Suppr超能文献

囊性纤维化患儿肺部疾病演变的区域性差异。

Regional differences in the evolution of lung disease in children with cystic fibrosis.

机构信息

Department of Pediatrics, University of Wisconsin-Madison, Madison, Wisconsin 53792-9988, USA.

出版信息

Pediatr Pulmonol. 2012 Jul;47(7):635-40. doi: 10.1002/ppul.21604. Epub 2011 Dec 7.

Abstract

Progression of lung disease is a major event in children with cystic fibrosis (CF), but regional differences in its evolution are unclear. We hypothesized that regional differences occur beginning in early childhood. We examined this issue by evaluating 132 patients followed in the Wisconsin Neonatal Screening Project between 1985 and 2010. We scored chest X-rays obtained every 1-2 years with the Wisconsin chest X-ray system, in which we divided the lungs into quadrants, and gave special attention to ratings for bronchiectasis (BX) and nodular/branching opacities. We compared the upper and lower quadrant scores, and upper right and left quadrant scores, as patients aged using a multivariable generalized estimation equation (GEE) model. We did a confirmatory analysis for a subset of 81 patients with chest computerized tomography (CT) images obtained in 2000 and scored using the Brody scoring system. The chest X-ray analysis shows that the upper quadrants have higher BX (P<0.001) and nodular/branching opacities (P<0.001) scores than the lower quadrants. CT analysis likewise reveals that the upper quadrants have more BX (P=0.02). Patients positive for mucoid PA showed significantly higher BX scores than patients with non-mucoid PA (P=0.001). Chest X-ray scoring also revealed that the upper right quadrant has more BX (P<0.001) than the upper left quadrant, and CT analysis was again confirmatory (P<0.001). We conclude that pediatric patients with CF develop more severe lung disease in the upper lobes than the lower lobes in association with mucoid PA infections and also have more severe lung disease on the right side than on the left side in the upper quadrants. A variety of potential explanations such as aspiration episodes may be clinically relevant and provide insights regarding therapies.

摘要

肺部疾病的进展是囊性纤维化(CF)患儿的主要事件,但疾病进展的区域差异尚不清楚。我们假设区域差异始于儿童早期。我们通过评估 1985 年至 2010 年间在威斯康星州新生儿筛查计划中接受随访的 132 例患者来研究这个问题。我们使用威斯康星州 X 射线系统对每 1-2 年获得的胸部 X 射线进行评分,该系统将肺部分为四个象限,并特别注意支气管扩张(BX)和结节/分支状不透明的评分。我们使用多变量广义估计方程(GEE)模型比较了患者年龄的上、下象限评分以及右上和左上象限评分。我们对 2000 年获得的 81 例胸部计算机断层扫描(CT)图像的子集进行了确认性分析,并使用 Brody 评分系统进行了评分。胸部 X 射线分析显示,上象限的 BX(P<0.001)和结节/分支状不透明评分(P<0.001)均高于下象限。CT 分析同样显示上象限的 BX 更多(P=0.02)。黏液性 PA 阳性患者的 BX 评分明显高于非黏液性 PA 患者(P=0.001)。胸部 X 射线评分还显示右上象限的 BX 多于左上象限(P<0.001),CT 分析再次证实(P<0.001)。我们的结论是,与黏液性 PA 感染相关,CF 儿科患者的上叶比下叶更容易发生更严重的肺部疾病,上叶的右上象限比左上象限更容易发生更严重的肺部疾病。各种潜在的解释,如吸入事件,可能具有临床相关性,并为治疗提供了深入了解。

相似文献

1
Regional differences in the evolution of lung disease in children with cystic fibrosis.
Pediatr Pulmonol. 2012 Jul;47(7):635-40. doi: 10.1002/ppul.21604. Epub 2011 Dec 7.
5
Ultrafast computerized tomography of the chest in cystic fibrosis: a new scoring system.
Pediatr Pulmonol. 1991;11(1):81-6. doi: 10.1002/ppul.1950110112.
6
PRAGMA-CF. A Quantitative Structural Lung Disease Computed Tomography Outcome in Young Children with Cystic Fibrosis.
Am J Respir Crit Care Med. 2015 May 15;191(10):1158-65. doi: 10.1164/rccm.201501-0061OC.
7
Scoring of chest CT in children with cystic fibrosis: state of the art.
Pediatr Radiol. 2014 Dec;44(12):1496-506. doi: 10.1007/s00247-013-2867-y. Epub 2014 Aug 28.

引用本文的文献

1
Quantifying Spatial Distribution of Ventilation Defects in Multiple Pulmonary Diseases With Hyperpolarized Xenon MRI.
J Magn Reson Imaging. 2025 Apr;61(4):1860-1873. doi: 10.1002/jmri.29627. Epub 2024 Oct 22.
3
Sensitive structural and functional measurements and 1-year pulmonary outcomes in pediatric cystic fibrosis.
J Cyst Fibros. 2021 May;20(3):533-539. doi: 10.1016/j.jcf.2020.11.019. Epub 2020 Dec 4.
4
mSphere of Influence: a Community To Study Communities.
mSphere. 2020 Feb 5;5(1):e00047-20. doi: 10.1128/mSphere.00047-20.
5
Cystic Fibrosis and Pseudomonas aeruginosa: the Host-Microbe Interface.
Clin Microbiol Rev. 2019 May 29;32(3). doi: 10.1128/CMR.00138-18. Print 2019 Jun 19.
6
Mucoid Pseudomonas aeruginosa and regional inflammation in the cystic fibrosis lung.
J Cyst Fibros. 2019 Nov;18(6):796-803. doi: 10.1016/j.jcf.2019.04.009. Epub 2019 Apr 26.
7
A Flow Cytometric Method for Isolating Cystic Fibrosis Airway Macrophages from Expectorated Sputum.
Am J Respir Cell Mol Biol. 2019 Jul;61(1):42-50. doi: 10.1165/rcmb.2018-0236MA.

本文引用的文献

1
Bronchoscopy in cystic fibrosis infants diagnosed by newborn screening.
Pediatr Pulmonol. 2011 Jul;46(7):696-700. doi: 10.1002/ppul.21434. Epub 2011 Mar 1.
2
Cystic Fibrosis Foundation evidence-based guidelines for management of infants with cystic fibrosis.
J Pediatr. 2009 Dec;155(6 Suppl):S73-93. doi: 10.1016/j.jpeds.2009.09.001.
4
Bronchiectasis in infants and preschool children diagnosed with cystic fibrosis after newborn screening.
J Pediatr. 2009 Nov;155(5):623-8.e1. doi: 10.1016/j.jpeds.2009.05.005. Epub 2009 Jul 19.
5
Computed tomography reflects lower airway inflammation and tracks changes in early cystic fibrosis.
Am J Respir Crit Care Med. 2007 May 1;175(9):943-50. doi: 10.1164/rccm.200603-343OC. Epub 2007 Feb 15.
7
Chest physiotherapy in infants with cystic fibrosis: to tip or not? A five-year study.
Pediatr Pulmonol. 2003 Mar;35(3):208-13. doi: 10.1002/ppul.10227.
10
Wisconsin cystic fibrosis chest radiograph scoring system: validation and standardization for application to longitudinal studies.
Pediatr Pulmonol. 2000 Jun;29(6):457-67. doi: 10.1002/(sici)1099-0496(200006)29:6<457::aid-ppul8>3.0.co;2-9.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验