TY - JOUR
T1 - Sepsis
T2 - Something old, something new, and a systems view
AU - Namas, Rami
AU - Zamora, Ruben
AU - Namas, Rajaie
AU - An, Gary
AU - Doyle, John
AU - Dick, Thomas E.
AU - Jacono, Frank J.
AU - Androulakis, Ioannis P.
AU - Nieman, Gary F.
AU - Chang, Steve
AU - Billiar, Timothy R.
AU - Kellum, John A.
AU - Angus, Derek C.
AU - Vodovotz, Yoram
N1 - Funding Information:
This work was supported, in part, by the National Institutes of Health grants R01GM67240 , P50GM53789 , R33HL089082 , R01HL080926 , R01AI080799 , R01HL76157 , 3R01GM034695-25S1 , and R01GM082974 ; National Institute on Disability and Rehabilitation Research grant H133E070024 ; the Veterans Administration Research Service; as well as grants from the Commonwealth of Pennsylvania, the Pittsburgh Lifesciences Greenhouse, and the Pittsburgh Tissue Engineering Initiative.
PY - 2012/6
Y1 - 2012/6
N2 - Sepsis is a clinical syndrome characterized by a multisystem response to a microbial pathogenic insult consisting of a mosaic of interconnected biochemical, cellular, and organ-organ interaction networks. A central thread that connects these responses is inflammation that, while attempting to defend the body and prevent further harm, causes further damage through the feed-forward, proinflammatory effects of damage-associated molecular pattern molecules. In this review, we address the epidemiology and current definitions of sepsis and focus specifically on the biologic cascades that comprise the inflammatory response to sepsis. We suggest that attempts to improve clinical outcomes by targeting specific components of this network have been unsuccessful due to the lack of an integrative, predictive, and individualized systems-based approach to define the time-varying, multidimensional state of the patient. We highlight the translational impact of computational modeling and other complex systems approaches as applied to sepsis, including in silico clinical trials, patient-specific models, and complexity-based assessments of physiology.
AB - Sepsis is a clinical syndrome characterized by a multisystem response to a microbial pathogenic insult consisting of a mosaic of interconnected biochemical, cellular, and organ-organ interaction networks. A central thread that connects these responses is inflammation that, while attempting to defend the body and prevent further harm, causes further damage through the feed-forward, proinflammatory effects of damage-associated molecular pattern molecules. In this review, we address the epidemiology and current definitions of sepsis and focus specifically on the biologic cascades that comprise the inflammatory response to sepsis. We suggest that attempts to improve clinical outcomes by targeting specific components of this network have been unsuccessful due to the lack of an integrative, predictive, and individualized systems-based approach to define the time-varying, multidimensional state of the patient. We highlight the translational impact of computational modeling and other complex systems approaches as applied to sepsis, including in silico clinical trials, patient-specific models, and complexity-based assessments of physiology.
KW - Inflammatory response
KW - Mathematical model
KW - Physiologic variability
KW - Sepsis
UR - http://www.scopus.com/inward/record.url?scp=84861199459&partnerID=8YFLogxK
U2 - 10.1016/j.jcrc.2011.05.025
DO - 10.1016/j.jcrc.2011.05.025
M3 - Article
AN - SCOPUS:84861199459
SN - 0883-9441
VL - 27
SP - 314.e1-314.e11
JO - Journal of Critical Care
JF - Journal of Critical Care
IS - 3
ER -