Effect of a microaerosol filter on spirometry in children with cystic fibrosis.
作者信息
Rogers D, Doull I J M
机构信息
Cystic Fibrosis/Respiratory Unit, Department of Child Health, University Hospital of Wales, Cardiff, UK.
出版信息
Acta Paediatr. 2002;91(11):1257-9. doi: 10.1080/080352502320777522.
PMID:12463328
Abstract
AIM
To measure the effect of an in-line microaerosol filter on spirometric values in cystic fibrosis (CF).
METHODS
Twenty-six subjects with CF undertook a randomized, open, cross-over comparison of spirometry with and without an in-line filter.
RESULTS
The filter had no significant effect on spirometric parameters nor was there any order effect. Measurement error was unrelated to the magnitude of the measurement.
CONCLUSION
In-line microaerosol filters do not affect spirometric values or variability in children with CF.
摘要
相似文献
1
Effect of a microaerosol filter on spirometry in children with cystic fibrosis.
Acta Paediatr. 2002;91(11):1257-9. doi: 10.1080/080352502320777522.
2
Improved air trapping evaluation in chest computed tomography in children with cystic fibrosis using real-time spirometric monitoring and biofeedback.使用实时肺量计监测和生物反馈技术改善囊性纤维化患儿胸部 CT 中的空气潴留评估。
J Cyst Fibros. 2013 Dec;12(6):559-66. doi: 10.1016/j.jcf.2013.05.012. Epub 2013 Jun 27.
3
Spirometry in early childhood in cystic fibrosis patients.囊性纤维化患者幼儿期的肺功能测定
Chest. 2007 Feb;131(2):356-61. doi: 10.1378/chest.06-1351.
4
Correlation between parameters of volumetric capnography and spirometry during a submaximal exercise protocol on a treadmill in patients with cystic fibrosis and healthy controls.在平板跑步机上进行次最大运动方案时，囊性纤维化患者和健康对照者的容积二氧化碳图参数与肺量计检查参数的相关性。
Pulmonology. 2019 Jan-Feb;25(1):21-31. doi: 10.1016/j.pulmoe.2018.04.006. Epub 2018 Jun 25.
5
Spirometry in 3- to 6-year-old children with cystic fibrosis.3至6岁囊性纤维化患儿的肺功能测定
Am J Respir Crit Care Med. 2002 Jul 1;166(1):67-71. doi: 10.1164/rccm.200111-056OC.
6
Multiple-breath inert gas washout and spirometry versus structural lung disease in cystic fibrosis.囊性纤维化患者的多呼吸惰性气体冲洗和肺量测定与结构性肺病的关系
Thorax. 2008 Feb;63(2):129-34. doi: 10.1136/thx.2007.077784. Epub 2007 Aug 3.
7
Small airway involvement in cystic fibrosis lung disease: routine spirometry as an early and sensitive marker.囊性纤维化肺病中小气道受累：常规肺功能检查作为早期和敏感的标志物。
Pediatr Pulmonol. 2013 Nov;48(11):1081-8. doi: 10.1002/ppul.22777. Epub 2013 Feb 8.
8
A comparison of spirometric variables in cystic fibrosis and bronchiectasis over 4 years.4年间囊性纤维化和支气管扩张症患者肺量计变量的比较
Respir Med. 1993 Jul;87(5):395-6. doi: 10.1016/0954-6111(93)90055-5.
9
Effect of oral glycine on the clinical, spirometric and inflammatory status in subjects with cystic fibrosis: a pilot randomized trial.口服甘氨酸对囊性纤维化患者临床、肺功能和炎症状态的影响：一项初步随机试验。
BMC Pulm Med. 2017 Dec 15;17(1):206. doi: 10.1186/s12890-017-0528-x.
10
Decline in lung function does not predict future decline in lung function in cystic fibrosis patients.肺功能下降并不能预测囊性纤维化患者未来的肺功能下降情况。
Pediatr Pulmonol. 2015 Sep;50(9):856-62. doi: 10.1002/ppul.23227. Epub 2015 Jun 18.
Zotero 插件