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评价奥洛他定和左西替利嗪在 24 小时内的抗组胺作用:组胺离子电渗法诱导皮肤反应的双盲、随机、交叉、安慰剂对照比较。

Evaluation of the antihistamine effects of olopatadine and levocetirizine during a 24-h period: a double-blind, randomized, cross-over, placebo-controlled comparison in skin responses induced by histamine iontophoresis.

机构信息

Department of Dermatology, Aichi Medical University, Nagakute, Japan.

出版信息

J Dermatol. 2013 Dec;40(12):987-92. doi: 10.1111/1346-8138.12326. Epub 2013 Dec 4.

Abstract

The antihistamine effects of olopatadine and levocetirizine, in standard-dose application described in their information (5 mg twice a day for olopatadine; 5 mg once daily for levocetirizine), were examined from 11.5 to 24 h after application. The test was designed in a double-blind, randomized, cross-over, placebo-controlled study of 12 healthy volunteers on histamine-induced flare and wheal response using an iontophoresis technique. The suppressive effect of olopatadine on the wheals induced by a 0.1-mA histamine iontophoresis lasted for 24 h after dosing. Both drugs inhibited flare induced by histamine iontophoresis almost completely until 24 h after the first administration. Suppression of the 0.2-mA-induced wheal response by levocetirizine, taken once daily, decreased with time, although 0.1-mA-induced flare was almost completely suppressed by the drug. Olopatadine completely suppressed even the wheal response induced by a 0.2-mA histamine iontophoresis. Compared with the placebo, the two drugs significantly suppressed the subjective itching assessed by visual analog scale at all intervals. There were no significant differences in subjective drowsiness and objective cognitive function between drug- and placebo-treated subjects. These results demonstrate that olopatadine seems to be more potent than levocetirizine when administrated in a standard dose. In conclusion, mild to moderate urticaria could be controlled by standard application as described in their information. On the other hand, severe urticaria could be managed by a standard application of olopatadine, but levocetirizine may need an additional dose to control severe urticaria.

摘要

奥洛他定和左西替利嗪的抗组胺作用,在其说明书中标准剂量的应用(奥洛他定 5mg,每日 2 次;左西替利嗪 5mg,每日 1 次),在应用后 11.5 至 24 小时进行了检查。该试验采用双盲、随机、交叉、安慰剂对照研究设计,共纳入 12 名健康志愿者,使用离子电渗技术评估组胺诱导的风团和红晕反应。奥洛他定对 0.1mA 组胺离子电渗引起的风团的抑制作用在给药后 24 小时内持续存在。两种药物在首次给药后 24 小时内几乎完全抑制组胺离子电渗引起的红斑。左西替利嗪每日 1 次给药抑制 0.2mA 诱导的风团反应随时间逐渐减弱,尽管药物对 0.1mA 诱导的红斑几乎完全抑制。奥洛他定甚至完全抑制了 0.2mA 组胺离子电渗引起的风团反应。与安慰剂相比,两种药物在所有时间间隔均显著抑制视觉模拟量表评估的主观瘙痒。药物和安慰剂治疗组之间的主观嗜睡和客观认知功能无显著差异。这些结果表明,奥洛他定在标准剂量给药时似乎比左西替利嗪更有效。总之,按照说明书中的标准用法,轻度至中度荨麻疹可以得到控制。另一方面,严重的荨麻疹可以通过标准剂量的奥洛他定来控制,但左西替利嗪可能需要额外的剂量来控制严重的荨麻疹。

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