Stalmans Ingeborg, Lemij Hans, Clarke Jonathan, Baudouin Christophe
Department of Ophthalmology, UZ Leuven, Leuven, Belgium.
Glaucoma Service, Rotterdam Eye Hospital, Rotterdam, the Netherlands.
Clin Ophthalmol. 2020 Oct 30;14:3675-3680. doi: 10.2147/OPTH.S269586. eCollection 2020.
Ocular Surface Disease (OSD) and hyperemia are the most common adverse events of topical ocular medications. While active compounds may cause allergic reactions or irritation, preservatives, which are intended to prevent bacterial growth, are toxic as well. Therefore, the most recent glaucoma medications no longer contain preservatives. Despite this, local tolerability may still impact treatment compliance and patient quality of life. We conducted an observational, multi-center, international, cross-sectional study in 793 treated and stabilized glaucoma patients to assess patient satisfaction and local tolerability of their treatment. The vast majority (93.7%) of patients was satisfied or very satisfied with their treatment in terms of tolerability and only 6.3% were dissatisfied. However, ophthalmological examination showed a high frequency of ocular signs: conjunctival hyperemia (32%), OSD (42.5%) and positive conjunctival fluorescein staining (10.3%). Additionally, patients reported symptoms upon instillation (31.4%) and between instillations (57.3%); 25.1% of patients were using tear substitutes. All signs and symptoms were significantly (p<0.001) associated with patient dissatisfaction. A logistic regression model indicated that dissatisfaction was higher in patients with symptoms upon instillation and in those using tear substitutes (OR: 3.03 and 4.63, respectively). The mean patient tolerability score to treatment was 82.7±16.1 on a 100-point visual analogue scale. In conclusion, even if patients may be highly satisfied with their current treatment, most of them present ocular signs and symptoms. A treatment change should be considered in case of clinical signs or patient-reported symptoms.
眼表疾病(OSD)和充血是局部眼用药物最常见的不良事件。虽然活性成分可能会引起过敏反应或刺激,但用于防止细菌生长的防腐剂也具有毒性。因此,最新的青光眼药物不再含有防腐剂。尽管如此,局部耐受性仍可能影响治疗依从性和患者生活质量。我们对793名接受治疗且病情稳定的青光眼患者进行了一项观察性、多中心、国际性横断面研究,以评估患者对其治疗的满意度和局部耐受性。绝大多数(93.7%)患者在耐受性方面对其治疗感到满意或非常满意,只有6.3%的患者不满意。然而,眼科检查显示眼部体征的发生率很高:结膜充血(32%)、眼表疾病(42.5%)和结膜荧光素染色阳性(10.3%)。此外,患者报告了滴眼时(31.4%)和两次滴眼之间(57.3%)的症状;25.1%的患者正在使用泪液替代物。所有体征和症状均与患者不满意显著相关(p<0.001)。逻辑回归模型表明,滴眼时出现症状的患者和使用泪液替代物的患者不满意程度更高(比值比分别为:3.03和4.63)。在100分的视觉模拟量表上,患者对治疗的平均耐受性评分为82.7±16.1。总之,即使患者可能对其当前治疗高度满意,但大多数患者仍存在眼部体征和症状。如果出现临床体征或患者报告的症状,应考虑改变治疗方案。