Abstract
The technical, statistical, and methodological challenges of handling human genomic information and translating it into reliable tools applicable in clinical decision-making must overcome one major hurdle preventing the widespread use of genomics in clinical medicine, and that is translating basic science discoveries into new and better patient-centered treatments. Over the past 30 years a cadre of clinicians and researchers alike has described the genomic and proteomic response to inflammation and severe injury in leukocyte populations from humans with cancer and trauma. Now is the time to take advantage of the large scientific database of information and use it to implement a diagnostic test for predicting outcome and appropriateness for therapy in the critically ill trauma patient, cancer patient, or acute care surgery patient. The future of improved outcomes is rooted in new genomic diagnostics that can accurately identify patients who may benefit from therapies aimed at disease prevention and not just therapeutic reaction. Rather than focus on disease treatment, we as physicians should focus on patient-centered disease identification before the symptomatology and sequelae are manifest and rampant. By applying genomics and other high-throughput technologies, clinicians and researchers will have a robust platform for using the human transcriptome as a reliable and convenient diagnostic tool to not only treat but also prevent disease in the clinical setting.
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Delano, M.J., Maier, R.V. (2015). Genomics in Surgery, Trauma, and Critical Care: How Do We Control the Future?. In: Latifi, R., Rhee, P., Gruessner, R. (eds) Technological Advances in Surgery, Trauma and Critical Care. Springer, New York, NY. https://doi.org/10.1007/978-1-4939-2671-8_3
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DOI: https://doi.org/10.1007/978-1-4939-2671-8_3
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