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Neurophysiological and behavioral measures of pain during neonatal hip examination

INTRODUCTION: The aim of this study was to test the hypothesis that neonatal hip examination causes pain in newborns. Pain assessment using instruments such as the Premature Infant Pain Profile‐Revised (PIPP‐R) scale is recommended, but recently physiological and neurophysiological measures, for exa...

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Autores principales: Pettersson, Miriam, Olsson, Emma, Ohlin, Andreas, Eriksson, Mats
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8974883/
https://www.ncbi.nlm.nih.gov/pubmed/35546870
http://dx.doi.org/10.1002/pne2.12006
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author Pettersson, Miriam
Olsson, Emma
Ohlin, Andreas
Eriksson, Mats
author_facet Pettersson, Miriam
Olsson, Emma
Ohlin, Andreas
Eriksson, Mats
author_sort Pettersson, Miriam
collection PubMed
description INTRODUCTION: The aim of this study was to test the hypothesis that neonatal hip examination causes pain in newborns. Pain assessment using instruments such as the Premature Infant Pain Profile‐Revised (PIPP‐R) scale is recommended, but recently physiological and neurophysiological measures, for example, near‐infrared spectroscopy (NIRS) and galvanic skin response (GSR), have been used as well. METHODS: Heart auscultation and hip examination were performed, and the response of the newborn was registered by NIRS optodes, GSR electrodes, and a pulse oximeter probe attached to the infant. The face of the newborn was filmed. Heart auscultation was used as a nonpainful reference. RESULTS: The pain scores for hip examination were higher than for the heart auscultation. Near‐infrared spectroscopy showed a significant higher increase from baseline in oxygenated hemoglobin (HbO(2)) on both sides of the cortex at hip examination compared with at heart auscultation (P = .011 and P = .017). Mean PIPP‐R scores for the hip examination compared with heart auscultation increased from 3.0 to 8.1 (P = .000). The GSR analyses of hip examination compared with heart auscultation showed a significant increase in area under small peaks during the hip examination (P = .016), however, not when measured in peaks per second (P = .104). Interrater reliability was calculated for the NIRS interpretations, with an intraclass correlation coefficient (ICC) range of 0.93‐1.0 (P = .000). DISCUSSION: Pain in newborns can have negative consequences, and pain prevention and treatment are therefore important. We conclude that neonatal hip examinations are painful and that the pain should be treated, for example, with oral sweet solution. This is a change from present routines during neonatal hip examination and is hoped to lead to a change in national guidelines.
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spelling pubmed-89748832022-05-10 Neurophysiological and behavioral measures of pain during neonatal hip examination Pettersson, Miriam Olsson, Emma Ohlin, Andreas Eriksson, Mats Paediatr Neonatal Pain Original Articles INTRODUCTION: The aim of this study was to test the hypothesis that neonatal hip examination causes pain in newborns. Pain assessment using instruments such as the Premature Infant Pain Profile‐Revised (PIPP‐R) scale is recommended, but recently physiological and neurophysiological measures, for example, near‐infrared spectroscopy (NIRS) and galvanic skin response (GSR), have been used as well. METHODS: Heart auscultation and hip examination were performed, and the response of the newborn was registered by NIRS optodes, GSR electrodes, and a pulse oximeter probe attached to the infant. The face of the newborn was filmed. Heart auscultation was used as a nonpainful reference. RESULTS: The pain scores for hip examination were higher than for the heart auscultation. Near‐infrared spectroscopy showed a significant higher increase from baseline in oxygenated hemoglobin (HbO(2)) on both sides of the cortex at hip examination compared with at heart auscultation (P = .011 and P = .017). Mean PIPP‐R scores for the hip examination compared with heart auscultation increased from 3.0 to 8.1 (P = .000). The GSR analyses of hip examination compared with heart auscultation showed a significant increase in area under small peaks during the hip examination (P = .016), however, not when measured in peaks per second (P = .104). Interrater reliability was calculated for the NIRS interpretations, with an intraclass correlation coefficient (ICC) range of 0.93‐1.0 (P = .000). DISCUSSION: Pain in newborns can have negative consequences, and pain prevention and treatment are therefore important. We conclude that neonatal hip examinations are painful and that the pain should be treated, for example, with oral sweet solution. This is a change from present routines during neonatal hip examination and is hoped to lead to a change in national guidelines. John Wiley and Sons Inc. 2019-09-13 /pmc/articles/PMC8974883/ /pubmed/35546870 http://dx.doi.org/10.1002/pne2.12006 Text en © 2019 The Authors. Paediatric and Neonatal Pain published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Pettersson, Miriam
Olsson, Emma
Ohlin, Andreas
Eriksson, Mats
Neurophysiological and behavioral measures of pain during neonatal hip examination
title Neurophysiological and behavioral measures of pain during neonatal hip examination
title_full Neurophysiological and behavioral measures of pain during neonatal hip examination
title_fullStr Neurophysiological and behavioral measures of pain during neonatal hip examination
title_full_unstemmed Neurophysiological and behavioral measures of pain during neonatal hip examination
title_short Neurophysiological and behavioral measures of pain during neonatal hip examination
title_sort neurophysiological and behavioral measures of pain during neonatal hip examination
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8974883/
https://www.ncbi.nlm.nih.gov/pubmed/35546870
http://dx.doi.org/10.1002/pne2.12006
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