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通过年度CT评估严重α1-抗胰蛋白酶缺乏症患者肺气肿的进展情况。

Progress of emphysema in severe alpha 1-antitrypsin deficiency as assessed by annual CT.

作者信息

Dirksen A, Friis M, Olesen K P, Skovgaard L T, Sørensen K

机构信息

Department of Respiratory Medicine, Bispebjerg Hospital, Copenhagen, Denmark.

出版信息

Acta Radiol. 1997 Sep;38(5):826-32. doi: 10.1080/02841859709172418.

Abstract

PURPOSE

To assess serial CT as a measure of the progress of emphysema in patients with severe alpha 1-antitrypsin deficiency (phenotype PiZ).

MATERIAL AND METHODS

In a randomized placebo-controlled study of alpha 1-antitrypsin augmentation therapy, 22 patients with moderate emphysema were followed for 2-4 years with an annual lung CT. The images were analysed by means of semiautomatic lung detection, and the degree of emphysema was quantitated by the density-mask and the percentile methods. The influence of lung volume was standardised by a regression model.

RESULTS

A highly significant decline in Hounsfield units (HU) was found in low-density areas, corresponding to a mean (SE) annual loss of lung tissue of 2.1 (0.4) g/l lung volume. Analysis of a single slice at 5 cm below the level of the carina gave comparable results: 2.4 (0.4) g/l.

CONCLUSION

Serial CT is a sensitive measure of the progress of emphysema in patients with severe alpha 1-antitrypsin deficiency.

摘要

目的

评估连续CT作为重度α1-抗胰蛋白酶缺乏症(PiZ表型)患者肺气肿进展的一种测量方法。

材料与方法

在一项α1-抗胰蛋白酶增强疗法的随机安慰剂对照研究中,对22例中度肺气肿患者进行了为期2至4年的年度肺部CT随访。通过半自动肺部检测对图像进行分析,并采用密度掩码法和百分位数法对肺气肿程度进行定量。通过回归模型对肺容积的影响进行标准化。

结果

在低密度区域发现亨氏单位(HU)显著下降,相当于肺组织平均(标准误)每年损失2.1(0.4)g/升肺容积。在隆突水平以下5 cm处分析单个层面得到了类似结果:2.4(0.4)g/升。

结论

连续CT是重度α1-抗胰蛋白酶缺乏症患者肺气肿进展的一种敏感测量方法。

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