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首页> 外文期刊>Critical care medicine >Dexamethasone in children mechanically ventilated for lower respiratory tract infection caused by respiratory syncytial virus: A randomized controlled trial.
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Dexamethasone in children mechanically ventilated for lower respiratory tract infection caused by respiratory syncytial virus: A randomized controlled trial.

机译:机械通气的儿童地塞米松用于呼吸道合胞病毒引起的下呼吸道感染:一项随机对照试验。

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OBJECTIVE:: To determine the efficacy of dexamethasone in the treatment of mechanically ventilated children with respiratory syncytial virus-severe lower respiratory tract infection. DESIGN:: International, multicenter, randomized, double-blind, placebo-controlled trial. SETTING:: Twelve pediatric intensive care units. SUBJECTS:: Children (<2 yrs) mechanically ventilated for respiratory syncytial virus lower respiratory tract infection. Children were prestratified for severity of oxygen abnormalities on admission. INTERVENTION:: Intravenous dexamethasone (0.6 mg/kg/day, 48 hrs) or placebo. MEASUREMENTS AND MAIN RESULTS:: A superiority approach was used in the subgroup of patients with mild oxygen abnormalities (arterial partial pressure of oxygen/fractional inspired oxygen concentration [PaO2/Fio2] >200 mm Hg and/or mean arterial pressure 10 cm H2O). Primary outcome was the duration of mechanical ventilation. In the subgroup with mild oxygenation abnormalities, 45 of the 89 included patients received dexamethasone and 44 placebo; in the subgroup with severe oxygenation abnormalities, 28 of the 56 included patients received dexamethasone and 28 placebo. Baseline characteristics in both treatment arms were similar for both subgroups. After the third interim analysis, the trial was stopped early for futility taking the slow enrollment into account. At that time, the median duration (interquartile range) of mechanical ventilation was 137 (91-195) hrs in the dexamethasone- and 139 (117-188) hrs in the placebo-treated patients in the subgroup with mild oxygenation abnormalities (p = .6). In the subgroup with severe oxygenation abnormalities, it was 171 (136-212) hrs in the dexamethasone- and 170 (125-201) hrs in the placebo-treated patients (p = .6). CONCLUSION:: In this prematurely ended trial in children mechanically ventilated for severe respiratory syncytial virus-lower respiratory tract infection, we found no evidence of a beneficial effect of dexamethasone in children with mild oxygenation abnormalities. Neither was evidence found that dexamethasone may prolong mechanical ventilation in those with severe oxygenation abnormalities.
机译:目的:确定地塞米松治疗机械通气患呼吸道合胞病毒严重下呼吸道感染的儿童的疗效。设计::国际,多中心,随机,双盲,安慰剂对照试验。地点:十二个儿科重症监护室。受试者:机械呼吸(小于2岁)的儿童因呼吸道合胞病毒下呼吸道感染。入院时对儿童的氧气异常严重程度进行了预先分类。干预::静脉地塞米松(0.6 mg / kg /天,48小时)或安慰剂。测量和主要结果:优度方法用于轻度氧气异常(氧气的动脉分压/分数吸氧浓度[PaO2 / Fio2]> 200 mm Hg和/或平均动脉压 10 cm H2O)的患者,采用非劣效方法。主要结局是机械通气的持续时间。在轻度氧合异常的亚组中,89例患者中有45例接受了地塞米松治疗,44例接受了安慰剂治疗。在严重氧合异常的亚组中,56名患者中有28名接受了地塞米松治疗,28名接受了安慰剂治疗。两个亚组的两个治疗组的基线特征相似。在进行第三次中期分析后,考虑到注册缓慢,该试验因徒劳无功而提前终止。那时,地塞米松组机械通气的中位时间(四分位范围)为137(91-195)小时,而轻度充氧异常的亚组安慰剂治疗患者为139(117-188)小时(p = .6)。在具有严重氧合异常的亚组中,地塞米松治疗为171(136-212)小时,安慰剂治疗患者为170(125-201)小时(p = .6)。结论:在这项针对严重呼吸道合胞病毒-下呼吸道感染而进行机械通气的儿童的过早结束的试验中,我们没有发现地塞米松对轻度充氧异常儿童的有益作用的证据。没有证据表明地塞米松可以延长严重氧合异常患者的机械通气时间。

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