Prompt Administration of Antibiotics and Fluids in the Treatment of Sepsis: A Murine Trial

被引:26
作者
Lewis, Anthony J. [1 ]
Griepentrog, John E. [1 ]
Zhang, Xianghong [1 ]
Angus, Derek C. [2 ,3 ]
Seymour, Christopher W. [2 ,3 ]
Rosengart, Matthew R. [1 ,2 ,3 ]
机构
[1] Univ Pittsburgh, Dept Surg, 497 Scaife Hall, Pittsburgh, PA 15260 USA
[2] Univ Pittsburgh, Dept Crit Care Med, Pittsburgh, PA 15260 USA
[3] Univ Pittsburgh, Dept Crit Care Med, Clin Res Invest & Syst Modeling Acute Illness Ctr, Pittsburgh, PA 15260 USA
基金
美国国家卫生研究院;
关键词
animal model; antibiotics; resuscitation; sepsis; telemetry; SEPTIC SHOCK; CRITICAL DETERMINANT; UNITED-STATES; MORTALITY; SURVIVAL; MODEL; INITIATION; CYTOKINE; CARE; EPIDEMIOLOGY;
D O I
10.1097/CCM.0000000000003004
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Objectives: Sepsis, the acute organ dysfunction caused by a dysregulated host response to infection, poses a serious public health burden. Current management includes early detection, initiation of antibiotics and fluids, and source control as necessary. Although observational data suggest that delays of even a few hours in the initiation of antibiotics or IV fluids is associated with survival, these findings are controversial. There are no randomized data in humans, and prior animal studies studied time from experimental manipulation, not from the onset of clinical features of sepsis. Using a recently developed murine cecal ligation and puncture model that precisely monitors physiologic deterioration, we hypothesize that incremental hourly delays in the first dose of antibiotics, in the first bolus of fluid resuscitation, or a combination of the two at a clinically relevant point of physiologic deterioration during polymicrobial sepsis will shorten survival. Design: Randomized laboratory animal experimental trial. Setting: University basic science laboratory. Subjects: Male C57BL/6J, female C57BL/6J, aged (40-50wk old) male C57BL/6J, and BALB/C mice. Interventions: Mice (n = 200) underwent biotelemetry-enhanced cecal ligation and puncture and were randomized after meeting validated criteria for acute physiologic deterioration. Treatment groups consisted of a single dose of imipenem/cilastatin, a single bolus of 30mL/kg fluid resuscitation, or a combination of the two. Mice were allocated to receive treatment at the time of meeting deterioration criteria, after a 2-hour delay or after a 4-hour delay. Measurements and Main Results: Hourly delays in the initiation of antibiotic therapy led to progressively shortened survival in our model (p < 0.001). The addition of fluid resuscitation was unable to rescue animals, which received treatment 4 hours after meeting enrollment criteria. Systemic inflammation was increased, and host physiology was increasingly deranged with hourly delays to antibiotics. Conclusions: We conclude that antibiotic therapy is highly time sensitive, and efforts should be made to deliver this critical therapy as early as possible in sepsis, perhaps extending into the first point of medical contact outside the hospital.
引用
收藏
页码:E426 / E434
页数:9
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