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两种电子肺活量计与水封式肺活量计的临床比较。

Clinical comparison of two electronic spirometers with a water-sealed spirometer.

作者信息

Shanks D E, Morris J F

出版信息

Chest. 1976 Apr;69(4):461-6. doi: 10.1378/chest.69.4.461.

Abstract

Two electronic spirometers which use a hot-wire anemometer to measure air flow were clinically compared with a water-sealed spirometer. The forced vital capacity (FVC), the forced expiratory volume in one second (FEV1), the FEV1/FVC%, the mean forced expiratory flow between 200 and 1,200 ml of the FVC, the mean forced expiratory flow during the middle half of the FVC, the mean forced expiratory flow between 75 and 85 percent of the FVC, and the maximum voluntary ventilation were determined for a group of 67 subjects. Techniques are described for connecting the spirometers in series to permit evaluation by human subjects or by syringe injection. High correlation coefficients generally were obtained when comparing the electronic spirometers with the water-sealed spirometer, but the actual range of percent difference was greater than 11 percent in all spirometric tests. The results indicate the need for systematic evaluation of electronic spirometers to characterize their deviation from accented standards. Frequent calibration is necessary to maintain consistent performance.

摘要

将两台采用热线风速仪测量气流的电子肺活量计与一台水封式肺活量计进行了临床比较。对67名受试者测定了用力肺活量(FVC)、一秒用力呼气量(FEV1)、FEV1/FVC%、FVC中200至1200毫升之间的平均用力呼气流量、FVC中间一半时间的平均用力呼气流量、FVC的75%至85%之间的平均用力呼气流量以及最大自主通气量。描述了将肺活量计串联连接以允许受试者或通过注射器注射进行评估的技术。在将电子肺活量计与水封式肺活量计进行比较时,通常获得较高的相关系数,但在所有肺活量测试中,实际百分比差异范围均大于11%。结果表明需要对电子肺活量计进行系统评估,以确定其与公认标准的偏差。需要经常校准以保持一致的性能。

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