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Therapeutic Drug Monitoring and Pharmacogenetic Testing as Guides to Psychotropic Drug Dose Adjustment: An Observational Study

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  • معلومة اضافية
    • Contributors:
      Groupe de Recherche sur les formes Injectables et les Technologies Associées - ULR 7365 (GRITA); Université de Lille-Centre Hospitalier Régional Universitaire CHU Lille (CHRU Lille); Lille Neurosciences & Cognition - U 1172 (LilNCog); Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Lille-Centre Hospitalier Régional Universitaire CHU Lille (CHRU Lille); Laboratoire de Biométrie et Biologie Evolutive - UMR 5558 (LBBE); Université Claude Bernard Lyon 1 (UCBL); Université de Lyon-Université de Lyon-VetAgro Sup - Institut national d'enseignement supérieur et de recherche en alimentation, santé animale, sciences agronomiques et de l'environnement (VAS)-Centre National de la Recherche Scientifique (CNRS); Laboratoire Sciences Cognitives et Sciences Affectives - UMR 9193 (SCALab); Université de Lille-Centre National de la Recherche Scientifique (CNRS); Impact de l'environnement chimique sur la santé humaine - ULR 4483 (IMPECS); Département de Pharmacologie Médicale Lille (Pôle Recherche); Centre Hospitalier Régional Universitaire CHU Lille (CHRU Lille)-Faculté de Médecine Henri Warembourg - Université de Lille; CHU Lille, Institut de Pharmacie; Groupe de Recherche Interdiscipinaire Innovation et Optimisation Thérapeutique - EA 4481 (GRIIOT); Université de Lille, Droit et Santé
    • بيانات النشر:
      HAL CCSD
      MDPI
    • الموضوع:
      2023
    • Collection:
      Université de Lyon: HAL
    • نبذة مختصرة :
      International audience ; To avoid the failures in therapy with psychotropic drugs, treatments can be personalized by applying the results of therapeutic drug monitoring and pharmacogenetic testing. The objective of the present single-center observational study was to describe the changes in psychotropic drug management prompted by therapeutic drug monitoring and pharmacogenetic testing, and to compare the effective drug concentration based on metabolic status with the dose predicted using an in silico decision tool for drug–drug interactions. The study was conducted in psychiatry wards at Lille University Hospital (Lille, France) between 2016 and 2020. Patients with data for at least one therapeutic drug monitoring session or pharmacogenetic test were included. Blood tests were performed for 490 inpatients (mainly indicated by treatment monitoring or failure) and mainly concerned clozapine (21.4%) and quetiapine (13.7%). Of the 617 initial therapeutic drug monitoring tests, 245 (40%) complied with good sampling practice. Of the patients, 51% had a drug concentration within the therapeutic range. Regardless of the drug concentration, the drug management did not change in 83% of cases. Thirty patients underwent pharmacogenetic testing (twenty-seven had also undergone therapeutic drug monitoring) for treatment failure; the plasma drug concentration was outside the reference range in 93% of cases. The patient’s metabolic status explained the treatment failure in 12 cases (40%), and prompted a switch to a drug metabolized by another CYP450 pathway in 5 cases (42%). Of the six tests that could be analyzed with the in silico decision tool, all of the drug concentrations after adjustment were included in the range estimated by the tool. Knowledge of a patient’s drug concentration and metabolic status (for CYD2D6 and CYP2C19) can help clinicians to optimize psychotropic drug adjustment. Drug management can be optimized with good sampling practice, support from a multidisciplinary team (a physician, a geneticist, and ...
    • Relation:
      hal-04549351; https://hal.science/hal-04549351; https://hal.science/hal-04549351/document; https://hal.science/hal-04549351/file/TDM_PG_testing_Pharmaceuticals2024.pdf
    • الرقم المعرف:
      10.3390/ph17010021
    • الدخول الالكتروني :
      https://doi.org/10.3390/ph17010021
      https://hal.science/hal-04549351
      https://hal.science/hal-04549351/document
      https://hal.science/hal-04549351/file/TDM_PG_testing_Pharmaceuticals2024.pdf
    • Rights:
      info:eu-repo/semantics/OpenAccess
    • الرقم المعرف:
      edsbas.97C40AC2