Using pharmacogenetics to structure individual pain management protocols in total knee arthroplasty.
Aged
Aged, 80 and over
Analgesics, Opioid
/ therapeutic use
Anti-Inflammatory Agents, Non-Steroidal
/ therapeutic use
Arthroplasty, Replacement, Knee
Female
Humans
Male
Middle Aged
Pain Management
/ methods
Pain, Postoperative
/ drug therapy
Pharmacogenomic Testing
Pilot Projects
Prospective Studies
Single-Blind Method
knee arthroplasty
pain management
pharmacogenetics
Journal
The bone & joint journal
ISSN: 2049-4408
Titre abrégé: Bone Joint J
Pays: England
ID NLM: 101599229
Informations de publication
Date de publication:
Jun 2020
Jun 2020
Historique:
entrez:
2
6
2020
pubmed:
2
6
2020
medline:
19
6
2020
Statut:
ppublish
Résumé
The purpose of this study was to use pharmacogenetics to determine the frequency of genetic variants in our total knee arthroplasty (TKA) patients that could affect postoperative pain medications. Pharmacogenetic testing evaluates patient DNA to determine if a drug is expected to have a normal clinical effect, heightened effect, or no effect at all on the patient. It also predicts whether patients are likely to experience side effects from medicine. We further sought to determine if changing the multimodal programme based on these results would improve pain control or reduce side effects. In this pilot study, buccal samples were collected from 31 primary TKA patients. Pharmacogenetics testing examined genetic variants in genes Genetic variants involving one or more medications in the multimodal pain protocol occurred in 13 of the 31 patients (42%). In total, eight patients (26%) had variants affecting more than one of the medications. For the 25 patients who recorded pain and medication logs, the mean pain levels and morphine equivalents (MEQs) consumed in the first ten days were higher in the control group than in the custom-guided group (p = 0.019 for pain and p = 0.655 for MEQ). Overall, 42% of patients had a variant involving one of the pain medications prescribed in our perioperative pain program for TKA. Ongoing research will help determine if using these data to modify a patient's medication will improve outcomes. Cite this article:
Identifiants
pubmed: 32475277
doi: 10.1302/0301-620X.102B6.BJJ-2019-1539.R1
doi:
Substances chimiques
Analgesics, Opioid
0
Anti-Inflammatory Agents, Non-Steroidal
0
Types de publication
Journal Article
Randomized Controlled Trial
Langues
eng
Sous-ensembles de citation
IM