Department of Ophthalmology, Queen's University, Kingston, Ont.
Department of Ophthalmology, Queen's University, Kingston, Ont.
Can J Ophthalmol. 2018 Dec;53(6):605-608. doi: 10.1016/j.jcjo.2018.01.020. Epub 2018 Jul 14.
To evaluate a novel, simple, noninvasive method (known as the "bitter taste test") of establishing nasolacrimal duct patency in healthy asymptomatic eyes.
Double-blind, randomized controlled pilot study.
Healthy asymptomatic medical students, residents, and allied health staff at our institution.
Participants, aged 18-35 years (n = 28) with assumed normal lacrimal function, were randomized to the interventional group (100 parts per million denatonium benzoate in sterile water, n = 14) or to the control group (sterile water only, n = 14). All participants were pretreated with topical tetracaine in their right conjunctival cul-de sac, followed by 3 drops of the experimental solution spaced 1 minute apart. The primary outcome was whether participants reported a strong, persistent bitter taste. The secondary outcome was the time-to-taste. All participants received lacrimal irrigation. The Fisher's exact test was done using GraphPad online software.
All participants in the interventional group reported the presence of the bitter solution. None of the participants in the control group reported bitterness (p < 0.001, Fisher's exact test). Time-to-taste was within 15 minutes for 71% of the intervention group (n = 10); within 30 minutes for 79% (n = 11); and within 2 hours for 100% (n = 14). The bitterness typically persisted for 1-2 hours. All participants had normal lacrimal systems to irrigation. No adverse events were reported.
The bitter taste test demonstrates a promising ability to assess nasolacrimal duct patency under physiologic conditions in healthy participants. Further research is needed to validate this method in a clinical sample of patients with nasolacrimal duct obstruction.
评估一种新颖、简单、非侵入性的方法(称为“苦味测试”),用于确定健康无症状眼睛的鼻泪管通畅性。
双盲、随机对照初步研究。
本机构的健康无症状医学生、住院医师和辅助卫生人员。
参与者为年龄在 18-35 岁之间(n=28)、假定泪液功能正常的无症状者,随机分为干预组(100ppm 苯甲地那铵在无菌水中,n=14)或对照组(仅无菌水,n=14)。所有参与者均在右眼结膜囊内预先用局部盐酸丁卡因处理,然后间隔 1 分钟滴入 3 滴实验溶液。主要结局是参与者是否报告强烈、持续的苦味。次要结局是味觉出现的时间。所有参与者均接受泪道冲洗。Fisher 确切检验使用 GraphPad 在线软件进行。
干预组的所有参与者均报告存在苦味溶液。对照组的参与者均未报告苦味(p<0.001,Fisher 确切检验)。71%(n=10)的干预组在 15 分钟内出现味觉;79%(n=11)在 30 分钟内出现味觉;100%(n=14)在 2 小时内出现味觉。苦味通常持续 1-2 小时。所有参与者的泪道系统对冲洗均正常。未报告不良事件。
苦味测试在健康参与者的生理条件下评估鼻泪管通畅性方面具有有前景的能力。需要进一步研究来验证该方法在鼻泪管阻塞患者的临床样本中的有效性。