Early Use of Norepinephrine in Septic Shock Resuscitation (CENSER) A Randomized Trial

被引:167
|
作者
Permpikul, Chairat [1 ]
Tongyoo, Surat [1 ]
Viarasilpa, Tanuwong [1 ]
Trainarongsakul, Thavinee [1 ]
Chakorn, Tipa [2 ]
Udompanturak, Suthipol [3 ]
机构
[1] Mahidol Univ, Siriraj Hosp, Fac Med, Dept Med, Bangkok, Thailand
[2] Mahidol Univ, Siriraj Hosp, Fac Med, Dept Emergency Med, Bangkok, Thailand
[3] Mahidol Univ, Siriraj Hosp, Fac Med, Off Res & Dev, Bangkok, Thailand
关键词
septic shock; norepinephrine; resuscitation; early norepinephrine administration; sepsis with hypotension; GOAL-DIRECTED THERAPY; SEVERE SEPSIS; BLOOD-FLOW;
D O I
10.1164/rccm.201806-1034OC
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Rationale: Recent retrospective evidence suggests the efficacy of early norepinephrine administration during resuscitation; however, prospective data to support this assertion are scarce. Objectives: To conduct a phase II trial evaluating the hypothesis that early low-dose norepinephrine in adults with sepsis with hypotension increases shock control by 6 hours compared with standard care. Methods: This single-center, randomized, double-blind, placebo-controlled clinical trial was conducted at Siriraj Hospital, Bangkok, Thailand. The study enrolled 310 adults diagnosed with sepsis with hypotension. The patients were randomly divided into two groups: early norepinephrine (n = 155) and standard treatment (n = 155). The primary outcome was shock control rate (defined as achievement of mean arterial blood pressure >= 65mm Hg, with urine flow >= 0.5 ml/kg/h for 2 consecutive hours, or decreased serum lactate >= 10% from baseline) by 6 hours after diagnosis. Measurements and Main Results: The patients in both groups were well matched in background characteristics and disease severity. Median time from emergency room arrival to norepinephrine administration was significantly shorter in the early norepinephrine group (93 vs. 192 min; P < 0.001). Shock control rate by 6 hours was significantly higher in the early norepinephrine group (118/155 [76.1%] vs. 75/155 [48.4%]; P < 0.001). The 28-day mortality was not different between groups: 24/155 (15.5%) in the early norepinephrine group versus 34/155 (21.9%) in the standard treatment group (P= 0.15). The early norepinephrine group was associated with lower incidences of cardiogenic pulmonary edema (22/155 [14.4%] vs. 43/155 [27.7%]; P = 0.004) and new-onset arrhythmia (17/155 [11%] vs. 31/155 [20%]; P= 0.03). Conclusions: Early norepinephrine was significantly associated with increased shock control by 6 hours. Further studies are needed before this approach is introduced in clinical resuscitation practice.
引用
收藏
页码:1097 / 1105
页数:9
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