Inhaled aztreonam lysine in the management of Pseudomonas aeruginosa in patients with cystic fibrosis: real-life effectiveness

Inés Jiménez-Lozano, Carmen Luna-Paredes, Emilio Monte-Boquet, Aurora Fernández-Polo, Carme Cañete-Ramírez, María Roch-Santed, Silvia Gartner, Antonio Álvarez-Fernández
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Abstract

Background Inhaled antibiotics have achieved or stabilised the clinical condition of patients with cystic fibrosis (CF) and chronic Pseudomonas aeruginosa infection. We aimed to determine the effectiveness of aztreonam lysine inhaled solution (AZLI) in patients with CF and chronic P. aeruginosa infection. Methods A retrospective observational study was conducted on patients with CF and chronic P. aeruginosa infection who received AZLI between July 2012 and September 2018 inclusive in three Spanish hospitals in a routine clinical practice setting. The primary endpoint was the absolute change in the percentage of predicted forced expiratory volume in 1 second (FEV1) compared with the previous 12 months, at the start of AZLI treatment and 12 months after starting the drug. Other variables analysed were exacerbations, hospitalisations, type and route of antibiotics prescribed, weight and body mass index (BMI) and adverse drug reactions. Results In a cohort of 52 patients, AZLI treatment led to stabilisation of FEV1, changing from a mean (SD) value of 55.60 (21.3)% at the start of treatment to 56.8 (20.4)% after 12 months of treatment (p=0.5296) in patients who had not previously received the drug. In addition, it significantly reduced exacerbations from a median (P25; P75) of 2.0 (1.0; 3.0) in the 12 months prior to AZLI to 1.0 (1.0; 2.0) in the 12 months after treatment initiation (p=0.0350). AZLI also reduced the need for other antibiotics and prevented a decrease in BMI, with an adequate safety profile. Conclusions AZLI achieved stabilisation of lung function measured by FEV1 in patients with CF and chronic P. aeruginosa infection, along with an adequate safety profile. Data are available upon reasonable request. no applicable.
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吸入阿曲南赖氨酸治疗囊性纤维化患者的铜绿假单胞菌:实际效果
背景 吸入抗生素可使囊性纤维化(CF)和慢性铜绿假单胞菌感染患者的临床病情好转或稳定。我们旨在确定阿曲南赖氨酸吸入溶液(AZLI)对 CF 和慢性铜绿假单胞菌感染患者的疗效。方法 对 2012 年 7 月至 2018 年 9 月(含)期间在西班牙三家医院常规临床实践环境中接受 AZLI 治疗的 CF 和慢性铜绿假单胞菌感染患者进行了一项回顾性观察研究。主要终点是与前12个月相比,AZLI治疗开始时和开始用药12个月后1秒用力呼气容积(FEV1)预测值百分比的绝对变化。其他分析变量包括病情恶化、住院治疗、处方抗生素的类型和途径、体重和体重指数(BMI)以及药物不良反应。结果 在一组 52 例患者中,AZLI 治疗使 FEV1 趋于稳定,治疗开始时的平均值(标度)为 55.60 (21.3)%,而在治疗 12 个月后,以前未接受过该药物治疗的患者的平均值(标度)为 56.8 (20.4)%(P=0.5296)。此外,AZLI 还显著降低了病情恶化的发生率,治疗前 12 个月的中位数(P25;P75)为 2.0(1.0;3.0),治疗开始后 12 个月的中位数(P25;P75)为 1.0(1.0;2.0)(P=0.0350)。AZLI 还减少了对其他抗生素的需求,并防止了体重指数的下降,同时具有充分的安全性。结论 AZLI 可稳定 CF 和慢性铜绿假单胞菌感染患者的 FEV1 肺功能,并具有良好的安全性。如有合理要求,可提供相关数据。
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