Persistent Inflammation, Immunosuppression and Catabolism Syndrome

被引:133
|
作者
Mira, Juan C. [1 ]
Brakenridge, Scott C. [2 ]
Moldawer, Lyle L. [2 ]
Moore, Frederick A. [2 ]
机构
[1] Univ Florida, Coll Med, Dept Surg, Sepsis & Crit Illness Res Ctr, 1600 Southwest Archer Rd,POB 100019, Gainesville, FL 32610 USA
[2] Univ Florida, Coll Med, Dept Surg, Sepsis & Crit Illness Res Ctr, 1600 Southwest Archer Rd,POB 100286, Gainesville, FL 32610 USA
关键词
Shock; Multiple organ failure; Trauma; Sepsis; Chronic critical illness; Cachexia; Myeloid-derived suppressor cells e; PICS; MULTIPLE-ORGAN FAILURE; LONG-TERM SURVIVAL; INNATE IMMUNE-RESPONSES; SUPPRESSOR-CELLS; CRITICALLY-ILL; SEVERE SEPSIS; TRAUMA; INFECTION; MORTALITY; IMMUNOTHERAPY;
D O I
10.1016/j.ccc.2016.12.001
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Following advances in critical care, in-hospital multiple organ failure related mortality is declining. Consequently, incidence of chronic critical illness is increasing. These patients linger in the intensive care unit, have high resource utilization, and poor long-term outcomes. Within this population, the authors propose that a substantial subset of patients have a new phenotype: persistent inflammation, immunosuppression, and catabolism syndrome. There is evidence that myelodysplasia with expansion of myeloid-derived suppressor cells, innate and adaptive immune suppression, and protein catabolism with malnutrition are major contributors. Optimal care of these patients will require novel multimodality interventions.
引用
收藏
页码:245 / +
页数:15
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