2014
DOI: 10.1111/pme.12380
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Personalized Oxycodone Dosing: Using Pharmacogenetic Testing and Clinical Pharmacokinetics to Reduce Toxicity Risk and Increase Effectiveness

Abstract: Personalized oxycodone dosing is a new tool for a clinician treating chronic pain patients requiring oxycodone. By expressing a patient's CYP2D6 phenotype pharmacokinetically, a clinician (at least theoretically) can improve the safety and efficacy of oxycodone and decrease the risk for iatrogenically induced overdose or death. Pharmacokinomics provides a general framework for the integration of pharmacogenetics with clinical pharmacokinetics into clinical practice for gene-based prescribing.

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Cited by 37 publications
(27 citation statements)
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“…(14) Further, pharmacogenetics data suggest that opioids including hydrocodone, oxycodone, and codeine may be ineffective in up to 10% of the Caucasian population. (30,31,32) As a result, best practice recommendations note that opioid analgesics should be reserved for the minority of situations in which optimal doses of NSAIDs and/or acetaminophen/aspirin provide insufficient pain management. (14,29)…”
Section: Discussionmentioning
confidence: 99%
“…(14) Further, pharmacogenetics data suggest that opioids including hydrocodone, oxycodone, and codeine may be ineffective in up to 10% of the Caucasian population. (30,31,32) As a result, best practice recommendations note that opioid analgesics should be reserved for the minority of situations in which optimal doses of NSAIDs and/or acetaminophen/aspirin provide insufficient pain management. (14,29)…”
Section: Discussionmentioning
confidence: 99%
“…Indeed, we commonly observe in clinical practice that the first several pain assessment-treatment-evaluation cycles often require a co-adaptation between the patient and the healthcare delivery system to identify which analgesic strategies optimally provide sustained, successful pain management. 20,21 Rather than rewarding healthcare delivery systems for offering a non-selective “kitchen sink” approach to postoperative pain management principally predicated on high-dose opioid analgesia, which can lead to substantial increases in patient safety events with insignificant decreases in pain intensity across the hospital population, it may be advantageous to encourage expedited assessment-treatment-evaluation cycles to hasten the co-adaptation and personalization of analgesic strategies to individual patients. The time to SuPPR thus partially considers the adaptability of the healthcare system to an individual patient’s needs in requiring a sustained improvement, rather than a linear trend that may feature a decreasing overall trend in pain intensity yet still permit repeated episodes of severe pain.…”
Section: Discussionmentioning
confidence: 99%
“…In our patient dose selection of anesthetic and ancillary medication based on clinical experience, convenience, cost, pharmacokinetic and pharmacodynamic properties of the drugs [8]. In addition to these approach, combine clinical pharmacokinetics with pharmacogenetics based approaches are also emerging for dose selection of medications [9]. These patients should be given adequate premedication to reduce stress.…”
Section: Discussionmentioning
confidence: 99%