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Improvement in patient and physician notification of cardiac rhythm device report transmissions

Background Cardiac rhythm devices (CRD) require complex management to identify potential device or patient issues. While easy to obtain, report processing is complex and time consuming. In our population, a majority of reports were performed outside of institutional protocols and no method for elect...

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Autores principales: Czosek, Richard J, Brown, James, Proctor, Diane, Koch, Paula, Martin, Michelle, Rust, Mary, Anderson, Jeffrey B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5699127/
https://www.ncbi.nlm.nih.gov/pubmed/29450294
http://dx.doi.org/10.1136/bmjoq-2017-000155
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author Czosek, Richard J
Brown, James
Proctor, Diane
Koch, Paula
Martin, Michelle
Rust, Mary
Anderson, Jeffrey B
author_facet Czosek, Richard J
Brown, James
Proctor, Diane
Koch, Paula
Martin, Michelle
Rust, Mary
Anderson, Jeffrey B
author_sort Czosek, Richard J
collection PubMed
description Background Cardiac rhythm devices (CRD) require complex management to identify potential device or patient issues. While easy to obtain, report processing is complex and time consuming. In our population, a majority of reports were performed outside of institutional protocols and no method for electrophysiology (EP) notification for unscheduled reports existed. These process breakdowns led to potential issues with safety and associated loss of work efficiency. Objective Our aim was to decrease the percentage of reports without EP notification from 30% to 10% over a 9-month time period. Methods We created a detailed process map of in-office and home device reporting. Failure mode and effects analysis (FMEA)/Pareto charts were used to determine the mechanistic underpinnings of notification failures and identify areas for process improvement. Multiple interventions were implemented using the Plan-Do-Study-Act (PDSA) technique. Process run charts and control charts were used to evaluate ongoing changes. Results Our FMEA identified failures related to (1) lack of physician understanding of the device reporting system, (2) lack of an easy to use method of EP notification and (3) lack of patient understanding of report notification. Pareto charts identified the most frequent failures to be associated with specific cardiology subspecialties as well as reports sent from home. We performed multiple interventions including(1) creation of an easy to use method of EP notification used by patients and medical staff, (2) physician education and (3) patient education. Compared with baseline reporting, there was a decrease from 30% to <10% of device reports obtained without EP notification. This process improvement additionally resulted in a 34% reduction in time required for device processing. Conclusions Development of a unified EP reporting system and quality improvement methodology resulted in improved CRD report notification and improved efficiency for staff. These process changes resulted in improvement across differing cardiac subspecialty providers and patients.
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spelling pubmed-56991272018-02-15 Improvement in patient and physician notification of cardiac rhythm device report transmissions Czosek, Richard J Brown, James Proctor, Diane Koch, Paula Martin, Michelle Rust, Mary Anderson, Jeffrey B BMJ Open Qual Original Article Background Cardiac rhythm devices (CRD) require complex management to identify potential device or patient issues. While easy to obtain, report processing is complex and time consuming. In our population, a majority of reports were performed outside of institutional protocols and no method for electrophysiology (EP) notification for unscheduled reports existed. These process breakdowns led to potential issues with safety and associated loss of work efficiency. Objective Our aim was to decrease the percentage of reports without EP notification from 30% to 10% over a 9-month time period. Methods We created a detailed process map of in-office and home device reporting. Failure mode and effects analysis (FMEA)/Pareto charts were used to determine the mechanistic underpinnings of notification failures and identify areas for process improvement. Multiple interventions were implemented using the Plan-Do-Study-Act (PDSA) technique. Process run charts and control charts were used to evaluate ongoing changes. Results Our FMEA identified failures related to (1) lack of physician understanding of the device reporting system, (2) lack of an easy to use method of EP notification and (3) lack of patient understanding of report notification. Pareto charts identified the most frequent failures to be associated with specific cardiology subspecialties as well as reports sent from home. We performed multiple interventions including(1) creation of an easy to use method of EP notification used by patients and medical staff, (2) physician education and (3) patient education. Compared with baseline reporting, there was a decrease from 30% to <10% of device reports obtained without EP notification. This process improvement additionally resulted in a 34% reduction in time required for device processing. Conclusions Development of a unified EP reporting system and quality improvement methodology resulted in improved CRD report notification and improved efficiency for staff. These process changes resulted in improvement across differing cardiac subspecialty providers and patients. BMJ Publishing Group 2017-10-09 /pmc/articles/PMC5699127/ /pubmed/29450294 http://dx.doi.org/10.1136/bmjoq-2017-000155 Text en © Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/ 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 and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
spellingShingle Original Article
Czosek, Richard J
Brown, James
Proctor, Diane
Koch, Paula
Martin, Michelle
Rust, Mary
Anderson, Jeffrey B
Improvement in patient and physician notification of cardiac rhythm device report transmissions
title Improvement in patient and physician notification of cardiac rhythm device report transmissions
title_full Improvement in patient and physician notification of cardiac rhythm device report transmissions
title_fullStr Improvement in patient and physician notification of cardiac rhythm device report transmissions
title_full_unstemmed Improvement in patient and physician notification of cardiac rhythm device report transmissions
title_short Improvement in patient and physician notification of cardiac rhythm device report transmissions
title_sort improvement in patient and physician notification of cardiac rhythm device report transmissions
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5699127/
https://www.ncbi.nlm.nih.gov/pubmed/29450294
http://dx.doi.org/10.1136/bmjoq-2017-000155
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