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在囊性纤维化跨膜传导调节因子调节剂治疗时代,对囊性纤维化儿童铜绿假单胞菌抗生素敏感性的三年纵向评估。

A Three-year Longitudinal Assessment of Pseudomonas aeruginosa Antibiotic Susceptibility in Children With Cystic Fibrosis in the Era of Cystic Fibrosis Transmembrane Conductance Regulator Modulator Therapy.

作者信息

Stout Dayna, Bradley John S, Fireizen Yaron, Akong Kathryn, Ramchandar Nanda

机构信息

From the Division of Infectious Diseases, Rady Childrens Hospital San Diego, San Diego.

Department of Pediatrics, University of California, San Diego School of Medicine, La Jolla.

出版信息

Pediatr Infect Dis J. 2025 Mar 1;44(3):e77-e80. doi: 10.1097/INF.0000000000004580. Epub 2024 Oct 4.

DOI:10.1097/INF.0000000000004580
PMID:39733270
Abstract

Cystic fibrosis is a genetic disease characterized by chronic lung infection, often with Pseudomonas aeruginosa , requiring repeated antibiotic treatment for pulmonary exacerbations. In the era of cystic fibrosis transmembrane conductance regulator modulator therapy, we assessed susceptibility to antipseudomonal antibiotics in modulator-eligible and modulator-ineligible children over 3 years and found that P. aeruginosa isolates largely remained susceptible to standard parenteral but not oral antimicrobial agents.

摘要

囊性纤维化是一种遗传性疾病,其特征为慢性肺部感染,常由铜绿假单胞菌引起,肺部病情加重时需要反复使用抗生素治疗。在囊性纤维化跨膜传导调节因子调节剂治疗时代,我们评估了3岁以上符合使用调节剂条件和不符合使用调节剂条件的儿童对抗铜绿假单胞菌抗生素的敏感性,发现铜绿假单胞菌分离株对标准肠外抗菌药物大多仍敏感,但对口服抗菌药物不敏感。

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