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Efficacy and tolerability of subcutaneous repository corticotropin injection in refractory ocular inflammatory diseases.

Authors :
Yavari, Negin
Ghoraba, Hashem
Or, Christopher
Thng, Zheng Xian
Mohammadi, S. Saeed
Karaca, Irmak
Mobasserian, Azadeh
Akhavanrezayat, Amir
Le, Anthony
Lyu, Xun
Khatri, Anadi
Yoo, Woong Sun
Feky, Dalia El
Than, Ngoc Trong Tuong
Elaraby, Osama
Saengsirinavin, Aim-On
Zhang, Xiaoyan
Anover, Frances Andrea
Gupta, Ankur Sudhir
Halim, Muhammad Sohail
Source :
Journal of Ophthalmic Inflammation & Infection. 10/24/2024, Vol. 14 Issue 1, p1-8. 8p.
Publication Year :
2024

Abstract

Background: Repository corticotropin injection (RCI) has been suggested to exert immunomodulatory and anti-inflammatory effects in ocular inflammation. The index retrospective study aimed to evaluate the efficacy and tolerability of subcutaneous RCI in patients with active scleritis or uveitis. Main body: Medical records of patients who were diagnosed with different types of active scleritis or uveitis and received RCI for more than six months at a tertiary eye center were reviewed. Patient characteristics including age, sex, comorbidities, clinical findings, treatment details, and adverse events were recorded. A total of 17 eyes of 17 patients were included. Median age was 43 years old and 53% of patients were male. Mean treatment duration was 25.4 ± 15.5 months. Indications for RCI therapy were scleritis (7 anterior and 1 posterior) (47.8%), panuveitis (17.4%), retinal vasculitis (17.4%), chronic/recurrent anterior uveitis (13%), and posterior uveitis (4.35%). RCI was initiated at a dose of 40 to 80 units 3 times weekly. Given the adequate control of inflammation, RCI was successfully discontinued in four patients (23.5%). Prior to RCI therapy, 14 (82.3%) patients were on oral prednisone at an average of 10 mg daily (range 2.5–40 mg), and two (11.7%) patients discontinued prednisone immediately before initiating RCI due to side effects. After six months of therapy, the prednisone dose was reduced in four (23.5%) patients to an average of 3 mg daily (range 1–5 mg) and was stopped in eight (53%) patients. Concomitant immunomodulatory therapies (IMTs) included mycophenolate mofetil (23.5%) and methotrexate (23.5%), and adalimumab (23.5%). Ten patients were on IMTs prior to using RCI, and during the course of treatment, IMT was stopped in two patients and reduced in one. Side effects included insomnia (23%), hypertension (11.7%), lower extremity edema (11.7%), hyperglycemia (11.7%), weight gain (11.7%), and infection (5.8%). Conclusion: RCI may be considered as a potential therapy with acceptable tolerability for patients with non-infectious scleritis or uveitis. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
18695760
Volume :
14
Issue :
1
Database :
Academic Search Index
Journal :
Journal of Ophthalmic Inflammation & Infection
Publication Type :
Academic Journal
Accession number :
180501698
Full Text :
https://doi.org/10.1186/s12348-024-00428-8