Improved survival of critically ill trauma patients treated with recombinant human erythropoletin

被引:60
作者
Napolitano, Lena M. [1 ]
Fabian, Timothy C. [2 ]
Kelly, Kathleen M. [3 ]
Bailey, Jeffrey A. [4 ]
Block, Ernest F. [5 ]
Langholff, Wayne [6 ]
Enny, Christopher [3 ]
Corwin, Howard L. [7 ]
机构
[1] Univ Michigan, Med Ctr, Dept Surg, Ann Arbor, MI 48109 USA
[2] Univ Tennessee, Hlth Sci Ctr, Dept Surg, Memphis, TN USA
[3] OrthoBiotech Clin Affairs LLC, Bridgewater, NJ USA
[4] St Louis Univ, Med Ctr, Dept Surg, St Louis, MO 63110 USA
[5] Orlando Reg Med Ctr Inc, Dept Surg, Orlando, FL USA
[6] OrthoBiotech Biometr, Bridgewater, NJ USA
[7] Dartmouth Hitchcock Med Ctr, Dept Med & Anesthesiol, Lebanon, NH 03766 USA
来源
JOURNAL OF TRAUMA-INJURY INFECTION AND CRITICAL CARE | 2008年 / 65卷 / 02期
关键词
trauma; anemia; intensive care unit; epoetin alfa; mortality; outcome;
D O I
10.1097/TA.0b013e31817f2c6e
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Background A randomized, double-blind, placebo-controlled, multicenter trial (EPO-2, N = 1,302) in anemic critically ill patients demonstrated a 29-day survival benefit in the trauma subgroup receiving epoetin alfa (mortality 8.9% vs. 4.1%). A second similarly designed trial (EPO-3, N = 1,460) confirmed this survival benefit in the epoetin alfa-treated trauma cohort (mortality 6.7% vs. 3.5%). This analysis presents trauma cohort data from both trials for evaluation of the impact of baseline factors including trauma-specific variables on outcomes. Methods: Patients received 40,000 U epoetin alfa or placebo weekly, for a total of 4 (EPO-2) or 3 (EPO-3) doses, starting on ICU day 3. Kaplan-Meier survival curves for the two groups were compared using the log-rank test. Univariate and multivariate Cox proportional hazard regression methods were used to evaluate relationship between baseline factors and mortality. Results: Demographic and trauma variables at baseline were comparable. Mortality was consistently reduced by approximate to 50% in both studies (EPO-2-day 29 unadjusted HR: 0.46, 95% CI: 0.24-0.89; EPO-3-day 29 unadjusted HR: 0.51, 95% CI: 0.27-0.98.). Adjusting for baseline and trauma variables had minimal effect on hazard ratios for mortality at day 29 (EPO-2-day 29 adjusted HR: 0.50, 95% CI: 0.26-0.97; EPO-3-day 29 adjusted HR: 0.38, 95% CI: 0.19-0.74) and day 140 (EPO-3-adjusted HR: 0.39, 95% CI: 0.21-0.72). In EPO-3, there appeared to be an increase in clinically relevant thrombovascular events in the epoetin alfa treated group (16.4% vs. 12.5%, RR: 1.3, 95% Cl: 0.93-1.85) but not in EPO-2 (11.1 % vs. 13.3 %, R R: 0.84, 95% CI: 0.56-1.28). Conclusion: Epoetin alfa demonstrated a survival advantage in both of the critically ill trauma patient cohorts of two prospective, randomized clinical trials, which was not affected by baseline factors including trauma-specific variables. A definitive study in trauma subjects is warranted.
引用
收藏
页码:285 / 297
页数:13
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