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肺活量计作为基层医疗中 COPD 筛查试验的准确性。

Accuracy of Vitalograph lung monitor as a screening test for COPD in primary care.

机构信息

Institute of Applied Health Research, University of Birmingham, Birmingham, UK.

Warwick Medical School - Health Sciences, University of Warwick, Coventry, UK.

出版信息

NPJ Prim Care Respir Med. 2020 Jan 3;30(1):2. doi: 10.1038/s41533-019-0158-2.

Abstract

Microspirometry may be useful as the second stage of a screening pathway among patients reporting respiratory symptoms. We assessed sensitivity and specificity of the Vitalograph® lung monitor compared with post-bronchodilator confirmatory spirometry (ndd Easy on-PC) among primary care chronic obstructive pulmonary disease (COPD) patients within the Birmingham COPD cohort. We report a case-control analysis within 71 general practices in the UK. Eligible patients were aged ≥40 years who were either on a clinical COPD register or reported chronic respiratory symptoms on a questionnaire. Participants performed pre- and post-bronchodilator microspirometry, prior to confirmatory spirometry. Out of the 544 participants, COPD was confirmed in 337 according to post-bronchodilator confirmatory spirometry. Pre-bronchodilator, using the LLN as a cut-point, the lung monitor had a sensitivity of 50.5% (95% CI 45.0%, 55.9%) and a specificity of 99.0% (95% CI 96.6%, 99.9%) in our sample. Using a fixed ratio of FEV/FEV < 0.7 to define obstruction in the lung monitor, sensitivity increased (58.8%; 95% CI 53.0, 63.8) while specificity was virtually identical (98.6%; 95% CI 95.8, 99.7). Within our sample, the optimal cut-point for the lung monitor was FEV/FEV < 0.78, with sensitivity of 82.8% (95% CI 78.3%, 86.7%) and specificity of 85.0% (95% CI 79.4%, 89.6%). Test performance of the lung monitor was unaffected by bronchodilation. The lung monitor could be used in primary care without a bronchodilator using a simple ratio of FEV/FEV as part of a screening pathway for COPD among patients reporting respiratory symptoms.

摘要

微肺活量测定法可作为报告呼吸症状的患者的筛选途径的第二阶段,可能会有所帮助。我们评估了 Vitalograph®肺监测仪与支气管扩张剂后确认的肺活量测定法(ndd Easy on-PC)在伯明翰 COPD 队列中的初级保健慢性阻塞性肺疾病(COPD)患者中的敏感性和特异性。我们报告了英国 71 家普通诊所内的病例对照分析。合格的患者年龄≥40 岁,要么在临床 COPD 登记册中,要么在问卷中报告有慢性呼吸道症状。患者在进行确认性肺活量测定法之前,先进行支气管扩张剂前和支气管扩张剂后的微肺活量测定法。在 544 名参与者中,根据支气管扩张剂后确认的肺活量测定法,337 名患者被确诊为 COPD。使用 LLN 作为截断值,在支气管扩张剂前,肺监测仪在我们的样本中的敏感性为 50.5%(95%CI 45.0%,55.9%),特异性为 99.0%(95%CI 96.6%,99.9%)。使用固定的 FEV/FEV<0.7 比值来定义肺监测仪中的阻塞,敏感性增加(58.8%;95%CI 53.0,63.8),而特异性几乎相同(98.6%;95%CI 95.8,99.7)。在我们的样本中,肺监测仪的最佳截断值为 FEV/FEV<0.78,敏感性为 82.8%(95%CI 78.3%,86.7%),特异性为 85.0%(95%CI 79.4%,89.6%)。肺监测仪的测试性能不受支气管扩张剂的影响。在没有支气管扩张剂的情况下,肺监测仪可在初级保健中使用,作为报告呼吸症状的患者 COPD 筛查途径的一部分,使用 FEV/FEV 的简单比值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a50/6941963/150729e50253/41533_2019_158_Fig1_HTML.jpg

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