Hafezi Farhad, Hosny Mohammed, Shetty Rohit, Knyazer Boris, Chen Shihao, Wang Qinmei, Hashemi Hassan, Torres-Netto Emilio A
Center for Applied Biotechnology and Molecular Medicine (CABMM), University of Zurich, Zurich, Switzerland.
ELZA Institute, Dietikon, Switzerland.
Eye Vis (Lond). 2022 Jan 7;9(1):2. doi: 10.1186/s40662-021-00272-0.
Infectious keratitis is a major cause of global blindness. We tested whether standalone photoactivated chromophore corneal cross-linking (PACK-CXL) may be an effective first-line treatment in early to moderate infectious keratitis, compared with standard antimicrobial treatment.
This is a randomized, controlled, multinational phase 3 clinical trial. Participants in five centers in Egypt, India, Iran, Israel, and China, aged ≥ 18 years, with infectious keratitis of presumed bacterial, fungal, or mixed origin, were randomly assigned (1:1) to PACK-CXL, or antimicrobial therapy. Outcomes measures included healing, defined as time to re-epithelialization of the corneal epithelial defect in the absence of inflammatory activity in the anterior chamber and clearance of stromal infiltrates. Treatment success was defined as the complete resolution of signs of infection.
Between July 21, 2016, and March 4, 2020, participants were randomly assigned to receive PACK-CXL (n = 18) or antimicrobial therapy per American Academy of Ophthalmology (AAO) guidelines (n = 21). No participants were lost to follow-up. Four eyes were excluded from the epithelialization time analysis due to treatment failure: two in the antimicrobial therapy group, and two in the PACK-CXL group. Success rates were 88.9% (16/18 patients) in the PACK-CXL group and 90.5% (19/21 patients) in the medication group. There was no significant difference in time to complete corneal re-epithelialization (P = 0.828) between both treatment groups.
PACK-CXL may be an alternative to antimicrobial drugs for first-line and standalone treatment of early to moderate infectious keratitis of bacterial or fungal origin. Trial registration This trial is registered at ClinicalTrials.gov, trial registration number: NCT02717871.
感染性角膜炎是全球失明的主要原因。我们测试了与标准抗菌治疗相比,单独使用光活化发色团角膜交联术(PACK-CXL)是否可能是早期至中度感染性角膜炎的有效一线治疗方法。
这是一项随机、对照、多中心3期临床试验。来自埃及、印度、伊朗、以色列和中国五个中心的年龄≥18岁、患有推测为细菌、真菌或混合来源的感染性角膜炎的参与者被随机分配(1:1)接受PACK-CXL或抗菌治疗。结局指标包括愈合,定义为无前房炎症活动且基质浸润清除时角膜上皮缺损重新上皮化的时间。治疗成功定义为感染体征完全消退。
在2016年7月21日至2020年3月4日期间,参与者被随机分配接受PACK-CXL(n = 18)或按照美国眼科学会(AAO)指南接受抗菌治疗(n = 21)。没有参与者失访。由于治疗失败,4只眼被排除在上皮化时间分析之外:抗菌治疗组2只,PACK-CXL组2只。PACK-CXL组的成功率为88.9%(16/18例患者),药物治疗组为90.5%(19/21例患者)。两个治疗组之间角膜完全重新上皮化的时间无显著差异(P = 0.828)。
PACK-CXL可能是细菌性或真菌性早期至中度感染性角膜炎一线单独治疗中抗菌药物的替代方法。试验注册 本试验已在ClinicalTrials.gov注册,试验注册号:NCT02717871。