Ferdjallah Asmaa, Nelson Kristina M, Meyer Kailey, Jennissen Cathryn A, Ebens Christen L
J Pediatr Pharmacol Ther. 2021;26(8):863-867. doi: 10.5863/1551-6776-26.8.863. Epub 2021 Nov 10.
Prolonged neutropenia increases the risk for lethal invasive fungal infections (IFIs) such as those caused by species. Isavuconazonium sulfate is a new triazole that lacks pediatric dosing recommendations. Clinical courses of 4 pediatric patients with IFIs in the peri-allogeneic hematopoietic cell transplantation (alloHCT) period between 2015 and 2017 were reviewed. The reviews included previously unreported pharmacokinetic and safety data, and the IFIs included . Isavuconazonium sulfate was initiated with a loading dose followed by daily dosing, adjusted to a goal trough concentration of >3 mg/L based on adult literature. This target was achieved at a median of 7 days, demonstrating varying rates of metabolism. Renal insufficiency, electrolyte disturbances, and transaminitis were noted, although attribution was confounded by other alloHCT complications. One patient survived infection-free to hospital discharge and 1 of 3 deceased patients had evidence of an unresolved IFI (case 2). Case 2 was subtherapeutic for 39% of the duration of treatment, compared with others at an average of 29%, suggesting this target trough to be clinically relevant because case 2 demonstrated positive sinus and nasal cultures for on autopsy. We recommend initiation of isavuconazonium 10 mg/kg with a maximum dose of 372 mg. A loading dose of 10 mg/kg is used every 8 hours for 6 doses followed by 10 mg/kg dosing every 24 hours. Monitoring must continue beyond steady state. If early monitoring is not possible, we recommend a first drug level at week 3. If dose increases are required, a partial reload has been more successful instead of increasing daily doses. Further larger studies are needed to demonstrate optimum dosing in pediatric patients.
长期中性粒细胞减少会增加致命性侵袭性真菌感染(IFI)的风险,例如由某些菌种引起的感染。硫酸艾沙康唑是一种新的三唑类药物,目前缺乏儿科用药推荐。回顾了2015年至2017年间4例异基因造血细胞移植(alloHCT)期间发生IFI的儿科患者的临床病程。这些回顾包括先前未报告的药代动力学和安全性数据,IFI包括……硫酸艾沙康唑开始时给予负荷剂量,随后每日给药,根据成人文献调整至目标谷浓度>3mg/L。该目标在中位7天达到,显示出不同的代谢率。尽管其他alloHCT并发症混淆了归因,但仍注意到肾功能不全、电解质紊乱和转氨酶升高。1例患者无感染存活至出院,3例死亡患者中有1例有未解决的IFI证据(病例2)。病例2在治疗持续时间的39%低于治疗水平,而其他患者平均为29%,这表明该目标谷浓度具有临床相关性,因为病例2尸检时鼻窦和鼻腔培养显示……阳性。我们建议开始使用硫酸艾沙康唑,剂量为10mg/kg,最大剂量为372mg。每8小时使用10mg/kg的负荷剂量,共6剂,随后每24小时给予10mg/kg剂量。监测必须持续超过稳态。如果无法进行早期监测,我们建议在第3周进行首次药物水平检测。如果需要增加剂量,部分重新加载比增加每日剂量更成功。需要进一步的大型研究来证明儿科患者的最佳给药方案。