| Literature DB >> 32328757 |
Jean-François Korobelnik1,2, Anat Loewenstein3, Bora Eldem4, Antonia M Joussen5, Adrian Koh6, George N Lambrou7, Paolo Lanzetta8,9,10, Xiaoxin Li11, Monica Lövestam-Adrian12, Rafael Navarro13, Annabelle A Okada14, Ian Pearce15, Francisco J Rodríguez16, David T Wong17, Lihteh Wu18.
Abstract
PURPOSE: There is an urgent need to address how to best provide ophthalmic care for patients with retinal disease receiving intravitreal injections with anti-vascular endothelial growth factor agents during the ongoing global COVID-19 pandemic. This article provides guidance for ophthalmologists on how to deliver the best possible care for patients while minimizing the risk of infection.Entities:
Keywords: COVID-19; Coronavirus; Ophthalmology; Recommendations; Retinal disease; Vision Academy
Mesh:
Substances:
Year: 2020 PMID: 32328757 PMCID: PMC7179379 DOI: 10.1007/s00417-020-04703-x
Source DB: PubMed Journal: Graefes Arch Clin Exp Ophthalmol ISSN: 0721-832X Impact factor: 3.117
The Royal College of Ophthalmologists’ medical retinal management plans during COVID-19 [7]
| For patients already under review by the hospital eye service | For new patients |
|---|---|
| Wet AMD: Maintain all patients on 8 weekly anti-VEGF therapy with no clinic review unless they mention a significant drop in vision at their injection visit. Such patients may need OCT and visual acuity assessments and management changed, if deemed appropriate | Wet AMD: Diagnosis confirmed with OCT and OCT-A, if available. Confirmed new wet AMD cases should be treated with a loading phase of 3 injections of anti-VEGF and then continued on 8 weekly with no clinic review. Consent is taken on the day of first injection |
| DME: Defer anti-VEGF injections and review in clinic after 4 months. Exceptions are eyes with severe NPDR and active PDR that may require anti-VEGF agents and PRP. Virtual review with OCT and wide-field color photography is the preferred option to review these patients | DME: Defer treatment for 6 months unless associated with R3. R3 patients should be treated with PRP |
| BRVO: Defer review in clinic by 4 months | BRVO: Defer review in clinic by 4 months |
| CRVO: For patients with macular edema due to CRVO who have had at least 6 injections, consider PRP if required. Otherwise, review in clinic in 4 months | CRVO: Provide 6 mandated loading phases if visual impairment due to macular edema and then review in clinic. If, in the opinion of the clinician, there is no hope of visual improvement, an alternative approach is an extensive PRP laser to reduce the risk of rubeotic glaucoma. However, visual outcomes are likely to be poorer with this approach |
Cited with permission from the Royal College of Ophthalmologists (RCOphth). The RCOphth COVID-19 team have prepared guidance as a temporary response to the clinical management of patients during the ongoing COVID-19 pandemic and in parallel with Public Health England COVID-19 guidance. These publications are not meant to substitute patient care under normal circumstances. RCOphth clinical guidelines are to be used for the standard long-term care of patients
These considerations are for the UK only and may not be valid for other countries
AMD age-related macular degeneration, BRVO branch retinal vein occlusion, CRVO central retinal vein occlusion, DME diabetic macular edema, NPDR non-proliferative diabetic retinopathy, OCT optical coherence tomography, OCT-A optical coherence tomography angiography, PDR proliferative diabetic retinopathy, PRP panretinal photocoagulation, VEGF vascular endothelial growth factor
Fig. 1Example of a slit lamp set-up equipped with a protective shield (image courtesy of Professor Anat Loewenstein)