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Clinical Decision Support to Improve Dosing Weight Use in Infants with Neonatal Abstinence Syndrome

INTRODUCTION: Opioid abuse in the United States is a public health emergency. From 2000 to 2009, prenatal maternal opiate use increased from 1.19 to 5.63 per 1,000 births, with up to 80% of in utero opioid-exposed infants requiring pharmacotherapy. This study aimed to increase the percentage of neon...

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Autores principales: Bertoni, C. Briana, Prusakov, Pavel, Merandi, Jenna, Bartman, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6708646/
https://www.ncbi.nlm.nih.gov/pubmed/31572886
http://dx.doi.org/10.1097/pq9.0000000000000184
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author Bertoni, C. Briana
Prusakov, Pavel
Merandi, Jenna
Bartman, Thomas
author_facet Bertoni, C. Briana
Prusakov, Pavel
Merandi, Jenna
Bartman, Thomas
author_sort Bertoni, C. Briana
collection PubMed
description INTRODUCTION: Opioid abuse in the United States is a public health emergency. From 2000 to 2009, prenatal maternal opiate use increased from 1.19 to 5.63 per 1,000 births, with up to 80% of in utero opioid-exposed infants requiring pharmacotherapy. This study aimed to increase the percentage of neonatal abstinence syndrome (NAS) medication orders based on birth weight (BW) in neonates admitted to a neonatal intensive care unit with a principal diagnosis of NAS from 29% to 90%, within 4 months of project initiation, and to sustain this for 6 months. METHODS: This project occurred at an academic medical center with 5,000 deliveries per year and a 49-bed Level III neonatal intensive care unit. We used the Institute for Healthcare Improvement methodology, largely focusing interventions on clinical decision support (CDS) tools. We plotted all measures on Shewhart charts, and Nelson rules differentiated special versus common cause variation. RESULTS: The percent of orders based on BW increased from 29% to 78% after implementing multiple interventions focused primarily on CDS. However, this later decreased to 48% as workarounds began. There was also a significant decrease in the length of stay variability, which persisted throughout the project. DISCUSSION: CDS is a helpful tool to guide prescribing behavior; however, workarounds can negate its usefulness. Standardized use of BW for weight-based NAS medication prescribing can decrease the length of stay variability. Further studies are needed using a human factors approach to minimize workarounds in CDS and potentially decrease the length of stay in neonates with NAS.
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spelling pubmed-67086462019-09-30 Clinical Decision Support to Improve Dosing Weight Use in Infants with Neonatal Abstinence Syndrome Bertoni, C. Briana Prusakov, Pavel Merandi, Jenna Bartman, Thomas Pediatr Qual Saf Individual QI Projects from Single Institutions INTRODUCTION: Opioid abuse in the United States is a public health emergency. From 2000 to 2009, prenatal maternal opiate use increased from 1.19 to 5.63 per 1,000 births, with up to 80% of in utero opioid-exposed infants requiring pharmacotherapy. This study aimed to increase the percentage of neonatal abstinence syndrome (NAS) medication orders based on birth weight (BW) in neonates admitted to a neonatal intensive care unit with a principal diagnosis of NAS from 29% to 90%, within 4 months of project initiation, and to sustain this for 6 months. METHODS: This project occurred at an academic medical center with 5,000 deliveries per year and a 49-bed Level III neonatal intensive care unit. We used the Institute for Healthcare Improvement methodology, largely focusing interventions on clinical decision support (CDS) tools. We plotted all measures on Shewhart charts, and Nelson rules differentiated special versus common cause variation. RESULTS: The percent of orders based on BW increased from 29% to 78% after implementing multiple interventions focused primarily on CDS. However, this later decreased to 48% as workarounds began. There was also a significant decrease in the length of stay variability, which persisted throughout the project. DISCUSSION: CDS is a helpful tool to guide prescribing behavior; however, workarounds can negate its usefulness. Standardized use of BW for weight-based NAS medication prescribing can decrease the length of stay variability. Further studies are needed using a human factors approach to minimize workarounds in CDS and potentially decrease the length of stay in neonates with NAS. Wolters Kluwer Health 2019-06-28 /pmc/articles/PMC6708646/ /pubmed/31572886 http://dx.doi.org/10.1097/pq9.0000000000000184 Text en Copyright © 2019 the Author(s). Published by Wolters Kluwer Health, Inc. 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) (http://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
Bertoni, C. Briana
Prusakov, Pavel
Merandi, Jenna
Bartman, Thomas
Clinical Decision Support to Improve Dosing Weight Use in Infants with Neonatal Abstinence Syndrome
title Clinical Decision Support to Improve Dosing Weight Use in Infants with Neonatal Abstinence Syndrome
title_full Clinical Decision Support to Improve Dosing Weight Use in Infants with Neonatal Abstinence Syndrome
title_fullStr Clinical Decision Support to Improve Dosing Weight Use in Infants with Neonatal Abstinence Syndrome
title_full_unstemmed Clinical Decision Support to Improve Dosing Weight Use in Infants with Neonatal Abstinence Syndrome
title_short Clinical Decision Support to Improve Dosing Weight Use in Infants with Neonatal Abstinence Syndrome
title_sort clinical decision support to improve dosing weight use in infants with neonatal abstinence syndrome
topic Individual QI Projects from Single Institutions
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6708646/
https://www.ncbi.nlm.nih.gov/pubmed/31572886
http://dx.doi.org/10.1097/pq9.0000000000000184
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