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已确诊的成人呼吸窘迫综合征经皮质类固醇治疗成功。

Established adult respiratory distress syndrome successfully treated with corticosteroids.

作者信息

Hooper R G, Kearl R A

机构信息

Charles E. Barrow Heart Lung Center, St. Luke's Medical Center, Phoenix, Ariz., USA.

出版信息

South Med J. 1996 Apr;89(4):359-64. doi: 10.1097/00007611-199604000-00001.

Abstract

In 1990, we described the treatment of established adult respiratory distress syndrome (ARDS) with a sustained course of adrenocortical steroids (ACS). This report updates our experience with an uncontrolled prospective series. Patients with ARDS of more than 3 days' duration were initially given ACS in intravenous dosages of 125 to 250 mg every 6 hours, with tapering every 3 to 4 days. ARDS was present for 3 to 40 days before treatment. The PO2/FIO2 ranged from 45 to 211 (mean, 109) and the injury index from 2 to 4 (mean, 3.25). Nineteen gallium Ga 67 citrate lung scans were obtained in 18 patients. The scans showed diffuse abnormality in all 19 studies, but added no new diagnostic information. We have treated 26 patients, and overall survival was 81% (21/26). When complicating features were present, survival was 64% (9/14). Our uncontrolled, observational experience in treating established ARDS suggests that a sustained course of ACS may improve survival in these severely ill patients.

摘要

1990年,我们描述了采用持续疗程的肾上腺皮质类固醇(ACS)治疗已确诊的成人呼吸窘迫综合征(ARDS)。本报告更新了我们在一项非对照前瞻性系列研究中的经验。病程超过3天的ARDS患者最初静脉注射ACS,剂量为每6小时125至250毫克,每3至4天逐渐减量。治疗前ARDS已存在3至40天。氧分压/吸入氧浓度比值为45至211(平均109),损伤指数为2至4(平均3.25)。18例患者进行了19次枸橼酸镓Ga 67肺扫描。所有19次扫描均显示弥漫性异常,但未提供新的诊断信息。我们共治疗了26例患者,总体生存率为81%(21/26)。存在并发症时,生存率为64%(9/14)。我们在治疗已确诊ARDS方面的非对照观察经验表明,持续疗程的ACS可能会提高这些重症患者的生存率。

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