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本文引用的文献

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Radiographic fibrosis score predicts survival in systemic sclerosis-associated interstitial lung disease.放射纤维化评分可预测系统性硬皮病相关间质性肺疾病的生存情况。
Respirology. 2018 Apr;23(4):385-391. doi: 10.1111/resp.13175. Epub 2017 Sep 19.
2
Mapping and predicting mortality from systemic sclerosis.系统性硬化症患者死亡率的预测与评估。
Ann Rheum Dis. 2017 Nov;76(11):1897-1905. doi: 10.1136/annrheumdis-2017-211448. Epub 2017 Aug 23.
3
Treatment of Rapidly Progressive Systemic Sclerosis: Current and Futures Perspectives.快速进展性系统性硬化症的治疗:现状与未来展望
Expert Opin Orphan Drugs. 2016;4(1):31-47. doi: 10.1517/21678707.2016.1114454. Epub 2015 Nov 23.
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Pulmonary involvement in systemic sclerosis.系统性硬皮病的肺部受累。
Autoimmun Rev. 2016 Nov;15(11):1094-1108. doi: 10.1016/j.autrev.2016.07.025. Epub 2016 Aug 4.
5
Interstitial lung disease in systemic sclerosis: progress in screening and early diagnosis.系统性硬化症中的间质性肺疾病:筛查与早期诊断的进展
Curr Opin Rheumatol. 2016 Nov;28(6):613-8. doi: 10.1097/BOR.0000000000000323.
6
Effect of Iterative Reconstruction on the Detection of Systemic Sclerosis-related Interstitial Lung Disease: Clinical Experience in 55 Patients.迭代重建对系统性硬化症相关间质性肺病检测的影响:55 例临床经验。
Radiology. 2016 Apr;279(1):297-305. doi: 10.1148/radiol.2015150849. Epub 2015 Nov 18.
7
Brief Report: Pulmonary Function Tests: High Rate of False-Negative Results in the Early Detection and Screening of Scleroderma-Related Interstitial Lung Disease.简报:肺功能检查:在硬皮病相关间质性肺病的早期检测和筛查中,存在大量假阴性结果。
Arthritis Rheumatol. 2015 Dec;67(12):3256-61. doi: 10.1002/art.39405.
8
Visual vs Fully Automatic Histogram-Based Assessment of Idiopathic Pulmonary Fibrosis (IPF) Progression Using Sequential Multidetector Computed Tomography (MDCT).使用序列多排螺旋计算机断层扫描(MDCT)对特发性肺纤维化(IPF)进展进行基于直方图的视觉评估与全自动评估对比
PLoS One. 2015 Jun 25;10(6):e0130653. doi: 10.1371/journal.pone.0130653. eCollection 2015.
9
Predictive value of serial high-resolution computed tomography analyses and concurrent lung function tests in systemic sclerosis.系统性硬化症中系列高分辨率 CT 分析和同期肺功能检测的预测价值。
Arthritis Rheumatol. 2015 May;67(8):2205-12. doi: 10.1002/art.39166.
10
Screening for interstitial lung disease in systemic sclerosis: performance of high-resolution CT with limited number of slices: a prospective study.系统性硬化症中肺间质疾病的筛查:有限切片数的高分辨率 CT 的性能:一项前瞻性研究。
Ann Rheum Dis. 2014 Dec;73(12):2069-73. doi: 10.1136/annrheumdis-2014-205637. Epub 2014 Sep 30.

断层扫描减少的计算机断层扫描对系统性硬化症患者肺纤维化基于直方图的密度测定评估的影响。

The impact of slice-reduced computed tomography on histogram-based densitometry assessment of lung fibrosis in patients with systemic sclerosis.

作者信息

Nguyen-Kim Thi Dan Linh, Maurer Britta, Suliman Yossra A, Morsbach Fabian, Distler Oliver, Frauenfelder Thomas

机构信息

Institute of Diagnostic and Interventional Radiology, Raemistrasse, Zurich, Switzerland.

Division of Rheumatology University Hospital Zurich, Raemistrasse, Zurich, Switzerland.

出版信息

J Thorac Dis. 2018 Apr;10(4):2142-2152. doi: 10.21037/jtd.2018.04.39.

DOI:10.21037/jtd.2018.04.39
PMID:29850118
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5949494/
Abstract

BACKGROUND

To evaluate usability of slice-reduced sequential computed tomography (CT) compared to standard high-resolution CT (HRCT) in patients with systemic sclerosis (SSc) for qualitative and quantitative assessment of interstitial lung disease (ILD) with respect to (I) detection of lung parenchymal abnormalities, (II) qualitative and semiquantitative visual assessment, (III) quantification of ILD by histograms and (IV) accuracy for the 20%-cut off discrimination.

METHODS

From standard chest HRCT of 60 SSc patients sequential 9-slice-computed tomography (reduced HRCT) was retrospectively reconstructed. ILD was assessed by visual scoring and quantitative histogram parameters. Results from standard and reduced HRCT were compared using non-parametric tests and analysed by univariate linear regression analyses.

RESULTS

With respect to the detection of parenchymal abnormalities, only the detection of intrapulmonary bronchiectasis was significantly lower in reduced HRCT compared to standard HRCT (P=0.039). No differences were found comparing visual scores for fibrosis severity and extension from standard and reduced HRCT (P=0.051-0.073). All scores correlated significantly (P<0.001) to histogram parameters derived from both, standard and reduced HRCT. Significant higher values of kurtosis and skewness for reduced HRCT were found (both P<0.001). In contrast to standard HRCT histogram parameters from reduced HRCT showed significant discrimination at cut-off 20% fibrosis (sensitivity 88% kurtosis and skewness; specificity 81% kurtosis and 86% skewness; cut-off kurtosis ≤26, cut-off skewness ≤4; both P<0.001).

CONCLUSIONS

Reduced HRCT is a robust method to assess lung fibrosis in SSc with minimal radiation dose with no difference in scoring assessment of lung fibrosis severity and extension in comparison to standard HRCT. In contrast to standard HRCT histogram parameters derived from the approach of reduced HRCT could discriminate at a threshold of 20% lung fibrosis with high sensitivity and specificity. Hence it might be used to detect early disease progression of lung fibrosis in context of monitoring and treatment of SSc patients.

摘要

背景

为了评估与标准高分辨率计算机断层扫描(HRCT)相比,层厚缩减的序贯计算机断层扫描(CT)在系统性硬化症(SSc)患者中对间质性肺疾病(ILD)进行定性和定量评估的可用性,具体涉及(I)肺实质异常的检测,(II)定性和半定量视觉评估,(III)通过直方图对ILD进行量化,以及(IV)20%截断值判别的准确性。

方法

从60例SSc患者的标准胸部HRCT中回顾性重建层厚缩减为9层的计算机断层扫描(缩减HRCT)。通过视觉评分和定量直方图参数评估ILD。使用非参数检验比较标准HRCT和缩减HRCT的结果,并通过单变量线性回归分析进行分析。

结果

在肺实质异常检测方面,与标准HRCT相比,缩减HRCT仅肺内支气管扩张的检测率显著降低(P = 0.039)。比较标准HRCT和缩减HRCT的纤维化严重程度和范围的视觉评分未发现差异(P = 0.051 - 0.073)。所有评分与标准HRCT和缩减HRCT得出的直方图参数均显著相关(P < 0.001)。发现缩减HRCT的峰度和偏度值显著更高(均P < 0.001)。与标准HRCT不同,缩减HRCT的直方图参数在20%纤维化截断值时显示出显著判别能力(峰度和偏度的敏感性为88%;峰度的特异性为81%,偏度的特异性为86%;截断峰度≤26,截断偏度≤4;均P < 0.001)。

结论

缩减HRCT是一种评估SSc患者肺纤维化的可靠方法,辐射剂量最小,与标准HRCT相比,在肺纤维化严重程度和范围的评分评估上无差异。与标准HRCT不同,缩减HRCT方法得出的直方图参数能够在20%肺纤维化阈值时以高敏感性和特异性进行判别。因此,它可用于在SSc患者的监测和治疗中检测肺纤维化的早期疾病进展。