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Shifting Landscape of Airway Infection in Early Cystic Fibrosis.

作者信息

Hoppe Jordana E, Sagel Scott D

机构信息

Department of PediatricsChildren's Hospital Colorado and University of Colorado School of MedicineAurora, Colorado.

出版信息

Am J Respir Crit Care Med. 2019 Sep 1;200(5):528-529. doi: 10.1164/rccm.201903-0529ED.

DOI:10.1164/rccm.201903-0529ED
PMID:30875233
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6727166/
Abstract
摘要

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本文引用的文献

1
Changing Prevalence of Lower Airway Infections in Young Children with Cystic Fibrosis.囊性纤维化患儿下呼吸道感染患病率的变化。
Am J Respir Crit Care Med. 2019 Sep 1;200(5):590-599. doi: 10.1164/rccm.201810-1919OC.
2
Clinical outcomes in U.S. infants with cystic fibrosis from 2001 to 2012.2001 年至 2012 年美国囊性纤维化婴儿的临床结局。
Pediatr Pulmonol. 2018 Nov;53(11):1492-1497. doi: 10.1002/ppul.24165. Epub 2018 Sep 26.
3
The myriad challenges of respiratory fungal infection in cystic fibrosis.囊性纤维化患者呼吸道真菌感染的诸多挑战。
Pediatr Pulmonol. 2018 Nov;53(S3):S75-S85. doi: 10.1002/ppul.24126. Epub 2018 Jul 10.
4
Risk factors for persistent Aspergillus respiratory isolation in cystic fibrosis.囊性纤维化患者中持续性烟曲霉呼吸道定植的危险因素。
J Cyst Fibros. 2018 Sep;17(5):624-630. doi: 10.1016/j.jcf.2018.01.008. Epub 2018 Feb 12.
5
Early Respiratory Bacterial Detection and Antistaphylococcal Antibiotic Prophylaxis in Young Children with Cystic Fibrosis.早期呼吸道细菌检测和抗葡萄球菌抗生素预防在囊性纤维化的幼儿。
Ann Am Thorac Soc. 2018 Jan;15(1):42-48. doi: 10.1513/AnnalsATS.201705-376OC.
6
Retrospective observational study of French patients with cystic fibrosis and a Gly551Asp-CFTR mutation after 1 and 2years of treatment with ivacaftor in a real-world setting.回顾性观察研究：在真实环境中，1 年和 2 年后使用 ivacaftor 治疗法治疗囊性纤维化和 Gly551Asp-CFTR 突变的法国患者。
J Cyst Fibros. 2018 Jan;17(1):89-95. doi: 10.1016/j.jcf.2017.07.001. Epub 2017 Jul 12.
7
Restoring Cystic Fibrosis Transmembrane Conductance Regulator Function Reduces Airway Bacteria and Inflammation in People with Cystic Fibrosis and Chronic Lung Infections.恢复囊性纤维化跨膜传导调节因子功能可减少囊性纤维化和慢性肺部感染患者的气道细菌及炎症。
Am J Respir Crit Care Med. 2017 Jun 15;195(12):1617-1628. doi: 10.1164/rccm.201609-1954OC.
8
Chronic Aspergillus fumigatus colonization of the pediatric cystic fibrosis airway is common and may be associated with a more rapid decline in lung function.小儿囊性纤维化气道慢性烟曲霉定植很常见，且可能与肺功能下降更快有关。
Med Mycol. 2016 Jul 1;54(5):537-43. doi: 10.1093/mmy/myv119. Epub 2016 Jan 17.
9
Pseudomonas aeruginosa in cystic fibrosis patients with G551D-CFTR treated with ivacaftor.接受依伐卡托治疗的携带G551D-CFTR的囊性纤维化患者中的铜绿假单胞菌
Clin Infect Dis. 2015 Mar 1;60(5):703-12. doi: 10.1093/cid/ciu944. Epub 2014 Nov 25.
10
Effect of bronchoalveolar lavage-directed therapy on Pseudomonas aeruginosa infection and structural lung injury in children with cystic fibrosis: a randomized trial.支气管肺泡灌洗导向治疗对囊性纤维化患儿铜绿假单胞菌感染和结构性肺损伤的影响：一项随机试验。
JAMA. 2011 Jul 13;306(2):163-71. doi: 10.1001/jama.2011.954.