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REDucing Unnecessary Coagulation Testing in the Emergency Department (REDUCED)

The PT/INR (prothrombin time/international normalized ratio) and aPTT (activated partial thromboplastin time) were tests developed in the early 20th century for specific and unique indications. Despite this, they are often ordered together routinely. The objective of this study was to determine if a...

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Autores principales: Fralick, Michael, Hicks, Lisa K, Chaudhry, Hina, Goldberg, Nicola, Ackery, Alun, Nisenbaum, Rosane, Sholzberg, Michelle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: British Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5411723/
https://www.ncbi.nlm.nih.gov/pubmed/28469907
http://dx.doi.org/10.1136/bmjquality.u221651.w8161
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author Fralick, Michael
Hicks, Lisa K
Chaudhry, Hina
Goldberg, Nicola
Ackery, Alun
Nisenbaum, Rosane
Sholzberg, Michelle
author_facet Fralick, Michael
Hicks, Lisa K
Chaudhry, Hina
Goldberg, Nicola
Ackery, Alun
Nisenbaum, Rosane
Sholzberg, Michelle
author_sort Fralick, Michael
collection PubMed
description The PT/INR (prothrombin time/international normalized ratio) and aPTT (activated partial thromboplastin time) were tests developed in the early 20th century for specific and unique indications. Despite this, they are often ordered together routinely. The objective of this study was to determine if a multimodal intervention could reduce PT/INR and aPTT testing in the emergency department (ED). This was a prospective multi-pronged quality improvement study at St. Michael's Hospital. The initiative involved stakeholder engagement, uncoupling of PT/INR and aPTT testing, teaching, and most importantly a revision to the ED order panels. After changes to order panels, weekly rates of PT/INR and aPTT testing per 100 ED patients decreased (17.2 vs 38.4, rate ratio=0.45 (95% CI 0.43-0.47), p<0.001; 16.6 vs 37.8, rate ratio=0.44 (95% CI 0.42-0.46), p<0.001, respectively). Rate of creatinine testing per 100 ED patients, our internal control, increased during the same period (54.0 vs 49.7, rate ratio=1.09 (95% CI 1.06-1.12); p<0.0001) while the weekly rate per 100 ED patients receiving blood transfusions slightly decreased (0.5 vs 0.7, rate ratio=0.66 (95% CI 0.49-0.87), p=0.0034). We found that a simple process change to order panels was associated with meaningful reductions in coagulation testing without obvious adverse effects.
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spelling pubmed-54117232017-05-03 REDucing Unnecessary Coagulation Testing in the Emergency Department (REDUCED) Fralick, Michael Hicks, Lisa K Chaudhry, Hina Goldberg, Nicola Ackery, Alun Nisenbaum, Rosane Sholzberg, Michelle BMJ Qual Improv Rep BMJ Quality Improvement Programme The PT/INR (prothrombin time/international normalized ratio) and aPTT (activated partial thromboplastin time) were tests developed in the early 20th century for specific and unique indications. Despite this, they are often ordered together routinely. The objective of this study was to determine if a multimodal intervention could reduce PT/INR and aPTT testing in the emergency department (ED). This was a prospective multi-pronged quality improvement study at St. Michael's Hospital. The initiative involved stakeholder engagement, uncoupling of PT/INR and aPTT testing, teaching, and most importantly a revision to the ED order panels. After changes to order panels, weekly rates of PT/INR and aPTT testing per 100 ED patients decreased (17.2 vs 38.4, rate ratio=0.45 (95% CI 0.43-0.47), p<0.001; 16.6 vs 37.8, rate ratio=0.44 (95% CI 0.42-0.46), p<0.001, respectively). Rate of creatinine testing per 100 ED patients, our internal control, increased during the same period (54.0 vs 49.7, rate ratio=1.09 (95% CI 1.06-1.12); p<0.0001) while the weekly rate per 100 ED patients receiving blood transfusions slightly decreased (0.5 vs 0.7, rate ratio=0.66 (95% CI 0.49-0.87), p=0.0034). We found that a simple process change to order panels was associated with meaningful reductions in coagulation testing without obvious adverse effects. British Publishing Group 2017-05-02 /pmc/articles/PMC5411723/ /pubmed/28469907 http://dx.doi.org/10.1136/bmjquality.u221651.w8161 Text en © 2017, 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 under the terms of the Creative Commons Attribution Non-commercial License, which permits use, distribution, and reproduction in any medium, provided the original work is properly cited, the use is non commercial and is otherwise in compliance with the license. See: http://creativecommons.org/licenses/by-nc/2.0/http://creativecommons.org/licenses/by-nc/2.0/legalcode
spellingShingle BMJ Quality Improvement Programme
Fralick, Michael
Hicks, Lisa K
Chaudhry, Hina
Goldberg, Nicola
Ackery, Alun
Nisenbaum, Rosane
Sholzberg, Michelle
REDucing Unnecessary Coagulation Testing in the Emergency Department (REDUCED)
title REDucing Unnecessary Coagulation Testing in the Emergency Department (REDUCED)
title_full REDucing Unnecessary Coagulation Testing in the Emergency Department (REDUCED)
title_fullStr REDucing Unnecessary Coagulation Testing in the Emergency Department (REDUCED)
title_full_unstemmed REDucing Unnecessary Coagulation Testing in the Emergency Department (REDUCED)
title_short REDucing Unnecessary Coagulation Testing in the Emergency Department (REDUCED)
title_sort reducing unnecessary coagulation testing in the emergency department (reduced)
topic BMJ Quality Improvement Programme
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5411723/
https://www.ncbi.nlm.nih.gov/pubmed/28469907
http://dx.doi.org/10.1136/bmjquality.u221651.w8161
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