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利巴韦林对其他情况良好但患有呼吸道合胞病毒相关呼吸衰竭婴儿的疗效。儿科重症研究组。

Effectiveness of ribavirin in otherwise well infants with respiratory syncytial virus-associated respiratory failure. Pediatric Critical Study Group.

作者信息

Moler F W, Steinhart C M, Ohmit S E, Stidham G L

机构信息

Department of Pediatrics and Communicable Diseases, University of Michigan, Ann Arbor, USA.

出版信息

J Pediatr. 1996 Mar;128(3):422-8. doi: 10.1016/s0022-3476(96)70294-9.

Abstract

OBJECTIVE

To examine ribavirin's effectiveness in otherwise well infants with respiratory syncytial virus (RSV)-associated respiratory failure.

DESIGN

Prospective multicenter cohort study.

SETTING

Pediatric critical care units affiliated with the Pediatric Critical Care Study Group; 38 centers from the United States and Canada participated.

PATIENTS

Infants with RSV-associated respiratory failure undergoing mechanical ventilation.

INTERVENTIONS

None.

MEASUREMENTS AND MAIN RESULTS

Data collected included demographic information; dates of hospitalization, intensive care, and mechanical ventilation; all patient diagnoses; reason for tracheal intubation; dates of ribavirin use before and during mechanical ventilation; time in hours after intubation until ribavirin administration; Pediatric Risk of Mortality (PRISM) score; and outcome. A total of 439 patients received mechanical ventilation for RSV-associated respiratory failure; 223 were classified as previously well and met entry criteria. Ninety-one infants (41%) received ribavirin during mechanical ventilation. The PRISM scores during the initial 24 hours of intensive care and blood gas measurements before intubation were similar for patients who received ribavirin versus those who did not. Use of ribavirin during mechanical ventilation was associated with prolonged duration of mechanical ventilation (p < 0.01) in a multivariate model that controlled for patient age, gender, prematurity status, and use of ribavirin before intubation. Subgroup analysis of mechanical ventilation days for previously well patients was 5.0 +/- 4.2 in the no-ribavirin group versus 6.4 +/- 5.0 in the ribavirin group (p < 0.05) and for well premature infants was 6.3 +/- 4.9 in the no-ribavirin group versus 9.0 +/- 6.3 in the ribavirin group (p < 0.01). The mortality rates for the term and the premature groups were similar for treated and untreated patients.

CONCLUSIONS

Ribavirin administration during mechanical ventilation to previously well infants with RSV infection was not associated with reductions in either mortality rates or duration of mechanical ventilation. Additional clinical effectiveness studies are required to define specific groups in which the use of aerosolized ribavirin is indicated.

摘要

目的

研究利巴韦林对其他方面健康但患有呼吸道合胞病毒(RSV)相关呼吸衰竭的婴儿的疗效。

设计

前瞻性多中心队列研究。

地点

隶属于儿科重症监护研究组的儿科重症监护病房;美国和加拿大的38个中心参与。

患者

患有RSV相关呼吸衰竭且正在接受机械通气的婴儿。

干预措施

无。

测量指标及主要结果

收集的数据包括人口统计学信息;住院、重症监护和机械通气日期;所有患者诊断结果;气管插管原因;机械通气前及通气期间使用利巴韦林的日期;插管后至使用利巴韦林的小时数;儿科死亡风险(PRISM)评分;以及结局。共有439例患者因RSV相关呼吸衰竭接受机械通气;223例被归类为之前健康且符合入选标准。91例婴儿(41%)在机械通气期间接受了利巴韦林治疗。接受利巴韦林治疗的患者与未接受治疗的患者相比,在重症监护最初24小时内的PRISM评分以及插管前的血气测量结果相似。在控制了患者年龄、性别、早产状态以及插管前利巴韦林使用情况的多变量模型中,机械通气期间使用利巴韦林与机械通气时间延长相关(p < 0.01)。对之前健康患者的机械通气天数进行亚组分析,未使用利巴韦林组为5.0±4.2天,使用利巴韦林组为6.4±5.0天(p < 0.05);对于健康早产儿,未使用利巴韦林组为6.3±4.9天,使用利巴韦林组为9.0±6.3天(p < 0.01)。足月组和早产组中,接受治疗和未接受治疗患者的死亡率相似。

结论

对之前健康且感染RSV的婴儿在机械通气期间使用利巴韦林,与死亡率降低或机械通气时间缩短均无关。需要进行更多临床疗效研究来确定适合使用雾化利巴韦林的特定人群。

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