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Pathway map development for medical device event reporting in operating theatres: a human factors approach to improving the existing system

OBJECTIVES: This study aimed to develop the actual pathway to reporting and information transfer in operating theatres in relation to medical technology malfunction/failure. This with the aim of understanding the differences with the pathway published by NHS Improvement and identification of points...

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Autores principales: Tase, Arkeliana, Micocci, Massimo, Buckle, Peter, Ni, Melody, Hanna, George
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9980347/
https://www.ncbi.nlm.nih.gov/pubmed/36873658
http://dx.doi.org/10.1136/bmjsit-2022-000155
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author Tase, Arkeliana
Micocci, Massimo
Buckle, Peter
Ni, Melody
Hanna, George
author_facet Tase, Arkeliana
Micocci, Massimo
Buckle, Peter
Ni, Melody
Hanna, George
author_sort Tase, Arkeliana
collection PubMed
description OBJECTIVES: This study aimed to develop the actual pathway to reporting and information transfer in operating theatres in relation to medical technology malfunction/failure. This with the aim of understanding the differences with the pathway published by NHS Improvement and identification of points for improvement. DESIGN: This is a qualitative study involving stakeholder interviews with doctors, nurses, manufacturers, medical device safety officer and Medicines and Healthcare products Regulatory Agency. SETTING: Data were collected on reporting pathway used in operating theatres. Clinical staff who took part worked in different trusts throughout UK while manufacturers provided devices in UK and EU/USA. PARTICIPANTS: Semistructured interviews were completed with 15 clinicians and 13 manufacturers. Surveys were completed by 38 clinicians and 5 manufacturers. Recognised methods of pathway development were used. The Lean Six Sigma principles adapted to healthcare were used to develop suggestions for improvement. MAIN OUTCOME MEASURES: To identify the differences between the set pathway to reporting and information transfer to what is occurring on a day-to-day basis as reported by staff. Identify points in the pathway where improvements could be applied. RESULTS: The developed pathway demonstrated great complexity of the current reporting system for medical devices. It identified numerous areas that give rise to problems and multiple biases in decision making. This highlighted the core issues leading to under-reporting and lack of knowledge on device performance and patient risk. Suggestions for improvement were deduced based on end user requirements and identified problems. CONCLUSIONS: This study has provided a detailed understanding of the key problem areas that exist within the current reporting system for medical devices and technology. The developed pathway sets to address the key problems to improve reporting outcomes. The identification of pathway differences between ‘work as done’ and ‘work as imagined’ can lead to development of quality improvements that could be systematically applied.
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spelling pubmed-99803472023-03-03 Pathway map development for medical device event reporting in operating theatres: a human factors approach to improving the existing system Tase, Arkeliana Micocci, Massimo Buckle, Peter Ni, Melody Hanna, George BMJ Surg Interv Health Technol Original Research OBJECTIVES: This study aimed to develop the actual pathway to reporting and information transfer in operating theatres in relation to medical technology malfunction/failure. This with the aim of understanding the differences with the pathway published by NHS Improvement and identification of points for improvement. DESIGN: This is a qualitative study involving stakeholder interviews with doctors, nurses, manufacturers, medical device safety officer and Medicines and Healthcare products Regulatory Agency. SETTING: Data were collected on reporting pathway used in operating theatres. Clinical staff who took part worked in different trusts throughout UK while manufacturers provided devices in UK and EU/USA. PARTICIPANTS: Semistructured interviews were completed with 15 clinicians and 13 manufacturers. Surveys were completed by 38 clinicians and 5 manufacturers. Recognised methods of pathway development were used. The Lean Six Sigma principles adapted to healthcare were used to develop suggestions for improvement. MAIN OUTCOME MEASURES: To identify the differences between the set pathway to reporting and information transfer to what is occurring on a day-to-day basis as reported by staff. Identify points in the pathway where improvements could be applied. RESULTS: The developed pathway demonstrated great complexity of the current reporting system for medical devices. It identified numerous areas that give rise to problems and multiple biases in decision making. This highlighted the core issues leading to under-reporting and lack of knowledge on device performance and patient risk. Suggestions for improvement were deduced based on end user requirements and identified problems. CONCLUSIONS: This study has provided a detailed understanding of the key problem areas that exist within the current reporting system for medical devices and technology. The developed pathway sets to address the key problems to improve reporting outcomes. The identification of pathway differences between ‘work as done’ and ‘work as imagined’ can lead to development of quality improvements that could be systematically applied. BMJ Publishing Group 2023-03-01 /pmc/articles/PMC9980347/ /pubmed/36873658 http://dx.doi.org/10.1136/bmjsit-2022-000155 Text en © Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Original Research
Tase, Arkeliana
Micocci, Massimo
Buckle, Peter
Ni, Melody
Hanna, George
Pathway map development for medical device event reporting in operating theatres: a human factors approach to improving the existing system
title Pathway map development for medical device event reporting in operating theatres: a human factors approach to improving the existing system
title_full Pathway map development for medical device event reporting in operating theatres: a human factors approach to improving the existing system
title_fullStr Pathway map development for medical device event reporting in operating theatres: a human factors approach to improving the existing system
title_full_unstemmed Pathway map development for medical device event reporting in operating theatres: a human factors approach to improving the existing system
title_short Pathway map development for medical device event reporting in operating theatres: a human factors approach to improving the existing system
title_sort pathway map development for medical device event reporting in operating theatres: a human factors approach to improving the existing system
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9980347/
https://www.ncbi.nlm.nih.gov/pubmed/36873658
http://dx.doi.org/10.1136/bmjsit-2022-000155
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