真实世界干眼症患者队列中的眼部神经性疼痛:救盲干眼症登记研究

Damien Tuan-Man Le , Himal Kandel , Ngozi C Chidi-Egboka , Gerd Geerling , Saaeha Rauz , Alberto Recchioni , Chris HL Lim , Stephanie L Watson
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摘要

目的比较有眼部神经痛和无眼部神经痛的干眼症(DED)患者的人口统计学特征、临床体征和问卷评分。根据临床医生对眼部神经性疼痛的诊断以及泪膜和眼表学会干眼研讨会 II 的定义,将患者分为两组。比较了患者的人口统计学特征、眼表疾病指数(OSDI)和眼舒适指数(OCI)评分、干眼症体征以及患者健康问卷-4(PHQ-4)评分、平均筛查时间和治疗依从性。统计分析包括描述性统计、曼-惠特尼 U 检验、独立性卡方检验和费雪精确检验。结果 分析了 298 名有 DED 症状和体征的患者(26 名有眼神经痛)的数据。患者的人口统计学特征无统计学差异(p*>0.0063)。眼神经痛患者在 OSDI(P*<0.0031)和 OCI(P*<0.0039)中的最终得分、领域得分和疼痛相关问题得分较低,在 PHQ-4 中的焦虑和抑郁得分较高(P*<0.0083)。来自 SSDER 的真实世界数据显示,在 DED 队列中,患者人口统计学和临床体征很难区分眼神经痛患者。眼神经痛患者的 OSDI 和 OCI 评分明显更差,表明症状严重程度更高。虽然这突出了症状差异,但仍需进一步研究,以确定 OSDI 和 OCI 评分是否有助于识别 DED 中的眼神经痛。
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Ocular neuropathic pain in a real-world patient cohort with dry eye disease: A save sight dry eye registry study

Purpose

To compare patient demographics, clinical signs, and questionnaire scores in dry eye disease (DED) patients with and without ocular neuropathic pain.

Methods

A cross-sectional cohort study was performed using the Save Sight Dry Eye Registry (SSDER). Patients were divided into two groups based on a clinician diagnosis of ocular neuropathic pain and Tear Film and Ocular Surface Society Dry Eye Workshop II definitions. Patient demographics, Ocular Surface Disease Index (OSDI) and Ocular Comfort Index (OCI) scores, and DED signs were compared along with Patient Health Questionnaire-4 (PHQ-4) scores, average screen time and treatment compliance. Statistical analyses included descriptive statistics, Mann-Whitney U test, Chi-squared test of independence, and Fisher's exact test. P-values were Bonferroni corrected (p*).

Results

Data from 298 patients with DED symptoms and signs (26 with ocular neuropathic pain) were analysed. There was no statistical difference in patient demographics (p*>0.0063). Patients with ocular neuropathic pain had worse final, domain, and pain-related question scores for the OSDI (p*<0.0031) and OCI (p*<0.0039) and had higher scores for anxiety and depression for the PHQ-4 (p*<0.0083). Patients with ocular neuropathic pain had a lower rate and severity of meibomian gland dysfunction (p*<0.0063).

Conclusion

Real-world data from the SSDER demonstrated patient demographics and clinical signs poorly differentiated patients with ocular neuropathic pain within a DED cohort. Patients with ocular neuropathic pain reported significantly worse OSDI and OCI scores, indicating greater symptom severity. While this highlighted symptom differences, further research is required to determine whether OSDI and OCI scores can assist in identifying ocular neuropathic pain in DED.
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