Visual and Anatomical Outcomes of a Single Intravitreal Dexamethasone in Diabetic Macular Edema: An 8 Year Real-World Study

Author:

Faes Livia1,Mishra Amit V.1,Lipkova Veronika2ORCID,Balaskas Konstantinos1,Quek Chrystie1ORCID,Hamilton Robin1,Held Ulrike3,Sim Dawn14,Sivaprasad Sobha1ORCID,Fu Dun Jack12

Affiliation:

1. NIHR Biomedical Research Centre, Moorfields Eye Hospital NHS Foundation Trust, UCL Institute of Ophthalmology, London EC1V 9EL, UK

2. Kings College London, London WC2R 2LS, UK

3. Epidemiology, Biostatistics and Prevention Institute, University of Zurich, 8057 Zurich, Switzerland

4. Genentech Roche, 1 DNA Way, South San Francisco, CA 940980, USA

Abstract

Importance: Diabetic macular edema (DME) is a major cause of vision loss in patients with diabetes mellitus. Intravitreal dexamethasone is a treatment option for patients unsuitable for or non-responsive to anti-angiogenic agents. Objective: To quantify visual and anatomical outcomes from an initial intravitreal dexamethasone injection over the expected 6-month period of dexamethasone release by the implant. Design and enrolment: This is a retrospective cohort study using electronic medical records of patients reviewed between 1 January 2012 and 1 April 2022. Setting: A tertiary eye-care center in London, United Kingdom; Moorfields Eye Hospital National Healthcare System Foundation Trust. Participants: The cohort comprised 418 adult patients with DME who received an initial treatment of 700 µg intravitreal dexamethasone in the study period. Of these, 240 patients met the inclusion criteria of ≥2 hospital visits following initial injection (≥1 beyond 6 months) and no previous ocular corticosteroid treatment or missing assessment at baseline. Exposure(s): Intravitreal dexamethasone implant (700 µg). Main Outcome(s) and Measure(s): Probability of a positive visual outcome, defined as ≥5 or ≥10 Early Treatment Diabetic Retinopathy Study (ETDRS)-letter gain after treatment when compared to baseline (Kaplan–Meier models). Results: From the initial intravitreal dexamethasone injection alone, we observed a >75% chance of gaining ≥5 ETDRS letters and >50% chance of gaining ≥10 ETDRS letters within 6 months. There was less than a 50% chance of sustaining either positive visual outcome beyond 4 months. Conclusions and Relevance: Most patients can be expected to have a positive visual outcome following an initial injection of dexamethasone implants that subsides within 4 months. Real-world re-treatment was observed to be delayed until after visual benefits were lost in half of the cohort. Further research will be needed to study the effects of delays in re-treatment.

Funder

Abbvie investigator-initiated-study

NIHR Biomedical Research Centre at Moorfields Eye Hospital National Health Service (NHS) Foundation Trust, the University College London Institute of Ophthalmology

Allergan

Bayer

Novartis

Roche

Boehringer Ingelheim

Optos

EyeBiotech

Biogen

Apellis

Publisher

MDPI AG

Subject

General Medicine

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