Adjuntive nicergoline therapy for severe persistent corneal epithelial defects.

Valeria Oliva-Biénzobas , Enrique O. Graue-Hernandez , Guillermo Raul Vera-Duarte , Jesus Cabral-Macías , Juan Serna-Ojeda , Victor Boullosa , Arturo Ramirez-Miranda , Vishal Jhanji , Victor L. Perez , Alejandro Navas
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Abstract

Purpose

The aim of this study was to determine the effect of nicergoline in patients with persistent corneal epithelial defects.

Methods

This is a prospective, non-comparative interventional study. The study included ten eyes of 9 patients with persistent corneal epithelial defects unresponsive to conventional therapy. Patients were treated with 10 mg nicergoline orally twice daily for at least two weeks. Slit-lamp examination, photography, corneal fluorescein dye testing, and best-corrected visual acuity were performed before and after treatment.

Results

Two male and seven female patients with persistent corneal epithelial defects unresponsive to conventional therapy treated with oral nicergoline were included. The average age was 60.9 years (51–76 years). The most frequent diagnoses associated with persistent corneal defects were neurotrophic (3 patients) and exposure ulcer (2 patients). In eight eyes (72.7 %), epithelial defects entirely healed between 10 and 28 days of treatment with nicergoline (mean resolution time 17 days). Epithelial defects persisted in 2 eyes (27.3 %).

Conclusion

Nicergoline represents a potential therapeutic option in patients with abnormal corneal healing responses. Further studies and clinical trials must be conducted to prove safety and efficacy as a treatment for persistent corneal epithelium defects in humans.
尼麦角林辅助治疗严重持续性角膜上皮缺损。
目的本研究的目的是确定尼麦角林对持续性角膜上皮缺损患者的疗效。方法本研究为前瞻性、非比较性介入研究。该研究包括9例持续性角膜上皮缺损患者的10只眼,对常规治疗无反应。患者口服尼麦角林10mg,每日两次,持续治疗至少两周。治疗前后进行裂隙灯检查、摄影、角膜荧光素染色试验、最佳矫正视力检查。结果对口服尼麦角林常规治疗无反应的持续性角膜上皮缺损患者2男7女。平均年龄为60.9岁(51 ~ 76岁)。与持续性角膜缺损相关的最常见诊断是神经营养性(3例)和暴露性溃疡(2例)。8只眼(72.7%)上皮缺损在尼麦角林治疗10 - 28天内完全愈合(平均消退时间为17天)。2只眼(27.3%)存在上皮缺损。结论尼麦角林是治疗角膜愈合反应异常患者的一种潜在的治疗选择。必须进行进一步的研究和临床试验,以证明其作为治疗人类持续性角膜上皮缺陷的安全性和有效性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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