Since the completion of the Human Genome and Hap Map Project the era of personalized medicine is upon us. Sequencing of the entire human genome has brought about a progression of knowledge regarding drug therapies, genetic predisposition and environmental impact such as epigenetics. Every individual has a distinctive genetic code. Pharmacogenomics is the study of how disparities in the human genome ultimately affect the response to medications and offer different views into the variability observed within individuals prescribed opioids for pain management (Jannetto & Bratanow, 2011). Pharmacogenomics seeks to link differences in gene structure or genotype (polymorphisms) with pharmacologic differences in drug action (phenotype) (Galinkin, et al, 2010). Pharmacogenomics primarily is split into two parts describing genetic variants involving pharmacokinetics (absorption, distribution, metabolism and elimination of a drug) and pharmacodynamics (an activity of the drug at the target site/receptor of a drug (Janicki, 2013; Jannetto & Bratanow, 2011).
Opioids are standard treatments for chronic and post-operative pain. Reports of prescription opiate misuse in adolescence and adult population is predominant in the media. The concern in healthcare providers and families is fear of exposure to prescribed opioid prescription drugs may be a catalyst for addiction Hence, pain pharmacogenomics has held promise to provide information on one’s genome , identify patients at risk for complications or inadequate response to pain pharmacotherapy . The purpose of this presentation is to explore the genetic science involved with drug and individual variability which can aid nurses to support patient/families in developing guidelines towards a personalized pain management plan based upon one's genome.
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