Characterization of serous retinal detachments in uveitis patients with optical coherence tomography

被引:11
作者
Annamieka Simmons-Rear
Steven Yeh
Brian T. Chan-Kai
Andreas K. Lauer
Christina J. Flaxel
Justine R. Smith
James T. Rosenbaum
Eric B. Suhler
机构
[1] Casey Eye Institute, Oregon Health and Science University, Portland, OR
[2] Emory Eye Center, Emory University, Atlanta, GA
[3] Cullen Eye Institute, Baylor College of Medicine, Houston, TX
[4] Veterans Affairs Medical Center, Portland, OR
关键词
Acute posterior multifocal placoid pigment epitheliopathy; Choroidal neovascularization; Hypotony maculopathy; Macular edema; OCT; Optical coherence tomography; Pars planitis; Sarcoidosis; Serous retinal detachment; Uveitis; Vogt-Koyanagi-Harada syndrome;
D O I
10.1007/s12348-012-0084-8
中图分类号
学科分类号
摘要
Objectives: To determine the prevalence of serous retinal detachments (SRD) using optical coherence tomography (OCT) in a large database of patients with uveitis from a tertiary referral setting, to describe clinical features of patients with SRD, and to ascertain retinal architectural features found in association with SRD. Main outcome measures: Prevalence of SRD in uveitis patients imaged with OCT, correlation of visual acuity with SRD, anatomic subtypes of uveitis identified, and association of SRD with various subtypes of macular edema (focal and diffuse) and retinal architectural abnormalities. Design: Retrospective, single-setting cross-sectional study of all OCTs in a digital imaging base ordered on patients from a tertiary referral uveitis clinic between July 2006 and March 2008. Results: SRD were identified in 17 of 111 uveitis patients (15 %) reviewed; bilateral SRD were found in 5 of 17 patients (29 %). Intermediate uveitis was the most common disease association (47 %), but other conditions identified included Vogt-Koyanagi-Harada syndrome, multifocal choroiditis/panuveitis, and sarcoidosis. Retinal architectural features identified in association with SRD included focal macular edema (59 %), diffuse macular edema (50 %), any intraretinal edema (77 %), both diffuse and focal macular edema (32 %), and retinal pigment epithelial alteration (27 %). Moderate or severe visual impairment, defined as visual acuity 20/50 or poorer was seen in 71 % of patients with SRD. Poorer visual acuity was correlated with increased central subfield thickness in patients with SRD (r2 = 0.41, p < 0.001). Conclusion: SRD were present in 15 % of the uveitis patients reviewed. Moderate to severe vision impairment was present in the majority of eyes (71 %) with SRD. Diffuse macular edema and focal cystoid macular edema were the OCT features most commonly associated with SRD. Intermediate and panuveitis were the most common anatomic sites of inflammation. A variety of pathogenic mechanisms, both inflammatory and non-inflammatory, may be involved in SRD in uveitis patients; identification of the precise mechanism is important for appropriate therapy. © 2012 The Author(s).
引用
收藏
页码:191 / 197
页数:6
相关论文
共 15 条
[1]  
Lardenoye C.W., van Kooij B., Rothova A., Impact of macular edema on visual acuity in uveitis, Ophthalmology, 113, pp. 1446-1449, (2006)
[2]  
Catier A., Tadayoni R., Paques M., Et al., Characterization of macular edema from various etiologies by optical coherence tomography, Am J Ophthalmol, 140, pp. 200-206, (2005)
[3]  
Markomichelakis N.N., Halkiadakis I., Pantelia E., Et al., Patterns of macular edema in patients with uveitis: qualitative and quantitative assessment using optical coherence tomography, Ophthalmology, 111, pp. 946-953, (2004)
[4]  
Sivaprasad S., Ikeji F., Xing W., Lightman S., Tomographic assessment of therapeutic response to uveitic macular oedema, Clin Exp Ophthalmol, 35, pp. 719-723, (2007)
[5]  
Tran T.H., de Smet M.D., Bodaghi B., Fardeau C., Cassoux N., Lehoang P., Uveitic macular oedema: correlation between optical coherence tomography patterns with visual acuity and fluorescein angiography, Br J Ophthalmol, 92, pp. 922-927, (2008)
[6]  
Ohno S., Minakawa R., Matsuda H., Clinical studies of Vogt-Koyanagi-Harada's disease, Jpn J Ophthalmol, 32, pp. 334-343, (1988)
[7]  
Usui Y., Goto H., Sakai J., Takeuchi M., Usui M., Rao N.A., Presumed Vogt-Koyanagi-Harada disease with unilateral ocular involvement: report of three cases, Graefes Arch Clin Exp Ophthalmol, 247, pp. 1127-1132, (2009)
[8]  
Khairallah M., Yahia S.B., Zaouali S., Jenzeri S., Attia S., Messaoud R., Acute choroidal ischemia associated with toxoplasmic retinochoroiditis, Retina, 27, pp. 947-951, (2007)
[9]  
Ozdemir H., Mudun B., Karacorlu M., Karacorlu S., Serous detachment of macula in Behcet disease, Retina, 25, pp. 361-362, (2005)
[10]  
Ducos de Lahitte G., Terrada C., Tran T.H., Et al., Maculopathy in uveitis of juvenile idiopathic arthritis: an optical coherence tomography study, Br J Ophthalmol, 92, pp. 64-69, (2008)