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Risk factors for muscular symptoms associated with atorvastatin therapy; evidence from an observational study in a group of Sri Lankan patients

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dc.contributor.author Wijekoon, C.N.
dc.contributor.author Wijekoon, P.W.M.C.S.B.
dc.contributor.author Wickramasinghe, M.C.
dc.contributor.author Paranavitane, S.A.
dc.contributor.author Kottage, A.
dc.contributor.author Sumanadasa, S.
dc.contributor.author Bulugahapitiya, U.
dc.contributor.author Senarath, U.
dc.date.accessioned 2017-11-02T02:21:35Z
dc.date.available 2017-11-02T02:21:35Z
dc.date.issued 2016
dc.identifier.citation Wijekoon, C.N., Wijekoon, P.W.M.C.S.B., Wickramasinghe, M.C., Paranavitane, S.A., Kottage, A., Sumanadasa, S., Bulugahapitiya, U., Senarath, U. (2016). "Risk factors for muscular symptoms associated with atorvastatin therapy; evidence from an observational study in a group of Sri Lankan patients", Proceedings of 49th Annual Academic Sessions 2016, Ceylon College of Physicians, p. 112 en_US, si_LK
dc.identifier.uri http://dr.lib.sjp.ac.lk/handle/123456789/6388
dc.description.abstract Attached en_US, si_LK
dc.description.abstract OBJECTIVES Occurrence of muscular symptoms with statin therapy is well-recognized. It could adversely affect quality of life and exercise tolerance. Objective of this study was to describe the risk factors for muscular symptoms associated with atorvastatin therapy in a group of Sri Lankan patients. METHOD Consecutive patients receiving atorvastatin at outpatient clinics of a tertiary-care hospital who were screened for a clinical trial on management of statin myopathy, were studied. Those with muscle symptoms (pain, tenderness, stiffness, cramps, weakness) started after initiation of atorvastatin were included. Potential risk factors were detected with clinical assessment and/or investigations. Details were recorded using an interviewer administered questionnaire. Data were analysed with SPSS version-19.0 RESULTS 456 patients were studied; 64.7% were females; mean age was 63.4±10years. 57.5%, ^ . 16.7% and 15.4% had diabetes, hypothyroidism and chronic kidney disease (CKD), respectively. 46.5% and 45.8% were on lOmg and 20mg of atorvastatin, respectively. Majority (56%) were on atorvastatin for >48 months. 29.4% had at least one muscle symptom; 2.9% had elevated creatine phosphokinase. Results of multiple logistic regression indicated that female gender (OR:1.7; 95% Cl: 1.1-2.9; p=0.03), diabetes (OR:3.0; 95% Cl: 1.3-6.7; p=0.008) and treatment duration of £48months (OR:2.2; 95% Cl: 1.1-4.8; p=0.04) were independent risk factors for muscular symptoms associated with atorvastatin therapy. Age, atorvastatin dose, co-medications, history of hypothyroidism and CKD were not found to be significant risk factors. CONCLUSION In the study population, one third had muscular symptoms associated with atorvastatin therapy; female gender, diabetes and treatment for >48months were independent risk factors.
dc.language.iso en_US en_US, si_LK
dc.publisher Proceedings of 49th Annual Academic Sessions 2016, Ceylon College of Physicians en_US, si_LK
dc.title Risk factors for muscular symptoms associated with atorvastatin therapy; evidence from an observational study in a group of Sri Lankan patients en_US, si_LK
dc.type Article en_US, si_LK


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