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延长甲泼尼龙治疗对未缓解的急性呼吸窘迫综合征的影响:一项随机对照试验。

Effect of prolonged methylprednisolone therapy in unresolving acute respiratory distress syndrome: a randomized controlled trial.

作者信息

Meduri G U, Headley A S, Golden E, Carson S J, Umberger R A, Kelso T, Tolley E A

机构信息

Baptist Memorial Hospitals, Veterans Affairs Medical Center, University of Tennessee, Memphis, USA.

出版信息

JAMA. 1998 Jul 8;280(2):159-65. doi: 10.1001/jama.280.2.159.

Abstract

CONTEXT

No pharmacological therapeutic protocol has been found effective in modifying the clinical course of acute respiratory distress syndrome (ARDS) and mortality remains greater than 50%.

OBJECTIVE

To determine the effects of prolonged methylprednisolone therapy on lung function and mortality in patients with unresolving ARDS.

DESIGN

Randomized, double-blind, placebo-controlled trial.

SETTING

Medical intensive care units of 4 medical centers.

PARTICIPANTS

Twenty-four patients with severe ARDS who had failed to improve lung injury score (LIS) by the seventh day of respiratory failure.

INTERVENTIONS

Sixteen patients received methylprednisolone and 8 received placebo. Methylprednisolone dose was initially 2 mg/kg per day and the duration of treatment was 32 days. Four patients whose LIS failed to improve by at least 1 point after 10 days of treatment were blindly crossed over to the alternative treatment.

MAIN OUTCOME MEASURES

Primary outcome measures were improvement in lung function and mortality. Secondary outcome measures were improvement in multiple organ dysfunction syndrome (MODS) and development of nosocomial infections.

RESULTS

Physiological characteristics at the onset of ARDS were similar in both groups. At study entry (day 9 [SD, 3] of ARDS), the 2 groups had similar LIS, ratios of PaO2 to fraction of inspired oxygen (FIO2), and MODS scores. Changes observed by study day 10 for methylprednisolone vs placebo were as follows: reduced LIS (mean [SEM], 1.7 [0.1] vs 3.0 [0.2]; P<.001); improved ratio of PaO2 to FIO2 (mean [SEM], 262 [19] vs 148 [35]; P<.001); decreased MODS score (mean [SEM], 0.7 [0.2] vs 1.8 [0.3]; P<.001); and successful extubation (7 vs 0; P=.05). For the treatment group vs the placebo group, mortality associated with the intensive care unit was 0 (0%) of 16 vs 5 (62%) of 8 (P=.002) and hospital-associated mortality was 2 (12%) of 16 vs 5 (62%) of 8 (P=.03). The rate of infections per day of treatment was similar in both groups, and pneumonia was frequently detected in the absence of fever.

CONCLUSIONS

In this study, prolonged administration of methylprednisolone in patients with unresolving ARDS was associated with improvement in lung injury and MODS scores and reduced mortality.

摘要

背景

尚未发现有药理学治疗方案能有效改变急性呼吸窘迫综合征(ARDS)的临床病程,其死亡率仍高于50%。

目的

确定延长甲泼尼龙治疗对未缓解的ARDS患者肺功能和死亡率的影响。

设计

随机、双盲、安慰剂对照试验。

地点

4个医疗中心的医学重症监护病房。

参与者

24例严重ARDS患者,这些患者在呼吸衰竭第7天时肺损伤评分(LIS)未改善。

干预措施

16例患者接受甲泼尼龙治疗,8例患者接受安慰剂治疗。甲泼尼龙初始剂量为每日2mg/kg,治疗持续32天。4例患者在治疗10天后LIS未改善至少1分,被随机交叉接受替代治疗。

主要结局指标

主要结局指标为肺功能改善和死亡率。次要结局指标为多器官功能障碍综合征(MODS)改善和医院感染的发生情况。

结果

两组ARDS发病时的生理特征相似。在研究入组时(ARDS第9天[标准差,3天]),两组的LIS、动脉血氧分压与吸入氧分数(FIO2)比值及MODS评分相似。在研究第10天时,甲泼尼龙组与安慰剂组相比观察到的变化如下:LIS降低(均值[标准误],1.7[0.1]对3.0[0.2];P<0.001);动脉血氧分压与FIO2比值改善(均值[标准误],262[19]对148[35];P<0.001);MODS评分降低(均值[标准误],0.7[0.2]对1.8[0.3];P<0.001);成功脱机(7例对0例;P=0.05)。治疗组与安慰剂组相比,重症监护病房相关死亡率为16例中的0例(0%)对8例中的5例(62%)(P=0.002),医院相关死亡率为16例中的2例(12%)对8例中的5例(62%)(P=0.03)。两组每日治疗的感染率相似,且在无发热情况下常检测到肺炎。

结论

在本研究中,对未缓解的ARDS患者延长甲泼尼龙给药与肺损伤和MODS评分改善及死亡率降低相关。

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