Please use this identifier to cite or link to this item: https://www.um.edu.mt/library/oar/handle/123456789/112164
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dc.contributor.authorWest, Lorna Marie-
dc.contributor.authorBrincat, Alison-
dc.contributor.authorMercieca, Mark-
dc.contributor.authorFsadni, Demis-
dc.contributor.authorRapa, Ian-
dc.contributor.authorCordina, Maria-
dc.date.accessioned2023-08-01T10:20:04Z-
dc.date.available2023-08-01T10:20:04Z-
dc.date.issued2018-
dc.identifier.citationWest, L. M., Brincat, A., Mercieca, M., Fsadni, D., Rapa, I., & Cordina, M. (2018). Applying lean methodology to improve parenteral chemotherapy and monoclonal antibody documentation processes based on Normalisation Process Theory. European Journal of Hospital Pharmacy, 25(1), 32-37.en_GB
dc.identifier.urihttps://www.um.edu.mt/library/oar/handle/123456789/112164-
dc.description.abstractObjective: To determine the impact of lean thinking on the original time required to prepare the necessary documentation in relation to the preparation of parenteral chemotherapy/monoclonal antibodies.en_GB
dc.description.abstractMethod: Four pharmacists and one pharmacy technician from the oncology hospital (Malta) all participated in eight focus groups linked to the different constructs of Normalisation Process Theory (NPT): coherence, cognitive participation, collective action and reflexive monitoring. The value stream documentation process was mapped by analysing all steps in the process where each activity must add value for the patient; tools of lean thinking were applied. Points causing delay in processing were considered critical; possible changes to minimise time waste were discussed and implemented. Time spent on critical points was measured by timing in minutes each step of the process 1 month before and after the changes had been implemented and calculating the mean±SD. An audit was performed comparing the process with standard operating procedures to determine whether any steps required quality improvement.en_GB
dc.description.abstractResults: Three critical points were identified: time required to search for pharmacy patient medication records for chemotherapy/monoclonal antibodies required on the day; time to generate preparation labels; and time to generate worksheets. Overall, a total of 122 ±8.6 min ( p=0.06) were saved per day, a 37% decrease from the original documentation time. Five deficiencies were identified in the documentation process audit; corrective action was proposed.en_GB
dc.description.abstractConclusions: By applying lean thinking, non-value added steps leading to time waste in the documentation process were eliminated. This concept could be implemented by using NPT as part of a strategic system to reduce waste.en_GB
dc.language.isoenen_GB
dc.publisherBMJ Groupen_GB
dc.rightsinfo:eu-repo/semantics/restrictedAccessen_GB
dc.subjectParenteral therapy -- Standardsen_GB
dc.subjectChemotherapyen_GB
dc.subjectMedical care -- Documentation -- Evaluationen_GB
dc.subjectMonoclonal antibodies -- Documentationen_GB
dc.titleApplying lean methodology to improve parenteral chemotherapy and monoclonal antibody documentation processes based on normalisation process theoryen_GB
dc.typearticleen_GB
dc.rights.holderThe copyright of this work belongs to the author(s)/publisher. The rights of this work are as defined by the appropriate Copyright Legislation or as modified by any successive legislation. Users may access this work and can make use of the information contained in accordance with the Copyright Legislation provided that the author must be properly acknowledged. Further distribution or reproduction in any format is prohibited without the prior permission of the copyright holder.en_GB
dc.description.reviewedpeer-revieweden_GB
dc.identifier.doi10.1136/ejhpharm-2016-001046-
dc.publication.titleEuropean Journal of Hospital Pharmacyen_GB
Appears in Collections:Scholarly Works - FacM&SCPT



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