Objective The first 3 months after symptom onset represent an important therapeutic window for rheumatoid arthritis (RA). This study investigates the extent and causes of delay in assessment of patients with RA in eight European countries.
Method Data on the following levels of delay were collected from 10 centres (Berlin, Birmingham, Heraklion, Lund, Prague, Stockholm, Umeå, Vienna, Warsaw and Zurich): (1) from onset of RA symptoms to request to see healthcare professional (HCP); (2) from request to see HCP to assessment by that HCP; (3) from initial assessment by HCP to referral to rheumatologist; and (4) from referral to rheumatologist to assessment by that rheumatologist.
Results Data were collected from 482 patients with RA. The median delay across the 10 centres from symptom onset to assessment by the rheumatologist was 24 weeks, with the percentage of patients seen within 12 weeks of symptom onset ranging from 8% to 42%. There were important differences in the levels underlying the total delays at individual centres.
Conclusions This research highlights the contribution of patients, professionals and health systems to treatment delay for patients with RA in Europe. Although some centres have strengths in minimising certain types of delay, interventions are required in all centres to ensure timely treatment for patients.
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Funding This work has been supported by a grant from the European Community's Sixth Framework Programme (AutoCure). The Prague centre was supported by a grant NR 10065-4 from the Internal Grant Agency of the Ministry of Health of the Czech Republic.
Ethics approval This study was conducted with the approval of the research ethics committee in the Czech Republic. In the other countries the regulatory authorities determined that the collection of these anonymous data constituted a service evaluation for which approval from a research ethics committee was not necessary.
Provenance and peer review Not commissioned; externally peer reviewed.
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