Ajou University repository

Clinical pharmacokinetic study of tacrolimus in continuous intravenous administration for lung transplantationoa mark
  • Sohn, You Min ;
  • Ko, Ryoung Eun ;
  • Park, Hyo Jung ;
  • Choo, Eunjung ;
  • Jung, Minji ;
  • Lee, Sukhyang ;
  • Jeon, Kyeongman
Citations

SCOPUS

2

Citation Export

Publication Year
2023-06-01
Publisher
AME Publishing Company
Citation
Journal of Thoracic Disease, Vol.15, pp.3431-3436
Keyword
intravenous infusionlung transplantationTacrolimustherapeutic drug monitoring
All Science Classification Codes (ASJC)
Pulmonary and Respiratory Medicine
Abstract
Tacrolimus is a cornerstone of immunosuppression after lung transplantation. However, there are no clear guidelines on how to administer the drug and the duration to achieve the required therapeutic range in the early phase of lung transplantation. This is a single-center cohort study of adult patients who had lung transplantation. Tacrolimus was administered beginning with a low dose of 0.01 mg/kg/day immediately after transplantation. In addition, the designated clinical pharmacist conducted a daily intervention with trough concentrations to achieve the target of 10–15 ng/mL. Time in the therapeutic range (TTRin, %), time to the therapeutic range (TTRto, days), and coefficient of variation (CoV) of tacrolimus were evaluated for the 2-week post-transplant period. A total of 67 adult patients who had received first-time lung transplantation were included in the analysis. The median percentage of tacrolimus TTRin was 35.7% (21.4–42.9%) for the 2-week postoperative period. The median day of TTRto was 7 days (5–9 days), and the median tacrolimus trough concentration was 10.02 ng/mL (7.87–12.26 ng/mL) for the 2-week postoperative period. The median CoV of tacrolimus was 49.7% (40.8–61.6%). Acute kidney injury following tacrolimus infusion occurred in 23 (34.3%) patients, but there was no neurotoxicity or acute cellular rejection within 1 month of the postoperative period. In conclusion, continuous intravenous administration with the daily measure and dose titration of tacrolimus trough concentrations allowed the therapeutic range of tacrolimus to be reached within 1 week without significant adverse events, although the pharmacokinetic parameters were highly variable over time.
Language
eng
URI
https://dspace.ajou.ac.kr/dev/handle/2018.oak/33564
DOI
https://doi.org/10.21037/jtd-22-1760
Fulltext

Type
Article
Funding
Funding: This work was supported by a Samsung Medical
Show full item record

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

Related Researcher

Lee, Sukhyang Image
Lee, Sukhyang이숙향
Division of Pharmacy Sciences
Read More

Total Views & Downloads

File Download

  • There are no files associated with this item.