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利巴韦林治疗实验性呼吸道合胞病毒感染。一项针对年轻人的对照双盲研究。

Ribavirin treatment of experimental respiratory syncytial viral infection. A controlled double-blind study in young adults.

作者信息

Hall C B, Walsh E E, Hruska J F, Betts R F, Hall W J

出版信息

JAMA. 1983 May 20;249(19):2666-70.

PMID:6341640
Abstract

The effect of ribavirin aerosol on experimental respiratory syncytial virus (RSV) infection was evaluated in a double-blind controlled study of 16 young adult volunteers. Two days after intranasal inoculation with RSV, half of the subjects were treated with a small-particle aerosol of ribavirin and half with placebo for a total of 12 hours each day for three days. Seven of eight placebo-treated and six of eight ribavirin-treated subjects became infected. Viral shedding was diminished in the ribavirin-treated group. The proportion of infected volunteers still shedding virus on days 6 through 9 was significantly less than in the placebo-treated group. Ribavirin appeared to have no effect on minor upper respiratory tract signs, but systemic complaints and fever occurred significantly less often in the ribavirin-treated group. Ribavirin aerosol therapy was well tolerated and produced no significant changes in pulmonary function test results or signs of toxicity. This suggests that such therapy might be further evaluated in infants with RSV lower respiratory tract disease.

摘要

在一项针对16名年轻成年志愿者的双盲对照研究中,评估了利巴韦林气雾剂对实验性呼吸道合胞病毒(RSV)感染的影响。在经鼻接种RSV两天后,一半受试者接受利巴韦林小颗粒气雾剂治疗,另一半接受安慰剂治疗,每天各治疗12小时,持续三天。接受安慰剂治疗的8名受试者中有7名被感染,接受利巴韦林治疗的8名受试者中有6名被感染。利巴韦林治疗组的病毒排出量减少。在第6至9天仍有病毒排出的受感染志愿者比例明显低于安慰剂治疗组。利巴韦林似乎对轻微的上呼吸道症状没有影响,但利巴韦林治疗组全身不适和发热的发生率明显较低。利巴韦林气雾剂治疗耐受性良好,肺功能测试结果或毒性体征未出现显著变化。这表明这种治疗方法可能需要在患有RSV下呼吸道疾病的婴儿中进一步评估。

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