4.7 Article

Drug utilization in patients with OA: a population-based study

Journal

RHEUMATOLOGY
Volume 54, Issue 5, Pages 860-867

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/rheumatology/keu403

Keywords

osteoarthritis; pharmaceutical therapy; population-based cohort; Catalonia; pharmacoepidemiology; drug utilization; electronic health records

Categories

Funding

  1. Bioiberica
  2. Oxford National Institute for Health Research Musculoskeletal Biomedical Research Unit
  3. Medical Research Council [U1475000001, MC_U147585819, G0400491, MC_U147585824, MC_UU_12011/1, MC_UP_A620_1014, MC_U147585827] Funding Source: researchfish
  4. National Institute for Health Research [NF-SI-0513-10085, NF-SI-0508-10082] Funding Source: researchfish
  5. MRC [MC_U147585819, G0400491, MC_U147585827] Funding Source: UKRI

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Objective. Patients with OA use different drugs in their search for relief. We aimed to study the prevalence of use and combinations of different medications for OA in a population-based cohort of OA patients in Catalonia, Spain, while characterizing users of each of the drugs available, with a particular focus on cardiovascular risk factors. Methods. Data were obtained from the Sistema d'Informaci per al Desenvolupament de l'Investigaci en Atenci PrimA ria (SIDIAP) database, which includes electronic medical records and pharmacy invoice data for > 5 million people from Catalonia. Study participants were those with a clinical diagnosis of OA in 2006-10. Drugs studied included oral and topical NSAIDs, analgesics (paracetamol, metamizole), opioids (tramadol, fentanyl), cyclooxygenase 2 (COX-2) inhibitors and symptomatic slow-acting drugs in OA. Drug utilization was described using medication possession ratios (MPRs), equivalent to the proportion of days covered with the drug of interest. The annual incidence of new users in the first year after OA diagnosis from 2006 to 2010 was estimated for all studied drugs among newly diagnosed OA patients using Poisson regression. Results. We identified 238 536 study participants. The most common regimen of treatment consisted of at least three drugs (53.9% of patients). The drugs most frequently used regularly (MPR a parts per thousand yen50%) were chondroitin (21.2%), glucosamine (15.8%) and oral NSAIDs (14.4%). The incidence of the use of opioids, COX-2 inhibitors and chondroitin increased over the 5 year period, whereas all others decreased. Conclusion. Drug combinations are common in the treatment of OA patients, who are thus exposed to potential drug interactions, with unknown impacts on their health. The increasing use of opioids and COX-2 inhibitors is noteworthy because of the potential impact on safety and costs.

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