Department of Ophthalmology, Ocular Surface Center of Excellence, Bascom Palmer Eye Institute, University of Miami Miller School of Medicine, Miami, Florida.
Department of Ophthalmology, Ocular Surface Center of Excellence, Bascom Palmer Eye Institute, University of Miami Miller School of Medicine, Miami, Florida; Department Microbiology & Immunology, University of Miami Miller School of Medicine, Miami, Florida.
Am J Ophthalmol. 2018 May;189:65-70. doi: 10.1016/j.ajo.2018.02.009. Epub 2018 Feb 19.
To describe the safety and efficacy of autologous serum tears (AST) in managing ocular surface disease resistant to conventional therapy in patients with systemic autoimmune disease(s).
Retrospective, interventional case series.
Records of patients from 2009 to 2015 with systemic autoimmune disease treated with AST (20%-50%) for chronic surface disease were analyzed. Standardized measures of subjective dry eye symptoms, objective dry eye staining of the cornea, and slit-lamp findings including punctate epithelial erosion (PEE), filamentary keratopathy (FK), and corneal epithelial defects (KED) were compared during first and last visit. We attempted to standardize outcomes by creating a scale from 1 to 4 for subjective and objective components: worsening (1), no improvement (2), partial improvement (3), and complete resolution (4).
Fifty-one patients (101 eyes) were included. The mean age was 59.8 ± 13.2 years (72.5% female). Average use of AST was 14.3 ± 11.7 months. Complete objective improvement of initial slit-lamp findings was achieved in 30% and partial improvement in 55% of eyes. Presence of PEE, FK, and KED decreased from 92.1% to 52.5% (P < .001), from 22.8% to 9.9% (P = .02), and from 5% to 2% (P = .44) of the eyes, respectively. Full subjective improvement of symptoms was achieved in 34.6%, partial in 50.5%, and none in 14.9% of patients. No adverse side effects were noted during follow-up.
AST are a safe and effective adjunct therapy in improving both objective signs and subjective symptoms of ocular surface disorders associated with systemic autoimmune disease(s).
描述自体血清(AST)在治疗对常规治疗有抵抗力的系统性自身免疫性疾病患者的眼表疾病中的安全性和疗效。
回顾性、干预性病例系列研究。
分析了 2009 年至 2015 年间接受 AST(20%-50%)治疗慢性表面疾病的系统性自身免疫性疾病患者的记录。比较了首次和末次就诊时的主观干眼症状、角膜客观干眼染色、裂隙灯检查结果(包括点状上皮糜烂[PEE]、丝状角膜病变[FK]和角膜上皮缺损[KED])的标准化测量值。我们试图通过为主观和客观成分创建从 1 到 4 的量表来标准化结果:恶化(1)、无改善(2)、部分改善(3)和完全缓解(4)。
共纳入 51 例(101 只眼)患者。平均年龄为 59.8±13.2 岁(72.5%为女性)。AST 的平均使用时间为 14.3±11.7 个月。30%的眼睛初始裂隙灯检查结果完全改善,55%的眼睛部分改善。PEE、FK 和 KED 的存在率从 92.1%降至 52.5%(P<.001),从 22.8%降至 9.9%(P=.02),从 5%降至 2%(P=.44)。34.6%的患者症状完全改善,50.5%的患者症状部分改善,14.9%的患者症状无改善。在随访期间未观察到不良反应。
AST 是一种安全有效的辅助治疗方法,可改善与系统性自身免疫性疾病相关的眼表疾病的客观体征和主观症状。