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A comparison of the effect of carbomer-, cellulose- and mineral oil-based artificial tear formulations.

机译:卡波姆,纤维素和矿物油基人造泪液配方效果的比较。

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PURPOSE. To compare the efficacy, safety, and local tolerance between carbomer-based artificial tears, cellulose-, and mineral oil-based artificial tears. METHODS. A randomized, open-label, parallel-group comparative 28-day study was designed for 67 patients who were randomized into three treatment groups. Measurements included the scoring of total subjective symptoms and objective signs, Schirmer-Jones test values, and tear break-up time (BUT) at baseline, and after 2 and 4 weeks of treatment. Safety of study treatment was also assessed. Outcomes measured at baseline and 2 and 4 weeks follow-up included the scoring of total subjective symptoms and objective signs, Schirmer-Jones test values, and tear BUT, subjective assessments, and safety. RESULTS. There were no differences regarding total scores, Schirmer-Jones test, or tear BUT at baseline among these three groups at 2 and 4 weeks. Patients in all three treatment groups experienced a significant improvement from baseline in total scores and Schirmer-Jones test values after treatment. Subjective assessment was better with carbomer-based treatment. CONCLUSIONS. Each artificial tear formulation successfully relieved symptoms and signs of keratoconjunctivitis sicca. The tolerance of carbomer-based artificial tears was comparable to that of cellulose- and mineral oil-based artificial tears.
机译:目的。比较基于卡波姆的人造泪液,基于纤维素和矿物油的人造泪液的功效,安全性和局部耐受性。方法。设计了一项随机,开放标签,平行组比较28天的研究,研究对象为67位随机分为三个治疗组的患者。测量包括总的主观症状和客观症状的评分,Schirmer-Jones测试值以及基线以及治疗2和4周后的泪液破裂时间(BUT)。还评估了研究治疗的安全性。在基线以及随访2和4周时测量的结果包括总主观症状和客观体征,Schirmer-Jones测试值和泪液BUT评分,主观评估和安全性。结果。在第2周和第4周,这三组的总分,Schirmer-Jones检验或基线泪液BUT均无差异。在治疗后,所有三个治疗组的患者总得分和Schirmer-Jones测试值均较基线有显着改善。以卡波姆为基础的治疗的主观评估更好。结论。每种人工泪液制剂都能成功缓解干燥性角膜结膜炎的症状和体征。卡波姆基人造眼泪的耐受性与纤维素基和矿物油基人造眼泪的耐受性相当。

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