lntravitreal glucocorticoids in posterior retina conditions
Rodríguez B, Pichon-Riviere A, Augustovski F, García Martí S, Alcaraz A, Bardach A, Ciapponi A, López A, Rey-Ares L
Record ID 32016001108
Spanish
Authors' objectives:
To assess the available evidence on the efficacy, safety and coverage policy related aspects regarding the use of intravitreal glucocorticoids in patients with conditions of the posterior retina.
Authors' recommendations:
Evidence of moderate quality suggests that the use of intravitreal glucocorticoids might be similarly effective, and in some cases, less effective than the antiangiogenic therapy (aflibercept, bevacizumab, ranibizumab) or laser in diabetic macular edema and retinal vein occlusion and systemic therapy in non-infectious uveitis. Its use is also associated to a higher risk of cataract and increase in ocular hypertension. Its main advantage would be fewer injections. That is why clinical practice guidelines and coverage policies usually consider its use only as an option for patients with diabetic macular edema, retinal vein occlusion or non-infectious uveitis refractory to other therapies or when other therapies cannot be used. The United States health sponsors surveyed consider the use of dexamethasone implant or fluocinolone implant in compliance with certain requirement. In contrast, Australian government does not cover it.
Details
Project Status:
Completed
Year Published:
2016
URL for published report:
www.iecs.org.ar/home-ets/
English language abstract:
An English language summary is available
Publication Type:
Not Assigned
Country:
Argentina
MeSH Terms
- Intravitreal Injections
- Fundus Oculi
- Glucocorticoids
- Vitreous Body
- Drug Implants
Contact
Organisation Name:
Institute for Clinical Effectiveness and Health Policy
Contact Address:
Dr. Emilio Ravignani 2024, Buenos Aires - Argentina, C1414 CABA
Contact Name:
info@iecs.org.ar
Contact Email:
info@iecs.org.ar
Copyright:
<p>Institute for Clinical Effectiveness and Health Policy (IECS)</p>
This is a bibliographic record of a published health technology assessment from a member of INAHTA or other HTA producer. No evaluation of the quality of this assessment has been made for the HTA database.