Gwon A, Vaughan E R, Cheetham J K, DeGryse R
Allergan Pharmaceuticals, Inc., Irvine, CA.
CLAO J. 1994 Apr;20(2):131-8.
Ocular pain is often treated with systemic analgesics, which are associated with some undesirable side effects. Because nonsteroidal anti-inflammatory drugs are thought to be peripheral analgesics, we decided to evaluate the local analgesic effect of flurbiprofen. After an initial study in 29 patients demonstrated that 0.03% flurbiprofen ophthalmic solution did not affect corneal sensitivity, a second trial was designed to test the analgesic efficacy and safety of this agent. In a multicenter, randomized, double-masked, parallel-group clinical trial, topically applied 0.03% flurbiprofen sodium ophthalmic solution was compared with its vehicle in 105 patients (53 females, 52 males) undergoing elective unilateral radial keratotomy. All patients received flurbiprofen or its vehicle before and every four hours after surgery for 14 days. Mean pain intensity variables were lower in the flurbiprofen group than the vehicle group after surgery. Clinically significant differences in pain relief (mean difference > or = 1 unit), favoring flurbiprofen, were seen at hours 2, 3, and 4, and on days 1 through 4, and on day 7. Statistically significant differences were seen at hours 2, 3, and 4. Sixteen patients (eight in each group) had adverse effects, most commonly transient burning. These studies suggest that topical 0.03% flurbiprofen safely and effectively relieves ocular pain without affecting corneal sensation.
眼痛通常采用全身镇痛药治疗,但这些药物会带来一些不良副作用。由于非甾体抗炎药被认为是外周镇痛药,我们决定评估氟比洛芬的局部镇痛效果。在对29例患者进行的初步研究表明0.03%氟比洛芬滴眼液不影响角膜敏感性后,设计了第二项试验来测试该药物的镇痛效果和安全性。在一项多中心、随机、双盲、平行组临床试验中,将局部应用的0.03%氟比洛芬钠滴眼液与其赋形剂在105例(53例女性,52例男性)接受择期单侧放射状角膜切开术的患者中进行比较。所有患者在手术前以及手术后14天内每4小时接受一次氟比洛芬或其赋形剂治疗。术后氟比洛芬组的平均疼痛强度变量低于赋形剂组。在术后第2、3和4小时,以及第1至4天和第7天,在疼痛缓解方面(平均差异≥1个单位)出现了有利于氟比洛芬的临床显著差异。在第2、3和4小时出现了统计学显著差异。16例患者(每组8例)出现不良反应,最常见的是短暂烧灼感。这些研究表明,局部应用0.0