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Diagnostic accuracy of a pocket screening spirometer in diagnosing chronic obstructive pulmonary disease in general practice: a cross sectional validation study using tertiary care as a reference (CROSBI ID 251707)

Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija

Labor, Marina ; Vrbica, Žarko ; Gudelj, Ivan ; Labor, Slavica ; Plavec, Davor Diagnostic accuracy of a pocket screening spirometer in diagnosing chronic obstructive pulmonary disease in general practice: a cross sectional validation study using tertiary care as a reference // BMC family practice, 17 (2016), 112-122. doi: 10.1186/s12875-016-0518-8

Podaci o odgovornosti

Labor, Marina ; Vrbica, Žarko ; Gudelj, Ivan ; Labor, Slavica ; Plavec, Davor

engleski

Diagnostic accuracy of a pocket screening spirometer in diagnosing chronic obstructive pulmonary disease in general practice: a cross sectional validation study using tertiary care as a reference

Background: COPD-6 (TM) is a lung function testing device for a rapid pre-spirometry testing to screen-out at-risk individuals not having COPD and indicating those at risk. The aim of this study was to validate COPD-6 (TM) lung function testing (index test) in general practice in discriminating patients with COPD out of the population at risk - smokers/ex-smokers with no previous diagnosis of COPD, using measurements at tertiary care as reference standard. Methods: Consecutive 227 subjects (115 women, 185 smokers/42 ex-smokers, >= 20 pack-years) with no previous diagnosis of COPD, aged 52.5 (SD 6.8) years from 26 general practitioners (GPs) were recruited, lung function tested with COPD-6 (TM), referred to the tertiary institution for repeated COPD-6 (TM) testing followed by spirometry with a bronchodilator (salbutamol), examination, and pulmonologist consultation for the diagnosis and severity of COPD. Results: COPD was diagnosed in 43 subjects (18.9 %), with an AUC of 0.827 (95 % CI 0.769-0.875, P < 0.001) for the diagnosis of COPD when lung function was measured using COPD-6 (TM) in GP's office with a specificity of 100 % (95 % CI, 97.95-100 %) but a very low sensitivity of 32.56 % (95 % CI, 20.49-47.48 %). Significant agreement for forced expiratory volume in 1 s measured at GP's office and at lung function lab was found (mean difference 0.01 L, p = 0.667) but not for other measured parameters (p < 0.001 for all). Conclusions: Our study results point out that active case finding in a population at risk for COPD should be instituted (almost 20 % of undiagnosed COPD). Based on our results lung function testing with COPD-6 (TM) can substitute spirometry testing in cases where it is not readily available to the patient/physician taken into account that the traditional FEV1/FEV6 cutoff value of <0.7 is not the only criterion for diagnosis and/or further referral.

LUNG-FUNCTION ; COPD ; RISK ; AGE ; PREVALENCE ; PIKO-6(R) ; IMPACT ; COHORT ; ADULTS ;

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Podaci o izdanju

17

2016.

112-122

objavljeno

1471-2296

10.1186/s12875-016-0518-8

Povezanost rada

Kliničke medicinske znanosti

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