Adherence to gastroprotection during cyclooxygenase 2 inhibitor treatment and the risk of upper gastrointestinal tract events: A population-based study
Autor: | Miriam C. J. M. Sturkenboom, Eva M. van Soest, Giampiero Mazzaglia, Jay L. Goldstein, Vera E. Valkhoff, Gianluca Trifirò, Ernst J. Kuipers, Sonia Hernandez-Diaz, R Schade, Mariam Molokhia |
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Přispěvatelé: | Valkhoff, V, van Soest, E, Mazzaglia, G, Molokhia, M, Schade, R, Trifiro, G, Goldstein, J, Hernandez-Diaz, S, Kuipers, E, Sturkenboom, M, Medical Informatics, Gastroenterology & Hepatology |
Jazyk: | angličtina |
Rok vydání: | 2012 |
Předmět: |
Male
Nonsteroidal Antiinflammatory Drug DATABASES law.invention Cohort Studies Upper Gastrointestinal Tract Naproxen Randomized controlled trial Risk Factors law NAPROXENTHERAPY Immunology and Allergy Medicine Pharmacology (medical) Registries Netherlands Aged 80 and over biology Incidence NONSTEROIDAL ANTIINFLAMMATORY DRUGS Middle Aged Italy Rheumatoid arthritis Cohort Female Gastrointestinal Hemorrhage Double-Blind DOUBLE-BLINDPREVENTION medicine.medical_specialty Immunology Database ULCER COMPLICATIONS Rheumatology Ulcer Complication Rheumatic Diseases Internal medicine Humans Upper gastrointestinal Stomach Ulcer Medical prescription Aged Retrospective Studies Rheumatoid-Arthriti Cyclooxygenase 2 Inhibitors Toxicity business.industry Prevention Proton Pump Inhibitors Odds ratio medicine.disease NONSTEROIDAL ANTIINFLAMMATORY DRUGS RANDOMIZED CONTROLLED-TRIAL RHEUMATOID-ARTHRITIS ULCER COMPLICATIONS DOUBLE-BLINDPREVENTION DATABASES TOXICITY NAPROXENTHERAPY United Kingdom Confidence interval RHEUMATOID-ARTHRITIS Surgery Logistic Models Case-Control Studies Randomized Controlled-Trial biology.protein Patient Compliance Cyclooxygenase Therapy business |
Zdroj: | Arthritis & Rheumatism, 64(8), 2792-2802. John Wiley & Sons Ltd. |
ISSN: | 0004-3591 |
Popis: | Objective Guidelines recommend coprescription of gastroprotective agents (GPAs) in patients receiving cyclooxygenase 2 inhibitors (coxibs) who are at high risk of upper gastrointestinal (UGI) tract complications (i.e., patients with a previous complicated ulcer or with multiple risk factors). Suboptimal GPA adherence has been shown to diminish the gastroprotective effect during use of nonselective nonsteroidal antiinflammatory drugs, but little is known about the effect of GPA adherence during coxib treatment. We undertook this study to determine the association between GPA adherence and UGI tract events among patients receiving coxibs. Methods Using primary care data from 3 databases, we conducted a casecontrol study in a cohort of patients age =50 years who were newly starting treatment with coxibs and concomitantly taking GPAs. Patients who had a UGI tract event (bleeding or symptomatic ulcer) were matched to event-free controls for age, sex, database, and calendar date. Coxib treatment intervals were defined as consecutive coxib prescriptions with intervening gaps not exceeding the duration of the previous coxib prescription. Adherence to GPAs was calculated as the proportion of days of coxib treatment covered by a GPA prescription. Odds ratios (ORs) with 95% confidence intervals (95% CIs) were calculated using conditional logistic regression analysis. Results The coxib plus GPAtreated cohort consisted of 14,416 coxib-treated patients who received GPAs for at least 1 day, yielding 16,442 coxib treatment intervals in which a GPA was coprescribed. Most patients were treated with coxibs for 80% adherence to GPAs. For every 10% decrease in GPA adherence, the risk of UGI tract events increased by 9% (OR 1.09 [95% CI 1.001.18]). Conclusion Decreasing GPA adherence among coxib-treated patients is associated with an increased risk of UGI tract events. |
Databáze: | OpenAIRE |
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