Department of pediatric nephrology, Dr Behçet Uz child disease and pediatric surgery training and research hospital, İzmir, Turkey.
Department of pediatric infectious diseases, Dr Behçet Uz children's diseases and surgery training and research hospital, İzmir, Turkey.
Nephrol Ther. 2021 Dec;17(7):507-511. doi: 10.1016/j.nephro.2021.06.007. Epub 2021 Sep 15.
Amphotericin B is a broad-spectrum antifungal agent and is the backbone of the treatment for medically important opportunistic fungal pathogens in children. This study aimed to compare the nephrotoxicity associated with L-AmB in children with acute lymphoblastic leukemia and acute myeloid leukemia.
A total of 112 pediatric acute lymphoblastic leukemia or acute myeloid leukemia patients who received treatment with L-AmB (Ambisome®) at the University of Health Sciences Dr Behcet Uz Children's Hospital over 7 years were included. The incidence of hypokalemia, decreased estimated glomerular filtration rate and presence of acute kidney injury was recorded.
The average L-AmB treatment duration was 17.1±15.0 days. Five patients (4.4%) of the patients had grade I acute renal injury according to KDIGO criteria and 16 patients (14.2%) had increased risk for kidney injury according to RIFLE criteria. There were no patients with eGFR decrease above 50% and no renal injury and failure were observed during L-AmB treatment. The rate of patients with hypokalemia in the pre-treatment was 17.9% and the post-L-AmB group was 50.0%. The rate of hypokalemia was higher in the post-treatment group (P=0.0015). Among the 112 patients, only two patients (1.7%) required cessation of L-AmB treatment due to resistant hypokalemia despite supplementation.
Hypokalemia was more common compared to glomerulotoxicity and acute renal injury (according to KDIGO and RIFLE criteria) in pediatric leukemia patients treated with L-AmB. Hypokalemia developed in nearly half of the patients and the study shows the need for randomized controlled trials and strategies for hypokalemia associated with L-AmB treatment.
两性霉素 B 是一种广谱抗真菌药物,是治疗儿童重要机会性真菌病原体的基础。本研究旨在比较儿童急性淋巴细胞白血病和急性髓细胞白血病患者使用两性霉素 B(Ambisome®)相关的肾毒性。
共纳入 112 名在健康科学大学贝赫切特·乌兹儿童医院接受两性霉素 B(Ambisome®)治疗的儿科急性淋巴细胞白血病或急性髓细胞白血病患者。记录低钾血症、估计肾小球滤过率下降和急性肾损伤的发生率。
平均两性霉素 B 治疗时间为 17.1±15.0 天。根据 KDIGO 标准,5 名患者(4.4%)为 I 级急性肾损伤,16 名患者(14.2%)根据 RIFLE 标准存在肾脏损伤风险增加。没有患者出现 eGFR 下降超过 50%,也没有在两性霉素 B 治疗期间观察到肾损伤和衰竭。治疗前低钾血症患者的发生率为 17.9%,治疗后为 50.0%。治疗后低钾血症发生率更高(P=0.0015)。在 112 名患者中,仅有 2 名患者(1.7%)因补充后仍存在耐药性低钾血症而停止两性霉素 B 治疗。
与肾小球毒性和急性肾损伤(根据 KDIGO 和 RIFLE 标准)相比,低钾血症在接受两性霉素 B 治疗的儿童白血病患者中更为常见。近一半的患者出现低钾血症,研究表明需要进行随机对照试验和制定与两性霉素 B 治疗相关的低钾血症策略。