Resuscitating the microcirculation in sepsis: The central role of nitric oxide, emerging concepts for novel therapies, and challenges for clinical trials

被引:194
作者
Trzeciak, Stephen [1 ,3 ]
Cinel, Ismail [3 ]
Dellinger, R. Phillip [3 ]
Shapiro, Nathan I.
Arnold, Ryan C. [1 ]
Parrillo, Joseph E. [2 ,3 ]
Hollenberg, Steven M. [2 ,3 ]
机构
[1] Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Cooper Univ Hosp, Dept Emergency Med, Camden, NJ 08103 USA
[2] Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Cooper Univ Hosp, Dept Med,Div Cardiovasc Dis, Camden, NJ 08103 USA
[3] Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Cooper Univ Hosp, Dept Med,Div Crit Care Med, Camden, NJ 08103 USA
关键词
microcirculation; sepsis; severe sepsis; septic shock; resuscitation; endothelium; nitric oxide; multi-organ failure;
D O I
10.1111/j.1553-2712.2008.00109.x
中图分类号
R4 [临床医学];
学科分类号
1002 [临床医学]; 100602 [中西医结合临床];
摘要
Microcirculatory dysfunction is a critical element of the pathogenesis of severe sepsis and septic shock. In this Bench-to-Bedside review, we present: 1) the central role of the microcirculation in the pathophysiology of sepsis; 2) new translational research techniques of in vivo video microscopy for assessment of microcirculatory flow in human subjects; 3) clinical investigations that reported associations between microcirculatory dysfunction and outcome in septic patients; 4) the potential role of novel agents to "rescue" the microcirculation in sepsis; 5) current challenges facing this emerging field of clinical investigation; and 6) a framework for the design of future clinical trials aimed to determine the impact of novel agents on microcirculatory flow and organ failure in patients with sepsis. We specifically focus this review on the central role and vital importance of the nitric oxide (NO) molecule in maintaining microcirculatory homeostasis and patency, especially when the microcirculation sustains an insult (as with sepsis). We also present the scientific rationale for clinical trials of exogenous NO administration to treat microcirculatory dysfunction and augment microcirculatory blood flow in early sepsis therapy.
引用
收藏
页码:399 / 413
页数:15
相关论文
共 151 条
[1]
Mechanisms of sepsis-induced organ dysfunction [J].
Abraham, Edward ;
Singer, Mervyn .
CRITICAL CARE MEDICINE, 2007, 35 (10) :2408-2416
[2]
The role of the endothelium in severe sepsis and multiple organ dysfunction syndrome [J].
Aird, WC .
BLOOD, 2003, 101 (10) :3765-3777
[3]
Endothelium as an organ system [J].
Aird, WC .
CRITICAL CARE MEDICINE, 2004, 32 (05) :S271-S279
[4]
Vascular bed-specific hemostasis: Role of endothelium in pathogenesis [J].
Aird, WC .
CRITICAL CARE MEDICINE, 2001, 29 (07) :S28-S34
[5]
Epidemiology of severe sepsis in the United States: Analysis of incidence, outcome, and associated costs of care [J].
Angus, DC ;
Linde-Zwirble, WT ;
Lidicker, J ;
Clermont, G ;
Carcillo, J ;
Pinsky, MR .
CRITICAL CARE MEDICINE, 2001, 29 (07) :1303-1310
[6]
Caring for the critically ill patient - Challenges and opportunities [J].
Angus, Derek C. .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2007, 298 (04) :456-458
[7]
Abnormal tissue oxygenation and cardiovascular changes in endotoxemia [J].
Anning, PB ;
Sair, M ;
Winlove, CP ;
Evans, TW .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1999, 159 (06) :1710-1715
[8]
INHIBITION OF NITRIC-OXIDE SYNTHESIS CAUSES MYOCARDIAL-ISCHEMIA IN ENDOTOXEMIC RATS [J].
AVONTUUR, JAM ;
BRUINING, HA ;
INCE, C .
CIRCULATION RESEARCH, 1995, 76 (03) :418-425
[9]
ENDOTHELIUM-DEPENDENT INHIBITION OF PLATELET-AGGREGATION [J].
AZUMA, H ;
ISHIKAWA, M ;
SEKIZAKI, S .
BRITISH JOURNAL OF PHARMACOLOGY, 1986, 88 (02) :411-415
[10]
BAKER CH, 1984, CIRC SHOCK, V12, P165