Hall C B, McBride J T, Gala C L, Hildreth S W, Schnabel K C
JAMA. 1985 Dec 6;254(21):3047-51.
Aerosolized ribavirin was evaluated in the treatment of respiratory syncytial virus lower respiratory tract disease in 53 infants, 36 of whom had underlying diseases. Of the total infants, 26 were studied in a double-blind, placebo-controlled manner; 14 received ribavirin and 12 received placebo, a water aerosol, for an average of five days. When the infants with bronchopulmonary dysplasia and congenital heart disease treated with ribavirin were compared with those receiving placebo, the treated infants showed a significantly faster rate of improvement in their illness severity score. The degree of improvement in the total group of infants receiving ribavirin compared with those receiving placebo was similarly greater, and at the end of therapy significantly greater improvement was also demonstrated in their arterial blood gas values and in the amount of virus shed from their nasal washes. No toxic or adverse effects of the aerosol therapy were observed in any of the 53 infants studied, and resistance to ribavirin did not develop in any of the respiratory syncytial virus strains isolated, despite prolonged treatment in some of the more ill infants.
对53名婴儿使用雾化利巴韦林治疗呼吸道合胞病毒引起的下呼吸道疾病,其中36名婴儿有基础疾病。在所有婴儿中,26名采用双盲、安慰剂对照方式进行研究;14名接受利巴韦林治疗,12名接受安慰剂(一种水雾剂)治疗,平均治疗5天。将接受利巴韦林治疗的支气管肺发育不良和先天性心脏病婴儿与接受安慰剂治疗的婴儿进行比较时,接受治疗的婴儿疾病严重程度评分改善速度明显更快。与接受安慰剂的婴儿相比,接受利巴韦林治疗的婴儿总体改善程度同样更大,并且在治疗结束时,他们的动脉血气值和鼻腔冲洗液中排出的病毒量也显示出明显更大的改善。在所研究的53名婴儿中,未观察到雾化治疗的任何毒性或不良反应,并且尽管对一些病情较重的婴儿进行了长时间治疗,但在所分离出的任何呼吸道合胞病毒菌株中均未产生对利巴韦林的耐药性。