Department of Pharmacology, Osmania Medical College, Hyderabad, Telangana, India.
Indian J Pharmacol. 2020 Nov-Dec;52(6):476-481. doi: 10.4103/ijp.IJP_174_20.
Vernal conjunctivitis comprises 0.5% of allergic eye diseases. The study is intended to collate the effectiveness of drugs by observing the reduction in signs and symptoms.
The objective of the study is to evaluate the effectiveness and safety of olopatadine 0.1% ophthalmic drops with bepotastine besilate 1.5% ophthalmic drops in patients with vernal keratoconjunctivitis (VKC).
A randomized, open-label, comparative study conducted in Sarojini Devi Eye Hospital, Telangana. The study included 50 patients diagnosed with VKC, of which Group A and Group B were given olopatadine 0.1% ophthalmic drops and bepotastine besilate 1.5% ophthalmic drops, respectively, twice a day for 8 weeks. The reduction in signs and symptoms in both groups was compared. The observations and results were tabulated accordingly, and data were analyzed using the SPSS. The unpaired t-test is used as the test of significance in between two groups. P value is statistically significant when it is less than 0.05.
Overall, 50 cases were included in the study, 72% of total patients were in the age group of 5-10 years, and 28% were in the age group of 11-15 years. There were 39 males and 11 females. After 8 weeks of follow-up, the mean reduction in the scoring of symptoms and signs provided better and quicker relief of watering, ocular discomfort, and conjunctival hyperemia with bepotastine 1.5% eye drops. Olopatadine 0.1% eye drops provided faster improvement in papillary hypertrophy. Both drugs were equally effective in reducing itching. Laboratory findings of absolute eosinophil count had no statistical significance in between the two groups.
In this study, based on the evaluation of therapeutic performance, bepotastine eye drops proved quicker relief of symptoms and signs compared to olopatadine eye drops but was not statistically significant which would prove beneficial for the patients.
春季结膜炎占过敏性眼病的 0.5%。本研究旨在通过观察体征和症状的减轻来比较药物的疗效。
本研究旨在评估奥洛他定 0.1%滴眼液联合贝美素噻吗洛尔 1.5%滴眼液治疗春季角结膜炎(VKC)患者的有效性和安全性。
这是一项在泰伦加纳邦 Sarojini Devi 眼科医院进行的随机、开放标签、对照研究。该研究纳入了 50 名被诊断为 VKC 的患者,其中 A 组和 B 组分别使用奥洛他定 0.1%滴眼液和贝美素噻吗洛尔 1.5%滴眼液,每天两次,持续 8 周。比较两组患者体征和症状的减轻情况。对观察结果进行制表,并使用 SPSS 进行数据分析。采用配对 t 检验比较两组间差异,P 值小于 0.05 时具有统计学意义。
本研究共纳入 50 例患者,其中 72%的患者年龄在 5-10 岁之间,28%的患者年龄在 11-15 岁之间。男性 39 例,女性 11 例。经过 8 周的随访,贝美素噻吗洛尔 1.5%滴眼液在评分症状和体征的均值减轻方面提供了更好、更快的缓解,包括流泪、眼部不适和结膜充血;奥洛他定 0.1%滴眼液则更快改善乳头肥大。两种药物在减轻瘙痒方面同样有效。两组患者的绝对嗜酸性粒细胞计数的实验室检查结果无统计学差异。
本研究基于治疗效果评估,贝美素噻吗洛尔滴眼液在缓解症状和体征方面比奥洛他定滴眼液更快,但无统计学意义,这对患者可能有益。