Minkus Caroline L, Pistilli Maxwell, Dreger Kurt A, Fitzgerald Tonetta D, Payal Abhishek R, Begum Hosne, Kaçmaz R Oktay, Jabs Douglas A, Nussenblatt Robert B, Rosenbaum James T, Levy-Clarke Grace A, Sen H Nida, Suhler Eric B, Thorne Jennifer E, Bhatt Nirali P, Foster C Stephen, Buchanich Jeanine M, Kempen John H
From the Department of Ophthalmology and Visual Neurosciences, University of Minnesota, Minneapolis, Minnesota; Department of Ophthalmology, Northwestern University Feinberg School of Medicine, Chicago, Illinois; Department of Ophthalmology, Massachusetts Eye and Ear Infirmary, Boston, Massachusetts; Department of Ophthalmology, Harvard Medical School, Boston, Massachusetts.
Department of Ophthalmology, the Perelman School of Medicine, the University of Pennsylvania, Philadelphia, Pennsylvania.
Am J Ophthalmol. 2021 Sep;229:200-209. doi: 10.1016/j.ajo.2021.02.032. Epub 2021 Mar 10.
To determine the incidence of and predictive factors for cataract in intermediate uveitis.
Retrospective cohort study.
Patients were identified from the Systemic Immunosuppressive Therapy for Eye Diseases Cohort Study, in which medical records were reviewed to determine demographic and clinical data of every eye/patient at every visit at 5 participating US tertiary care uveitis centers. The primary outcome was development of vision-compromising cataract as defined by a decrease in visual acuity to 20/40 or less, or requiring cataract surgery. Survival analysis assessed visually defined cataract to avoid bias due to timing of surgery vis-à-vis inflammatory status.
Among 2,190 eyes of 1,302 patients with intermediate uveitis, the cumulative incidence of cataract formation was 7.6% by 1 year (95% confidence interval [CI] = 6.2%-9.1%), increasing to 36.6% by 10 years (95% CI = 31.2%-41.6%). Increased cataract risk was observed in eyes with concurrent anterior uveitis causing posterior synechiae (hazard ratio = 2.68, 95% CI = 2.00-3.59, P < .001), and in eyes with epiretinal membrane formation (hazard ratio = 1.54, 95% CI = 1.15-2.07, P = .004). Higher dose corticosteroid therapy was associated with significantly higher incidence of cataract, especially time-updated use of topical corticosteroids ≥2 times/d or ≥4 periocular corticosteroid injections. Low-dose corticosteroid medications (oral prednisone 7.5 mg daily or less, or topical corticosteroid drops <2 times/d) were not associated with increased cataract risk.
Our study found that the incidence of clinically important cataract in intermediate uveitis is moderate. The risk is higher with markers of severity and with higher doses of corticosteroid medications, the latter being potentially modifiable.
确定中间葡萄膜炎患者白内障的发病率及预测因素。
回顾性队列研究。
从眼病全身免疫抑制治疗队列研究中识别患者,该研究对美国5个三级医疗葡萄膜炎中心的每位患者每次就诊时每只眼睛的人口统计学和临床数据进行了回顾。主要结局是视力受损性白内障的发生,定义为视力下降至20/40或更低,或需要进行白内障手术。生存分析评估视力定义的白内障,以避免因手术时间与炎症状态相关而产生的偏差。
在1302例中间葡萄膜炎患者的2190只眼中,1年时白内障形成的累积发病率为7.6%(95%置信区间[CI]=6.2%-9.1%),10年时增至36.6%(95%CI=31.2%-41.6%)。在并发前葡萄膜炎导致后粘连的眼中观察到白内障风险增加(风险比=2.68,95%CI=2.00-3.59,P<.001),以及在有视网膜前膜形成的眼中(风险比=1.54,95%CI=1.15-2.07,P=.004)。更高剂量的皮质类固醇治疗与白内障的显著更高发病率相关,尤其是每日使用局部皮质类固醇≥2次或≥4次眼周皮质类固醇注射的时间更新使用。低剂量皮质类固醇药物(口服泼尼松每日7.5mg或更少,或局部皮质类固醇滴眼液<2次/天)与白内障风险增加无关。
我们的研究发现,中间葡萄膜炎中具有临床意义的白内障发病率中等。病情严重程度指标和更高剂量的皮质类固醇药物会增加风险,后者可能是可改变的。