2005
DOI: 10.1136/ard.2005.043497
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The CORRONA database

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Cited by 74 publications
(64 citation statements)
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“…Arthritis registries were first created in the 1980s. The RA registries may vary according to the characteristics of the patients, and may be based on rheumatic diseases, [15][16][17] registries. In the TLAR registry, all patients older than 18 years of age with any kind of therapy or disease stage were recorded and monitored, and their real-life data was collected.…”
Section: Discussionmentioning
confidence: 99%
“…Arthritis registries were first created in the 1980s. The RA registries may vary according to the characteristics of the patients, and may be based on rheumatic diseases, [15][16][17] registries. In the TLAR registry, all patients older than 18 years of age with any kind of therapy or disease stage were recorded and monitored, and their real-life data was collected.…”
Section: Discussionmentioning
confidence: 99%
“…CORRONA is an independent, prospective, observational registry of patients with arthritis who were enrolled by participating rheumatologists at both academic and private practice sites 26,27 with data gathered from both patients and their treating rheumatologists. As of March 3, 2014, data have been collected from > 39,956 patients and > 600 participating rheumatologists, yielding > 111,303 patient-years of followup.…”
Section: Methodsmentioning
confidence: 99%
“…Data from the CORRONA registry were analyzed to assess RTX treatment outcomes in usual care settings. Data were collected from both patients and their treating rheumatologists using questionnaires that gathered information on disease severity and activity (including components of the American College of Rheumatology response criteria), comorbidities, use of medications including DMARD, and adverse events 26,27 . Only reported first-time users of RTX were considered; patients who restarted the drug were excluded.…”
Section: Study Populationmentioning
confidence: 99%
“…The registry has data on approximately 44,500 patients with RA, 337,500 patient visits, and approximately 152,200 patient-years (PY) of follow-up observation time, with mean time of patient follow-up of 4.2 years (median 3.5 years). Data collection, which began in 2001, is performed at clinical visits with follow-ups as frequent as every 3--6 months [28,29]. The current analysis is a descriptive study of long-term adalimumab effectiveness.…”
Section: Study Settingmentioning
confidence: 99%