Center for Translational Ocular Immunology, Department of Ophthalmology, Tufts Medical Center, Tufts University School of Medicine, Boston, USA; Cornea Service, New England Eye Center, Department of Ophthalmology, Tufts Medical School, Tufts University School of Medicine, Boston, USA.
Center for Translational Ocular Immunology, Department of Ophthalmology, Tufts Medical Center, Tufts University School of Medicine, Boston, USA.
Ocul Surf. 2020 Oct;18(4):814-820. doi: 10.1016/j.jtos.2020.08.006. Epub 2020 Aug 27.
Neuropathic corneal pain (NCP) is a recently acknowledged disease entity. However, there is no consensus in potential treatment strategies, particularly in patients with a centralized component of pain. This study aims to assess the efficacy and tolerability of the tricyclic antidepressant, nortriptyline, among NCP patients.
Patients with clinically diagnosed NCP and a centralized component of pain, treated with oral nortriptyline, who had recorded pain scores as assessed by the ocular pain assessment survey at the first and last visit were included. Patients were excluded if they had any other ocular pathology that might result in pain or had less than 4 weeks of nortriptyline use. Demographics, time between visits, concomitant medications, systemic and ocular co-morbidities, duration of NCP, side effects, ocular pain scores, and quality of life (QoL) assessment were recorded.
Thirty patients with a mean age of 53.1 ± 18.5 were included. Male to female ratio was 8:22. Mean ocular pain in the past 24 h improved from 5.7 ± 2.1 to 3.6 ± 2.1 after 10.5 ± 9.1 months (p < 0.0001). Twelve patients (40.0%) had equal to or more than 50% improvement, 6 patients (20.0%) had 30-49% improvement, 6 patients (20.0%) had 1-29% improvement, 4 patients (13.3%) did not improve, while 2 patients (6.7%) reported increase in pain levels. Mean QoL improved from 6.0 ± 2.5 to 4.3 ± 2.4 (p = 0.019). Eight patients (26.6%) discontinued treatment due to persistent side effects, despite improvement by 22.4%.
Nortriptyline was effective in relieving NCP symptoms in patients with centralized component and insufficient response to other systemic and topical therapies who tolerated the drug for at least 4 weeks. Nortriptyline may be used in the management of patients with NCP.
神经病理性角膜疼痛(NCP)是一种最近被认可的疾病实体。然而,在潜在的治疗策略方面尚无共识,尤其是在疼痛具有集中成分的患者中。本研究旨在评估三环类抗抑郁药,去甲替林,在 NCP 患者中的疗效和耐受性。
纳入了接受口服去甲替林治疗且临床诊断为 NCP 且具有疼痛集中成分的患者,这些患者在首次和末次就诊时记录了眼部疼痛评估调查评估的疼痛评分。如果患者有任何其他可能导致疼痛的眼部疾病,或者使用去甲替林不足 4 周,则将其排除在外。记录了患者的人口统计学资料、就诊间隔时间、合并用药、全身和眼部合并症、NCP 持续时间、副作用、眼部疼痛评分和生活质量(QoL)评估。
共纳入 30 名平均年龄为 53.1±18.5 岁的患者。男女比例为 8:22。在过去 24 小时内的平均眼部疼痛从 5.7±2.1 改善至治疗后 10.5±9.1 个月时的 3.6±2.1(p<0.0001)。12 名患者(40.0%)的改善程度等于或大于 50%,6 名患者(20.0%)的改善程度为 30-49%,6 名患者(20.0%)的改善程度为 1-29%,4 名患者(13.3%)没有改善,而 2 名患者(6.7%)报告疼痛水平增加。平均 QoL 从 6.0±2.5 改善至 4.3±2.4(p=0.019)。尽管有 22.4%的患者因持续的副作用而停药,但仍有 8 名患者(26.6%)因持续的副作用而停药。
去甲替林对具有集中成分且对其他全身和局部治疗反应不足的 NCP 患者的症状缓解有效,这些患者至少耐受药物 4 周。去甲替林可用于 NCP 患者的治疗。