±0.08 logMAR) or improved vision from last recorded preevent assessment at latest follow-up, whereas 15/42 eyes (35.7%) showed ≥0.30 logMAR (≥15 letters) VA reduction. Patients with no VA loss were on average slightly younger and had a higher proportion of nonocclusive events. Conclusion: Most RV/RO events reported after brolucizumab in early real-world practice occurred in women. Among eyes with VA measurements, approximately half experienced VA loss; overall, about one-third had VA reduction of ≥0.30 logMAR at latest follow-up, with indications of regional variations.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Ophthalmology,General Medicine

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