Effect of Early Vasopressin vs Norepinephrine on Kidney Failure in Patients With Septic Shock The VANISH Randomized Clinical Trial

被引:394
|
作者
Gordon, Anthony C. [1 ]
Mason, Alexina J. [2 ]
Thirunavukkarasu, Neeraja [3 ]
Perkins, Gavin D. [4 ]
Cecconi, Maurizio [5 ]
Cepkova, Magda [6 ]
Pogson, David G. [7 ]
Aya, Hollmann D. [5 ]
Anjum, Aisha [3 ]
Frazier, Gregory J. [3 ]
Santhakumaran, Shalini [3 ]
Ashby, Deborah [3 ]
Brett, Stephen J. [8 ]
机构
[1] Imperial Coll London, Sect Anaesthet Pain Med & Intens Care Med, Dept Surg & Canc, London W6 8RF, England
[2] London Sch Hyg & Trop Med, Fac Publ Hlth & Policy, London, England
[3] Imperial Coll London, Sch Publ Hlth, Imperial Clin Trials Unit, London W6 8RF, England
[4] Univ Warwick, Warwick Med Sch, Warwick Clin Trials Unit, Coventry, W Midlands, England
[5] St Georges Univ Hosp Natl Hlth Serv Fdn Trust, Anaesthesia & Intens Care Med, London, England
[6] Whittington Hlth Natl Hlth Serv, Intens Care Unit, London, England
[7] Portsmouth Hosp Natl Hlth Serv Trust, Acad Dept Crit Care, Portsmouth, Hants, England
[8] Imperial Coll Healthcare Natl Hlth Serv Trust, Ctr Perioperat & Crit Care Res, London, England
来源
基金
美国国家卫生研究院;
关键词
INFUSION; CORTICOSTEROIDS; THERAPY; INJURY; SEPSIS;
D O I
10.1001/jama.2016.10485
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
IMPORTANCE Norepinephrine is currently recommended as the first-line vasopressor in septic shock; however, early vasopressin use has been proposed as an alternative. OBJECTIVE To compare the effect of early vasopressin vs norepinephrine on kidney failure in patients with septic shock. DESIGN, SETTING, AND PARTICIPANTS A factorial (2x2), double-blind, randomized clinical trial conducted in 18 general adult intensive care units in the United Kingdom between February 2013 and May 2015, enrolling adult patients who had septic shock requiring vasopressors despite fluid resuscitation within a maximum of 6 hours after the onset of shock. INTERVENTIONS Patients were randomly allocated to vasopressin (titrated up to 0.06 U/min) and hydrocortisone (n = 101), vasopressin and placebo (n = 104), norepinephrine and hydrocortisone (n = 101), or norepinephrine and placebo (n = 103). MAIN OUTCOMES AND MEASURES The primary outcomewas kidney failure-free days during the 28-day period after randomization, measured as (1) the proportion of patients who never developed kidney failure and (2) median number of days alive and free of kidney failure for patients who did not survive, who experienced kidney failure, or both. Rates of renal replacement therapy, mortality, and serious adverse events were secondary outcomes. RESULTS A total of 409 patients (median age, 66 years; men, 58.2%) were included in the study, with a median time to study drug administration of 3.5 hours after diagnosis of shock. The number of survivors who never developed kidney failure was 94 of 165 patients (57.0%) in the vasopressin group and 93 of 157 patients (59.2%) in the norepinephrine group (difference, -2.3%[95% CI, -13.0% to 8.5%]). The median number of kidney failure-free days for patients who did not survive, who experienced kidney failure, or both was 9 days (interquartile range [IQR], 1 to -24) in the vasopressin group and 13 days (IQR, 1 to -25) in the norepinephrine group (difference, -4 days [95% CI, -11 to 5]). There was less use of renal replacement therapy in the vasopressin group than in the norepinephrine group (25.4% for vasopressin vs 35.3% for norepinephrine; difference, -9.9% [95% CI, -19.3% to -0.6%]). There was no significant difference in mortality rates between groups. In total, 22 of 205 patients (10.7%) had a serious adverse event in the vasopressin group vs 17 of 204 patients (8.3%) in the norepinephrine group (difference, 2.5%[95% CI, -3.3% to 8.2%]). CONCLUSIONS AND RELEVANCE Among adults with septic shock, the early use of vasopressin compared with norepinephrine did not improve the number of kidney failure-free days. Although these findings do not support the use of vasopressin to replace norepinephrine as initial treatment in this situation, the confidence interval included a potential clinically important benefit for vasopressin, and larger trials may be warranted to assess this further.
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收藏
页码:509 / 518
页数:10
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