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Reducing Medication Errors

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Reducing Medication Errors In Hospitals
Patient centered care and patient safety are the most important roles in nursing. “Serious medication errors are common in hospitals and often occur during order transcription or administration of medication” (Poon et al., 2010. p. 1). According to Seibert (2014), medication errors and related deaths cost the health care system billions of dollars yearly and that at least one error a day happens in all hospitals. “An estimated 450,000 adverse drug events medication errors that result in patient harm occur annually, approximately 25% of which are preventable” (Seibert, 2014. p. 1).
One important aspect of nursing is drug administration. It is a multidisciplinary task including doctors, pharmacist …show more content…
P – patients being administered medication in hospitals I - electronic medication systems with barcodes, C - paper based systems to administer medication, O – Reducing Medication errors.
Research Design
According to Houser (2015), quasi-experimental designs are studies of cause and effect that use convenience samples. “The most common quasi-experimental design is the nonequivalent comparison group before/after design” (Houser, 2015. p. 331). Subjects are not chosen randomly as with traditional research design, but are placed in groups of one or two.
The research design used in this article is a before and after quasi-experimental study that compared medication errors using traditional paper charting before implementing electronic medication administration systems with barcodes. “Errors that involved early or late administration of medications were classified as timing errors and all others as nontiming errors” (Poon et al., 2010. p. 1). …show more content…
p. 211). Direct and indirect are two types of observational research. Two trained research nurses used direct observation to measure medication error rates. They “observed order transcription and medication administration in each study unit 2 to 4 weeks before the bar-code eMAR rollout and then 4 to 8 weeks afterward” (Poon et al., 2010. p. 3). Research nurses shadowed staff nurses for four hours and were not privy to the medication ordered by physicians or details about the medication administered by the nurses. “After completing the observation session, the research nurses, assisted by research pharmacists, reviewed the physicians’ orders and either the paper record of medication administration (on units without the bar-code eMAR) or the eMAR (on units with the bar-code eMAR)” (Poon et al., 2010. p. 3). They determined if there were errors in transcription from doctor’s order or from medication administered during the observation period. “Each error was further adjudicated independently by two members of a multidisciplinary panel consisting of physicians, nurses, and pharmacists to confirm the presence of an error and the potential for that error to lead to patient harm (a subgroup known as potential adverse drug events)” (Poon et al., 2010. p.

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