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Plan-Do-Study-Act Methodology: Refining an Inpatient Pediatric Sepsis Screening Process

Pediatric sepsis remains a leading cause of death of children in the United States. Timely recognition and treatment are critical to prevent the onset of severe sepsis and septic shock. Electronic screening tools aid providers in identifying patients at risk for sepsis. Our overall project goal was...

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Autores principales: Nuss, Kathryn E., Kunar, Jillian S., Ahrens, Erin A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7470006/
https://www.ncbi.nlm.nih.gov/pubmed/33062902
http://dx.doi.org/10.1097/pq9.0000000000000338
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author Nuss, Kathryn E.
Kunar, Jillian S.
Ahrens, Erin A.
author_facet Nuss, Kathryn E.
Kunar, Jillian S.
Ahrens, Erin A.
author_sort Nuss, Kathryn E.
collection PubMed
description Pediatric sepsis remains a leading cause of death of children in the United States. Timely recognition and treatment are critical to prevent the onset of severe sepsis and septic shock. Electronic screening tools aid providers in identifying patients at risk for sepsis. Our overall project goal was to decrease the number of sepsis-related emergent transfers to the pediatric intensive care unit by optimizing sepsis screening tools, interruptive alerts, and a new paper tool and huddle process using Plan-Do-Study-Act (PDSA) methodology. METHODS: Our team utilized historical data to develop inpatient electronic sepsis screening tools to identify pediatric patients at risk for sepsis. Using PDSA iterative cycles over 3 months, we tested the design of an interruptive alert, paper tool, and a new sepsis huddle process. RESULTS: During the PDSA, the clinical teams conducted huddles on all patients who received an interruptive alert (n = 35). Eighty percent of huddles had a 5.7 minute average response time and an average duration of 5.3 minutes. Completion of the huddle outcome notes occurred 83% of the time, and 70% had feedback related to the alert, paper form, and huddle process. The number of days between sepsis-related emergent transfers to the pediatric intensive care unit increased from a median of 17.5 to 57.5 days, with a single point as high as 195 days between events. CONCLUSIONS: The inpatient sepsis team learned valuable lessons using PDSA methodology. The results of the iterative cycles allowed the team to optimize and refine the tests of change. System-wide implementation benefited from the application of this quality improvement tool.
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spelling pubmed-74700062020-10-14 Plan-Do-Study-Act Methodology: Refining an Inpatient Pediatric Sepsis Screening Process Nuss, Kathryn E. Kunar, Jillian S. Ahrens, Erin A. Pediatr Qual Saf Individual QI Projects from Single Institutions Pediatric sepsis remains a leading cause of death of children in the United States. Timely recognition and treatment are critical to prevent the onset of severe sepsis and septic shock. Electronic screening tools aid providers in identifying patients at risk for sepsis. Our overall project goal was to decrease the number of sepsis-related emergent transfers to the pediatric intensive care unit by optimizing sepsis screening tools, interruptive alerts, and a new paper tool and huddle process using Plan-Do-Study-Act (PDSA) methodology. METHODS: Our team utilized historical data to develop inpatient electronic sepsis screening tools to identify pediatric patients at risk for sepsis. Using PDSA iterative cycles over 3 months, we tested the design of an interruptive alert, paper tool, and a new sepsis huddle process. RESULTS: During the PDSA, the clinical teams conducted huddles on all patients who received an interruptive alert (n = 35). Eighty percent of huddles had a 5.7 minute average response time and an average duration of 5.3 minutes. Completion of the huddle outcome notes occurred 83% of the time, and 70% had feedback related to the alert, paper form, and huddle process. The number of days between sepsis-related emergent transfers to the pediatric intensive care unit increased from a median of 17.5 to 57.5 days, with a single point as high as 195 days between events. CONCLUSIONS: The inpatient sepsis team learned valuable lessons using PDSA methodology. The results of the iterative cycles allowed the team to optimize and refine the tests of change. System-wide implementation benefited from the application of this quality improvement tool. Lippincott Williams & Wilkins 2020-09-02 /pmc/articles/PMC7470006/ /pubmed/33062902 http://dx.doi.org/10.1097/pq9.0000000000000338 Text en Copyright © 2020 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.
spellingShingle Individual QI Projects from Single Institutions
Nuss, Kathryn E.
Kunar, Jillian S.
Ahrens, Erin A.
Plan-Do-Study-Act Methodology: Refining an Inpatient Pediatric Sepsis Screening Process
title Plan-Do-Study-Act Methodology: Refining an Inpatient Pediatric Sepsis Screening Process
title_full Plan-Do-Study-Act Methodology: Refining an Inpatient Pediatric Sepsis Screening Process
title_fullStr Plan-Do-Study-Act Methodology: Refining an Inpatient Pediatric Sepsis Screening Process
title_full_unstemmed Plan-Do-Study-Act Methodology: Refining an Inpatient Pediatric Sepsis Screening Process
title_short Plan-Do-Study-Act Methodology: Refining an Inpatient Pediatric Sepsis Screening Process
title_sort plan-do-study-act methodology: refining an inpatient pediatric sepsis screening process
topic Individual QI Projects from Single Institutions
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7470006/
https://www.ncbi.nlm.nih.gov/pubmed/33062902
http://dx.doi.org/10.1097/pq9.0000000000000338
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