Gilger Brian C, Stoppini Riccardo, Wilkie David A, Clode Alison B, Pinto Nelson H, Hempstead Julie, Gerding Joseph, Salmon Jacklyn H
Department of Clinical Sciences, North Carolina State University, 1060 William Moore Drive, Raleigh, NC, 27607, USA.
Vet Ophthalmol. 2014 Jul;17 Suppl 1:23-30. doi: 10.1111/vop.12087. Epub 2013 Aug 1.
To describe the use of episcleral silicone matrix cyclosporine (ESMC) drug delivery devices in horses with immune-mediated keratitis (IMMK) with evaluation of tolerability and efficacy in long-term control of inflammation.
Retrospective study. ESMC implants (1.2 cm length, 30% wt/wt cyclosporine (CsA) in silicone; with approximately 2 μg/day steady-state release for at least 400 days) were used.
Nineteen horses (20 eyes) received two or more ESMC implants for superficial stromal (n = 9), midstromal (n = 3), or endothelial (n = 5) IMMK. Three additional horses received two or more ESMC implants for pigmentary keratouveitis (PK). Nine eyes of eight horses with superficial and five eyes of five horses with endothelial IMMK were well controlled after placement of ESMC implants (mean follow-up 176.8 and 207.2 days, respectively). Horses with midstromal IMMK and PK were not controlled with ESMC implants alone, but instead required frequent use of other medications or surgery to control the disease. The mean duration of disease prior to ESMC implantation of horses with midstromal IMMK was 495 ± 203.9 days, compared with 121.6 ± 92.7 days with superficial IMMK. ESMC implants were well tolerated by all horses without documented loss of the device.
Results from this preliminary retrospective study suggest that the ESMC implants were well tolerated and associated with treatment success with superficial and endothelial IMMK, especially if placed early in the disease process. Further study is needed to determine the duration of efficacy, number of implants required, and better therapies for chronic midstromal IMMK and pigmentary keratouveitis.
描述巩膜上硅胶基质环孢素(ESMC)给药装置在免疫介导性角膜炎(IMMK)马匹中的应用,并评估其在长期控制炎症方面的耐受性和疗效。
回顾性研究。使用ESMC植入物(长度1.2厘米,硅胶中含30%重量/重量的环孢素(CsA);稳态释放量约为每天2微克,至少持续400天)。
19匹马(20只眼)接受了两个或更多ESMC植入物,用于浅表基质性(n = 9)、基质中层(n = 3)或内皮性(n = 5)IMMK。另外3匹马接受了两个或更多ESMC植入物用于色素性角膜葡萄膜炎(PK)。8匹患有浅表IMMK的马的9只眼和5匹患有内皮性IMMK的马的5只眼在植入ESMC植入物后得到了良好控制(平均随访时间分别为176.8天和207.2天)。基质中层IMMK和PK的马匹仅使用ESMC植入物无法得到控制,而是需要频繁使用其他药物或手术来控制疾病。基质中层IMMK马匹在植入ESMC之前的平均病程为495 ± 203.9天,而浅表IMMK马匹为121.6 ± 92.7天。所有马匹对ESMC植入物耐受性良好,未记录到装置丢失情况。
这项初步回顾性研究的结果表明,ESMC植入物耐受性良好,与浅表和内皮性IMMK的治疗成功相关,尤其是在疾病过程早期植入时。需要进一步研究来确定疗效持续时间、所需植入物数量以及针对慢性基质中层IMMK和色素性角膜葡萄膜炎的更好治疗方法。