Janai H K, Stutman H R, Zaleska M, Rub B, Eyzaguirre M, Marks M I, Nussbaum E
Division of Pediatric Infectious Diseases, Memorial Miller Children's Hospital, Long Beach, CA 90801-1428.
Pediatr Infect Dis J. 1993 Mar;12(3):214-8. doi: 10.1097/00006454-199303000-00008.
To assess the effect of ribavirin on pulmonary function in infants with respiratory syncytial virus bronchiolitis, we performed a randomized (nonmatched), double blinded, placebo-controlled study of 19 infants with RSV bronchiolitis. Infants with underlying respiratory, cardiac or immunologic disease were excluded. Patients were given ribavirin (10) or placebo (9) via an aerosol generator for 18 hours/day for 3 days. Pulmonary function (dynamic compliance, total lung resistance) was calculated using a pneumotachographic method on Days 1, 2 and 7. Differences between groups on clinical criteria were not found. Approximately one-half of each group showed increased compliance and decreased lung resistance after 24 to 48 hours of therapy. By Day 7 compliance had increased 30% in the placebo group and 210% in the ribavirin-treated infants (P = 0.05). Significant differences in the rate of change of lung resistance were not seen by Day 7. We conclude that previously noted improvements in the early course of respiratory syncytial virus bronchiolitis treated with ribavirin do not appear to be a result of measurable changes in pulmonary function. However, paradoxical increases in airway resistance were not found in patients treated with ribavirin.
为评估利巴韦林对呼吸道合胞病毒细支气管炎患儿肺功能的影响,我们对19例呼吸道合胞病毒细支气管炎患儿进行了一项随机(非配对)、双盲、安慰剂对照研究。排除有潜在呼吸道、心脏或免疫疾病的患儿。通过雾化发生器给予患儿利巴韦林(10例)或安慰剂(9例),每天18小时,持续3天。在第1、2和7天,采用呼吸流速描记法计算肺功能(动态顺应性、总肺阻力)。未发现两组在临床标准上存在差异。每组约一半的患儿在治疗24至48小时后顺应性增加,肺阻力降低。到第7天,安慰剂组的顺应性增加了30%,利巴韦林治疗的患儿增加了210%(P = 0.05)。到第7天,未观察到肺阻力变化率的显著差异。我们得出结论,先前指出的利巴韦林治疗呼吸道合胞病毒细支气管炎早期过程中的改善似乎不是肺功能可测量变化的结果。然而,接受利巴韦林治疗的患者未发现气道阻力反常增加。