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A Quality Improvement Initiative to Reduce Blood Culture Contamination in the Neonatal Unit

Peripheral blood culture contamination (BCC) can lead to an initiation of unnecessary antimicrobial treatment, further laboratory tests, increased length of stay, and increased costs. This study describes a 12-month quality improvement (QI) program to reduce the BCC rate in a neonatal unit by 50%. M...

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Autores principales: Allen, Elizabeth, Cavallaro, Angela, Keir, Amy K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8143735/
https://www.ncbi.nlm.nih.gov/pubmed/34046542
http://dx.doi.org/10.1097/pq9.0000000000000413
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author Allen, Elizabeth
Cavallaro, Angela
Keir, Amy K.
author_facet Allen, Elizabeth
Cavallaro, Angela
Keir, Amy K.
author_sort Allen, Elizabeth
collection PubMed
description Peripheral blood culture contamination (BCC) can lead to an initiation of unnecessary antimicrobial treatment, further laboratory tests, increased length of stay, and increased costs. This study describes a 12-month quality improvement (QI) program to reduce the BCC rate in a neonatal unit by 50%. METHODS: The QI team focused on standardizing processes to align with best practices using process mapping and cause and effect diagrams. Plan-Do-Study-Act (PDSA) 1: inoculation of blood culture bottles with the introduction of transfer device; PDSA 2: preparation of the skin for peripheral intravenous cannula insertion; PDSA 3: aseptic technique education package; and PDSA 4: optimizing blood volume of blood collected for culture. The team used statistical process control methodology to detect special cause variation. RESULTS: Compliance with the standard processes as part of PSDA 1 improved from a mean level of 50% to 100% and for PDSA 2 improved from a mean level of 50% to 95%. After implementation of PDSA 3, scores on a relevant knowledge test increased from a mean of 39% (pretraining test; n = 10) to 92% (posttraining test; n = 10) (P < 0.001). Postimplementation of the processes for PDSA 4, a minimum of 1 mL was collected in 94% of blood culture collection events (n = 450) (mean 1.1 mL; range 0.5–3.5 mL). Special cause variation occurred after the implementation of the PDSA cycles. During the baseline period, the BCC rate was 2.0% and decreased to 1.0% postinterventions implementation. CONCLUSIONS: Interventions focused on standardizing practices around collection of blood cultures in neonates were associated with fewer contaminants. This study is reported according to the SQUIRE 2.0 guidelines.
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spelling pubmed-81437352021-05-26 A Quality Improvement Initiative to Reduce Blood Culture Contamination in the Neonatal Unit Allen, Elizabeth Cavallaro, Angela Keir, Amy K. Pediatr Qual Saf Individual QI projects from single institutions Peripheral blood culture contamination (BCC) can lead to an initiation of unnecessary antimicrobial treatment, further laboratory tests, increased length of stay, and increased costs. This study describes a 12-month quality improvement (QI) program to reduce the BCC rate in a neonatal unit by 50%. METHODS: The QI team focused on standardizing processes to align with best practices using process mapping and cause and effect diagrams. Plan-Do-Study-Act (PDSA) 1: inoculation of blood culture bottles with the introduction of transfer device; PDSA 2: preparation of the skin for peripheral intravenous cannula insertion; PDSA 3: aseptic technique education package; and PDSA 4: optimizing blood volume of blood collected for culture. The team used statistical process control methodology to detect special cause variation. RESULTS: Compliance with the standard processes as part of PSDA 1 improved from a mean level of 50% to 100% and for PDSA 2 improved from a mean level of 50% to 95%. After implementation of PDSA 3, scores on a relevant knowledge test increased from a mean of 39% (pretraining test; n = 10) to 92% (posttraining test; n = 10) (P < 0.001). Postimplementation of the processes for PDSA 4, a minimum of 1 mL was collected in 94% of blood culture collection events (n = 450) (mean 1.1 mL; range 0.5–3.5 mL). Special cause variation occurred after the implementation of the PDSA cycles. During the baseline period, the BCC rate was 2.0% and decreased to 1.0% postinterventions implementation. CONCLUSIONS: Interventions focused on standardizing practices around collection of blood cultures in neonates were associated with fewer contaminants. This study is reported according to the SQUIRE 2.0 guidelines. Lippincott Williams & Wilkins 2021-05-19 /pmc/articles/PMC8143735/ /pubmed/34046542 http://dx.doi.org/10.1097/pq9.0000000000000413 Text en Copyright © 2021 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
Allen, Elizabeth
Cavallaro, Angela
Keir, Amy K.
A Quality Improvement Initiative to Reduce Blood Culture Contamination in the Neonatal Unit
title A Quality Improvement Initiative to Reduce Blood Culture Contamination in the Neonatal Unit
title_full A Quality Improvement Initiative to Reduce Blood Culture Contamination in the Neonatal Unit
title_fullStr A Quality Improvement Initiative to Reduce Blood Culture Contamination in the Neonatal Unit
title_full_unstemmed A Quality Improvement Initiative to Reduce Blood Culture Contamination in the Neonatal Unit
title_short A Quality Improvement Initiative to Reduce Blood Culture Contamination in the Neonatal Unit
title_sort quality improvement initiative to reduce blood culture contamination in the neonatal unit
topic Individual QI projects from single institutions
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8143735/
https://www.ncbi.nlm.nih.gov/pubmed/34046542
http://dx.doi.org/10.1097/pq9.0000000000000413
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