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一种在肺功能测试中评估支气管扩张剂反应性的统计方法。

A statistical approach for assessment of bronchodilator responsiveness in pulmonary function testing.

作者信息

Hansen J E, Casaburi R, Goldberg A S

机构信息

Department of Medicine, Harbor-UCLA Medical Center.

出版信息

Chest. 1993 Oct;104(4):1119-26. doi: 10.1378/chest.104.4.1119.

DOI:10.1378/chest.104.4.1119
PMID:8404178
Abstract

OBJECTIVE

Because published criteria for bronchodilator responsiveness are based on population variability and compare only the single best measures before and after intervention, we hypothesized that the variability of the FEV1 and FEV3 of each patient would better determine that patient's responsiveness.

DESIGN AND INTERVENTIONS

Five 3-s forced expiratory maneuvers were used for each of 3 sequential portions of the study: baseline, after nebulized saline solution, and after nebulized albuterol.

SETTING

Clinical pulmonary function laboratory in a county/university teaching hospital.

PATIENTS

Fifty consecutive adult patients with obstruction referred for routine testing and thought to be able to complete the study. (The primary diagnoses were found to be equally divided between asthma, bronchitis, and emphysema; equal numbers had very severe, severe, moderate, mild, or minimal obstruction.)

MEASUREMENTS AND RESULTS

The primary finding was that 36 patients were found to be responders (consistent and statistically significant FEV1 and FEV3 improvement after albuterol). The 14 identified as nonresponders would have been so categorized by all other published criteria. For assessing responsiveness, we found FEV3 measures preferable to vital capacity measures, because the latter depends on the duration of the maneuver.

CONCLUSIONS

The percentage of responders identified is higher than recognized by any other published criteria. Most criteria would not have identified the responders with very severe or minimal airways obstruction.

摘要

目的

由于已发表的支气管扩张剂反应性标准基于人群变异性,且仅比较干预前后的单一最佳测量值,我们推测每位患者的第一秒用力呼气容积(FEV1)和用力呼气3秒容积(FEV3)的变异性能更好地确定该患者的反应性。

设计与干预措施

在研究的3个连续阶段中,每个阶段对每位患者进行5次3秒的用力呼气动作:基线期、雾化吸入生理盐水后、雾化吸入沙丁胺醇后。

研究地点

县/大学教学医院的临床肺功能实验室。

患者

连续50例因常规检查前来就诊且被认为能够完成研究的成年阻塞性肺病患者。(初步诊断发现,哮喘、支气管炎和肺气肿患者数量相等;极重度、重度、中度、轻度或极轻度阻塞的患者数量也相等。)

测量与结果

主要发现是,36例患者被判定为反应者(吸入沙丁胺醇后FEV1和FEV3有持续且具有统计学意义的改善)。按照所有其他已发表的标准,另外14例被判定为无反应者也会被归为此类。在评估反应性方面,我们发现FEV3测量值优于肺活量测量值,因为后者取决于动作持续时间。

结论

本研究确定的反应者比例高于其他任何已发表标准所认可的比例。大多数标准无法识别出气道阻塞极重度或极轻度的反应者。

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