Sabatino David C, Lange Nicholas W, Salerno David M, Scheffert Jenna
Department of Pharmacy, NewYork-Presbyterian Hospital, New York, New York, USA.
Clin Transplant. 2023 Jan;37(1):e14826. doi: 10.1111/ctr.14826. Epub 2022 Oct 26.
Posaconazole is used for prophylaxis and treatment of invasive fungal infections in lung transplant recipients (LTR). Previous studies have not described the relationship between elevated posaconazole trough concentrations and adverse drug reactions in this population.
This IRB-approved, retrospective cohort study at NewYork-Presbyterian Hospital included LTR who had posaconazole trough concentrations measured. The primary aim of this study was to evaluate elevated posaconazole trough concentrations and changes in liver function tests as well as QTc interval. A secondary aim of this study was to identify patient factors associated with elevated posaconazole trough levels.
A total of 109 LTR were included. The average age was 58.1 years (IQR, 48-65), the majority were male (56%). A total of 932 trough levels were assessed with a median number of 8 (IQR, 5-15) levels per patient. The median posaconazole trough concentration was 1.7 mg/L (IQR, 1.1-2.5). Hepatotoxicity, as defined by common terminology criteria for adverse events (CTCAE), was observed in 73.4% of subjects, with the majority classified as grade 1 (67.5%). However, there was no correlation between elevated posaconazole levels and aspartate aminotransferase (r = .03), alanine aminotransferase (r = .04), alkaline phosphatase (r = .04), and total bilirubin (r = .02). There was also no correlation between posaconazole trough concentrations and QTc interval (r = .03).
This analysis demonstrates that no correlation exists between whole blood posaconazole levels and hepatotoxicity or QTc prolongation. Based on these results, posaconazole dose reductions may not be warranted for posaconazole levels that are significantly above the therapeutic target to avert risk for hepatotoxicity or QTc prolongation.
泊沙康唑用于肺移植受者(LTR)侵袭性真菌感染的预防和治疗。既往研究未描述该人群中泊沙康唑谷浓度升高与药物不良反应之间的关系。
这项在纽约长老会医院开展的、经机构审查委员会批准的回顾性队列研究纳入了检测泊沙康唑谷浓度的LTR。本研究的主要目的是评估泊沙康唑谷浓度升高以及肝功能检查和QTc间期的变化。本研究的次要目的是确定与泊沙康唑谷水平升高相关的患者因素。
共纳入109例LTR。平均年龄为58.1岁(四分位间距,48 - 65岁),大多数为男性(56%)。共评估了932次谷浓度,每位患者的中位数为8次(四分位间距,5 - 15次)。泊沙康唑谷浓度中位数为1.7 mg/L(四分位间距,1.1 - 2.5)。根据不良事件通用术语标准(CTCAE)定义的肝毒性在73.4%的受试者中观察到,大多数分类为1级(67.5%)。然而,泊沙康唑水平升高与天冬氨酸氨基转移酶(r = 0.03)、丙氨酸氨基转移酶(r = 0.04)、碱性磷酸酶(r = 0.04)和总胆红素(r = 0.02)之间无相关性。泊沙康唑谷浓度与QTc间期之间也无相关性(r = 0.03)。
该分析表明全血泊沙康唑水平与肝毒性或QTc延长之间不存在相关性。基于这些结果,对于显著高于治疗靶点的泊沙康唑水平,可能无需降低泊沙康唑剂量以避免肝毒性或QTc延长风险。