Intravitreal Corticosteroid Implantation in Diabetic Macular Edema: Updated European Consensus Guidance on Monitoring and Managing Intraocular Pressure.

Autor: Goñi FJ; Ophthalmology Department, Mollet Hospital, Ronda dels Pinetons 6, 08100 Mollet del Vallès, Barcelona, Spain. francisgoni@yahoo.com., Barton K; Glaucoma Service, Moorfields Eye Hospital, London, UK., Dias JA; Hospital CUF Sintra, Lisbon, Portugal., Diestelhorst M; Center for Ophthalmology, University of Cologne, Cologne, Germany., Garcia-Feijoo J; Ophthalmology Department, Complutense University, San Carlos Hospital, Madrid, Spain., Hommer A; Sanatorium Hera, Vienna, Austria., Kodjikian L; Department of Ophthalmology, Croix-Rousse University Hospital, Lyon, France.; UMR-CNRS 5510 Matéis, University Lyon 1, Villeurbane, France., Nicolò M; University Eye Clinic, DINOGMI, Ospedale Policlinico San Martino IRCCS, Genoa, Italy.
Jazyk: angličtina
Zdroj: Ophthalmology and therapy [Ophthalmol Ther] 2022 Feb; Vol. 11 (1), pp. 15-34. Date of Electronic Publication: 2022 Jan 05.
DOI: 10.1007/s40123-021-00427-1
Abstrakt: Intravitreal therapy for diabetic macular edema can, in susceptible patients, increase intraocular pressure (IOP). As uncontrolled IOP can potentially be sight threatening, monitoring is an essential component of patient management. It can be challenging for retina specialists to ensure that monitoring is rigorous enough to detect and resolve any potential problems at the earliest opportunity without it also being overburdensome for patients who have the lowest risk of developing an IOP rise. We have developed dynamic algorithms that: (1) tailor the frequency and extent of monitoring according to individual susceptibility and current IOP and (2) assist retina specialists in deciding when they should consider a referral to a glaucoma specialist. One algorithm is for patients with a relatively low susceptibility to developing an IOP rise (those whose baseline IOP is < 22 mmHg and who do not have a history of IOP events). Depending on their first post-implantation IOP check, the algorithm classifies them as: low risk if IOP remains < 22 mmHg; medium risk if IOP is 22-25 mmHg and any rise from baseline is < 10 mmHg; or high risk if IOP is > 25 mmHg or any rise from baseline is ≥ 10 mmHg. Thereafter, the algorithm guides on the frequency and extent of monitoring required in each of these groups and, if IOP rises or falls during treatment, patients may move up or down the risk groups accordingly. A different algorithm is provided for patients who are more susceptible to developing an IOP rise (those with a baseline IOP of ≥ 22 mmHg or a prior history of an IOP event). These patients need monitoring more closely so this algorithm has only medium- or high-risk classifications. These algorithms update the previous monitoring guidance by Goñi et al. (Goñi et al. in Ophthalmol Ther 5:47-61, 2016).
(© 2022. The Author(s).)
Databáze: MEDLINE
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