Targeted case finding for chronic obstructive pulmonary disease versus routine practice in primary care (TargetCOPD): a cluster-randomised controlled trial

Summary Background Many individuals with chronic obstructive pulmonary disease (COPD) remain undiagnosed worldwide. Health-care organisations are implementing case-finding programmes without good evidence of which are the most effective and cost-effective approaches. We assessed the effectiveness an...

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Veröffentlicht in:The lancet respiratory medicine 2016-09, Vol.4 (9), p.720-730
Hauptverfasser: Jordan, Rachel E, Dr, Adab, Peymané, Prof, Sitch, Alice, MSc, Enocson, Alexandra, PhD, Blissett, Deirdre, MSc, Jowett, Sue, PhD, Marsh, Jen, PhD, Riley, Richard D, Prof, Miller, Martin R, Prof, Cooper, Brendan G, PhD, Turner, Alice M, PhD, Jolly, Kate, Prof, Ayres, Jon G, Prof, Haroon, Shamil, PhD, Stockley, Robert, DSc, Greenfield, Sheila, Prof, Siebert, Stanley, Prof, Daley, Amanda J, PhD, Cheng, K K, Prof, Fitzmaurice, David, Prof
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Sprache:eng
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Zusammenfassung:Summary Background Many individuals with chronic obstructive pulmonary disease (COPD) remain undiagnosed worldwide. Health-care organisations are implementing case-finding programmes without good evidence of which are the most effective and cost-effective approaches. We assessed the effectiveness and cost-effectiveness of two alternative approaches to targeted case finding for COPD compared with routine practice. Methods In this cluster-randomised controlled trial, participating general practices in the West Midlands, UK, were randomly assigned (1:1), via a computer-generated block randomisation sequence, to either a targeted case-finding group or a routine care group. Eligible patients were ever-smokers aged 40–79 years without a previously recorded diagnosis of COPD. Patients in the targeted case-finding group were further randomly assigned (1:1) via their household to receive either a screening questionnaire at the general practitioner (GP) consultation (opportunistic) or a screening questionnaire at the GP consultation plus a mailed questionnaire (active). Respondents reporting relevant respiratory symptoms were invited for post-bronchodilator spirometry. Patients, clinicians, and investigators were not masked to allocation, but group allocation was concealed from the researchers who performed the spirometry assessments. Primary outcomes were the percentage of the eligible population diagnosed with COPD within 1 year (defined as post-bronchodilator forced expiratory volume in 1 s [FEV1 ] to forced vital capacity [FVC] ratio
ISSN:2213-2600
2213-2619
DOI:10.1016/S2213-2600(16)30149-7