Department of Ophthalmology, Hallym University College of Medicine, Seoul, Republic of Korea.
PLoS One. 2019 Apr 17;14(4):e0215297. doi: 10.1371/journal.pone.0215297. eCollection 2019.
To longitudinally evaluate the visual function and structure of patients taking ethambutol by various modalities and identify useful tests for detection of subclinical ethambutol-induced optic toxicity.
This retrospective study enrolled 84 patients with newly diagnosed tuberculosis treated with ethambutol. Best-corrected visual acuity (BCVA), color vision, contrast sensitivity, fundus and retinal nerve fiber layer (RNFL) photography, automated visual field (VF) test, and optical coherence tomography (OCT) were performed: prior to starting; every month during administration, and 1 month after stoppage. We longitudinally compared visual function and structure with the baseline and identified the occurrence of subclinical toxicity.
BCVA, color vision, and contrast sensitivity showed no change from the baseline. Mean temporal RNFL thickness was significantly increased at 6 months (p = 0.014). Subclinical toxicity was found in 22 eyes of 14 patients (i.e., 13% of 168 eyes), in the forms of VFI decrease (VF index, 9 eyes of 6 patients), quadrant RNFL thickness increase (5 eyes of 4 patients), and VF pattern defect (12 eyes of 6 patients). 73% of the patients showed recovery to the baseline at 1 month post-stoppage. The risk factors for occurrence of subclinical toxicity were age, cumulative dose, and medication duration.
Mean temporal RNFL thickness increased after administration. The VFI, quadrant RNFL thickness, and VF pattern defect could prove useful in assessment of subclinical toxicity. Medication duration was shown to be a strong risk factor for occurrence of subclinical toxicity.
通过多种方式对服用乙胺丁醇的患者进行纵向评估视觉功能和结构,确定用于检测亚临床乙胺丁醇诱导的视神经毒性的有用测试。
这项回顾性研究纳入了 84 例新诊断为结核病并接受乙胺丁醇治疗的患者。在开始前、治疗期间每月以及停药后 1 个月,对最佳矫正视力(BCVA)、色觉、对比敏感度、眼底和视网膜神经纤维层(RNFL)照相、自动视野(VF)测试和光学相干断层扫描(OCT)进行检测。我们将视觉功能和结构与基线进行纵向比较,并确定亚临床毒性的发生情况。
BCVA、色觉和对比敏感度与基线相比无变化。6 个月时平均颞侧 RNFL 厚度显著增加(p = 0.014)。14 例患者的 22 只眼(即 168 只眼中的 13%)发现亚临床毒性,表现为 VFI 降低(VF 指数,6 例患者的 9 只眼)、象限 RNFL 厚度增加(4 例患者的 5 只眼)和 VF 模式缺陷(6 例患者的 12 只眼)。73%的患者在停药后 1 个月恢复至基线。亚临床毒性发生的危险因素为年龄、累积剂量和用药时间。
用药后平均颞侧 RNFL 厚度增加。VF 指数、象限 RNFL 厚度和 VF 模式缺陷可用于评估亚临床毒性。用药时间是亚临床毒性发生的一个强危险因素。