Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/57459
Title: The relationship of postoperative tramadol activity with the CYP2D6*17 genome in total knee artroplasty patients
Other Titles: Total diz artroplastisi uygulanan hastalarda postoperatif tramadol etkinliğinin CYP2D6*17 genomu ile ilişkisi
Authors: Ök, N.
Gürbüz, M.E.
Köseler, A.
Keywords: CYP2D6*1/*17
postoperartive pain
Total knee arthroplasty CYP2D6
Tramadol
Publisher: Pamukkale University
Abstract: Purpose: In our study, we examined the effect of tramadol maintenance on the VAS score in geriatric patients. We observed them until the postoperative 60th minute. We investigated the incidence of pain in patients who underwent knee arthroplasty in the study. Our aim was to examine the effect of the *17 allele of the CYP2D6 genome on postoperative tramadol activity. Materials and methods: In our study we examined 110 patients who underwent total knee arthroplasty in the Department of Orthopedics and Traumatology at our facility, along with 100 healthy individuals without complaints who served as the control group. Each patient received a 100 mg dose of intravenous tramadol (Contramal). The postoperative VAS scores of the patients were recorded at 0-15-30-45-60 minutes. Results: The average age of the patients was 62.36 years. In our study, 86.4% of the patients were female, while this rate was 46% in the control group. We found that 3.65% of individuals (*17 carriers) possessed the *17 allele in both the patient group (n=7) and the control group (n=7). At the postoperative 0th minute, the VAS score for patients in the *1/*1 group was 91.07, while for the *1/*17 group, it measured 95.0. There was no statistically significant difference between the genomes (p>0.050). Likewise, no statistically significant difference was found between the genomes at the postoperative 15th, 30th, 45th, and 60th minutes (p>0.050). However, we observed a statistically significant decrease in the postoperative VAS score between 0-60 minutes in both groups, indicating time-dependent variation (p=0.000). Conclusion: When examining diverse literature on tramadol classification as intermediate metabolizer (IM) or extensive metabolizer (EM) concerning the *17 allele, our study indicates that the *17 allele should be regarded as both extensive metabolizer (EM) and normal metabolizer (NM). © 2024, Pamukkale University. All rights reserved.
URI: https://doi.org/10.31362/patd.1351539
https://hdl.handle.net/11499/57459
ISSN: 1309-9833
Appears in Collections:Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu

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