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Review

Potential role of pharmacogenomics testing in the setting of enhanced recovery pathways after surgery

, , , &
Pages 145-154 | Published online: 26 Jul 2019
 

Abstract

In 2001, a group of European academic surgeons created the Enhanced Recovery After Surgery (ERAS) study group and established the first official ERAS protocol. One of the most significant challenges during ERAS implementation is variability of drugs used throughout the perioperative period. Pharmacogenomic testing (blood or saliva) results (obtained within approximately 48 hrs) provide guidelines on how to prescribe the optimal drug with the optimal dosage to each patient based on an individual’s unique genetic profile. Pharmacogenomic testing of various methods of multimodal analgesia is an essential element of ERAS protocols spanning the entire perioperative period to ultimately optimize postoperative pain control. The key goal for anesthetic management in ERAS protocols is to facilitate rapid emergence by using the shortest acting agents available, thus accelerating recovery and reducing length of stay, hospital expenses, and postoperative complications. Postoperative nausea and vomiting (PONV) is an additional challenge that should be overcome to ensure an enhanced recovery and shorter length of stay with the use of antiemetics. Postoperative ileus (POI) can result in longer hospital stay with increasing susceptibility to associated morbidities along with an increase in associated hospitalization costs. Genetics-guided pharmacotherapy and its impact on clinical outcomes should be thoroughly studied for better understanding and managing drug administration in the settings of ERAS.

Acknowledgments

We acknowledge the contribution (editing the final version of the manuscript) of pre-med students Andrew Costa (The Ohio State University, Columbus, OH, USA) and Garegin Soghomonyan (Claremont McKenna College, Claremont, CA, USA).

Disclosure

Richard D Urman received research funding from CQuentia Inc. Sergio D Bergese reports personal fees from Baxter, outside the submitted work. The authors report no other conflicts of interest in this work.