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Pragmatic criteria to define chronic pseudomonas aeruginosa infection among adults with cystic fibrosis.

作者信息

Hoo Zhe Hui, Coates Elizabeth, Maguire Chin, Cantrill Hannah, Shafi Nadia, Nash Edward F, McGowan Angela, Bourke Stephen J, Flight William G, Daniels Thomas V, Nightingale Julia A, Allenby Mark I, Curley Rachael, Wildman Martin J

机构信息

School of Health and Related Research (ScHARR), University of Sheffield, Regent Court, 30 Regent Street,, Sheffield, S1 4DA, UK.

Sheffield Adult Cystic Fibrosis Centre, Brearley Outpatient, Sheffield Teaching Hospitals NHS Foundation Trust, Northern General Hospital, Herries Road, Sheffield, S5 7AU, UK.

出版信息

Eur J Clin Microbiol Infect Dis. 2018 Nov;37(11):2219-2222. doi: 10.1007/s10096-018-3358-8. Epub 2018 Aug 18.

DOI:10.1007/s10096-018-3358-8
PMID:30121804
Abstract
摘要

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本文引用的文献

1
Understanding Pseudomonas status among adults with cystic fibrosis: a real-world comparison of the Leeds criteria against clinicians' decision.了解成人囊性纤维化患者中的铜绿假单胞菌状况:利兹标准与临床医生决策的真实世界比较。
Eur J Clin Microbiol Infect Dis. 2018 Apr;37(4):735-743. doi: 10.1007/s10096-017-3168-4. Epub 2018 Jan 6.
2
Accurate reporting of adherence to inhaled therapies in adults with cystic fibrosis: methods to calculate "normative adherence".准确报告成年囊性纤维化患者吸入疗法的依从性:计算“规范依从性”的方法
Patient Prefer Adherence. 2016 May 23;10:887-900. doi: 10.2147/PPA.S105530. eCollection 2016.
3
Ciprofloxacin DPI: a randomised, placebo-controlled, phase IIb efficacy and safety study on cystic fibrosis.
环丙沙星 DPI:一项囊性纤维化的随机、安慰剂对照、IIb 期疗效和安全性研究。
BMJ Open Respir Res. 2015 Dec 2;2(1):e000100. doi: 10.1136/bmjresp-2015-000100. eCollection 2015.
4
How and why to monitor Pseudomonas aeruginosa infections in the long term at a cystic fibrosis centre.在囊性纤维化中心长期监测铜绿假单胞菌感染的方式及原因。
J Hosp Infect. 2016 Jan;92(1):54-60. doi: 10.1016/j.jhin.2015.09.010. Epub 2015 Oct 8.
5
Changing Epidemiology of the Respiratory Bacteriology of Patients With Cystic Fibrosis.囊性纤维化患者呼吸道细菌学的流行病学变化
Chest. 2016 Feb;149(2):390-400. doi: 10.1378/chest.15-0676. Epub 2016 Jan 12.
6
Cystic Fibrosis Foundation pulmonary guideline. pharmacologic approaches to prevention and eradication of initial Pseudomonas aeruginosa infection.囊性纤维化基金会肺部指南:预防和清除初始绿脓假单胞菌感染的药物治疗方法。
Ann Am Thorac Soc. 2014 Dec;11(10):1640-50. doi: 10.1513/AnnalsATS.201404-166OC.
7
Children and young adults with CF in the USA have better lung function compared with the UK.与英国相比,美国患有囊性纤维化的儿童和年轻人肺功能更好。
Thorax. 2015 Mar;70(3):229-36. doi: 10.1136/thoraxjnl-2014-205718. Epub 2014 Sep 25.
8
Cystic fibrosis pulmonary guidelines. Chronic medications for maintenance of lung health.囊性纤维化肺部治疗指南。用于维持肺部健康的慢性药物。
Am J Respir Crit Care Med. 2013 Apr 1;187(7):680-9. doi: 10.1164/rccm.201207-1160oe.
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Inhaled aztreonam lysine vs. inhaled tobramycin in cystic fibrosis: a comparative efficacy trial.吸入性阿佐霉素赖氨酸与吸入性妥布霉素治疗囊性纤维化的比较疗效试验。
J Cyst Fibros. 2013 Mar;12(2):130-40. doi: 10.1016/j.jcf.2012.07.006. Epub 2012 Sep 15.
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Early anti-pseudomonal acquisition in young patients with cystic fibrosis: rationale and design of the EPIC clinical trial and observational study'.早期抗假单胞菌在年轻囊性纤维化患者中的获得:EPIC 临床试验和观察研究的原理和设计'。
Contemp Clin Trials. 2009 May;30(3):256-68. doi: 10.1016/j.cct.2009.01.003. Epub 2009 Jan 15.