Prolonged glucocorticoid treatment is associated with improved ARDS outcomes: analysis of individual patients' data from four randomized trials and trial-level meta-analysis of the updated literature

被引:181
作者
Meduri, G. Umberto [1 ]
Bridges, Lisa [1 ]
Shih, Mei-Chiung [2 ,3 ]
Marik, Paul E. [4 ]
Siemieniuk, Reed A. C. [5 ,6 ]
Kocak, Mehmet [7 ]
机构
[1] Vet Affairs Med Ctr, Dept Med, Div Pulm Crit Care & Sleep Med, 111 1030 Jefferson Ave,Suite Room CW444, Memphis, TN 38104 USA
[2] Cooperat Studies Program Coordinating Ctr, Dept Vet Affairs, Palo Alto, CA USA
[3] Stanford Univ, Dept Hlth Res & Policy, Stanford, CA 94305 USA
[4] Eastern Virginia Med Sch, Dept Med, Div Pulm & Crit Care Med, Norfolk, VA 23501 USA
[5] McMaster Univ, Dept Clin Epidemiol & Biostat, Hamilton, ON, Canada
[6] Univ Toronto, Dept Med, Toronto, ON, Canada
[7] Univ Tennessee, Ctr Hlth Sci, Dept Prevent Med, Memphis, TN 38163 USA
关键词
Adult respiratory distress syndrome; Glucocorticoid treatment; Mechanical ventilation; Survival; RESPIRATORY-DISTRESS-SYNDROME; COMMUNITY-ACQUIRED PNEUMONIA; METHYLPREDNISOLONE TREATMENT; INFLAMMATORY CYTOKINES; SYSTEMIC INFLAMMATION; PERSISTENT ELEVATION; STEROID TREATMENT; CORTICOSTEROIDS; THERAPY; MANAGEMENT;
D O I
10.1007/s00134-015-4095-4
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
To investigate the effect of prolonged glucocorticoid treatment for patients with acute respiratory distress syndrome (ARDS). We conducted two sets of intention-to-treat analyses: (1) a primary analysis of individual patients' data (IPD) of four randomized controlled trials (RCTs) which investigated methylprednisolone treatment (n = 322) and (2) a trial-level meta-analysis incorporating four additional RCTs which investigated hydrocortisone treatment in early ARDS (n = 297). We standardized definitions to derive outcomes in all datasets. The primary outcome for the IPD analysis was time to achieving unassisted breathing (UAB) by study day 28. Secondary outcomes included mechanical ventilation (MV) and intensive care unit (ICU)-free days, hospital mortality, and time to hospital mortality by day 28. By study day 28, compared to the placebo group, the methylprednisolone group had fewer patients who died before achieving UAB (12 vs. 29 %; p < 0.001) and more patients who achieved UAB (80 vs. 50 %; p < 0.001). In the methylprednisolone group, time to achieving UAB was shorter [hazard ratio 2.59, 95 % confidence interval (CI) 1.95-3.43; p < 0.001], and hospital mortality was decreased (20 vs. 33 %; p = 0.006), leading to increased MV (13.3 +/- A 11.8 vs. 7.6 +/- A 5.7; p < 0.001) and ICU-free days (10.8 +/- A 0.71 vs. 6.4 +/- A 0.85; p < 0.001). In those patients randomized before day 14 of ARDS onset, the trial-level meta-analysis indicated decreased hospital mortality (36 vs. 49 %; risk ratio 0.76, 95 % CI 0.59-0.98, I (2) = 17 %, p = 0.035; moderate certainty). Treatment was not associated with increased risk for infections (risk ratio 0.77, 95 % CI 0.56-1.08, I (2) = 26 %; p = 0.13; moderate certainty). Prolonged methylprednisolone treatment accelerates the resolution of ARDS, improving a broad spectrum of interrelated clinical outcomes and decreasing hospital mortality and healthcare utilization.
引用
收藏
页码:829 / 840
页数:12
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