Lin Liangmo, Fu Xiangjun, Hong Mianhui
Pharmacy, Hainan General Hospital, Haikou, CHN.
Hematology, Hainan General Hospital, Haikou, CHN.
Cureus. 2023 Sep 28;15(9):e46107. doi: 10.7759/cureus.46107. eCollection 2023 Sep.
Voriconazole (VRZ) is a commonly used antifungal drug. However, the drug has nonlinear metabolic kinetic characteristics. Many factors can affect the plasma drug concentration, thus affecting the safety and effectiveness of VRZ.
The aim of this study is to characterize the correlation between prealbumin (PA) or CRP and VRZ overexposure and adverse reactions.
Patients who received VRZ as a treatment and performed therapeutic drug monitoring (TDM) were included. Biomarkers and combined medications were analyzed to find out factors that were related to VRZ trough concentrations (C) and overexposure (C>5.0 mg/L). Receiver operating characteristic (ROC) curves were used to determine the cut-off levels. Patients were divided into three groups according to different PA and CRP levels. Then, the incidence rate of VRZ adverse reactions between groups was analyzed.
A total of 123 patients were included in the study. PA was negatively correlated, while CRP was positively correlated with VRZ concentrations. Lower PA or higher CRP was related to VRZ overexposure with a cut-off level of 145.5 mg/L and 102.23 mg/L, respectively. Patients in Group 2 (PA <145.5 mg/L and CRP >102.23 mg/L) had an incidence rate of adverse reactions up to 70.27%, while the incidence rates in Group 1 (PA >145.5 mg/L and CRP <102.23 mg/L) and Group 3 (PA <145.5 mg/L and CRP <102.23 mg/L or PA >145.5 mg/L and CRP >102.23 mg/L) were 15.38% and 32.43%, respectively.
PA and CRP were both related to VRZ concentrations and overexposure. The risk of VRZ overexposure and adverse reactions significantly increased in patients with PA <145.5 mg/L and CRP >102.23 mg/L at the same time.
伏立康唑(VRZ)是一种常用的抗真菌药物。然而,该药物具有非线性代谢动力学特征。许多因素会影响血浆药物浓度,进而影响伏立康唑的安全性和有效性。
本研究旨在明确前白蛋白(PA)或C反应蛋白(CRP)与伏立康唑暴露过量及不良反应之间的相关性。
纳入接受伏立康唑治疗并进行治疗药物监测(TDM)的患者。分析生物标志物和联合用药情况,以找出与伏立康唑谷浓度(C)及暴露过量(C>5.0 mg/L)相关的因素。采用受试者工作特征(ROC)曲线确定临界值水平。根据不同的PA和CRP水平将患者分为三组。然后,分析各组间伏立康唑不良反应的发生率。
本研究共纳入123例患者。PA与伏立康唑浓度呈负相关,而CRP与伏立康唑浓度呈正相关。较低的PA或较高的CRP与伏立康唑暴露过量相关,临界值水平分别为145.5 mg/L和102.23 mg/L。第2组(PA<145.5 mg/L且CRP>102.23 mg/L)患者的不良反应发生率高达70.27%,而第1组(PA>145.5 mg/L且CRP<102.23 mg/L)和第3组(PA<145.5 mg/L且CRP<102.23 mg/L或PA>145.5 mg/L且CRP>102.23 mg/L)的发生率分别为15.38%和32.43%。
PA和CRP均与伏立康唑浓度及暴露过量有关。PA<145.5 mg/L且CRP>102.23 mg/L的患者同时发生伏立康唑暴露过量和不良反应的风险显著增加。