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肺活量计校准检查:3.5% 是否足够好?

Spirometer calibration checks: is 3.5% good enough?

作者信息

McCormack Meredith C, Shade David, Wise Robert A

机构信息

Division of Pulmonary and Critical Care Medicine, Johns Hopkins University, 1830 East Monument Street, Baltimore, MD 21205, USA.

出版信息

Chest. 2007 May;131(5):1486-93. doi: 10.1378/chest.06-1522.

Abstract

BACKGROUND

Current standards for spirometry require daily calibration checks to come within 3.5% of the inserted volume but do not require evaluation of trends over time. We examined the current guidelines and candidate quality control rules to determine the best method for identifying spirometers with suboptimal performance.

METHODS

Daily calibration checks on seven volume spirometers recorded over 4 to 11 years were reviewed. Current guidelines and candidate quality control rules were applied to determine how well each detected suboptimal spirometer performance.

RESULTS

Overall, 98% of 7,497 calibration checks were within 3.5%. However, based on visual inspection of calibration check data plots, spirometers 3 and 5 demonstrated systematic sources of error, drift, and bias. The +/- 3.5% criteria did not identify these spirometers. The application of +/- 2% criteria identified these spirometers (9% out-of control values in spirometers 3 and 5 vs < 5% in other spirometers). A rule stipulating out-of-control conditions when four consecutive checks exceeded 1% deviation identified suboptimal spirometers (14% and 20% out-of-control values) but maintained low error detection rates in other spirometers (< or = 2%). Other candidate rules were less effective or required longer times to error detection.

CONCLUSIONS

The current recommendation that calibration checks come within +/- 3.5% of the inserted volume did not detect subtle errors. Alternative candidate rules were more effective in detecting errors and maintained low overall error-detection rates. Our findings emphasize the need for laboratories to systematically review calibration checks over time and suggest that more stringent guidelines for calibration checks may be warranted for volume spirometers. Although our general approach may also be appropriate for flow-type spirometers, the details are likely to differ since flow-type spirometers are a much more varied category of equipment.

摘要

背景

目前的肺量计标准要求每日校准检查结果与插入体积的偏差在3.5%以内,但并不要求评估随时间的变化趋势。我们研究了当前的指南和候选质量控制规则,以确定识别性能欠佳的肺量计的最佳方法。

方法

回顾了4至11年期间对7台容量型肺量计进行的每日校准检查记录。应用当前指南和候选质量控制规则来确定每种方法检测性能欠佳的肺量计的效果如何。

结果

总体而言,7497次校准检查中有98%在3.5%以内。然而,通过对校准检查数据图的目视检查,发现肺量计3和5存在系统性误差、漂移和偏差来源。±3.5%的标准未能识别出这些肺量计。应用±2%的标准识别出了这些肺量计(肺量计3和5中有9%的失控值,而其他肺量计中<5%)。一条规定当连续四次检查超过1%偏差时为失控状态的规则识别出了性能欠佳的肺量计(失控值分别为14%和20%),但在其他肺量计中保持了较低的误差检测率(≤2%)。其他候选规则效果较差或需要更长时间才能检测到误差。

结论

目前关于校准检查结果应在插入体积的±3.5%以内的建议未能检测到细微误差。替代候选规则在检测误差方面更有效,且总体误差检测率较低。我们的研究结果强调实验室需要随着时间的推移系统地审查校准检查,并表明可能有必要对容量型肺量计采用更严格的校准检查指南。虽然我们的一般方法可能也适用于流量型肺量计,但细节可能会有所不同,因为流量型肺量计是一类更为多样的设备。

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