Patient safety related to medication infusion devices has received considerable attention recently. Critical adverse patient outcomes have resulted from misprogrammed delivery devices, inherent flaws in device design, and human error. A key strategy to improving patient safety is the development of an interdisciplinary team in product selection and the inclusion of registered nurses in the process. Such a process would include salient elements of each professional viewpoint and consider product impact on practice. No formal product selection guidelines exist which consider patient safety. This article outlines the process undertaken at University Health Network in the selection of its most recent patient-controlled analgesia device. Various available products were excluded from the selection process based on the interdisciplinary review. (C) 2007 by the American Society for Pain Management Nursing.
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Duke Clin Res Inst, Durham, NC USA
Duke Univ, Med Ctr, Dept Med, Div Cardiol, Durham, NC 27710 USA
Duke Margolis Ctr Hlth Policy, Durham, NC USAUniv Montreal, Montreal Heart Inst, 5000 Belanger St, Montreal, PQ H1T 1C8, Canada
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Natl Canc Ctr, Res Inst, Div Genome Biol, Tokyo 104, Japan
Natl Canc Ctr, Exploratory Oncol Res & Clin Trial Ctr, Div Translat Res, Tokyo, JapanNatl Canc Ctr, Res Inst, Div Genome Biol, Tokyo 104, Japan