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Predicting the Risk of Gastrointestinal Bleeding
Due to Nonsteroidal Antiinflammatory Drugs:
NSAID Electronic Assessment of Risk
T. CRAIG CHEETHAM, GERALD LEVY, and MICHELE SPENCE
ABSTRACT.
Methods. We conducted a retrospective cohort analysis using computer-stored information from a large group-model health maintenance organization. All patients who received one or more prescriptions for a single NSAID over a 9 month period were eligible. Historical and risk factor data was obtained for age, sex, prior GI bleeds, use of GI medications, prednisone use, and use of disease modifying antirheumatic drugs (DMARD). We tested a model (eSCORE) that is based on a previous risk stratification method. The primary outcome was a hospital admission for a GI bleed (GI event). Results. A total of 303,211 NSAID patient-users met eligibility requirements. Serious GI events occurred in 302 patients, for a rate of 0.68% (0.68 events per 100 patient-years' exposure). All the risk factors except DMARD use were associated with a significant increase in the GI event rate. Higher eSCORE points were associated with increased GI event rates. Conclusion. The study supports the concept that the rate of GI events can be predicted by a defined set of easily assessed patient criteria using the eSCORE. Stratification of patients by risk score can guide the physician to appropriate therapeutic options, with the potential of protecting patients at greatest risk for a GI event. (J Rheumatol 2003;30:2241-4) Key Indexing Terms:
ANTIINFLAMMATORY AGENTS
From Pharmacy Strategy and Operations, Kaiser Permanente, Downey, California; and the Southern California Permanente Medical Group, Division of Rheumatology, Downey, CA, USA. T.C. Cheetham, PharmD, MS, Kaiser Permanente Drug Information Service; G.D. Levy, MD, MBA, Southern California Permanente Medical Group; M. Spence, PhD, Kaiser Permanente Drug Information Service. Address reprint requests to T.C. Cheetham, Kaiser Permanente Drug Information Service, 9521 Dalen Street, Downey, CA 90242. Submitted May 31, 2002; revision accepted February 25, 2003. |