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A Comparison of Morphine Delivery in Neonatal Opioid Withdrawal

Current estimates of the prevalence of opioid withdrawal in newborns from the 2012 Better Outcomes Registry and Network Ontario reveal that more than 4 births per 1000 display recognizable symptoms of neonatal abstinence syndrome (NAS). With a growing consensus surrounding aspects of newborn opioid...

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Autores principales: Chisamore, Brian, Labana, Safaa, Blitz, Sandra, Ordean, Alice
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Libertas Academica 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5038613/
https://www.ncbi.nlm.nih.gov/pubmed/27695339
http://dx.doi.org/10.4137/SART.S34550
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author Chisamore, Brian
Labana, Safaa
Blitz, Sandra
Ordean, Alice
author_facet Chisamore, Brian
Labana, Safaa
Blitz, Sandra
Ordean, Alice
author_sort Chisamore, Brian
collection PubMed
description Current estimates of the prevalence of opioid withdrawal in newborns from the 2012 Better Outcomes Registry and Network Ontario reveal that more than 4 births per 1000 display recognizable symptoms of neonatal abstinence syndrome (NAS). With a growing consensus surrounding aspects of newborn opioid withdrawal care, clinicians might agree that all infants exposed to maternal opioids require supportive observation and care to ensure appropriate adaptation and growth in the newborn period and, likewise, that there exists a smaller percentage of newborns who require additional pharmacotherapy. However, due to the dearth of comparative studies of NAS tools, there remains a lack of evidence to support the use of a specific NAS method of scoring or treatment. Two types of NAS treatment protocols currently in use include a symptom-only versus weight-based protocols. Our Neonatal Intensive Care Unit (NICU) has used both models. A formal structured NAS tool and weight-based morphine delivery system began in our NICU in 1999. We audited all newborns with known exposure to maternal opioids in our NICU from the years 2000 to 2014. The Finnegan scoring tool was used throughout all years of the chart audit. Modifications made to the Finnegan scoring tool from the MOTHER study were adapted for use in our NICU at the same time as adopting the Johns Hopkins model of symptom-only based morphine delivery in 2006. The objective of this comparative study using a retrospective chart audit is to compare length of stay (LOS) and total accumulative morphine dose across these two morphine delivery protocols. Our audit revealed that there were a significantly higher proportion of newborns in the symptom-only model that received morphine and, perhaps accordingly, also had a significantly higher LOS compared to those in the weight-based model. Comparing only those infants who did receive morphine, the comparative total accumulative dose of morphine and LOS were not significantly different between the weight-based and symptom-only morphine delivery models.
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spelling pubmed-50386132016-09-30 A Comparison of Morphine Delivery in Neonatal Opioid Withdrawal Chisamore, Brian Labana, Safaa Blitz, Sandra Ordean, Alice Subst Abuse Original Research Current estimates of the prevalence of opioid withdrawal in newborns from the 2012 Better Outcomes Registry and Network Ontario reveal that more than 4 births per 1000 display recognizable symptoms of neonatal abstinence syndrome (NAS). With a growing consensus surrounding aspects of newborn opioid withdrawal care, clinicians might agree that all infants exposed to maternal opioids require supportive observation and care to ensure appropriate adaptation and growth in the newborn period and, likewise, that there exists a smaller percentage of newborns who require additional pharmacotherapy. However, due to the dearth of comparative studies of NAS tools, there remains a lack of evidence to support the use of a specific NAS method of scoring or treatment. Two types of NAS treatment protocols currently in use include a symptom-only versus weight-based protocols. Our Neonatal Intensive Care Unit (NICU) has used both models. A formal structured NAS tool and weight-based morphine delivery system began in our NICU in 1999. We audited all newborns with known exposure to maternal opioids in our NICU from the years 2000 to 2014. The Finnegan scoring tool was used throughout all years of the chart audit. Modifications made to the Finnegan scoring tool from the MOTHER study were adapted for use in our NICU at the same time as adopting the Johns Hopkins model of symptom-only based morphine delivery in 2006. The objective of this comparative study using a retrospective chart audit is to compare length of stay (LOS) and total accumulative morphine dose across these two morphine delivery protocols. Our audit revealed that there were a significantly higher proportion of newborns in the symptom-only model that received morphine and, perhaps accordingly, also had a significantly higher LOS compared to those in the weight-based model. Comparing only those infants who did receive morphine, the comparative total accumulative dose of morphine and LOS were not significantly different between the weight-based and symptom-only morphine delivery models. Libertas Academica 2016-09-26 /pmc/articles/PMC5038613/ /pubmed/27695339 http://dx.doi.org/10.4137/SART.S34550 Text en © 2016 the author(s), publisher and licensee Libertas Academica Ltd. This is an open-access article distributed under the terms of the Creative Commons CC-BY-NC 3.0 License.
spellingShingle Original Research
Chisamore, Brian
Labana, Safaa
Blitz, Sandra
Ordean, Alice
A Comparison of Morphine Delivery in Neonatal Opioid Withdrawal
title A Comparison of Morphine Delivery in Neonatal Opioid Withdrawal
title_full A Comparison of Morphine Delivery in Neonatal Opioid Withdrawal
title_fullStr A Comparison of Morphine Delivery in Neonatal Opioid Withdrawal
title_full_unstemmed A Comparison of Morphine Delivery in Neonatal Opioid Withdrawal
title_short A Comparison of Morphine Delivery in Neonatal Opioid Withdrawal
title_sort comparison of morphine delivery in neonatal opioid withdrawal
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5038613/
https://www.ncbi.nlm.nih.gov/pubmed/27695339
http://dx.doi.org/10.4137/SART.S34550
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