Maquera-Afaray Julio, Luna-Vilchez Medalit, Salazar-Mesones Blanca, Portillo-Alvarez Diana, Uribe-Ramirez Luis, Taipe-Sedano Graciela, Santillán-Salas Carlos, López José W
Unidad de Atención Integral Especializada (JM-A, ML-V, BS-M, DP-A, LU-R, GT-S, CS-S, JWL), Instituto Nacional de Salud del Niño San Borja, Lima, Perú.
Facultad de Ciencias de la Salud (JM-A), Universidad Privada de Tacna, Tacna, Perú.
J Pediatr Pharmacol Ther. 2022;27(1):57-62. doi: 10.5863/1551-6776-27.1.57. Epub 2021 Dec 22.
Prophylaxis with posaconazole (PP) is effective in the prevention of invasive fungal infections in immunocompromised adult patients. However, evaluation of its effectiveness and safety in children is limited. The aim of the study was to describe the use of posaconazole as antifungal prophylaxis in children.
We reviewed the medical records of immunocompromised patients younger than 13 years with hematologic diseases and post hematopoietic stem cell transplant (HSCT) who received antifungal PP at the Instituto Nacional de Salud del Niño San Borja (INSN-SB) in Lima, Peru, from January 2014 to December 2018.
Fifty-six courses of PP were identified in 47 patients with a median age of 7.5 years (IQR, 4-10), 51.6% (n = 24) of whom were female. The main underlying medical conditions were aplastic anemia (n = 19, 33.9%), acute lymphoblastic leukemia (n = 18, 32.1%), acute myeloid leukemia (n = 14, 25.0%), and 34.1% had undergone HSCT. The median dose of posaconazole was 13.62 mg/kg/day (IQR, 12.0-16.8), and the median duration of PP was 24 days (IQR, 16-82). Gastrointestinal symptoms included abdominal pain (17.9%), nausea (16.1%), diarrhea (7.1%), and vomiting (3.6%). Elevated alanine aminotransferase and aspartate aminotransferase levels were observed in 9/35 patients (25.7%) and 10/51 (19.6%) patients, respectively. Five cases of breakthrough fungal infection were identified (8.9%).
Patients younger than 13 years who received PP showed an increase in transaminase values, and the development of breakthrough fungal infections.
泊沙康唑预防性用药(PP)对预防免疫功能低下的成年患者侵袭性真菌感染有效。然而,其在儿童中的有效性和安全性评估有限。本研究的目的是描述泊沙康唑在儿童中作为抗真菌预防性用药的使用情况。
我们回顾了2014年1月至2018年12月在秘鲁利马的圣博尔哈国家儿童健康研究所(INSN-SB)接受抗真菌PP治疗的13岁以下血液系统疾病和造血干细胞移植(HSCT)后免疫功能低下患者的病历。
在47例患者中确定了56个PP疗程,中位年龄为7.5岁(四分位间距,4 - 10岁),其中51.6%(n = 24)为女性。主要潜在疾病为再生障碍性贫血(n = 19,33.9%)、急性淋巴细胞白血病(n = 18,32.1%)、急性髓细胞白血病(n = 14,25.0%),34.1%接受过HSCT。泊沙康唑的中位剂量为13.62 mg/kg/天(四分位间距,12.0 - 16.8),PP的中位疗程为24天(四分位间距,16 - 82天)。胃肠道症状包括腹痛(17.9%)、恶心(16.1%)、腹泻(7.1%)和呕吐(3.6%)。分别在9/35例患者(25.7%)和10/51例患者(19.6%)中观察到丙氨酸氨基转移酶和天冬氨酸氨基转移酶水平升高。确定了5例突破性真菌感染病例(8.9%)。
接受PP治疗的13岁以下患者转氨酶值升高,且出现了突破性真菌感染。