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العنوان
New trends in the management of non infectious uveitis
المؤلف
Mohamed Mahmoud Amin,Karim
هيئة الاعداد
باحث / Karim Mohamed Mahmoud Amin
مشرف / Hoda Mohamed Saber Naeim
مشرف / Ahmed Abd El Meguid Abd El Latif
الموضوع
General organization of immune system-
تاريخ النشر
2009 .
عدد الصفحات
189.p:
اللغة
الإنجليزية
الدرجة
ماجستير
التخصص
طب العيون
تاريخ الإجازة
1/1/2009
مكان الإجازة
جامعة عين شمس - كلية الطب - Ophthalmology
الفهرس
Only 14 pages are availabe for public view

from 190

from 190

Abstract

Uveitis is an inflammation of the uveal tract, which lines the inside of the eye behind the cornea. Much of the uvea lies between the retina and tough, outer sclera. The uveal tract has three parts: the iris, the ciliary body, and the choroid. Uveitis is categorized according to the part of the uveal tract that is affected. Anterior uveitis is an inflammation of the front part of the uveal tract; it includes inflammation of the iris (iritis) and inflammation of the iris and the ciliary body (iridocyclitis). Posterior uveitis is an inflammation of the part of the uveal tract behind the lens of the eye. It includes inflammation of the choroid (choroiditis) and inflammation of the choroid and retina (chorioretinitis). Uveitis that affects the entire uveal tract is called panuveitis or diffuse uveitis.
Many cases will resolve rapidly, but a significant number of patients develop persistent disease with inflammatory damage to ocular structures resulting in severe visual impairment. The main causes of sight loss are cystoid macular edema, cataract, and glaucoma.

Approximately 5-20% of legal blindness in developed countries is due to uveitis, and it has been estimated that uveitis accounts for 10-15% of all cases of total blindness in the USA. Acute anterior uveitis is the commonest subtype and carries the best visual outcome, with a worse visual prognosis seen in patients with posterior uveitis and panuveitis.
For many years, uveitis was considered a single disease entity; therefore, the approach to treatment varied very little. As knowledge of the disease process grew and the sophistication of immunologic and microbiologic testing increased, the fact that uveitis entails a multitude of diseases became clear. Although some diseases are local ocular immune phenomena, many of them are systemic diseases with ocular manifestations. Because the spectrum of disease pathogenesis ranges from autoimmunity to neoplasia to viruses, the practitioner of uveitis requires an understanding of internal medicine, infectious diseases, rheumatology, and immunology.
In non-infectious causes, therapy is usually aimed at dampening down the immune response with corticosteroids being the first line treatment. In sight threatening disease immunosuppressive agents as methotrexate, cyclosporine and cyclophosphamide may need to be added to improve or preserve sight.
Another new treatment modality is the use of intraocular pharmacotherapy via intravitreal injection and surgically placed implants as (Retisert) that shows a significant reduction in recurrence rate and improvement in visual acuity for approximately 3 years after implant
Autoimmune uveitis is a treatable condition that may require the use of systemic immunomodulatory medications to halt its progression. Although corticosteroids remain the primary initial treatment for patients with uveitis, use of non-corticosteroid immunomodulatory agents in selected patients with uveitis allows for improved control and decreased risk of corticosteroid-induced side effects.
Based on the increasing knowledge of the immune mechanisms that underlie autoimmune diseases, a new group of “biologicals” has been generated. These are immunologically active proteins focussing on specific cells, receptors or ligands. They target those immune responses that are involved in uveitis, either by blocking inflammatory cytokines (anti-TNF therapies such as etanercept, infliximab or adalimumab), by affecting T-helper cells (anti-IL2 receptor such as daclizumab) or suppressing the autoantigen-specific immune response by induction of mucosal tolerance (oral tolerance).
The impressive efficacy of TNFα-targeted therapies in sight-threatening, otherwise treatment-refractory uveitis is an argument in favor of expanding the role of these agents in non-infectious ocular inflammation. Introduction of these agents earlier in the course of the disease may prevent the structural damage that results in permanent visual impairment. The rapid action of anti-TNFα agents could also be utilized as a rescue therapy in acute severe relapse, particularly in patients who have contraindications to high dose corticosteroids.
Surgical management of noninfectious uveitis in the form of pars plana vitrectomy should be put into consideration in cases of posterior uveitis unresponsive to medical treatment.