Duschet P, Schwarz T, Soyer P, Henk A, Hausmaninger H, Gschnait F
Department of Dermatology, Hospital Vienna Lainz, Austria.
Int J Dermatol. 1988 Apr;27(3):193-7. doi: 10.1111/j.1365-4362.1988.tb04932.x.
Sixty-four patients received systemic alpha-interferon (10 million units subcutaneously daily) and 63 received systemic acyclovir (5 mg/kg body weight intravenously thrice daily) in a randomized study of acute herpes zoster. Start of healing, complete healing, development of new skin lesions in the primarily affected and in other dermatomes, and degree and duration of pain were evaluated. Both drugs proved equally clinically efficient without statistically different findings between the two groups; herpes zoster neuralgia was not prevented by either interferon or acyclovir therapy. Minor clinical side effects occurred slightly more frequently during interferon treatment and included fever and nausea. Transient and moderate leukopenia was observed in nearly all patients in the interferon group.
在一项急性带状疱疹的随机研究中,64例患者接受全身性α干扰素(每日皮下注射1000万单位),63例患者接受全身性阿昔洛韦(每日静脉注射3次,每次5mg/kg体重)。评估愈合开始时间、完全愈合情况、主要受累皮区和其他皮节出现新皮肤损害的情况以及疼痛程度和持续时间。两种药物在临床上均显示出同等疗效,两组之间无统计学差异;干扰素或阿昔洛韦治疗均不能预防带状疱疹后神经痛。干扰素治疗期间轻微临床副作用的发生频率略高,包括发热和恶心。几乎所有干扰素组患者均出现短暂性中度白细胞减少。