Imaging Lung Function Abnormalities in Primary Ciliary Dyskinesia Using Hyperpolarized Gas Ventilation MRI.
作者信息
Smith Laurie J, West Noreen, Hughes David, Marshall Helen, Johns Christopher S, Stewart Neil J, Chan Ho-Fung, Rao Madhwesha, Capener David J, Bray Jody, Collier Guilhem J, Hughes Paul J C, Norquay Graham, Schofield Lynne, Chetcuti Phil, Moya Eduardo, Wild Jim M
机构信息
1 University of Sheffield Sheffield, United Kingdom.
2 Sheffield Children's Hospital NHS Foundation Trust Sheffield, United Kingdom and.
出版信息
Ann Am Thorac Soc. 2018 Dec;15(12):1487-1490. doi: 10.1513/AnnalsATS.201711-890RL.
Abstract
摘要
相似文献
1
Imaging Lung Function Abnormalities in Primary Ciliary Dyskinesia Using Hyperpolarized Gas Ventilation MRI.使用超极化气体通气MRI成像原发性纤毛运动障碍中的肺功能异常。
Ann Am Thorac Soc. 2018 Dec;15(12):1487-1490. doi: 10.1513/AnnalsATS.201711-890RL.
2
Structural and Functional Lung Impairment in Primary Ciliary Dyskinesia. Assessment with Magnetic Resonance Imaging and Multiple Breath Washout in Comparison to Spirometry.原发性纤毛运动障碍的结构性和功能性肺损伤。磁共振成像和多呼吸冲洗与肺活量测定法的评估比较。
Ann Am Thorac Soc. 2018 Dec;15(12):1434-1442. doi: 10.1513/AnnalsATS.201712-967OC.
3
Semiautomated Ventilation Defect Quantification in Exercise-induced Bronchoconstriction Using Hyperpolarized Helium-3 Magnetic Resonance Imaging: A Repeatability Study.使用超极化氦-3磁共振成像对运动诱发支气管收缩中的通气缺陷进行半自动定量分析：一项重复性研究
Acad Radiol. 2016 Sep;23(9):1104-14. doi: 10.1016/j.acra.2016.04.005. Epub 2016 Jun 2.
4
Hyperpolarized 3helium magnetic resonance ventilation imaging of the lung in cystic fibrosis: comparison with high resolution CT and spirometry.囊性纤维化患者肺部的超极化3氦磁共振通气成像：与高分辨率CT和肺量计的比较
Eur Radiol. 2006 Nov;16(11):2483-90. doi: 10.1007/s00330-006-0311-5. Epub 2006 Jul 27.
5
Primary ciliary dyskinesia: can we identify patients with the most severe phenotype?原发性纤毛运动障碍：我们能否识别出具有最严重表型的患者？
Minerva Med. 2021 Aug;112(4):518-520. doi: 10.23736/S0026-4806.19.06054-3. Epub 2019 Jun 25.
6
Lung structure-function correlation in patients with primary ciliary dyskinesia.原发性纤毛运动障碍患者的肺结构-功能相关性。
Thorax. 2015 Apr;70(4):339-45. doi: 10.1136/thoraxjnl-2014-206578. Epub 2015 Feb 11.
7
Applications of hyperpolarized helium-3 gas magnetic resonance imaging in pediatric lung disease.超极化氦-3气体磁共振成像在儿科肺部疾病中的应用。
Top Magn Reson Imaging. 2003 Jun;14(3):231-6. doi: 10.1097/00002142-200306000-00003.
8
Assessment of lung disease in children with cystic fibrosis using hyperpolarized 3-Helium MRI: comparison with Shwachman score, Chrispin-Norman score and spirometry.使用超极化3-氦磁共振成像评估囊性纤维化患儿的肺部疾病：与施瓦克曼评分、克里斯平-诺曼评分及肺量计检查结果的比较
Eur Radiol. 2007 Apr;17(4):1018-24. doi: 10.1007/s00330-006-0392-1. Epub 2006 Aug 29.
9
Detection of early subclinical lung disease in children with cystic fibrosis by lung ventilation imaging with hyperpolarised gas MRI.应用超极化气体 MRI 肺通气成像检测囊性纤维化患儿的早期亚临床肺部疾病。
Thorax. 2017 Aug;72(8):760-762. doi: 10.1136/thoraxjnl-2016-208948. Epub 2017 Mar 6.
10
Comparison of Multiple Breath Washout and Spirometry in Children with Primary Ciliary Dyskinesia and Cystic Fibrosis and Healthy Controls.原发性纤毛运动障碍和囊性纤维化患儿与健康对照者的多次呼吸冲洗和肺量测定比较。
Ann Am Thorac Soc. 2020 Sep;17(9):1085-1093. doi: 10.1513/AnnalsATS.201905-375OC.
引用本文的文献
1
Multiple breath washout in primary ciliary dyskinesia: a systematic review of the literature.原发性纤毛运动障碍中的多次呼吸冲洗：文献系统评价
Eur Respir Rev. 2025 Jun 18;34(176). doi: 10.1183/16000617.0002-2025. Print 2025 Apr.
2
Pulmonary MRI in Newborns and Children.新生儿和儿童的肺部磁共振成像
J Magn Reson Imaging. 2025 May;61(5):2094-2115. doi: 10.1002/jmri.29669. Epub 2024 Dec 6.
3
Primary Ciliary Dyskinesia: A Clinical Review.原发性纤毛运动障碍：临床综述。
Cells. 2024 Jun 4;13(11):974. doi: 10.3390/cells13110974.
4
Lung Function in Children with Primary Ciliary Dyskinesia.原发性纤毛运动障碍患儿的肺功能
Children (Basel). 2023 Feb 2;10(2):290. doi: 10.3390/children10020290.
5
Image Phenotyping of Preterm-Born Children Using Hyperpolarized Xe Lung Magnetic Resonance Imaging and Multiple-Breath Washout.应用超极化氙气肺部磁共振成像和多次呼吸冲洗对早产儿进行图像表型分析。
Am J Respir Crit Care Med. 2023 Jan 1;207(1):89-100. doi: 10.1164/rccm.202203-0606OC.
6
Lower airway clinical outcome measures for use in primary ciliary dyskinesia research: a scoping review.用于原发性纤毛运动障碍研究的下呼吸道临床结局指标：一项范围综述
ERJ Open Res. 2021 Nov 29;7(4). doi: 10.1183/23120541.00320-2021. eCollection 2021 Oct.
本文引用的文献
1
Longitudinal Assessment of Children with Mild Cystic Fibrosis Using Hyperpolarized Gas Lung Magnetic Resonance Imaging and Lung Clearance Index.使用超极化气体肺磁共振成像和肺清除指数对轻度囊性纤维化儿童进行纵向评估。
Am J Respir Crit Care Med. 2018 Feb 1;197(3):397-400. doi: 10.1164/rccm.201705-0894LE.
2
Lung structure and function similarities between primary ciliary dyskinesia and mild cystic fibrosis: a pilot study.原发性纤毛运动障碍与轻度囊性纤维化之间的肺结构和功能相似性：一项初步研究。
Ital J Pediatr. 2017 Apr 12;43(1):34. doi: 10.1186/s13052-017-0351-2.
3
Detection of early subclinical lung disease in children with cystic fibrosis by lung ventilation imaging with hyperpolarised gas MRI.应用超极化气体 MRI 肺通气成像检测囊性纤维化患儿的早期亚临床肺部疾病。
Thorax. 2017 Aug;72(8):760-762. doi: 10.1136/thoraxjnl-2016-208948. Epub 2017 Mar 6.
4
Correlation of Lung Clearance Index with Hyperpolarized Xe Magnetic Resonance Imaging in Pediatric Subjects with Cystic Fibrosis.肺清除指数与超极化氙磁共振成像在囊性纤维化儿科患者中的相关性
Am J Respir Crit Care Med. 2017 Oct 15;196(8):1073-1075. doi: 10.1164/rccm.201611-2228LE.
5
Use of hyperpolarized helium-3 MRI to assess response to ivacaftor treatment in patients with cystic fibrosis.使用超极化氦-3磁共振成像评估囊性纤维化患者对依伐卡托治疗的反应。
J Cyst Fibros. 2017 Mar;16(2):267-274. doi: 10.1016/j.jcf.2016.12.004. Epub 2017 Jan 26.
6
The international primary ciliary dyskinesia cohort (iPCD Cohort): methods and first results.国际原发性纤毛运动障碍队列研究（iPCD队列）：方法与初步结果
Eur Respir J. 2017 Jan 4;49(1). doi: 10.1183/13993003.01181-2016. Print 2017 Jan.
7
European Respiratory Society guidelines for the diagnosis of primary ciliary dyskinesia.欧洲呼吸学会原发性纤毛运动障碍诊断指南。
Eur Respir J. 2017 Jan 4;49(1). doi: 10.1183/13993003.01090-2016. Print 2017 Jan.
8
Hyperpolarized Xe for investigation of mild cystic fibrosis lung disease in pediatric patients.超极化氙用于小儿轻度囊性纤维化肺病的研究。
J Cyst Fibros. 2017 Mar;16(2):275-282. doi: 10.1016/j.jcf.2016.07.008. Epub 2016 Jul 29.
9
Clinical characteristics, functional respiratory decline and follow-up in adult patients with primary ciliary dyskinesia.原发性纤毛运动障碍成年患者的临床特征、功能呼吸下降及随访。
Thorax. 2017 Feb;72(2):154-160. doi: 10.1136/thoraxjnl-2015-207891. Epub 2016 Jul 5.
10
Lung morphology assessment of cystic fibrosis using MRI with ultra-short echo time at submillimeter spatial resolution.利用亚毫米空间分辨率的超高回波时间 MRI 评估囊性纤维化的肺部形态。
Eur Radiol. 2016 Nov;26(11):3811-3820. doi: 10.1007/s00330-016-4218-5. Epub 2016 Feb 2.
Zotero 插件