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Off-label Use of Ceftazidime/Avibactam in Neonatal Intensive Care Unit: A Real-life Experience and Literature Review

医学 头孢他啶/阿维巴坦 头孢他啶 不利影响 肺炎克雷伯菌 新生儿重症监护室 肺炎 抗生素 胎龄 儿科 重症监护医学 内科学 铜绿假单胞菌 怀孕 微生物学 生物化学 化学 遗传学 大肠杆菌 细菌 基因 生物
作者
Argyro Ftergioti,Melania Degli Antoni,Angeliki Kontou,Maria Kourti,Kalliopi Pantzartzi,Charalampos Zarras,Eleni Agakidou,Kosmas Sarafidis,Emmanuel Roilides,Εlias Iosifidis
出处
期刊:Pediatric Infectious Disease Journal [Ovid Technologies (Wolters Kluwer)]
卷期号:43 (5): e149-e154 被引量:2
标识
DOI:10.1097/inf.0000000000004247
摘要

Background: Multi/extensively drug-resistant bacterial infections have recently increased and new antimicrobial options are needed for difficult-to-treat infections. Ceftazidime/avibactam (CZA) has been approved for patients 3 months to 18 years of age, but real-life data on its off-label use in neonates and young infants are still scarce. Materials: We report demographic, clinical and microbiologic data as well as outcome and safety of all cases of infants treated with CZA between January 1, 2021 and September 30, 2022 in a tertiary neonatal intensive care unit. We also review all neonatal cases previously reported. Results: Twenty-one patients [17 males, with median gestational age 29 +2 (IQR 6 +6 ) weeks] received 31 CZA courses at a dose of 20–50 mg/kg/dose of ceftazidime q8h for suspected or proved multi/extensively drug-resistant infections. Median postnatal age at the onset of treatment was 44 days (IQR: 94 days). Twelve bacteremias, 2 urinary tract infections and 1 ventilator-acquired pneumonia were recorded. Twelve (39%) treatments were targeted, while 19 (61%) were empirically started due to known colonization with Klebsiella pneumoniae carbapenemase-producing Gram-negative bacteria. All patients had received multiple antibiotics prior and concomitantly with CZA. The most common pathogen identified at targeted administrations was carbapenem-resistant Klebsiella pneumoniae (83%). No serious adverse events attributed to the drug were detected. Twenty-one courses of CZA administration to 20 neonates with a median gestational age of 28.5 (IQR 3.5) weeks were previously reported without significant related adverse events. Conclusions: Favorable clinical and microbiologic responses in neonatal intensive care unit patients treated with CZA off-label were observed without significant and unexpected adverse events in critically ill neonates.
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