You have accessJournal of UrologyCME1 Apr 2023MP19-08 DETERMINANTS OF BETA-3 AGONIST PRESCRIPTION FOR OVERACTIVE BLADDER ACCORDING TO THE AUA QUALITY REGISTRY Max Bowman, Katherine Shapiro, Camille Velez, Rachel Mbassa, Raymond Fang, Benjamin Brucker, and Michelle van Kuiken Max BowmanMax Bowman More articles by this author , Katherine ShapiroKatherine Shapiro More articles by this author , Camille VelezCamille Velez More articles by this author , Rachel MbassaRachel Mbassa More articles by this author , Raymond FangRaymond Fang More articles by this author , Benjamin BruckerBenjamin Brucker More articles by this author , and Michelle van KuikenMichelle van Kuiken More articles by this author View All Author Informationhttps://doi.org/10.1097/JU.0000000000003244.08AboutPDF ToolsAdd to favoritesDownload CitationsTrack CitationsPermissionsReprints ShareFacebookLinked InTwitterEmail Abstract INTRODUCTION AND OBJECTIVE: First-line treatment for overactive bladder (OAB) is behavioral therapy, followed by oral anticholinergics (ACH) or beta-3 agonists (B3). B3 agonists are better tolerated, but prescription rates between the two classes vary greatly. Using the AUA Quality (AQUA) Registry, we aim to determine which factors are associated with receiving a B3 agonist versus an ACH as the first prescription for OAB. METHODS: In this cross-sectional study, we queried the AQUA registry from 2014-2020 for adults with new diagnosis of OAB, including frequency, urgency, nocturia, and urge incontinence, examining the prescription rate and choice of first medication prescribed. Patients with neurogenic bladder or incomplete data were excluded. Insurance, age, race/ethnicity, gender, practice type, metropolitan status, and year of prescription were examined via multivariate analysis to determine which were associated with prescription of B3 agonists. RESULTS: 641,122 patients were diagnosed with OAB during the study period, and 112,021 (17.5%) received medication. Compared to those with private insurance, patients with Medicaid, Medicare, and other/self-pay were less likely to receive a B3 (OR 0.81, 0.91, and 0.68, respectively; p<0.001). Odds of receiving B3 increased over age 50: 51-64 (OR 1.11), 65-79 (OR 1.29), and >80 (OR 1.62) (p<0.001 for all). Compared to white patients, black (OR 0.87, p<0.001), Asian (OR 0.91, p=0.05) and those of other races (OR 0.84, p=0.005) had lower odds of receiving B3 agonists. Additionally, patients in rural areas (OR 0.85, p<0.001) and those seen in academic practices were less likely to receive B3 therapy than those seen in multispecialty, single specialty, or solo practices (Table 1). Patient gender was not associated with a difference in B3 prescription. CONCLUSIONS: Factors associated with increased B3 agonist prescription included white race, older age, having private or military insurance, and residence in a metropolitan area. Non-white patients, younger patients, those residing in rural areas, and those seen in academic practices were less likely to receive B3 prescription as their first choice of medication. These findings indicate that factors other than the patient’s disease affect treatment offered. Source of Funding: None © 2023 by American Urological Association Education and Research, Inc.FiguresReferencesRelatedDetails Volume 209Issue Supplement 4April 2023Page: e267 Advertisement Copyright & Permissions© 2023 by American Urological Association Education and Research, Inc.MetricsAuthor Information Max Bowman More articles by this author Katherine Shapiro More articles by this author Camille Velez More articles by this author Rachel Mbassa More articles by this author Raymond Fang More articles by this author Benjamin Brucker More articles by this author Michelle van Kuiken More articles by this author Expand All Advertisement PDF downloadLoading ...
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