Bernard G R, Luce J M, Sprung C L, Rinaldo J E, Tate R M, Sibbald W J, Kariman K, Higgins S, Bradley R, Metz C A
Department of Medicine and Biomedical Engineering, Vanderbilt School of Medicine, Nashville, TN 37232.
N Engl J Med. 1987 Dec 17;317(25):1565-70. doi: 10.1056/NEJM198712173172504.
Corticosteroids are widely used as therapy for the adult respiratory distress syndrome (ARDS) without proof of efficacy. We conducted a prospective, randomized, double-blind, placebo-controlled trial of methylprednisolone therapy in 99 patients with refractory hypoxemia, diffuse bilateral infiltrates on chest radiography and absence of congestive heart failure documented by pulmonary-artery catheterization. The causes of ARDS included sepsis (27 percent), aspiration pneumonia (18 percent), pancreatitis (4 percent), shock (2 percent), fat emboli (1 percent), and miscellaneous causes or more than one cause (42 percent). Fifty patients received methylprednisolone (30 mg per kilogram of body weight every six hours for 24 hours), and 49 received placebo according to the same schedule. Serial measurements were made of pulmonary shunting, the ratio of partial pressure of arterial oxygen to partial pressure of alveolar oxygen, the chest radiograph severity score, total thoracic compliance, and pulmonary-artery pressure. We observed no statistical differences between groups in these characteristics upon entry or during the five days after entry. Forty-five days after entry there were no differences between the methylprednisolone and placebo groups in mortality (respectively, 30 of 50 [60 percent; 95 percent confidence interval, 46 to 74] and 31 of 49 [63 percent; 95 percent confidence interval, 49 to 77]; P = 0.74) or in the reversal of ARDS (18 of 50 [36 percent] vs. 19 of 49 [39 percent]; P = 0.77). However, the relatively wide confidence intervals in the mortality data make it impossible to exclude a small effect of treatment. Infectious complications were similar in the methylprednisolone group (8 of 50 [16 percent]) and the placebo group (5 of 49 [10 percent]; P = 0.60). Our data suggest that in patients with established ARDS due to sepsis, aspiration, or a mixed cause, high-dose methylprednisolone does not affect outcome.
皮质类固醇被广泛用作成人呼吸窘迫综合征(ARDS)的治疗方法,但尚无疗效证据。我们对99例难治性低氧血症、胸部X线片显示双侧弥漫性浸润且经肺动脉导管检查证实无充血性心力衰竭的患者进行了一项前瞻性、随机、双盲、安慰剂对照试验,以研究甲基强的松龙的治疗效果。ARDS的病因包括败血症(27%)、吸入性肺炎(18%)、胰腺炎(4%)、休克(2%)、脂肪栓塞(1%)以及其他病因或多种病因并存(42%)。50例患者接受甲基强的松龙治疗(每6小时每千克体重30毫克,共24小时),49例患者按照相同方案接受安慰剂治疗。对肺分流、动脉血氧分压与肺泡氧分压之比、胸部X线片严重程度评分、总胸壁顺应性和肺动脉压进行了系列测量。我们观察到两组在入组时或入组后的五天内,这些特征没有统计学差异。入组45天后,甲基强的松龙组和安慰剂组在死亡率(分别为50例中的30例[60%;95%可信区间,46至74]和49例中的31例[63%;95%可信区间,49至77];P = 0.74)或ARDS逆转情况(50例中的18例[36%]对49例中的19例[39%];P = 0.77)方面没有差异。然而,死亡率数据中相对较宽的可信区间使得无法排除治疗有小的效果。甲基强的松龙组(50例中的8例[16%])和安慰剂组(49例中的5例[10%];P = 0.60)的感染并发症相似。我们的数据表明,对于因败血症、吸入或混合病因导致的已确诊ARDS患者,大剂量甲基强的松龙不影响治疗结果。