Medication Error Reporting Law
Contents |
DataSetsGEO ProfilesGSSGTRHomoloGeneMedGenMeSHNCBI Web SiteNLM CatalogNucleotideOMIMPMCPopSetProbeProteinProtein ClustersPubChem BioAssayPubChem CompoundPubChem SubstancePubMedPubMed HealthSNPSparcleSRAStructureTaxonomyToolKitToolKitAllToolKitBookToolKitBookghUniGeneSearch termSearch Browse Titles Limits Advanced Help NCBI Bookshelf. medication error definition A service of the National Library of Medicine, National
Medication Error Reporting Procedure
Institutes of Health.Hughes RG, editor. Patient Safety and Quality: An Evidence-Based Handbook for Nurses.
Medication Errors In Nursing
Rockville (MD): Agency for Healthcare Research and Quality (US); 2008 Apr. Patient Safety and Quality: An Evidence-Based Handbook for Nurses.Show detailsHughes RG, editor.Rockville
Medication Errors Statistics
(MD): Agency for Healthcare Research and Quality (US); 2008 Apr.ContentsSearch term < PrevNext > Chapter 35Error Reporting and DisclosureZane Robinson Wolf; Ronda G. Hughes.Author InformationZane Robinson Wolf;1 Ronda G. Hughes.21 Zane Robinson Wolf, Ph.D., R.N., F.A.A.N., dean and professor, La Salle University School of Nursing and types of medication errors Health Sciences. E-mail: ude.ellasal@flow2 Ronda G. Hughes, Ph.D., M.H.S., R.N., senior health scientist administrator, Agency for Healthcare Research and Quality. E-mail: vog.shh.qrha@sehguH.adnoRBackgroundThis chapter examines reporting of health care errors (e.g., verbal, written, or other form of communication and/or recording of near miss and patient safety events that generally involves some form of reporting system) and these events’ disclosure (e.g., communication of errors to patients and their families), including the ethical aspects of error-reporting mechanisms. The potential benefits of intrainstitutional and Web-based databases might assist nurses and other providers to prevent similar hazards and improve patient safety. Clinicians’ fears of lawsuits and their self-perceptions of incompetence could be dispelled by organizational cultures emphasizing safety rather than blame. This chapter focuses on the assertion that reporting errors that result in patient harm as well as seemingly trivial erro
Design support from Skysoft Consulting ©QuPS.org Terms of Use ©QuPS.org Privacy Policy
advocate for learning from the experiences of others—to take certain aspects of another’s experience and incorporate them into your own work and life for https://www.ismp.org/newsletters/acutecare/articles/20100325.asp the purpose of improvement. It is in this spirit of learning that we share with readers our support of a state-wide initiative in California (CA) to reduce medication-related errors that can be used as an example for all US hospitals to voluntarily adopt a similar initiative. As a condition of licensure, every general acute care hospital in CA was medication error required to adopt a Medication Error Reduction Plan (MERP; not to be confused with the ISMP MERP [Medication Errors Reporting Program]) to substantially reduce medication–related errors (http://law.justia.com/california/codes/hsc/1339.63.html) by January 1, 2002. The plans were required to include the implementation of technology proven to reduce errors. The submitted plans were approved by the California Department of Public Health (CDPH), and medication error reporting each hospital was required to implement its plan before January 1, 2005. Each hospital must review and approve the plan annually. MERP Components Table 1 Details regarding the required components in the hospital’s MERP are provided in Table 1. In brief, each hospital must adopt a methodology to assess, improve, and evaluate medication safety, with particular attention paid to prescribing, prescription order communication, product labeling, product packaging and nomenclature, compounding, dispensing, distribution, administration, education, monitoring, and use. This methodology must include a system or process to proactively identify actual or potential medication-related errors as well as concurrent and retrospective review of clinical care. The regulation defines a “medication-related error” as any preventable medication-related event that adversely affects a patient and is related to professional practice or healthcare products, procedures, and systems, including but not limited to the elements listed above in bold text. A multidisciplinary process that includes pharmacists, nurses, physicians, and administrative leaders must be established to regularly analyze all identified actual or potential medication-related errors—not just aggregate reports about these conditions or ev
be down. Please try the request again. Your cache administrator is webmaster. Generated Thu, 20 Oct 2016 15:09:23 GMT by s_wx1126 (squid/3.5.20)