Bonini S, Barney N P, Schiavone M, Centofanti M, Berruto A, Bonini S, Allansmith M R
Department of Ophthalmology, University of Rome, Tor Vergata, Italy.
Eye (Lond). 1992;6 ( Pt 6):648-52. doi: 10.1038/eye.1992.139.
A double-masked, randomised, placebo-controlled study was conducted to evaluate the effectiveness of nedocromil 2% eyedrops, a mast cell stabilizer, in 20 symptomatic patients with vernal conjunctivitis. A 1-week baseline period was followed by 6 weeks of treatment. Clinical examination and cytological evaluation of tear fluid were performed weekly, and the patients recorded their subjective assessment on a daily diary card. The nedocromil group showed significantly less hyperaemia in the course of treatment than did the placebo group, and significantly less itching at all visits compared with baseline itching. In the nedocromil-treated group, but not in the placebo group, the number of neutrophils, eosinophils and lymphocytes in tears decreased significantly during some treatment weeks when compared with baseline. The overall assessment of treatment efficacy by both clinician and patient was significantly in favour of nedocromil treatment over placebo.
开展了一项双盲、随机、安慰剂对照研究,以评估肥大细胞稳定剂2%奈多罗米滴眼液对20例有症状的春季结膜炎患者的疗效。1周基线期后进行6周治疗。每周进行临床检查和泪液细胞学评估,患者在每日日记卡上记录主观评估。奈多罗米组在治疗过程中的充血明显少于安慰剂组,与基线瘙痒相比,在所有就诊时的瘙痒也明显减轻。在奈多罗米治疗组中,与基线相比,某些治疗周期间泪液中的中性粒细胞、嗜酸性粒细胞和淋巴细胞数量显著减少,而安慰剂组未出现这种情况。临床医生和患者对治疗效果的总体评估均明显倾向于奈多罗米治疗而非安慰剂治疗。