Effect of Aspirin on Development of ARDS in At-Risk Patients Presenting to the Emergency Department The LIPS-A Randomized Clinical Trial

被引:171
作者
Kor, Daryl J. [1 ]
Carter, Rickey E. [2 ]
Park, Pauline K. [3 ]
Festic, Emir [4 ]
Banner-Goodspeed, Valerie M. [5 ]
Hinds, Richard [1 ]
Talmor, Daniel [6 ]
Gajic, Ognjen [7 ]
Ware, Lorraine B. [8 ,9 ]
Gong, Michelle Ng [10 ]
机构
[1] Mayo Clin, Coll Med, Dept Anesthesiol, Rochester, MN 55905 USA
[2] Mayo Clin, Coll Med, Dept Hlth Sci Res, Div Biomed Stat & Informat, Rochester, MN 55905 USA
[3] Univ Michigan, Sch Med, Dept Surg, Ann Arbor, MI USA
[4] Mayo Clin, Coll Med, Dept Med, Jacksonville, FL 32224 USA
[5] Beth Israel Deaconess Med Ctr, Boston, MA 02215 USA
[6] Harvard Univ, Beth Israel Deaconess Med Ctr, Dept Anaesthesia, Sch Med, Boston, MA 02215 USA
[7] Mayo Clin, Coll Med, Dept Med, Rochester, MN 55905 USA
[8] Vanderbilt Univ, Sch Med, Dept Pathol & Med, Nashville, TN 37212 USA
[9] Vanderbilt Univ, Sch Med, Dept Microbiol & Immunol, Nashville, TN 37212 USA
[10] Albert Einstein Coll Med, Dept Med, Bronx, NY 10467 USA
来源
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION | 2016年 / 315卷 / 22期
关键词
ACUTE LUNG INJURY; RESPIRATORY-DISTRESS-SYNDROME; INTENSIVE-CARE-UNIT; 15-EPI-LIPOXIN A(4); THERAPY; MORTALITY; PREVENTION; RESOLUTION; PLATELETS;
D O I
10.1001/jama.2016.6330
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
IMPORTANCE Management of acute respiratory distress syndrome (ARDS) remains largely supportive. Whether early intervention can prevent development of ARDS remains unclear. OBJECTIVE To evaluate the efficacy and safety of early aspirin administration for the prevention of ARDS. DESIGN, SETTING, AND PARTICIPANTS A multicenter, double-blind, placebo-controlled, randomized clinical trial conducted at 16 US academic hospitals. Between January 2, 2012, and November 17, 2014, 7673 patients at risk for ARDS (Lung Injury Prediction Score >= 4) in the emergency department were screened and 400 were randomized. Ten patients were excluded, leaving 390 in the final modified intention-to-treat analysis cohort. INTERVENTIONS Administration of aspirin, 325-mg loading dose followed by 81 mg/d (n = 195) or placebo (n = 195) within 24 hours of emergency department presentation and continued to hospital day 7, discharge, or death. MAIN OUTCOMES AND MEASURES The primary outcome was the development of ARDS by study day 7. Secondary measures included ventilator-free days, hospital and intensive care unit length of stay, 28-day and 1-year survival, and change in serum biomarkers associated with ARDS. A final a level of.0737 (a = .10 overall) was required for statistical significance of the primary outcome. RESULTS Among 390 analyzed patients (median age, 57 years; 187 [48%] women), median (IQR) hospital length of stay was 6 (3-10) days. Administration of aspirin, compared with placebo, did not significantly reduce the incidence of ARDS at 7 days (OR, 1.24; 92.6% CI, 0.67-2.31). No significant differences were seen in secondary outcomes or adverse events. [GRAPHICS] CONCLUSIONS AND RELEVANCE Among at-risk patients presenting to the ED, the use of aspirin compared with placebo did not reduce the risk of ARDS at 7 days. The findings of this phase 2b trial do not support continuation to a larger phase 3 trial.
引用
收藏
页码:2406 / 2414
页数:9
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