TY - JOUR
T1 - Linezolid therapeutic drug monitoring in patients with hepatic impairment
AU - Meng, Dandan
AU - Chen, Lihong
AU - Dong, Yalin
AU - Han, Xinyan
AU - Dou, Linjie
AU - Zhang, Di
AU - Dong, Haiyan
N1 - Publisher Copyright:
© 2021, Editorial Department of Chinese Journal of Infection. All rights reserved.
PY - 2021
Y1 - 2021
N2 - Objective To investigate the distribution profile of trough plasma concentration (Cmin) of linezolid in patients with hepatic impairment and the factors affecting concentration variation, and to evaluate treatment efficacy and linezolid-induced thrombocytopenia. Methods Hepatic impairment patients who received standard dose of linezolid (600 mg, q12 h) were stratified according to baseline hepatic function as defined by Child-Pugh-Turcotte score criteria: mild hepatic impairment (Child-Pugh-Turcotte Class A), moderate hepatic impairment (Child-Pugh-Turcotte Class B) and severe hepatic impairment (Child-Pugh-Turcotte Class C). Linezolid Cmin was measured by high-performance liquid chromatography. Data pertaining to linezolid were collected. Multivariate linear regression models were used to investigate the effect of variables on linezolid Cmin. Bacterial eradication rate and incidence of linezolid-induced thrombocytopenia were analyzed in terms of hepatic impairment. Results Plasma samples were collected from 30 patients. Severe hepatic impairment patients showed significantly higher linezolid Cmin than the patients with mild or moderate hepatic impairment [(19.3 ± 6.5) mg/L vs (7.5 ± 3.2) mg/L, P < 0.05; (19.3 ± 6.5) mg/L vs (11.6 ± 3.2) mg/L, P < 0.05]. Supratherapeutic linezolid Cmin was observed in 11.8%, 42.1%, and 66.7% of the patients with mild, moderate, or severe hepatic impairment, respectively. Age(≥65 years), Charlson comorbidity score(≥4 points), and severe hepatic impairment had a significant effect on linezolid Cmin (P < 0.05). Bacterial eradication rate and the incidence of linezolid-induced thrombocytopenia was 70.0% and 30.0% respectively in patients with hepatic impairment. Conclusions Standard dosing regimen of linezolid still achieves high plasma concentration in patients with hepatic impairment. Plasma concentrations of linezolid should be closely monitored in patients with hepatic impairment to ensure the safety and efficacy of linezolid therapy.
AB - Objective To investigate the distribution profile of trough plasma concentration (Cmin) of linezolid in patients with hepatic impairment and the factors affecting concentration variation, and to evaluate treatment efficacy and linezolid-induced thrombocytopenia. Methods Hepatic impairment patients who received standard dose of linezolid (600 mg, q12 h) were stratified according to baseline hepatic function as defined by Child-Pugh-Turcotte score criteria: mild hepatic impairment (Child-Pugh-Turcotte Class A), moderate hepatic impairment (Child-Pugh-Turcotte Class B) and severe hepatic impairment (Child-Pugh-Turcotte Class C). Linezolid Cmin was measured by high-performance liquid chromatography. Data pertaining to linezolid were collected. Multivariate linear regression models were used to investigate the effect of variables on linezolid Cmin. Bacterial eradication rate and incidence of linezolid-induced thrombocytopenia were analyzed in terms of hepatic impairment. Results Plasma samples were collected from 30 patients. Severe hepatic impairment patients showed significantly higher linezolid Cmin than the patients with mild or moderate hepatic impairment [(19.3 ± 6.5) mg/L vs (7.5 ± 3.2) mg/L, P < 0.05; (19.3 ± 6.5) mg/L vs (11.6 ± 3.2) mg/L, P < 0.05]. Supratherapeutic linezolid Cmin was observed in 11.8%, 42.1%, and 66.7% of the patients with mild, moderate, or severe hepatic impairment, respectively. Age(≥65 years), Charlson comorbidity score(≥4 points), and severe hepatic impairment had a significant effect on linezolid Cmin (P < 0.05). Bacterial eradication rate and the incidence of linezolid-induced thrombocytopenia was 70.0% and 30.0% respectively in patients with hepatic impairment. Conclusions Standard dosing regimen of linezolid still achieves high plasma concentration in patients with hepatic impairment. Plasma concentrations of linezolid should be closely monitored in patients with hepatic impairment to ensure the safety and efficacy of linezolid therapy.
KW - hepatic impairment
KW - linezolid
KW - therapeutic drug monitoring
KW - thrombocytopenia
UR - https://www.scopus.com/pages/publications/105000503872
U2 - 10.16718/j.1009-7708.2021.03.006
DO - 10.16718/j.1009-7708.2021.03.006
M3 - 文章
AN - SCOPUS:105000503872
SN - 1009-7708
VL - 21
SP - 275
EP - 281
JO - Chinese Journal of Infection and Chemotherapy
JF - Chinese Journal of Infection and Chemotherapy
IS - 3
ER -