Department of Pharmacy, Toho University Omori Medical Center, Tokyo, Japan.
Department of Pharmacy, Tokyo Women's Medical University Hospital, Tokyo, Japan.
J Infect Chemother. 2021 Feb;27(2):151-160. doi: 10.1016/j.jiac.2020.11.014. Epub 2020 Dec 26.
This systematic review and meta-analysis was designed to determine the optimal trough concentration of voriconazole for children with invasive fungal infections (IFIs).
We searched electronic databases (PubMed, Cochrane Central Register of Controlled Trials, ClinicalTrials.gov and Japana Centra Revuo Medicina) for clinical studies describing the voriconazole trough concentration. We used stepwise cut-off values of 1.0-2.0 mg/L for efficacy and 3.0-6.0 mg/L for safety. The efficacy outcomes were treatment success and all-cause mortality, and the safety outcomes were hepatotoxicity, neurotoxicity and all-cause adverse events.
Nine studies involving 211 patients were included in the analysis. The probability of treatment success against IFIs was significantly increased at cut-off values of ≥1.0 mg/L (odds ratio [OR] = 2.65, 95% confidence interval [CI] = 1.20-5.87). Our analysis did not find any relationship between the trough concentration and survival. Concerning safety, the occurrence of any outcomes did not significantly differ according to the voriconazole trough concentrations at any cut-off value. However, in a subgroup analysis of Asian study locations, a significantly higher risk of hepatotoxicity was demonstrated at voriconazole trough cut-off values ≥ 3.0 mg/L (OR = 8.40, 95% CI = 1.36-51.92). Although a significant correlation between the voriconazole concentration and hepatotoxicity was evident in regression curve analysis, (y = 0.1198e), no correlation was demonstrated for neurotoxicity (y = 0.3913e).
Our findings suggest that the optimal trough concentration for increasing clinical success and minimizing hepatotoxicity during voriconazole therapy in children with IFIs, particularly for Asian populations, is 1.0-3.0 mg/L.
本系统评价和荟萃分析旨在确定儿童侵袭性真菌感染(IFI)患者伏立康唑的最佳谷浓度。
我们检索了电子数据库(PubMed、Cochrane 中央对照试验注册库、ClinicalTrials.gov 和 Japana Centra Revuo Medicina),以获取描述伏立康唑谷浓度的临床研究。我们使用逐步的截止值 1.0-2.0mg/L 来评估疗效,使用 3.0-6.0mg/L 来评估安全性。疗效结局包括治疗成功率和全因死亡率,安全性结局包括肝毒性、神经毒性和全因不良事件。
共有 9 项研究,涉及 211 例患者纳入分析。在截止值≥1.0mg/L 时,抗 IFI 治疗成功率显著增加(比值比 [OR] = 2.65,95%置信区间 [CI] = 1.20-5.87)。我们的分析未发现谷浓度与生存之间存在任何关系。关于安全性,在任何截止值下,谷浓度与任何结局的发生均无显著差异。然而,在亚洲研究地点的亚组分析中,伏立康唑谷浓度≥3.0mg/L 时,肝毒性的发生风险显著增加(OR = 8.40,95%CI = 1.36-51.92)。虽然回归曲线分析(y=0.1198e)表明伏立康唑浓度与肝毒性之间存在显著相关性,但在神经毒性方面(y=0.3913e)未显示出相关性。
我们的研究结果表明,对于儿童 IFI 患者,特别是亚洲人群,在伏立康唑治疗中增加临床成功率和最小化肝毒性的最佳谷浓度为 1.0-3.0mg/L。