The Safety and Efficacy of Noncorticosteroid Triple Immunosuppressive Therapy in the Treatment of Refractory Chronic Noninfectious Uveitis in Childhood

2013 ◽  
Vol 41 (1) ◽  
pp. 136-139 ◽  
Author(s):  
Jessica A. Little ◽  
Ethan S. Sen ◽  
Helen Strike ◽  
Annie Hinchcliffe ◽  
Catherine M. Guly ◽  
...  

Objective.To assess the safety and efficacy of noncorticosteroid triple immunosuppressive therapy in the treatment of refractory chronic noninfectious childhood uveitis.Methods.Subjects were retrospectively selected from a database. Patients were included if they were diagnosed with chronic, noninfectious uveitis at 16 years of age or under and treated with triple immunosuppressive therapy for at least 6 months (following failure of a combination of 2 immunosuppressants). Patient demographics, diagnoses, duration of uveitis, drug dosages, active joint inflammation, and ophthalmologic data were recorded. Efficacy outcomes for triple therapy were recorded at 6 months.Results.Thirteen patients with bilateral uveitis were included. Using Standardized Uveitis Nomenclature (SUN) criteria, at 6 months only 11 eyes (42%) had a 2-step improvement in anterior chamber cell inflammation (n = 26). In addition, 2 patients required additional oral corticosteroid treatment. There were 4 significant infectious adverse events during a total of 21.9 patient-years (PY) on triple therapy (0.18 events per PY).Conclusion.In this group of children with refractory uveitis, addition of a third immunosuppressive agent did not confer substantial benefit in redressing ocular inflammation and was associated with significant infections in a minority of patients.

Pharmaceutics ◽  
2019 ◽  
Vol 11 (8) ◽  
pp. 413 ◽  
Author(s):  
Hsiu-Chao Lin ◽  
Madonna Rica Anggelia ◽  
Chih-Chi Cheng ◽  
Kuan-Lin Ku ◽  
Hui-Yun Cheng ◽  
...  

Tacrolimus is an immunosuppressive agent for acute rejection after allotransplantation. However, the low aqueous solubility of tacrolimus poses difficulties in formulating an injection dosage. Polypeptide thermosensitive hydrogels can maintain a sustained release depot to deliver tacrolimus. The copolymers, which consist of poloxamer and poly(l-alanine) with l-lysine segments at both ends (P–Lys–Ala–PLX), are able to carry tacrolimus in an in situ gelled form with acceptable biocompatibility, biodegradability, and low gelling concentrations from 3 to 7 wt %. By adding Pluronic F-127 to formulate a mixed hydrogel system, the drug release rate can be adjusted to maintain suitable drug levels in animals with transplants. Under this formulation, the in vitro release of tacrolimus was stable for more than 100 days, while in vivo release of tacrolimus in mouse model showed that rejection from skin allotransplantation was prevented for at least three weeks with one single administration. Using these mixed hydrogel systems for sustaining delivery of tacrolimus demonstrates advancement in immunosuppressive therapy.


2018 ◽  
Vol 28 (11) ◽  
pp. 1375-1377 ◽  
Author(s):  
Ali Orgun ◽  
Hazım A. Gursu ◽  
Ibrahim I. Cetin

AbstractSteroids are used in the treatment of acute rheumatic fever with moderate-to-severe carditis. Corticosteroids have several cardiovascular side affects that are more common in adults than in children. Corticosteroid-related bradycardia is a rarely seen side effect. Children with bradycardia following oral corticosteroid use are rarely reported previously. We present a child who developed bradycardia after oral corticosteroid treatment and concurrent Wolff–Parkinson–White pattern.


BMJ ◽  
1969 ◽  
Vol 4 (5676) ◽  
pp. 138-141 ◽  
Author(s):  
T. Lehner ◽  
C. Lyne

2015 ◽  
Vol 54 (2) ◽  
pp. 119-126 ◽  
Author(s):  
Chisa Kondo ◽  
Masanori Atsukawa ◽  
Akihito Tsubota ◽  
Noritomo Shimada ◽  
Hiroshi Abe ◽  
...  

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