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a prescription for improving drug formulary decision making改善药物处方规定的决策
Policy Forum A Prescription for Improving Drug Formulary Decision Making Gordon D. Schiff1,2*, William L. Galanter2,3,4, Jay Duhig2,5, Michael J. Koronkowski2,5, Amy E. Lodolce2,5, Pam Pontikes2,6, John Busker2,6, Daniel Touchette2,5, Surrey Walton2,5, Bruce L. Lambert2,4,5 1 Brigham and Woman’s Hospital, Harvard Medical School, Boston, Massachusetts, United States of America, 2 Center for Education and Research on Therapeutics, University of Illinois at Chicago, Chicago, Illinois, United States of America, 3 University of Illinois at Chicago, College of Medicine, Chicago, Illinois, United States of America, 4 Department of Pharmacy Practice, University of Illinois at Chicago, Chicago, Illinois, United States of America, 5 University of Illinois at Chicago, Department of Pharmacy Administration, Chicago, Illinois, United States of America, 6 John H. Stroger Jr. Hospital of Cook County, Chicago, Illinois, United States of America Introduction efficacious, safest, and cost-effective ther- faced with packed meeting agendas that apies, while serving as a firewall to protect never seemed to permit sufficient time to Drug formularies are a ubiquitous, against prescribing overly driven by mar- thoroughly explore decision pros and heterogeneous yet often contentious fea- keting claims [11–13,16–21]. Through the cons, monitoring requirements, and opti- ture of both US and international drug decision-making activities of the formulary mal usage for proposed new drugs, we policy [1–6]. Formularies represent the process, knowledge and leverage may be observed that discussions were often fundamental
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