So Ha-Rim, Park Hae Young Lopilly, Chung So-Hyang, Kim Hyun-Seung, Byun Yong-Soo
Department of Ophthalmology, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, 222, Banpo-daero, Seocho-gu, Seoul 06591, Korea.
J Clin Med. 2020 Dec 1;9(12):3904. doi: 10.3390/jcm9123904.
Autologous serum eyedrops (ASE) are effective in treating various ocular surface diseases, including damages induced by long-term use of preserved glaucoma eyedrops. However, there has been no study on whether ASE is effective without stopping the causative eyedrops. This retrospective observational study included 55 patients with ocular-surface diseases caused by long-term use of preserved glaucoma eyedrops: 18 patients who used ASEs for 2 months without discontinuing the use of glaucoma eyedrops (Group 1), 22 patients who used ASEs for 2 months, discontinuing the use of glaucoma eyedrops for the first month (Group 2) and 15 patients who used non-preservative artificial tears for 2 months, discontinuing the use of glaucoma eyedrops for the first month (Group 3). There were no intergroup differences in the baseline values of the Schirmer I test results, tear breakup time (TBUT), ocular surface staining (OSS) score, loss of the meibomian gland, meibum quality and ocular-surface disease index (OSDI). Group 1 showed significant differences in TBUT, OSS score and OSDI at 2 months when compared to the baseline values before treatment, while Group 2 showed significant differences in those values at both 1 and 2 months. There were no differences in any of the parameters at baseline, 1 month or 2 months in Group 3. Our result suggested that ASE is effective for treating ocular surface diseases caused by glaucoma eyedrops containing preservatives and its effects can be expected without interruption of glaucoma eyedrop treatment.
自体血清滴眼液(ASE)在治疗各种眼表疾病方面有效,包括长期使用含防腐剂的青光眼滴眼液引起的损伤。然而,尚无关于不停止使用致病滴眼液时ASE是否有效的研究。这项回顾性观察研究纳入了55例因长期使用含防腐剂的青光眼滴眼液而导致眼表疾病的患者:18例患者在不停止使用青光眼滴眼液的情况下使用ASE 2个月(第1组),22例患者使用ASE 2个月,在第一个月停止使用青光眼滴眼液(第2组),15例患者使用不含防腐剂的人工泪液2个月,在第一个月停止使用青光眼滴眼液(第3组)。在Schirmer I试验结果、泪膜破裂时间(TBUT)、眼表染色(OSS)评分、睑板腺缺失、睑脂质量和眼表疾病指数(OSDI)的基线值方面,各组之间没有差异。与治疗前的基线值相比,第1组在2个月时TBUT、OSS评分和OSDI有显著差异,而第2组在1个月和2个月时这些值均有显著差异。第3组在基线、1个月或2个月时的任何参数均无差异。我们的结果表明,ASE对治疗由含防腐剂的青光眼滴眼液引起的眼表疾病有效,并且在不中断青光眼滴眼液治疗的情况下即可预期其效果。