Zaloga Alexandra R, Khalili Ashley, Ayres Brandon D, Finklea Brenton D, Meghpara Beeran B, Rapuano Christopher J, Syed Zeba A
Sidney Kimmel Medical College, Thomas Jefferson University, Philadelphia, PA, USA.
Cornea Service, Wills Eye Hospital, Philadelphia, PA, USA.
Oman J Ophthalmol. 2025 Jun 24;18(2):198-204. doi: 10.4103/ojo.ojo_311_24. eCollection 2025 May-Aug.
The study aimed to report the outcomes of patients treated with cenegermin 0.002% for neurotrophic keratopathy (NK) following penetrating keratoplasty (PK).
This retrospective case series included patients evaluated at a tertiary care hospital who completed an 8-week course of cenegermin for NK within 12 months following PK. The primary outcome measure was NK stage, while secondary outcomes included complete epithelial healing, epithelial defect size, and best-corrected visual acuity (BCVA) at baseline and four time points during and following treatment. We also evaluated disease progression.
Fourteen eyes of 14 patients were included and demonstrated significant improvement in NK stage at 4 weeks (1.1 ± 0.7; = 0.006) and 8 weeks after treatment initiation (0.9 ± 0.7; = 0.002) and 1 month (0.6 ± 0.5; < 0.001) and 6 months after treatment completion (0.8 ± 0.9; = 0.002) compared to baseline (1.6 ± 0.5). Complete epithelial healing was noted 1 month (42.9%; = 0.016) and 6 months after treatment completion (38.5%; = 0.016). Epithelial defect size improved to <5 mm at all points ( < 0.05) during and after treatment compared to baseline (37.24 mm). Improvement in BCVA was not significant at any time point. Two (14.3%) patients experienced disease progression up to 6 months of follow-up.
Following an 8-week course of cenegermin, patients with a history of PK demonstrated improvement in NK stage, epithelial healing, and reduced epithelial defect size lasting 6 months after treatment completion. Patients with prior PK and NK may be considered candidates for cenegermin treatment.
本研究旨在报告穿透性角膜移植术(PK)后使用0.002%西奈吉明治疗神经营养性角膜病变(NK)患者的治疗结果。
本回顾性病例系列纳入了在一家三级护理医院接受评估的患者,这些患者在PK后12个月内完成了为期8周的西奈吉明治疗NK的疗程。主要结局指标为NK分期,次要结局包括基线时以及治疗期间和治疗后的四个时间点的完全上皮愈合、上皮缺损大小和最佳矫正视力(BCVA)。我们还评估了疾病进展情况。
纳入了14例患者的14只眼,与基线时(1.6±0.5)相比,治疗开始后4周(1.1±0.7;P = 0.006)、8周(0.9±0.7;P = 0.002)、治疗完成后1个月(0.6±0.5;P<0.001)和6个月(0.8±0.9;P = 0.002)时NK分期有显著改善。治疗完成后1个月(42.9%;P = 0.016)和6个月(38.5%;P = 0.016)时观察到完全上皮愈合。与基线时(37.24 mm)相比,治疗期间和治疗后所有时间点上皮缺损大小均改善至<5 mm(P<0.05)。BCVA在任何时间点均无显著改善。两名(14.3%)患者在随访至6个月时出现疾病进展。
在接受为期8周的西奈吉明治疗后,有PK病史的患者在治疗完成后6个月内NK分期、上皮愈合情况改善,上皮缺损大小减小。既往有PK和NK的患者可考虑作为西奈吉明治疗的候选者。