- Open Access
"Metabolic staging" after major trauma - a guide for clinical decision making?
© Stahel et al; licensee BioMed Central Ltd. 2010
Received: 11 June 2010
Accepted: 17 June 2010
Published: 17 June 2010
Metabolic changes after major trauma have a complex underlying pathophysiology. The early posttraumatic stress response is associated with a state of hyperinflammation, with increased oxygen consumption and energy expenditure. This hypercatabolic state must be recognized early and mandates an early nutritional management strategy. A proactive concept of early enteral "immunonutrition" in severely injured patients, is aimed at counterbalancing the negative aspects of hyperinflammation and hypercatabolism in order to reduce the risk of late complications, including infections and posttraumatic organ failure. Recently, the concept of "metabolic staging" has been advocated, which takes into account the distinct inflammatory phases and metabolic phenotypes after major trauma, including the "ischemia/reperfusion phenotype", the "leukocytic phenotype", and the "angiogenic phenotype". The potential clinical impact of metabolic staging, and of an appropriately adapted "metabolic control" and nutritional support, remains to be determined.
In a recent article published in the Journal, Aller and colleagues propose a modern perspective on the metabolic events associated with the inflammatory response to major trauma, which should guide therapeutic strategies . The authors classified the metabolic changes after injury into three distinct phenotypes: (1) the "ischemia/reperfusion phenotype"; (2) the "leukocytic phenotype"; and (3) the "angiogenic phenotype". Using this innovative classification concept, the authors explain the metabolic alterations in association with the "classical" progression of posttraumatic inflammation. The first ("ischemia/reperfusion") phenotype represents the immediate, nervous system-related alteration in response to injury, in which neuronal and humoral responses and edema formation predominate. This phase is characterized by regulating the metabolic supply to cells via the least elaborate mechanism: diffusion. The second ("leukocytic") phenotype, is characterized as the intermediate (or "immune") phase of the metabolic response to trauma. This phase is characterized by leukocytic and bacterial infiltration of previously damaged tissues, which occurs in an edematous, oxygen-poor environment. The resulting post-shock hypercatabolism and hypermetabolism is related to a hyperdynamic response with increased body temperature, increased oxygen consumption, glycogenolysis, lipolysis, proteolysis and futile substrate cycling. The third ("angiogenic") phenotype is defined as the late (or "endocrine") phase of systemic response to injury. This phase is characterized by a return of oxidative metabolism, favoring angiogenesis in damaged tissues and organs. This process creates a capillary bed that facilitates tissue repair and regeneration.
In 1942, Cuthbertson was the first to describe distinct phases of the metabolic changes which occur after major trauma [2, 3]. He characterized the "ebb" and the "flow" phases of posttraumatic metabolic alterations. The "ebb" phase is associated with a decline in body temperature and oxygen consumption, presumably aimed at reducing posttraumatic energy depletion. The brief duration of this phase limits its clinical relevance. In contrast, the "flow" phase occurs after resuscitation from a state of shock, which leads to an increased metabolic turnover, activation of the innate immune system and induction of the hepatic acute-phase response. This hypercatabolic condition leads to a significantly increased oxygen consumption and energy expenditure. The state of hypercatabolism has been associated with severe complications after major trauma, related to hyperglycemia, hypoproteinemia, and immunosuppression. The presence and significance of these metabolic alterations must be recognized and managed early in multiply injured patients [4, 5]. The catabolic state requires an adjusted energetic balance with early protein substitution and hypercaloric nutrition. Early enteral nutrition has been advocated as the concept of choice for nutrition of polytraumatized and severely ill patients. In this regard, prospective randomized controlled trials in the 1980s have clearly demonstrated the positive effect of an early full enteral nutrition with a decreased posttraumatic infection rate, a shorter duration of hospital stay, and an improved overall outcome [6, 7]. The concept of "immunonutrition" is exemplified by the enteral supplementation of glutamine, an essential amino acid which exerts metabolic benefits beyond its nutritional value by mediating immunological effects, such as induction of neutrophil phagocytic activity and oxidative burst . In addition, glutamine is a precursor to the reducing agent glutathione and thus contributes to antioxidant effects and cellular protection from ischemia/reperfusion-mediated injury . A prospective, randomized, double-blind controlled clinical trial demonstrated that glutamine supplementation reduces the incidence of multiple organ failure and death attributed to infections in critically ill patients . In addition to glutamine, Ω- fatty acids have become an important nutritional supplementation for severely injured patients . These long-chain polyunsaturated fatty acids derived from fish oil were shown to have potent anti-inflammatory properties, related to the attenuation of arachidonic acid-derived metabolites like thromboxane A 2 and leukotriene B 4, inhibition of leukocyte activation and chemotaxis, and attenuation of pro-inflammatory gene expression levels. Other nutritional supplements that promote anabolism in trauma patients include phospholipids, leptins, and anabolic hormones, such as thyroid hormones, growth hormone, and insulin. For example, growth hormone substitution has been shown to promote protein anabolism in severely injured patients.
The authors propose a third, "angiogenic phenotype" . But, again, the focus on angiogenesis may be somewhat myopic. On one hand, discerning the angiogenic phase from the leukocyte will be difficult as the two processes overlap. On the other hand, the nutritional needs are largely dictated by the metabolic state described in the leukocyte phase.
Based on these distinct pathophysiological phases of posttraumatic metabolic alterations, the authors deduce the need for a "metabolic staging" after severe trauma . This implies the adjustment of the nutritional needs, which should be adjusted in a staged fashion to the different metabolic phases after major trauma. The authors conclude that a better understanding of these pathophysiological events may provide the treating clinician with novel and innovative therapeutic approaches, which include providing the most appropriate metabolic support dependent on the predominant phase and phenotype of metabolic alterations. The potential clinical impact and the feasibility of a, likely over-simplified, concept of "metabolic staging" in the guidance and decision making for the nutritional support of severely injured patients remains elusive.
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