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Incidence of deepening of upper eyelid sulcus after topical use of tafluprost ophthalmic solution in Japanese patients

机译:日本患者局部使用他氟前列素滴眼液后上眼睑沟加深的发生率

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Purpose: To investigate the incidence of deepening of upper eyelid sulcus (DUES) with topical use of tafluprost in Japanese glaucoma patients.Methods: This study was a prospective, open-label, non-controlled case series conducted at a single center. Thirty-six primary open-angle glaucoma Japanese patients who had no history of surgery were enrolled. The patients were prescribed 0.0015% topical tafluprost once daily to one eye that had the more severe visual field disorder, and observed during outpatient visits before and at 30, 60, and 90 days after starting treatment. At every visit, three examiners judged the presence of DUES unanimously by facial photographs including eyebrows and lower eyelids. The primary outcome variable was the incidence of DUES at the end of day 90 in the study as assessed by observer-masked facial photography. The patients were also asked if they noticed any subjective symptom of DUES. Gender, refraction, and intraocular pressure were evaluated as potential risk factors.Results: Thirty-two patients completed this clinical trial. DUES were identified objectively in 19% (6/32) of the patients after 90 days of treatment. The incidence was not related to gender, refraction, baseline or post-treatment intraocular pressure, or intraocular pressure reduction. Finally, 17% (1/6) of patients with objectively diagnosed DUES noticed the presence of DUES by themselves. No patient dropped out of the study because of DUES.Conclusion: Similar to other prostaglandin analogs, topical use of tafluprost ophthalmic solution is associated with DUES as a local adverse reaction.
机译:目的:调查在日本青光眼患者中局部使用他氟前列素加重上睑睑沟(DUES)的发生率。方法:本研究是在单个中心进行的前瞻性,开放标签,非对照病例系列。纳入了36例无手术史的原发性开角型青光眼日本患者。每天对一只患有较严重视野障碍的眼睛开一次0.0015%的局部用药tafluprost,并在开始治疗前和治疗后30、60和90天进行门诊就诊。每次访问时,三名检查员均通过眉毛和下眼睑的面部照片一致地判断DUES的存在。主要结果变量是研究中90天结束时DUES的发生率,这是由观察者掩盖的面部摄影评估得出的。还询问患者是否注意到DUES的任何主观症状。性别,屈光度和眼压被评估为潜在危险因素。结果:32例患者完成了该临床试验。治疗90天后,客观上确定了19%(6/32)的DUES。发生率与性别,验光,基线或治疗后眼内压或眼内压降低无关。最后,客观诊断为DUES的患者中有17%(1/6)自己注意到了DUES的存在。没有患者因DUES退出研究。结论:与其他前列腺素类似物相似,局部使用塔氟前列素滴眼液与DUES有关,是局部不良反应。

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