Conrad D A, Christenson J C, Waner J L, Marks M I
Pediatr Infect Dis J. 1987 Feb;6(2):152-8. doi: 10.1097/00006454-198702000-00003.
Thirty-three infants with predisposing conditions and/or severely symptomatic with respiratory syncytial virus (RSV) infection were treated with aerosolized ribavirin during a 12-week period at Oklahoma Children's Memorial Hospital. These patients were compared with 97 untreated patients with RSV infection hospitalized during the same epidemic. Despite preconditions which selected for a more seriously ill treatment group, patients who received ribavirin showed prompter resolution of the illness than did untreated controls. Greatest clinical improvement in treated patients occurred between the first and second days of ribavirin therapy; mean ribavirin treatment duration was 4.5 days. Ten of 22 ribavirin-treated patients continued to excrete RSV after conclusion of antiviral therapy. No adverse hematologic, renal or metabolic effects occurred with ribavirin therapy. Our experience with ribavirin therapy during a major epidemic confirms and extends the results of previous controlled evaluations demonstrating this treatment safe and effective in high risk and seriously ill infants with RSV bronchiolitis and bronchopneumonia.
在俄克拉荷马州儿童纪念医院为期12周的时间里,33名患有易感疾病和/或呼吸道合胞病毒(RSV)感染症状严重的婴儿接受了雾化利巴韦林治疗。这些患者与同一疫情期间住院的97名未接受治疗的RSV感染患者进行了比较。尽管选择治疗组的前提条件是病情更严重,但接受利巴韦林治疗的患者比未治疗的对照组病情缓解得更快。接受治疗的患者在利巴韦林治疗的第一天和第二天之间临床改善最为明显;利巴韦林的平均治疗时长为4.5天。22名接受利巴韦林治疗的患者中有10名在抗病毒治疗结束后仍继续排出RSV。利巴韦林治疗未产生不良血液学、肾脏或代谢影响。我们在一次重大疫情期间使用利巴韦林治疗的经验证实并扩展了先前对照评估的结果,表明该治疗方法对患有RSV细支气管炎和支气管肺炎的高危和重症婴儿是安全有效的。