The host response to sepsis and developmental impact
- PMID: 20421258
- PMCID: PMC2894560
- DOI: 10.1542/peds.2009-3301
The host response to sepsis and developmental impact
Abstract
Invasion of the human by a pathogen necessitates an immune response to control and eradicate the microorganism. When this response is inadequately regulated, systemic manifestations can result in physiologic changes described as "sepsis." Recognition, diagnosis, and management of sepsis remain among the greatest challenges shared by the fields of neonatology and pediatric critical care medicine. Sepsis remains among the leading causes of death in both developed and underdeveloped countries and has an incidence that is predicted to increase each year. Despite these sobering statistics, promising therapies derived from preclinical models have universally failed to obviate the substantial mortality and morbidity associated with sepsis. Thus, there remains a need for well-designed epidemiologic and mechanistic studies of neonatal and pediatric sepsis to improve our understanding of the causes (both early and late) of deaths attributed to the syndrome. In reviewing the definitions and epidemiology, developmental influences, and regulation of the host response to sepsis, it is anticipated that an improved understanding of this host response will assist clinician-investigators in identifying improved therapeutic strategies.
References
-
- Geroulanos S, Douka ET. Historical perspective of the word “sepsis”. Intensive Care Med. 2006;32(12):2077. - PubMed
-
- Steppan J, Hofer S, Funke B, Brenner T, Henrich M, Martin E, et al. Sepsis and Major Abdominal Surgery Lead to Flaking of the Endothelial Glycocalix. J Surg Res. 2009 - PubMed
-
- Thomas L. Germs. N Engl J Med. 1972;287:553–555. - PubMed
-
- Bone RC, Sibbald WJ, Sprung CL. The ACCP-SCCM consensus conference on sepsis and organ failure. Chest. 1992;101(6):1481–1483. - PubMed
-
- Bone RC, Sprung CL, Sibbald WJ. Definitions for sepsis and organ failure. Crit Care Med. 1992;20(6):724–726. - PubMed
Publication types
MeSH terms
Substances
Grants and funding
- R01 GM066839/GM/NIGMS NIH HHS/United States
- R01GM066839/GM/NIGMS NIH HHS/United States
- 1RC1HL100474-01/HL/NHLBI NIH HHS/United States
- R01HL097361/HL/NHLBI NIH HHS/United States
- R01GM064619/GM/NIGMS NIH HHS/United States
- RC1 HL100474/HL/NHLBI NIH HHS/United States
- R01 HL097361/HL/NHLBI NIH HHS/United States
- R01 GM064619/GM/NIGMS NIH HHS/United States
- K12HD047349/HD/NICHD NIH HHS/United States
- UL1RR024986/RR/NCRR NIH HHS/United States
- K08 HD062142/HD/NICHD NIH HHS/United States
- K12 HD047349/HD/NICHD NIH HHS/United States
- UL1 RR024986/RR/NCRR NIH HHS/United States
- K08 GM077432/GM/NIGMS NIH HHS/United States
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
