14 research outputs found
Effects of a self-management arthritis programme with an added exercise component for osteoarthritic knee : randomized controlled trial
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Reducing medication errors : development of a new model of drug administration for enhancing safe nursing practice
Aims: Medication error is a persistent and far-reaching clinical problem. Unsafe medication practices often occur due to unresolved medication errors, poor compliance with rules and policies, and the low clinical applicability of such rules and policies. This study, conducted in a Hong Kong hospital, aimed at addressing these concerns and developing a new model for drug administration and enhancing safe clinical practice based on research evidence. The current drug administrative procedure of \u27three checks\u27 and \u27five rights\u27 was reviewed to examine adherence and applicability in clinical settings. Methods: The study adopted a mixed method, with both quantitative and qualitative research designs. Data collection involved a review of medication incidents involving nurses that occurred over a 1-year period at the hospital, focus group interviews of nurses (n = 29), questionnaires for nurses (n = 466) and nurse managers (n = 12), observational studies of nurses (n = 46; 210 observations), and individual interviews (n = 3). Results: The common causes of medication errors were non-compliance with policies or procedures, doctor\u27s illegible writing, wrong transcription of drug administration times, failure to check for the right patient, wrong identification of drugs, and distractions. Many nurses regarded the \u27golden rule\u27 of \u27three checks\u27 and \u27five rights\u27 for drug administration as impractical and not viable because of time constraints, manpower shortage, and heavy workloads. Research data from questionnaires and observation studies validated the appropriateness of \u27five rights\u27 in preventing medication errors, but also supported a reduction of the \u27three checks\u27 practice to \u27two checks\u27. Conclusion: A new model of drug administration that is more practical, applicable, and safe in clinical practice is proposed. It is suggested that this model, which adopts \u27two checks\u27 and \u27five rights\u27 for drug administration, be tested further as a model that can save nurses\u27 time, enhance effective checking, and reduce medication error incidents
Predictors of functioning in people suffering from first-episode psychosis 1 year into entering early intervention service in Hong Kong
A large retrospective cohort study of cefazolin compared with flucloxacillin for methicillin-susceptible Staphylococcus aureus bacteraemia.
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A culture system to study oligodendrocyte myelination processes using engineered nanofibers
Current methods for studying central nervous system myelination necessitate permissive axonal substrates conducive to myelin wrapping by oligodendrocytes. We have developed a neuron-free culture system in which electron-spun nanofibers of varying sizes su
Myelin-based inhibitors of oligodendrocyte myelination: clues from axonal growth and regeneration
The differentiation of and myelination by oligodendrocytes (OLs) are exquisitely regulated by a series of intrinsic and extrinsic mechanisms. As each OL can make differing numbers of myelin segments with variable lengths along similar axon tracts, myelination can be viewed as a graded process shaped by inhibitory/inductive cues during development. Myelination by OLs is a prime example of an adaptive process determined by the microenvironment and architecture of the central nervous system (CNS). in this review, we discuss how myelin formation by OLs may be controlled by the heterogeneous microenvironment of the CNS. Then we address recent findings demonstrating that neighboring OLs may compete for available axon space, and highlight our current understanding of myelin-based inhibitors of axonal regeneration that are potentially responsible for the reciprocal dialogue between OLs and determine the numbers and lengths of myelin internodes. Understanding the mechanisms that control the spatiotemporal regulation of myelinogenic potential during development may provide valuable insight into therapeutic strategies for promoting remyelination in an inhibitory microenvironment