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Defining adverse events during trauma resuscitation: a modified RAND Delphi study

BACKGROUND: The majority of preventable adverse event (AEs) in trauma care occur during the initial phase of resuscitation, often within the trauma bay. However, there is significant heterogeneity in reporting these AEs that limits performance comparisons between hospitals and trauma systems. The ob...

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Autores principales: Nolan, Brodie, Petrosoniak, Andrew, Hicks, Christopher M, Cripps, Michael W, Dumas, Ryan P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8527130/
https://www.ncbi.nlm.nih.gov/pubmed/34746435
http://dx.doi.org/10.1136/tsaco-2021-000805
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author Nolan, Brodie
Petrosoniak, Andrew
Hicks, Christopher M
Cripps, Michael W
Dumas, Ryan P
author_facet Nolan, Brodie
Petrosoniak, Andrew
Hicks, Christopher M
Cripps, Michael W
Dumas, Ryan P
author_sort Nolan, Brodie
collection PubMed
description BACKGROUND: The majority of preventable adverse event (AEs) in trauma care occur during the initial phase of resuscitation, often within the trauma bay. However, there is significant heterogeneity in reporting these AEs that limits performance comparisons between hospitals and trauma systems. The objective of this study was to create a taxonomy of AEs that occur during trauma resuscitation and a corresponding classification system to assign a degree of harm. METHODS: This study used a modified RAND Delphi methodology to establish a taxonomy of AEs in trauma and a degree of harm classification system. A systematic review informed the preliminary list of AEs. An interdisciplinary panel of 22 trauma experts rated these AEs through two rounds of online surveys and a final consensus meeting. Consensus was defined as 80% for each AE and the final checklist. RESULTS: The Delphi panel consisted of 22 multidisciplinary trauma experts. A list of 57 evidence-informed AEs was revised and expanded during the modified Delphi process into a finalized list of 67 AEs. Each AE was classified based on degree of harm on a scale from I (no harm) to V (death). DISCUSSION: This study developed a taxonomy of 67 AEs that occur during the initial phases of a trauma resuscitation with a corresponding degree of harm classification. This taxonomy serves to support a standardized evaluation of trauma care between centers and regions. LEVEL OF EVIDENCE: Level 5.
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spelling pubmed-85271302021-11-04 Defining adverse events during trauma resuscitation: a modified RAND Delphi study Nolan, Brodie Petrosoniak, Andrew Hicks, Christopher M Cripps, Michael W Dumas, Ryan P Trauma Surg Acute Care Open Original Research BACKGROUND: The majority of preventable adverse event (AEs) in trauma care occur during the initial phase of resuscitation, often within the trauma bay. However, there is significant heterogeneity in reporting these AEs that limits performance comparisons between hospitals and trauma systems. The objective of this study was to create a taxonomy of AEs that occur during trauma resuscitation and a corresponding classification system to assign a degree of harm. METHODS: This study used a modified RAND Delphi methodology to establish a taxonomy of AEs in trauma and a degree of harm classification system. A systematic review informed the preliminary list of AEs. An interdisciplinary panel of 22 trauma experts rated these AEs through two rounds of online surveys and a final consensus meeting. Consensus was defined as 80% for each AE and the final checklist. RESULTS: The Delphi panel consisted of 22 multidisciplinary trauma experts. A list of 57 evidence-informed AEs was revised and expanded during the modified Delphi process into a finalized list of 67 AEs. Each AE was classified based on degree of harm on a scale from I (no harm) to V (death). DISCUSSION: This study developed a taxonomy of 67 AEs that occur during the initial phases of a trauma resuscitation with a corresponding degree of harm classification. This taxonomy serves to support a standardized evaluation of trauma care between centers and regions. LEVEL OF EVIDENCE: Level 5. BMJ Publishing Group 2021-10-19 /pmc/articles/PMC8527130/ /pubmed/34746435 http://dx.doi.org/10.1136/tsaco-2021-000805 Text en © Author(s) (or their employer(s)) 2021. 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
Nolan, Brodie
Petrosoniak, Andrew
Hicks, Christopher M
Cripps, Michael W
Dumas, Ryan P
Defining adverse events during trauma resuscitation: a modified RAND Delphi study
title Defining adverse events during trauma resuscitation: a modified RAND Delphi study
title_full Defining adverse events during trauma resuscitation: a modified RAND Delphi study
title_fullStr Defining adverse events during trauma resuscitation: a modified RAND Delphi study
title_full_unstemmed Defining adverse events during trauma resuscitation: a modified RAND Delphi study
title_short Defining adverse events during trauma resuscitation: a modified RAND Delphi study
title_sort defining adverse events during trauma resuscitation: a modified rand delphi study
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8527130/
https://www.ncbi.nlm.nih.gov/pubmed/34746435
http://dx.doi.org/10.1136/tsaco-2021-000805
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