首页> 外文期刊>Journal of cataract and refractive surgery >Topical cyclosporine A for postoperative photorefractive keratectomy and laser in situ keratomileusis
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Topical cyclosporine A for postoperative photorefractive keratectomy and laser in situ keratomileusis

机译:局部环孢霉素A用于术后屈光性角膜切除术和激光原位角膜磨镶术

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摘要

Purpose: To compare the stability and predictability of the refractive outcomes in eyes treated with photorefractive keratectomy (PRK) or laser in situ keratomileusis (LASIK) with and without postoperative use of topical cyclosporine A emulsion. Setting: Naval Medical Center San Diego Refractive Surgery Center, San Diego, California, USA. Design: Randomized clinical trial. Methods: Patients had PRK or LASIK and were randomized, pairwise, to a standard postoperative treatment regimen with or without the addition of topical cyclosporine A 0.05% emulsion twice daily for 3 months postoperatively. Visual acuity, mesopic contrast acuity, refractions, and ocular symptoms were assessed through the 3-month examination. Tear-film samples (cytokines and chemokines) were analyzed preoperatively and 1 week and 1 and 3 months postoperatively. Results: The PRK group comprised 70 patients and the LASIK group, 54 patients. The addition of topical cyclosporine A twice a day after PRK or LASIK did not confer special benefits in terms of achievement of target refraction, final uncorrected distance visual acuity (UDVA), or rate of visual recovery (all P>.05, multivariate analysis of variance [MANOVA]). There was no significant difference in tear-film composition based on measurement of matrix metalloproteinase-9, interleukin (IL)-6, or IL-8 recovery (all P>.05, MANOVA). Conclusion: The addition of topical cyclosporine A twice daily for 3 months after PRK or LASIK did not provide a significant benefit in the rate of visual recovery, final UDVA, or patient symptoms, nor did it significantly change measured inflammatory mediators (cytokines) present in the tear film. Financial Disclosure: No author has a financial or proprietary interest in any material or method mentioned.
机译:目的:比较接受屈光性角膜切除术(PRK)或激光原位角膜磨镶术(LASIK)以及术后是否使用局部环孢素A乳剂治疗的眼睛的屈光结果的稳定性和可预测性。地点:美国加利福尼亚州圣地亚哥,海军医学中心圣地亚哥屈光手术中心。设计:随机临床试验。方法:患有PRK或LASIK的患者,在术后3个月内,每天两次,随机分为标准的术后治疗方案,每天加两次或不加局部环孢素A 0.05%乳剂。通过3个月的检查评估视力,中视对比力,屈光度和眼部症状。术前,术后1周,术后1和3个月分析泪膜样品(细胞因子和趋化因子)。结果:PRK组包括70例患者,LASIK组为54例患者。 PRK或LASIK术后每天两次外用环孢素A不能达到目标屈光,最终未矫正的远视力(UDVA)或视力恢复率(所有P> 0.05)方差[MANOVA])。根据基质金属蛋白酶9,白介素(IL)-6或IL-8回收率的测定,泪膜组成没有显着差异(所有P> .05,MANOVA)。结论:PRK或LASIK术后3个月每天两次局部使用环孢素A不能显着改善视力恢复率,最终UDVA或患者症状,也不能显着改变患者体内测得的炎症介质(细胞因子)。泪膜。财务披露:没有任何作者对所提及的任何材料或方法有财务或专有利益。

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