Survivors Versus Nonsurvivors Postburn Differences in Inflammatory and Hypermetabolic Trajectories

被引:100
作者
Jeschke, Marc G. [2 ,6 ,7 ,8 ]
Gauglitz, Gerd G. [5 ]
Finnerty, Celeste C. [1 ,2 ,3 ,4 ]
Kraft, Robert [1 ,2 ]
Mlcak, Ronald P. [1 ,2 ]
Herndon, David N. [1 ,2 ]
机构
[1] Shriners Hosp Children, Galveston, TX 77550 USA
[2] Univ Texas Med Branch, Dept Surg, Galveston, TX 77555 USA
[3] Univ Texas Med Branch, Inst Translat Sci, Galveston, TX 77555 USA
[4] Univ Texas Med Branch, Sealy Ctr Mol Med, Galveston, TX 77555 USA
[5] Univ Munich, Dept Dermatol & Allergy, Munich, Germany
[6] Univ Toronto, Sunnybrook Hlth Sci Ctr, Ross Tilley Burn Ctr, Toronto, ON M4N 3M5, Canada
[7] Univ Toronto, Sunnybrook Res Inst, Dept Surg, Toronto, ON M4N 3M5, Canada
[8] Univ Toronto, Dept Immunol, Div Plast Surg, Toronto, ON M4N 3M5, Canada
基金
美国国家卫生研究院;
关键词
burn size; critical care; hypermetabolism; inflammation; mortality; survival; pediatric; INTENSIVE INSULIN THERAPY; SEVERELY BURNED CHILDREN; PEDIATRIC-PATIENTS; METABOLIC-RESPONSE; MUSCLE CATABOLISM; MORTALITY; INJURY; SIZE; HYPERGLYCEMIA; ASSOCIATION;
D O I
10.1097/SLA.0b013e31828dfbf1
中图分类号
R61 [外科手术学];
学科分类号
摘要
Objective: To evaluate whether a panel of common biomedical markers can be utilized as trajectories to determine survival in pediatric burn patients. Background: Despite major advances in clinical care, of the more than 1 million people burned in the United States each year, more than 4500 die as a result of their burn injuries. The ability to predict patient outcome or anticipate clinical trajectories using plasma protein expression would allow personalization of clinical care to optimize the potential for patient survival. Methods: A total of 230 severely burned children with burns exceeding 30% of the total body surface, requiring at least 1 surgical procedure were enrolled in this prospective cohort study. Demographics, clinical outcomes, and inflammatory and acute-phase responses (serum cytokines, hormones, and proteins) were determined at admission and at 11 time points for up to 180 days postburn. Statistical analysis was performed using a 1-way analysis of variance, the Student t test, (2) test, and Mann-Whitney test where appropriate. Results: Survivors and nonsurvivors exhibited profound differences in critical markers of inflammation and metabolism at each time point. Nonsurvivors had significantly higher serum levels of interleukin (IL)-6, IL-8, granulocyte colony-stimulating factor, monocyte chemoattractant protein-1, C-reactive protein, glucose, insulin, blood urea nitrogen, creatinine, and bilirubin (P < 0.05). Furthermore, nonsurvivors exhibited a vastly increased hypermetabolic response that was associated with increases in organ dysfunction and sepsis when compared with survivors (P < 0.05). Conclusions: Nonsurvivors have different trajectories in inflammatory, metabolic, and acute phase responses allowing differentiation of nonsurvivors from survivors and now possibly allowing novel predictive models to improve and personalize burn outcomes.
引用
收藏
页码:814 / 823
页数:10
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