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Do traditional risk factors for knee osteoarthritis predict pain flares in knee osteoarthritis?.

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dc.contributor.author Atukorala, I. en_US
dc.contributor.author Pathmeswaran, A. en_US
dc.contributor.author Chang, T. en_US
dc.contributor.author Zhang, Y. en_US
dc.contributor.author Hunter, D.J. en_US
dc.date.accessioned 2017-11-08T09:56:43Z en_US
dc.date.available 2017-11-08T09:56:43Z en_US
dc.date.issued 2016 en_US
dc.identifier.citation Annals of the Rheumatic Diseases. 2016; 75 (Suppl 2): 835 en_US
dc.identifier.issn 1063-4584 (Print) en_US
dc.identifier.issn 1468-2060 (Electronic) en_US
dc.identifier.uri http://repository.kln.ac.lk/handle/123456789/17966 en_US
dc.description Poster Presentation(Osteoarthritis) Abstract (SAT 0452), Annual European Congress of Rheumatology of the European League Against Rheumatism (EULAR 2016), June 08-11 2016, London. United Kingdom en_US
dc.description.abstract BACKGROUND: Knee pain is the main cause of disability and reduced function in knee osteoarthritis (KOA). Though knee pain in osteoarthritis was previously perceived as a chronic condition it is now established that KOA pain fluctuates. There is emerging evidence that time variant risk factors-such as knee injury, buckling and mood- are associated with knee pain flares. But, it is not known whether conventional risk factors associated with KOA - age, gender, body mass index-are associated with pain flares in KOA. OBJECTIVES: This study examines whether conventional time invariant risk factors for KOA and baseline pain felt by the patient are associated with KOA pain flares. METHODS: Study participants were selected from a 3-month web-based longitudinal follow up study developed to identify risk factors for KOA pain flares. Participants were requested to complete online questionnaire at days 0, 30, 60 and 90 (control period assessment points) and at time points whenever they experienced knee pain flare (case period assessment points) during the follow up period. A KOA pain flare was defined as current pain with a greater than 2 point increase (on a 0-10 point numeric rating scale) from the mildest KOA pain intensity reported at day 0. The association of pain flares with traditional risk factors for knee osteoarthritis -gender, weight, height, body mass index- was assessed by negative binomial regression. The duration of knee osteoarthritis, baseline pain intensity (lowest pain and highest pain scores at baseline) were similarly evaluated. The best explanatory variable was decided by forward selection. RESULTS: 345 persons (61.2% females) with multiple KOA pain flares were selected. Their mean age was 62.1years (SD +/-8.2). The mean body mass index was 29.8kg/m2 (SD +/-6.5). The participants rated their baseline pain (on a numeric rating scale) as being 4.41 (SD+/- 2.02) and their worst pain as being 7.91 (SD +/-1.74). An average of 1.92 (SD 2.59) flares were documented during the 3-month period. The levels of baseline pain - usual and worst pain felt at baseline- were the only parameters significantly associated with KOA pain flares (Table 1). CONCLUSIONS: The baseline pain scores were the strongest predictors of pain flares of knee osteoarthritis. The traditional risk factors associated with knee osteoarthritis did not usefully predict pain flares. The traditional time invariant risk factors may not be associated with short term variability in pain though they are associated with long term outcomes of knee osteoarthritis. It is postulated that as knee pain is already present, time invariant risk factors that contributed to the original symptom causation are not associated with pain flare. (Table Presented). en_US
dc.description.sponsorship The European League Against Rheumatism (EULAR) en_US
dc.language.iso en_US en_US
dc.publisher BMJ Publishing en_US
dc.subject Osteoarthritis en_US
dc.subject.mesh Osteoarthritis, Knee en
dc.subject.mesh Risk Factors en
dc.subject.mesh Follow-Up Studies en_US
dc.subject.mesh Longitudinal Studies en_US
dc.title Do traditional risk factors for knee osteoarthritis predict pain flares in knee osteoarthritis?. en_US
dc.type Conference Abstract en_US


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