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镰状细胞性状患者的肺容积与弥散能力

Lung volumes and diffusion capacity in sickle cell trait.

作者信息

Stinson J M, McPherson G L

出版信息

J Natl Med Assoc. 1986 Jun;78(6):505-7.

Abstract

Patients with sickle cell anemia have a restrictive ventilatory pattern, with reduction in diffusion capacity of the lung (DLco) and lung volumes. Diffusion capacity and lung volumes are reported as either normal or reduced in subjects with sickle cell trait. Thirteen subjects with sickle cell trait, age range 25 to 79 years, were compared with 13 normal subjects matched for age, sex, height, and smoking patterns. There was no significant difference in mean values of DLco or lung volume for the two groups. Neither was there a consistent difference for age-matched individuals. Normal lung function in sickle cell trait as opposed to sickle cell disease is probably related to the fact that the former have fewer, if any, pulmonary infectious and infarctive episodes.

摘要

镰状细胞贫血患者存在限制性通气模式,肺弥散功能(DLco)和肺容积降低。镰状细胞性状患者的弥散功能和肺容积报告为正常或降低。将13名年龄在25至79岁之间的镰状细胞性状受试者与13名年龄、性别、身高和吸烟模式相匹配的正常受试者进行比较。两组的DLco或肺容积平均值无显著差异。年龄匹配的个体之间也没有一致的差异。与镰状细胞病相反,镰状细胞性状患者的肺功能正常可能与以下事实有关:前者肺部感染和梗死发作较少(如果有的话)。

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