Bench-to-bedside review: Sepsis, severe sepsis and septic shock - does the nature of the infecting organism matter?

被引:48
作者
Gao, Hongmei [1 ]
Evans, Timothy W. [1 ]
Finney, Simon J. [1 ]
机构
[1] Royal Brompton Hosp, Adult Intens Care Unit, London SW3 6NP, England
关键词
D O I
10.1186/cc6862
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
International guidelines concerning the management of patients with sepsis, septic shock and multiple organ failure make no reference to the nature of the infecting organism. Indeed, most clinical signs of sepsis are nonspecific. In contrast, in vitro data suggest that there are mechanistic differences between bacterial, viral and fungal sepsis, and imply that pathogenetic differences may exist between subclasses such as Gram-negative and Gram-positive bacteria. These differences are reflected in different cytokine profiles and mortality rates associated with Gram-positive and Gram-negative sepsis in humans. They also suggest that putative anti-mediator therapies may act differently according to the nature of an infecting organism. Data from some clinical trials conducted in severe sepsis support this hypothesis. It is likely that potential new therapies targeting, for example, Toll-like receptor pathways will require knowledge of the infecting organism. The advent of new technologies that accelerate the identification of infectious agents and their antimicrobial sensitivities may allow better tailored anti-mediator therapies and administration of antibiotics with narrow spectra and known efficacy.
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页数:6
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共 59 条
[1]   Divergent trophoblast responses to bacterial products mediated by TLRs [J].
Abrahams, VM ;
Bole-Aldo, P ;
Kim, YM ;
Straszewski-Chavez, SL ;
Chaiworapongsa, T ;
Romero, R ;
Mor, G .
JOURNAL OF IMMUNOLOGY, 2004, 173 (07) :4286-4296
[2]  
*ACCESS, CONTR COMP ER TETR P
[3]   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
[4]  
[Anonymous], A study to evaluate the efficacy and safety of pemigatinib versus chemotherapy in unresectable or metastatic cholangiocarcinoma (FIGHT -302)
[5]  
[Anonymous], STUDY SAFETY EFFICAC
[6]   Efficacy and safety of recombinant human activated protein C for severe sepsis. [J].
Bernard, GR ;
Vincent, JL ;
Laterre, P ;
LaRosa, SP ;
Dhainaut, JF ;
Lopez-Rodriguez, A ;
Steingrub, JS ;
Garber, GE ;
Helterbrand, JD ;
Ely, EW ;
Fisher, CJ .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 344 (10) :699-709
[7]   LBP, CD14, TLR4 and the murine innate immune response to a peritoneal Salmonella infection [J].
Bernheiden, M ;
Heinrich, JM ;
Minigo, G ;
Schütt, C ;
Stelter, F ;
Freeman, M ;
Golenbock, D ;
Jack, RS .
JOURNAL OF ENDOTOXIN RESEARCH, 2001, 7 (06) :447-450
[8]   Plasma interferon-γ and interleukin-10 concentrations in systemic meningococcal disease compared with severe systemic Gram-positive septic shock [J].
Bjerre, A ;
Brusletto, B ;
Hoiby, EA ;
Kierulf, P ;
Brandtzaeg, P .
CRITICAL CARE MEDICINE, 2004, 32 (02) :433-438
[9]   DEFINITIONS FOR SEPSIS AND ORGAN FAILURE AND GUIDELINES FOR THE USE OF INNOVATIVE THERAPIES IN SEPSIS [J].
BONE, RC ;
BALK, RA ;
CERRA, FB ;
DELLINGER, RP ;
FEIN, AM ;
KNAUS, WA ;
SCHEIN, RMH ;
SIBBALD, WJ .
CHEST, 1992, 101 (06) :1644-1655
[10]  
BRUNBUISSON C, 1994, ARCH INTERN MED, V154, P2484