2015
DOI: 10.3109/13814788.2015.1084279
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A general practice perspective on early rheumatoid arthritis management: A qualitative study from Flanders

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Cited by 21 publications
(34 citation statements)
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References 31 publications
(41 reference statements)
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“…GP have previously self‐reported potential causes of delayed referral in early RA. These include the symptoms of early RA being insufficiently clear, the time‐intensive nature of examining the condition, a lack of self‐confidence in the condition, diagnostic uncertainty and inconclusive tests, low RA incidence in the community and confusion with other rheumatic diseases, such as osteoarthritis and gout . Although patient delay exerted the largest influence on overall delay, GP delay did independently predict overall delay in this cohort.…”
Section: Discussionmentioning
confidence: 89%
“…GP have previously self‐reported potential causes of delayed referral in early RA. These include the symptoms of early RA being insufficiently clear, the time‐intensive nature of examining the condition, a lack of self‐confidence in the condition, diagnostic uncertainty and inconclusive tests, low RA incidence in the community and confusion with other rheumatic diseases, such as osteoarthritis and gout . Although patient delay exerted the largest influence on overall delay, GP delay did independently predict overall delay in this cohort.…”
Section: Discussionmentioning
confidence: 89%
“…International guidelines recommend the involvement of general practitioners (GPs) in the RA multidisciplinary team [ 9 ]. Various studies have investigated the relationship between GPs and rheumatologists regarding the referral of patients with inflammatory rheumatic diseases from primary care to rheumatology clinics [ 79 82 ]. According to the results of a survey among Flemish GPs, decisions about intensive treatment initiation in early RA should be made by rheumatologists [ 79 ].…”
Section: Resultsmentioning
confidence: 99%
“…A non-responsive treatment population can be found for csDMARDS treatment regimens [86], and despite their high effectiveness in many patients, bDMARDS such as TNF-α inhibitors also give variable therapy responses and still a considerable number of patients do not respond [87,88]. Of course the remaining important delay in diagnosis and appropriate treatment initiation [89][90][91], difficulties with the implementation of sufficiently intensive treatment schedules [82][83][84] as well as adverse reactions to DMARDs, comorbidities, discrepancies in treatment goals between patients and health professionals [89] and psychosocial factors can be held partly responsible for this, but the leading cause of the unmet need remains insufficient biological disease control with current therapeutics. It might be that current therapies are simply not sufficiently potent to deal with the particular pathophysiological processes responsible for persistent disease activity in certain individuals or that they fail to hit the right targets.…”
Section: Lack Of Treatment Response For Patient Subpopulationmentioning
confidence: 99%
“…This was the case for 42,9 % of the 5'UTR fusions and 50% of the fusions to the coding region. The clones that had an in-frame fusion to the 5'UTR contained part of the translated 5'UTR followed by the full length protein, which could range in size between 91 donors. Ferritin has been found to be specifically upregulated in RA synovium [133,134].…”
Section: Construction Of a Novel Ra Cdna Phage Display Librarymentioning
confidence: 99%