Characteristics of studies evaluating handheld flow meters (4 studies)14 22 23 26
Characteristic | Range/number of studies | |
---|---|---|
Study designs | Cross-sectional test accuracy study | 4 |
Participants | 305–2464 | |
Mean age (years) | 52.0–65.3 | |
Male (%) | 43.3–99.7 | |
Required smoking status | Only current/ex-smokers | 3 |
Included never-smokers | 1 | |
Required respiratory symptoms | 0 | |
Setting | General practice(s) | 4 |
Number of centres | 4–25 | |
Multicentre | 4 | |
Recruitment strategy | Active | 1 |
Opportunistic | 2 | |
Active and opportunistic | 1 | |
Handheld flow meter | ||
Device | Piko-6 | 3 |
COPD-6 | 1 | |
Operator | Nurse | 2 |
GP | 1 | |
Not reported | 1 | |
Use of BD | Pre-BD | 3 |
Post-BD | 1 | |
Test threshold | FEV1/FEV6< | 0.70–0.75 |
Reference test—spirometry | ||
Post-BD | 4 | |
Definition of airflow obstruction | Post-BD FEV1/FVC <0.7 | 4 |
Included symptoms in definition of COPD | 0 | |
Spirometry quality control | Yes | 2 |
No | 1 | |
Unclear | 1 | |
Range of results | ||
Sensitivity | 79–86% | |
Specificity | 71–99% | |
Severity of new COPD cases | ≥80% | 35–48% |
(FEV1% predicted)3 | 50–80% | 48–65% |
<50% | 0–16% |
BD, bronchodilator; COPD, chronic obstructive pulmonary disease; FEV1, forced expiratory volume in 1 s; FVC, forced vital capacity; GP, general practitioner.